Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23186 |
|---|---|
| ensemblid | ENSG00000089902.10 |
| hgncid | 17441 |
| symbol | RCOR1 |
| name | REST corepressor 1 |
| refseq_nuc | NM_015156.4 |
| refseq_prot | NP_055971.2 |
| ensembl_nuc | ENST00000262241.7 |
| ensembl_prot | ENSP00000262241.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 102592649 |
| end | 102730561 |
| strand | + |
| ver | v1.2 |
| region | chr14:102592649-102730561 |
| region5000 | chr14:102587649-102735561 |
| regionname0 | RCOR1_chr14_102592649_102730561 |
| regionname5000 | RCOR1_chr14_102587649_102735561 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 485 | 290 | 88 | 67 | 93 | 14 | 26 | 75 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0002 | 0/0 | 485 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0003 | 0/0 | 485 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1458 | 284 | 85 | 64 | 93 | 14 | 26 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| c0002 | 0/0 | 1458 | 3 | 1 | 2 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| c0003 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| c0004 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| c0005 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| c0006 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| c0007 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4294 | 60 | 3 | 15 | 33 | 3 | 5 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0002 | 0/0 | 4294 | 55 | 14 | 9 | 28 | 0 | 4 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0003 | 0/0 | 4294 | 40 | 17 | 11 | 3 | 3 | 6 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0004 | 0/0 | 4294 | 23 | 0 | 9 | 11 | 0 | 3 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0005 | 0/0 | 4294 | 16 | 12 | 4 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0006 | 0/0 | 4295 | 14 | 1 | 8 | 0 | 5 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0007 | 0/0 | 4294 | 8 | 1 | 3 | 4 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0008 | 0/0 | 4295 | 7 | 6 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0009 | 1/0 | 4294 | 7 | 6 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0010 | 0/0 | 4294 | 5 | 0 | 0 | 5 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0011 | 0/0 | 4295 | 4 | 2 | 2 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0012 | 0/0 | 4295 | 4 | 4 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0013 | 0/0 | 4294 | 3 | 1 | 1 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0014 | 0/0 | 4294 | 3 | 3 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0015 | 0/0 | 4294 | 2 | 0 | 0 | 0 | 1 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0016 | 0/0 | 4294 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0017 | 0/0 | 4295 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0018 | 0/0 | 4295 | 2 | 1 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0019 | 0/0 | 4295 | 2 | 1 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0020 | 0/0 | 4295 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0021 | 0/0 | 4295 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0022 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0023 | 0/0 | 4294 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0024 | 0/0 | 4294 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0025 | 0/0 | 4294 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0026 | 0/0 | 4294 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0027 | 0/0 | 4294 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0028 | 0/0 | 4294 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0029 | 0/0 | 4294 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0030 | 0/0 | 4295 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0031 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0032 | 0/0 | 4294 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0033 | 0/0 | 4294 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0034 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0035 | 0/0 | 4294 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0036 | 0/0 | 4294 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0037 | 0/0 | 4294 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0038 | 0/0 | 4295 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0039 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0040 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0041 | 0/0 | 4294 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0042 | 0/0 | 4294 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0043 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0044 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0045 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0046 | 0/0 | 4295 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0047 | 0/0 | 4295 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0048 | 0/0 | 4295 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0049 | 0/0 | 4294 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0050 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| t0051 | 0/0 | 4294 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1458 | 284 | 85 | 64 | 93 | 14 | 26 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0002 | 0/0 | 1458 | 3 | 1 | 2 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0003 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0004 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0005 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0002c0007 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0003c0006 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5751 | 58 | 3 | 14 | 32 | 3 | 5 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0002 | 0/0 | 5751 | 55 | 14 | 9 | 28 | 0 | 4 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0003 | 0/0 | 5751 | 38 | 16 | 10 | 3 | 3 | 6 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0004 | 0/0 | 5751 | 23 | 0 | 9 | 11 | 0 | 3 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0005 | 0/0 | 5751 | 15 | 11 | 4 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0006 | 0/0 | 5752 | 14 | 1 | 8 | 0 | 5 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0007 | 0/0 | 5751 | 8 | 1 | 3 | 4 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0008 | 0/0 | 5752 | 7 | 6 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0009 | 1/0 | 5751 | 7 | 6 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0010 | 0/0 | 5751 | 5 | 0 | 0 | 5 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0011 | 0/0 | 5752 | 3 | 2 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0012 | 0/0 | 5752 | 3 | 3 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0013 | 0/0 | 5751 | 3 | 1 | 1 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0014 | 0/0 | 5751 | 3 | 3 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0015 | 0/0 | 5751 | 2 | 0 | 0 | 0 | 1 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0016 | 0/0 | 5751 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0017 | 0/0 | 5752 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0018 | 0/0 | 5752 | 2 | 1 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0019 | 0/0 | 5752 | 2 | 1 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0020 | 0/0 | 5752 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0021 | 0/0 | 5752 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0022 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0023 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0024 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0025 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0026 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0027 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0028 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0029 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0030 | 0/0 | 5752 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0031 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0032 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0033 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0034 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0035 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0036 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0038 | 0/0 | 5752 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0039 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0040 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0041 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0042 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0043 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0044 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0045 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0046 | 0/0 | 5752 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0047 | 0/0 | 5752 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0048 | 0/0 | 5752 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0049 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0050 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0001t0051 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0002t0003 | 0/0 | 5751 | 2 | 1 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0002t0011 | 0/0 | 5752 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0003t0005 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0004t0012 | 0/0 | 5752 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0001c0005t0037 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0002c0007t0001 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| a0003c0006t0001 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | copy fasta | chr14 | 102587649 | 102735561 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0006g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0009g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0009g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0010g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0011g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0013g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0013g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0013g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0014g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0014g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0014g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0015g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0015g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0016g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0016g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0017g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0017g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0018g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0019g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0019g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0020g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0020g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0021g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0022g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0023g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0024g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0025g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0026g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0027g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0028g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0029g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0030g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0031g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0032g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0033g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0034g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0035g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0036g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0038g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0039g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0040g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0041g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0042g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0043g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0044g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0045g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0046g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0047g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0048g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0049g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0050g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0001t0051g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0002t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0003t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0004t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0001c0005t0037g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0002c0007t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| a0003c0006t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0256 | EUR | GBR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0101 | EUR | GBR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0038 | EUR | FIN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0267 | EUR | FIN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00323 | hp1 | a0001 | c0001 | t0028 | g0080 | EUR | FIN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0264 | EUR | FIN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CHS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0132 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00733 | hp1 | a0001 | c0001 | t0013 | g0291 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00735 | hp1 | a0001 | c0001 | t0024 | g0062 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0265 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01099 | hp2 | a0001 | c0001 | t0049 | g0159 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01167 | hp2 | a0001 | c0005 | t0037 | g0149 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0271 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0273 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0047 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0280 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0138 | AMR | PUR | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01255 | hp1 | a0001 | c0001 | t0019 | g0258 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0270 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01261 | hp1 | a0001 | c0002 | t0011 | g0054 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0272 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0051 | EUR | IBS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0257 | EUR | IBS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01884 | hp1 | a0001 | c0001 | t0045 | g0203 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0121 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0145 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0234 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0261 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0055 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0275 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01993 | hp1 | a0001 | c0001 | t0025 | g0088 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0220 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0058 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02080 | hp1 | a0001 | c0001 | t0010 | g0067 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02080 | hp2 | a0001 | c0001 | t0042 | g0228 | EAS | KHV | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0274 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CDX | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0277 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0235 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02300 | hp2 | a0003 | c0006 | t0001 | g0068 | AMR | PEL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0144 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02451 | hp2 | a0001 | c0001 | t0046 | g0150 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0193 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0263 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0290 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02738 | hp1 | a0001 | c0001 | t0029 | g0115 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02809 | hp1 | a0001 | c0001 | t0034 | g0039 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02818 | hp2 | a0001 | c0003 | t0005 | g0117 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0276 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0268 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0269 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0292 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0147 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0194 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03130 | hp2 | a0001 | c0001 | t0018 | g0195 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03139 | hp1 | a0001 | c0001 | t0044 | g0202 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03139 | hp2 | a0001 | c0004 | t0012 | g0151 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0156 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03209 | hp2 | a0001 | c0001 | t0040 | g0213 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0157 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0199 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03486 | hp2 | a0001 | c0001 | t0050 | g0142 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0184 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03492 | hp1 | a0001 | c0001 | t0023 | g0078 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03540 | hp2 | a0001 | c0001 | t0020 | g0289 | AFR | GWD | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03579 | hp1 | a0001 | c0001 | t0021 | g0279 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03669 | hp2 | a0001 | c0001 | t0051 | g0247 | SAS | PJL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03927 | hp1 | a0001 | c0001 | t0047 | g0226 | SAS | BEB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0046 | SAS | BEB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | BEB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | BEB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04115 | hp1 | a0001 | c0001 | t0036 | g0174 | SAS | STU | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | BEB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04184 | hp2 | a0001 | c0001 | t0035 | g0251 | SAS | BEB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04199 | hp1 | a0001 | c0001 | t0013 | g0123 | SAS | STU | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0185 | SAS | STU | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04204 | hp1 | a0001 | c0001 | t0015 | g0124 | SAS | STU | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | STU | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0153 | AFR | YRI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0143 | AFR | YRI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | YRI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | YRI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18939 | hp2 | a0001 | c0001 | t0010 | g0104 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18945 | hp2 | a0001 | c0001 | t0032 | g0057 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18954 | hp1 | a0001 | c0001 | t0007 | g0219 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18962 | hp2 | a0001 | c0001 | t0041 | g0214 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18967 | hp2 | a0001 | c0001 | t0016 | g0282 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18971 | hp1 | a0001 | c0001 | t0026 | g0069 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18979 | hp1 | a0001 | c0001 | t0018 | g0239 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0113 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18980 | hp2 | a0001 | c0001 | t0048 | g0179 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19000 | hp2 | a0001 | c0001 | t0030 | g0125 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19010 | hp2 | a0001 | c0001 | t0016 | g0281 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | LWK | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | LWK | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | LWK | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | LWK | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19066 | hp1 | a0002 | c0007 | t0001 | g0141 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19066 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0034 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0064 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0152 | AFR | ASW | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20129 | hp2 | a0001 | c0001 | t0039 | g0158 | AFR | ASW | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20752 | hp2 | a0001 | c0001 | t0033 | g0255 | EUR | TSI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0266 | EUR | TSI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0035 | EUR | TSI | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0260 | AMR | CLM | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0278 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0136 | AFR | ACB | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03471 | hp1 | a0001 | c0001 | t0038 | g0155 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG03471 | hp2 | a0001 | c0001 | t0031 | g0001 | AFR | MSL | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG06807 | hp1 | a0001 | c0001 | t0043 | g0146 | AFR | USA | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | USA | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18955 | hp1 | a0001 | c0001 | t0027 | g0099 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0262 | AFR | USA | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0253 | AFR | USA | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0259 | AFR | LWK | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0103 | REF | REF | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0250 | REF | REF | RCOR1_chr14_102587649_102735561 | RCOR1 | chr14 | 102587649 | 102735561 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102593118
|
C | G | 1 | a0002 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.232C>G | p.Pro78Ala | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 1/12 | 470/5751 | 232/1458 | 78/485 | chr14 | 102593118 | ||
| chr14:102722346
|
A | G | 1 | a0003 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.1349A>G | p.Asn450Ser | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/12 | 1587/5751 | 1349/1458 | 450/485 | chr14 | 102722346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102593012
|
C | A | 1 | a0001c0003 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.126C>A | p.Ala42Ala | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 1/12 | 364/5751 | 126/1458 | 42/485 | chr14 | 102593012 | ||
| chr14:102707396
|
T | C | 1 | a0001c0004 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.544T>C | p.Leu182Leu | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/12 | 782/5751 | 544/1458 | 182/485 | chr14 | 102707396 | ||
| chr14:102707419
|
C | A | 1 | a0001c0005 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.567C>A | p.Thr189Thr | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/12 | 805/5751 | 567/1458 | 189/485 | chr14 | 102707419 | ||
| chr14:102722401
|
C | T | 1 | a0001c0002 | 3 | HG01261.hp1 HG01975.hp1 HG02486.hp2 |
synonymous_variant | LOW | c.1404C>T | p.Pro468Pro | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/12 | 1642/5751 | 1404/1458 | 468/485 | chr14 | 102722401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102592833
|
C | T | 1 | a0001c0001t0051 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 1/12 | 54 | chr14 | 102592833 | |||||
| chr14:102592862
|
T | A | 3 | a0001c0001t0008a0001c0001t0021a0001c0001t0022 | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-25T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 1/12 | 25 | chr14 | 102592862 | |||||
| chr14:102592883
|
G | A | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(19): Show | 131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
5_prime_UTR_variant | MODIFIER | c.-4G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 1/12 | 4 | chr14 | 102592883 | |||||
| chr14:102726534
|
T | G | 1 | a0001c0001t0035 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 28 | chr14 | 102726534 | |||||
| chr14:102726554
|
G | A | 1 | a0001c0001t0023 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*48G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 48 | chr14 | 102726554 | |||||
| chr14:102726691
|
G | A | 13 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(10): Show | 75 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*185G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 185 | chr14 | 102726691 | |||||
| chr14:102726721
|
A | C | 1 | a0001c0001t0050 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 215 | chr14 | 102726721 | |||||
| chr14:102726734
|
G | A | 1 | a0001c0001t0021 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 228 | chr14 | 102726734 | |||||
| chr14:102726794
|
C | A | 1 | a0001c0001t0050 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 288 | chr14 | 102726794 | |||||
| chr14:102726962
|
T | C | 3 | a0001c0001t0031a0001c0001t0050a0001c0005t0037 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*456T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 456 | chr14 | 102726962 | |||||
| chr14:102726999
|
C | T | 7 | a0001c0001t0006a0001c0001t0008a0001c0001t0019others(4): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*493C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 493 | chr14 | 102726999 | |||||
| chr14:102727021
|
T | C | 1 | a0001c0001t0024 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 515 | chr14 | 102727021 | |||||
| chr14:102727181
|
T | C | 1 | a0001c0001t0038 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*675T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 675 | chr14 | 102727181 | |||||
| chr14:102727198
|
A | G | 1 | a0001c0001t0034 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 692 | chr14 | 102727198 | |||||
| chr14:102727281
|
A | AC | 16 | a0001c0001t0006a0001c0001t0008a0001c0001t0011others(13): Show | 43 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*783dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 784 | INFO_REALIGN_3_PRIME | chr14 | 102727281 | ||||
| chr14:102727309
|
G | T | 2 | a0001c0001t0005a0001c0003t0005 | 16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*803G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 803 | chr14 | 102727309 | |||||
| chr14:102727481
|
G | A | 1 | a0001c0001t0017 | 2 | HG03209.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*975G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 975 | chr14 | 102727481 | |||||
| chr14:102727680
|
A | G | 1 | a0001c0001t0050 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1174 | chr14 | 102727680 | |||||
| chr14:102727784
|
T | G | 1 | a0001c0001t0046 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1278 | chr14 | 102727784 | |||||
| chr14:102727819
|
T | C | 1 | a0001c0005t0037 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1313T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1313 | chr14 | 102727819 | |||||
| chr14:102727828
|
A | G | 1 | a0001c0001t0014 | 3 | HG02615.hp1 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1322A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1322 | chr14 | 102727828 | |||||
| chr14:102727829
|
T | C | 3 | a0001c0001t0031a0001c0001t0039a0001c0005t0037 | 3 | HG01167.hp2 HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1323T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1323 | chr14 | 102727829 | |||||
| chr14:102727896
|
C | T | 1 | a0001c0001t0045 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1390 | chr14 | 102727896 | |||||
| chr14:102728067
|
T | A | 1 | a0001c0005t0037 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1561 | chr14 | 102728067 | |||||
| chr14:102728086
|
T | C | 1 | a0001c0001t0047 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1580T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1580 | chr14 | 102728086 | |||||
| chr14:102728089
|
G | T | 1 | a0001c0001t0029 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1583G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1583 | chr14 | 102728089 | |||||
| chr14:102728104
|
G | C | 1 | a0001c0001t0040 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1598 | chr14 | 102728104 | |||||
| chr14:102728203
|
T | C | 1 | a0001c0001t0016 | 2 | NA18967.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1697T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1697 | chr14 | 102728203 | |||||
| chr14:102728215
|
A | G | 3 | a0001c0001t0031a0001c0001t0050a0001c0005t0037 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1709A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1709 | chr14 | 102728215 | |||||
| chr14:102728223
|
A | G | 1 | a0001c0001t0006 | 14 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1717A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1717 | chr14 | 102728223 | |||||
| chr14:102728249
|
C | T | 1 | a0001c0001t0044 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1743 | chr14 | 102728249 | |||||
| chr14:102728316
|
T | C | 1 | a0001c0001t0041 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1810T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1810 | chr14 | 102728316 | |||||
| chr14:102728341
|
C | T | 1 | a0001c0005t0037 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1835C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1835 | chr14 | 102728341 | |||||
| chr14:102728411
|
G | A | 1 | a0001c0001t0025 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1905G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 1905 | chr14 | 102728411 | |||||
| chr14:102728509
|
A | T | 1 | a0001c0001t0031 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2003 | chr14 | 102728509 | |||||
| chr14:102728661
|
A | G | 19 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(16): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2155A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2155 | chr14 | 102728661 | |||||
| chr14:102728752
|
C | T | 1 | a0001c0001t0028 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2246C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2246 | chr14 | 102728752 | |||||
| chr14:102729015
|
G | A | 1 | a0001c0001t0026 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2509G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2509 | chr14 | 102729015 | |||||
| chr14:102729028
|
G | C | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(13): Show | 103 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2522G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2522 | chr14 | 102729028 | |||||
| chr14:102729157
|
T | C | 1 | a0001c0005t0037 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2651T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2651 | chr14 | 102729157 | |||||
| chr14:102729407
|
C | T | 4 | a0001c0001t0012a0001c0001t0038a0001c0001t0046others(1): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2901C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2901 | chr14 | 102729407 | |||||
| chr14:102729452
|
A | G | 1 | a0001c0001t0031 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2946A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2946 | chr14 | 102729452 | |||||
| chr14:102729458
|
G | A | 1 | a0001c0001t0039 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2952G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2952 | chr14 | 102729458 | |||||
| chr14:102729460
|
G | A | 1 | a0001c0001t0027 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2954G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 2954 | chr14 | 102729460 | |||||
| chr14:102729508
|
T | C | 1 | a0001c0001t0010 | 5 | HG02027.hp1 HG02080.hp1 NA18939.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3002T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3002 | chr14 | 102729508 | |||||
| chr14:102729513
|
G | T | 3 | a0001c0001t0004a0001c0001t0032a0001c0001t0048 | 25 | HG00609.hp1 HG00735.hp2 HG01261.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3007G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3007 | chr14 | 102729513 | |||||
| chr14:102729526
|
C | T | 1 | a0001c0001t0039 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3020C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3020 | chr14 | 102729526 | |||||
| chr14:102729626
|
A | G | 3 | a0001c0001t0031a0001c0001t0050a0001c0005t0037 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3120A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3120 | chr14 | 102729626 | |||||
| chr14:102729629
|
A | G | 3 | a0001c0001t0031a0001c0001t0050a0001c0005t0037 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3123A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3123 | chr14 | 102729629 | |||||
| chr14:102729710
|
A | G | 1 | a0001c0001t0043 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3204A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3204 | chr14 | 102729710 | |||||
| chr14:102729718
|
C | T | 3 | a0001c0001t0015a0001c0001t0028a0001c0001t0033 | 4 | HG00099.hp2 HG00323.hp1 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3212C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3212 | chr14 | 102729718 | |||||
| chr14:102729789
|
A | G | 1 | a0001c0001t0031 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3283A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3283 | chr14 | 102729789 | |||||
| chr14:102729889
|
C | T | 1 | a0001c0001t0029 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3383C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3383 | chr14 | 102729889 | |||||
| chr14:102730097
|
A | G | 1 | a0001c0001t0042 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3591A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 3591 | chr14 | 102730097 | |||||
| chr14:102730536
|
A | G | 1 | a0001c0001t0020 | 2 | HG02630.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4030A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 12/12 | 4030 | chr14 | 102730536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102593569
|
C | T | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.361+244C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102593569 | ||||||
| chr14:102593576
|
G | A | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+251G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102593576 | ||||||
| chr14:102593621
|
C | T | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.361+296C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102593621 | ||||||
| chr14:102593633
|
G | C | 1 | a0001c0001t0009g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.361+308G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102593633 | ||||||
| chr14:102593743
|
C | G | 8 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(5): Show | 8 | HG02040.hp2 NA18967.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+418C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102593743 | ||||||
| chr14:102593782
|
C | T | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.361+457C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102593782 | ||||||
| chr14:102594081
|
C | T | 26 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.361+756C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594081 | ||||||
| chr14:102594128
|
G | A | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+803G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594128 | ||||||
| chr14:102594166
|
A | G | 8 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(5): Show | 8 | HG02040.hp2 NA18967.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+841A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594166 | ||||||
| chr14:102594231
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.361+906C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594231 | ||||||
| chr14:102594267
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.361+942A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594267 | ||||||
| chr14:102594269
|
C | T | 40 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.361+944C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594269 | ||||||
| chr14:102594300
|
G | A | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+975G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594300 | ||||||
| chr14:102594360
|
GAT | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.361+1037_361+1038d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102594360 | |||||
| chr14:102594426
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.361+1101A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594426 | ||||||
| chr14:102594625
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG01123.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.361+1300T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594625 | ||||||
| chr14:102594659
|
A | G | 1 | a0001c0001t0038g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.361+1334A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102594659 | ||||||
| chr14:102595158
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.361+1833T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595158 | ||||||
| chr14:102595171
|
A | G | 1 | a0002c0007t0001g0141 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.361+1846A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595171 | ||||||
| chr14:102595267
|
C | G | 1 | a0001c0001t0007g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.361+1942C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595267 | ||||||
| chr14:102595527
|
C | G | 1 | a0001c0001t0005g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361+2202C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595527 | ||||||
| chr14:102595653
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+2328C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595653 | ||||||
| chr14:102595720
|
C | T | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.361+2395C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595720 | ||||||
| chr14:102595785
|
C | T | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.361+2460C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595785 | ||||||
| chr14:102595834
|
C | G | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.361+2509C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595834 | ||||||
| chr14:102595874
|
C | T | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.361+2549C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595874 | ||||||
| chr14:102595890
|
T | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+2565T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595890 | ||||||
| chr14:102595932
|
T | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+2607T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102595932 | ||||||
| chr14:102596009
|
T | G | 2 | a0001c0001t0006g0256a0001c0001t0006g0257 | 2 | HG00099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.361+2684T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596009 | ||||||
| chr14:102596041
|
T | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+2716T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596041 | ||||||
| chr14:102596104
|
A | T | 1 | a0001c0001t0012g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.361+2779A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596104 | ||||||
| chr14:102596104
|
AT | A | 10 | a0001c0001t0003g0003a0001c0001t0009g0002a0001c0001t0009g0143others(7): Show | 10 | HG01255.hp1 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+2793delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102596104 | |||||
| chr14:102596220
|
T | C | 245 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.361+2895T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596220 | ||||||
| chr14:102596250
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.361+2925C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596250 | ||||||
| chr14:102596593
|
C | G | 1 | a0001c0001t0009g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.361+3268C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596593 | ||||||
| chr14:102596602
|
T | C | 1 | a0001c0001t0005g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.361+3277T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596602 | ||||||
| chr14:102596645
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+3320A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102596645 | ||||||
| chr14:102596875
|
C | CT | 8 | a0001c0001t0001g0135a0001c0001t0002g0252a0001c0001t0004g0215others(5): Show | 8 | HG01243.hp2 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+3565dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102596875 | |||||
| chr14:102596875
|
CT | C | 49 | a0001c0001t0001g0005a0001c0001t0006g0256a0001c0001t0006g0257others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.361+3565delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102596875 | |||||
| chr14:102597019
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.361+3694C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597019 | ||||||
| chr14:102597020
|
G | A | 30 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0181others(27): Show | 30 | HG00609.hp1 HG00735.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.361+3695G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597020 | ||||||
| chr14:102597197
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0254 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.361+3872T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597197 | ||||||
| chr14:102597376
|
T | C | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+4051T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597376 | ||||||
| chr14:102597584
|
T | C | 48 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.361+4259T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597584 | ||||||
| chr14:102597620
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+4295C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597620 | ||||||
| chr14:102597624
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.361+4299C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597624 | ||||||
| chr14:102597628
|
C | CT | 9 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(6): Show | 9 | HG00733.hp1 HG01099.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+4329dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597628
|
C | CTT | 6 | a0001c0001t0006g0264a0001c0001t0006g0265a0001c0001t0006g0266others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+4328_361+4329d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597628
|
C | CTTT | 17 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0270others(14): Show | 17 | HG00099.hp1 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.361+4327_361+4329d others(5): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597628
|
CT | C | 158 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0061others(155): Show | 158 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.361+4329delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597628
|
CTT | C | 67 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(64): Show | 67 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.361+4328_361+4329d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597628
|
CTTT | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0002g0218others(9): Show | 12 | HG01256.hp1 HG01891.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.361+4327_361+4329d others(5): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597628
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0006 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.361+4319_361+4329d others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597628
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+4317_361+4329d others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597628 | |||||
| chr14:102597671
|
A | G | 1 | a0001c0001t0032g0057 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.361+4346A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597671 | ||||||
| chr14:102597766
|
C | T | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | NA19009.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.361+4441C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597766 | ||||||
| chr14:102597817
|
A | AT | 41 | a0001c0001t0004g0188a0001c0001t0006g0256a0001c0001t0006g0257others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.361+4506dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597817 | |||||
| chr14:102597885
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0003g0008a0001c0001t0003g0127 | 3 | HG01074.hp2 HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.361+4560C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597885 | ||||||
| chr14:102597929
|
TCTC | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+4607_361+4609d others(5): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102597929 | |||||
| chr14:102597955
|
C | G | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+4630C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102597955 | ||||||
| chr14:102598101
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.361+4776C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598101 | ||||||
| chr14:102598113
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+4788C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598113 | ||||||
| chr14:102598122
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.361+4797A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598122 | ||||||
| chr14:102598447
|
C | CT | 47 | a0001c0001t0001g0009a0001c0001t0002g0248a0001c0001t0003g0003others(44): Show | 47 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.361+5140dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102598447 | |||||
| chr14:102598447
|
CT | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+5140delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102598447 | |||||
| chr14:102598471
|
G | A | 1 | a0001c0001t0040g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.361+5146G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598471 | ||||||
| chr14:102598516
|
G | A | 1 | a0001c0001t0007g0034 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.361+5191G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598516 | ||||||
| chr14:102598529
|
G | A | 1 | a0001c0001t0019g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.361+5204G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598529 | ||||||
| chr14:102598562
|
C | T | 1 | a0001c0001t0029g0115 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.361+5237C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598562 | ||||||
| chr14:102598572
|
C | T | 9 | a0001c0001t0008g0263a0001c0001t0008g0268a0001c0001t0008g0269others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+5247C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598572 | ||||||
| chr14:102598573
|
GA | G | 141 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.361+5249delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598573 | ||||||
| chr14:102598584
|
A | G | 2 | a0001c0002t0003g0055a0001c0002t0011g0054 | 2 | HG01261.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.361+5259A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598584 | ||||||
| chr14:102598593
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.361+5268G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598593 | ||||||
| chr14:102598714
|
C | T | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.361+5389C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598714 | ||||||
| chr14:102598789
|
C | T | 1 | a0001c0001t0004g0215 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.361+5464C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598789 | ||||||
| chr14:102598868
|
G | C | 1 | a0001c0001t0010g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.361+5543G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102598868 | ||||||
| chr14:102599305
|
A | G | 29 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.361+5980A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599305 | ||||||
| chr14:102599432
|
A | G | 9 | a0001c0001t0008g0263a0001c0001t0008g0268a0001c0001t0008g0269others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+6107A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599432 | ||||||
| chr14:102599460
|
T | A | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.361+6135T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599460 | ||||||
| chr14:102599554
|
T | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+6229T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599554 | ||||||
| chr14:102599704
|
T | C | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.361+6379T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599704 | ||||||
| chr14:102599802
|
TG | T | 4 | a0001c0001t0005g0053a0001c0001t0005g0114a0001c0001t0005g0126others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+6478delG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599802 | ||||||
| chr14:102599807
|
TG | T | 137 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.361+6483delG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599807 | ||||||
| chr14:102599808
|
G | T | 34 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0003g0052others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.361+6483G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599808 | ||||||
| chr14:102599813
|
T | G | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.361+6488T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102599813 | ||||||
| chr14:102600076
|
A | T | 1 | a0001c0001t0001g0110 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.361+6751A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600076 | ||||||
| chr14:102600206
|
CCT | C | 14 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.361+6886_361+6887d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102600206 | |||||
| chr14:102600233
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+6908G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600233 | ||||||
| chr14:102600234
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+6909C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600234 | ||||||
| chr14:102600407
|
T | G | 37 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.361+7082T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600407 | ||||||
| chr14:102600568
|
A | AT | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0002g0254others(14): Show | 17 | HG00280.hp2 HG01167.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+7262dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102600568 | |||||
| chr14:102600568
|
AT | A | 7 | a0001c0001t0001g0005a0001c0001t0003g0014a0001c0001t0003g0160others(4): Show | 7 | HG01168.hp2 HG01257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+7262delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102600568 | |||||
| chr14:102600617
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.361+7292C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600617 | ||||||
| chr14:102600728
|
G | A | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+7403G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600728 | ||||||
| chr14:102600812
|
T | G | 1 | a0001c0001t0003g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.361+7487T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600812 | ||||||
| chr14:102600814
|
C | T | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+7489C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600814 | ||||||
| chr14:102600861
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361+7536C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102600861 | ||||||
| chr14:102601078
|
A | G | 29 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.361+7753A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601078 | ||||||
| chr14:102601150
|
C | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.361+7825C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601150 | ||||||
| chr14:102601247
|
A | C | 1 | a0001c0001t0002g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.361+7922A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601247 | ||||||
| chr14:102601275
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | NA18940.hp1 NA18952.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.361+7950A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601275 | ||||||
| chr14:102601276
|
G | GCCTCCT | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | NA18940.hp1 NA18952.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.361+7951_361+7952i others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601276 | ||||||
| chr14:102601338
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+8013A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601338 | ||||||
| chr14:102601370
|
C | A | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.361+8045C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601370 | ||||||
| chr14:102601423
|
T | G | 37 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.361+8098T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601423 | ||||||
| chr14:102601475
|
A | G | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+8150A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601475 | ||||||
| chr14:102601617
|
G | C | 1 | a0001c0001t0004g0215 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.361+8292G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601617 | ||||||
| chr14:102601652
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+8327G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601652 | ||||||
| chr14:102601775
|
T | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+8450T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601775 | ||||||
| chr14:102601803
|
C | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+8478C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601803 | ||||||
| chr14:102601868
|
C | G | 1 | a0001c0001t0003g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.361+8543C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102601868 | ||||||
| chr14:102602158
|
CA | C | 125 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.361+8848delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102602158 | |||||
| chr14:102602184
|
G | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+8859G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602184 | ||||||
| chr14:102602275
|
C | T | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+8950C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602275 | ||||||
| chr14:102602384
|
CTTTTCTT others(4): Show |
C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+9064_361+9074d others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102602384 | |||||
| chr14:102602394
|
CTTTT | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.361+9085_361+9088d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102602394 | |||||
| chr14:102602431
|
CTT | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+9107_361+9108d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602431 | ||||||
| chr14:102602482
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.361+9157T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602482 | ||||||
| chr14:102602529
|
G | A | 1 | a0001c0001t0009g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.361+9204G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602529 | ||||||
| chr14:102602544
|
C | T | 1 | a0001c0001t0010g0104 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.361+9219C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602544 | ||||||
| chr14:102602549
|
A | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+9224A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602549 | ||||||
| chr14:102602561
|
G | A | 4 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+9236G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602561 | ||||||
| chr14:102602655
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.361+9330C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602655 | ||||||
| chr14:102602726
|
G | A | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+9401G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602726 | ||||||
| chr14:102602736
|
C | T | 1 | a0001c0001t0017g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.361+9411C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602736 | ||||||
| chr14:102602895
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.361+9570G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102602895 | ||||||
| chr14:102603152
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.361+9827G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603152 | ||||||
| chr14:102603361
|
G | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG01123.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.361+10036G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603361 | ||||||
| chr14:102603524
|
G | T | 1 | a0001c0001t0002g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.361+10199G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603524 | ||||||
| chr14:102603552
|
G | A | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+10227G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603552 | ||||||
| chr14:102603675
|
C | T | 24 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.361+10350C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603675 | ||||||
| chr14:102603691
|
G | A | 2 | a0001c0001t0002g0212a0001c0001t0040g0213 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.361+10366G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603691 | ||||||
| chr14:102603744
|
C | T | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.361+10419C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603744 | ||||||
| chr14:102603985
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+10660C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102603985 | ||||||
| chr14:102604023
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+10698A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604023 | ||||||
| chr14:102604053
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.361+10728C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604053 | ||||||
| chr14:102604289
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.361+10964A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604289 | ||||||
| chr14:102604298
|
A | C | 1 | a0001c0001t0004g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.361+10973A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604298 | ||||||
| chr14:102604488
|
C | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+11163C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604488 | ||||||
| chr14:102604508
|
A | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+11183A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604508 | ||||||
| chr14:102604619
|
G | A | 2 | a0001c0001t0013g0291a0001c0001t0039g0158 | 2 | HG00733.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.361+11294G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604619 | ||||||
| chr14:102604766
|
G | T | 2 | a0001c0001t0005g0138a0001c0001t0013g0123 | 2 | HG01243.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.361+11441G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604766 | ||||||
| chr14:102604938
|
G | A | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.361+11613G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102604938 | ||||||
| chr14:102605067
|
C | CA | 8 | a0001c0001t0002g0162a0001c0001t0002g0204a0001c0001t0002g0205others(5): Show | 8 | HG01081.hp1 HG02056.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+11764dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102605067 | |||||
| chr14:102605067
|
CA | C | 139 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(136): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.361+11764delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102605067 | |||||
| chr14:102605067
|
CAA | C | 40 | a0001c0001t0001g0009a0001c0001t0003g0028a0001c0001t0006g0256others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.361+11763_361+1176 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102605067 | |||||
| chr14:102605067
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+11755_361+1176 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102605067 | |||||
| chr14:102605108
|
A | C | 1 | a0001c0001t0015g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.361+11783A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605108 | ||||||
| chr14:102605177
|
G | A | 1 | a0001c0001t0005g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.361+11852G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605177 | ||||||
| chr14:102605321
|
A | G | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.361+11996A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605321 | ||||||
| chr14:102605479
|
A | T | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.361+12154A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605479 | ||||||
| chr14:102605488
|
G | T | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.361+12163G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605488 | ||||||
| chr14:102605523
|
A | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+12198A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605523 | ||||||
| chr14:102605524
|
G | A | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.361+12199G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605524 | ||||||
| chr14:102605549
|
T | C | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.361+12224T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605549 | ||||||
| chr14:102605923
|
G | T | 1 | a0001c0001t0035g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361+12598G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605923 | ||||||
| chr14:102605924
|
T | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+12599T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605924 | ||||||
| chr14:102605994
|
C | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+12669C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102605994 | ||||||
| chr14:102606212
|
C | T | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.361+12887C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606212 | ||||||
| chr14:102606215
|
C | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+12890C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606215 | ||||||
| chr14:102606320
|
C | G | 1 | a0001c0001t0003g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.361+12995C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606320 | ||||||
| chr14:102606336
|
A | G | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.361+13011A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606336 | ||||||
| chr14:102606437
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0131 | 2 | HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.361+13112G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606437 | ||||||
| chr14:102606546
|
C | A | 1 | a0001c0001t0003g0037 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.361+13221C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606546 | ||||||
| chr14:102606627
|
G | GT | 18 | a0001c0001t0001g0063a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 18 | HG00738.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.361+13318dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102606627 | |||||
| chr14:102606934
|
G | GT | 38 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0201others(35): Show | 38 | HG00609.hp1 HG00735.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.361+13626dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102606934 | |||||
| chr14:102606934
|
G | GTT | 31 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0004g0165others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.361+13625_361+1362 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102606934 | |||||
| chr14:102606934
|
GT | G | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0009g0002others(9): Show | 12 | HG01255.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.361+13626delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102606934 | |||||
| chr14:102606934
|
GTT | G | 141 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.361+13625_361+1362 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102606934 | |||||
| chr14:102606956
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+13631C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606956 | ||||||
| chr14:102606988
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+13663C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102606988 | ||||||
| chr14:102607032
|
C | T | 4 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0215others(1): Show | 4 | HG00609.hp1 NA18944.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+13707C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607032 | ||||||
| chr14:102607074
|
T | C | 16 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0181others(13): Show | 16 | HG01261.hp2 HG01358.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.361+13749T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607074 | ||||||
| chr14:102607092
|
T | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+13767T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607092 | ||||||
| chr14:102607148
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.361+13823G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607148 | ||||||
| chr14:102607188
|
C | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+13863C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607188 | ||||||
| chr14:102607196
|
G | A | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+13871G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607196 | ||||||
| chr14:102607738
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+14413C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607738 | ||||||
| chr14:102607967
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+14642A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102607967 | ||||||
| chr14:102608027
|
G | T | 6 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0002g0205others(3): Show | 6 | HG01081.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+14702G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608027 | ||||||
| chr14:102608153
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.361+14828C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608153 | ||||||
| chr14:102608299
|
G | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.361+14974G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608299 | ||||||
| chr14:102608411
|
T | C | 2 | a0001c0001t0016g0281a0001c0001t0016g0282 | 2 | NA18967.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.361+15086T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608411 | ||||||
| chr14:102608461
|
G | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.361+15136G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608461 | ||||||
| chr14:102608613
|
T | G | 2 | a0001c0001t0005g0138a0001c0001t0013g0123 | 2 | HG01243.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.361+15288T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608613 | ||||||
| chr14:102608615
|
A | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.361+15290A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608615 | ||||||
| chr14:102608729
|
T | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.361+15404T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608729 | ||||||
| chr14:102608733
|
A | AT | 10 | a0001c0001t0005g0053a0001c0001t0005g0059a0001c0001t0005g0114others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.361+15418dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102608733 | |||||
| chr14:102608755
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+15430G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608755 | ||||||
| chr14:102608919
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+15594C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608919 | ||||||
| chr14:102608980
|
A | G | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+15655A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102608980 | ||||||
| chr14:102609025
|
C | CT | 10 | a0001c0001t0002g0162a0001c0001t0002g0211a0001c0001t0002g0248others(7): Show | 10 | HG01952.hp1 HG01981.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.361+15724dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102609025 | |||||
| chr14:102609025
|
CT | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(44): Show | 47 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.361+15724delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102609025 | |||||
| chr14:102609025
|
CTTTTT | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+15720_361+1572 others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102609025 | |||||
| chr14:102609049
|
T | A | 1 | a0001c0001t0003g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.361+15724T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609049 | ||||||
| chr14:102609050
|
A | T | 1 | a0001c0001t0029g0115 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.361+15725A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609050 | ||||||
| chr14:102609071
|
C | T | 8 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198others(5): Show | 8 | HG02109.hp1 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+15746C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609071 | ||||||
| chr14:102609200
|
T | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(160): Show | 163 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.361+15875T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609200 | ||||||
| chr14:102609286
|
G | T | 5 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+15961G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609286 | ||||||
| chr14:102609295
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+15970G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609295 | ||||||
| chr14:102609374
|
G | C | 1 | a0001c0001t0036g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.361+16049G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609374 | ||||||
| chr14:102609515
|
C | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+16190C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609515 | ||||||
| chr14:102609540
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.361+16215A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609540 | ||||||
| chr14:102609789
|
G | T | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+16464G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609789 | ||||||
| chr14:102609862
|
G | A | 8 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(5): Show | 8 | HG02451.hp2 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+16537G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609862 | ||||||
| chr14:102609905
|
C | T | 2 | a0001c0001t0002g0172a0001c0005t0037g0149 | 2 | HG01167.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.361+16580C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609905 | ||||||
| chr14:102609922
|
G | T | 2 | a0001c0001t0002g0182a0001c0001t0041g0214 | 2 | NA18952.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.361+16597G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609922 | ||||||
| chr14:102609999
|
A | C | 1 | a0001c0001t0002g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.361+16674A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102609999 | ||||||
| chr14:102610021
|
T | C | 1 | a0001c0001t0003g0041 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.361+16696T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610021 | ||||||
| chr14:102610258
|
T | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+16933T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610258 | ||||||
| chr14:102610470
|
A | T | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+17145A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610470 | ||||||
| chr14:102610487
|
C | T | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.361+17162C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610487 | ||||||
| chr14:102610488
|
C | A | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.361+17163C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610488 | ||||||
| chr14:102610489
|
A | T | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.361+17164A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610489 | ||||||
| chr14:102610490
|
G | A | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.361+17165G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610490 | ||||||
| chr14:102610496
|
T | G | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.361+17171T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610496 | ||||||
| chr14:102610497
|
C | A | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.361+17172C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610497 | ||||||
| chr14:102610498
|
A | T | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.361+17173A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610498 | ||||||
| chr14:102610591
|
G | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(160): Show | 163 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.361+17266G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610591 | ||||||
| chr14:102610601
|
T | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(160): Show | 163 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.361+17276T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610601 | ||||||
| chr14:102610905
|
G | A | 162 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(159): Show | 162 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.361+17580G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610905 | ||||||
| chr14:102610972
|
TA | T | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.361+17648delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102610972 | ||||||
| chr14:102611109
|
G | C | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.361+17784G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611109 | ||||||
| chr14:102611157
|
C | T | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+17832C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611157 | ||||||
| chr14:102611181
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.361+17856C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611181 | ||||||
| chr14:102611234
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.361+17909G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611234 | ||||||
| chr14:102611275
|
G | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.361+17950G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611275 | ||||||
| chr14:102611312
|
T | G | 162 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(159): Show | 162 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.361+17987T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611312 | ||||||
| chr14:102611365
|
G | A | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.361+18040G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611365 | ||||||
| chr14:102611703
|
C | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.361+18378C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611703 | ||||||
| chr14:102611736
|
A | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.361+18411A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102611736 | ||||||
| chr14:102612021
|
C | T | 245 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.361+18696C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612021 | ||||||
| chr14:102612050
|
T | C | 1 | a0001c0001t0006g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.361+18725T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612050 | ||||||
| chr14:102612082
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.361+18757C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612082 | ||||||
| chr14:102612100
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.361+18775T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612100 | ||||||
| chr14:102612215
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.361+18890T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612215 | ||||||
| chr14:102612344
|
C | G | 1 | a0001c0001t0010g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.361+19019C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612344 | ||||||
| chr14:102612352
|
C | T | 29 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.361+19027C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612352 | ||||||
| chr14:102612395
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.361+19070G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612395 | ||||||
| chr14:102612433
|
A | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+19108A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612433 | ||||||
| chr14:102612436
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+19111C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612436 | ||||||
| chr14:102612453
|
C | G | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+19128C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612453 | ||||||
| chr14:102612494
|
C | T | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.361+19169C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612494 | ||||||
| chr14:102612578
|
C | T | 1 | a0001c0002t0011g0054 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361+19253C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612578 | ||||||
| chr14:102612648
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+19323A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612648 | ||||||
| chr14:102612825
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.361+19500C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612825 | ||||||
| chr14:102612941
|
G | A | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+19616G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102612941 | ||||||
| chr14:102612958
|
C | CA | 21 | a0001c0001t0001g0029a0001c0001t0002g0200a0001c0001t0003g0105others(18): Show | 21 | HG00639.hp2 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.361+19648dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102612958 | |||||
| chr14:102613050
|
T | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.361+19725T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613050 | ||||||
| chr14:102613140
|
C | T | 1 | a0001c0001t0024g0062 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.361+19815C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613140 | ||||||
| chr14:102613224
|
C | T | 1 | a0001c0001t0009g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.361+19899C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613224 | ||||||
| chr14:102613251
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+19926G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613251 | ||||||
| chr14:102613301
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.361+19976C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613301 | ||||||
| chr14:102613378
|
A | G | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.361+20053A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613378 | ||||||
| chr14:102613380
|
G | A | 1 | a0001c0001t0007g0219 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.361+20055G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613380 | ||||||
| chr14:102613388
|
C | G | 124 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.361+20063C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613388 | ||||||
| chr14:102613435
|
A | AT | 6 | a0001c0001t0001g0100a0001c0001t0001g0135a0001c0001t0002g0211others(3): Show | 6 | HG00639.hp2 HG01256.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+20125dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102613435 | |||||
| chr14:102613435
|
AT | A | 9 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0056others(6): Show | 9 | HG01496.hp2 HG02451.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+20125delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102613435 | |||||
| chr14:102613479
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+20154C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613479 | ||||||
| chr14:102613622
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.361+20297C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613622 | ||||||
| chr14:102613695
|
C | G | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.361+20370C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613695 | ||||||
| chr14:102613700
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+20375A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613700 | ||||||
| chr14:102613723
|
C | CT | 11 | a0001c0001t0002g0211a0001c0001t0005g0053a0001c0001t0005g0059others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.361+20412dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102613723 | |||||
| chr14:102613847
|
C | T | 1 | a0001c0001t0014g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.361+20522C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613847 | ||||||
| chr14:102613884
|
TC | T | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+20560delC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102613884 | ||||||
| chr14:102613885
|
C | CT | 8 | a0001c0001t0001g0108a0001c0001t0002g0164a0001c0001t0002g0211others(5): Show | 8 | HG00423.hp2 HG00733.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+20584dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102613885 | |||||
| chr14:102613885
|
CT | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(126): Show | 129 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.361+20584delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102613885 | |||||
| chr14:102613885
|
CTT | C | 16 | a0001c0001t0001g0016a0001c0001t0003g0014a0001c0001t0003g0042others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.361+20583_361+2058 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102613885 | |||||
| chr14:102614224
|
CT | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.361+20917delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102614224 | |||||
| chr14:102614332
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.361+21007C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102614332 | ||||||
| chr14:102614424
|
C | A | 1 | a0001c0001t0003g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.361+21099C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102614424 | ||||||
| chr14:102614445
|
C | T | 2 | a0001c0001t0007g0024a0001c0001t0007g0048 | 2 | NA18960.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.361+21120C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102614445 | ||||||
| chr14:102614647
|
A | T | 1 | a0001c0001t0003g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361+21322A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102614647 | ||||||
| chr14:102614834
|
A | AT | 6 | a0001c0001t0001g0089a0001c0001t0004g0177a0001c0001t0004g0216others(3): Show | 6 | HG00733.hp1 HG00735.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+21524dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102614834 | |||||
| chr14:102614934
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(141): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.361+21609C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102614934 | ||||||
| chr14:102614952
|
C | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(141): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.361+21627C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102614952 | ||||||
| chr14:102614978
|
C | T | 1 | a0001c0001t0006g0275 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.361+21653C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102614978 | ||||||
| chr14:102615082
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.361+21757T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615082 | ||||||
| chr14:102615083
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.361+21758G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615083 | ||||||
| chr14:102615091
|
A | T | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.361+21766A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615091 | ||||||
| chr14:102615128
|
G | GC | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+21810dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102615128 | |||||
| chr14:102615156
|
C | CA | 38 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.361+21832dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102615156 | |||||
| chr14:102615227
|
G | A | 1 | a0001c0001t0006g0257 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.361+21902G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615227 | ||||||
| chr14:102615300
|
A | AT | 45 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0129others(42): Show | 45 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.361+21986dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102615300 | |||||
| chr14:102615361
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG01123.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.361+22036C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615361 | ||||||
| chr14:102615381
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+22056A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615381 | ||||||
| chr14:102615391
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+22066C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615391 | ||||||
| chr14:102615447
|
C | CT | 11 | a0001c0001t0001g0018a0001c0001t0001g0112a0001c0001t0001g0133others(8): Show | 11 | HG01515.hp1 HG02300.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.361+22140dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102615447 | |||||
| chr14:102615740
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+22415C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615740 | ||||||
| chr14:102615741
|
G | A | 2 | a0001c0001t0002g0245a0001c0001t0002g0248 | 2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.361+22416G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615741 | ||||||
| chr14:102615792
|
T | A | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+22467T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615792 | ||||||
| chr14:102615984
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0011g0047 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.361+22659C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102615984 | ||||||
| chr14:102616086
|
C | T | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.361+22761C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616086 | ||||||
| chr14:102616206
|
A | ATG | 7 | a0001c0001t0002g0164a0001c0001t0002g0192a0001c0001t0002g0207others(4): Show | 7 | HG00423.hp2 HG02015.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+22923_361+2292 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATG | A | 21 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0229others(18): Show | 21 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.361+22923_361+2292 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTG | A | 10 | a0001c0001t0002g0243a0001c0001t0006g0265a0001c0001t0006g0266others(7): Show | 10 | HG00280.hp2 HG01081.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+22921_361+2292 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTG | A | 14 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0209others(11): Show | 14 | HG01099.hp2 HG01123.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.361+22919_361+2292 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTGT others(1): Show |
A | 6 | a0001c0001t0002g0212a0001c0001t0006g0256a0001c0001t0006g0257others(3): Show | 6 | HG00099.hp1 HG01123.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+22917_361+2292 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTGT others(3): Show |
A | 13 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0002g0205others(10): Show | 13 | HG01081.hp1 HG02486.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.361+22915_361+2292 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTGT others(5): Show |
A | 8 | a0001c0001t0003g0003a0001c0001t0003g0037a0001c0001t0003g0040others(5): Show | 8 | HG01167.hp2 HG03209.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+22913_361+2292 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTGT others(7): Show |
A | 51 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0003g0008others(48): Show | 51 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.361+22911_361+2292 others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTGT others(9): Show |
A | 19 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(16): Show | 19 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.361+22909_361+2292 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTGT others(13): Show |
A | 2 | a0001c0001t0003g0006a0001c0001t0005g0118 | 2 | HG00733.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.361+22905_361+2292 others(24): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616206
|
ATGTGTGT others(17): Show |
A | 75 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.361+22901_361+2292 others(28): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616206 | |||||
| chr14:102616210
|
GTGTGTGT others(33): Show |
G | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.361+22899_361+2293 others(44): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616210 | |||||
| chr14:102616240
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.361+22915G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616240 | ||||||
| chr14:102616240
|
G | GTGTGTA | 20 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0181others(17): Show | 20 | HG00609.hp1 HG01261.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.361+22920_361+2292 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616240 | |||||
| chr14:102616240
|
G | GTGTGTGT others(1): Show |
4 | a0001c0001t0004g0170a0001c0001t0004g0177a0001c0001t0004g0180others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+22922_361+2292 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616240 | |||||
| chr14:102616240
|
G | GTGTGTGT others(5): Show |
3 | a0001c0001t0002g0182a0001c0001t0004g0215a0001c0001t0041g0214 | 3 | NA18952.hp1 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.361+22924_361+2292 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102616240 | |||||
| chr14:102616248
|
G | A | 185 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.361+22923G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616248 | ||||||
| chr14:102616356
|
A | G | 1 | a0001c0001t0025g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.361+23031A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616356 | ||||||
| chr14:102616542
|
A | G | 1 | a0001c0001t0003g0046 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.361+23217A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616542 | ||||||
| chr14:102616744
|
G | A | 1 | a0001c0003t0005g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.361+23419G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616744 | ||||||
| chr14:102616916
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.361+23591A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616916 | ||||||
| chr14:102616963
|
A | G | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+23638A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616963 | ||||||
| chr14:102616985
|
T | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+23660T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102616985 | ||||||
| chr14:102617562
|
G | A | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+24237G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102617562 | ||||||
| chr14:102617587
|
C | CT | 22 | a0001c0001t0002g0162a0001c0001t0002g0198a0001c0001t0002g0211others(19): Show | 22 | HG02015.hp2 HG02027.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.361+24284dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102617587 | |||||
| chr14:102617587
|
CTT | C | 57 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0106others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.361+24283_361+2428 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102617587 | |||||
| chr14:102617587
|
CTTT | C | 130 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.361+24282_361+2428 others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102617587 | |||||
| chr14:102617593
|
T | C | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+24268T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102617593 | ||||||
| chr14:102617632
|
C | G | 2 | a0001c0001t0024g0062a0001c0001t0033g0255 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.361+24307C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102617632 | ||||||
| chr14:102617714
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.361+24389C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102617714 | ||||||
| chr14:102617839
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0034g0039 | 2 | HG01515.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.361+24514C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102617839 | ||||||
| chr14:102617957
|
G | GTTTCTTT others(4): Show |
5 | a0001c0001t0002g0182a0001c0001t0004g0176a0001c0001t0004g0177others(2): Show | 5 | HG00735.hp2 HG02015.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+24647_361+2465 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102617957 | |||||
| chr14:102617972
|
C | CT | 19 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0002g0211others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.361+24663dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102617972 | |||||
| chr14:102617972
|
CT | C | 22 | a0001c0001t0002g0248a0001c0001t0009g0002a0001c0001t0009g0143others(19): Show | 22 | HG00733.hp1 HG01099.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.361+24663delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102617972 | |||||
| chr14:102617981
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.361+24656T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102617981 | ||||||
| chr14:102618104
|
G | A | 4 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(1): Show | 4 | HG03139.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+24779G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618104 | ||||||
| chr14:102618119
|
G | A | 9 | a0001c0001t0008g0263a0001c0001t0008g0268a0001c0001t0008g0269others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+24794G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618119 | ||||||
| chr14:102618163
|
G | A | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+24838G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618163 | ||||||
| chr14:102618229
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+24904G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618229 | ||||||
| chr14:102618257
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+24932G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618257 | ||||||
| chr14:102618385
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+25060A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618385 | ||||||
| chr14:102618441
|
G | C | 1 | a0001c0001t0003g0035 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.361+25116G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618441 | ||||||
| chr14:102618557
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.361+25232G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618557 | ||||||
| chr14:102618580
|
C | T | 1 | a0001c0001t0009g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.361+25255C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618580 | ||||||
| chr14:102618726
|
G | A | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+25401G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102618726 | ||||||
| chr14:102619076
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.361+25751C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619076 | ||||||
| chr14:102619104
|
A | ATCTGTCT others(1): Show |
45 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.361+25795_361+2580 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102619104 | |||||
| chr14:102619104
|
A | ATCTGTCT others(5): Show |
20 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.361+25791_361+2580 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102619104 | |||||
| chr14:102619368
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+26043C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619368 | ||||||
| chr14:102619437
|
A | ATCTG | 4 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(1): Show | 4 | HG03139.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+26124_361+2612 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102619437 | |||||
| chr14:102619466
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+26141A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619466 | ||||||
| chr14:102619473
|
C | CT | 12 | a0001c0001t0002g0164a0001c0001t0002g0205a0001c0001t0002g0212others(9): Show | 12 | HG00423.hp2 HG00673.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.361+26172dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102619473 | |||||
| chr14:102619473
|
CTTTTTTT others(4): Show |
C | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+26162_361+2617 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102619473 | |||||
| chr14:102619473
|
CTTTTTTT others(6): Show |
C | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+26160_361+2617 others(17): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102619473 | |||||
| chr14:102619535
|
T | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0210 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.361+26210T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619535 | ||||||
| chr14:102619558
|
G | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.361+26233G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619558 | ||||||
| chr14:102619679
|
C | G | 2 | a0001c0001t0006g0256a0001c0001t0006g0257 | 2 | HG00099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.361+26354C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619679 | ||||||
| chr14:102619719
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0003g0008a0001c0001t0003g0127 | 3 | HG01074.hp2 HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.361+26394G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619719 | ||||||
| chr14:102619768
|
ACTGTGCC others(4): Show |
A | 1 | a0001c0001t0006g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361+26448_361+2645 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102619768 | |||||
| chr14:102619863
|
C | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+26538C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619863 | ||||||
| chr14:102619941
|
G | A | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+26616G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619941 | ||||||
| chr14:102619952
|
T | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+26627T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102619952 | ||||||
| chr14:102620019
|
T | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+26694T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620019 | ||||||
| chr14:102620148
|
G | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+26823G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620148 | ||||||
| chr14:102620236
|
T | TAC | 38 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.361+26926_361+2692 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102620236 | |||||
| chr14:102620251
|
A | C | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+26926A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620251 | ||||||
| chr14:102620253
|
C | A | 40 | a0001c0001t0003g0052a0001c0001t0006g0256a0001c0001t0006g0257others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.361+26928C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620253 | ||||||
| chr14:102620361
|
A | G | 3 | a0001c0001t0002g0212a0001c0001t0040g0213a0001c0001t0045g0203 | 3 | HG01884.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.361+27036A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620361 | ||||||
| chr14:102620388
|
A | AG | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.361+27064dupG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102620388 | |||||
| chr14:102620611
|
A | G | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.361+27286A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620611 | ||||||
| chr14:102620711
|
T | C | 2 | a0001c0001t0002g0229a0001c0001t0002g0230 | 2 | NA19011.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.361+27386T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620711 | ||||||
| chr14:102620833
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG00423.hp1 NA18972.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.361+27508T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620833 | ||||||
| chr14:102620965
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.361+27640A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102620965 | ||||||
| chr14:102621074
|
A | G | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.361+27749A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102621074 | ||||||
| chr14:102621191
|
T | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+27866T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102621191 | ||||||
| chr14:102621318
|
G | A | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.361+27993G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102621318 | ||||||
| chr14:102621367
|
C | CT | 23 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0181others(20): Show | 23 | HG00733.hp1 HG01261.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.361+28068dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102621367 | |||||
| chr14:102621367
|
CT | C | 43 | a0001c0001t0001g0005a0001c0001t0001g0084a0001c0001t0001g0089others(40): Show | 43 | HG00099.hp1 HG00639.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.361+28068delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102621367 | |||||
| chr14:102621367
|
CTT | C | 92 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.361+28067_361+2806 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102621367 | |||||
| chr14:102621367
|
CTTT | C | 26 | a0001c0001t0001g0012a0001c0001t0001g0063a0001c0001t0001g0065others(23): Show | 26 | HG01257.hp2 HG01943.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.361+28066_361+2806 others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102621367 | |||||
| chr14:102621367
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+28059_361+2806 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102621367 | |||||
| chr14:102621535
|
C | T | 27 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.361+28210C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102621535 | ||||||
| chr14:102621585
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01516.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.361+28260G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102621585 | ||||||
| chr14:102621710
|
TAAATG | T | 126 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.361+28388_361+2839 others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102621710 | |||||
| chr14:102621845
|
G | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+28520G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102621845 | ||||||
| chr14:102622060
|
T | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+28735T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622060 | ||||||
| chr14:102622182
|
T | TA | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+28858dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102622182 | |||||
| chr14:102622195
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+28870A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622195 | ||||||
| chr14:102622198
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+28873C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622198 | ||||||
| chr14:102622200
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+28875T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622200 | ||||||
| chr14:102622201
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+28876T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622201 | ||||||
| chr14:102622203
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+28878T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622203 | ||||||
| chr14:102622206
|
C | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+28881C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622206 | ||||||
| chr14:102622211
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+28886C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622211 | ||||||
| chr14:102622711
|
C | T | 1 | a0001c0001t0015g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.361+29386C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622711 | ||||||
| chr14:102622873
|
G | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.361+29548G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102622873 | ||||||
| chr14:102623108
|
G | A | 4 | a0001c0001t0005g0059a0001c0001t0005g0119a0001c0001t0005g0120others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+29783G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623108 | ||||||
| chr14:102623380
|
TTTATTTA | T | 19 | a0001c0001t0006g0270a0001c0001t0006g0274a0001c0001t0008g0263others(16): Show | 19 | HG00733.hp1 HG01175.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.361+30065_361+3007 others(11): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623380 | |||||
| chr14:102623384
|
TTTA | T | 15 | a0001c0001t0006g0256a0001c0001t0006g0260a0001c0001t0006g0261others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.361+30065_361+3006 others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623384 | |||||
| chr14:102623384
|
TTTATTAT others(3): Show |
T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+30062_361+3007 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623384 | |||||
| chr14:102623386
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.361+30061T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623386 | ||||||
| chr14:102623387
|
A | AT | 3 | a0001c0001t0006g0257a0001c0001t0006g0272a0001c0003t0005g0117 | 3 | HG01433.hp2 HG01516.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.361+30064dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623387 | |||||
| chr14:102623387
|
A | ATTAATTA others(20): Show |
1 | a0001c0001t0002g0233 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.361+30065_361+3006 others(31): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623387 | |||||
| chr14:102623387
|
A | ATTAT | 24 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0218others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.361+30097_361+3010 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623387 | |||||
| chr14:102623387
|
A | ATTATTTA others(1): Show |
3 | a0001c0001t0005g0053a0001c0001t0005g0114a0001c0001t0005g0140 | 3 | HG01167.hp1 HG01169.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.361+30093_361+3010 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623387 | |||||
| chr14:102623387
|
A | ATTATTTA others(5): Show |
1 | a0001c0001t0005g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.361+30089_361+3010 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623387 | |||||
| chr14:102623387
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.361+30062A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623387 | ||||||
| chr14:102623387
|
ATTAT | A | 30 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0200others(27): Show | 30 | HG01081.hp1 HG01943.hp2 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.361+30097_361+3010 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623387 | |||||
| chr14:102623387
|
ATTATTTA others(1): Show |
A | 5 | a0001c0001t0004g0185a0001c0001t0020g0289a0001c0001t0020g0290others(2): Show | 5 | HG01099.hp2 HG01167.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+30093_361+3010 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102623387 | |||||
| chr14:102623390
|
A | T | 3 | a0001c0001t0002g0212a0001c0001t0040g0213a0001c0001t0045g0203 | 3 | HG01884.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.361+30065A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623390 | ||||||
| chr14:102623391
|
T | A | 3 | a0001c0001t0002g0212a0001c0001t0040g0213a0001c0001t0045g0203 | 3 | HG01884.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.361+30066T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623391 | ||||||
| chr14:102623430
|
A | G | 1 | a0001c0001t0004g0180 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.361+30105A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623430 | ||||||
| chr14:102623465
|
A | G | 2 | a0001c0001t0005g0053a0001c0001t0005g0114 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.361+30140A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623465 | ||||||
| chr14:102623471
|
C | T | 126 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.361+30146C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623471 | ||||||
| chr14:102623483
|
A | G | 1 | a0001c0001t0015g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.361+30158A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623483 | ||||||
| chr14:102623700
|
G | A | 1 | a0001c0001t0014g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.361+30375G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623700 | ||||||
| chr14:102623731
|
A | T | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.361+30406A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623731 | ||||||
| chr14:102623856
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.361+30531A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623856 | ||||||
| chr14:102623931
|
C | T | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | NA19009.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.361+30606C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102623931 | ||||||
| chr14:102624031
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.361+30706A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624031 | ||||||
| chr14:102624141
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+30816A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624141 | ||||||
| chr14:102624143
|
C | A | 1 | a0001c0001t0006g0264 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.361+30818C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624143 | ||||||
| chr14:102624143
|
C | G | 2 | a0001c0001t0002g0217a0001c0001t0002g0254 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.361+30818C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624143 | ||||||
| chr14:102624270
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+30945G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624270 | ||||||
| chr14:102624336
|
T | G | 8 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0021others(5): Show | 8 | HG02258.hp1 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+31011T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624336 | ||||||
| chr14:102624546
|
G | C | 1 | a0001c0001t0004g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.361+31221G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624546 | ||||||
| chr14:102624652
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+31327G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624652 | ||||||
| chr14:102624773
|
G | GA | 7 | a0001c0001t0001g0089a0001c0001t0002g0162a0001c0001t0002g0223others(4): Show | 7 | HG02615.hp1 HG02735.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+31461dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102624773 | |||||
| chr14:102624783
|
A | C | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+31458A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624783 | ||||||
| chr14:102624851
|
T | G | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+31526T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624851 | ||||||
| chr14:102624966
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.361+31641C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102624966 | ||||||
| chr14:102625035
|
T | TA | 15 | a0001c0001t0002g0222a0001c0001t0009g0002a0001c0001t0009g0143others(12): Show | 15 | HG01891.hp1 HG02015.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.361+31716dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102625035 | |||||
| chr14:102625036
|
A | AAAAAAAA others(58): Show |
1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+31716_361+3171 others(69): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102625036 | |||||
| chr14:102625042
|
G | A | 289 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.361+31717G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625042 | ||||||
| chr14:102625103
|
C | G | 163 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(160): Show | 163 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.361+31778C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625103 | ||||||
| chr14:102625231
|
C | CT | 153 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.361+31930dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102625231 | |||||
| chr14:102625231
|
C | CTT | 17 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(14): Show | 17 | HG00423.hp1 HG01361.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+31929_361+3193 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102625231 | |||||
| chr14:102625283
|
T | G | 1 | a0001c0001t0002g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.361+31958T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625283 | ||||||
| chr14:102625310
|
G | A | 19 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(16): Show | 19 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.361+31985G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625310 | ||||||
| chr14:102625331
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+32006A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625331 | ||||||
| chr14:102625360
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.361+32035C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625360 | ||||||
| chr14:102625449
|
T | C | 19 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(16): Show | 19 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.361+32124T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625449 | ||||||
| chr14:102625524
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+32199C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625524 | ||||||
| chr14:102625793
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.361+32468G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625793 | ||||||
| chr14:102625899
|
C | T | 3 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0048g0179 | 3 | HG00609.hp1 NA18944.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.361+32574C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625899 | ||||||
| chr14:102625908
|
T | A | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+32583T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102625908 | ||||||
| chr14:102626255
|
C | T | 4 | a0001c0001t0005g0059a0001c0001t0005g0119a0001c0001t0005g0120others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+32930C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102626255 | ||||||
| chr14:102626301
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+32976A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102626301 | ||||||
| chr14:102626420
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.361+33095A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102626420 | ||||||
| chr14:102626531
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+33206T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102626531 | ||||||
| chr14:102626739
|
G | T | 1 | a0001c0001t0002g0222 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.361+33414G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102626739 | ||||||
| chr14:102626886
|
C | A | 1 | a0001c0001t0002g0222 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.361+33561C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102626886 | ||||||
| chr14:102626926
|
A | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+33601A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102626926 | ||||||
| chr14:102627095
|
T | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+33770T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627095 | ||||||
| chr14:102627137
|
T | C | 291 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.361+33812T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627137 | ||||||
| chr14:102627170
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+33845A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627170 | ||||||
| chr14:102627255
|
G | GT | 12 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0081others(9): Show | 12 | HG00609.hp2 HG00738.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.361+33933dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627255 | |||||
| chr14:102627295
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+33970A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627295 | ||||||
| chr14:102627300
|
C | CAAATTTT others(76): Show |
1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+33976_361+3405 others(87): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627300 | |||||
| chr14:102627394
|
C | T | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.361+34069C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627394 | ||||||
| chr14:102627434
|
A | G | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+34109A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627434 | ||||||
| chr14:102627476
|
G | A | 2 | a0001c0001t0005g0121a0001c0001t0005g0137 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.361+34151G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627476 | ||||||
| chr14:102627575
|
T | G | 1 | a0001c0001t0002g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.361+34250T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627575 | ||||||
| chr14:102627635
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+34310C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627635 | ||||||
| chr14:102627656
|
T | TA | 22 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0079others(19): Show | 22 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.361+34346dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627656 | |||||
| chr14:102627656
|
TA | T | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+34346delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627656 | |||||
| chr14:102627665
|
A | G | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+34340A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627665 | ||||||
| chr14:102627717
|
T | C | 1 | a0001c0001t0015g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.361+34392T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627717 | ||||||
| chr14:102627739
|
C | T | 2 | a0001c0001t0002g0212a0001c0001t0040g0213 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.361+34414C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627739 | ||||||
| chr14:102627900
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+34575G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627900 | ||||||
| chr14:102627949
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+34624A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102627949 | ||||||
| chr14:102627960
|
G | GGT | 182 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.361+34656_361+3465 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627960 | |||||
| chr14:102627960
|
G | GGTGT | 6 | a0001c0001t0001g0016a0001c0001t0004g0215a0001c0001t0007g0024others(3): Show | 6 | HG01516.hp2 HG03471.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+34654_361+3465 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627960 | |||||
| chr14:102627960
|
G | GGTGTGT | 7 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(4): Show | 7 | HG03139.hp2 HG03209.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+34652_361+3465 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627960 | |||||
| chr14:102627960
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+34646_361+3465 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627960 | |||||
| chr14:102627960
|
G | GGTGTGTG others(7): Show |
7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+34644_361+3465 others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102627960 | |||||
| chr14:102628021
|
A | C | 1 | a0001c0001t0028g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.361+34696A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628021 | ||||||
| chr14:102628068
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+34743A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628068 | ||||||
| chr14:102628085
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+34760G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628085 | ||||||
| chr14:102628146
|
C | T | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+34821C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628146 | ||||||
| chr14:102628241
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | NA18972.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.361+34916C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628241 | ||||||
| chr14:102628439
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+35114C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628439 | ||||||
| chr14:102628444
|
C | T | 6 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0041others(3): Show | 6 | HG00733.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+35119C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628444 | ||||||
| chr14:102628517
|
C | A | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+35192C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628517 | ||||||
| chr14:102628538
|
C | CA | 13 | a0001c0001t0001g0134a0001c0001t0002g0243a0001c0001t0005g0137others(10): Show | 13 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.361+35226dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102628538 | |||||
| chr14:102628538
|
C | CAA | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+35225_361+3522 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102628538 | |||||
| chr14:102628893
|
C | CT | 34 | a0001c0001t0002g0225a0001c0001t0002g0284a0001c0001t0003g0045others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.361+35585dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102628893 | |||||
| chr14:102628915
|
C | T | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+35590C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628915 | ||||||
| chr14:102628925
|
C | G | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.361+35600C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628925 | ||||||
| chr14:102628931
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.361+35606C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628931 | ||||||
| chr14:102628999
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.361+35674T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102628999 | ||||||
| chr14:102629007
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.361+35682C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629007 | ||||||
| chr14:102629092
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+35767C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629092 | ||||||
| chr14:102629308
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+35983C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629308 | ||||||
| chr14:102629315
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+35990C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629315 | ||||||
| chr14:102629315
|
C | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.361+35990C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629315 | ||||||
| chr14:102629375
|
C | T | 1 | a0001c0001t0021g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.361+36050C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629375 | ||||||
| chr14:102629387
|
C | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.361+36062C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629387 | ||||||
| chr14:102629419
|
A | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+36094A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629419 | ||||||
| chr14:102629442
|
T | TC | 18 | a0001c0001t0002g0162a0001c0001t0002g0168a0001c0001t0002g0211others(15): Show | 18 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.361+36128dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102629442 | |||||
| chr14:102629442
|
TC | T | 154 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.361+36128delC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102629442 | |||||
| chr14:102629448
|
C | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.361+36123C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629448 | ||||||
| chr14:102629449
|
C | G | 1 | a0001c0001t0002g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.361+36124C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629449 | ||||||
| chr14:102629466
|
A | G | 13 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(10): Show | 13 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.361+36141A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102629466 | ||||||
| chr14:102630005
|
G | A | 1 | a0001c0001t0028g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.361+36680G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630005 | ||||||
| chr14:102630015
|
T | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+36690T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630015 | ||||||
| chr14:102630114
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+36789T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630114 | ||||||
| chr14:102630160
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.361+36835A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630160 | ||||||
| chr14:102630242
|
T | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+36917T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630242 | ||||||
| chr14:102630269
|
C | T | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.361+36944C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630269 | ||||||
| chr14:102630318
|
C | A | 1 | a0001c0001t0003g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.361+36993C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630318 | ||||||
| chr14:102630334
|
G | T | 1 | a0001c0003t0005g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.361+37009G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630334 | ||||||
| chr14:102630352
|
C | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.361+37027C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630352 | ||||||
| chr14:102630353
|
G | A | 1 | a0001c0001t0004g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.361+37028G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630353 | ||||||
| chr14:102630502
|
A | C | 2 | a0001c0001t0006g0270a0001c0001t0006g0272 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.361+37177A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630502 | ||||||
| chr14:102630606
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.361+37281C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630606 | ||||||
| chr14:102630641
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37316G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630641 | ||||||
| chr14:102630643
|
T | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37318T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630643 | ||||||
| chr14:102630649
|
C | A | 45 | a0001c0001t0001g0009a0001c0001t0003g0003a0001c0001t0003g0006others(42): Show | 45 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.361+37324C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630649 | ||||||
| chr14:102630652
|
ATCCAGAA others(22): Show |
A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37328_361+3735 others(33): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630652 | ||||||
| chr14:102630656
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.361+37331A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630656 | ||||||
| chr14:102630682
|
G | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37357G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630682 | ||||||
| chr14:102630689
|
C | G | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37364C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630689 | ||||||
| chr14:102630690
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37365G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630690 | ||||||
| chr14:102630743
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37418G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630743 | ||||||
| chr14:102630752
|
A | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37427A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630752 | ||||||
| chr14:102630753
|
T | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37428T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630753 | ||||||
| chr14:102630765
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.361+37440G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630765 | ||||||
| chr14:102630765
|
G | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37440G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630765 | ||||||
| chr14:102630827
|
A | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37502A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630827 | ||||||
| chr14:102630837
|
T | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37512T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630837 | ||||||
| chr14:102630897
|
G | C | 4 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+37572G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630897 | ||||||
| chr14:102630909
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37584G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630909 | ||||||
| chr14:102630910
|
T | G | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37585T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630910 | ||||||
| chr14:102630911
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37586G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630911 | ||||||
| chr14:102630921
|
A | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37596A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630921 | ||||||
| chr14:102630947
|
T | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37622T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630947 | ||||||
| chr14:102630948
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37623G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630948 | ||||||
| chr14:102630953
|
C | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+37628C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630953 | ||||||
| chr14:102630983
|
G | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37658G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630983 | ||||||
| chr14:102630985
|
A | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37660A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630985 | ||||||
| chr14:102630989
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37664G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630989 | ||||||
| chr14:102630994
|
T | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37669T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630994 | ||||||
| chr14:102630996
|
A | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37671A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630996 | ||||||
| chr14:102630999
|
G | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37674G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102630999 | ||||||
| chr14:102631000
|
C | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37675C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631000 | ||||||
| chr14:102631206
|
C | CT | 20 | a0001c0001t0003g0022a0001c0001t0009g0002a0001c0001t0009g0143others(17): Show | 20 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.361+37895dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102631206 | |||||
| chr14:102631226
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+37901G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631226 | ||||||
| chr14:102631226
|
G | C | 1 | a0001c0001t0002g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.361+37901G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631226 | ||||||
| chr14:102631298
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37973G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631298 | ||||||
| chr14:102631300
|
T | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+37975T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631300 | ||||||
| chr14:102631371
|
T | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+38046T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631371 | ||||||
| chr14:102631395
|
G | A | 4 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(1): Show | 4 | HG03139.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+38070G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631395 | ||||||
| chr14:102631488
|
C | T | 3 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0276 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.361+38163C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631488 | ||||||
| chr14:102631575
|
A | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.361+38250A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631575 | ||||||
| chr14:102631650
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+38325A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631650 | ||||||
| chr14:102631695
|
A | C | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.361+38370A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631695 | ||||||
| chr14:102631740
|
A | G | 10 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0196others(7): Show | 10 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+38415A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631740 | ||||||
| chr14:102631745
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+38420C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631745 | ||||||
| chr14:102631812
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+38487T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631812 | ||||||
| chr14:102631817
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+38492T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631817 | ||||||
| chr14:102631865
|
A | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+38540A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631865 | ||||||
| chr14:102631870
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+38545G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631870 | ||||||
| chr14:102631946
|
T | A | 1 | a0001c0001t0003g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361+38621T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102631946 | ||||||
| chr14:102632105
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+38780G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632105 | ||||||
| chr14:102632218
|
GT | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(144): Show | 147 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.361+38909delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632218 | |||||
| chr14:102632218
|
GTT | G | 33 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.361+38908_361+3890 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632218 | |||||
| chr14:102632231
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+38906T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632231 | ||||||
| chr14:102632379
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.361+39054G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632379 | ||||||
| chr14:102632611
|
A | ATCCTT | 9 | a0001c0001t0002g0192a0001c0001t0002g0196a0001c0001t0002g0197others(6): Show | 9 | HG02055.hp2 HG02922.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+39353_361+3935 others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632611
|
A | ATCCTTTC others(3): Show |
4 | a0001c0001t0013g0292a0001c0001t0017g0156a0001c0001t0018g0195others(1): Show | 4 | HG01167.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+39348_361+3935 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632611
|
A | ATCCTTTC others(8): Show |
2 | a0001c0001t0004g0178a0001c0001t0048g0179 | 2 | HG00609.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.361+39343_361+3935 others(19): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632611
|
ATCCTT | A | 48 | a0001c0001t0002g0164a0001c0001t0002g0168a0001c0001t0002g0172others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.361+39353_361+3935 others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632611
|
ATCCTTTC others(3): Show |
A | 17 | a0001c0001t0002g0206a0001c0001t0002g0223a0001c0001t0002g0224others(14): Show | 17 | HG00733.hp1 HG01243.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+39348_361+3935 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632611
|
ATCCTTTC others(8): Show |
A | 14 | a0001c0001t0002g0198a0001c0001t0002g0200a0001c0001t0002g0221others(11): Show | 14 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.361+39343_361+3935 others(19): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632611
|
ATCCTTTC others(13): Show |
A | 11 | a0001c0001t0002g0237a0001c0001t0005g0053a0001c0001t0005g0114others(8): Show | 11 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.361+39338_361+3935 others(24): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632611
|
ATCCTTTC others(18): Show |
A | 2 | a0001c0001t0002g0245a0001c0001t0002g0248 | 2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.361+39333_361+3935 others(29): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632611 | |||||
| chr14:102632633
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.361+39308C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632633 | ||||||
| chr14:102632654
|
CTTTCCTT others(19): Show |
C | 2 | a0001c0001t0008g0263a0001c0001t0019g0259 | 2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.361+39338_361+3936 others(30): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632654 | |||||
| chr14:102632659
|
CTTTCCTT others(14): Show |
C | 6 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0276others(3): Show | 6 | HG01099.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+39343_361+3936 others(25): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632659 | |||||
| chr14:102632660
|
TTTCCTTT others(7): Show |
T | 2 | a0001c0001t0002g0249a0001c0001t0050g0142 | 2 | HG01433.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.361+39338_361+3935 others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632660 | |||||
| chr14:102632664
|
CTTTCCTT others(9): Show |
C | 4 | a0001c0001t0006g0257a0001c0001t0008g0277a0001c0001t0008g0278others(1): Show | 4 | HG01175.hp2 HG01516.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+39348_361+3936 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632664 | |||||
| chr14:102632665
|
TTTCCTTT others(2): Show |
T | 9 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0001g0085others(6): Show | 9 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+39343_361+3935 others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632665 | |||||
| chr14:102632669
|
CTTTCCTT others(4): Show |
C | 2 | a0001c0001t0006g0266a0001c0001t0009g0147 | 2 | HG02976.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.361+39353_361+3936 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632669 | |||||
| chr14:102632670
|
TTTCC | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(38): Show | 41 | HG00673.hp2 HG00735.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.361+39348_361+3935 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632670 | |||||
| chr14:102632674
|
C | CT | 29 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(26): Show | 29 | HG00099.hp2 HG00738.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.361+39352dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632674 | |||||
| chr14:102632674
|
C | CTTTCCT | 25 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0060others(22): Show | 25 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.361+39370_361+3937 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632674 | |||||
| chr14:102632674
|
C | CTTTCCTT others(4): Show |
13 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0076others(10): Show | 13 | HG00280.hp1 HG00733.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.361+39357_361+3935 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632674 | |||||
| chr14:102632674
|
C | CTTTCCTT others(9): Show |
1 | a0001c0001t0011g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.361+39357_361+3935 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632674 | |||||
| chr14:102632674
|
CTTTCCT | C | 16 | a0001c0001t0002g0212a0001c0001t0006g0256a0001c0001t0006g0260others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.361+39370_361+3937 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632674 | |||||
| chr14:102632680
|
T | TTTCC | 9 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(6): Show | 9 | HG01952.hp1 HG02273.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+39357_361+3935 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632680 | |||||
| chr14:102632680
|
T | TTTCCTTT others(2): Show |
3 | a0001c0001t0003g0105a0001c0001t0007g0034a0001c0001t0011g0047 | 3 | HG01175.hp1 HG02055.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.361+39357_361+3935 others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632680 | |||||
| chr14:102632686
|
T | C | 2 | a0001c0001t0009g0002a0001c0001t0031g0001 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.361+39361T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632686 | ||||||
| chr14:102632692
|
TTTTCC | T | 3 | a0001c0001t0001g0077a0001c0001t0008g0277a0001c0001t0008g0278 | 3 | HG02109.hp2 HG02258.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.361+39381_361+3938 others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632692 | |||||
| chr14:102632697
|
C | CT | 16 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0002g0218others(13): Show | 16 | HG00609.hp2 HG01175.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.361+39375dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632697 | |||||
| chr14:102632697
|
CTTTCCTT others(4): Show |
C | 1 | a0001c0001t0015g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.361+39386_361+3939 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632697 | |||||
| chr14:102632702
|
C | T | 2 | a0001c0001t0009g0002a0001c0001t0031g0001 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.361+39377C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632702 | ||||||
| chr14:102632702
|
CTTTCCT | C | 6 | a0001c0001t0001g0161a0001c0001t0009g0143a0001c0001t0009g0144others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+39386_361+3939 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632702 | |||||
| chr14:102632706
|
C | T | 13 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(10): Show | 13 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.361+39381C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632706 | ||||||
| chr14:102632708
|
T | C | 13 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(10): Show | 13 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.361+39383T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632708 | ||||||
| chr14:102632715
|
TTCCTTTC others(22): Show |
T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+39391_361+3941 others(33): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632715 | ||||||
| chr14:102632716
|
T | C | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+39391T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632716 | ||||||
| chr14:102632718
|
C | CT | 13 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(10): Show | 13 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.361+39396dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632718 | |||||
| chr14:102632718
|
C | T | 5 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+39393C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632718 | ||||||
| chr14:102632720
|
T | C | 5 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+39395T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632720 | ||||||
| chr14:102632724
|
T | C | 5 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+39399T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632724 | ||||||
| chr14:102632725
|
T | C | 5 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+39400T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632725 | ||||||
| chr14:102632728
|
T | C | 19 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(16): Show | 19 | HG01175.hp1 HG01891.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.361+39403T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632728 | ||||||
| chr14:102632729
|
T | C | 5 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+39404T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632729 | ||||||
| chr14:102632729
|
T | TCTCCC | 3 | a0001c0001t0002g0162a0001c0001t0002g0224a0001c0001t0004g0215 | 3 | HG02738.hp2 NA18971.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.361+39443_361+3944 others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632729 | |||||
| chr14:102632729
|
T | TCTCCCCT others(3): Show |
1 | a0001c0001t0009g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.361+39438_361+3944 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632729 | |||||
| chr14:102632729
|
TCTCCC | T | 44 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0201others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.361+39443_361+3944 others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632729 | |||||
| chr14:102632729
|
TCTCCCCT others(3): Show |
T | 130 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(127): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.361+39438_361+3944 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632729 | |||||
| chr14:102632729
|
TCTCCCCT others(13): Show |
T | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.361+39428_361+3944 others(24): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632729 | |||||
| chr14:102632730
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(11): Show | 14 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.361+39405C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632730 | ||||||
| chr14:102632734
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(11): Show | 14 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.361+39409C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632734 | ||||||
| chr14:102632735
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(11): Show | 14 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.361+39410C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632735 | ||||||
| chr14:102632738
|
C | T | 13 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(10): Show | 13 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.361+39413C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632738 | ||||||
| chr14:102632739
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(11): Show | 14 | HG01175.hp1 HG01952.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.361+39414C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632739 | ||||||
| chr14:102632740
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+39415C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632740 | ||||||
| chr14:102632743
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+39418C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632743 | ||||||
| chr14:102632744
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+39419C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632744 | ||||||
| chr14:102632763
|
C | T | 1 | a0001c0001t0019g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.361+39438C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632763 | ||||||
| chr14:102632782
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.361+39457C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632782 | ||||||
| chr14:102632792
|
C | CTCTCTCG | 27 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.361+39474_361+3948 others(11): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102632792 | |||||
| chr14:102632792
|
C | G | 1 | a0001c0001t0019g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.361+39467C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632792 | ||||||
| chr14:102632798
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+39473C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102632798 | ||||||
| chr14:102633222
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+39897A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633222 | ||||||
| chr14:102633538
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+40213T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633538 | ||||||
| chr14:102633554
|
C | T | 1 | a0001c0001t0001g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.361+40229C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633554 | ||||||
| chr14:102633611
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+40286C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633611 | ||||||
| chr14:102633612
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+40287T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633612 | ||||||
| chr14:102633616
|
AGCAACTT others(41): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+40292_361+4033 others(52): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633616 | ||||||
| chr14:102633669
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+40344A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633669 | ||||||
| chr14:102633670
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.361+40345G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633670 | ||||||
| chr14:102633685
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.361+40360G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633685 | ||||||
| chr14:102633696
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.361+40371C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633696 | ||||||
| chr14:102633719
|
A | G | 1 | a0001c0001t0033g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.361+40394A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633719 | ||||||
| chr14:102633991
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.361+40666T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102633991 | ||||||
| chr14:102634011
|
G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(141): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.361+40686G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634011 | ||||||
| chr14:102634039
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+40714G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634039 | ||||||
| chr14:102634045
|
C | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+40720C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634045 | ||||||
| chr14:102634335
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.361+41010A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634335 | ||||||
| chr14:102634377
|
A | AAACC | 5 | a0001c0001t0002g0192a0001c0001t0002g0206a0001c0001t0002g0207others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+41069_361+4107 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634377 | |||||
| chr14:102634388
|
C | A | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.361+41063C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634388 | ||||||
| chr14:102634416
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.361+41091C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634416 | ||||||
| chr14:102634601
|
C | CAT | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.361+41276_361+4127 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634601 | ||||||
| chr14:102634601
|
C | CATAT | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.361+41276_361+4127 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634601 | ||||||
| chr14:102634601
|
C | CGT | 5 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+41287_361+4128 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634601 | |||||
| chr14:102634602
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0107 | 2 | HG04115.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.361+41277G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634602 | ||||||
| chr14:102634618
|
A | ATG | 3 | a0001c0001t0001g0107a0001c0001t0005g0059a0001c0001t0005g0120 | 3 | HG02622.hp1 HG03225.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.361+41303_361+4130 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634618 | |||||
| chr14:102634634
|
GTGTATAT others(9): Show |
G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+41324_361+4133 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634634 | |||||
| chr14:102634636
|
G | GTA | 9 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0003g0014others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+41325_361+4132 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634636 | |||||
| chr14:102634636
|
GTA | G | 4 | a0001c0001t0003g0003a0001c0001t0003g0037a0001c0001t0003g0040others(1): Show | 4 | HG01099.hp2 NA18951.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+41325_361+4132 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634636 | |||||
| chr14:102634638
|
A | G | 11 | a0001c0001t0001g0083a0001c0001t0002g0217a0001c0001t0002g0218others(8): Show | 11 | HG00639.hp2 HG00673.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.361+41313A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634638 | ||||||
| chr14:102634640
|
A | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.361+41315A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634640 | ||||||
| chr14:102634663
|
TAC | T | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+41347_361+4134 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634663 | |||||
| chr14:102634671
|
C | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.361+41346C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634671 | ||||||
| chr14:102634708
|
A | T | 2 | a0001c0001t0002g0212a0001c0001t0040g0213 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.361+41383A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634708 | ||||||
| chr14:102634848
|
C | T | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+41523C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634848 | ||||||
| chr14:102634871
|
A | AT | 38 | a0001c0001t0005g0121a0001c0001t0005g0137a0001c0001t0006g0256others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.361+41561dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634871 | |||||
| chr14:102634871
|
A | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01099.hp1 HG01257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.361+41546A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634871 | ||||||
| chr14:102634871
|
AT | A | 10 | a0001c0001t0004g0169a0001c0001t0009g0002a0001c0001t0009g0143others(7): Show | 10 | HG01891.hp1 HG01943.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+41561delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102634871 | |||||
| chr14:102634949
|
C | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.361+41624C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634949 | ||||||
| chr14:102634974
|
A | T | 1 | a0001c0001t0004g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.361+41649A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634974 | ||||||
| chr14:102634998
|
A | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+41673A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102634998 | ||||||
| chr14:102635054
|
G | C | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.361+41729G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635054 | ||||||
| chr14:102635082
|
C | T | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.361+41757C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635082 | ||||||
| chr14:102635199
|
C | A | 2 | a0001c0001t0005g0138a0001c0001t0013g0123 | 2 | HG01243.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.361+41874C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635199 | ||||||
| chr14:102635265
|
C | T | 1 | a0001c0003t0005g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.361+41940C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635265 | ||||||
| chr14:102635369
|
T | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361+42044T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635369 | ||||||
| chr14:102635486
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.361+42161A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635486 | ||||||
| chr14:102635943
|
C | T | 1 | a0001c0001t0032g0057 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.361+42618C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635943 | ||||||
| chr14:102635978
|
T | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0037a0001c0001t0003g0040 | 3 | NA18951.hp1 NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.361+42653T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635978 | ||||||
| chr14:102635982
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.361+42657G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102635982 | ||||||
| chr14:102636033
|
C | T | 1 | a0001c0001t0002g0233 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.361+42708C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636033 | ||||||
| chr14:102636127
|
A | G | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.361+42802A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636127 | ||||||
| chr14:102636174
|
G | A | 1 | a0001c0001t0035g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361+42849G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636174 | ||||||
| chr14:102636218
|
G | A | 1 | a0001c0001t0022g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.361+42893G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636218 | ||||||
| chr14:102636224
|
A | C | 1 | a0001c0001t0003g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.361+42899A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636224 | ||||||
| chr14:102636261
|
A | T | 2 | a0001c0001t0038g0155a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.361+42936A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636261 | ||||||
| chr14:102636262
|
T | A | 2 | a0001c0001t0002g0245a0001c0001t0002g0248 | 2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.361+42937T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636262 | ||||||
| chr14:102636587
|
A | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+43262A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636587 | ||||||
| chr14:102636744
|
C | T | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.361+43419C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636744 | ||||||
| chr14:102636768
|
G | A | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+43443G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636768 | ||||||
| chr14:102636880
|
T | TG | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+43557dupG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102636880 | |||||
| chr14:102636974
|
A | G | 1 | a0001c0001t0019g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.361+43649A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102636974 | ||||||
| chr14:102637024
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.361+43699T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637024 | ||||||
| chr14:102637107
|
T | G | 1 | a0001c0001t0002g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.361+43782T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637107 | ||||||
| chr14:102637107
|
TTTTG | T | 4 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0201others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+43798_361+4380 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102637107 | |||||
| chr14:102637127
|
T | G | 1 | a0001c0002t0003g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.361+43802T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637127 | ||||||
| chr14:102637131
|
A | AT | 34 | a0001c0001t0002g0231a0001c0001t0005g0004a0001c0001t0005g0116others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.361+43819dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102637131 | |||||
| chr14:102637131
|
AT | A | 8 | a0001c0001t0002g0241a0001c0001t0009g0002a0001c0001t0009g0143others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+43819delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102637131 | |||||
| chr14:102637136
|
T | A | 1 | a0001c0001t0002g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.361+43811T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637136 | ||||||
| chr14:102637137
|
T | A | 1 | a0001c0001t0003g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.361+43812T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637137 | ||||||
| chr14:102637138
|
T | A | 1 | a0001c0001t0005g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361+43813T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637138 | ||||||
| chr14:102637195
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.361+43870C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637195 | ||||||
| chr14:102637252
|
G | C | 1 | a0001c0001t0004g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.361+43927G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637252 | ||||||
| chr14:102637316
|
G | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+43991G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637316 | ||||||
| chr14:102637407
|
C | T | 1 | a0001c0001t0046g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.361+44082C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637407 | ||||||
| chr14:102637408
|
T | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.361+44083T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637408 | ||||||
| chr14:102637539
|
C | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.361+44214C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637539 | ||||||
| chr14:102637661
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-44234G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637661 | ||||||
| chr14:102637668
|
C | T | 1 | a0001c0002t0003g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.362-44227C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637668 | ||||||
| chr14:102637965
|
T | G | 1 | a0001c0001t0027g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.362-43930T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102637965 | ||||||
| chr14:102638068
|
C | G | 2 | a0001c0001t0003g0093a0001c0001t0011g0047 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.362-43827C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102638068 | ||||||
| chr14:102638362
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-43533C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102638362 | ||||||
| chr14:102638470
|
C | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.362-43425C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102638470 | ||||||
| chr14:102638471
|
G | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0135 | 2 | HG02040.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.362-43424G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102638471 | ||||||
| chr14:102638758
|
C | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-43137C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102638758 | ||||||
| chr14:102639021
|
T | C | 1 | a0001c0001t0046g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-42874T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639021 | ||||||
| chr14:102639264
|
CT | C | 76 | a0001c0001t0001g0076a0001c0001t0002g0242a0001c0001t0003g0003others(73): Show | 76 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.362-42613delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639264 | |||||
| chr14:102639264
|
CTT | C | 113 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.362-42614_362-4261 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639264 | |||||
| chr14:102639455
|
T | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.362-42440T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639455 | ||||||
| chr14:102639497
|
T | TTTTA | 34 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0063others(31): Show | 34 | HG00735.hp1 HG01175.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.362-42347_362-4234 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639497
|
T | TTTTATTT others(1): Show |
8 | a0001c0001t0001g0098a0001c0001t0002g0284a0001c0001t0002g0285others(5): Show | 8 | HG01993.hp1 HG01993.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-42351_362-4234 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639497
|
TTTTA | T | 83 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(80): Show | 83 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.362-42347_362-4234 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639497
|
TTTTATTT others(1): Show |
T | 30 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0082others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.362-42351_362-4234 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639497
|
TTTTATTT others(5): Show |
T | 14 | a0001c0001t0001g0066a0001c0001t0005g0053a0001c0001t0005g0059others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.362-42355_362-4234 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639497
|
TTTTATTT others(9): Show |
T | 2 | a0001c0001t0002g0200a0001c0001t0013g0291 | 2 | HG00733.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.362-42359_362-4234 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639497
|
TTTTATTT others(13): Show |
T | 4 | a0001c0001t0005g0116a0001c0001t0005g0132a0001c0001t0005g0138others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-42363_362-4234 others(24): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639497
|
TTTTATTT others(29): Show |
T | 1 | a0001c0001t0005g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.362-42379_362-4234 others(40): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639497 | |||||
| chr14:102639662
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.362-42233T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639662 | ||||||
| chr14:102639816
|
A | AGC | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-42079_362-4207 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639816 | ||||||
| chr14:102639822
|
A | C | 186 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.362-42073A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639822 | ||||||
| chr14:102639822
|
A | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-42073A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639822 | ||||||
| chr14:102639827
|
A | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-42068A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639827 | ||||||
| chr14:102639831
|
T | TATTC | 3 | a0001c0001t0002g0218a0001c0001t0014g0194a0001c0001t0014g0199 | 3 | HG03098.hp1 HG03453.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.362-42033_362-4203 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639831 | |||||
| chr14:102639831
|
TATTC | T | 178 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.362-42033_362-4203 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639831 | |||||
| chr14:102639831
|
TATTCATT others(5): Show |
T | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362-42041_362-4203 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102639831 | |||||
| chr14:102639870
|
C | T | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.362-42025C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639870 | ||||||
| chr14:102639882
|
C | G | 1 | a0001c0001t0003g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.362-42013C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639882 | ||||||
| chr14:102639887
|
C | G | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-42008C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639887 | ||||||
| chr14:102639903
|
A | G | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.362-41992A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102639903 | ||||||
| chr14:102640184
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.362-41711G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640184 | ||||||
| chr14:102640223
|
C | T | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.362-41672C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640223 | ||||||
| chr14:102640274
|
A | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.362-41621A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640274 | ||||||
| chr14:102640611
|
G | A | 1 | a0001c0001t0034g0039 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.362-41284G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640611 | ||||||
| chr14:102640628
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.362-41267G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640628 | ||||||
| chr14:102640639
|
C | T | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-41256C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640639 | ||||||
| chr14:102640651
|
CACTT | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-41242_362-4123 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102640651 | |||||
| chr14:102640738
|
A | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-41157A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640738 | ||||||
| chr14:102640783
|
AAACCCCG others(4): Show |
A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-41110_362-4110 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102640783 | |||||
| chr14:102640798
|
G | T | 1 | a0001c0001t0046g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-41097G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640798 | ||||||
| chr14:102640815
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0135 | 2 | HG02040.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.362-41080C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640815 | ||||||
| chr14:102640903
|
T | G | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-40992T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102640903 | ||||||
| chr14:102641194
|
G | A | 1 | a0001c0001t0005g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.362-40701G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102641194 | ||||||
| chr14:102641311
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.362-40584T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102641311 | ||||||
| chr14:102641370
|
C | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-40525C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102641370 | ||||||
| chr14:102641589
|
G | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-40306G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102641589 | ||||||
| chr14:102641611
|
A | T | 40 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.362-40284A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102641611 | ||||||
| chr14:102641754
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.362-40141A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102641754 | ||||||
| chr14:102641883
|
A | G | 1 | a0001c0003t0005g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.362-40012A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102641883 | ||||||
| chr14:102642141
|
C | T | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.362-39754C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642141 | ||||||
| chr14:102642184
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-39711C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642184 | ||||||
| chr14:102642237
|
A | T | 1 | a0001c0001t0002g0248 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.362-39658A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642237 | ||||||
| chr14:102642243
|
C | CTTTG | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.362-39651_362-3964 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102642243 | |||||
| chr14:102642315
|
T | G | 1 | a0001c0001t0051g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.362-39580T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642315 | ||||||
| chr14:102642354
|
C | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-39541C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642354 | ||||||
| chr14:102642505
|
C | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.362-39390C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642505 | ||||||
| chr14:102642659
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.362-39236G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642659 | ||||||
| chr14:102642730
|
G | A | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.362-39165G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642730 | ||||||
| chr14:102642805
|
C | G | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-39090C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642805 | ||||||
| chr14:102642823
|
T | G | 1 | a0001c0001t0002g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.362-39072T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642823 | ||||||
| chr14:102642869
|
C | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-39026C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102642869 | ||||||
| chr14:102643085
|
A | G | 1 | a0001c0001t0003g0040 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.362-38810A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643085 | ||||||
| chr14:102643090
|
G | GACCTCA | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-38805_362-3880 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643090 | ||||||
| chr14:102643091
|
G | C | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-38804G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643091 | ||||||
| chr14:102643094
|
A | G | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-38801A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643094 | ||||||
| chr14:102643283
|
CAA | C | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-38605_362-3860 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102643283 | |||||
| chr14:102643331
|
A | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.362-38564A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643331 | ||||||
| chr14:102643404
|
A | T | 1 | a0001c0001t0002g0248 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.362-38491A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643404 | ||||||
| chr14:102643426
|
A | G | 1 | a0001c0001t0010g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.362-38469A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643426 | ||||||
| chr14:102643491
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.362-38404C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643491 | ||||||
| chr14:102643554
|
G | C | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-38341G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643554 | ||||||
| chr14:102643916
|
T | A | 2 | a0001c0001t0007g0024a0001c0001t0007g0048 | 2 | NA18960.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.362-37979T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643916 | ||||||
| chr14:102643963
|
T | A | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.362-37932T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102643963 | ||||||
| chr14:102644002
|
T | A | 2 | a0001c0001t0002g0212a0001c0001t0040g0213 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.362-37893T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644002 | ||||||
| chr14:102644025
|
A | G | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.362-37870A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644025 | ||||||
| chr14:102644193
|
A | G | 46 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.362-37702A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644193 | ||||||
| chr14:102644238
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0135 | 2 | HG02040.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.362-37657G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644238 | ||||||
| chr14:102644296
|
A | T | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.362-37599A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644296 | ||||||
| chr14:102644430
|
A | G | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.362-37465A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644430 | ||||||
| chr14:102644559
|
C | T | 4 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0201others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-37336C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644559 | ||||||
| chr14:102644619
|
C | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-37276C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644619 | ||||||
| chr14:102644818
|
G | A | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-37077G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644818 | ||||||
| chr14:102644916
|
C | T | 3 | a0001c0001t0002g0212a0001c0001t0040g0213a0001c0001t0045g0203 | 3 | HG01884.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.362-36979C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102644916 | ||||||
| chr14:102645021
|
T | C | 125 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.362-36874T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645021 | ||||||
| chr14:102645112
|
A | C | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.362-36783A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645112 | ||||||
| chr14:102645128
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-36767C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645128 | ||||||
| chr14:102645170
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.362-36725T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645170 | ||||||
| chr14:102645247
|
T | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-36648T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645247 | ||||||
| chr14:102645396
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.362-36499A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645396 | ||||||
| chr14:102645460
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-36435G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645460 | ||||||
| chr14:102645486
|
T | C | 38 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.362-36409T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645486 | ||||||
| chr14:102645729
|
C | T | 2 | a0001c0001t0005g0053a0001c0001t0005g0114 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.362-36166C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645729 | ||||||
| chr14:102645737
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-36158C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645737 | ||||||
| chr14:102645862
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-36033G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102645862 | ||||||
| chr14:102646090
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.362-35805A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102646090 | ||||||
| chr14:102646231
|
C | T | 1 | a0001c0002t0003g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.362-35664C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102646231 | ||||||
| chr14:102646254
|
T | C | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-35641T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102646254 | ||||||
| chr14:102646637
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.362-35258A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102646637 | ||||||
| chr14:102646872
|
C | T | 3 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145 | 3 | HG01891.hp1 HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.362-35023C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102646872 | ||||||
| chr14:102647077
|
G | C | 291 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.362-34818G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647077 | ||||||
| chr14:102647215
|
G | A | 284 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.362-34680G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647215 | ||||||
| chr14:102647385
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0011g0047 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.362-34510C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647385 | ||||||
| chr14:102647736
|
T | G | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-34159T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647736 | ||||||
| chr14:102647754
|
T | C | 165 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(162): Show | 165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.362-34141T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647754 | ||||||
| chr14:102647774
|
A | T | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-34121A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647774 | ||||||
| chr14:102647793
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-34102C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647793 | ||||||
| chr14:102647823
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-34072C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647823 | ||||||
| chr14:102647832
|
C | T | 1 | a0001c0001t0041g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.362-34063C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647832 | ||||||
| chr14:102647990
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-33905A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102647990 | ||||||
| chr14:102648109
|
T | C | 1 | a0001c0001t0002g0284 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.362-33786T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102648109 | ||||||
| chr14:102648177
|
C | T | 2 | a0001c0001t0003g0006a0001c0001t0003g0046 | 2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.362-33718C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102648177 | ||||||
| chr14:102648284
|
G | A | 1 | a0001c0001t0010g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.362-33611G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102648284 | ||||||
| chr14:102648608
|
A | G | 97 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(94): Show | 97 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.362-33287A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102648608 | ||||||
| chr14:102648831
|
T | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-33064T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102648831 | ||||||
| chr14:102648877
|
C | A | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362-33018C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102648877 | ||||||
| chr14:102649064
|
AAC | A | 10 | a0001c0001t0002g0218a0001c0001t0002g0223a0001c0001t0002g0230others(7): Show | 10 | HG00673.hp1 HG01192.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.362-32829_362-3282 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102649064 | |||||
| chr14:102649065
|
AC | A | 76 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(73): Show | 76 | HG00423.hp2 HG00609.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.362-32829delC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649065 | ||||||
| chr14:102649066
|
C | A | 12 | a0001c0001t0002g0192a0001c0001t0002g0207a0001c0001t0002g0211others(9): Show | 12 | HG02055.hp2 HG02148.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.362-32829C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649066 | ||||||
| chr14:102649066
|
C | CA | 6 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0013g0291others(3): Show | 6 | HG00733.hp1 HG01167.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-32819dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102649066 | |||||
| chr14:102649067
|
A | C | 4 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(1): Show | 4 | HG03139.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-32828A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649067 | ||||||
| chr14:102649113
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.362-32782A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649113 | ||||||
| chr14:102649160
|
C | G | 1 | a0001c0001t0003g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.362-32735C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649160 | ||||||
| chr14:102649188
|
A | G | 1 | a0001c0001t0009g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.362-32707A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649188 | ||||||
| chr14:102649368
|
T | C | 1 | a0001c0001t0028g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.362-32527T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649368 | ||||||
| chr14:102649925
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.362-31970C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102649925 | ||||||
| chr14:102650005
|
T | C | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.362-31890T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650005 | ||||||
| chr14:102650067
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-31828G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650067 | ||||||
| chr14:102650067
|
G | C | 1 | a0001c0001t0002g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.362-31828G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650067 | ||||||
| chr14:102650195
|
C | T | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-31700C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650195 | ||||||
| chr14:102650197
|
C | CA | 32 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0083others(29): Show | 32 | HG00609.hp1 HG00673.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.362-31681dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102650197 | |||||
| chr14:102650197
|
C | CAA | 6 | a0001c0001t0004g0187a0001c0001t0009g0143a0001c0001t0009g0144others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-31682_362-3168 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102650197 | |||||
| chr14:102650197
|
CA | C | 34 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.362-31681delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102650197 | |||||
| chr14:102650210
|
A | G | 1 | a0001c0001t0019g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.362-31685A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650210 | ||||||
| chr14:102650252
|
T | G | 1 | a0001c0001t0002g0238 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.362-31643T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650252 | ||||||
| chr14:102650261
|
C | T | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.362-31634C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650261 | ||||||
| chr14:102650386
|
A | ATGGG | 36 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.362-31489_362-3148 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102650386 | |||||
| chr14:102650386
|
ATGGG | A | 20 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0065others(17): Show | 20 | HG02027.hp1 HG02040.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.362-31489_362-3148 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102650386 | |||||
| chr14:102650483
|
G | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-31412G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650483 | ||||||
| chr14:102650580
|
T | C | 1 | a0001c0001t0004g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.362-31315T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650580 | ||||||
| chr14:102650691
|
A | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-31204A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650691 | ||||||
| chr14:102650748
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-31147A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650748 | ||||||
| chr14:102650942
|
C | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-30953C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650942 | ||||||
| chr14:102650989
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-30906A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102650989 | ||||||
| chr14:102651052
|
A | G | 166 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(163): Show | 166 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.362-30843A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651052 | ||||||
| chr14:102651109
|
T | C | 2 | a0001c0001t0010g0064a0001c0001t0010g0104 | 2 | NA18939.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.362-30786T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651109 | ||||||
| chr14:102651291
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-30604A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651291 | ||||||
| chr14:102651330
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.362-30565G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651330 | ||||||
| chr14:102651336
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.362-30559T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651336 | ||||||
| chr14:102651381
|
C | T | 3 | a0001c0001t0002g0221a0001c0001t0002g0237a0001c0001t0018g0239 | 3 | NA18979.hp1 NA19070.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.362-30514C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651381 | ||||||
| chr14:102651514
|
C | G | 38 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.362-30381C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651514 | ||||||
| chr14:102651552
|
C | CA | 10 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(7): Show | 10 | HG01099.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.362-30331dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102651552 | |||||
| chr14:102651575
|
A | G | 2 | a0001c0001t0024g0062a0001c0001t0033g0255 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.362-30320A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651575 | ||||||
| chr14:102651595
|
G | A | 291 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.362-30300G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651595 | ||||||
| chr14:102651706
|
G | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-30189G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651706 | ||||||
| chr14:102651934
|
G | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.362-29961G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102651934 | ||||||
| chr14:102652236
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.362-29659G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102652236 | ||||||
| chr14:102652486
|
G | GTT | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-29406_362-2940 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102652486 | |||||
| chr14:102652552
|
G | A | 1 | a0001c0001t0004g0180 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.362-29343G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102652552 | ||||||
| chr14:102652644
|
C | G | 1 | a0001c0001t0014g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.362-29251C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102652644 | ||||||
| chr14:102652837
|
A | G | 2 | a0001c0001t0003g0014a0001c0001t0003g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.362-29058A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102652837 | ||||||
| chr14:102652880
|
A | C | 1 | a0001c0001t0014g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.362-29015A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102652880 | ||||||
| chr14:102652993
|
C | T | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.362-28902C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102652993 | ||||||
| chr14:102653023
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.362-28872C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653023 | ||||||
| chr14:102653073
|
G | C | 146 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(143): Show | 146 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.362-28822G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653073 | ||||||
| chr14:102653079
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.362-28816C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653079 | ||||||
| chr14:102653088
|
C | T | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-28807C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653088 | ||||||
| chr14:102653304
|
C | T | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.362-28591C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653304 | ||||||
| chr14:102653327
|
T | C | 1 | a0001c0001t0026g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.362-28568T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653327 | ||||||
| chr14:102653369
|
C | A | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.362-28526C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653369 | ||||||
| chr14:102653374
|
G | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-28521G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653374 | ||||||
| chr14:102653427
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.362-28468C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653427 | ||||||
| chr14:102653463
|
C | T | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-28432C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653463 | ||||||
| chr14:102653503
|
T | G | 1 | a0001c0001t0003g0070 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.362-28392T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653503 | ||||||
| chr14:102653683
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-28212C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653683 | ||||||
| chr14:102653867
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-28028G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653867 | ||||||
| chr14:102653920
|
C | CTTCT | 8 | a0001c0001t0001g0010a0001c0001t0001g0066a0001c0001t0001g0091others(5): Show | 8 | HG00738.hp1 HG02895.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-27912_362-2790 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
C | CTTCTTTC others(5): Show |
4 | a0001c0001t0003g0003a0001c0001t0003g0037a0001c0001t0026g0069others(1): Show | 4 | HG02738.hp1 NA18951.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-27920_362-2790 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
C | CTTCTTTC others(9): Show |
1 | a0001c0001t0003g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.362-27924_362-2790 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
C | CTTCTTTC others(13): Show |
2 | a0001c0001t0001g0109a0001c0001t0003g0023 | 2 | HG02976.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.362-27928_362-2790 others(24): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
C | CTTCTTTC others(17): Show |
1 | a0001c0001t0001g0087 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.362-27932_362-2790 others(28): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
C | CTTCTTTC others(21): Show |
1 | a0001c0001t0001g0005 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.362-27936_362-2790 others(32): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
CTTCT | C | 12 | a0001c0001t0001g0029a0001c0001t0001g0074a0001c0001t0001g0082others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.362-27912_362-2790 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
CTTCTTTC others(1): Show |
C | 14 | a0001c0001t0001g0111a0001c0001t0002g0205a0001c0001t0002g0237others(11): Show | 14 | HG00323.hp1 HG01515.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.362-27916_362-2790 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
CTTCTTTC others(5): Show |
C | 13 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0073others(10): Show | 13 | HG00639.hp1 HG01074.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-27920_362-2790 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
CTTCTTTC others(9): Show |
C | 2 | a0001c0001t0001g0079a0001c0001t0007g0253 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.362-27924_362-2790 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
CTTCTTTC others(17): Show |
C | 2 | a0001c0001t0003g0015a0001c0002t0011g0054 | 2 | HG01261.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.362-27932_362-2790 others(28): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
CTTCTTTC others(21): Show |
C | 2 | a0001c0001t0005g0053a0001c0001t0005g0114 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.362-27936_362-2790 others(32): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653920
|
CTTCTTTC others(25): Show |
C | 11 | a0001c0001t0005g0004a0001c0001t0005g0059a0001c0001t0005g0119others(8): Show | 11 | HG00639.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.362-27940_362-2790 others(36): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653920 | |||||
| chr14:102653924
|
T | C | 2 | a0001c0001t0002g0246a0001c0001t0027g0099 | 2 | HG02027.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.362-27971T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653924 | ||||||
| chr14:102653941
|
TTCTTTCT others(31): Show |
T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-27952_362-2791 others(42): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653941 | |||||
| chr14:102653942
|
TCTTTCTT others(34): Show |
T | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-27952_362-2791 others(45): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653942 | ||||||
| chr14:102653944
|
TTTCTTTC others(4): Show |
T | 1 | a0001c0001t0004g0215 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.362-27948_362-2793 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653944 | |||||
| chr14:102653944
|
TTTCTTTC others(28): Show |
T | 24 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.362-27948_362-2791 others(39): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653944 | |||||
| chr14:102653945
|
TTCTTTCT others(27): Show |
T | 11 | a0001c0001t0006g0274a0001c0001t0008g0280a0001c0001t0012g0153others(8): Show | 11 | HG01099.hp2 HG01175.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-27948_362-2791 others(38): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653945 | |||||
| chr14:102653948
|
TTTCTTTC others(24): Show |
T | 6 | a0001c0001t0005g0116a0001c0001t0005g0118a0001c0001t0005g0120others(3): Show | 6 | HG02647.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-27944_362-2791 others(35): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653948 | |||||
| chr14:102653949
|
TTCTTTCT others(23): Show |
T | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.362-27944_362-2791 others(34): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653949 | |||||
| chr14:102653949
|
TTCTTTCT others(27): Show |
T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-27944_362-2791 others(38): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653949 | |||||
| chr14:102653950
|
TCTTTCTT others(26): Show |
T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-27944_362-2791 others(37): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653950 | ||||||
| chr14:102653957
|
T | C | 1 | a0001c0001t0004g0215 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.362-27938T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653957 | ||||||
| chr14:102653957
|
TTCTTTCT others(3): Show |
T | 1 | a0001c0001t0040g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.362-27936_362-2792 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653957 | |||||
| chr14:102653957
|
TTCTTTCT others(19): Show |
T | 1 | a0001c0001t0014g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.362-27936_362-2791 others(30): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653957 | |||||
| chr14:102653959
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.362-27936C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653959 | ||||||
| chr14:102653960
|
TTTCTTTC others(16): Show |
T | 1 | a0001c0002t0003g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.362-27932_362-2791 others(27): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653960 | |||||
| chr14:102653961
|
TTCTTTCT others(15): Show |
T | 2 | a0001c0001t0002g0172a0001c0001t0002g0181 | 2 | HG02004.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.362-27932_362-2791 others(26): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653961 | |||||
| chr14:102653962
|
TCTTTCTT others(14): Show |
T | 2 | a0001c0001t0035g0251a0001c0001t0042g0228 | 2 | HG02080.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.362-27932_362-2791 others(25): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653962 | ||||||
| chr14:102653963
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.362-27932C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653963 | ||||||
| chr14:102653965
|
TTCTTTCT others(11): Show |
T | 8 | a0001c0001t0002g0218a0001c0001t0002g0224a0001c0001t0002g0229others(5): Show | 8 | HG00735.hp2 HG01496.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-27928_362-2791 others(22): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653965 | |||||
| chr14:102653966
|
TCTTTCTT others(10): Show |
T | 4 | a0001c0001t0002g0242a0001c0001t0004g0185a0001c0001t0007g0220others(1): Show | 4 | HG01243.hp1 HG01993.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-27928_362-2791 others(21): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653966 | ||||||
| chr14:102653967
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.362-27928C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653967 | ||||||
| chr14:102653968
|
TTTCTTTC others(8): Show |
T | 6 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0241others(3): Show | 6 | HG00735.hp1 HG01175.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-27924_362-2791 others(19): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653968 | |||||
| chr14:102653969
|
TTCTTTCT others(7): Show |
T | 23 | a0001c0001t0002g0168a0001c0001t0002g0182a0001c0001t0002g0209others(20): Show | 23 | HG00673.hp1 HG01934.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.362-27924_362-2791 others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653969 | |||||
| chr14:102653970
|
TCTTTCTT others(6): Show |
T | 11 | a0001c0001t0002g0164a0001c0001t0002g0198a0001c0001t0002g0225others(8): Show | 11 | HG00423.hp2 HG01261.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.362-27924_362-2791 others(17): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653970 | ||||||
| chr14:102653971
|
C | T | 2 | a0001c0001t0002g0212a0001c0001t0040g0213 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.362-27924C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653971 | ||||||
| chr14:102653971
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0004g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.362-27920_362-2790 others(17): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653971 | |||||
| chr14:102653972
|
TTTCTTTC others(4): Show |
T | 6 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0110others(3): Show | 6 | HG00673.hp2 HG00738.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-27920_362-2791 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653972 | |||||
| chr14:102653973
|
TTCTTTCT others(3): Show |
T | 10 | a0001c0001t0002g0204a0001c0001t0002g0208a0001c0001t0002g0217others(7): Show | 10 | HG01081.hp1 HG02015.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.362-27920_362-2791 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653973 | |||||
| chr14:102653974
|
TCTTTCTT others(2): Show |
T | 8 | a0001c0001t0002g0162a0001c0001t0002g0200a0001c0001t0002g0221others(5): Show | 8 | HG01192.hp1 HG01358.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.362-27920_362-2791 others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653974 | ||||||
| chr14:102653975
|
C | T | 2 | a0001c0001t0002g0212a0001c0001t0040g0213 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.362-27920C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653975 | ||||||
| chr14:102653977
|
TTCTTTC | T | 7 | a0001c0001t0002g0163a0001c0001t0002g0232a0001c0001t0002g0236others(4): Show | 7 | HG01123.hp1 HG02040.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.362-27916_362-2791 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653977 | |||||
| chr14:102653979
|
C | T | 3 | a0001c0001t0002g0212a0001c0001t0038g0155a0001c0001t0040g0213 | 3 | HG01891.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.362-27916C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653979 | ||||||
| chr14:102653980
|
TTTC | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0061others(7): Show | 10 | HG02735.hp1 HG02922.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.362-27912_362-2791 others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653980 | |||||
| chr14:102653983
|
C | CTTTCTTT others(3): Show |
1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.362-27909_362-2790 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653983 | |||||
| chr14:102653983
|
C | CTTTCTTT others(6): Show |
2 | a0001c0001t0001g0072a0001c0001t0001g0084 | 2 | HG01257.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.362-27909_362-2790 others(17): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653983 | |||||
| chr14:102653983
|
C | CTTTCTTT others(8): Show |
1 | a0001c0001t0002g0197 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.362-27909_362-2790 others(19): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653983 | |||||
| chr14:102653983
|
C | CTTTCTTT others(14): Show |
1 | a0001c0001t0001g0100 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.362-27909_362-2790 others(25): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653983 | |||||
| chr14:102653983
|
C | CTTTCTTT others(34): Show |
1 | a0001c0001t0001g0063 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.362-27909_362-2790 others(45): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653983 | |||||
| chr14:102653983
|
C | G | 1 | a0001c0001t0003g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.362-27912C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653983 | ||||||
| chr14:102653983
|
C | T | 66 | a0001c0001t0002g0205a0001c0001t0002g0212a0001c0001t0002g0237others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.362-27912C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653983 | ||||||
| chr14:102653984
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.362-27911T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653984 | ||||||
| chr14:102653984
|
T | TTTCTTTC others(4): Show |
2 | a0001c0001t0002g0201a0001c0001t0003g0070 | 2 | HG01256.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.362-27909_362-2790 others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653984 | |||||
| chr14:102653984
|
T | TTTCTTTC others(8): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0085 | 2 | HG00423.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.362-27909_362-2790 others(19): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653984 | |||||
| chr14:102653984
|
T | TTTCTTTC others(44): Show |
1 | a0001c0001t0003g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.362-27909_362-2790 others(55): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653984 | |||||
| chr14:102653984
|
T | TTTCTTTC others(56): Show |
2 | a0001c0001t0003g0030a0001c0001t0003g0105 | 2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.362-27909_362-2790 others(67): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653984 | |||||
| chr14:102653984
|
T | TTTCTTTG others(52): Show |
1 | a0001c0001t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.362-27909_362-2790 others(63): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653984 | |||||
| chr14:102653985
|
T | TTCTTTCT others(3): Show |
1 | a0001c0001t0007g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.362-27909_362-2790 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102653985 | |||||
| chr14:102653986
|
T | TCTTTCTT others(14): Show |
1 | a0001c0001t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.362-27909_362-2790 others(25): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653986 | ||||||
| chr14:102653986
|
T | TCTTTCTT others(34): Show |
1 | a0001c0001t0001g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.362-27909_362-2790 others(45): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653986 | ||||||
| chr14:102653987
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0109a0001c0001t0003g0023 | 3 | HG02976.hp1 NA18967.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.362-27908T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653987 | ||||||
| chr14:102653988
|
T | C | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-27907T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102653988 | ||||||
| chr14:102654025
|
G | T | 1 | a0001c0001t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362-27870G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102654025 | ||||||
| chr14:102654078
|
C | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-27817C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102654078 | ||||||
| chr14:102654727
|
A | T | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.362-27168A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102654727 | ||||||
| chr14:102654786
|
G | GT | 15 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0084others(12): Show | 15 | HG01074.hp1 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.362-27089dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102654786 | |||||
| chr14:102654786
|
G | GTT | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-27090_362-2708 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102654786 | |||||
| chr14:102654786
|
GT | G | 132 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0168others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.362-27089delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102654786 | |||||
| chr14:102654794
|
T | G | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.362-27101T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102654794 | ||||||
| chr14:102654806
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.362-27089T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102654806 | ||||||
| chr14:102654819
|
C | CT | 44 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.362-27067dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102654819 | |||||
| chr14:102654895
|
G | A | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-27000G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102654895 | ||||||
| chr14:102655007
|
T | A | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-26888T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655007 | ||||||
| chr14:102655044
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-26851C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655044 | ||||||
| chr14:102655110
|
CT | C | 172 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(169): Show | 172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.362-26760delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655110 | |||||
| chr14:102655110
|
CTT | C | 32 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0002g0206others(29): Show | 32 | HG01099.hp2 HG01167.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.362-26761_362-2676 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655110 | |||||
| chr14:102655110
|
CTTT | C | 20 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(17): Show | 20 | HG00099.hp1 HG01081.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.362-26762_362-2676 others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655110 | |||||
| chr14:102655110
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0186 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.362-26769_362-2676 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655110 | |||||
| chr14:102655135
|
T | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-26760T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655135 | ||||||
| chr14:102655168
|
A | G | 2 | a0001c0001t0002g0217a0001c0001t0002g0254 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.362-26727A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655168 | ||||||
| chr14:102655226
|
A | G | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-26669A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655226 | ||||||
| chr14:102655447
|
T | A | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-26448T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655447 | ||||||
| chr14:102655542
|
C | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-26353C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655542 | ||||||
| chr14:102655544
|
A | G | 1 | a0001c0001t0007g0219 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.362-26351A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655544 | ||||||
| chr14:102655738
|
A | G | 3 | a0001c0001t0002g0192a0001c0001t0002g0207a0001c0001t0002g0211 | 3 | HG02055.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.362-26157A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655738 | ||||||
| chr14:102655813
|
T | C | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-26082T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655813 | ||||||
| chr14:102655951
|
T | TCA | 69 | a0001c0001t0001g0082a0001c0001t0002g0162a0001c0001t0002g0164others(66): Show | 69 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.362-25908_362-2590 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
T | TCACA | 47 | a0001c0001t0001g0033a0001c0001t0001g0074a0001c0001t0001g0075others(44): Show | 47 | HG00423.hp1 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.362-25910_362-2590 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
T | TCACACA | 47 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0060others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-25912_362-2590 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
T | TCACACAC others(1): Show |
46 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(43): Show | 46 | HG00323.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.362-25914_362-2590 others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
T | TCACACAC others(3): Show |
10 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0083others(7): Show | 10 | HG00673.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.362-25916_362-2590 others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
T | TCACACAC others(5): Show |
3 | a0001c0001t0006g0267a0001c0001t0006g0275a0001c0001t0010g0058 | 3 | HG00280.hp2 HG01981.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.362-25918_362-2590 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0007 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.362-25922_362-2590 others(20): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
TCA | T | 7 | a0001c0001t0002g0212a0001c0001t0003g0003a0001c0001t0003g0037others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-25908_362-2590 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
TCACA | T | 34 | a0001c0001t0001g0009a0001c0001t0003g0006a0001c0001t0003g0008others(31): Show | 34 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.362-25910_362-2590 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
TCACACA | T | 3 | a0001c0001t0003g0028a0001c0001t0007g0024a0001c0001t0007g0048 | 3 | HG03017.hp2 NA18960.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.362-25912_362-2590 others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
TCACACAC others(5): Show |
T | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0003g0020 | 3 | HG01496.hp2 NA18972.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.362-25918_362-2590 others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655951
|
TCACACAC others(7): Show |
T | 1 | a0001c0001t0005g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.362-25920_362-2590 others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102655951 | |||||
| chr14:102655970
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-25925C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102655970 | ||||||
| chr14:102656137
|
A | T | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-25758A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656137 | ||||||
| chr14:102656207
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.362-25688T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656207 | ||||||
| chr14:102656254
|
C | A | 2 | a0001c0001t0016g0281a0001c0001t0016g0282 | 2 | NA18967.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.362-25641C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656254 | ||||||
| chr14:102656303
|
C | G | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-25592C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656303 | ||||||
| chr14:102656340
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0254 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.362-25555T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656340 | ||||||
| chr14:102656351
|
C | G | 2 | a0001c0001t0002g0217a0001c0001t0002g0254 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.362-25544C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656351 | ||||||
| chr14:102656362
|
C | G | 2 | a0001c0001t0002g0164a0001c0001t0002g0233 | 2 | HG00423.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.362-25533C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656362 | ||||||
| chr14:102656399
|
G | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.362-25496G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656399 | ||||||
| chr14:102656556
|
C | T | 2 | a0001c0001t0020g0289a0001c0001t0020g0290 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362-25339C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656556 | ||||||
| chr14:102656607
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.362-25288G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656607 | ||||||
| chr14:102656777
|
C | CT | 15 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0004g0165others(12): Show | 15 | HG01261.hp2 HG01358.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.362-25114dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102656777 | |||||
| chr14:102656782
|
C | T | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-25113C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656782 | ||||||
| chr14:102656784
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.362-25111T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656784 | ||||||
| chr14:102656941
|
C | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.362-24954C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656941 | ||||||
| chr14:102656981
|
G | A | 1 | a0001c0001t0004g0180 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.362-24914G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656981 | ||||||
| chr14:102656992
|
C | T | 1 | a0001c0001t0005g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.362-24903C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102656992 | ||||||
| chr14:102657006
|
C | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-24889C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102657006 | ||||||
| chr14:102657067
|
A | C | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-24828A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102657067 | ||||||
| chr14:102657098
|
C | CT | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-24785dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102657098 | |||||
| chr14:102657151
|
T | TAC | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-24743_362-2474 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102657151 | |||||
| chr14:102657708
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.362-24187C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102657708 | ||||||
| chr14:102657789
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.362-24106G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102657789 | ||||||
| chr14:102657837
|
C | CA | 8 | a0001c0001t0001g0018a0001c0001t0003g0028a0001c0001t0003g0041others(5): Show | 8 | HG01167.hp2 HG01515.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.362-24037dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102657837 | |||||
| chr14:102657837
|
CA | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.362-24037delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102657837 | |||||
| chr14:102657837
|
CAA | C | 92 | a0001c0001t0001g0095a0001c0001t0002g0162a0001c0001t0002g0163others(89): Show | 92 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.362-24038_362-2403 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102657837 | |||||
| chr14:102657837
|
CAAA | C | 6 | a0001c0001t0002g0192a0001c0001t0002g0230a0001c0001t0004g0166others(3): Show | 6 | HG01975.hp2 HG02922.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-24039_362-2403 others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102657837 | |||||
| chr14:102657837
|
CAAAA | C | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-24040_362-2403 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102657837 | |||||
| chr14:102657945
|
G | A | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.362-23950G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102657945 | ||||||
| chr14:102657960
|
A | T | 1 | a0001c0001t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362-23935A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102657960 | ||||||
| chr14:102658234
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0072a0001c0001t0001g0102others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-23661C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658234 | ||||||
| chr14:102658432
|
G | C | 1 | a0001c0001t0002g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.362-23463G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658432 | ||||||
| chr14:102658509
|
T | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-23386T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658509 | ||||||
| chr14:102658557
|
T | C | 10 | a0001c0001t0005g0053a0001c0001t0005g0059a0001c0001t0005g0114others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.362-23338T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658557 | ||||||
| chr14:102658609
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-23286A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658609 | ||||||
| chr14:102658644
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-23251C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658644 | ||||||
| chr14:102658649
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.362-23246C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658649 | ||||||
| chr14:102658722
|
A | C | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-23173A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658722 | ||||||
| chr14:102658722
|
A | G | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.362-23173A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658722 | ||||||
| chr14:102658742
|
C | G | 75 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.362-23153C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102658742 | ||||||
| chr14:102659025
|
T | G | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-22870T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659025 | ||||||
| chr14:102659096
|
G | C | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-22799G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659096 | ||||||
| chr14:102659178
|
G | C | 1 | a0001c0001t0002g0218 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.362-22717G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659178 | ||||||
| chr14:102659345
|
A | G | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-22550A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659345 | ||||||
| chr14:102659354
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-22541G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659354 | ||||||
| chr14:102659387
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-22508A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659387 | ||||||
| chr14:102659560
|
T | A | 1 | a0001c0001t0003g0040 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.362-22335T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659560 | ||||||
| chr14:102659632
|
T | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-22263T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659632 | ||||||
| chr14:102659657
|
T | G | 1 | a0001c0001t0006g0260 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.362-22238T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659657 | ||||||
| chr14:102659764
|
C | T | 164 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(161): Show | 164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.362-22131C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659764 | ||||||
| chr14:102659808
|
C | T | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.362-22087C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102659808 | ||||||
| chr14:102660002
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.362-21893T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660002 | ||||||
| chr14:102660071
|
A | G | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-21824A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660071 | ||||||
| chr14:102660191
|
G | T | 1 | a0001c0001t0003g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.362-21704G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660191 | ||||||
| chr14:102660233
|
A | T | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-21662A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660233 | ||||||
| chr14:102660353
|
CT | C | 124 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(121): Show | 124 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.362-21530delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102660353 | |||||
| chr14:102660403
|
G | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-21492G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660403 | ||||||
| chr14:102660484
|
G | A | 1 | a0001c0001t0036g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.362-21411G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660484 | ||||||
| chr14:102660575
|
T | G | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-21320T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660575 | ||||||
| chr14:102660645
|
A | T | 39 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.362-21250A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660645 | ||||||
| chr14:102660674
|
A | G | 1 | a0001c0001t0005g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.362-21221A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660674 | ||||||
| chr14:102660972
|
C | T | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.362-20923C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102660972 | ||||||
| chr14:102661015
|
T | C | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-20880T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661015 | ||||||
| chr14:102661112
|
T | C | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-20783T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661112 | ||||||
| chr14:102661172
|
C | T | 67 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(64): Show | 67 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.362-20723C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661172 | ||||||
| chr14:102661216
|
T | C | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-20679T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661216 | ||||||
| chr14:102661280
|
G | T | 4 | a0001c0001t0004g0173a0001c0001t0004g0175a0001c0001t0004g0184others(1): Show | 4 | HG01496.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-20615G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661280 | ||||||
| chr14:102661487
|
T | C | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-20408T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661487 | ||||||
| chr14:102661951
|
G | A | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-19944G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661951 | ||||||
| chr14:102661958
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.362-19937A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102661958 | ||||||
| chr14:102662041
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.362-19854G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662041 | ||||||
| chr14:102662136
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-19759G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662136 | ||||||
| chr14:102662309
|
C | T | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-19586C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662309 | ||||||
| chr14:102662408
|
T | C | 5 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-19487T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662408 | ||||||
| chr14:102662414
|
A | G | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-19481A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662414 | ||||||
| chr14:102662440
|
G | T | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-19455G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662440 | ||||||
| chr14:102662571
|
G | A | 1 | a0001c0001t0036g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.362-19324G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662571 | ||||||
| chr14:102662757
|
T | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-19138T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102662757 | ||||||
| chr14:102663104
|
G | A | 97 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(94): Show | 97 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.362-18791G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102663104 | ||||||
| chr14:102663117
|
T | C | 1 | a0001c0001t0005g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.362-18778T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102663117 | ||||||
| chr14:102663608
|
G | T | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-18287G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102663608 | ||||||
| chr14:102663980
|
T | G | 1 | a0001c0001t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362-17915T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102663980 | ||||||
| chr14:102664014
|
T | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.362-17881T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102664014 | ||||||
| chr14:102664278
|
G | GT | 8 | a0001c0001t0001g0077a0001c0001t0002g0217a0001c0001t0003g0014others(5): Show | 8 | HG01993.hp2 HG02015.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.362-17609dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102664278 | |||||
| chr14:102664358
|
A | G | 1 | a0001c0001t0004g0166 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.362-17537A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102664358 | ||||||
| chr14:102664761
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.362-17134T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102664761 | ||||||
| chr14:102664870
|
A | C | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-17025A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102664870 | ||||||
| chr14:102664962
|
G | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-16933G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102664962 | ||||||
| chr14:102665014
|
T | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.362-16881T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102665014 | ||||||
| chr14:102665088
|
C | T | 4 | a0001c0001t0001g0129a0001c0001t0015g0101a0001c0001t0015g0124others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-16807C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102665088 | ||||||
| chr14:102665311
|
C | CT | 102 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0002g0163others(99): Show | 102 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.362-16565dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102665311 | |||||
| chr14:102665311
|
C | CTT | 26 | a0001c0001t0002g0162a0001c0001t0002g0217a0001c0001t0002g0241others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.362-16566_362-1656 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102665311 | |||||
| chr14:102665311
|
CT | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0102others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-16565delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102665311 | |||||
| chr14:102665329
|
TTA | T | 6 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-16565_362-1656 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102665329 | ||||||
| chr14:102665331
|
A | T | 123 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(120): Show | 123 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.362-16564A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102665331 | ||||||
| chr14:102665386
|
T | C | 128 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.362-16509T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102665386 | ||||||
| chr14:102665433
|
G | C | 128 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.362-16462G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102665433 | ||||||
| chr14:102665473
|
G | A | 1 | a0001c0001t0003g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.362-16422G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102665473 | ||||||
| chr14:102666372
|
T | C | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.362-15523T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102666372 | ||||||
| chr14:102666723
|
G | A | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-15172G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102666723 | ||||||
| chr14:102667048
|
T | C | 148 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(145): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.362-14847T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102667048 | ||||||
| chr14:102667159
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-14736C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102667159 | ||||||
| chr14:102667227
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.362-14668G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102667227 | ||||||
| chr14:102667454
|
T | C | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-14441T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102667454 | ||||||
| chr14:102667789
|
GC | G | 47 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.362-14104delC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102667789 | |||||
| chr14:102667794
|
C | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.362-14101C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102667794 | ||||||
| chr14:102667884
|
G | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-14011G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102667884 | ||||||
| chr14:102667973
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.362-13922G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102667973 | ||||||
| chr14:102668129
|
T | G | 1 | a0001c0001t0002g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.362-13766T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102668129 | ||||||
| chr14:102668133
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.362-13762A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102668133 | ||||||
| chr14:102668190
|
C | G | 1 | a0001c0001t0004g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.362-13705C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102668190 | ||||||
| chr14:102668703
|
AT | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-13183delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102668703 | |||||
| chr14:102668767
|
T | G | 284 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.362-13128T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102668767 | ||||||
| chr14:102668832
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-13063C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102668832 | ||||||
| chr14:102669099
|
C | T | 99 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(96): Show | 99 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-12796C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669099 | ||||||
| chr14:102669169
|
C | T | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.362-12726C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669169 | ||||||
| chr14:102669178
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-12717A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669178 | ||||||
| chr14:102669264
|
G | A | 1 | a0001c0001t0003g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.362-12631G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669264 | ||||||
| chr14:102669307
|
C | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-12588C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669307 | ||||||
| chr14:102669309
|
G | GA | 128 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(125): Show | 128 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.362-12572dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102669309 | |||||
| chr14:102669309
|
G | GAA | 6 | a0001c0001t0009g0002a0001c0001t0009g0144a0001c0001t0009g0148others(3): Show | 6 | HG00733.hp1 HG02451.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-12573_362-1257 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102669309 | |||||
| chr14:102669312
|
A | G | 1 | a0001c0001t0013g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.362-12583A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669312 | ||||||
| chr14:102669324
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-12571G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669324 | ||||||
| chr14:102669472
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.362-12423T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669472 | ||||||
| chr14:102669738
|
G | C | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.362-12157G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669738 | ||||||
| chr14:102669808
|
T | C | 1 | a0001c0001t0051g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.362-12087T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669808 | ||||||
| chr14:102669822
|
G | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-12073G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669822 | ||||||
| chr14:102669896
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-11999G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669896 | ||||||
| chr14:102669959
|
T | G | 5 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0238others(2): Show | 5 | HG00673.hp1 HG01192.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.362-11936T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102669959 | ||||||
| chr14:102670061
|
C | T | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-11834C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102670061 | ||||||
| chr14:102670106
|
A | G | 101 | a0001c0001t0001g0095a0001c0001t0002g0162a0001c0001t0002g0163others(98): Show | 101 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.362-11789A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102670106 | ||||||
| chr14:102670463
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-11432A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102670463 | ||||||
| chr14:102670655
|
C | T | 1 | a0001c0001t0003g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.362-11240C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102670655 | ||||||
| chr14:102670739
|
T | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-11156T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102670739 | ||||||
| chr14:102670741
|
T | TTA | 98 | a0001c0001t0001g0060a0001c0001t0001g0134a0001c0001t0002g0164others(95): Show | 98 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.362-11138_362-1113 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102670741 | |||||
| chr14:102670741
|
T | TTATA | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0244 | 3 | HG01123.hp1 HG01192.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.362-11140_362-1113 others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102670741 | |||||
| chr14:102670741
|
TTA | T | 71 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0095others(68): Show | 71 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.362-11138_362-1113 others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102670741 | |||||
| chr14:102670743
|
A | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | NA18972.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.362-11152A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102670743 | ||||||
| chr14:102670869
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-11026G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102670869 | ||||||
| chr14:102671172
|
C | G | 1 | a0001c0001t0003g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.362-10723C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671172 | ||||||
| chr14:102671500
|
A | G | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.362-10395A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671500 | ||||||
| chr14:102671502
|
C | T | 1 | a0001c0001t0020g0290 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362-10393C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671502 | ||||||
| chr14:102671535
|
A | G | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.362-10360A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671535 | ||||||
| chr14:102671686
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.362-10209C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671686 | ||||||
| chr14:102671749
|
C | T | 3 | a0001c0001t0010g0058a0001c0001t0010g0067a0001c0001t0010g0113 | 3 | HG02027.hp1 HG02080.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.362-10146C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671749 | ||||||
| chr14:102671776
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-10119A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671776 | ||||||
| chr14:102671855
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-10040A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671855 | ||||||
| chr14:102671861
|
C | G | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.362-10034C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671861 | ||||||
| chr14:102671882
|
A | G | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.362-10013A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671882 | ||||||
| chr14:102671901
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-9994C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671901 | ||||||
| chr14:102671983
|
A | G | 1 | a0001c0001t0007g0034 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.362-9912A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102671983 | ||||||
| chr14:102672067
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-9828A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672067 | ||||||
| chr14:102672282
|
G | A | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-9613G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672282 | ||||||
| chr14:102672310
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.362-9585C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672310 | ||||||
| chr14:102672545
|
A | G | 1 | a0001c0001t0046g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-9350A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672545 | ||||||
| chr14:102672789
|
A | T | 12 | a0001c0001t0006g0260a0001c0001t0006g0261a0001c0001t0006g0264others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.362-9106A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672789 | ||||||
| chr14:102672794
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-9101C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672794 | ||||||
| chr14:102672850
|
A | G | 2 | a0001c0001t0002g0217a0001c0001t0002g0254 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.362-9045A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672850 | ||||||
| chr14:102672907
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-8988A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672907 | ||||||
| chr14:102672977
|
T | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-8918T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102672977 | ||||||
| chr14:102673091
|
T | G | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.362-8804T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673091 | ||||||
| chr14:102673184
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.362-8711C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673184 | ||||||
| chr14:102673325
|
C | T | 4 | a0001c0001t0003g0014a0001c0001t0003g0041a0001c0001t0003g0042others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-8570C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673325 | ||||||
| chr14:102673334
|
A | AT | 36 | a0001c0001t0001g0091a0001c0001t0001g0135a0001c0001t0002g0196others(33): Show | 36 | HG00280.hp2 HG00639.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.362-8541dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102673334 | |||||
| chr14:102673334
|
AT | A | 19 | a0001c0001t0002g0224a0001c0001t0002g0286a0001c0001t0003g0037others(16): Show | 19 | HG00733.hp1 HG01993.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-8541delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102673334 | |||||
| chr14:102673354
|
T | A | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.362-8541T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673354 | ||||||
| chr14:102673375
|
G | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-8520G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673375 | ||||||
| chr14:102673421
|
C | T | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.362-8474C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673421 | ||||||
| chr14:102673497
|
C | T | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-8398C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673497 | ||||||
| chr14:102673549
|
A | G | 1 | a0001c0001t0003g0035 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.362-8346A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673549 | ||||||
| chr14:102673612
|
G | A | 1 | a0001c0003t0005g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.362-8283G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673612 | ||||||
| chr14:102673630
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-8265C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673630 | ||||||
| chr14:102673708
|
C | T | 1 | a0001c0001t0003g0015 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.362-8187C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673708 | ||||||
| chr14:102673775
|
C | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0084others(2): Show | 5 | NA18971.hp1 NA18980.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.362-8120C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673775 | ||||||
| chr14:102673867
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0111others(1): Show | 4 | HG00423.hp1 NA18972.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-8028C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673867 | ||||||
| chr14:102673892
|
G | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-8003G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673892 | ||||||
| chr14:102673904
|
C | T | 30 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0181others(27): Show | 30 | HG00609.hp1 HG00735.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.362-7991C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673904 | ||||||
| chr14:102673917
|
C | T | 164 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(161): Show | 164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.362-7978C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102673917 | ||||||
| chr14:102674011
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-7884A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102674011 | ||||||
| chr14:102674059
|
T | G | 1 | a0001c0001t0003g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.362-7836T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102674059 | ||||||
| chr14:102674074
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-7821A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102674074 | ||||||
| chr14:102674585
|
A | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-7310A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102674585 | ||||||
| chr14:102674662
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-7233G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102674662 | ||||||
| chr14:102674797
|
G | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.362-7098G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102674797 | ||||||
| chr14:102674954
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.362-6941C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102674954 | ||||||
| chr14:102675047
|
C | CA | 23 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0075others(20): Show | 23 | HG01175.hp1 HG01891.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.362-6824dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102675047 | |||||
| chr14:102675047
|
C | CAA | 8 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(5): Show | 8 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.362-6825_362-6824d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102675047 | |||||
| chr14:102675047
|
CA | C | 55 | a0001c0001t0001g0016a0001c0001t0002g0168a0001c0001t0002g0172others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.362-6824delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102675047 | |||||
| chr14:102675047
|
CAA | C | 68 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(65): Show | 68 | HG00423.hp2 HG00673.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.362-6825_362-6824d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102675047 | |||||
| chr14:102675239
|
G | A | 9 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0225others(6): Show | 9 | HG00673.hp1 HG01192.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.362-6656G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102675239 | ||||||
| chr14:102675453
|
A | C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-6442A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102675453 | ||||||
| chr14:102675684
|
T | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-6211T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102675684 | ||||||
| chr14:102675698
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.362-6197C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102675698 | ||||||
| chr14:102675798
|
G | T | 127 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.362-6097G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102675798 | ||||||
| chr14:102675822
|
C | A | 3 | a0001c0001t0002g0221a0001c0001t0002g0237a0001c0001t0018g0239 | 3 | NA18979.hp1 NA19070.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.362-6073C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102675822 | ||||||
| chr14:102675885
|
C | T | 5 | a0001c0001t0002g0192a0001c0001t0002g0206a0001c0001t0002g0207others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.362-6010C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102675885 | ||||||
| chr14:102676031
|
GT | G | 20 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0089others(17): Show | 20 | HG01167.hp1 HG01169.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.362-5847delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676031 | |||||
| chr14:102676031
|
GTT | G | 9 | a0001c0001t0002g0246a0001c0001t0004g0216a0001c0001t0005g0119others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.362-5848_362-5847d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676031 | |||||
| chr14:102676031
|
GTTT | G | 120 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(117): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.362-5849_362-5847d others(5): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676031 | |||||
| chr14:102676048
|
T | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0009g0002others(8): Show | 11 | HG01167.hp2 HG01516.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-5847T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676048 | ||||||
| chr14:102676163
|
C | G | 2 | a0001c0001t0002g0212a0001c0001t0040g0213 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.362-5732C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676163 | ||||||
| chr14:102676219
|
C | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-5676C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676219 | ||||||
| chr14:102676226
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.362-5669C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676226 | ||||||
| chr14:102676269
|
GCTTCCCA others(120): Show |
G | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-5606_362-5480d others(2): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676269 | |||||
| chr14:102676298
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-5597C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676298 | ||||||
| chr14:102676336
|
G | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-5559G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676336 | ||||||
| chr14:102676343
|
A | AC | 22 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0200others(19): Show | 22 | HG01192.hp1 HG01433.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.362-5545dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676343 | |||||
| chr14:102676351
|
A | C | 125 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(122): Show | 125 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.362-5544A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676351 | ||||||
| chr14:102676352
|
C | G | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | NA19009.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.362-5543C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676352 | ||||||
| chr14:102676365
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.362-5530C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676365 | ||||||
| chr14:102676379
|
G | A | 1 | a0001c0001t0040g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.362-5516G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676379 | ||||||
| chr14:102676400
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.362-5495C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676400 | ||||||
| chr14:102676405
|
T | A | 127 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.362-5490T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676405 | ||||||
| chr14:102676416
|
A | G | 74 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(71): Show | 74 | HG00423.hp2 HG00673.hp1 HG01123.hp1 others(71): Show |
intron_variant | MODIFIER | c.362-5479A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676416 | ||||||
| chr14:102676439
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.362-5456C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676439 | ||||||
| chr14:102676442
|
A | C | 1 | a0001c0001t0004g0190 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.362-5453A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676442 | ||||||
| chr14:102676452
|
C | T | 9 | a0001c0001t0004g0177a0001c0001t0009g0002a0001c0001t0009g0143others(6): Show | 9 | HG00735.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.362-5443C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676452 | ||||||
| chr14:102676457
|
G | A | 9 | a0001c0001t0004g0177a0001c0001t0009g0002a0001c0001t0009g0143others(6): Show | 9 | HG00735.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.362-5438G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676457 | ||||||
| chr14:102676457
|
G | GGGGCGGG others(174): Show |
1 | a0001c0001t0002g0162 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.362-5436_362-5435i others(183): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676457 | |||||
| chr14:102676471
|
C | CCCCCCCA others(164): Show |
6 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0021others(3): Show | 6 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-5380_362-5379i others(173): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676471 | |||||
| chr14:102676471
|
C | CCCCCCCA others(168): Show |
2 | a0001c0001t0001g0134a0001c0001t0003g0127 | 2 | HG01074.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676471 | |||||
| chr14:102676471
|
C | CCCCCCCA others(167): Show |
4 | a0001c0001t0003g0008a0001c0001t0003g0050a0001c0001t0007g0024others(1): Show | 4 | HG01952.hp1 HG02273.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676471 | |||||
| chr14:102676471
|
C | CCCCCCCA others(166): Show |
5 | a0001c0001t0003g0006a0001c0001t0003g0023a0001c0001t0003g0028others(2): Show | 5 | HG00733.hp2 HG02004.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(175): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676471 | |||||
| chr14:102676471
|
C | CCCCCCCA others(165): Show |
8 | a0001c0001t0003g0014a0001c0001t0003g0035a0001c0001t0003g0036others(5): Show | 8 | HG00639.hp1 HG01515.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(174): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676471 | |||||
| chr14:102676471
|
C | CCCCCCCA others(164): Show |
3 | a0001c0001t0003g0030a0001c0001t0003g0032a0001c0001t0003g0105 | 3 | HG02055.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(173): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676471 | |||||
| chr14:102676471
|
C | T | 11 | a0001c0001t0002g0162a0001c0001t0004g0177a0001c0001t0009g0002others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-5424C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676471 | ||||||
| chr14:102676493
|
A | AGGGCGGC others(175): Show |
1 | a0001c0001t0016g0282 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.362-5379_362-5378i others(184): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | AGGGCGGC others(171): Show |
1 | a0001c0001t0002g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(180): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | AGGGCGGC others(170): Show |
2 | a0001c0001t0002g0168a0001c0001t0047g0226 | 2 | HG01934.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(179): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | AGGGCGGC others(169): Show |
3 | a0001c0001t0002g0249a0001c0001t0004g0169a0001c0001t0004g0183 | 3 | HG01433.hp1 HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(178): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | AGGGCGGC others(168): Show |
1 | a0001c0001t0004g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | AGGGCGGC others(167): Show |
1 | a0001c0001t0018g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | AGGGCGGC others(164): Show |
1 | a0001c0001t0013g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.362-5380_362-5379i others(173): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | AGGGCGGC others(120): Show |
1 | a0001c0001t0006g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.362-5389_362-5388i others(129): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676493 | |||||
| chr14:102676493
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0004g0177 | 2 | HG00735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.362-5402A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676493 | ||||||
| chr14:102676506
|
G | GGGCAGAG others(119): Show |
28 | a0001c0001t0002g0204a0001c0001t0006g0256a0001c0001t0006g0257others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.362-5389_362-5388i others(128): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676506 | ||||||
| chr14:102676506
|
G | GGGCGGGG others(4): Show |
8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-5389_362-5388i others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676506 | ||||||
| chr14:102676507
|
A | ACCCCCCC others(165): Show |
3 | a0001c0001t0003g0020a0001c0001t0003g0026a0001c0001t0011g0025 | 3 | HG01496.hp2 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.362-5380_362-5379i others(174): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(169): Show |
1 | a0001c0001t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.362-5379_362-5378i others(178): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(169): Show |
1 | a0001c0001t0001g0009 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(178): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(168): Show |
5 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096others(2): Show | 5 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(169): Show |
8 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0077others(5): Show | 8 | HG01099.hp1 HG01928.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(178): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(168): Show |
4 | a0001c0001t0003g0015a0001c0001t0003g0044a0001c0001t0003g0056others(1): Show | 4 | HG01192.hp2 HG02486.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(167): Show |
5 | a0001c0001t0001g0060a0001c0001t0001g0097a0001c0001t0001g0103others(2): Show | 5 | HG01358.hp1 HG02273.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(168): Show |
15 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0016others(12): Show | 15 | HG00099.hp2 HG01168.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(167): Show |
2 | a0001c0001t0003g0052a0001c0001t0011g0049 | 2 | HG02145.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(166): Show |
16 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0072others(13): Show | 16 | HG00323.hp1 HG00609.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(175): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(167): Show |
16 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0079others(13): Show | 16 | HG00423.hp1 HG01256.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(168): Show |
1 | a0001c0001t0001g0010 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(166): Show |
9 | a0001c0001t0003g0003a0001c0001t0003g0037a0001c0001t0003g0038others(6): Show | 9 | HG00280.hp1 HG00738.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(175): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(165): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0045g0203 | 3 | HG01884.hp1 HG02735.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(174): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(166): Show |
4 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0108others(1): Show | 4 | HG04115.hp2 NA19009.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(175): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(165): Show |
1 | a0001c0001t0003g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(174): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(165): Show |
2 | a0001c0001t0003g0031a0001c0001t0003g0041 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(174): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(165): Show |
1 | a0001c0001t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(174): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | ACCCCCCC others(167): Show |
1 | a0001c0001t0029g0115 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676507 | |||||
| chr14:102676507
|
A | G | 36 | a0001c0001t0002g0204a0001c0001t0006g0256a0001c0001t0006g0257others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.362-5388A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676507 | ||||||
| chr14:102676508
|
C | A | 36 | a0001c0001t0002g0204a0001c0001t0006g0256a0001c0001t0006g0257others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.362-5387C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676508 | ||||||
| chr14:102676508
|
C | CCCCCCCC others(164): Show |
1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(173): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(172): Show |
2 | a0001c0001t0016g0281a0001c0001t0042g0228 | 2 | HG02080.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(181): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(171): Show |
3 | a0001c0001t0002g0212a0001c0001t0004g0178a0001c0001t0044g0202 | 3 | HG00609.hp1 HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(180): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(171): Show |
1 | a0001c0001t0002g0164 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.362-5379_362-5378i others(180): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(170): Show |
3 | a0001c0001t0002g0206a0001c0001t0004g0165a0001c0001t0048g0179 | 3 | HG02630.hp2 NA18955.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(179): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(169): Show |
13 | a0001c0001t0002g0192a0001c0001t0002g0211a0001c0001t0002g0232others(10): Show | 13 | HG00673.hp1 HG01243.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(178): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(174): Show |
1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.362-5379_362-5378i others(183): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(168): Show |
1 | a0001c0001t0002g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(168): Show |
25 | a0001c0001t0002g0163a0001c0001t0002g0181a0001c0001t0002g0207others(22): Show | 25 | HG01123.hp1 HG01975.hp2 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(168): Show |
1 | a0001c0001t0004g0215 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(177): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(167): Show |
12 | a0001c0001t0002g0172a0001c0001t0002g0200a0001c0001t0002g0224others(9): Show | 12 | HG01361.hp2 HG01496.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(167): Show |
1 | a0001c0001t0002g0233 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(176): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(166): Show |
13 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0208others(10): Show | 13 | HG01167.hp2 HG01358.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(175): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(165): Show |
10 | a0001c0001t0002g0196a0001c0001t0002g0201a0001c0001t0002g0210others(7): Show | 10 | HG01884.hp2 HG01928.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(174): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(164): Show |
12 | a0001c0001t0002g0222a0001c0001t0002g0231a0001c0001t0002g0252others(9): Show | 12 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.362-5379_362-5378i others(173): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(163): Show |
2 | a0001c0001t0005g0137a0001c0003t0005g0117 | 2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.362-5379_362-5378i others(172): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676508
|
C | CCCCCCCC others(163): Show |
1 | a0001c0001t0005g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.362-5380_362-5379i others(172): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676508 | |||||
| chr14:102676509
|
C | A | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-5386C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676509 | ||||||
| chr14:102676509
|
C | CCCCCCCC others(568): Show |
1 | a0001c0001t0036g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.362-5379_362-5378i others(577): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676509 | |||||
| chr14:102676515
|
CCACCTCC others(513): Show |
C | 1 | a0001c0001t0046g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-5378_362-4859d others(2): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676515 | |||||
| chr14:102676516
|
CACCTCCC others(511): Show |
C | 3 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0038g0155 | 3 | HG03471.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.362-5375_362-4858d others(2): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676516 | |||||
| chr14:102676517
|
A | C | 2 | a0001c0001t0012g0154a0001c0004t0012g0151 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.362-5378A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676517 | ||||||
| chr14:102676517
|
A | G | 7 | a0001c0001t0002g0182a0001c0001t0013g0291a0001c0001t0013g0292others(4): Show | 7 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.362-5378A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676517 | ||||||
| chr14:102676518
|
CCTCCCTC others(510): Show |
C | 2 | a0001c0001t0012g0154a0001c0004t0012g0151 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.362-5375_362-4859d others(2): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676518 | |||||
| chr14:102676555
|
G | T | 5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5340G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676555 | ||||||
| chr14:102676581
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.362-5314C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676581 | ||||||
| chr14:102676601
|
C | G | 10 | a0001c0001t0005g0053a0001c0001t0005g0059a0001c0001t0005g0114others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.362-5294C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676601 | ||||||
| chr14:102676605
|
C | T | 6 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(3): Show | 6 | HG00733.hp1 HG02738.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-5290C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676605 | ||||||
| chr14:102676626
|
T | C | 7 | a0001c0001t0002g0182a0001c0001t0013g0291a0001c0001t0013g0292others(4): Show | 7 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.362-5269T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676626 | ||||||
| chr14:102676626
|
T | TG | 124 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(121): Show | 124 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.362-5263dupG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676626 | |||||
| chr14:102676627
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.362-5268G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676627 | ||||||
| chr14:102676633
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-5262C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676633 | ||||||
| chr14:102676659
|
GGGGCGGC others(41): Show |
G | 4 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(1): Show | 4 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-5224_362-5177d others(50): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676659 | |||||
| chr14:102676669
|
G | GCCGACCC others(110): Show |
2 | a0001c0001t0002g0182a0001c0001t0041g0214 | 2 | NA18952.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.362-5225_362-5224i others(119): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676669 | |||||
| chr14:102676671
|
T | A | 2 | a0001c0001t0002g0182a0001c0001t0041g0214 | 2 | NA18952.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.362-5224T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676671 | ||||||
| chr14:102676671
|
T | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-5224T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676671 | ||||||
| chr14:102676674
|
G | T | 2 | a0001c0001t0002g0182a0001c0001t0041g0214 | 2 | NA18952.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.362-5221G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676674 | ||||||
| chr14:102676675
|
C | G | 2 | a0001c0001t0002g0182a0001c0001t0041g0214 | 2 | NA18952.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.362-5220C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676675 | ||||||
| chr14:102676675
|
CGGGGGGC others(42): Show |
C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-5214_362-5166d others(51): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676675 | |||||
| chr14:102676723
|
C | T | 1 | a0001c0001t0011g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.362-5172C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676723 | ||||||
| chr14:102676733
|
A | AC | 35 | a0001c0001t0001g0135a0001c0001t0002g0162a0001c0001t0002g0168others(32): Show | 35 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.362-5154dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676733 | |||||
| chr14:102676747
|
C | A | 5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5148C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676747 | ||||||
| chr14:102676769
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-5126C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676769 | ||||||
| chr14:102676780
|
G | GC | 5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5115_362-5114i others(3): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676780 | ||||||
| chr14:102676792
|
C | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.362-5103C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676792 | ||||||
| chr14:102676806
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.362-5089G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676806 | ||||||
| chr14:102676823
|
A | ACCTCCCG others(42): Show |
7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-5049_362-5048i others(51): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676823 | |||||
| chr14:102676846
|
C | CAGGTGGG others(42): Show |
5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5049_362-5048i others(51): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676846 | ||||||
| chr14:102676847
|
G | A | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-5048G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676847 | ||||||
| chr14:102676852
|
A | G | 240 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.362-5043A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676852 | ||||||
| chr14:102676877
|
T | C | 7 | a0001c0001t0009g0147a0001c0001t0013g0291a0001c0001t0013g0292others(4): Show | 7 | HG00733.hp1 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-5018T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676877 | ||||||
| chr14:102676882
|
G | T | 5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-5013G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676882 | ||||||
| chr14:102676900
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.362-4995G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676900 | ||||||
| chr14:102676926
|
C | T | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-4969C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676926 | ||||||
| chr14:102676934
|
G | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-4961G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676934 | ||||||
| chr14:102676935
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-4960C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676935 | ||||||
| chr14:102676939
|
TGGCCGGG others(71): Show |
T | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-4947_362-4870d others(80): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676939 | |||||
| chr14:102676950
|
AG | A | 5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-4941delG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102676950 | |||||
| chr14:102676955
|
C | T | 5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-4940C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102676955 | ||||||
| chr14:102677014
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-4881G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677014 | ||||||
| chr14:102677017
|
C | T | 132 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.362-4878C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677017 | ||||||
| chr14:102677022
|
G | A | 5 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(2): Show | 5 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-4873G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677022 | ||||||
| chr14:102677035
|
A | ATCCCCCC others(91): Show |
1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-4860_362-4859i others(100): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677035 | ||||||
| chr14:102677035
|
A | ATCCCCCC others(91): Show |
4 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0001t0017g0156others(1): Show | 4 | HG00733.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-4860_362-4859i others(100): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677035 | ||||||
| chr14:102677035
|
A | C | 3 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0038g0155 | 3 | HG03471.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.362-4860A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677035 | ||||||
| chr14:102677041
|
C | G | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-4854C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677041 | ||||||
| chr14:102677042
|
A | G | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-4853A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677042 | ||||||
| chr14:102677057
|
G | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-4838G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677057 | ||||||
| chr14:102677111
|
C | A | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-4784C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677111 | ||||||
| chr14:102677116
|
A | C | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-4779A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677116 | ||||||
| chr14:102677134
|
C | T | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.362-4761C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677134 | ||||||
| chr14:102677143
|
T | C | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-4752T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677143 | ||||||
| chr14:102677148
|
G | A | 2 | a0001c0001t0005g0121a0001c0001t0005g0137 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.362-4747G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677148 | ||||||
| chr14:102677161
|
A | AC | 37 | a0001c0001t0001g0065a0001c0001t0001g0098a0001c0001t0001g0106others(34): Show | 37 | HG00609.hp1 HG00733.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.362-4725dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102677161 | |||||
| chr14:102677190
|
C | A | 1 | a0001c0001t0002g0192 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.362-4705C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677190 | ||||||
| chr14:102677190
|
CGGCTGGC others(42): Show |
C | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-4690_362-4642d others(51): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102677190 | |||||
| chr14:102677198
|
C | T | 127 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.362-4697C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677198 | ||||||
| chr14:102677212
|
A | AC | 11 | a0001c0001t0001g0106a0001c0001t0001g0135a0001c0001t0002g0162others(8): Show | 11 | HG01261.hp2 HG01361.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.362-4676dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102677212 | |||||
| chr14:102677220
|
T | C | 1 | a0001c0001t0047g0226 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.362-4675T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677220 | ||||||
| chr14:102677225
|
C | A | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-4670C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677225 | ||||||
| chr14:102677275
|
C | A | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-4620C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677275 | ||||||
| chr14:102677289
|
A | C | 1 | a0001c0001t0009g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.362-4606A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677289 | ||||||
| chr14:102677290
|
A | G | 291 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.362-4605A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677290 | ||||||
| chr14:102677308
|
C | T | 1 | a0001c0001t0015g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.362-4587C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677308 | ||||||
| chr14:102677321
|
T | C | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-4574T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677321 | ||||||
| chr14:102677329
|
CA | C | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-4565delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677329 | ||||||
| chr14:102677330
|
A | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-4565A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677330 | ||||||
| chr14:102677330
|
A | G | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-4565A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677330 | ||||||
| chr14:102677339
|
A | AC | 71 | a0001c0001t0001g0012a0001c0001t0001g0077a0001c0001t0001g0084others(68): Show | 71 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.362-4546dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102677339 | |||||
| chr14:102677339
|
A | ACCCCCCA others(119): Show |
1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-4550_362-4549i others(128): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102677339 | |||||
| chr14:102677343
|
C | A | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-4552C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677343 | ||||||
| chr14:102677361
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.362-4534G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677361 | ||||||
| chr14:102677376
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-4519C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677376 | ||||||
| chr14:102677450
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.362-4445G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677450 | ||||||
| chr14:102677493
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-4402C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677493 | ||||||
| chr14:102677542
|
G | T | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-4353G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677542 | ||||||
| chr14:102677595
|
A | G | 3 | a0001c0001t0002g0204a0001c0001t0020g0289a0001c0001t0020g0290 | 3 | HG01081.hp1 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362-4300A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677595 | ||||||
| chr14:102677623
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-4272C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677623 | ||||||
| chr14:102677700
|
G | C | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.362-4195G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677700 | ||||||
| chr14:102677727
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-4168A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677727 | ||||||
| chr14:102677793
|
C | CG | 7 | a0001c0001t0002g0164a0001c0001t0002g0244a0001c0001t0003g0056others(4): Show | 7 | HG00423.hp2 HG01192.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.362-4098dupG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102677793 | |||||
| chr14:102677850
|
G | A | 3 | a0001c0001t0002g0204a0001c0001t0020g0289a0001c0001t0020g0290 | 3 | HG01081.hp1 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362-4045G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677850 | ||||||
| chr14:102677882
|
T | TCACGCCA others(21): Show |
1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.362-4012_362-3985d others(30): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102677882 | |||||
| chr14:102677886
|
G | A | 1 | a0001c0001t0003g0015 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.362-4009G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677886 | ||||||
| chr14:102677918
|
A | G | 5 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-3977A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102677918 | ||||||
| chr14:102678036
|
C | CA | 23 | a0001c0001t0001g0071a0001c0001t0001g0107a0001c0001t0001g0111others(20): Show | 23 | HG01081.hp1 HG01255.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.362-3848dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102678036 | |||||
| chr14:102678036
|
CA | C | 82 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0168others(79): Show | 82 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.362-3848delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102678036 | |||||
| chr14:102678071
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.362-3824C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678071 | ||||||
| chr14:102678073
|
C | T | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-3822C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678073 | ||||||
| chr14:102678076
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01516.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.362-3819G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678076 | ||||||
| chr14:102678157
|
C | T | 1 | a0001c0001t0009g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.362-3738C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678157 | ||||||
| chr14:102678182
|
GGGAGACC others(6): Show |
G | 1 | a0001c0001t0005g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.362-3700_362-3688d others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102678182 | |||||
| chr14:102678216
|
G | A | 1 | a0001c0001t0007g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.362-3679G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678216 | ||||||
| chr14:102678220
|
C | CGAGAGG | 125 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0168others(122): Show | 125 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.362-3657_362-3652d others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102678220 | |||||
| chr14:102678220
|
CGAGAGG | C | 3 | a0001c0001t0001g0079a0001c0001t0013g0292a0001c0005t0037g0149 | 3 | HG01167.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.362-3657_362-3652d others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102678220 | |||||
| chr14:102678246
|
G | A | 19 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(16): Show | 19 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.362-3649G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678246 | ||||||
| chr14:102678301
|
TTTTG | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0111others(1): Show | 4 | HG00423.hp1 NA18972.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-3582_362-3579d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102678301 | |||||
| chr14:102678348
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.362-3547G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678348 | ||||||
| chr14:102678958
|
A | C | 4 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0201others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-2937A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678958 | ||||||
| chr14:102678962
|
T | A | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-2933T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102678962 | ||||||
| chr14:102679070
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-2825G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679070 | ||||||
| chr14:102679308
|
T | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0233 | 2 | HG00423.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.362-2587T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679308 | ||||||
| chr14:102679309
|
T | A | 147 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.362-2586T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679309 | ||||||
| chr14:102679310
|
A | T | 5 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-2585A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679310 | ||||||
| chr14:102679564
|
C | T | 3 | a0001c0001t0005g0116a0001c0001t0013g0291a0001c0001t0013g0292 | 3 | HG00733.hp1 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.362-2331C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679564 | ||||||
| chr14:102679627
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.362-2268C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679627 | ||||||
| chr14:102679628
|
G | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-2267G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679628 | ||||||
| chr14:102679649
|
T | G | 1 | a0001c0001t0004g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.362-2246T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679649 | ||||||
| chr14:102679768
|
G | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-2127G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102679768 | ||||||
| chr14:102680037
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.362-1858A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680037 | ||||||
| chr14:102680052
|
A | G | 1 | a0001c0001t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362-1843A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680052 | ||||||
| chr14:102680196
|
A | G | 1 | a0001c0002t0003g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.362-1699A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680196 | ||||||
| chr14:102680603
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362-1292C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680603 | ||||||
| chr14:102680864
|
T | A | 3 | a0001c0001t0010g0058a0001c0001t0010g0067a0001c0001t0010g0113 | 3 | HG02027.hp1 HG02080.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.362-1031T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680864 | ||||||
| chr14:102680869
|
C | T | 3 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0048g0179 | 3 | HG00609.hp1 NA18944.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.362-1026C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680869 | ||||||
| chr14:102680875
|
C | G | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.362-1020C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680875 | ||||||
| chr14:102680969
|
T | C | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-926T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102680969 | ||||||
| chr14:102681015
|
G | T | 2 | a0001c0001t0004g0169a0001c0001t0004g0183 | 2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.362-880G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681015 | ||||||
| chr14:102681111
|
T | A | 14 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.362-784T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681111 | ||||||
| chr14:102681163
|
A | G | 1 | a0001c0001t0014g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.362-732A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681163 | ||||||
| chr14:102681247
|
A | G | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-648A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681247 | ||||||
| chr14:102681311
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.362-584C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681311 | ||||||
| chr14:102681346
|
C | T | 14 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.362-549C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681346 | ||||||
| chr14:102681347
|
G | A | 3 | a0001c0001t0013g0291a0001c0001t0013g0292a0001c0005t0037g0149 | 3 | HG00733.hp1 HG01167.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.362-548G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681347 | ||||||
| chr14:102681418
|
G | T | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.362-477G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681418 | ||||||
| chr14:102681482
|
ATAGT | A | 4 | a0001c0001t0006g0260a0001c0001t0006g0261a0001c0001t0006g0264others(1): Show | 4 | HG00323.hp2 HG01123.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-410_362-407del others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102681482 | |||||
| chr14:102681835
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0110 | 2 | NA18944.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.362-60C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | chr14 | 102681835 | ||||||
| chr14:102682059
|
A | G | 1 | a0001c0001t0004g0166 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.445+81A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682059 | ||||||
| chr14:102682130
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0110 | 2 | NA18944.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.445+152T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682130 | ||||||
| chr14:102682259
|
A | G | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.445+281A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682259 | ||||||
| chr14:102682392
|
A | G | 128 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.445+414A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682392 | ||||||
| chr14:102682600
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.445+622G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682600 | ||||||
| chr14:102682642
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0082 | 2 | HG00609.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.445+664T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682642 | ||||||
| chr14:102682822
|
T | C | 8 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(5): Show | 8 | HG02451.hp2 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+844T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682822 | ||||||
| chr14:102682972
|
A | G | 1 | a0001c0001t0033g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.445+994A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102682972 | ||||||
| chr14:102683060
|
T | C | 1 | a0001c0001t0032g0057 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.445+1082T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683060 | ||||||
| chr14:102683086
|
C | T | 1 | a0001c0001t0042g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.445+1108C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683086 | ||||||
| chr14:102683110
|
T | G | 148 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(145): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.445+1132T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683110 | ||||||
| chr14:102683138
|
G | A | 19 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(16): Show | 19 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+1160G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683138 | ||||||
| chr14:102683178
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.445+1200G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683178 | ||||||
| chr14:102683264
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.445+1286G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683264 | ||||||
| chr14:102683401
|
C | T | 1 | a0001c0001t0006g0260 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.445+1423C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683401 | ||||||
| chr14:102683427
|
A | G | 1 | a0001c0001t0004g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.445+1449A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683427 | ||||||
| chr14:102683522
|
C | A | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.445+1544C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683522 | ||||||
| chr14:102683526
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.445+1548C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683526 | ||||||
| chr14:102683659
|
G | A | 19 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(16): Show | 19 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+1681G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683659 | ||||||
| chr14:102683671
|
C | T | 1 | a0001c0001t0051g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.445+1693C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683671 | ||||||
| chr14:102683702
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0135 | 2 | HG02040.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.445+1724G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683702 | ||||||
| chr14:102683720
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.445+1742C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102683720 | ||||||
| chr14:102684070
|
A | G | 148 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(145): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.445+2092A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684070 | ||||||
| chr14:102684073
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.445+2095C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684073 | ||||||
| chr14:102684120
|
T | G | 5 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0002g0205others(2): Show | 5 | HG01081.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+2142T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684120 | ||||||
| chr14:102684125
|
C | G | 1 | a0001c0001t0002g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.445+2147C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684125 | ||||||
| chr14:102684196
|
G | C | 1 | a0001c0001t0002g0241 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.445+2218G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684196 | ||||||
| chr14:102684207
|
C | T | 1 | a0001c0001t0026g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.445+2229C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684207 | ||||||
| chr14:102684286
|
A | G | 165 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(162): Show | 165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.445+2308A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684286 | ||||||
| chr14:102684458
|
C | T | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.445+2480C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684458 | ||||||
| chr14:102684467
|
A | G | 2 | a0001c0001t0010g0064a0001c0001t0010g0104 | 2 | NA18939.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.445+2489A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684467 | ||||||
| chr14:102684707
|
T | TG | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.445+2733dupG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102684707 | |||||
| chr14:102684921
|
G | A | 1 | a0001c0001t0015g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.445+2943G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102684921 | ||||||
| chr14:102685062
|
T | TTG | 128 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.445+3100_445+3101d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102685062 | |||||
| chr14:102685078
|
G | T | 1 | a0001c0001t0033g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.445+3100G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102685078 | ||||||
| chr14:102685188
|
A | G | 2 | a0001c0001t0002g0245a0001c0001t0002g0248 | 2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.445+3210A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102685188 | ||||||
| chr14:102685275
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01516.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.445+3297C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102685275 | ||||||
| chr14:102685350
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0082 | 2 | HG00609.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.445+3372G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102685350 | ||||||
| chr14:102685485
|
C | CT | 21 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0085others(18): Show | 21 | HG00423.hp1 HG01074.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.445+3521dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102685485 | |||||
| chr14:102685669
|
A | G | 1 | a0001c0001t0026g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.445+3691A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102685669 | ||||||
| chr14:102685917
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.445+3939C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102685917 | ||||||
| chr14:102686154
|
T | G | 19 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(16): Show | 19 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+4176T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686154 | ||||||
| chr14:102686282
|
TATTTTAG others(4): Show |
T | 1 | a0001c0001t0051g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.445+4312_445+4322d others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102686282 | |||||
| chr14:102686420
|
T | C | 1 | a0001c0001t0044g0202 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.445+4442T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686420 | ||||||
| chr14:102686424
|
A | G | 1 | a0001c0001t0038g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.445+4446A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686424 | ||||||
| chr14:102686448
|
T | G | 6 | a0001c0001t0001g0063a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG00738.hp1 HG01928.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+4470T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686448 | ||||||
| chr14:102686693
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.445+4715A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686693 | ||||||
| chr14:102686732
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.445+4754C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686732 | ||||||
| chr14:102686827
|
A | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+4849A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686827 | ||||||
| chr14:102686878
|
T | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.445+4900T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102686878 | ||||||
| chr14:102687080
|
G | A | 1 | a0001c0001t0019g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.445+5102G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102687080 | ||||||
| chr14:102687178
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.445+5200C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102687178 | ||||||
| chr14:102687564
|
A | G | 1 | a0001c0001t0034g0039 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.445+5586A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102687564 | ||||||
| chr14:102687656
|
T | C | 1 | a0001c0001t0042g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.445+5678T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102687656 | ||||||
| chr14:102687854
|
A | G | 109 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(106): Show | 109 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.445+5876A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102687854 | ||||||
| chr14:102687927
|
A | G | 4 | a0001c0001t0009g0143a0001c0001t0009g0144a0001c0001t0009g0145others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+5949A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102687927 | ||||||
| chr14:102687964
|
C | CT | 14 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(11): Show | 14 | HG01099.hp1 HG01167.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+6005dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102687964 | |||||
| chr14:102687964
|
CT | C | 120 | a0001c0001t0001g0084a0001c0001t0002g0162a0001c0001t0002g0163others(117): Show | 120 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.445+6005delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102687964 | |||||
| chr14:102687964
|
CTT | C | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.445+6004_445+6005d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102687964 | |||||
| chr14:102687964
|
CTTT | C | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.445+6003_445+6005d others(5): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102687964 | |||||
| chr14:102687980
|
T | C | 109 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(106): Show | 109 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.445+6002T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102687980 | ||||||
| chr14:102688006
|
G | A | 1 | a0001c0001t0043g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.445+6028G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102688006 | ||||||
| chr14:102688127
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.445+6149C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102688127 | ||||||
| chr14:102688440
|
A | T | 10 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(7): Show | 10 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.445+6462A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102688440 | ||||||
| chr14:102688560
|
C | T | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.445+6582C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102688560 | ||||||
| chr14:102688651
|
A | G | 19 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(16): Show | 19 | HG00733.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+6673A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102688651 | ||||||
| chr14:102688782
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.445+6804G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102688782 | ||||||
| chr14:102688794
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.445+6816C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102688794 | ||||||
| chr14:102689077
|
A | G | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.445+7099A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102689077 | ||||||
| chr14:102689128
|
G | A | 5 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+7150G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102689128 | ||||||
| chr14:102689207
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.445+7229C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102689207 | ||||||
| chr14:102689257
|
A | G | 133 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.445+7279A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102689257 | ||||||
| chr14:102689300
|
T | G | 170 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(167): Show | 170 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.445+7322T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102689300 | ||||||
| chr14:102689317
|
AT | A | 3 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0048g0179 | 3 | HG00609.hp1 NA18944.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.445+7341delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102689317 | |||||
| chr14:102689352
|
G | T | 8 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(5): Show | 8 | HG02451.hp2 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+7374G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102689352 | ||||||
| chr14:102689774
|
C | G | 3 | a0001c0001t0004g0173a0001c0001t0004g0184a0001c0001t0004g0185 | 3 | HG03490.hp1 HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.445+7796C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102689774 | ||||||
| chr14:102690032
|
C | T | 9 | a0001c0001t0008g0263a0001c0001t0008g0268a0001c0001t0008g0269others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+8054C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690032 | ||||||
| chr14:102690045
|
A | AT | 36 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.445+8077dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102690045 | |||||
| chr14:102690138
|
G | GT | 7 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0026others(4): Show | 7 | HG02258.hp1 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.445+8163dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102690138 | |||||
| chr14:102690248
|
A | C | 11 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(8): Show | 11 | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.445+8270A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690248 | ||||||
| chr14:102690249
|
C | T | 151 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.445+8271C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690249 | ||||||
| chr14:102690286
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.445+8308A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690286 | ||||||
| chr14:102690439
|
A | G | 16 | a0001c0001t0002g0168a0001c0001t0002g0172a0001c0001t0002g0181others(13): Show | 16 | HG01261.hp2 HG01358.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.445+8461A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690439 | ||||||
| chr14:102690596
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.445+8618G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690596 | ||||||
| chr14:102690822
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.445+8844G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690822 | ||||||
| chr14:102690968
|
T | C | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.445+8990T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690968 | ||||||
| chr14:102690975
|
A | T | 1 | a0001c0001t0043g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.445+8997A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102690975 | ||||||
| chr14:102691088
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.445+9110C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691088 | ||||||
| chr14:102691150
|
C | T | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.445+9172C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691150 | ||||||
| chr14:102691285
|
CAATA | C | 111 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(108): Show | 111 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.445+9313_445+9316d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102691285 | |||||
| chr14:102691319
|
G | GGA | 114 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.445+9345_445+9346d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102691319 | |||||
| chr14:102691399
|
C | T | 2 | a0001c0001t0003g0021a0001c0001t0011g0025 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.445+9421C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691399 | ||||||
| chr14:102691407
|
G | A | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.445+9429G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691407 | ||||||
| chr14:102691447
|
A | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.445+9469A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691447 | ||||||
| chr14:102691516
|
G | A | 3 | a0001c0001t0002g0192a0001c0001t0002g0207a0001c0001t0002g0211 | 3 | HG02055.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.445+9538G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691516 | ||||||
| chr14:102691551
|
T | C | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.445+9573T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691551 | ||||||
| chr14:102691563
|
A | T | 3 | a0001c0001t0002g0245a0001c0001t0002g0248a0001c0001t0002g0285 | 3 | NA18969.hp1 NA19004.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.445+9585A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691563 | ||||||
| chr14:102691640
|
T | A | 1 | a0001c0001t0001g0010 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.446-9638T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691640 | ||||||
| chr14:102691760
|
T | C | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-9518T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691760 | ||||||
| chr14:102691772
|
A | T | 11 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-9506A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691772 | ||||||
| chr14:102691775
|
T | C | 11 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-9503T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691775 | ||||||
| chr14:102691848
|
T | C | 2 | a0001c0001t0006g0256a0001c0005t0037g0149 | 2 | HG00099.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.446-9430T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691848 | ||||||
| chr14:102691868
|
C | T | 1 | a0001c0001t0042g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.446-9410C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691868 | ||||||
| chr14:102691920
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.446-9358A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691920 | ||||||
| chr14:102691933
|
T | C | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.446-9345T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102691933 | ||||||
| chr14:102692119
|
T | G | 4 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(1): Show | 4 | HG03139.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-9159T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692119 | ||||||
| chr14:102692325
|
C | G | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.446-8953C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692325 | ||||||
| chr14:102692378
|
A | G | 1 | a0001c0001t0005g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.446-8900A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692378 | ||||||
| chr14:102692440
|
A | AAC | 79 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(76): Show | 79 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.446-8807_446-8806d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
A | AACAC | 18 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0017others(15): Show | 18 | HG00423.hp1 HG01099.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.446-8809_446-8806d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
A | AACACAC | 5 | a0001c0001t0003g0052a0001c0001t0010g0064a0001c0001t0010g0104others(2): Show | 5 | HG00733.hp1 HG02818.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-8811_446-8806d others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
A | AACACACA others(1): Show |
3 | a0001c0001t0005g0121a0001c0001t0005g0137a0001c0001t0010g0067 | 3 | HG01884.hp2 HG02080.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.446-8813_446-8806d others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
A | AACACACA others(3): Show |
31 | a0001c0001t0005g0059a0001c0001t0005g0116a0001c0001t0005g0118others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.446-8815_446-8806d others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
A | AACACACA others(5): Show |
6 | a0001c0001t0005g0004a0001c0001t0005g0140a0001c0001t0006g0261others(3): Show | 6 | HG01175.hp2 HG01934.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.446-8817_446-8806d others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
A | AACACACA others(7): Show |
4 | a0001c0001t0005g0053a0001c0001t0005g0114a0001c0001t0005g0126others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-8819_446-8806d others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
A | AACACACA others(9): Show |
1 | a0001c0001t0006g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.446-8821_446-8806d others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
AAC | A | 8 | a0001c0001t0001g0072a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 8 | HG01099.hp1 HG01257.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-8807_446-8806d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
AACAC | A | 9 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(6): Show | 9 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-8809_446-8806d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
AACACACA others(1): Show |
A | 8 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(5): Show | 8 | HG02451.hp2 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-8813_446-8806d others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692440
|
AACACACA others(5): Show |
A | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | NA19009.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.446-8817_446-8806d others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692440 | |||||
| chr14:102692557
|
C | T | 1 | a0001c0003t0005g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.446-8721C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692557 | ||||||
| chr14:102692567
|
A | G | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.446-8711A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692567 | ||||||
| chr14:102692595
|
G | T | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.446-8683G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692595 | ||||||
| chr14:102692710
|
C | CTCCT | 85 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(82): Show | 85 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.446-8525_446-8522d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
C | CTCCTTCC others(1): Show |
67 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0071others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.446-8529_446-8522d others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
C | CTCCTTCC others(5): Show |
32 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0084others(29): Show | 32 | HG00099.hp1 HG01168.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.446-8533_446-8522d others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
C | CTCCTTCC others(9): Show |
18 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0131others(15): Show | 18 | HG00673.hp1 HG00738.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.446-8537_446-8522d others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
C | CTCCTTCC others(13): Show |
5 | a0001c0001t0001g0100a0001c0001t0002g0164a0001c0001t0002g0207others(2): Show | 5 | HG00423.hp2 HG01928.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-8541_446-8522d others(22): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
CTCCT | C | 21 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0090others(18): Show | 21 | HG00673.hp2 HG01243.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.446-8525_446-8522d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
CTCCTTCC others(1): Show |
C | 8 | a0001c0001t0001g0029a0001c0001t0003g0006a0001c0001t0003g0046others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-8529_446-8522d others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
CTCCTTCC others(5): Show |
C | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.446-8533_446-8522d others(14): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
CTCCTTCC others(13): Show |
C | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.446-8541_446-8522d others(22): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692710
|
CTCCTTCC others(17): Show |
C | 1 | a0001c0001t0003g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.446-8545_446-8522d others(26): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692710 | |||||
| chr14:102692737
|
C | T | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.446-8541C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692737 | ||||||
| chr14:102692739
|
TCCTTCCT others(7): Show |
T | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.446-8538_446-8525d others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692739 | ||||||
| chr14:102692757
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.446-8521T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692757 | ||||||
| chr14:102692760
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.446-8518T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692760 | ||||||
| chr14:102692768
|
C | CT | 17 | a0001c0001t0002g0204a0001c0001t0003g0014a0001c0001t0003g0042others(14): Show | 17 | HG01081.hp1 HG01081.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.446-8493dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692768 | |||||
| chr14:102692768
|
CT | C | 10 | a0001c0001t0002g0222a0001c0001t0012g0152a0001c0001t0012g0153others(7): Show | 10 | HG01993.hp1 HG02015.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-8493delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102692768 | |||||
| chr14:102692800
|
C | G | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.446-8478C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692800 | ||||||
| chr14:102692822
|
T | G | 38 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(35): Show | 38 | HG00639.hp2 HG00733.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.446-8456T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102692822 | ||||||
| chr14:102693016
|
T | C | 1 | a0001c0001t0018g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.446-8262T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102693016 | ||||||
| chr14:102693289
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.446-7989G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102693289 | ||||||
| chr14:102693290
|
G | A | 10 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(7): Show | 10 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-7988G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102693290 | ||||||
| chr14:102693609
|
G | A | 10 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(7): Show | 10 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-7669G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102693609 | ||||||
| chr14:102693967
|
A | G | 3 | a0001c0001t0005g0053a0001c0001t0005g0114a0001c0001t0005g0140 | 3 | HG01167.hp1 HG01169.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.446-7311A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102693967 | ||||||
| chr14:102694279
|
T | C | 10 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(7): Show | 10 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-6999T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694279 | ||||||
| chr14:102694341
|
C | T | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.446-6937C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694341 | ||||||
| chr14:102694349
|
T | C | 10 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(7): Show | 10 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-6929T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694349 | ||||||
| chr14:102694380
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.446-6898C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694380 | ||||||
| chr14:102694402
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-6876A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694402 | ||||||
| chr14:102694570
|
C | T | 9 | a0001c0001t0006g0260a0001c0001t0009g0002a0001c0001t0009g0143others(6): Show | 9 | HG01123.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-6708C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694570 | ||||||
| chr14:102694594
|
A | G | 1 | a0001c0001t0003g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.446-6684A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694594 | ||||||
| chr14:102694832
|
A | G | 10 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(7): Show | 10 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-6446A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694832 | ||||||
| chr14:102694864
|
T | G | 1 | a0001c0001t0004g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.446-6414T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694864 | ||||||
| chr14:102694869
|
T | C | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.446-6409T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694869 | ||||||
| chr14:102694911
|
T | C | 1 | a0001c0001t0042g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.446-6367T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694911 | ||||||
| chr14:102694988
|
C | G | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.446-6290C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694988 | ||||||
| chr14:102694989
|
A | T | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.446-6289A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102694989 | ||||||
| chr14:102695134
|
T | G | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.446-6144T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102695134 | ||||||
| chr14:102695143
|
G | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.446-6135G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102695143 | ||||||
| chr14:102695399
|
A | AG | 291 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.446-5878dupG | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102695399 | |||||
| chr14:102695444
|
T | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.446-5834T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102695444 | ||||||
| chr14:102695614
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.446-5664C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102695614 | ||||||
| chr14:102695711
|
A | AT | 10 | a0001c0001t0001g0065a0001c0001t0001g0109a0001c0001t0001g0110others(7): Show | 10 | HG00733.hp1 HG02738.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-5548dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102695711 | |||||
| chr14:102695711
|
AT | A | 12 | a0001c0001t0001g0061a0001c0001t0006g0267a0001c0001t0009g0002others(9): Show | 12 | HG00280.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.446-5548delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102695711 | |||||
| chr14:102695851
|
T | C | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.446-5427T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102695851 | ||||||
| chr14:102696037
|
G | C | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.446-5241G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696037 | ||||||
| chr14:102696098
|
A | C | 2 | a0001c0001t0005g0059a0001c0001t0005g0120 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.446-5180A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696098 | ||||||
| chr14:102696168
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.446-5110T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696168 | ||||||
| chr14:102696422
|
G | C | 38 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(35): Show | 38 | HG00639.hp2 HG00733.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.446-4856G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696422 | ||||||
| chr14:102696443
|
G | A | 3 | a0001c0001t0002g0221a0001c0001t0002g0237a0001c0001t0018g0239 | 3 | NA18979.hp1 NA19070.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.446-4835G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696443 | ||||||
| chr14:102696585
|
C | T | 12 | a0001c0001t0006g0260a0001c0001t0006g0261a0001c0001t0006g0264others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.446-4693C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696585 | ||||||
| chr14:102696660
|
A | G | 1 | a0001c0001t0002g0248 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.446-4618A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696660 | ||||||
| chr14:102696711
|
T | C | 1 | a0001c0001t0046g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.446-4567T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102696711 | ||||||
| chr14:102696808
|
C | CT | 50 | a0001c0001t0001g0102a0001c0001t0002g0162a0001c0001t0002g0229others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.446-4447dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102696808 | |||||
| chr14:102696808
|
CT | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0060others(23): Show | 26 | HG00323.hp1 HG00733.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.446-4447delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102696808 | |||||
| chr14:102696808
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.446-4456_446-4447d others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102696808 | |||||
| chr14:102697042
|
G | C | 38 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(35): Show | 38 | HG00639.hp2 HG00733.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.446-4236G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697042 | ||||||
| chr14:102697118
|
A | G | 103 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.446-4160A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697118 | ||||||
| chr14:102697355
|
C | T | 1 | a0001c0001t0004g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.446-3923C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697355 | ||||||
| chr14:102697369
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0025g0088 | 3 | HG01993.hp1 NA18969.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.446-3909G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697369 | ||||||
| chr14:102697371
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.446-3907G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697371 | ||||||
| chr14:102697644
|
T | TC | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.446-3633dupC | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102697644 | |||||
| chr14:102697723
|
A | AT | 7 | a0001c0001t0001g0082a0001c0001t0002g0198a0001c0001t0002g0200others(4): Show | 7 | HG00609.hp2 HG02630.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-3539dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102697723 | |||||
| chr14:102697752
|
G | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.446-3526G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697752 | ||||||
| chr14:102697783
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.446-3495C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697783 | ||||||
| chr14:102697874
|
C | A | 1 | a0001c0001t0029g0115 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.446-3404C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697874 | ||||||
| chr14:102697901
|
A | G | 3 | a0001c0001t0002g0192a0001c0001t0002g0207a0001c0001t0002g0211 | 3 | HG02055.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.446-3377A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102697901 | ||||||
| chr14:102698128
|
G | A | 2 | a0001c0001t0031g0001a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.446-3150G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102698128 | ||||||
| chr14:102698344
|
A | G | 97 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(94): Show | 97 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.446-2934A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102698344 | ||||||
| chr14:102698591
|
C | T | 1 | a0001c0001t0015g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.446-2687C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102698591 | ||||||
| chr14:102698709
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.446-2569G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102698709 | ||||||
| chr14:102698808
|
G | C | 25 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.446-2470G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102698808 | ||||||
| chr14:102698849
|
A | G | 6 | a0001c0001t0001g0063a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG00738.hp1 HG01928.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.446-2429A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102698849 | ||||||
| chr14:102698925
|
CT | C | 72 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0002g0162others(69): Show | 72 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.446-2342delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102698925 | |||||
| chr14:102698940
|
A | G | 1 | a0001c0001t0006g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.446-2338A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102698940 | ||||||
| chr14:102699027
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0044g0202 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.446-2251C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699027 | ||||||
| chr14:102699079
|
G | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.446-2199G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699079 | ||||||
| chr14:102699104
|
G | C | 10 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(7): Show | 10 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-2174G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699104 | ||||||
| chr14:102699177
|
G | A | 70 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(67): Show | 70 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.446-2101G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699177 | ||||||
| chr14:102699178
|
C | T | 70 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(67): Show | 70 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.446-2100C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699178 | ||||||
| chr14:102699314
|
A | G | 1 | a0001c0001t0036g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.446-1964A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699314 | ||||||
| chr14:102699432
|
T | C | 1 | a0001c0001t0003g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.446-1846T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699432 | ||||||
| chr14:102699549
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.446-1729T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699549 | ||||||
| chr14:102699598
|
C | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.446-1680C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699598 | ||||||
| chr14:102699645
|
G | C | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.446-1633G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699645 | ||||||
| chr14:102699755
|
A | AT | 10 | a0001c0001t0001g0109a0001c0001t0002g0164a0001c0001t0002g0233others(7): Show | 10 | HG00323.hp2 HG00423.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.446-1509dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102699755 | |||||
| chr14:102699755
|
AT | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0005g0004others(26): Show | 29 | HG00609.hp2 HG00639.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.446-1509delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102699755 | |||||
| chr14:102699765
|
T | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.446-1513T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699765 | ||||||
| chr14:102699778
|
T | G | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.446-1500T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699778 | ||||||
| chr14:102699863
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.446-1415C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102699863 | ||||||
| chr14:102700006
|
G | A | 2 | a0001c0001t0003g0006a0001c0001t0003g0046 | 2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.446-1272G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700006 | ||||||
| chr14:102700050
|
A | C | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.446-1228A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700050 | ||||||
| chr14:102700091
|
A | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.446-1187A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700091 | ||||||
| chr14:102700224
|
T | C | 2 | a0001c0001t0003g0006a0001c0001t0003g0046 | 2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.446-1054T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700224 | ||||||
| chr14:102700227
|
C | CTTTTTCT others(15): Show |
2 | a0001c0001t0005g0119a0001c0001t0005g0122 | 2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.446-1049_446-1028d others(24): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102700227 | |||||
| chr14:102700315
|
G | A | 2 | a0001c0001t0031g0001a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.446-963G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700315 | ||||||
| chr14:102700372
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.446-906C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700372 | ||||||
| chr14:102700405
|
A | G | 2 | a0001c0001t0003g0035a0001c0001t0003g0038 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.446-873A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700405 | ||||||
| chr14:102700600
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.446-678C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700600 | ||||||
| chr14:102700644
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.446-634C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700644 | ||||||
| chr14:102700822
|
G | GT | 8 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(5): Show | 8 | HG02451.hp2 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-455dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102700822 | |||||
| chr14:102700831
|
C | T | 7 | a0001c0001t0002g0182a0001c0001t0012g0152a0001c0001t0012g0153others(4): Show | 7 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-447C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700831 | ||||||
| chr14:102700948
|
C | T | 1 | a0001c0001t0036g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.446-330C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102700948 | ||||||
| chr14:102701010
|
C | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.446-268C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102701010 | ||||||
| chr14:102701232
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-46A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 3/11 | chr14 | 102701232 | ||||||
| chr14:102701339
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+9A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102701339 | ||||||
| chr14:102701598
|
G | C | 1 | a0001c0001t0034g0039 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.498+268G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102701598 | ||||||
| chr14:102701750
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.498+420C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102701750 | ||||||
| chr14:102701751
|
G | A | 15 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.498+421G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102701751 | ||||||
| chr14:102701854
|
A | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.498+524A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102701854 | ||||||
| chr14:102701877
|
A | G | 1 | a0001c0001t0045g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.498+547A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102701877 | ||||||
| chr14:102702198
|
T | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0037a0001c0001t0003g0040 | 3 | NA18951.hp1 NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.498+868T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102702198 | ||||||
| chr14:102702209
|
T | C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.498+879T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102702209 | ||||||
| chr14:102702920
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.498+1590A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102702920 | ||||||
| chr14:102702937
|
A | G | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.498+1607A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102702937 | ||||||
| chr14:102703086
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.498+1756T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102703086 | ||||||
| chr14:102703096
|
G | A | 1 | a0001c0001t0004g0169 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.498+1766G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102703096 | ||||||
| chr14:102703195
|
G | A | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1865G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102703195 | ||||||
| chr14:102703768
|
A | C | 1 | a0001c0001t0001g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.498+2438A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102703768 | ||||||
| chr14:102703768
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.498+2438A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102703768 | ||||||
| chr14:102703906
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0011g0047 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.498+2576C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102703906 | ||||||
| chr14:102703972
|
A | C | 1 | a0001c0001t0002g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.498+2642A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102703972 | ||||||
| chr14:102704028
|
A | G | 8 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0021others(5): Show | 8 | HG02258.hp1 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+2698A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704028 | ||||||
| chr14:102704255
|
C | T | 4 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(1): Show | 4 | HG03139.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+2925C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704255 | ||||||
| chr14:102704428
|
A | G | 161 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(158): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.499-2923A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704428 | ||||||
| chr14:102704518
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.499-2833G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704518 | ||||||
| chr14:102704525
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0081others(9): Show | 12 | HG00609.hp2 HG00738.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-2826G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704525 | ||||||
| chr14:102704535
|
A | G | 14 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(11): Show | 14 | HG00733.hp1 HG01167.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.499-2816A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704535 | ||||||
| chr14:102704592
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.499-2759C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704592 | ||||||
| chr14:102704638
|
G | T | 4 | a0001c0001t0005g0053a0001c0001t0005g0114a0001c0001t0005g0126others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-2713G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704638 | ||||||
| chr14:102704677
|
A | G | 161 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(158): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.499-2674A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704677 | ||||||
| chr14:102704690
|
G | A | 3 | a0001c0001t0009g0002a0001c0001t0009g0148a0001c0001t0043g0146 | 3 | HG03453.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.499-2661G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704690 | ||||||
| chr14:102704710
|
G | A | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.499-2641G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102704710 | ||||||
| chr14:102705131
|
C | A | 9 | a0001c0001t0001g0011a0001c0001t0012g0152a0001c0001t0012g0153others(6): Show | 9 | HG01074.hp1 HG01167.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.499-2220C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102705131 | ||||||
| chr14:102705141
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.499-2210G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102705141 | ||||||
| chr14:102705251
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.499-2100T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102705251 | ||||||
| chr14:102705284
|
G | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.499-2067G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102705284 | ||||||
| chr14:102705911
|
T | C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.499-1440T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102705911 | ||||||
| chr14:102706114
|
C | CA | 34 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0060others(31): Show | 34 | HG00738.hp2 HG01074.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.499-1209dupA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAA | 11 | a0001c0001t0001g0071a0001c0001t0003g0008a0001c0001t0003g0021others(8): Show | 11 | HG01099.hp2 HG02145.hp2 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-1210_499-1209d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAA | 7 | a0001c0001t0002g0192a0001c0001t0002g0207a0001c0001t0003g0013others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-1211_499-1209d others(5): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAA | 15 | a0001c0001t0002g0172a0001c0001t0002g0196a0001c0001t0002g0200others(12): Show | 15 | HG01261.hp2 HG01891.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.499-1212_499-1209d others(6): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAA | 10 | a0001c0001t0002g0182a0001c0001t0002g0208a0001c0001t0004g0169others(7): Show | 10 | HG01943.hp2 HG02300.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.499-1213_499-1209d others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAA | 10 | a0001c0001t0002g0163a0001c0001t0002g0209a0001c0001t0002g0283others(7): Show | 10 | HG01123.hp1 HG01358.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.499-1214_499-1209d others(8): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA | 20 | a0001c0001t0002g0181a0001c0001t0002g0198a0001c0001t0002g0204others(17): Show | 20 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.499-1215_499-1209d others(9): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(1): Show |
14 | a0001c0001t0002g0197a0001c0001t0002g0201a0001c0001t0002g0217others(11): Show | 14 | HG02015.hp2 HG02056.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.499-1216_499-1209d others(10): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(2): Show |
24 | a0001c0001t0002g0162a0001c0001t0002g0168a0001c0001t0002g0218others(21): Show | 24 | HG00639.hp2 HG01192.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.499-1217_499-1209d others(11): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(3): Show |
9 | a0001c0001t0002g0164a0001c0001t0002g0238a0001c0001t0002g0246others(6): Show | 9 | HG00423.hp2 HG00673.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.499-1218_499-1209d others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0223a0001c0001t0002g0232a0001c0001t0002g0242 | 3 | HG01243.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.499-1219_499-1209d others(13): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(6): Show |
6 | a0001c0001t0005g0114a0001c0001t0005g0119a0001c0001t0005g0120others(3): Show | 6 | HG01169.hp2 HG01928.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.499-1221_499-1209d others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0005g0053a0001c0001t0005g0059a0001c0003t0005g0117 | 3 | HG01167.hp1 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.499-1222_499-1209d others(16): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0005g0121a0001c0001t0005g0126 | 2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.499-1224_499-1209d others(18): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0005g0122a0001c0001t0005g0137 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.499-1225_499-1209d others(19): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0005g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.499-1209_499-1208i others(31): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
CA | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.499-1209delA | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706114
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0134a0001c0001t0004g0175 | 2 | HG01496.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.499-1221_499-1209d others(15): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706114 | |||||
| chr14:102706142
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0005g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499-1209_499-1208i others(34): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102706142 | ||||||
| chr14:102706241
|
T | C | 3 | a0001c0001t0020g0289a0001c0001t0020g0290a0001c0001t0050g0142 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.499-1110T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102706241 | ||||||
| chr14:102706303
|
T | A | 2 | a0001c0001t0050g0142a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.499-1048T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102706303 | ||||||
| chr14:102706347
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.499-1004A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102706347 | ||||||
| chr14:102706686
|
G | T | 1 | a0001c0003t0005g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.499-665G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102706686 | ||||||
| chr14:102706822
|
A | AAAT | 8 | a0001c0001t0002g0212a0001c0001t0002g0288a0001c0001t0003g0160others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.499-505_499-503dup others(3): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102706822 | |||||
| chr14:102706966
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.499-385A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102706966 | ||||||
| chr14:102707232
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0050g0142 | 2 | HG03486.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.499-119G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 4/11 | chr14 | 102707232 | ||||||
| chr14:102707665
|
G | T | 1 | a0001c0001t0003g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.660+153G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707665 | ||||||
| chr14:102707666
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.660+154G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707666 | ||||||
| chr14:102707820
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.660+308C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707820 | ||||||
| chr14:102707840
|
G | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.660+328G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707840 | ||||||
| chr14:102707861
|
T | A | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660+349T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707861 | ||||||
| chr14:102707881
|
C | T | 4 | a0001c0001t0003g0051a0001c0002t0003g0055a0001c0002t0003g0136others(1): Show | 4 | HG01261.hp1 HG01515.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+369C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707881 | ||||||
| chr14:102707946
|
C | T | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.660+434C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707946 | ||||||
| chr14:102707955
|
A | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.660+443A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707955 | ||||||
| chr14:102707956
|
A | C | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+444A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102707956 | ||||||
| chr14:102707967
|
CT | C | 139 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0083others(136): Show | 139 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.660+471delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 102707967 | |||||
| chr14:102708124
|
C | T | 1 | a0001c0001t0025g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.661-341C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102708124 | ||||||
| chr14:102708151
|
A | G | 14 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(11): Show | 14 | HG00733.hp1 HG01167.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.661-314A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102708151 | ||||||
| chr14:102708356
|
A | G | 3 | a0001c0001t0031g0001a0001c0001t0050g0142a0001c0005t0037g0149 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661-109A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102708356 | ||||||
| chr14:102708392
|
G | A | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.661-73G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 5/11 | chr14 | 102708392 | ||||||
| chr14:102708876
|
G | C | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.779+293G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102708876 | ||||||
| chr14:102708982
|
CTG | C | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.779+401_779+402del others(2): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102708982 | |||||
| chr14:102709050
|
G | C | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.779+467G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102709050 | ||||||
| chr14:102709517
|
A | G | 2 | a0001c0001t0031g0001a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.779+934A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102709517 | ||||||
| chr14:102709733
|
T | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0184 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.779+1150T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102709733 | ||||||
| chr14:102709803
|
A | G | 1 | a0001c0001t0003g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780-1132A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102709803 | ||||||
| chr14:102709901
|
A | T | 1 | a0001c0001t0022g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.780-1034A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102709901 | ||||||
| chr14:102710179
|
G | A | 3 | a0001c0001t0031g0001a0001c0001t0050g0142a0001c0005t0037g0149 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.780-756G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710179 | ||||||
| chr14:102710196
|
G | C | 3 | a0001c0001t0031g0001a0001c0001t0050g0142a0001c0005t0037g0149 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.780-739G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710196 | ||||||
| chr14:102710220
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.780-715C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710220 | ||||||
| chr14:102710298
|
A | G | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.780-637A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710298 | ||||||
| chr14:102710424
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.780-511A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710424 | ||||||
| chr14:102710600
|
A | G | 1 | a0001c0001t0009g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.780-335A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710600 | ||||||
| chr14:102710867
|
C | G | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.780-68C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710867 | ||||||
| chr14:102710886
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.780-49G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710886 | ||||||
| chr14:102710895
|
G | A | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.780-40G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 6/11 | chr14 | 102710895 | ||||||
| chr14:102711077
|
AT | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.858+66delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102711077 | |||||
| chr14:102711083
|
G | C | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.858+70G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711083 | ||||||
| chr14:102711307
|
A | G | 31 | a0001c0001t0005g0004a0001c0001t0005g0053a0001c0001t0005g0059others(28): Show | 31 | HG00639.hp2 HG00733.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.858+294A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711307 | ||||||
| chr14:102711356
|
A | G | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+343A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711356 | ||||||
| chr14:102711357
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.858+344T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711357 | ||||||
| chr14:102711370
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.858+357G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711370 | ||||||
| chr14:102711431
|
C | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.858+418C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711431 | ||||||
| chr14:102711523
|
A | C | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.858+510A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711523 | ||||||
| chr14:102711612
|
G | C | 1 | a0001c0001t0004g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.858+599G>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711612 | ||||||
| chr14:102711794
|
T | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.858+781T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711794 | ||||||
| chr14:102711856
|
T | G | 2 | a0001c0001t0004g0173a0001c0001t0004g0184 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.858+843T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102711856 | ||||||
| chr14:102712323
|
T | C | 3 | a0001c0001t0031g0001a0001c0001t0050g0142a0001c0005t0037g0149 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.858+1310T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102712323 | ||||||
| chr14:102712370
|
A | G | 28 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.858+1357A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102712370 | ||||||
| chr14:102712663
|
C | CT | 8 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0094others(5): Show | 8 | HG01433.hp1 HG02735.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.858+1666dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102712663 | |||||
| chr14:102712663
|
CT | C | 6 | a0001c0001t0001g0095a0001c0001t0003g0041a0001c0001t0009g0148others(3): Show | 6 | HG00733.hp1 HG01255.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.858+1666delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102712663 | |||||
| chr14:102712924
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.859-1499A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102712924 | ||||||
| chr14:102712947
|
G | GT | 48 | a0001c0001t0001g0033a0001c0001t0001g0065a0001c0001t0001g0075others(45): Show | 48 | HG00735.hp2 HG01175.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.859-1452dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102712947 | |||||
| chr14:102712947
|
GT | G | 30 | a0001c0001t0001g0029a0001c0001t0002g0163a0001c0001t0002g0181others(27): Show | 30 | HG00733.hp1 HG01123.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.859-1452delT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102712947 | |||||
| chr14:102712947
|
GTT | G | 57 | a0001c0001t0002g0164a0001c0001t0002g0192a0001c0001t0002g0196others(54): Show | 57 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.859-1453_859-1452d others(4): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102712947 | |||||
| chr14:102712947
|
GTTT | G | 18 | a0001c0001t0005g0004a0001c0001t0006g0256a0001c0001t0006g0257others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.859-1454_859-1452d others(5): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102712947 | |||||
| chr14:102712947
|
GTTTTT | G | 22 | a0001c0001t0005g0053a0001c0001t0005g0059a0001c0001t0005g0114others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.859-1456_859-1452d others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102712947 | |||||
| chr14:102712952
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.859-1471T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102712952 | ||||||
| chr14:102712958
|
T | G | 1 | a0001c0001t0020g0290 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.859-1465T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102712958 | ||||||
| chr14:102712959
|
T | G | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.859-1464T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102712959 | ||||||
| chr14:102713107
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.859-1316C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713107 | ||||||
| chr14:102713206
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.859-1217G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713206 | ||||||
| chr14:102713255
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.859-1168G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713255 | ||||||
| chr14:102713262
|
C | CT | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0004g0177others(3): Show | 6 | HG00735.hp2 HG01167.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-1147dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102713262 | |||||
| chr14:102713450
|
T | C | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-973T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713450 | ||||||
| chr14:102713524
|
C | T | 2 | a0001c0001t0031g0001a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.859-899C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713524 | ||||||
| chr14:102713542
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.859-881A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713542 | ||||||
| chr14:102713543
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.859-880A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713543 | ||||||
| chr14:102713629
|
G | A | 3 | a0001c0001t0009g0147a0001c0001t0031g0001a0001c0005t0037g0149 | 3 | HG01167.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.859-794G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713629 | ||||||
| chr14:102713725
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.859-698A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713725 | ||||||
| chr14:102713747
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.859-676A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102713747 | ||||||
| chr14:102714023
|
T | C | 2 | a0001c0001t0006g0271a0001c0001t0006g0273 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.859-400T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102714023 | ||||||
| chr14:102714090
|
C | G | 1 | a0001c0001t0004g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.859-333C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 7/11 | chr14 | 102714090 | ||||||
| chr14:102714707
|
G | A | 9 | a0001c0001t0008g0263a0001c0001t0008g0268a0001c0001t0008g0269others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1053+90G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102714707 | ||||||
| chr14:102714733
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1053+116C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102714733 | ||||||
| chr14:102714811
|
T | C | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1053+194T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102714811 | ||||||
| chr14:102714941
|
A | G | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1053+324A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102714941 | ||||||
| chr14:102714967
|
A | G | 2 | a0001c0001t0031g0001a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1053+350A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102714967 | ||||||
| chr14:102715072
|
A | AT | 11 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0002g0205others(8): Show | 11 | HG01081.hp1 HG01167.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1053+469dupT | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 102715072 | |||||
| chr14:102715130
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1053+513G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715130 | ||||||
| chr14:102715228
|
C | A | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1053+611C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715228 | ||||||
| chr14:102715290
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1053+673C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715290 | ||||||
| chr14:102715382
|
T | A | 1 | a0001c0001t0002g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1053+765T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715382 | ||||||
| chr14:102715477
|
G | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0025g0088 | 3 | HG01993.hp1 NA18969.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1053+860G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715477 | ||||||
| chr14:102715500
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1053+883G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715500 | ||||||
| chr14:102715648
|
G | A | 1 | a0001c0001t0004g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1053+1031G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715648 | ||||||
| chr14:102715986
|
C | T | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1053+1369C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102715986 | ||||||
| chr14:102716213
|
C | G | 9 | a0001c0001t0008g0263a0001c0001t0008g0268a0001c0001t0008g0269others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1053+1596C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102716213 | ||||||
| chr14:102716347
|
A | G | 2 | a0001c0001t0031g0001a0001c0005t0037g0149 | 2 | HG01167.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1053+1730A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102716347 | ||||||
| chr14:102716454
|
G | A | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1053+1837G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102716454 | ||||||
| chr14:102716580
|
A | G | 1 | a0001c0001t0004g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1053+1963A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102716580 | ||||||
| chr14:102716595
|
T | TATTGAAG others(22): Show |
8 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(5): Show | 8 | HG02451.hp2 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053+1980_1053+200 others(33): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 102716595 | |||||
| chr14:102716676
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1053+2059G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102716676 | ||||||
| chr14:102717086
|
T | C | 1 | a0001c0001t0003g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1053+2469T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717086 | ||||||
| chr14:102717179
|
A | G | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+2562A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717179 | ||||||
| chr14:102717356
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1053+2739G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717356 | ||||||
| chr14:102717446
|
G | T | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1053+2829G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717446 | ||||||
| chr14:102717560
|
G | A | 1 | a0001c0001t0036g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1053+2943G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717560 | ||||||
| chr14:102717679
|
T | G | 1 | a0001c0001t0026g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1053+3062T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717679 | ||||||
| chr14:102717720
|
G | A | 2 | a0001c0001t0006g0270a0001c0001t0006g0272 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1053+3103G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717720 | ||||||
| chr14:102717839
|
T | C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1054-3168T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717839 | ||||||
| chr14:102717994
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG01123.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1054-3013G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102717994 | ||||||
| chr14:102718017
|
A | G | 2 | a0001c0001t0016g0281a0001c0001t0016g0282 | 2 | NA18967.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1054-2990A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102718017 | ||||||
| chr14:102718232
|
A | G | 1 | a0001c0001t0003g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1054-2775A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102718232 | ||||||
| chr14:102718255
|
A | C | 1 | a0001c0001t0001g0071 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1054-2752A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102718255 | ||||||
| chr14:102718416
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1054-2591C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102718416 | ||||||
| chr14:102718587
|
T | G | 2 | a0001c0001t0003g0028a0001c0001t0003g0056 | 2 | HG03017.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1054-2420T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102718587 | ||||||
| chr14:102718792
|
G | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1054-2215G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102718792 | ||||||
| chr14:102718811
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1054-2196C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102718811 | ||||||
| chr14:102719098
|
T | G | 106 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0002g0162others(103): Show | 106 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.1054-1909T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719098 | ||||||
| chr14:102719132
|
A | G | 3 | a0001c0001t0004g0173a0001c0001t0004g0184a0001c0001t0004g0185 | 3 | HG03490.hp1 HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1054-1875A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719132 | ||||||
| chr14:102719172
|
T | C | 1 | a0001c0001t0038g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1054-1835T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719172 | ||||||
| chr14:102719236
|
T | TTTC | 3 | a0001c0001t0003g0003a0001c0001t0003g0037a0001c0001t0003g0040 | 3 | NA18951.hp1 NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1054-1753_1054-175 others(7): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 102719236 | |||||
| chr14:102719257
|
T | C | 1 | a0001c0001t0004g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1054-1750T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719257 | ||||||
| chr14:102719262
|
A | T | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1054-1745A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719262 | ||||||
| chr14:102719288
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1054-1719C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719288 | ||||||
| chr14:102719356
|
G | A | 3 | a0001c0001t0003g0046a0001c0001t0009g0148a0001c0001t0043g0146 | 3 | HG03927.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1054-1651G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719356 | ||||||
| chr14:102719394
|
C | T | 1 | a0001c0001t0005g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1054-1613C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719394 | ||||||
| chr14:102719419
|
C | T | 1 | a0001c0001t0004g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1054-1588C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719419 | ||||||
| chr14:102719812
|
A | G | 7 | a0001c0001t0009g0002a0001c0001t0009g0143a0001c0001t0009g0144others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054-1195A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719812 | ||||||
| chr14:102719989
|
T | C | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1054-1018T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102719989 | ||||||
| chr14:102720150
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054-857C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720150 | ||||||
| chr14:102720227
|
C | T | 3 | a0001c0001t0002g0283a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | NA18973.hp2 NA19012.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1054-780C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720227 | ||||||
| chr14:102720305
|
T | A | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1054-702T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720305 | ||||||
| chr14:102720356
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1054-651C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720356 | ||||||
| chr14:102720458
|
C | T | 1 | a0001c0001t0013g0292 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1054-549C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720458 | ||||||
| chr14:102720589
|
C | T | 4 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0201others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-418C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720589 | ||||||
| chr14:102720788
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1054-219C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720788 | ||||||
| chr14:102720892
|
A | G | 1 | a0001c0001t0051g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1054-115A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720892 | ||||||
| chr14:102720929
|
C | G | 1 | a0001c0001t0011g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1054-78C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720929 | ||||||
| chr14:102720932
|
T | C | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1054-75T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 8/11 | chr14 | 102720932 | ||||||
| chr14:102721430
|
C | T | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(2): Show | 5 | HG03139.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189+53C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721430 | ||||||
| chr14:102721444
|
A | G | 1 | a0001c0001t0003g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1189+67A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721444 | ||||||
| chr14:102721449
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1189+72G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721449 | ||||||
| chr14:102721563
|
A | T | 4 | a0001c0001t0031g0001a0001c0001t0050g0142a0001c0003t0005g0117others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189+186A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721563 | ||||||
| chr14:102721564
|
T | A | 1 | a0001c0001t0004g0190 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1189+187T>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721564 | ||||||
| chr14:102721607
|
A | G | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1189+230A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721607 | ||||||
| chr14:102721798
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1190-389A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721798 | ||||||
| chr14:102721858
|
T | C | 2 | a0001c0001t0013g0291a0001c0001t0013g0292 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1190-329T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102721858 | ||||||
| chr14:102722002
|
C | T | 6 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190-185C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102722002 | ||||||
| chr14:102722044
|
C | T | 1 | a0001c0005t0037g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1190-143C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 10/11 | chr14 | 102722044 | ||||||
| chr14:102722555
|
C | G | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1419+139C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102722555 | ||||||
| chr14:102722869
|
C | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1419+453C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102722869 | ||||||
| chr14:102722985
|
A | G | 2 | a0001c0001t0006g0270a0001c0001t0006g0272 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1419+569A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102722985 | ||||||
| chr14:102723177
|
G | T | 1 | a0001c0001t0002g0285 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1419+761G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723177 | ||||||
| chr14:102723255
|
C | G | 1 | a0001c0001t0013g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1419+839C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723255 | ||||||
| chr14:102723416
|
A | G | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1419+1000A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723416 | ||||||
| chr14:102723526
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1419+1110A>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723526 | ||||||
| chr14:102723557
|
C | T | 1 | a0001c0001t0011g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1419+1141C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723557 | ||||||
| chr14:102723636
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0050g0142 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1419+1220A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723636 | ||||||
| chr14:102723845
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1419+1429C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723845 | ||||||
| chr14:102723846
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1419+1430G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723846 | ||||||
| chr14:102723850
|
G | A | 3 | a0001c0001t0009g0002a0001c0001t0009g0148a0001c0001t0043g0146 | 3 | HG03453.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1419+1434G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102723850 | ||||||
| chr14:102724025
|
A | G | 76 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1419+1609A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724025 | ||||||
| chr14:102724061
|
G | T | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1419+1645G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724061 | ||||||
| chr14:102724201
|
A | G | 1 | a0001c0001t0003g0015 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1419+1785A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724201 | ||||||
| chr14:102724242
|
C | A | 9 | a0001c0001t0008g0263a0001c0001t0008g0268a0001c0001t0008g0269others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1419+1826C>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724242 | ||||||
| chr14:102724258
|
T | G | 3 | a0001c0001t0002g0212a0001c0001t0040g0213a0001c0001t0045g0203 | 3 | HG01884.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1419+1842T>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724258 | ||||||
| chr14:102724279
|
A | G | 1 | a0001c0001t0003g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1419+1863A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724279 | ||||||
| chr14:102724389
|
A | G | 1 | a0001c0001t0043g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1419+1973A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724389 | ||||||
| chr14:102724393
|
C | T | 3 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132 | 3 | HG00639.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1419+1977C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724393 | ||||||
| chr14:102724422
|
T | C | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1419+2006T>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724422 | ||||||
| chr14:102724429
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1419+2013C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724429 | ||||||
| chr14:102724506
|
A | G | 35 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0260others(32): Show | 35 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1420-1962A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724506 | ||||||
| chr14:102724575
|
C | T | 12 | a0001c0001t0005g0053a0001c0001t0005g0059a0001c0001t0005g0114others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420-1893C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724575 | ||||||
| chr14:102724628
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1420-1840C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724628 | ||||||
| chr14:102724879
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1420-1589A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102724879 | ||||||
| chr14:102725089
|
G | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1420-1379G>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725089 | ||||||
| chr14:102725134
|
A | G | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1420-1334A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725134 | ||||||
| chr14:102725143
|
A | G | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1420-1325A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725143 | ||||||
| chr14:102725320
|
A | C | 1 | a0001c0001t0003g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1420-1148A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725320 | ||||||
| chr14:102725331
|
A | G | 3 | a0001c0001t0031g0001a0001c0001t0050g0142a0001c0005t0037g0149 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1420-1137A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725331 | ||||||
| chr14:102725385
|
A | G | 1 | a0001c0001t0049g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1420-1083A>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725385 | ||||||
| chr14:102725629
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1420-839G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725629 | ||||||
| chr14:102725703
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1420-765G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725703 | ||||||
| chr14:102725725
|
G | A | 1 | a0001c0001t0004g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1420-743G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725725 | ||||||
| chr14:102725806
|
A | C | 12 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0012g0154others(9): Show | 12 | HG01099.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1420-662A>C | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725806 | ||||||
| chr14:102725956
|
C | G | 3 | a0001c0001t0031g0001a0001c0001t0050g0142a0001c0005t0037g0149 | 3 | HG01167.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1420-512C>G | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102725956 | ||||||
| chr14:102726019
|
C | T | 1 | a0001c0001t0050g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1420-449C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102726019 | ||||||
| chr14:102726274
|
C | T | 1 | a0001c0001t0039g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1420-194C>T | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102726274 | ||||||
| chr14:102726351
|
G | A | 1 | a0001c0001t0031g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1420-117G>A | RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | chr14 | 102726351 | ||||||
| chr14:102726418
|
GTTTACCT others(5): Show |
G | 5 | a0001c0001t0005g0004a0001c0001t0005g0116a0001c0001t0005g0132others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420-47_1420-36del others(12): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 102726418 |