Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84458 |
|---|---|
| ensemblid | ENSG00000196233.14 |
| hgncid | 29503 |
| symbol | LCOR |
| name | ligand dependent nuclear receptor corepressor |
| refseq_nuc | NM_001346516.2 |
| refseq_prot | NP_001333445.1 |
| ensembl_nuc | ENST00000421806.4 |
| ensembl_prot | ENSP00000490116.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 96832298 |
| end | 96995956 |
| strand | + |
| ver | v1.2 |
| region | chr10:96832298-96995956 |
| region5000 | chr10:96827298-97000956 |
| regionname0 | LCOR_chr10_96832298_96995956 |
| regionname5000 | LCOR_chr10_96827298_97000956 |
| 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 | 1557 | 157 | 41 | 32 | 61 | 3 | 18 | 51 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002 | 0/0 | 1557 | 58 | 11 | 5 | 34 | 1 | 7 | 27 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003 | 0/0 | 1557 | 33 | 0 | 2 | 27 | 0 | 4 | 23 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004 | 0/0 | 1557 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0005 | 0/0 | 1557 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0006 | 0/0 | 1557 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0007 | 0/0 | 1557 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0008 | 0/0 | 1557 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0009 | 0/0 | 1557 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0010 | 0/0 | 1557 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0011 | 0/0 | 1557 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0012 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0013 | 0/0 | 1160 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0014 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0015 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0016 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| 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 | 4674 | 129 | 35 | 29 | 47 | 3 | 13 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0002 | 0/0 | 4674 | 57 | 11 | 5 | 33 | 1 | 7 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0003 | 0/0 | 4674 | 33 | 0 | 2 | 27 | 0 | 4 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0004 | 0/0 | 4674 | 22 | 1 | 3 | 13 | 0 | 5 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0005 | 0/0 | 4674 | 9 | 8 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0006 | 0/0 | 4674 | 5 | 5 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0007 | 0/0 | 4674 | 5 | 5 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0008 | 0/0 | 4674 | 4 | 2 | 2 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0009 | 0/0 | 4674 | 3 | 3 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0010 | 0/0 | 4674 | 3 | 0 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0011 | 0/0 | 4674 | 3 | 0 | 1 | 0 | 0 | 2 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0012 | 0/0 | 4674 | 3 | 0 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0013 | 0/0 | 4674 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0014 | 0/0 | 4674 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0015 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0016 | 0/0 | 4674 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0017 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0018 | 0/0 | 4674 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0019 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0020 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0021 | 0/0 | 4674 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| c0022 | 0/0 | 4674 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| 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 | 0/0 | 11328 | 35 | 1 | 8 | 22 | 0 | 4 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0002 | 0/0 | 11324 | 15 | 1 | 3 | 10 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0003 | 1/0 | 11328 | 15 | 1 | 0 | 12 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0004 | 0/0 | 11324 | 13 | 0 | 0 | 11 | 0 | 2 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0005 | 0/0 | 11328 | 6 | 2 | 1 | 2 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0006 | 0/1 | 11327 | 6 | 1 | 1 | 2 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0007 | 0/0 | 11325 | 5 | 1 | 0 | 3 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0008 | 0/0 | 11328 | 5 | 0 | 1 | 4 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0009 | 0/0 | 11342 | 5 | 0 | 1 | 3 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0010 | 0/0 | 11324 | 4 | 0 | 0 | 4 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0011 | 0/0 | 11323 | 4 | 1 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0012 | 0/0 | 11329 | 4 | 1 | 1 | 1 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0013 | 0/0 | 11344 | 4 | 0 | 0 | 3 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0014 | 0/0 | 11342 | 4 | 0 | 0 | 4 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0015 | 0/0 | 11341 | 3 | 3 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0016 | 0/0 | 11333 | 3 | 3 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0017 | 0/0 | 11333 | 3 | 3 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0018 | 0/0 | 11334 | 3 | 0 | 3 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0019 | 0/0 | 11344 | 3 | 0 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0020 | 0/0 | 11343 | 3 | 0 | 0 | 0 | 0 | 3 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0021 | 0/0 | 11347 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0022 | 0/0 | 11333 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0023 | 0/0 | 11336 | 2 | 0 | 2 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0024 | 0/0 | 11323 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0025 | 0/0 | 11324 | 2 | 0 | 0 | 1 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0026 | 0/0 | 11328 | 2 | 0 | 2 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0027 | 0/0 | 11328 | 2 | 1 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0028 | 0/0 | 11330 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0029 | 0/0 | 11329 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0030 | 0/0 | 11329 | 2 | 0 | 1 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0031 | 0/0 | 11327 | 2 | 1 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0032 | 0/0 | 11329 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0033 | 0/0 | 11343 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0034 | 0/0 | 11341 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0035 | 0/0 | 11343 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0036 | 0/0 | 11342 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0037 | 0/0 | 11342 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0038 | 0/0 | 11328 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0039 | 0/0 | 11344 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0040 | 0/0 | 11360 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0041 | 0/0 | 11328 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0042 | 0/0 | 11357 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0043 | 0/0 | 11347 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0044 | 0/0 | 11352 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0045 | 0/0 | 11344 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0046 | 0/0 | 11347 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0047 | 0/0 | 11348 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0048 | 0/0 | 11342 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0049 | 0/0 | 11340 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0050 | 0/0 | 11347 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0051 | 0/0 | 11335 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0052 | 0/0 | 11350 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0053 | 0/0 | 11345 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0054 | 0/0 | 11350 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0055 | 0/0 | 11342 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0056 | 0/0 | 11343 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0057 | 0/0 | 11344 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0058 | 0/0 | 11346 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0059 | 0/0 | 11347 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0060 | 0/0 | 11342 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0061 | 0/0 | 11342 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0062 | 0/0 | 11341 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0063 | 0/0 | 11342 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0064 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0065 | 0/0 | 11339 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0066 | 0/0 | 11337 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0067 | 0/0 | 11336 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0068 | 0/0 | 11338 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0069 | 0/0 | 11339 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0070 | 0/0 | 11337 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0071 | 0/0 | 11337 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0072 | 0/0 | 11338 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0073 | 0/0 | 11334 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0074 | 0/0 | 11338 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0075 | 0/0 | 11335 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0076 | 0/0 | 11333 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0077 | 0/0 | 11334 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0078 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0079 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0080 | 0/0 | 11352 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0081 | 0/0 | 11328 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0082 | 0/0 | 11328 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0083 | 0/0 | 11327 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0084 | 0/0 | 11326 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0085 | 0/0 | 11329 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0086 | 0/0 | 11328 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0087 | 0/0 | 11322 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0088 | 0/0 | 11324 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0089 | 0/0 | 11325 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0090 | 0/0 | 11325 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0091 | 0/0 | 11327 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0092 | 0/0 | 11324 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0093 | 0/0 | 11324 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0094 | 0/0 | 11325 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0095 | 0/0 | 11325 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0096 | 0/0 | 11324 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0097 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0098 | 0/0 | 11329 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0099 | 0/0 | 11329 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0100 | 0/0 | 11328 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0101 | 0/0 | 11334 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0102 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0103 | 0/0 | 11329 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0104 | 0/0 | 11328 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0105 | 0/0 | 11328 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0106 | 0/0 | 11342 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0107 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0108 | 0/0 | 11326 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0109 | 0/0 | 11329 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0110 | 0/0 | 11328 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0111 | 0/0 | 11325 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0112 | 0/0 | 11329 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0113 | 0/0 | 11328 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0114 | 0/0 | 11328 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0115 | 0/0 | 11328 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0116 | 0/0 | 11330 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0117 | 0/0 | 11328 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0118 | 0/0 | 11328 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0119 | 0/0 | 11328 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0120 | 0/0 | 11330 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0121 | 0/0 | 11328 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0122 | 0/0 | 11324 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0123 | 0/0 | 11346 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0124 | 0/0 | 11343 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0125 | 0/0 | 11346 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0126 | 0/0 | 11341 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0127 | 0/0 | 11342 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0128 | 0/0 | 11344 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0129 | 0/0 | 11342 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0130 | 0/0 | 11345 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0131 | 0/0 | 11343 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0132 | 0/0 | 11344 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0133 | 0/0 | 11344 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0134 | 0/0 | 11340 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0135 | 0/0 | 11343 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0136 | 0/0 | 11342 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0137 | 0/0 | 11343 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0138 | 0/0 | 11341 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0139 | 0/0 | 11341 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0140 | 0/0 | 11342 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0141 | 0/0 | 11351 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0142 | 0/0 | 11325 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0143 | 0/0 | 11328 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0144 | 0/0 | 11328 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0145 | 0/0 | 11344 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0146 | 0/0 | 11340 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| t0147 | 0/0 | 11327 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| 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 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| 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 | 4674 | 129 | 35 | 29 | 47 | 3 | 13 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004 | 0/0 | 4674 | 22 | 1 | 3 | 13 | 0 | 5 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0007 | 0/0 | 4674 | 5 | 5 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0019 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002 | 0/0 | 4674 | 57 | 11 | 5 | 33 | 1 | 7 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0015 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003 | 0/0 | 4674 | 33 | 0 | 2 | 27 | 0 | 4 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005 | 0/0 | 4674 | 9 | 8 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0009 | 0/0 | 4674 | 3 | 3 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0005c0006 | 0/0 | 4674 | 5 | 5 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0006c0008 | 0/0 | 4674 | 4 | 2 | 2 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0007c0013 | 0/0 | 4674 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0007c0016 | 0/0 | 4674 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0008c0011 | 0/0 | 4674 | 3 | 0 | 1 | 0 | 0 | 2 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0009c0012 | 0/0 | 4674 | 3 | 0 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0010c0010 | 0/0 | 4674 | 3 | 0 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0011c0014 | 0/0 | 4674 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0012c0017 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0013c0018 | 0/0 | 4674 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0014c0020 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0015c0021 | 0/0 | 4674 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0016c0022 | 0/0 | 4674 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 16001 | 33 | 1 | 8 | 20 | 0 | 4 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0003 | 1/0 | 16001 | 14 | 1 | 0 | 11 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0005 | 0/0 | 16001 | 6 | 2 | 1 | 2 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0006 | 0/1 | 16000 | 5 | 1 | 1 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0012 | 0/0 | 16002 | 3 | 1 | 1 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0016 | 0/0 | 16006 | 3 | 3 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0017 | 0/0 | 16006 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0018 | 0/0 | 16007 | 3 | 0 | 3 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0022 | 0/0 | 16006 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0023 | 0/0 | 16009 | 2 | 0 | 2 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0026 | 0/0 | 16001 | 2 | 0 | 2 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0027 | 0/0 | 16001 | 2 | 1 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0028 | 0/0 | 16003 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0029 | 0/0 | 16002 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0030 | 0/0 | 16002 | 2 | 0 | 1 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0031 | 0/0 | 16000 | 2 | 1 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0032 | 0/0 | 16002 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0038 | 0/0 | 16001 | 2 | 2 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0051 | 0/0 | 16008 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0056 | 0/0 | 16016 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0065 | 0/0 | 16012 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0066 | 0/0 | 16010 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0067 | 0/0 | 16009 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0068 | 0/0 | 16011 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0069 | 0/0 | 16012 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0070 | 0/0 | 16010 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0071 | 0/0 | 16010 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0072 | 0/0 | 16011 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0073 | 0/0 | 16007 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0074 | 0/0 | 16011 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0075 | 0/0 | 16008 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0076 | 0/0 | 16006 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0077 | 0/0 | 16007 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0078 | 0/0 | 16000 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0079 | 0/0 | 16000 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0081 | 0/0 | 16001 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0093 | 0/0 | 15997 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0097 | 0/0 | 15999 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0098 | 0/0 | 16002 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0099 | 0/0 | 16002 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0100 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0101 | 0/0 | 16007 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0104 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0106 | 0/0 | 16015 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0107 | 0/0 | 16000 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0111 | 0/0 | 15998 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0112 | 0/0 | 16002 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0113 | 0/0 | 16001 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0114 | 0/0 | 16001 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0115 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0116 | 0/0 | 16003 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0117 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0118 | 0/0 | 16001 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0119 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0120 | 0/0 | 16003 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0121 | 0/0 | 16001 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0142 | 0/0 | 15998 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0143 | 0/0 | 16001 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0001t0144 | 0/0 | 16001 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0002 | 0/0 | 15997 | 5 | 0 | 1 | 4 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0007 | 0/0 | 15998 | 4 | 1 | 0 | 2 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0010 | 0/0 | 15997 | 3 | 0 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0011 | 0/0 | 15996 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0083 | 0/0 | 16000 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0084 | 0/0 | 15999 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0088 | 0/0 | 15997 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0089 | 0/0 | 15998 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0091 | 0/0 | 16000 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0094 | 0/0 | 15998 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0109 | 0/0 | 16002 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0110 | 0/0 | 16001 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0004t0122 | 0/0 | 15997 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0007t0102 | 0/0 | 16000 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0007t0103 | 0/0 | 16002 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0007t0105 | 0/0 | 16001 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0007t0108 | 0/0 | 15999 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0007t0147 | 0/0 | 16000 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0001c0019t0003 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0001 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0009 | 0/0 | 16015 | 4 | 0 | 1 | 2 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0013 | 0/0 | 16017 | 4 | 0 | 0 | 3 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0014 | 0/0 | 16015 | 4 | 0 | 0 | 4 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0015 | 0/0 | 16014 | 3 | 3 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0019 | 0/0 | 16017 | 3 | 0 | 0 | 3 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0020 | 0/0 | 16016 | 3 | 0 | 0 | 0 | 0 | 3 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0033 | 0/0 | 16016 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0034 | 0/0 | 16014 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0035 | 0/0 | 16016 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0036 | 0/0 | 16015 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0037 | 0/0 | 16015 | 2 | 0 | 1 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0039 | 0/0 | 16017 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0053 | 0/0 | 16018 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0055 | 0/0 | 16015 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0057 | 0/0 | 16017 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0058 | 0/0 | 16019 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0059 | 0/0 | 16020 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0061 | 0/0 | 16015 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0062 | 0/0 | 16014 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0063 | 0/0 | 16015 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0124 | 0/0 | 16016 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0126 | 0/0 | 16014 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0128 | 0/0 | 16017 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0129 | 0/0 | 16015 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0130 | 0/0 | 16018 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0131 | 0/0 | 16016 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0132 | 0/0 | 16017 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0133 | 0/0 | 16017 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0134 | 0/0 | 16013 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0135 | 0/0 | 16016 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0136 | 0/0 | 16015 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0137 | 0/0 | 16016 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0138 | 0/0 | 16014 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0139 | 0/0 | 16014 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0140 | 0/0 | 16015 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0002t0145 | 0/0 | 16017 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0002c0015t0009 | 0/0 | 16015 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0001 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0002 | 0/0 | 15997 | 5 | 0 | 0 | 5 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0004 | 0/0 | 15997 | 12 | 0 | 0 | 11 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0008 | 0/0 | 16001 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0010 | 0/0 | 15997 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0024 | 0/0 | 15996 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0025 | 0/0 | 15997 | 2 | 0 | 0 | 1 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0082 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0085 | 0/0 | 16002 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0086 | 0/0 | 16001 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0087 | 0/0 | 15995 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0090 | 0/0 | 15998 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0092 | 0/0 | 15997 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0095 | 0/0 | 15998 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0003c0003t0096 | 0/0 | 15997 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0021 | 0/0 | 16020 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0042 | 0/0 | 16030 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0043 | 0/0 | 16020 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0045 | 0/0 | 16017 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0046 | 0/0 | 16020 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0047 | 0/0 | 16021 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0048 | 0/0 | 16015 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0049 | 0/0 | 16013 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0005t0050 | 0/0 | 16020 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0009t0021 | 0/0 | 16020 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0009t0044 | 0/0 | 16025 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0004c0009t0064 | 0/0 | 16000 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0005c0006t0040 | 0/0 | 16033 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0005c0006t0041 | 0/0 | 16001 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0005c0006t0052 | 0/0 | 16023 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0005c0006t0054 | 0/0 | 16023 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0005c0006t0060 | 0/0 | 16015 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0006c0008t0002 | 0/0 | 15997 | 3 | 1 | 2 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0006c0008t0011 | 0/0 | 15996 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0007c0013t0080 | 0/0 | 16025 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0007c0013t0141 | 0/0 | 16024 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0007c0016t0146 | 0/0 | 16013 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0008c0011t0002 | 0/0 | 15997 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0008c0011t0004 | 0/0 | 15997 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0008c0011t0008 | 0/0 | 16001 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0009c0012t0007 | 0/0 | 15998 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0009c0012t0008 | 0/0 | 16001 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0010c0010t0002 | 0/0 | 15997 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0010c0010t0011 | 0/0 | 15996 | 2 | 0 | 0 | 2 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0011c0014t0123 | 0/0 | 16019 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0011c0014t0125 | 0/0 | 16019 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0012c0017t0127 | 0/0 | 16015 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0013c0018t0006 | 0/0 | 16000 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0014c0020t0012 | 0/0 | 16002 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0015c0021t0017 | 0/0 | 16006 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| a0016c0022t0028 | 0/0 | 16003 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | copy fasta | chr10 | 96827298 | 97000956 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0006g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0012g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0012g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0012g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0016g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0016g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0017g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0018g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0018g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0018g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0022g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0023g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0023g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0026g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0026g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0027g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0027g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0028g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0029g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0029g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0030g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0030g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0031g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0031g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0032g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0032g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0038g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0038g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0051g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0056g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0065g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0066g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0067g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0068g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0069g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0070g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0071g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0072g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0073g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0074g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0075g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0076g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0077g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0078g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0079g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0081g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0093g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0097g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0098g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0099g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0100g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0101g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0104g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0106g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0107g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0111g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0112g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0113g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0114g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0115g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0116g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0117g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0118g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0119g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0120g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0121g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0142g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0143g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0001t0144g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0010g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0010g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0083g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0084g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0088g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0089g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0091g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0094g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0109g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0110g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0004t0122g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0007t0102g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0007t0103g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0007t0105g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0007t0108g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0007t0147g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0001c0019t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0009g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0009g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0013g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0013g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0014g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0014g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0014g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0014g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0015g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0015g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0019g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0019g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0019g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0020g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0020g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0020g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0033g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0033g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0034g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0034g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0035g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0035g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0036g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0036g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0037g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0037g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0039g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0053g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0055g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0057g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0058g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0059g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0061g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0062g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0063g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0124g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0126g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0128g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0129g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0130g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0131g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0132g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0133g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0134g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0135g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0136g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0137g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0138g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0139g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0140g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0002t0145g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0002c0015t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0024g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0024g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0025g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0025g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0082g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0085g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0086g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0087g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0090g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0092g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0095g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0003c0003t0096g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0021g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0042g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0043g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0045g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0046g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0047g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0048g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0049g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0005t0050g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0009t0021g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0009t0044g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0004c0009t0064g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0005c0006t0040g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0005c0006t0041g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0005c0006t0052g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0005c0006t0054g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0005c0006t0060g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0006c0008t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0006c0008t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0006c0008t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0006c0008t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0007c0013t0080g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0007c0013t0141g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0007c0016t0146g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0008c0011t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0008c0011t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0008c0011t0008g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0009c0012t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0009c0012t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0009c0012t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0010c0010t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0010c0010t0011g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0010c0010t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0011c0014t0123g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0011c0014t0125g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0012c0017t0127g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0013c0018t0006g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0014c0020t0012g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0015c0021t0017g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| a0016c0022t0028g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0002 | c0002 | t0134 | g0095 | EUR | FIN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00323 | hp2 | a0001 | c0001 | t0031 | g0267 | EUR | FIN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00438 | hp2 | a0002 | c0002 | t0009 | g0076 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00544 | hp1 | a0001 | c0001 | t0104 | g0206 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00544 | hp2 | a0002 | c0002 | t0037 | g0071 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00558 | hp1 | a0002 | c0002 | t0138 | g0075 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00558 | hp2 | a0001 | c0004 | t0007 | g0019 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00621 | hp1 | a0002 | c0002 | t0135 | g0082 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00621 | hp2 | a0001 | c0001 | t0101 | g0247 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00639 | hp1 | a0001 | c0001 | t0067 | g0138 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00639 | hp2 | a0008 | c0011 | t0008 | g0201 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00642 | hp1 | a0002 | c0002 | t0036 | g0093 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00673 | hp1 | a0003 | c0003 | t0086 | g0050 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | CHS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00733 | hp1 | a0001 | c0001 | t0071 | g0132 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00733 | hp2 | a0006 | c0008 | t0002 | g0033 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00741 | hp1 | a0001 | c0001 | t0026 | g0223 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG00741 | hp2 | a0001 | c0001 | t0081 | g0231 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01070 | hp2 | a0001 | c0001 | t0076 | g0149 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01071 | hp1 | a0001 | c0001 | t0018 | g0151 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01071 | hp2 | a0001 | c0001 | t0093 | g0204 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01074 | hp1 | a0001 | c0001 | t0144 | g0257 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01081 | hp1 | a0001 | c0001 | t0066 | g0137 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01081 | hp2 | a0001 | c0001 | t0026 | g0242 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01099 | hp1 | a0001 | c0001 | t0113 | g0191 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01099 | hp2 | a0001 | c0004 | t0089 | g0055 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01106 | hp2 | a0001 | c0004 | t0084 | g0025 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01109 | hp1 | a0004 | c0005 | t0048 | g0167 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0225 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01167 | hp1 | a0002 | c0002 | t0034 | g0104 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01168 | hp1 | a0001 | c0001 | t0121 | g0264 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01168 | hp2 | a0002 | c0002 | t0037 | g0094 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01243 | hp1 | a0016 | c0022 | t0028 | g0219 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01243 | hp2 | a0001 | c0001 | t0120 | g0003 | AMR | PUR | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01257 | hp1 | a0006 | c0008 | t0002 | g0030 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01257 | hp2 | a0001 | c0001 | t0018 | g0150 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01258 | hp1 | a0001 | c0001 | t0030 | g0228 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01258 | hp2 | a0001 | c0001 | t0018 | g0152 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01261 | hp1 | a0001 | c0001 | t0023 | g0159 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01361 | hp1 | a0003 | c0003 | t0095 | g0053 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01361 | hp2 | a0001 | c0001 | t0023 | g0130 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01515 | hp1 | a0001 | c0001 | t0012 | g0252 | EUR | IBS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01515 | hp2 | a0001 | c0001 | t0074 | g0131 | EUR | IBS | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01884 | hp1 | a0007 | c0013 | t0080 | g0174 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01884 | hp2 | a0001 | c0001 | t0107 | g0178 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01928 | hp2 | a0001 | c0004 | t0002 | g0058 | AMR | PEL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01993 | hp1 | a0003 | c0003 | t0096 | g0279 | AMR | PEL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02027 | hp1 | a0001 | c0001 | t0116 | g0255 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02027 | hp2 | a0009 | c0012 | t0008 | g0021 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0136 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0254 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02071 | hp1 | a0009 | c0012 | t0008 | g0020 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02071 | hp2 | a0002 | c0002 | t0132 | g0088 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02074 | hp1 | a0003 | c0003 | t0090 | g0054 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02083 | hp1 | a0009 | c0012 | t0007 | g0063 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02083 | hp2 | a0001 | c0001 | t0115 | g0227 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02132 | hp2 | a0002 | c0002 | t0014 | g0065 | EAS | KHV | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02257 | hp1 | a0004 | c0005 | t0045 | g0168 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02257 | hp2 | a0001 | c0004 | t0007 | g0126 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02258 | hp1 | a0002 | c0002 | t0053 | g0108 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02258 | hp2 | a0001 | c0001 | t0022 | g0143 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0004 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02280 | hp2 | a0002 | c0002 | t0063 | g0117 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02300 | hp2 | a0002 | c0002 | t0009 | g0092 | AMR | PEL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02602 | hp1 | a0001 | c0004 | t0083 | g0024 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02602 | hp2 | a0001 | c0001 | t0030 | g0209 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02615 | hp1 | a0001 | c0007 | t0103 | g0179 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02615 | hp2 | a0001 | c0001 | t0073 | g0141 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02622 | hp1 | a0001 | c0001 | t0069 | g0129 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02622 | hp2 | a0006 | c0008 | t0002 | g0051 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02630 | hp1 | a0001 | c0001 | t0065 | g0148 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02630 | hp2 | a0001 | c0001 | t0027 | g0285 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02647 | hp1 | a0002 | c0002 | t0057 | g0119 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02647 | hp2 | a0001 | c0001 | t0056 | g0284 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02683 | hp1 | a0001 | c0004 | t0109 | g0027 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02683 | hp2 | a0013 | c0018 | t0006 | g0190 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02717 | hp1 | a0004 | c0005 | t0043 | g0124 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02717 | hp2 | a0001 | c0001 | t0038 | g0060 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02723 | hp2 | a0002 | c0002 | t0061 | g0118 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02735 | hp1 | a0008 | c0011 | t0004 | g0202 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02735 | hp2 | a0001 | c0004 | t0007 | g0041 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02738 | hp1 | a0003 | c0003 | t0085 | g0056 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02738 | hp2 | a0001 | c0001 | t0118 | g0249 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02809 | hp1 | a0001 | c0007 | t0105 | g0182 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02809 | hp2 | a0002 | c0002 | t0058 | g0107 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0273 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0146 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02886 | hp1 | a0001 | c0007 | t0102 | g0181 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02886 | hp2 | a0002 | c0002 | t0055 | g0109 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0176 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02895 | hp2 | a0007 | c0016 | t0146 | g0007 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02922 | hp1 | a0001 | c0001 | t0077 | g0127 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02922 | hp2 | a0005 | c0006 | t0040 | g0288 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02965 | hp1 | a0001 | c0007 | t0108 | g0180 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02965 | hp2 | a0006 | c0008 | t0011 | g0032 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02976 | hp1 | a0005 | c0006 | t0060 | g0287 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02976 | hp2 | a0001 | c0001 | t0111 | g0184 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03017 | hp2 | a0002 | c0002 | t0020 | g0116 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03041 | hp1 | a0002 | c0002 | t0059 | g0120 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03041 | hp2 | a0002 | c0002 | t0015 | g0102 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0145 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03195 | hp2 | a0004 | c0005 | t0046 | g0125 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03209 | hp1 | a0001 | c0001 | t0031 | g0272 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03209 | hp2 | a0001 | c0001 | t0143 | g0006 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03225 | hp1 | a0005 | c0006 | t0041 | g0163 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03225 | hp2 | a0002 | c0002 | t0015 | g0122 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03239 | hp1 | a0001 | c0004 | t0122 | g0011 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03453 | hp1 | a0004 | c0005 | t0021 | g0171 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03453 | hp2 | a0005 | c0006 | t0054 | g0164 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03516 | hp1 | a0001 | c0001 | t0032 | g0013 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03516 | hp2 | a0001 | c0001 | t0070 | g0139 | AFR | ESN | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03540 | hp1 | a0001 | c0001 | t0106 | g0286 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03540 | hp2 | a0001 | c0001 | t0079 | g0142 | AFR | GWD | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03579 | hp1 | a0001 | c0001 | t0097 | g0008 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03579 | hp2 | a0004 | c0009 | t0064 | g0166 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03654 | hp1 | a0002 | c0002 | t0009 | g0111 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03654 | hp2 | a0001 | c0004 | t0110 | g0043 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03688 | hp2 | a0001 | c0001 | t0051 | g0133 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03704 | hp1 | a0002 | c0002 | t0133 | g0074 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03704 | hp2 | a0008 | c0011 | t0002 | g0203 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03710 | hp2 | a0003 | c0003 | t0025 | g0045 | SAS | PJL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03834 | hp1 | a0002 | c0002 | t0020 | g0090 | SAS | BEB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03834 | hp2 | a0003 | c0003 | t0004 | g0177 | SAS | BEB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03942 | hp1 | a0001 | c0001 | t0114 | g0246 | SAS | BEB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03942 | hp2 | a0002 | c0002 | t0013 | g0096 | SAS | BEB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04115 | hp2 | a0001 | c0001 | t0072 | g0135 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04184 | hp1 | a0002 | c0002 | t0126 | g0160 | SAS | BEB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04184 | hp2 | a0001 | c0001 | t0112 | g0266 | SAS | BEB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04199 | hp1 | a0002 | c0002 | t0020 | g0091 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04199 | hp2 | a0003 | c0003 | t0092 | g0042 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0235 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG04228 | hp2 | a0001 | c0001 | t0068 | g0134 | SAS | STU | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18522 | hp1 | a0001 | c0001 | t0142 | g0061 | AFR | YRI | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18522 | hp2 | a0001 | c0001 | t0032 | g0012 | AFR | YRI | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18612 | hp1 | a0001 | c0001 | t0117 | g0224 | EAS | CHB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0036 | EAS | CHB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18747 | hp1 | a0003 | c0003 | t0004 | g0039 | EAS | CHB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18747 | hp2 | a0002 | c0002 | t0034 | g0114 | EAS | CHB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18906 | hp1 | a0005 | c0006 | t0052 | g0165 | AFR | YRI | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18906 | hp2 | a0001 | c0007 | t0147 | g0183 | AFR | YRI | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18939 | hp1 | a0003 | c0003 | t0004 | g0034 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18942 | hp1 | a0002 | c0002 | t0033 | g0080 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18942 | hp2 | a0001 | c0019 | t0003 | g0195 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18943 | hp1 | a0002 | c0002 | t0014 | g0101 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18943 | hp2 | a0001 | c0004 | t0002 | g0157 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18944 | hp1 | a0002 | c0002 | t0039 | g0084 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18945 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18947 | hp1 | a0010 | c0010 | t0011 | g0062 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18952 | hp1 | a0003 | c0003 | t0010 | g0162 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18952 | hp2 | a0002 | c0002 | t0013 | g0068 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18953 | hp1 | a0002 | c0002 | t0129 | g0070 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18957 | hp1 | a0003 | c0003 | t0024 | g0161 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18959 | hp2 | a0002 | c0002 | t0013 | g0083 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18960 | hp1 | a0001 | c0004 | t0011 | g0155 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18960 | hp2 | a0002 | c0002 | t0013 | g0067 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18961 | hp2 | a0003 | c0003 | t0024 | g0283 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18964 | hp1 | a0001 | c0001 | t0029 | g0239 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18964 | hp2 | a0001 | c0004 | t0002 | g0029 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18966 | hp1 | a0003 | c0003 | t0004 | g0156 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18966 | hp2 | a0001 | c0004 | t0010 | g0044 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18968 | hp2 | a0010 | c0010 | t0011 | g0015 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0282 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18970 | hp1 | a0001 | c0001 | t0028 | g0233 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18970 | hp2 | a0002 | c0002 | t0124 | g0085 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18971 | hp1 | a0003 | c0003 | t0004 | g0038 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18971 | hp2 | a0001 | c0001 | t0027 | g0188 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18972 | hp1 | a0001 | c0004 | t0007 | g0158 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18973 | hp1 | a0001 | c0004 | t0088 | g0016 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18978 | hp1 | a0002 | c0002 | t0145 | g0115 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18980 | hp2 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18982 | hp1 | a0001 | c0001 | t0100 | g0226 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18982 | hp2 | a0001 | c0004 | t0002 | g0009 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18983 | hp1 | a0003 | c0003 | t0004 | g0047 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18984 | hp1 | a0002 | c0002 | t0137 | g0097 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18984 | hp2 | a0003 | c0003 | t0087 | g0281 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18985 | hp1 | a0001 | c0004 | t0094 | g0017 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18985 | hp2 | a0001 | c0001 | t0029 | g0271 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18986 | hp1 | a0002 | c0002 | t0035 | g0098 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18986 | hp2 | a0003 | c0003 | t0008 | g0280 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18989 | hp2 | a0003 | c0003 | t0004 | g0028 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18990 | hp1 | a0011 | c0014 | t0125 | g0081 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18993 | hp1 | a0001 | c0004 | t0002 | g0154 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18998 | hp2 | a0002 | c0002 | t0019 | g0110 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18999 | hp1 | a0014 | c0020 | t0012 | g0211 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA18999 | hp2 | a0002 | c0002 | t0140 | g0064 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19001 | hp1 | a0003 | c0003 | t0025 | g0022 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19001 | hp2 | a0002 | c0002 | t0139 | g0099 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19005 | hp1 | a0012 | c0017 | t0127 | g0077 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19007 | hp1 | a0002 | c0002 | t0036 | g0072 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19007 | hp2 | a0003 | c0003 | t0004 | g0026 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19009 | hp1 | a0003 | c0003 | t0004 | g0052 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19010 | hp1 | a0002 | c0002 | t0014 | g0113 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19010 | hp2 | a0001 | c0004 | t0091 | g0018 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19012 | hp1 | a0003 | c0003 | t0004 | g0031 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19012 | hp2 | a0002 | c0002 | t0131 | g0103 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19030 | hp1 | a0004 | c0005 | t0047 | g0172 | AFR | LWK | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19030 | hp2 | a0001 | c0001 | t0075 | g0140 | AFR | LWK | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19043 | hp1 | a0004 | c0005 | t0050 | g0173 | AFR | LWK | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19043 | hp2 | a0004 | c0009 | t0044 | g0186 | AFR | LWK | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19055 | hp2 | a0001 | c0004 | t0010 | g0153 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19056 | hp1 | a0002 | c0002 | t0136 | g0105 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19056 | hp2 | a0003 | c0003 | t0004 | g0023 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19057 | hp2 | a0002 | c0002 | t0014 | g0089 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19060 | hp1 | a0002 | c0002 | t0033 | g0112 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19060 | hp2 | a0003 | c0003 | t0004 | g0035 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19064 | hp2 | a0002 | c0002 | t0009 | g0073 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19066 | hp1 | a0011 | c0014 | t0123 | g0079 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19067 | hp1 | a0002 | c0002 | t0128 | g0087 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19067 | hp2 | a0003 | c0003 | t0082 | g0037 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0048 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19070 | hp1 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19074 | hp2 | a0002 | c0002 | t0130 | g0066 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19076 | hp1 | a0001 | c0001 | t0119 | g0208 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19076 | hp2 | a0010 | c0010 | t0002 | g0014 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19081 | hp1 | a0002 | c0002 | t0019 | g0086 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19084 | hp2 | a0002 | c0015 | t0009 | g0106 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19085 | hp1 | a0001 | c0001 | t0099 | g0216 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19085 | hp2 | a0003 | c0003 | t0008 | g0040 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19087 | hp2 | a0001 | c0004 | t0010 | g0049 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19091 | hp1 | a0002 | c0002 | t0019 | g0069 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA20129 | hp1 | a0002 | c0002 | t0062 | g0121 | AFR | ASW | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | ASW | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01123 | hp1 | a0002 | c0002 | t0035 | g0100 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0262 | AMR | CLM | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02109 | hp1 | a0002 | c0002 | t0015 | g0123 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02109 | hp2 | a0001 | c0001 | t0038 | g0059 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02486 | hp1 | a0004 | c0009 | t0021 | g0187 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02486 | hp2 | a0001 | c0001 | t0078 | g0128 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02559 | hp1 | a0001 | c0001 | t0022 | g0144 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG02559 | hp2 | a0001 | c0001 | t0098 | g0010 | AFR | ACB | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03471 | hp1 | a0015 | c0021 | t0017 | g0147 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG03471 | hp2 | a0004 | c0005 | t0042 | g0170 | AFR | MSL | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | USA | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| HG06807 | hp2 | a0004 | c0005 | t0049 | g0169 | AFR | USA | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | USA | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| NA20300 | hp2 | a0007 | c0013 | t0141 | g0175 | AFR | USA | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0241 | REF | REF | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0185 | REF | REF | LCOR_chr10_96827298_97000956 | LCOR | chr10 | 96827298 | 97000956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:96981302
|
T | G | 1 | a0012 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.842T>G | p.Phe281Cys | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 1347/16001 | 842/4674 | 281/1557 | chr10 | 96981302 | ||
| chr10:96981392
|
T | C | 1 | a0010 | 3 | NA18947.hp1 NA18968.hp2 NA19076.hp2 |
missense_variant | MODERATE | c.932T>C | p.Met311Thr | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 1437/16001 | 932/4674 | 311/1557 | chr10 | 96981392 | ||
| chr10:96981536
|
A | G | 2 | a0003a0009 | 36 | HG00673.hp1 HG01361.hp1 HG01993.hp1 others(33): Show |
missense_variant | MODERATE | c.1076A>G | p.Asn359Ser | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 1581/16001 | 1076/4674 | 359/1557 | chr10 | 96981536 | ||
| chr10:96982286
|
A | G | 1 | a0008 | 3 | HG00639.hp2 HG02735.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.1826A>G | p.Glu609Gly | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2331/16001 | 1826/4674 | 609/1557 | chr10 | 96982286 | ||
| chr10:96982331
|
T | C | 1 | a0006 | 4 | HG00733.hp2 HG01257.hp1 HG02622.hp2 others(1): Show |
missense_variant | MODERATE | c.1871T>C | p.Leu624Pro | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2376/16001 | 1871/4674 | 624/1557 | chr10 | 96982331 | ||
| chr10:96982577
|
A | G | 1 | a0004 | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
missense_variant | MODERATE | c.2117A>G | p.Glu706Gly | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2622/16001 | 2117/4674 | 706/1557 | chr10 | 96982577 | ||
| chr10:96982591
|
C | G | 3 | a0004a0005a0007 | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
missense_variant | MODERATE | c.2131C>G | p.Pro711Ala | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2636/16001 | 2131/4674 | 711/1557 | chr10 | 96982591 | ||
| chr10:96982993
|
A | C | 3 | a0002a0011a0012 | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
missense_variant | MODERATE | c.2533A>C | p.Ile845Leu | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3038/16001 | 2533/4674 | 845/1557 | chr10 | 96982993 | ||
| chr10:96983056
|
A | C | 2 | a0004a0005 | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
missense_variant | MODERATE | c.2596A>C | p.Thr866Pro | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3101/16001 | 2596/4674 | 866/1557 | chr10 | 96983056 | ||
| chr10:96983162
|
G | C | 1 | a0009 | 3 | HG02027.hp2 HG02071.hp1 HG02083.hp1 |
missense_variant | MODERATE | c.2702G>C | p.Gly901Ala | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3207/16001 | 2702/4674 | 901/1557 | chr10 | 96983162 | ||
| chr10:96983480
|
A | G | 1 | a0016 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.3020A>G | p.Asp1007Gly | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3525/16001 | 3020/4674 | 1007/1557 | chr10 | 96983480 | ||
| chr10:96983942
|
C | A | 1 | a0013 | 1 | HG02683.hp2 | stop_gained | HIGH | c.3482C>A | p.Ser1161* | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3987/16001 | 3482/4674 | 1161/1557 | chr10 | 96983942 | ||
| chr10:96984410
|
G | A | 1 | a0014 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.3950G>A | p.Arg1317Gln | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4455/16001 | 3950/4674 | 1317/1557 | chr10 | 96984410 | ||
| chr10:96984505
|
G | A | 1 | a0011 | 2 | NA18990.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.4045G>A | p.Val1349Ile | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4550/16001 | 4045/4674 | 1349/1557 | chr10 | 96984505 | ||
| chr10:96985096
|
T | C | 1 | a0015 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.4636T>C | p.Cys1546Arg | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5141/16001 | 4636/4674 | 1546/1557 | chr10 | 96985096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:96980808
|
G | A | 1 | a0002c0015 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.348G>A | p.Glu116Glu | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 853/16001 | 348/4674 | 116/1557 | chr10 | 96980808 | ||
| chr10:96981117
|
G | A | 5 | a0004c0005a0004c0009a0005c0006others(2): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
synonymous_variant | LOW | c.657G>A | p.Thr219Thr | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 1162/16001 | 657/4674 | 219/1557 | chr10 | 96981117 | ||
| chr10:96982251
|
G | A | 1 | a0004c0009 | 3 | HG02486.hp1 HG03579.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.1791G>A | p.Lys597Lys | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2296/16001 | 1791/4674 | 597/1557 | chr10 | 96982251 | ||
| chr10:96982264
|
C | T | 5 | a0001c0004a0003c0003a0006c0008others(2): Show | 65 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(62): Show |
synonymous_variant | LOW | c.1804C>T | p.Leu602Leu | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2309/16001 | 1804/4674 | 602/1557 | chr10 | 96982264 | ||
| chr10:96982848
|
C | T | 10 | a0001c0004a0003c0003a0004c0005others(7): Show | 85 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(82): Show |
synonymous_variant | LOW | c.2388C>T | p.Leu796Leu | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2893/16001 | 2388/4674 | 796/1557 | chr10 | 96982848 | ||
| chr10:96983496
|
T | C | 1 | a0007c0016 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.3036T>C | p.Ser1012Ser | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3541/16001 | 3036/4674 | 1012/1557 | chr10 | 96983496 | ||
| chr10:96983619
|
T | C | 1 | a0001c0007 | 5 | HG02615.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
synonymous_variant | LOW | c.3159T>C | p.Asp1053Asp | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3664/16001 | 3159/4674 | 1053/1557 | chr10 | 96983619 | ||
| chr10:96984306
|
T | C | 1 | a0001c0019 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.3846T>C | p.Ser1282Ser | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4351/16001 | 3846/4674 | 1282/1557 | chr10 | 96984306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:96832350
|
C | G | 1 | a0001c0007t0147 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-453C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/8 | 116708 | chr10 | 96832350 | |||||
| chr10:96832371
|
G | C | 1 | a0002c0002t0039 | 1 | NA18944.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-432G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/8 | chr10 | 96832371 | ||||||
| chr10:96907707
|
A | G | 1 | a0007c0016t0146 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-224A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/8 | 41351 | chr10 | 96907707 | |||||
| chr10:96985576
|
C | T | 1 | a0002c0002t0145 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 442 | chr10 | 96985576 | |||||
| chr10:96985587
|
C | T | 1 | a0001c0001t0144 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 453 | chr10 | 96985587 | |||||
| chr10:96985947
|
C | T | 3 | a0001c0001t0038a0001c0001t0142a0001c0001t0143 | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*813C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 813 | chr10 | 96985947 | |||||
| chr10:96985955
|
C | T | 1 | a0007c0013t0141 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 821 | chr10 | 96985955 | |||||
| chr10:96986412
|
C | T | 31 | a0002c0002t0009a0002c0002t0013a0002c0002t0014others(28): Show | 49 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1278C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 1278 | chr10 | 96986412 | |||||
| chr10:96987106
|
A | G | 1 | a0001c0004t0122 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1972A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 1972 | chr10 | 96987106 | |||||
| chr10:96987241
|
G | A | 14 | a0004c0005t0021a0004c0005t0042a0004c0005t0043others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2107G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2107 | chr10 | 96987241 | |||||
| chr10:96987357
|
C | A | 83 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(80): Show | 110 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2223C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2223 | chr10 | 96987357 | |||||
| chr10:96987420
|
C | T | 1 | a0001c0001t0121 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2286C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2286 | chr10 | 96987420 | |||||
| chr10:96987565
|
A | G | 2 | a0001c0001t0032a0001c0001t0120 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2431A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2431 | chr10 | 96987565 | |||||
| chr10:96987748
|
G | A | 1 | a0001c0001t0081 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2614G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2614 | chr10 | 96987748 | |||||
| chr10:96987996
|
T | C | 126 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(123): Show | 187 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*2862T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 2862 | chr10 | 96987996 | |||||
| chr10:96988411
|
G | T | 2 | a0007c0013t0080a0007c0013t0141 | 2 | HG01884.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3277G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3277 | chr10 | 96988411 | |||||
| chr10:96988563
|
G | A | 1 | a0001c0001t0051 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3429G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3429 | chr10 | 96988563 | |||||
| chr10:96988695
|
A | G | 23 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(20): Show | 31 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3561A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3561 | chr10 | 96988695 | |||||
| chr10:96989072
|
C | T | 1 | a0007c0016t0146 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3938C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 3938 | chr10 | 96989072 | |||||
| chr10:96989219
|
G | A | 2 | a0001c0001t0099a0001c0001t0100 | 2 | NA18982.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4085G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4085 | chr10 | 96989219 | |||||
| chr10:96989276
|
T | A | 1 | a0003c0003t0082 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4142T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4142 | chr10 | 96989276 | |||||
| chr10:96989354
|
TG | T | 22 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(19): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4222delG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4222 | INFO_REALIGN_3_PRIME | chr10 | 96989354 | ||||
| chr10:96989408
|
A | G | 7 | a0002c0002t0014a0002c0002t0136a0002c0002t0137others(4): Show | 10 | HG00558.hp1 HG02132.hp2 NA18943.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4274A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4274 | chr10 | 96989408 | |||||
| chr10:96989417
|
T | C | 2 | a0005c0006t0040a0005c0006t0041 | 2 | HG02922.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4283T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4283 | chr10 | 96989417 | |||||
| chr10:96989490
|
A | G | 3 | a0001c0001t0077a0001c0001t0078a0001c0001t0079 | 3 | HG02486.hp2 HG02922.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4356A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4356 | chr10 | 96989490 | |||||
| chr10:96989669
|
A | G | 16 | a0001c0001t0097a0001c0001t0098a0004c0005t0021others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4535A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4535 | chr10 | 96989669 | |||||
| chr10:96989674
|
G | GAT | 4 | a0001c0001t0028a0001c0001t0116a0001c0007t0103others(1): Show | 4 | HG01243.hp1 HG02027.hp1 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4561_*4562dupAT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATAT | 5 | a0001c0001t0016a0001c0001t0017a0001c0001t0022others(2): Show | 9 | HG00621.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4557_*4562dupATAT others(2): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATATA others(3): Show |
2 | a0001c0001t0066a0001c0001t0071 | 2 | HG00733.hp1 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4553_*4562dupATAT others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATATA others(5): Show |
6 | a0001c0001t0065a0001c0001t0069a0002c0002t0055others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4551_*4562dupATAT others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATATA others(7): Show |
3 | a0002c0002t0019a0002c0002t0053a0004c0005t0048 | 5 | HG01109.hp1 HG02258.hp1 NA18998.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4549_*4562dupATAT others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATATA others(9): Show |
2 | a0004c0005t0045a0011c0014t0123 | 2 | HG02257.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4547_*4562dupATAT others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATATA others(11): Show |
1 | a0004c0005t0043 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4545_*4562dupATAT others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATATA others(13): Show |
1 | a0004c0005t0047 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4543_*4562dupATAT others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
G | GATATATA others(17): Show |
1 | a0004c0009t0044 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989674
|
GATAT | G | 5 | a0003c0003t0004a0003c0003t0025a0003c0003t0095others(2): Show | 17 | HG01361.hp1 HG01993.hp1 HG02735.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4559_*4562delATAT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4559 | INFO_REALIGN_3_PRIME | chr10 | 96989674 | ||||
| chr10:96989693
|
A | T | 1 | a0005c0006t0041 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4559A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4559 | chr10 | 96989693 | |||||
| chr10:96989693
|
ATATT | A | 12 | a0001c0001t0093a0001c0004t0002a0001c0004t0089others(9): Show | 22 | HG00733.hp2 HG01071.hp2 HG01099.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4561_*4564delATTT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4561 | INFO_REALIGN_3_PRIME | chr10 | 96989693 | ||||
| chr10:96989693
|
ATATTT | A | 5 | a0001c0004t0011a0001c0004t0088a0003c0003t0087others(2): Show | 6 | HG02965.hp2 NA18947.hp1 NA18960.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4561_*4565delATTT others(1): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4561 | INFO_REALIGN_3_PRIME | chr10 | 96989693 | ||||
| chr10:96989695
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0034 | 2 | HG01167.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(6): Show |
3 | a0002c0002t0033a0002c0002t0128a0002c0002t0129 | 4 | NA18942.hp1 NA18953.hp1 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(25): Show |
1 | a0005c0006t0040 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(28): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(17): Show |
1 | a0007c0013t0080 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(12): Show |
1 | a0004c0005t0050 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(15): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(14): Show |
1 | a0005c0006t0052 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(17): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(15): Show |
1 | a0007c0013t0141 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(9): Show |
1 | a0011c0014t0125 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(13): Show |
1 | a0005c0006t0054 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(7): Show |
2 | a0002c0002t0013a0002c0002t0039 | 5 | HG03942.hp2 NA18944.hp1 NA18952.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0056a0002c0002t0130 | 2 | HG02647.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(11): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(5): Show |
2 | a0002c0002t0035a0002c0002t0036 | 4 | HG00642.hp1 HG01123.hp1 NA18986.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(6): Show |
2 | a0002c0002t0131a0002c0002t0137 | 2 | NA18984.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(7): Show |
3 | a0002c0002t0057a0002c0002t0132a0002c0002t0145 | 3 | HG02071.hp2 HG02647.hp1 NA18978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0058 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(11): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(9): Show |
1 | a0002c0002t0059 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(4): Show |
2 | a0002c0002t0015a0002c0002t0138 | 4 | HG00558.hp1 HG02109.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(5): Show |
5 | a0002c0002t0009a0002c0002t0014a0002c0002t0139others(2): Show | 11 | HG00438.hp2 HG02132.hp2 HG02300.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(6): Show |
2 | a0002c0002t0020a0002c0002t0061 | 4 | HG02723.hp2 HG03017.hp2 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(7): Show |
1 | a0002c0002t0133 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(3): Show |
1 | a0002c0002t0134 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0062 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0106a0002c0002t0037a0002c0002t0140 | 4 | HG00544.hp2 HG01168.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0135 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | ATATATTT others(5): Show |
1 | a0002c0002t0063 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
A | T | 4 | a0001c0001t0119a0003c0003t0025a0004c0009t0064others(1): Show | 5 | HG03225.hp1 HG03579.hp2 HG03710.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4561A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4561 | chr10 | 96989695 | |||||
| chr10:96989695
|
AT | A | 9 | a0001c0001t0006a0001c0001t0031a0001c0001t0104others(6): Show | 14 | HG00323.hp2 HG00544.hp1 HG01167.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4585delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4585 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
ATTT | A | 6 | a0001c0001t0097a0001c0001t0111a0001c0001t0142others(3): Show | 9 | HG00558.hp2 HG01106.hp2 HG02083.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4583_*4585delTTT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4583 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989695
|
ATTTT | A | 3 | a0001c0004t0010a0003c0003t0010a0003c0003t0024 | 6 | NA18952.hp1 NA18957.hp1 NA18961.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4582_*4585delTTTT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4582 | INFO_REALIGN_3_PRIME | chr10 | 96989695 | ||||
| chr10:96989696
|
T | TA | 6 | a0001c0001t0012a0001c0001t0030a0001c0001t0099others(3): Show | 9 | HG01109.hp2 HG01258.hp1 HG01515.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989696 | |||||
| chr10:96989696
|
T | TATATATA | 6 | a0001c0001t0018a0001c0001t0051a0001c0001t0073others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(3): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989696 | |||||
| chr10:96989696
|
T | TATATATA others(2): Show |
3 | a0001c0001t0023a0001c0001t0067a0001c0001t0070 | 4 | HG00639.hp1 HG01261.hp1 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(5): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989696 | |||||
| chr10:96989696
|
T | TATATATA others(4): Show |
5 | a0001c0001t0068a0001c0001t0072a0001c0001t0074others(2): Show | 5 | HG01515.hp2 HG02895.hp2 HG04115.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989696 | |||||
| chr10:96989696
|
T | TATATATA others(6): Show |
1 | a0002c0002t0124 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989696 | |||||
| chr10:96989696
|
T | TATATATA others(12): Show |
3 | a0004c0005t0021a0004c0005t0046a0004c0009t0021 | 3 | HG02486.hp1 HG03195.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(15): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989696 | |||||
| chr10:96989696
|
T | TATATATA others(22): Show |
1 | a0004c0005t0042 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562_*4563insATAT others(25): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989696 | |||||
| chr10:96989697
|
T | A | 35 | a0001c0001t0001a0001c0001t0005a0001c0001t0016others(32): Show | 78 | HG00621.hp2 HG00642.hp2 HG00733.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*4563T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4563 | chr10 | 96989697 | |||||
| chr10:96989698
|
T | A | 23 | a0001c0001t0006a0001c0001t0012a0001c0001t0018others(20): Show | 32 | HG00544.hp1 HG00639.hp1 HG01070.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*4564T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4564 | chr10 | 96989698 | |||||
| chr10:96989699
|
T | A | 27 | a0001c0001t0005a0001c0001t0016a0001c0001t0017others(24): Show | 39 | HG00621.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4565T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4565 | chr10 | 96989699 | |||||
| chr10:96989700
|
T | A | 14 | a0001c0001t0067a0001c0001t0068a0001c0001t0070others(11): Show | 14 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4566T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4566 | chr10 | 96989700 | |||||
| chr10:96989701
|
T | A | 12 | a0001c0001t0016a0001c0001t0022a0001c0001t0027others(9): Show | 16 | HG01081.hp1 HG01109.hp1 HG02055.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4567T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4567 | chr10 | 96989701 | |||||
| chr10:96989702
|
T | A | 4 | a0001c0001t0067a0001c0001t0097a0001c0001t0099others(1): Show | 4 | HG00544.hp1 HG00639.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4568T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4568 | chr10 | 96989702 | |||||
| chr10:96989703
|
T | A | 6 | a0001c0001t0022a0001c0001t0065a0001c0001t0066others(3): Show | 7 | HG01081.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4569T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4569 | chr10 | 96989703 | |||||
| chr10:96989704
|
T | A | 1 | a0001c0001t0097 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4570T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4570 | chr10 | 96989704 | |||||
| chr10:96989705
|
T | A | 1 | a0001c0001t0098 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4571T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4571 | chr10 | 96989705 | |||||
| chr10:96989836
|
C | A | 16 | a0001c0001t0097a0001c0001t0098a0004c0005t0021others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4702C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4702 | chr10 | 96989836 | |||||
| chr10:96989846
|
G | A | 2 | a0002c0002t0058a0002c0002t0059 | 2 | HG02809.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4712G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 4712 | chr10 | 96989846 | |||||
| chr10:96990268
|
A | G | 131 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(128): Show | 192 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*5134A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5134 | chr10 | 96990268 | |||||
| chr10:96990282
|
G | T | 1 | a0007c0016t0146 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5148G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5148 | chr10 | 96990282 | |||||
| chr10:96990360
|
A | T | 1 | a0002c0002t0139 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5226A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5226 | chr10 | 96990360 | |||||
| chr10:96990599
|
G | C | 2 | a0001c0001t0081a0001c0001t0144 | 2 | HG00741.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5465G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5465 | chr10 | 96990599 | |||||
| chr10:96990626
|
G | A | 1 | a0001c0001t0107 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5492G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5492 | chr10 | 96990626 | |||||
| chr10:96990885
|
A | G | 14 | a0004c0005t0021a0004c0005t0042a0004c0005t0043others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5751A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5751 | chr10 | 96990885 | |||||
| chr10:96990893
|
C | G | 13 | a0001c0001t0018a0001c0001t0023a0001c0001t0026others(10): Show | 17 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5759C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5759 | chr10 | 96990893 | |||||
| chr10:96991022
|
T | TA | 23 | a0001c0001t0029a0001c0001t0032a0001c0001t0051others(20): Show | 25 | HG00544.hp1 HG01099.hp2 HG01106.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5911dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5912 | INFO_REALIGN_3_PRIME | chr10 | 96991022 | ||||
| chr10:96991022
|
T | TAA | 37 | a0001c0001t0106a0001c0001t0112a0001c0001t0120others(34): Show | 56 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5910_*5911dupAA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5912 | INFO_REALIGN_3_PRIME | chr10 | 96991022 | ||||
| chr10:96991022
|
T | TAAA | 5 | a0002c0002t0035a0002c0002t0053a0002c0002t0058others(2): Show | 6 | HG01123.hp1 HG02258.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5909_*5911dupAAA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5912 | INFO_REALIGN_3_PRIME | chr10 | 96991022 | ||||
| chr10:96991022
|
TA | T | 12 | a0001c0001t0076a0001c0001t0115a0001c0004t0088others(9): Show | 13 | HG01070.hp2 HG02083.hp2 HG02615.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5911delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 5911 | INFO_REALIGN_3_PRIME | chr10 | 96991022 | ||||
| chr10:96991585
|
G | A | 16 | a0001c0001t0097a0001c0001t0098a0004c0005t0021others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6451G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 6451 | chr10 | 96991585 | |||||
| chr10:96991686
|
C | T | 33 | a0001c0001t0093a0001c0004t0002a0001c0004t0007others(30): Show | 64 | HG00558.hp2 HG00639.hp2 HG00673.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*6552C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 6552 | chr10 | 96991686 | |||||
| chr10:96991762
|
G | A | 2 | a0001c0001t0099a0001c0001t0100 | 2 | NA18982.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6628G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 6628 | chr10 | 96991762 | |||||
| chr10:96991936
|
C | CTG | 16 | a0001c0001t0097a0001c0001t0098a0004c0005t0021others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6803_*6804insGT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 6804 | INFO_REALIGN_3_PRIME | chr10 | 96991936 | ||||
| chr10:96992119
|
C | T | 1 | a0005c0006t0054 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6985C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 6985 | chr10 | 96992119 | |||||
| chr10:96992352
|
A | G | 14 | a0004c0005t0021a0004c0005t0042a0004c0005t0043others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*7218A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 7218 | chr10 | 96992352 | |||||
| chr10:96992573
|
G | A | 1 | a0001c0004t0089 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7439G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 7439 | chr10 | 96992573 | |||||
| chr10:96992755
|
T | C | 2 | a0005c0006t0052a0005c0006t0054 | 2 | HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7621T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 7621 | chr10 | 96992755 | |||||
| chr10:96993079
|
A | G | 16 | a0001c0001t0097a0001c0001t0098a0004c0005t0021others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*7945A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 7945 | chr10 | 96993079 | |||||
| chr10:96993450
|
T | C | 2 | a0007c0013t0080a0007c0013t0141 | 2 | HG01884.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8316T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 8316 | chr10 | 96993450 | |||||
| chr10:96993453
|
A | C | 1 | a0001c0001t0068 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8319A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 8319 | chr10 | 96993453 | |||||
| chr10:96993454
|
G | C | 1 | a0001c0001t0068 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8320G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 8320 | chr10 | 96993454 | |||||
| chr10:96993490
|
A | G | 1 | a0007c0016t0146 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8356A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 8356 | chr10 | 96993490 | |||||
| chr10:96993760
|
T | TTA | 3 | a0001c0004t0088a0001c0004t0091a0001c0004t0094 | 3 | NA18973.hp1 NA18985.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8641_*8642dupTA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 8643 | INFO_REALIGN_3_PRIME | chr10 | 96993760 | ||||
| chr10:96993760
|
TTA | T | 16 | a0001c0001t0097a0001c0001t0098a0004c0005t0021others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8641_*8642delTA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 8641 | INFO_REALIGN_3_PRIME | chr10 | 96993760 | ||||
| chr10:96994012
|
A | G | 1 | a0002c0002t0055 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8878A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 8878 | chr10 | 96994012 | |||||
| chr10:96994423
|
G | A | 1 | a0001c0001t0117 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9289G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 9289 | chr10 | 96994423 | |||||
| chr10:96995168
|
G | A | 1 | a0007c0013t0141 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10034G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 10034 | chr10 | 96995168 | |||||
| chr10:96995276
|
T | C | 1 | a0001c0001t0143 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10142T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 10142 | chr10 | 96995276 | |||||
| chr10:96995323
|
G | A | 24 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(21): Show | 31 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*10189G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 10189 | chr10 | 96995323 | |||||
| chr10:96995365
|
C | T | 1 | a0001c0001t0093 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10231C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 10231 | chr10 | 96995365 | |||||
| chr10:96995732
|
G | T | 1 | a0001c0001t0113 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10598G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 10598 | chr10 | 96995732 | |||||
| chr10:96995814
|
C | G | 1 | a0003c0003t0086 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10680C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 8/8 | 10680 | chr10 | 96995814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:96832419
|
G | GCCGCCGC others(13): Show |
1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-404+29_-404+48dup others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 96832419 | |||||
| chr10:96832596
|
G | T | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-404+197G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96832596 | ||||||
| chr10:96832791
|
C | T | 2 | a0001c0001t0027g0285a0001c0001t0056g0284 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-404+392C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96832791 | ||||||
| chr10:96832864
|
C | G | 1 | a0003c0003t0024g0283 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-404+465C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96832864 | ||||||
| chr10:96832904
|
G | T | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-403-502G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96832904 | ||||||
| chr10:96832982
|
C | T | 4 | a0003c0003t0002g0282a0003c0003t0008g0280a0003c0003t0087g0281others(1): Show | 4 | HG01993.hp1 NA18969.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-403-424C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96832982 | ||||||
| chr10:96832984
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-403-422G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96832984 | ||||||
| chr10:96833086
|
T | C | 184 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(181): Show | 184 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.-403-320T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96833086 | ||||||
| chr10:96833281
|
G | T | 1 | a0003c0003t0004g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-403-125G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 1/7 | chr10 | 96833281 | ||||||
| chr10:96833520
|
C | T | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | NA18961.hp1 NA18978.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+41C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833520 | ||||||
| chr10:96833528
|
C | T | 1 | a0001c0001t0016g0176 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-330+49C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833528 | ||||||
| chr10:96833609
|
G | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+130G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833609 | ||||||
| chr10:96833671
|
G | T | 14 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.-330+192G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833671 | ||||||
| chr10:96833717
|
G | C | 1 | a0001c0001t0120g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-330+238G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833717 | ||||||
| chr10:96833727
|
A | G | 7 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0045g0168others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+248A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833727 | ||||||
| chr10:96833763
|
C | G | 3 | a0003c0003t0010g0162a0003c0003t0024g0161a0003c0003t0024g0283 | 3 | NA18952.hp1 NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-330+284C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833763 | ||||||
| chr10:96833832
|
A | G | 1 | a0002c0002t0126g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-330+353A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96833832 | ||||||
| chr10:96834152
|
T | C | 1 | a0001c0001t0016g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-330+673T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834152 | ||||||
| chr10:96834358
|
A | G | 8 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0045g0168others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.-330+879A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834358 | ||||||
| chr10:96834402
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-330+923C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834402 | ||||||
| chr10:96834454
|
G | C | 1 | a0003c0003t0002g0005 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-330+975G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834454 | ||||||
| chr10:96834466
|
A | G | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+987A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834466 | ||||||
| chr10:96834497
|
T | C | 1 | a0003c0003t0002g0005 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-330+1018T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834497 | ||||||
| chr10:96834893
|
G | A | 1 | a0001c0001t0143g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-330+1414G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834893 | ||||||
| chr10:96834896
|
T | G | 6 | a0001c0001t0107g0178a0001c0007t0102g0181a0001c0007t0103g0179others(3): Show | 6 | HG01884.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+1417T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834896 | ||||||
| chr10:96834943
|
C | G | 1 | a0001c0004t0007g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-330+1464C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834943 | ||||||
| chr10:96834944
|
G | A | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-330+1465G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96834944 | ||||||
| chr10:96835000
|
A | G | 9 | a0002c0002t0015g0122a0002c0002t0015g0123a0002c0002t0057g0119others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-330+1521A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835000 | ||||||
| chr10:96835076
|
C | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(282): Show | 285 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(282): Show |
intron_variant | MODIFIER | c.-330+1597C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835076 | ||||||
| chr10:96835087
|
G | C | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+1608G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835087 | ||||||
| chr10:96835091
|
G | A | 2 | a0004c0009t0021g0187a0004c0009t0044g0186 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-330+1612G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835091 | ||||||
| chr10:96835185
|
A | G | 4 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0047g0172others(1): Show | 4 | HG03453.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+1706A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835185 | ||||||
| chr10:96835201
|
CG | C | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+1723delG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835201 | ||||||
| chr10:96835495
|
A | G | 1 | a0007c0013t0141g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-330+2016A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835495 | ||||||
| chr10:96835569
|
G | T | 117 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(114): Show | 117 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.-330+2090G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96835569 | ||||||
| chr10:96836102
|
C | T | 1 | a0001c0001t0023g0159 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-330+2623C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836102 | ||||||
| chr10:96836218
|
T | C | 1 | a0001c0001t0016g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-330+2739T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836218 | ||||||
| chr10:96836296
|
G | A | 39 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(36): Show | 39 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.-330+2817G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836296 | ||||||
| chr10:96836312
|
G | A | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-330+2833G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836312 | ||||||
| chr10:96836525
|
G | C | 63 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(60): Show | 63 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-330+3046G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836525 | ||||||
| chr10:96836570
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+3091G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836570 | ||||||
| chr10:96836842
|
G | C | 1 | a0001c0001t0097g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-330+3363G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836842 | ||||||
| chr10:96836936
|
G | T | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-330+3457G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96836936 | ||||||
| chr10:96836993
|
C | CT | 32 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(29): Show | 32 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-330+3530dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96836993 | |||||
| chr10:96836993
|
C | CTT | 7 | a0001c0001t0023g0159a0001c0004t0002g0154a0001c0004t0002g0157others(4): Show | 7 | HG01261.hp1 NA18943.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+3529_-330+353 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96836993 | |||||
| chr10:96837015
|
G | A | 1 | a0001c0001t0027g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-330+3536G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837015 | ||||||
| chr10:96837036
|
G | T | 6 | a0001c0004t0002g0154a0001c0004t0002g0157a0001c0004t0007g0158others(3): Show | 6 | NA18943.hp2 NA18960.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+3557G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837036 | ||||||
| chr10:96837056
|
A | G | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+3577A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837056 | ||||||
| chr10:96837135
|
T | C | 1 | a0002c0002t0140g0064 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-330+3656T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837135 | ||||||
| chr10:96837139
|
C | T | 4 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+3660C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837139 | ||||||
| chr10:96837166
|
C | A | 3 | a0001c0001t0001g0189a0001c0004t0002g0009a0002c0002t0014g0065 | 3 | HG02132.hp2 NA18939.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-330+3687C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837166 | ||||||
| chr10:96837270
|
A | G | 63 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(60): Show | 63 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.-330+3791A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837270 | ||||||
| chr10:96837580
|
T | C | 1 | a0004c0005t0042g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-330+4101T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837580 | ||||||
| chr10:96837645
|
C | T | 5 | a0001c0001t0001g0274a0001c0001t0003g0265a0001c0001t0031g0267others(2): Show | 5 | HG00323.hp2 HG01168.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-330+4166C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837645 | ||||||
| chr10:96837663
|
A | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+4184A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837663 | ||||||
| chr10:96837743
|
T | C | 1 | a0003c0003t0008g0280 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-330+4264T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96837743 | ||||||
| chr10:96838029
|
G | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+4550G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838029 | ||||||
| chr10:96838246
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-330+4767A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838246 | ||||||
| chr10:96838302
|
C | T | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+4823C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838302 | ||||||
| chr10:96838393
|
A | G | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+4914A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838393 | ||||||
| chr10:96838405
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-330+4926C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838405 | ||||||
| chr10:96838517
|
A | G | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+5038A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838517 | ||||||
| chr10:96838638
|
A | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+5159A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838638 | ||||||
| chr10:96838796
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+5317A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96838796 | ||||||
| chr10:96839119
|
T | C | 41 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(38): Show | 41 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.-330+5640T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96839119 | ||||||
| chr10:96839273
|
T | G | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+5794T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96839273 | ||||||
| chr10:96839316
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+5837C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96839316 | ||||||
| chr10:96839408
|
G | C | 7 | a0001c0004t0007g0019a0001c0004t0088g0016a0001c0004t0091g0018others(4): Show | 7 | HG00558.hp2 NA18947.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-330+5929G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96839408 | ||||||
| chr10:96839485
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-330+6006A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96839485 | ||||||
| chr10:96840004
|
G | A | 2 | a0001c0001t0113g0191a0013c0018t0006g0190 | 2 | HG01099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-330+6525G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96840004 | ||||||
| chr10:96840683
|
T | C | 5 | a0002c0002t0013g0067a0002c0002t0013g0068a0002c0002t0019g0069others(2): Show | 5 | NA18952.hp2 NA18953.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-330+7204T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96840683 | ||||||
| chr10:96840773
|
A | G | 1 | a0002c0002t0140g0064 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-330+7294A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96840773 | ||||||
| chr10:96840791
|
A | C | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-330+7312A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96840791 | ||||||
| chr10:96840809
|
G | A | 1 | a0003c0003t0004g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-330+7330G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96840809 | ||||||
| chr10:96840830
|
C | T | 1 | a0002c0002t0014g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-330+7351C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96840830 | ||||||
| chr10:96841235
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0003g0193 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-330+7756G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841235 | ||||||
| chr10:96841303
|
A | T | 1 | a0001c0004t0002g0058 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-330+7824A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841303 | ||||||
| chr10:96841362
|
C | CT | 76 | a0001c0001t0001g0260a0001c0001t0005g0261a0001c0001t0005g0262others(73): Show | 76 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-330+7901dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96841362 | |||||
| chr10:96841362
|
C | CTT | 44 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(41): Show | 44 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-330+7900_-330+790 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96841362 | |||||
| chr10:96841362
|
CT | C | 60 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(57): Show | 60 | HG00673.hp1 HG00733.hp2 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.-330+7901delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96841362 | |||||
| chr10:96841400
|
A | G | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+7921A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841400 | ||||||
| chr10:96841447
|
A | G | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+7968A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841447 | ||||||
| chr10:96841650
|
C | T | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-330+8171C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841650 | ||||||
| chr10:96841661
|
A | G | 5 | a0001c0007t0102g0181a0001c0007t0103g0179a0001c0007t0105g0182others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-330+8182A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841661 | ||||||
| chr10:96841703
|
T | C | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+8224T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841703 | ||||||
| chr10:96841856
|
T | G | 1 | a0001c0007t0103g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-330+8377T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841856 | ||||||
| chr10:96841898
|
C | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+8419C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96841898 | ||||||
| chr10:96842038
|
C | T | 1 | a0002c0002t0033g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-330+8559C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842038 | ||||||
| chr10:96842039
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+8560G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842039 | ||||||
| chr10:96842147
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0003g0194a0001c0001t0003g0199others(1): Show | 4 | HG00673.hp2 NA18942.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+8668G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842147 | ||||||
| chr10:96842240
|
C | A | 6 | a0001c0001t0107g0178a0001c0007t0102g0181a0001c0007t0103g0179others(3): Show | 6 | HG01884.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+8761C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842240 | ||||||
| chr10:96842585
|
T | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+9106T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842585 | ||||||
| chr10:96842632
|
C | CT | 9 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0259others(6): Show | 9 | HG01070.hp1 HG01074.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-330+9169dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96842632 | |||||
| chr10:96842637
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+9158T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842637 | ||||||
| chr10:96842700
|
G | A | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-330+9221G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842700 | ||||||
| chr10:96842764
|
G | A | 4 | a0001c0001t0093g0204a0008c0011t0002g0203a0008c0011t0004g0202others(1): Show | 4 | HG00639.hp2 HG01071.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+9285G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842764 | ||||||
| chr10:96842797
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0003g0199 | 2 | HG00673.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-330+9318G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842797 | ||||||
| chr10:96842803
|
G | A | 1 | a0005c0006t0054g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-330+9324G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96842803 | ||||||
| chr10:96843439
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+9960G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96843439 | ||||||
| chr10:96843501
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+10022C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96843501 | ||||||
| chr10:96843550
|
A | T | 2 | a0003c0003t0002g0282a0003c0003t0087g0281 | 2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-330+10071A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96843550 | ||||||
| chr10:96843696
|
G | A | 1 | a0002c0002t0009g0073 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-330+10217G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96843696 | ||||||
| chr10:96843794
|
C | T | 1 | a0001c0001t0065g0148 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-330+10315C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96843794 | ||||||
| chr10:96844090
|
ACCCTCCC others(5): Show |
A | 9 | a0001c0001t0106g0286a0004c0009t0021g0187a0004c0009t0044g0186others(6): Show | 9 | HG02486.hp1 HG02922.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-330+10616_-330+10 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96844090 | |||||
| chr10:96844090
|
ACCCTCCC others(25): Show |
A | 9 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-330+10616_-330+10 others(38): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96844090 | |||||
| chr10:96844095
|
C | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+10616C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96844095 | ||||||
| chr10:96844123
|
C | A | 2 | a0009c0012t0008g0020a0009c0012t0008g0021 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-330+10644C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96844123 | ||||||
| chr10:96844124
|
C | G | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+10645C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96844124 | ||||||
| chr10:96844130
|
T | TTCCC | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+10664_-330+10 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96844130 | |||||
| chr10:96844311
|
T | A | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+10832T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96844311 | ||||||
| chr10:96844709
|
A | G | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+11230A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96844709 | ||||||
| chr10:96844920
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-330+11441G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96844920 | ||||||
| chr10:96845033
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+11554A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96845033 | ||||||
| chr10:96845112
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+11633T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96845112 | ||||||
| chr10:96845156
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+11677A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96845156 | ||||||
| chr10:96845160
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+11681C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96845160 | ||||||
| chr10:96845365
|
A | G | 1 | a0001c0004t0007g0019 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-330+11886A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96845365 | ||||||
| chr10:96845449
|
C | CT | 25 | a0001c0001t0001g0001a0001c0001t0001g0189a0001c0001t0001g0192others(22): Show | 25 | HG00621.hp2 HG01081.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.-330+12007dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
C | CTT | 23 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0003g0193others(20): Show | 23 | HG00733.hp2 HG01109.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-330+12006_-330+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
C | CTTT | 18 | a0001c0004t0002g0009a0001c0004t0007g0041a0003c0003t0001g0036others(15): Show | 18 | HG02071.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-330+12005_-330+12 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
C | CTTTT | 18 | a0001c0001t0001g0198a0001c0004t0002g0058a0001c0004t0007g0126others(15): Show | 18 | HG00673.hp1 HG01928.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.-330+12004_-330+12 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
C | CTTTTT | 6 | a0003c0003t0002g0057a0003c0003t0010g0162a0003c0003t0085g0056others(3): Show | 6 | HG01361.hp1 HG01993.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.-330+12003_-330+12 others(11): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
C | CTTTTTTT others(8): Show |
2 | a0001c0004t0089g0055a0003c0003t0090g0054 | 2 | HG01099.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-330+11993_-330+12 others(21): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CT | C | 37 | a0001c0001t0001g0196a0001c0001t0001g0213a0001c0001t0001g0215others(34): Show | 37 | HG00323.hp2 HG00639.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.-330+12007delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTT | C | 9 | a0001c0001t0001g0207a0001c0001t0104g0206a0001c0001t0107g0178others(6): Show | 9 | HG00544.hp1 HG01099.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-330+12006_-330+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTTTTTTT others(3): Show |
C | 1 | a0005c0006t0054g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-330+11998_-330+12 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTTTTTTT others(4): Show |
C | 1 | a0005c0006t0052g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-330+11997_-330+12 others(17): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0083g0024 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-330+11996_-330+12 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0077g0127a0001c0001t0078g0128a0001c0004t0007g0158others(2): Show | 5 | HG02486.hp2 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-330+11994_-330+12 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTTTTTTT others(8): Show |
C | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+11993_-330+12 others(21): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTTTTTTT others(9): Show |
C | 52 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(49): Show | 52 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-330+11992_-330+12 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845449
|
CTTTTTTT others(10): Show |
C | 2 | a0002c0002t0133g0074a0002c0002t0138g0075 | 2 | HG00558.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-330+11991_-330+12 others(23): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845449 | |||||
| chr10:96845553
|
GC | G | 8 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0045g0168others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.-330+12080delC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96845553 | |||||
| chr10:96845624
|
C | T | 1 | a0001c0001t0093g0204 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-330+12145C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96845624 | ||||||
| chr10:96845718
|
C | T | 1 | a0001c0001t0003g0240 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-330+12239C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96845718 | ||||||
| chr10:96846015
|
T | G | 4 | a0001c0001t0005g0222a0001c0001t0006g0241a0001c0001t0026g0223others(1): Show | 4 | HG00741.hp1 HG01081.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+12536T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846015 | ||||||
| chr10:96846267
|
T | A | 21 | a0002c0002t0001g0078a0002c0002t0009g0076a0002c0002t0013g0067others(18): Show | 21 | HG00438.hp2 HG00621.hp1 NA18747.hp2 others(18): Show |
intron_variant | MODIFIER | c.-330+12788T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846267 | ||||||
| chr10:96846589
|
G | A | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+13110G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846589 | ||||||
| chr10:96846657
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+13178C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846657 | ||||||
| chr10:96846658
|
G | A | 1 | a0001c0001t0117g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-330+13179G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846658 | ||||||
| chr10:96846659
|
T | C | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+13180T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846659 | ||||||
| chr10:96846748
|
C | A | 1 | a0001c0004t0110g0043 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-330+13269C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846748 | ||||||
| chr10:96846748
|
C | G | 3 | a0001c0001t0017g0145a0001c0001t0017g0146a0015c0021t0017g0147 | 3 | HG02818.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-330+13269C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846748 | ||||||
| chr10:96846849
|
C | T | 1 | a0002c0002t0015g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-330+13370C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96846849 | ||||||
| chr10:96847000
|
T | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+13521T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847000 | ||||||
| chr10:96847203
|
C | T | 1 | a0001c0001t0029g0239 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-330+13724C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847203 | ||||||
| chr10:96847347
|
C | CA | 9 | a0001c0001t0001g0250a0001c0001t0032g0012a0001c0001t0032g0013others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-330+13884dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96847347 | |||||
| chr10:96847406
|
T | TTTTA | 8 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0047g0172others(5): Show | 8 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.-330+13952_-330+13 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96847406 | |||||
| chr10:96847406
|
TTTTATTT others(1): Show |
T | 55 | a0001c0001t0001g0198a0001c0004t0002g0009a0001c0004t0002g0029others(52): Show | 55 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-330+13948_-330+13 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96847406 | |||||
| chr10:96847410
|
A | T | 18 | a0001c0001t0016g0004a0001c0001t0018g0150a0001c0001t0018g0151others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-330+13931A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847410 | ||||||
| chr10:96847431
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+13952T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847431 | ||||||
| chr10:96847523
|
T | A | 187 | a0001c0001t0001g0198a0001c0001t0016g0004a0001c0001t0016g0136others(184): Show | 187 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.-330+14044T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847523 | ||||||
| chr10:96847528
|
C | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+14049C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847528 | ||||||
| chr10:96847566
|
C | T | 1 | a0003c0003t0002g0057 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-330+14087C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847566 | ||||||
| chr10:96847598
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+14119C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847598 | ||||||
| chr10:96847726
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+14247A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847726 | ||||||
| chr10:96847871
|
G | A | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-330+14392G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847871 | ||||||
| chr10:96847925
|
C | T | 1 | a0001c0001t0073g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-330+14446C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847925 | ||||||
| chr10:96847966
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+14487C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96847966 | ||||||
| chr10:96848424
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+14945G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96848424 | ||||||
| chr10:96848526
|
C | T | 1 | a0002c0002t0053g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-330+15047C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96848526 | ||||||
| chr10:96848632
|
T | C | 1 | a0008c0011t0002g0203 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-330+15153T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96848632 | ||||||
| chr10:96849011
|
G | GT | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(83): Show | 86 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-330+15548dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849011 | |||||
| chr10:96849011
|
GT | G | 74 | a0001c0001t0017g0145a0001c0001t0017g0146a0001c0001t0032g0012others(71): Show | 74 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-330+15548delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849011 | |||||
| chr10:96849011
|
GTT | G | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+15547_-330+15 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849011 | |||||
| chr10:96849061
|
C | CT | 7 | a0001c0001t0012g0225a0001c0004t0002g0058a0001c0004t0088g0016others(4): Show | 7 | HG01109.hp2 HG01928.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+15612dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849061 | |||||
| chr10:96849061
|
CT | C | 109 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0196others(106): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-330+15612delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849061 | |||||
| chr10:96849061
|
CTT | C | 66 | a0001c0001t0001g0256a0001c0001t0006g0273a0001c0001t0016g0004others(63): Show | 66 | HG00558.hp1 HG00639.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.-330+15611_-330+15 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849061 | |||||
| chr10:96849061
|
CTTT | C | 44 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(41): Show | 44 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-330+15610_-330+15 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849061 | |||||
| chr10:96849061
|
CTTTTTTT others(7): Show |
C | 2 | a0002c0002t0014g0089a0002c0002t0145g0115 | 2 | NA18978.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-330+15599_-330+15 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849061 | |||||
| chr10:96849061
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-330+15598_-330+15 others(21): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849061 | |||||
| chr10:96849061
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+15597_-330+15 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849061 | |||||
| chr10:96849138
|
A | C | 1 | a0001c0001t0016g0176 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-330+15659A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849138 | ||||||
| chr10:96849302
|
T | G | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+15823T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849302 | ||||||
| chr10:96849342
|
G | A | 1 | a0002c0002t0020g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-330+15863G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849342 | ||||||
| chr10:96849365
|
G | A | 5 | a0002c0002t0013g0096a0002c0002t0020g0090a0002c0002t0020g0091others(2): Show | 5 | HG03017.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-330+15886G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849365 | ||||||
| chr10:96849429
|
T | C | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+15950T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849429 | ||||||
| chr10:96849432
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+15953A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849432 | ||||||
| chr10:96849727
|
A | G | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-330+16248A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849727 | ||||||
| chr10:96849845
|
T | C | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+16366T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96849845 | ||||||
| chr10:96849858
|
C | CT | 30 | a0001c0001t0001g0001a0001c0001t0001g0200a0001c0001t0001g0269others(27): Show | 30 | HG00438.hp1 HG01109.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-330+16401dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96849858 | |||||
| chr10:96850111
|
C | A | 2 | a0003c0003t0010g0162a0003c0003t0024g0161 | 2 | NA18952.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-330+16632C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850111 | ||||||
| chr10:96850220
|
G | C | 1 | a0001c0001t0032g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-330+16741G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850220 | ||||||
| chr10:96850236
|
C | T | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+16757C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850236 | ||||||
| chr10:96850312
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+16833G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850312 | ||||||
| chr10:96850490
|
T | A | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+17011T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850490 | ||||||
| chr10:96850709
|
A | G | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+17230A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850709 | ||||||
| chr10:96850733
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0005g0262 | 3 | HG01070.hp1 HG01074.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-330+17254C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850733 | ||||||
| chr10:96850837
|
A | G | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+17358A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850837 | ||||||
| chr10:96850946
|
C | A | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+17467C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96850946 | ||||||
| chr10:96851004
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-330+17525A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96851004 | ||||||
| chr10:96851078
|
A | G | 1 | a0002c0002t0019g0110 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-330+17599A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96851078 | ||||||
| chr10:96851358
|
G | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+17879G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96851358 | ||||||
| chr10:96851704
|
G | A | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-330+18225G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96851704 | ||||||
| chr10:96851751
|
C | T | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+18272C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96851751 | ||||||
| chr10:96851893
|
G | A | 1 | a0002c0002t0140g0064 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-330+18414G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96851893 | ||||||
| chr10:96852150
|
G | C | 187 | a0001c0001t0001g0198a0001c0001t0016g0004a0001c0001t0016g0136others(184): Show | 187 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.-330+18671G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852150 | ||||||
| chr10:96852210
|
A | G | 1 | a0001c0001t0093g0204 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-330+18731A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852210 | ||||||
| chr10:96852223
|
T | C | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+18744T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852223 | ||||||
| chr10:96852282
|
T | C | 1 | a0001c0004t0091g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-330+18803T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852282 | ||||||
| chr10:96852291
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-330+18812G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852291 | ||||||
| chr10:96852689
|
A | C | 1 | a0003c0003t0090g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-330+19210A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852689 | ||||||
| chr10:96852689
|
A | G | 1 | a0001c0001t0005g0218 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-330+19210A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852689 | ||||||
| chr10:96852799
|
G | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+19320G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852799 | ||||||
| chr10:96852942
|
T | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+19463T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852942 | ||||||
| chr10:96852953
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+19474A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96852953 | ||||||
| chr10:96853008
|
T | C | 1 | a0002c0002t0036g0072 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-330+19529T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96853008 | ||||||
| chr10:96853043
|
T | C | 2 | a0001c0004t0002g0154a0001c0004t0010g0153 | 2 | NA18993.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-330+19564T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96853043 | ||||||
| chr10:96853081
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+19602C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96853081 | ||||||
| chr10:96853297
|
C | A | 3 | a0001c0004t0002g0157a0001c0004t0011g0155a0003c0003t0004g0156 | 3 | NA18943.hp2 NA18960.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-330+19818C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96853297 | ||||||
| chr10:96854201
|
C | T | 19 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-330+20722C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96854201 | ||||||
| chr10:96854416
|
T | C | 1 | a0001c0004t0007g0019 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-330+20937T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96854416 | ||||||
| chr10:96854572
|
T | G | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-330+21093T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96854572 | ||||||
| chr10:96854575
|
C | T | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+21096C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96854575 | ||||||
| chr10:96854927
|
T | A | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+21448T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96854927 | ||||||
| chr10:96855215
|
G | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+21736G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855215 | ||||||
| chr10:96855345
|
A | AC | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+21868dupC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96855345 | |||||
| chr10:96855357
|
C | T | 1 | a0002c0002t0034g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-330+21878C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855357 | ||||||
| chr10:96855426
|
TTTTG | T | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+21967_-330+21 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96855426 | |||||
| chr10:96855566
|
C | G | 5 | a0004c0005t0043g0124a0004c0005t0045g0168a0004c0005t0046g0125others(2): Show | 5 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-330+22087C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855566 | ||||||
| chr10:96855584
|
A | G | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+22105A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855584 | ||||||
| chr10:96855636
|
A | G | 1 | a0001c0001t0005g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-330+22157A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855636 | ||||||
| chr10:96855818
|
C | T | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+22339C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855818 | ||||||
| chr10:96855895
|
C | T | 1 | a0001c0001t0107g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-330+22416C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855895 | ||||||
| chr10:96855897
|
A | G | 2 | a0001c0001t0026g0223a0001c0001t0026g0242 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-330+22418A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855897 | ||||||
| chr10:96855954
|
G | A | 4 | a0002c0002t0015g0102a0002c0002t0053g0108a0002c0002t0055g0109others(1): Show | 4 | HG02258.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+22475G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96855954 | ||||||
| chr10:96856004
|
A | C | 1 | a0001c0004t0083g0024 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-330+22525A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856004 | ||||||
| chr10:96856044
|
A | G | 4 | a0002c0002t0036g0072a0002c0002t0037g0071a0002c0002t0132g0088others(1): Show | 4 | HG00544.hp2 HG02071.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+22565A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856044 | ||||||
| chr10:96856079
|
G | GT | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-330+22609dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96856079 | |||||
| chr10:96856093
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+22614C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856093 | ||||||
| chr10:96856131
|
C | T | 2 | a0001c0001t0077g0127a0001c0001t0078g0128 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-330+22652C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856131 | ||||||
| chr10:96856231
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+22752C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856231 | ||||||
| chr10:96856232
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+22753G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856232 | ||||||
| chr10:96856351
|
G | A | 4 | a0001c0004t0002g0157a0001c0004t0007g0158a0001c0004t0011g0155others(1): Show | 4 | NA18943.hp2 NA18960.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+22872G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856351 | ||||||
| chr10:96856378
|
C | G | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+22899C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856378 | ||||||
| chr10:96856625
|
A | G | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-330+23146A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856625 | ||||||
| chr10:96856677
|
A | G | 1 | a0001c0001t0101g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-330+23198A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856677 | ||||||
| chr10:96856752
|
C | A | 1 | a0003c0003t0001g0036 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-330+23273C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856752 | ||||||
| chr10:96856964
|
A | T | 1 | a0003c0003t0090g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-330+23485A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856964 | ||||||
| chr10:96856997
|
CTT | C | 3 | a0002c0002t0015g0102a0002c0002t0055g0109a0002c0002t0058g0107 | 3 | HG02809.hp2 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-330+23519_-330+23 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96856997 | ||||||
| chr10:96857077
|
G | GAT | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+23607_-330+23 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96857077 | |||||
| chr10:96857094
|
ATATG | A | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-330+23617_-330+23 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96857094 | |||||
| chr10:96857236
|
A | C | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+23757A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857236 | ||||||
| chr10:96857363
|
A | T | 2 | a0001c0001t0097g0008a0001c0001t0098g0010 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-330+23884A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857363 | ||||||
| chr10:96857493
|
CCCCTGCA others(2435): Show |
C | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-330+24020_-330+26 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96857493 | |||||
| chr10:96857528
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+24049A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857528 | ||||||
| chr10:96857538
|
A | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+24059A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857538 | ||||||
| chr10:96857572
|
G | A | 1 | a0001c0001t0030g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-330+24093G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857572 | ||||||
| chr10:96857614
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+24135C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857614 | ||||||
| chr10:96857711
|
C | T | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-330+24232C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857711 | ||||||
| chr10:96857846
|
T | C | 2 | a0001c0004t0002g0009a0001c0004t0010g0049 | 2 | NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-330+24367T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857846 | ||||||
| chr10:96857862
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+24383A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857862 | ||||||
| chr10:96857884
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+24405C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96857884 | ||||||
| chr10:96858272
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-330+24793A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96858272 | ||||||
| chr10:96858608
|
T | C | 1 | a0004c0005t0047g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-330+25129T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96858608 | ||||||
| chr10:96858648
|
G | C | 1 | a0001c0001t0030g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-330+25169G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96858648 | ||||||
| chr10:96859278
|
C | T | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-330+25799C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96859278 | ||||||
| chr10:96859811
|
T | G | 62 | a0001c0001t0056g0284a0002c0002t0001g0078a0002c0002t0009g0073others(59): Show | 62 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-330+26332T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96859811 | ||||||
| chr10:96859844
|
C | T | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-330+26365C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96859844 | ||||||
| chr10:96859925
|
A | C | 3 | a0003c0003t0004g0031a0003c0003t0004g0047a0003c0003t0025g0022 | 3 | NA18983.hp1 NA19001.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-330+26446A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96859925 | ||||||
| chr10:96859958
|
A | G | 80 | a0001c0001t0056g0284a0001c0001t0106g0286a0002c0002t0001g0078others(77): Show | 80 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-330+26479A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96859958 | ||||||
| chr10:96860106
|
T | G | 59 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0002g0058others(56): Show | 59 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.-330+26627T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96860106 | ||||||
| chr10:96860243
|
A | G | 1 | a0001c0001t0003g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-330+26764A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96860243 | ||||||
| chr10:96860267
|
T | A | 1 | a0001c0001t0003g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-330+26788T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96860267 | ||||||
| chr10:96860300
|
A | G | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-330+26821A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96860300 | ||||||
| chr10:96861061
|
G | A | 1 | a0003c0003t0002g0057 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-330+27582G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861061 | ||||||
| chr10:96861126
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+27647A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861126 | ||||||
| chr10:96861155
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+27676C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861155 | ||||||
| chr10:96861248
|
C | T | 1 | a0001c0001t0113g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-330+27769C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861248 | ||||||
| chr10:96861305
|
A | G | 3 | a0004c0009t0021g0187a0004c0009t0044g0186a0004c0009t0064g0166 | 3 | HG02486.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-330+27826A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861305 | ||||||
| chr10:96861310
|
A | G | 21 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-330+27831A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861310 | ||||||
| chr10:96861339
|
T | A | 2 | a0001c0001t0106g0286a0005c0006t0060g0287 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-330+27860T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861339 | ||||||
| chr10:96861344
|
C | T | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-330+27865C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861344 | ||||||
| chr10:96861522
|
G | T | 2 | a0001c0004t0002g0058a0001c0004t0007g0126 | 2 | HG01928.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-330+28043G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861522 | ||||||
| chr10:96861665
|
G | A | 1 | a0004c0009t0021g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-330+28186G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861665 | ||||||
| chr10:96861706
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+28227C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861706 | ||||||
| chr10:96861742
|
C | T | 16 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-330+28263C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861742 | ||||||
| chr10:96861787
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-330+28308C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861787 | ||||||
| chr10:96861893
|
C | T | 1 | a0001c0001t0031g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-330+28414C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96861893 | ||||||
| chr10:96862161
|
C | T | 2 | a0001c0001t0097g0008a0001c0001t0098g0010 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-330+28682C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862161 | ||||||
| chr10:96862203
|
A | G | 1 | a0002c0002t0136g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-330+28724A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862203 | ||||||
| chr10:96862205
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+28726T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862205 | ||||||
| chr10:96862223
|
C | G | 1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-330+28744C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862223 | ||||||
| chr10:96862267
|
A | AT | 5 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0119g0208others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-330+28797dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96862267 | |||||
| chr10:96862276
|
T | G | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-330+28797T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862276 | ||||||
| chr10:96862300
|
G | A | 1 | a0003c0003t0004g0052 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-330+28821G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862300 | ||||||
| chr10:96862342
|
T | G | 3 | a0002c0002t0013g0067a0002c0002t0013g0068a0002c0002t0130g0066 | 3 | NA18952.hp2 NA18960.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-330+28863T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862342 | ||||||
| chr10:96862414
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+28935C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862414 | ||||||
| chr10:96862715
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+29236T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862715 | ||||||
| chr10:96862762
|
C | A | 1 | a0002c0002t0014g0101 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-330+29283C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862762 | ||||||
| chr10:96862808
|
A | AG | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-330+29330dupG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96862808 | |||||
| chr10:96862985
|
A | G | 14 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-330+29506A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96862985 | ||||||
| chr10:96863103
|
A | G | 2 | a0008c0011t0004g0202a0008c0011t0008g0201 | 2 | HG00639.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-330+29624A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863103 | ||||||
| chr10:96863104
|
T | A | 2 | a0008c0011t0004g0202a0008c0011t0008g0201 | 2 | HG00639.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-330+29625T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863104 | ||||||
| chr10:96863126
|
G | A | 2 | a0008c0011t0004g0202a0008c0011t0008g0201 | 2 | HG00639.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-330+29647G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863126 | ||||||
| chr10:96863206
|
G | GT | 75 | a0001c0001t0001g0250a0001c0001t0003g0220a0001c0001t0003g0243others(72): Show | 75 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-330+29742dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96863206 | |||||
| chr10:96863206
|
G | GTT | 11 | a0001c0001t0056g0284a0002c0002t0037g0071a0002c0002t0128g0087others(8): Show | 11 | HG00323.hp1 HG00544.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-330+29741_-330+29 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96863206 | |||||
| chr10:96863206
|
G | GTTT | 6 | a0004c0005t0043g0124a0004c0005t0046g0125a0004c0005t0048g0167others(3): Show | 6 | HG01109.hp1 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-330+29740_-330+29 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96863206 | |||||
| chr10:96863206
|
GT | G | 7 | a0001c0001t0001g0263a0001c0001t0012g0252a0001c0007t0102g0181others(4): Show | 7 | HG01515.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+29742delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96863206 | |||||
| chr10:96863207
|
T | G | 1 | a0001c0004t0089g0055 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-330+29728T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863207 | ||||||
| chr10:96863290
|
G | A | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-330+29811G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863290 | ||||||
| chr10:96863290
|
G | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+29811G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863290 | ||||||
| chr10:96863577
|
A | G | 2 | a0002c0002t0019g0086a0002c0002t0124g0085 | 2 | NA18970.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-330+30098A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863577 | ||||||
| chr10:96863617
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+30138T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863617 | ||||||
| chr10:96863778
|
T | C | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-330+30299T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96863778 | ||||||
| chr10:96864124
|
G | A | 1 | a0004c0005t0048g0167 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-330+30645G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96864124 | ||||||
| chr10:96864134
|
C | T | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-330+30655C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96864134 | ||||||
| chr10:96864522
|
G | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+31043G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96864522 | ||||||
| chr10:96864557
|
C | T | 1 | a0001c0004t0007g0158 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-330+31078C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96864557 | ||||||
| chr10:96864765
|
C | G | 2 | a0002c0002t0019g0110a0002c0002t0039g0084 | 2 | NA18944.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-330+31286C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96864765 | ||||||
| chr10:96865113
|
G | A | 21 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-330+31634G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865113 | ||||||
| chr10:96865115
|
A | G | 1 | a0001c0001t0005g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-330+31636A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865115 | ||||||
| chr10:96865236
|
G | A | 186 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(183): Show | 186 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-330+31757G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865236 | ||||||
| chr10:96865251
|
CTG | C | 9 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-330+31775_-330+31 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96865251 | |||||
| chr10:96865272
|
T | TA | 21 | a0001c0001t0106g0286a0002c0002t0019g0069a0004c0005t0021g0171others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-330+31801dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96865272 | |||||
| chr10:96865382
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+31903A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865382 | ||||||
| chr10:96865387
|
C | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+31908C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865387 | ||||||
| chr10:96865417
|
G | A | 68 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0038g0059others(65): Show | 68 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-330+31938G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865417 | ||||||
| chr10:96865530
|
T | TAGTTA | 21 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-330+32052_-330+32 others(11): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96865530 | |||||
| chr10:96865541
|
G | C | 1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-330+32062G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865541 | ||||||
| chr10:96865550
|
AC | A | 34 | a0001c0001t0001g0196a0001c0001t0001g0205a0001c0001t0001g0217others(31): Show | 34 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-330+32075delC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96865550 | |||||
| chr10:96865646
|
G | A | 2 | a0001c0001t0097g0008a0001c0001t0098g0010 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-330+32167G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865646 | ||||||
| chr10:96865651
|
G | C | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-330+32172G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865651 | ||||||
| chr10:96865874
|
C | CA | 18 | a0001c0001t0003g0243a0001c0001t0005g0218a0001c0001t0112g0266others(15): Show | 18 | HG00639.hp2 HG01109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-330+32414dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96865874 | |||||
| chr10:96865874
|
C | CAA | 6 | a0001c0001t0106g0286a0004c0009t0064g0166a0005c0006t0040g0288others(3): Show | 6 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+32413_-330+32 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96865874 | |||||
| chr10:96865874
|
CA | C | 163 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(160): Show | 163 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-330+32414delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96865874 | |||||
| chr10:96865904
|
A | G | 1 | a0001c0001t0067g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-330+32425A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865904 | ||||||
| chr10:96865929
|
G | A | 1 | a0001c0001t0003g0245 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-330+32450G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865929 | ||||||
| chr10:96865965
|
G | T | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-330+32486G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865965 | ||||||
| chr10:96865966
|
C | T | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-330+32487C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96865966 | ||||||
| chr10:96866054
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+32575G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866054 | ||||||
| chr10:96866148
|
G | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-330+32669G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866148 | ||||||
| chr10:96866216
|
C | T | 1 | a0002c0002t0128g0087 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-330+32737C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866216 | ||||||
| chr10:96866217
|
A | C | 1 | a0002c0002t0128g0087 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-330+32738A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866217 | ||||||
| chr10:96866242
|
A | G | 1 | a0001c0001t0099g0216 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-330+32763A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866242 | ||||||
| chr10:96866374
|
C | T | 1 | a0001c0001t0116g0255 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-330+32895C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866374 | ||||||
| chr10:96866702
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-330+33223G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866702 | ||||||
| chr10:96866788
|
C | T | 1 | a0001c0001t0117g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-330+33309C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866788 | ||||||
| chr10:96866898
|
T | G | 3 | a0002c0002t0015g0122a0002c0002t0015g0123a0002c0002t0061g0118 | 3 | HG02109.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-330+33419T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866898 | ||||||
| chr10:96866945
|
T | C | 3 | a0002c0002t0015g0122a0002c0002t0015g0123a0002c0002t0061g0118 | 3 | HG02109.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-330+33466T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96866945 | ||||||
| chr10:96867374
|
A | T | 17 | a0002c0002t0001g0078a0002c0002t0009g0076a0002c0002t0013g0083others(14): Show | 17 | HG00438.hp2 HG00621.hp1 NA18747.hp2 others(14): Show |
intron_variant | MODIFIER | c.-330+33895A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867374 | ||||||
| chr10:96867476
|
A | G | 2 | a0001c0004t0002g0009a0001c0004t0010g0049 | 2 | NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-330+33997A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867476 | ||||||
| chr10:96867526
|
G | C | 2 | a0008c0011t0004g0202a0008c0011t0008g0201 | 2 | HG00639.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-330+34047G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867526 | ||||||
| chr10:96867667
|
C | A | 1 | a0013c0018t0006g0190 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-330+34188C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867667 | ||||||
| chr10:96867712
|
C | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+34233C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867712 | ||||||
| chr10:96867895
|
T | C | 1 | a0001c0004t0007g0158 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-330+34416T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867895 | ||||||
| chr10:96867978
|
G | A | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-330+34499G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867978 | ||||||
| chr10:96867987
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0258 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-330+34508C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96867987 | ||||||
| chr10:96868089
|
T | G | 59 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0002g0058others(56): Show | 59 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.-330+34610T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868089 | ||||||
| chr10:96868120
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+34641G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868120 | ||||||
| chr10:96868278
|
C | CT | 24 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0106g0286others(21): Show | 24 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-330+34813dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96868278 | |||||
| chr10:96868285
|
T | C | 1 | a0001c0001t0023g0130 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-330+34806T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868285 | ||||||
| chr10:96868327
|
T | C | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-330+34848T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868327 | ||||||
| chr10:96868389
|
C | T | 1 | a0002c0002t0037g0094 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-330+34910C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868389 | ||||||
| chr10:96868475
|
T | C | 61 | a0001c0001t0097g0008a0001c0001t0098g0010a0001c0004t0002g0009others(58): Show | 61 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-330+34996T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868475 | ||||||
| chr10:96868533
|
G | A | 14 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-330+35054G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868533 | ||||||
| chr10:96868574
|
G | A | 1 | a0001c0001t0081g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-330+35095G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868574 | ||||||
| chr10:96868828
|
T | C | 6 | a0001c0001t0107g0178a0001c0007t0102g0181a0001c0007t0103g0179others(3): Show | 6 | HG01884.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+35349T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96868828 | ||||||
| chr10:96869135
|
A | G | 57 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(54): Show | 57 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.-330+35656A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96869135 | ||||||
| chr10:96869146
|
A | AT | 5 | a0002c0002t0009g0073a0002c0002t0036g0072a0002c0002t0037g0071others(2): Show | 5 | HG00544.hp2 HG02071.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-330+35668dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96869146 | |||||
| chr10:96869151
|
C | T | 1 | a0002c0002t0138g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-330+35672C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96869151 | ||||||
| chr10:96869153
|
C | T | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+35674C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96869153 | ||||||
| chr10:96869332
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-330+35853C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96869332 | ||||||
| chr10:96869569
|
C | CT | 24 | a0001c0004t0010g0049a0001c0007t0102g0181a0001c0007t0103g0179others(21): Show | 24 | HG00642.hp1 HG01109.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.-330+36106dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96869569 | |||||
| chr10:96869569
|
CT | C | 8 | a0001c0001t0001g0260a0001c0001t0003g0194a0001c0001t0005g0218others(5): Show | 8 | HG01070.hp2 HG01993.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-330+36106delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96869569 | |||||
| chr10:96869586
|
C | T | 4 | a0001c0001t0023g0130a0001c0001t0023g0159a0001c0001t0071g0132others(1): Show | 4 | HG00733.hp1 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+36107C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96869586 | ||||||
| chr10:96869927
|
A | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+36448A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96869927 | ||||||
| chr10:96870045
|
G | T | 184 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(181): Show | 184 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.-330+36566G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870045 | ||||||
| chr10:96870048
|
G | T | 1 | a0007c0013t0141g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-330+36569G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870048 | ||||||
| chr10:96870051
|
G | T | 1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-330+36572G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870051 | ||||||
| chr10:96870092
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-330+36613T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870092 | ||||||
| chr10:96870117
|
C | T | 1 | a0002c0002t0034g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-330+36638C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870117 | ||||||
| chr10:96870140
|
T | TGCCTCCT others(25): Show |
2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-330+36669_-330+36 others(38): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96870140 | |||||
| chr10:96870272
|
A | G | 1 | a0002c0002t0009g0073 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-330+36793A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870272 | ||||||
| chr10:96870831
|
A | G | 40 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(37): Show | 40 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-329-36434A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870831 | ||||||
| chr10:96870924
|
G | A | 1 | a0004c0005t0049g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-329-36341G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870924 | ||||||
| chr10:96870959
|
C | T | 9 | a0001c0001t0001g0274a0001c0001t0003g0265a0001c0001t0031g0267others(6): Show | 9 | HG00323.hp2 HG00741.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-329-36306C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96870959 | ||||||
| chr10:96871217
|
C | CT | 40 | a0001c0001t0003g0243a0001c0001t0016g0004a0001c0001t0016g0136others(37): Show | 40 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-329-36034dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96871217 | |||||
| chr10:96871439
|
G | T | 1 | a0004c0005t0043g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-329-35826G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96871439 | ||||||
| chr10:96871579
|
A | AT | 49 | a0001c0001t0001g0207a0001c0001t0006g0251a0001c0001t0012g0254others(46): Show | 49 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.-329-35671dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96871579 | |||||
| chr10:96871834
|
AAGG | A | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-329-35422_-329-35 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96871834 | |||||
| chr10:96871951
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0270 | 2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-329-35314C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96871951 | ||||||
| chr10:96872074
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-35191G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872074 | ||||||
| chr10:96872189
|
C | G | 1 | a0002c0002t0035g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-329-35076C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872189 | ||||||
| chr10:96872208
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-35057A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872208 | ||||||
| chr10:96872209
|
T | G | 2 | a0001c0001t0071g0132a0001c0001t0074g0131 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-329-35056T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872209 | ||||||
| chr10:96872226
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-35039G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872226 | ||||||
| chr10:96872229
|
G | A | 1 | a0001c0001t0005g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-329-35036G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872229 | ||||||
| chr10:96872289
|
G | A | 1 | a0001c0007t0108g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-329-34976G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872289 | ||||||
| chr10:96872294
|
A | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-34971A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872294 | ||||||
| chr10:96872310
|
C | T | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-329-34955C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872310 | ||||||
| chr10:96872556
|
G | A | 3 | a0003c0003t0010g0162a0003c0003t0024g0161a0003c0003t0024g0283 | 3 | NA18952.hp1 NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-329-34709G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872556 | ||||||
| chr10:96872950
|
TTA | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-34311_-329-34 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96872950 | |||||
| chr10:96872999
|
A | G | 1 | a0003c0003t0002g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-329-34266A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96872999 | ||||||
| chr10:96873068
|
A | AGT | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-329-34195_-329-34 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873068 | |||||
| chr10:96873303
|
A | G | 1 | a0016c0022t0028g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-329-33962A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873303 | ||||||
| chr10:96873340
|
A | G | 1 | a0001c0001t0078g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-329-33925A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873340 | ||||||
| chr10:96873557
|
T | C | 1 | a0002c0002t0019g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-329-33708T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873557 | ||||||
| chr10:96873557
|
TAC | T | 3 | a0001c0001t0001g0268a0001c0001t0098g0010a0001c0004t0002g0029 | 3 | HG02559.hp2 NA18964.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-329-33695_-329-33 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873557 | |||||
| chr10:96873567
|
CACACGT | C | 4 | a0003c0003t0002g0048a0003c0003t0002g0282a0003c0003t0004g0038others(1): Show | 4 | HG03834.hp2 NA18969.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-33697_-329-33 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873567 | ||||||
| chr10:96873567
|
CACACGTG others(1): Show |
C | 37 | a0001c0004t0002g0009a0001c0004t0002g0058a0001c0004t0007g0126others(34): Show | 37 | HG00733.hp2 HG01099.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.-329-33697_-329-33 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873567 | ||||||
| chr10:96873567
|
CACACGTG others(3): Show |
C | 13 | a0001c0004t0007g0019a0001c0004t0007g0041a0001c0004t0088g0016others(10): Show | 13 | HG00558.hp2 HG02735.hp2 HG03710.hp2 others(10): Show |
intron_variant | MODIFIER | c.-329-33697_-329-33 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873567 | ||||||
| chr10:96873568
|
A | G | 1 | a0001c0001t0005g0218 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-329-33697A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873568 | ||||||
| chr10:96873569
|
C | CGT | 3 | a0001c0001t0001g0270a0004c0005t0021g0171a0004c0005t0050g0173 | 3 | HG03453.hp1 HG03688.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-329-33696_-329-33 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873569 | ||||||
| chr10:96873569
|
C | CGTGTGT | 3 | a0001c0001t0001g0215a0004c0009t0021g0187a0004c0009t0044g0186 | 3 | HG02486.hp1 NA18990.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-329-33696_-329-33 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873569 | ||||||
| chr10:96873569
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0104g0206a0004c0009t0064g0166 | 2 | HG00544.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-329-33696_-329-33 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873569 | ||||||
| chr10:96873569
|
C | T | 1 | a0001c0001t0005g0218 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-329-33696C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873569 | ||||||
| chr10:96873569
|
CACGT | C | 3 | a0001c0001t0097g0008a0004c0005t0048g0167a0004c0005t0049g0169 | 3 | HG01109.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-329-33695_-329-33 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873569 | ||||||
| chr10:96873569
|
CACGTGT | C | 4 | a0003c0003t0082g0037a0004c0005t0045g0168a0007c0013t0080g0174others(1): Show | 4 | HG01884.hp1 HG02257.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-33695_-329-33 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873569 | ||||||
| chr10:96873569
|
CACGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0207 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-329-33695_-329-33 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873569 | ||||||
| chr10:96873570
|
A | G | 15 | a0001c0001t0001g0198a0001c0001t0001g0215a0001c0001t0001g0270others(12): Show | 15 | HG00544.hp1 HG02074.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-33695A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873570 | ||||||
| chr10:96873571
|
C | CACGTGTG others(5): Show |
1 | a0001c0001t0001g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-329-33694_-329-33 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873571 | ||||||
| chr10:96873571
|
C | CGT | 18 | a0001c0001t0001g0001a0001c0001t0001g0196a0001c0001t0001g0236others(15): Show | 18 | HG00642.hp2 HG01070.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.-329-33649_-329-33 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
C | CGTGT | 29 | a0001c0001t0001g0200a0001c0001t0001g0217a0001c0001t0001g0232others(26): Show | 29 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.-329-33651_-329-33 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
C | CGTGTGT | 16 | a0001c0001t0001g0197a0001c0001t0001g0213a0001c0001t0001g0250others(13): Show | 16 | HG00323.hp2 HG00639.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-329-33653_-329-33 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0253a0001c0001t0001g0269a0001c0001t0001g0275others(5): Show | 8 | HG02083.hp2 HG04115.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.-329-33655_-329-33 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
C | CGTGTGTG others(3): Show |
3 | a0001c0001t0005g0221a0001c0001t0006g0244a0001c0001t0027g0188 | 3 | NA18971.hp2 NA19074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-329-33657_-329-33 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-329-33659_-329-33 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
C | T | 15 | a0001c0001t0001g0198a0001c0001t0001g0215a0001c0001t0001g0270others(12): Show | 15 | HG00544.hp1 HG02074.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-33694C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873571 | ||||||
| chr10:96873571
|
CGT | C | 5 | a0001c0001t0001g0234a0001c0001t0114g0246a0001c0001t0144g0257others(2): Show | 5 | HG01074.hp1 HG02280.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-33649_-329-33 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
CGTGT | C | 30 | a0001c0001t0001g0230a0001c0001t0006g0229a0001c0001t0032g0012others(27): Show | 30 | HG00438.hp2 HG00558.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.-329-33651_-329-33 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
CGTGTGT | C | 35 | a0001c0001t0006g0273a0001c0001t0106g0286a0002c0002t0001g0078others(32): Show | 35 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-329-33653_-329-33 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
CGTGTGTG others(3): Show |
C | 4 | a0001c0001t0017g0145a0001c0001t0017g0146a0001c0001t0077g0127others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-33657_-329-33 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
CGTGTGTG others(5): Show |
C | 32 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(29): Show | 32 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.-329-33659_-329-33 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0071g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-329-33661_-329-33 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
CGTGTGTG others(9): Show |
C | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-33663_-329-33 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873571
|
CGTGTGTG others(19): Show |
C | 1 | a0001c0001t0012g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-329-33673_-329-33 others(32): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873571 | |||||
| chr10:96873574
|
G | A | 1 | a0014c0020t0012g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-329-33691G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873574 | ||||||
| chr10:96873575
|
T | C | 1 | a0014c0020t0012g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-329-33690T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873575 | ||||||
| chr10:96873576
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-33689G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873576 | ||||||
| chr10:96873578
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-33687G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873578 | ||||||
| chr10:96873582
|
G | A | 4 | a0001c0001t0017g0145a0001c0001t0017g0146a0001c0001t0077g0127others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-33683G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873582 | ||||||
| chr10:96873584
|
G | A | 34 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(31): Show | 34 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-329-33681G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873584 | ||||||
| chr10:96873586
|
G | A | 31 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(28): Show | 31 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-329-33679G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873586 | ||||||
| chr10:96873588
|
G | A | 1 | a0001c0001t0071g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-329-33677G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873588 | ||||||
| chr10:96873606
|
GTGTGTGT others(4): Show |
G | 1 | a0002c0002t0058g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-329-33657_-329-33 others(17): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96873606 | |||||
| chr10:96873891
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-329-33374G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96873891 | ||||||
| chr10:96874130
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0006g0229 | 2 | HG01167.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.-329-33135G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96874130 | ||||||
| chr10:96874185
|
T | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(90): Show | 93 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-329-33080T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96874185 | ||||||
| chr10:96874490
|
C | T | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-329-32775C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96874490 | ||||||
| chr10:96874527
|
C | T | 6 | a0001c0004t0002g0154a0001c0004t0002g0157a0001c0004t0007g0158others(3): Show | 6 | NA18943.hp2 NA18960.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-329-32738C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96874527 | ||||||
| chr10:96874710
|
T | C | 1 | a0004c0005t0050g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-329-32555T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96874710 | ||||||
| chr10:96875150
|
C | T | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-329-32115C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96875150 | ||||||
| chr10:96875245
|
G | A | 1 | a0001c0001t0027g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-329-32020G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96875245 | ||||||
| chr10:96875385
|
A | T | 48 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(45): Show | 48 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-329-31880A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96875385 | ||||||
| chr10:96875399
|
C | T | 39 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(36): Show | 39 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-329-31866C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96875399 | ||||||
| chr10:96875752
|
C | A | 1 | a0001c0001t0038g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-329-31513C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96875752 | ||||||
| chr10:96876013
|
TA | T | 9 | a0001c0001t0030g0209a0001c0001t0074g0131a0002c0002t0013g0083others(6): Show | 9 | HG01515.hp2 HG02602.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-329-31238delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96876013 | |||||
| chr10:96876055
|
A | AT | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-31204dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96876055 | |||||
| chr10:96876249
|
G | A | 1 | a0012c0017t0127g0077 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-329-31016G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96876249 | ||||||
| chr10:96876479
|
T | C | 1 | a0001c0001t0051g0133 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-329-30786T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96876479 | ||||||
| chr10:96876618
|
G | C | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-329-30647G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96876618 | ||||||
| chr10:96876753
|
G | A | 1 | a0001c0001t0012g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-329-30512G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96876753 | ||||||
| chr10:96876883
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0232a0001c0001t0001g0248others(2): Show | 5 | NA18959.hp1 NA18973.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-329-30382C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96876883 | ||||||
| chr10:96877246
|
A | G | 2 | a0001c0001t0032g0012a0001c0001t0120g0003 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-30019A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877246 | ||||||
| chr10:96877354
|
A | G | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-29911A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877354 | ||||||
| chr10:96877458
|
T | A | 1 | a0003c0003t0004g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-329-29807T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877458 | ||||||
| chr10:96877516
|
C | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-29749C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877516 | ||||||
| chr10:96877570
|
T | C | 3 | a0003c0003t0010g0162a0003c0003t0024g0161a0003c0003t0024g0283 | 3 | NA18952.hp1 NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-329-29695T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877570 | ||||||
| chr10:96877598
|
A | AT | 7 | a0001c0001t0001g0198a0001c0001t0001g0236a0001c0001t0005g0221others(4): Show | 7 | HG00642.hp2 HG01109.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-29636dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96877598 | |||||
| chr10:96877598
|
AT | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0189a0001c0001t0001g0192others(112): Show | 115 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.-329-29636delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96877598 | |||||
| chr10:96877598
|
ATT | A | 86 | a0001c0001t0001g0002a0001c0001t0003g0194a0001c0001t0003g0214others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.-329-29637_-329-29 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96877598 | |||||
| chr10:96877598
|
ATTT | A | 33 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(30): Show | 33 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-329-29638_-329-29 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96877598 | |||||
| chr10:96877598
|
ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0001g0253a0001c0001t0006g0244 | 2 | NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-329-29648_-329-29 others(19): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96877598 | |||||
| chr10:96877598
|
ATTTTTTT others(8): Show |
A | 1 | a0002c0002t0034g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-329-29650_-329-29 others(21): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96877598 | |||||
| chr10:96877813
|
G | A | 1 | a0004c0005t0049g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-329-29452G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877813 | ||||||
| chr10:96877892
|
T | A | 2 | a0003c0003t0004g0177a0003c0003t0085g0056 | 2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-329-29373T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877892 | ||||||
| chr10:96877893
|
G | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-329-29372G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877893 | ||||||
| chr10:96877902
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-329-29363C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877902 | ||||||
| chr10:96877932
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-29333G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96877932 | ||||||
| chr10:96878085
|
A | T | 1 | a0001c0001t0107g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-329-29180A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96878085 | ||||||
| chr10:96878119
|
T | C | 1 | a0003c0003t0025g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-329-29146T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96878119 | ||||||
| chr10:96878262
|
CT | C | 120 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(117): Show | 120 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-329-29001delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96878262 | |||||
| chr10:96878324
|
T | C | 188 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(185): Show | 188 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.-329-28941T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96878324 | ||||||
| chr10:96878457
|
A | G | 40 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(37): Show | 40 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-329-28808A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96878457 | ||||||
| chr10:96878941
|
C | T | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-28324C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96878941 | ||||||
| chr10:96879087
|
C | T | 1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-329-28178C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879087 | ||||||
| chr10:96879196
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(282): Show | 285 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(282): Show |
intron_variant | MODIFIER | c.-329-28069A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879196 | ||||||
| chr10:96879340
|
T | C | 188 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(185): Show | 188 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.-329-27925T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879340 | ||||||
| chr10:96879342
|
A | G | 1 | a0001c0004t0007g0019 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-329-27923A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879342 | ||||||
| chr10:96879479
|
C | T | 21 | a0001c0001t0056g0284a0001c0001t0106g0286a0004c0005t0021g0171others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-329-27786C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879479 | ||||||
| chr10:96879508
|
C | T | 56 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(53): Show | 56 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.-329-27757C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879508 | ||||||
| chr10:96879575
|
C | T | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-329-27690C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879575 | ||||||
| chr10:96879644
|
T | A | 2 | a0001c0001t0071g0132a0001c0001t0074g0131 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-329-27621T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879644 | ||||||
| chr10:96879677
|
C | T | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-329-27588C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879677 | ||||||
| chr10:96879716
|
G | T | 4 | a0001c0004t0007g0041a0001c0004t0083g0024a0001c0004t0084g0025others(1): Show | 4 | HG01099.hp2 HG01106.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-27549G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96879716 | ||||||
| chr10:96880007
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-27258A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880007 | ||||||
| chr10:96880089
|
G | A | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-329-27176G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880089 | ||||||
| chr10:96880126
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-27139C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880126 | ||||||
| chr10:96880443
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-329-26822G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880443 | ||||||
| chr10:96880490
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-329-26775C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880490 | ||||||
| chr10:96880673
|
C | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-26592C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880673 | ||||||
| chr10:96880687
|
C | G | 1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-329-26578C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880687 | ||||||
| chr10:96880702
|
A | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-26563A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880702 | ||||||
| chr10:96880743
|
C | G | 1 | a0001c0001t0078g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-329-26522C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880743 | ||||||
| chr10:96880865
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-329-26400T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880865 | ||||||
| chr10:96880872
|
C | T | 2 | a0003c0003t0004g0035a0003c0003t0008g0040 | 2 | NA19060.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-329-26393C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880872 | ||||||
| chr10:96880884
|
A | G | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-26381A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880884 | ||||||
| chr10:96880964
|
T | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-26301T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96880964 | ||||||
| chr10:96881150
|
A | G | 1 | a0004c0005t0049g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-329-26115A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881150 | ||||||
| chr10:96881152
|
G | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-26113G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881152 | ||||||
| chr10:96881237
|
G | T | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-329-26028G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881237 | ||||||
| chr10:96881462
|
GT | G | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-329-25792delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96881462 | |||||
| chr10:96881521
|
G | A | 186 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(183): Show | 186 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-329-25744G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881521 | ||||||
| chr10:96881561
|
A | G | 1 | a0001c0004t0091g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-329-25704A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881561 | ||||||
| chr10:96881643
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-329-25622G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881643 | ||||||
| chr10:96881791
|
A | G | 1 | a0001c0001t0030g0228 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-329-25474A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881791 | ||||||
| chr10:96881853
|
G | A | 1 | a0002c0002t0037g0094 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-329-25412G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96881853 | ||||||
| chr10:96882112
|
C | T | 1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-329-25153C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882112 | ||||||
| chr10:96882273
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-329-24992T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882273 | ||||||
| chr10:96882300
|
G | A | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-329-24965G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882300 | ||||||
| chr10:96882304
|
C | T | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-24961C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882304 | ||||||
| chr10:96882491
|
A | G | 43 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(40): Show | 43 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-329-24774A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882491 | ||||||
| chr10:96882651
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-329-24614A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882651 | ||||||
| chr10:96882664
|
C | T | 3 | a0001c0001t0016g0136a0001c0001t0073g0141a0001c0001t0075g0140 | 3 | HG02055.hp1 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-329-24601C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882664 | ||||||
| chr10:96882862
|
G | T | 1 | a0001c0001t0003g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-329-24403G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882862 | ||||||
| chr10:96882882
|
G | A | 1 | a0001c0001t0005g0261 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-329-24383G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882882 | ||||||
| chr10:96882997
|
G | C | 1 | a0001c0001t0079g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-329-24268G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96882997 | ||||||
| chr10:96883041
|
T | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-24224T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96883041 | ||||||
| chr10:96883179
|
G | A | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-24086G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96883179 | ||||||
| chr10:96883454
|
T | C | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-329-23811T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96883454 | ||||||
| chr10:96883464
|
A | G | 3 | a0003c0003t0004g0034a0003c0003t0004g0039a0003c0003t0082g0037 | 3 | NA18747.hp1 NA18939.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-329-23801A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96883464 | ||||||
| chr10:96883492
|
C | T | 1 | a0001c0001t0072g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-329-23773C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96883492 | ||||||
| chr10:96883972
|
G | A | 7 | a0001c0004t0007g0019a0001c0004t0088g0016a0001c0004t0091g0018others(4): Show | 7 | HG00558.hp2 NA18947.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-329-23293G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96883972 | ||||||
| chr10:96884018
|
A | C | 1 | a0002c0002t0014g0089 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-329-23247A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96884018 | ||||||
| chr10:96884038
|
TATA | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-23221_-329-23 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96884038 | |||||
| chr10:96884091
|
G | A | 2 | a0001c0004t0007g0041a0001c0004t0083g0024 | 2 | HG02602.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-329-23174G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96884091 | ||||||
| chr10:96884272
|
C | T | 61 | a0001c0001t0097g0008a0001c0001t0098g0010a0001c0004t0002g0009others(58): Show | 61 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-329-22993C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96884272 | ||||||
| chr10:96884316
|
G | A | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-329-22949G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96884316 | ||||||
| chr10:96884552
|
A | C | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-329-22713A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96884552 | ||||||
| chr10:96884552
|
A | G | 6 | a0001c0004t0002g0154a0001c0004t0002g0157a0001c0004t0007g0158others(3): Show | 6 | NA18943.hp2 NA18960.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-329-22713A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96884552 | ||||||
| chr10:96884613
|
G | A | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-22652G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96884613 | ||||||
| chr10:96885117
|
T | C | 2 | a0001c0004t0109g0027a0001c0004t0110g0043 | 2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-329-22148T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96885117 | ||||||
| chr10:96885129
|
G | C | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-22136G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96885129 | ||||||
| chr10:96885384
|
T | C | 11 | a0002c0002t0001g0078a0002c0002t0013g0083a0002c0002t0019g0086others(8): Show | 11 | NA18942.hp1 NA18944.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.-329-21881T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96885384 | ||||||
| chr10:96885421
|
TC | T | 3 | a0002c0002t0020g0091a0002c0002t0020g0116a0002c0002t0133g0074 | 3 | HG03017.hp2 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-329-21841delC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96885421 | |||||
| chr10:96885444
|
T | C | 1 | a0002c0002t0035g0098 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-329-21821T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96885444 | ||||||
| chr10:96885553
|
A | AT | 15 | a0001c0001t0001g0269a0001c0001t0003g0194a0002c0002t0013g0068others(12): Show | 15 | HG00558.hp1 HG00621.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-21688dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96885553 | |||||
| chr10:96885553
|
AT | A | 23 | a0001c0001t0001g0275a0001c0001t0003g0240a0001c0001t0106g0286others(20): Show | 23 | HG01109.hp1 HG02071.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-329-21688delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96885553 | |||||
| chr10:96885553
|
ATT | A | 63 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0038g0059others(60): Show | 63 | HG00673.hp1 HG00733.hp2 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.-329-21689_-329-21 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96885553 | |||||
| chr10:96885553
|
ATTT | A | 40 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(37): Show | 40 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-329-21690_-329-21 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96885553 | |||||
| chr10:96885595
|
G | C | 1 | a0006c0008t0002g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-329-21670G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96885595 | ||||||
| chr10:96885938
|
T | C | 50 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(47): Show | 50 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-329-21327T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96885938 | ||||||
| chr10:96886334
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-329-20931A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96886334 | ||||||
| chr10:96886525
|
T | C | 1 | a0003c0003t0004g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-329-20740T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96886525 | ||||||
| chr10:96886671
|
T | TA | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-20593dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96886671 | |||||
| chr10:96886789
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-20476C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96886789 | ||||||
| chr10:96886791
|
A | G | 2 | a0002c0002t0014g0089a0002c0002t0145g0115 | 2 | NA18978.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-329-20474A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96886791 | ||||||
| chr10:96886960
|
C | A | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-329-20305C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96886960 | ||||||
| chr10:96887197
|
T | C | 2 | a0001c0001t0077g0127a0001c0001t0078g0128 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-329-20068T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96887197 | ||||||
| chr10:96887207
|
T | C | 59 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0002g0058others(56): Show | 59 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.-329-20058T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96887207 | ||||||
| chr10:96887349
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-19916C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96887349 | ||||||
| chr10:96887421
|
G | A | 1 | a0001c0001t0117g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-329-19844G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96887421 | ||||||
| chr10:96887681
|
CT | C | 37 | a0001c0001t0003g0240a0001c0001t0016g0004a0001c0001t0016g0136others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-329-19569delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96887681 | |||||
| chr10:96887697
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-19568A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96887697 | ||||||
| chr10:96887805
|
C | T | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-19460C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96887805 | ||||||
| chr10:96887869
|
C | G | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-329-19396C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96887869 | ||||||
| chr10:96888133
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-329-19132G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888133 | ||||||
| chr10:96888279
|
C | T | 4 | a0002c0002t0053g0108a0002c0002t0055g0109a0002c0002t0058g0107others(1): Show | 4 | HG02258.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-18986C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888279 | ||||||
| chr10:96888363
|
C | CA | 65 | a0001c0001t0001g0001a0001c0001t0001g0189a0001c0001t0001g0192others(62): Show | 65 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-329-18874dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAA | 31 | a0001c0001t0001g0002a0001c0001t0001g0200a0001c0001t0001g0213others(28): Show | 31 | HG00438.hp1 HG00642.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-329-18875_-329-18 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAA | 6 | a0001c0001t0001g0205a0001c0001t0003g0199a0001c0001t0003g0210others(3): Show | 6 | HG00673.hp2 NA18947.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-329-18876_-329-18 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0023g0130a0001c0001t0023g0159a0001c0001t0068g0134others(2): Show | 5 | HG00733.hp1 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-329-18883_-329-18 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0077g0127a0001c0004t0002g0154 | 2 | HG02922.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-329-18884_-329-18 others(17): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0017g0146a0001c0001t0078g0128a0015c0021t0017g0147 | 3 | HG02486.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-329-18885_-329-18 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0065g0148a0001c0001t0072g0135a0001c0004t0002g0157others(1): Show | 4 | HG02630.hp1 HG04115.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-18886_-329-18 others(19): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0022g0144a0001c0001t0079g0142 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-329-18887_-329-18 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0016g0004a0001c0001t0022g0143a0001c0001t0067g0138 | 3 | HG00639.hp1 HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-329-18888_-329-18 others(21): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0073g0141a0001c0001t0075g0140 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-329-18889_-329-18 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0016g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-329-18890_-329-18 others(23): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(11): Show |
1 | a0001c0004t0011g0155 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-329-18891_-329-18 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0017g0145a0003c0003t0004g0156 | 2 | HG03195.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-329-18894_-329-18 others(27): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0016g0176 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-329-18897_-329-18 others(30): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0070g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-329-18874_-329-18 others(39): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
CA | C | 58 | a0001c0001t0032g0013a0001c0001t0069g0129a0001c0001t0120g0003others(55): Show | 58 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-329-18874delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
CAA | C | 58 | a0001c0001t0032g0012a0001c0001t0097g0008a0001c0001t0098g0010others(55): Show | 58 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-329-18875_-329-18 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
CAAAAAAA others(3): Show |
C | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-329-18883_-329-18 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0029g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-329-18884_-329-18 others(17): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888363
|
CAAAAAAA others(7): Show |
C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-18887_-329-18 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96888363 | |||||
| chr10:96888392
|
G | A | 1 | a0001c0001t0051g0133 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-329-18873G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888392 | ||||||
| chr10:96888418
|
T | C | 1 | a0002c0002t0014g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-329-18847T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888418 | ||||||
| chr10:96888447
|
T | C | 1 | a0002c0002t0009g0073 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-329-18818T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888447 | ||||||
| chr10:96888498
|
A | G | 3 | a0004c0009t0021g0187a0004c0009t0044g0186a0004c0009t0064g0166 | 3 | HG02486.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-329-18767A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888498 | ||||||
| chr10:96888523
|
G | A | 1 | a0001c0001t0016g0176 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-329-18742G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888523 | ||||||
| chr10:96888618
|
A | G | 1 | a0002c0002t0020g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-329-18647A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888618 | ||||||
| chr10:96888883
|
G | A | 1 | a0001c0001t0079g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-329-18382G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96888883 | ||||||
| chr10:96889085
|
A | T | 1 | a0001c0004t0084g0025 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-329-18180A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889085 | ||||||
| chr10:96889169
|
C | T | 1 | a0001c0004t0089g0055 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-329-18096C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889169 | ||||||
| chr10:96889299
|
G | T | 1 | a0001c0001t0038g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-329-17966G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889299 | ||||||
| chr10:96889389
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-329-17876T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889389 | ||||||
| chr10:96889430
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-329-17835T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889430 | ||||||
| chr10:96889539
|
C | T | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-329-17726C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889539 | ||||||
| chr10:96889625
|
C | G | 5 | a0001c0007t0102g0181a0001c0007t0103g0179a0001c0007t0105g0182others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-17640C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889625 | ||||||
| chr10:96889690
|
A | C | 1 | a0001c0004t0002g0009 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-329-17575A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889690 | ||||||
| chr10:96889747
|
A | G | 2 | a0004c0009t0021g0187a0004c0009t0044g0186 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-329-17518A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889747 | ||||||
| chr10:96889756
|
C | T | 1 | a0001c0001t0005g0218 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-329-17509C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889756 | ||||||
| chr10:96889833
|
T | A | 1 | a0002c0002t0014g0089 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-329-17432T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889833 | ||||||
| chr10:96889841
|
A | G | 1 | a0001c0007t0102g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-329-17424A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889841 | ||||||
| chr10:96889875
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-17390T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96889875 | ||||||
| chr10:96890485
|
A | T | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-16780A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96890485 | ||||||
| chr10:96890602
|
G | A | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | NA18961.hp1 NA18978.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-16663G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96890602 | ||||||
| chr10:96890885
|
G | T | 3 | a0001c0001t0016g0136a0001c0001t0073g0141a0001c0001t0075g0140 | 3 | HG02055.hp1 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-329-16380G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96890885 | ||||||
| chr10:96890964
|
A | G | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-329-16301A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96890964 | ||||||
| chr10:96891092
|
T | C | 1 | a0001c0001t0005g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-329-16173T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891092 | ||||||
| chr10:96891096
|
A | G | 1 | a0001c0004t0010g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-329-16169A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891096 | ||||||
| chr10:96891289
|
A | C | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-15976A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891289 | ||||||
| chr10:96891444
|
G | A | 65 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0097g0008others(62): Show | 65 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-329-15821G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891444 | ||||||
| chr10:96891482
|
C | CT | 85 | a0001c0001t0001g0189a0001c0001t0001g0207a0001c0001t0001g0232others(82): Show | 85 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-329-15763dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891482 | |||||
| chr10:96891482
|
C | CTT | 6 | a0002c0002t0014g0089a0002c0002t0055g0109a0002c0002t0061g0118others(3): Show | 6 | HG02027.hp2 HG02071.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-329-15764_-329-15 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891482 | |||||
| chr10:96891482
|
CT | C | 12 | a0001c0001t0001g0236a0001c0001t0003g0240a0001c0001t0065g0148others(9): Show | 12 | HG00642.hp2 HG01109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-329-15763delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891482 | |||||
| chr10:96891482
|
CTT | C | 42 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(39): Show | 42 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.-329-15764_-329-15 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891482 | |||||
| chr10:96891530
|
C | CT | 17 | a0001c0001t0111g0184a0002c0002t0014g0065a0002c0002t0014g0089others(14): Show | 17 | HG00323.hp1 HG00558.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.-329-15701dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
C | CTT | 14 | a0002c0002t0009g0076a0002c0002t0013g0067a0002c0002t0013g0068others(11): Show | 14 | HG00438.hp2 HG02071.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-329-15702_-329-15 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CT | C | 13 | a0001c0004t0002g0029a0001c0004t0088g0016a0001c0004t0094g0017others(10): Show | 13 | HG01257.hp1 HG02071.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-329-15701delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTT | C | 14 | a0001c0001t0056g0284a0001c0004t0002g0058a0001c0004t0010g0049others(11): Show | 14 | HG01928.hp2 HG02027.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-329-15702_-329-15 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTT | C | 40 | a0001c0001t0001g0217a0001c0001t0006g0273a0001c0001t0022g0144others(37): Show | 40 | HG00558.hp2 HG01099.hp2 HG01993.hp1 others(37): Show |
intron_variant | MODIFIER | c.-329-15703_-329-15 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTT | C | 44 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0196others(41): Show | 44 | HG00621.hp2 HG00741.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-329-15704_-329-15 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTT | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0198others(63): Show | 66 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-329-15705_-329-15 others(11): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTTT | C | 19 | a0001c0001t0001g0207a0001c0001t0003g0214a0001c0001t0016g0004others(16): Show | 19 | HG01071.hp2 HG01081.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-329-15706_-329-15 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0005g0261a0004c0005t0047g0172a0005c0006t0052g0165 | 3 | NA18906.hp1 NA18998.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-329-15710_-329-15 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTTTT others(4): Show |
C | 7 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(4): Show | 7 | HG02257.hp1 HG02717.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-329-15711_-329-15 others(17): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0106g0286a0004c0005t0048g0167a0004c0005t0049g0169others(6): Show | 9 | HG01109.hp1 HG02486.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-329-15712_-329-15 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTTTT others(6): Show |
C | 1 | a0006c0008t0002g0033 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-329-15713_-329-15 others(19): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTTTT others(8): Show |
C | 7 | a0001c0007t0102g0181a0001c0007t0103g0179a0001c0007t0105g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-15715_-329-15 others(21): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891530
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0004t0084g0025 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-329-15721_-329-15 others(27): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96891530 | |||||
| chr10:96891633
|
C | T | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-329-15632C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891633 | ||||||
| chr10:96891699
|
C | A | 1 | a0001c0001t0012g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-329-15566C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891699 | ||||||
| chr10:96891768
|
G | A | 1 | a0001c0007t0147g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-329-15497G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891768 | ||||||
| chr10:96891924
|
G | C | 186 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(183): Show | 186 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-329-15341G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96891924 | ||||||
| chr10:96892266
|
G | A | 1 | a0001c0001t0012g0225 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-329-14999G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96892266 | ||||||
| chr10:96892431
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-14834T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96892431 | ||||||
| chr10:96892512
|
T | A | 1 | a0001c0001t0107g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-329-14753T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96892512 | ||||||
| chr10:96892613
|
T | C | 21 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-329-14652T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96892613 | ||||||
| chr10:96892665
|
A | G | 2 | a0001c0001t0099g0216a0001c0001t0100g0226 | 2 | NA18982.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-329-14600A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96892665 | ||||||
| chr10:96892677
|
T | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-14588T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96892677 | ||||||
| chr10:96892945
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-14320G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96892945 | ||||||
| chr10:96893361
|
T | G | 2 | a0001c0001t0081g0231a0001c0001t0144g0257 | 2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-329-13904T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96893361 | ||||||
| chr10:96893424
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-13841C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96893424 | ||||||
| chr10:96893762
|
C | CA | 32 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(29): Show | 32 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-329-13487dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96893762 | |||||
| chr10:96893762
|
CA | C | 6 | a0002c0002t0037g0094a0003c0003t0004g0023a0003c0003t0025g0045others(3): Show | 6 | HG01168.hp2 HG01884.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.-329-13487delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96893762 | |||||
| chr10:96893815
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-329-13450T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96893815 | ||||||
| chr10:96894515
|
GC | G | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-329-12748delC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96894515 | |||||
| chr10:96894624
|
C | T | 2 | a0001c0001t0038g0059a0001c0001t0142g0061 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-329-12641C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96894624 | ||||||
| chr10:96894675
|
G | C | 3 | a0001c0007t0102g0181a0001c0007t0103g0179a0001c0007t0105g0182 | 3 | HG02615.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-329-12590G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96894675 | ||||||
| chr10:96894747
|
A | T | 5 | a0002c0002t0013g0096a0002c0002t0020g0090a0002c0002t0020g0091others(2): Show | 5 | HG03017.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-12518A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96894747 | ||||||
| chr10:96894841
|
A | G | 2 | a0001c0004t0002g0154a0001c0004t0010g0153 | 2 | NA18993.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-329-12424A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96894841 | ||||||
| chr10:96895057
|
T | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-329-12208T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96895057 | ||||||
| chr10:96895318
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-11947A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96895318 | ||||||
| chr10:96895678
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0006g0229 | 2 | HG01167.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.-329-11587T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96895678 | ||||||
| chr10:96895813
|
C | A | 4 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0047g0172others(1): Show | 4 | HG03453.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-11452C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96895813 | ||||||
| chr10:96895847
|
C | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-329-11418C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96895847 | ||||||
| chr10:96896132
|
G | A | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-11133G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96896132 | ||||||
| chr10:96896250
|
A | T | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-11015A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96896250 | ||||||
| chr10:96896352
|
A | C | 1 | a0001c0001t0069g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-329-10913A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96896352 | ||||||
| chr10:96896536
|
G | A | 1 | a0003c0003t0092g0042 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-329-10729G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96896536 | ||||||
| chr10:96896547
|
C | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-10718C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96896547 | ||||||
| chr10:96896932
|
A | G | 1 | a0001c0001t0119g0208 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-329-10333A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96896932 | ||||||
| chr10:96897052
|
TGAGAGAG others(1): Show |
T | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-329-10198_-329-10 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897052 | |||||
| chr10:96897069
|
G | GAGAGAA | 10 | a0001c0001t0097g0008a0004c0005t0021g0171a0004c0005t0042g0170others(7): Show | 10 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-329-10174_-329-10 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897069 | |||||
| chr10:96897069
|
GAGAGAAA others(5): Show |
G | 1 | a0003c0003t0010g0162 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-329-10180_-329-10 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897069 | |||||
| chr10:96897075
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-10190A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897075 | ||||||
| chr10:96897101
|
C | CA | 16 | a0001c0001t0006g0273a0001c0001t0031g0272a0001c0001t0074g0131others(13): Show | 16 | HG01109.hp1 HG01515.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-329-10148dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897101 | |||||
| chr10:96897101
|
C | CAA | 27 | a0001c0001t0016g0004a0001c0001t0016g0176a0001c0001t0017g0145others(24): Show | 27 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-329-10149_-329-10 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897101 | |||||
| chr10:96897101
|
C | CAAA | 8 | a0001c0001t0016g0136a0001c0001t0022g0143a0001c0001t0022g0144others(5): Show | 8 | HG00733.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-329-10150_-329-10 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897101 | |||||
| chr10:96897114
|
A | C | 2 | a0001c0001t0026g0223a0001c0001t0026g0242 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-329-10151A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897114 | ||||||
| chr10:96897500
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-329-9765C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897500 | ||||||
| chr10:96897520
|
A | C | 1 | a0001c0001t0027g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-329-9745A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897520 | ||||||
| chr10:96897648
|
T | C | 10 | a0001c0001t0016g0136a0001c0001t0016g0176a0001c0001t0017g0145others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-329-9617T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897648 | ||||||
| chr10:96897759
|
G | A | 61 | a0001c0001t0097g0008a0001c0001t0098g0010a0001c0004t0002g0009others(58): Show | 61 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-329-9506G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897759 | ||||||
| chr10:96897866
|
CT | C | 61 | a0001c0001t0001g0198a0001c0001t0001g0213a0001c0001t0001g0253others(58): Show | 61 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-329-9379delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897866 | |||||
| chr10:96897866
|
CTT | C | 11 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(8): Show | 11 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-329-9380_-329-937 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897866 | |||||
| chr10:96897866
|
CTTTTTTT others(3): Show |
C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-9388_-329-937 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96897866 | |||||
| chr10:96897873
|
T | A | 2 | a0002c0002t0058g0107a0002c0002t0059g0120 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-329-9392T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897873 | ||||||
| chr10:96897984
|
C | T | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-9281C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96897984 | ||||||
| chr10:96898167
|
T | C | 2 | a0002c0002t0058g0107a0002c0002t0059g0120 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-329-9098T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96898167 | ||||||
| chr10:96898258
|
G | T | 1 | a0001c0001t0003g0214 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-329-9007G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96898258 | ||||||
| chr10:96898593
|
T | G | 5 | a0001c0001t0016g0004a0001c0001t0022g0143a0001c0001t0022g0144others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-8672T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96898593 | ||||||
| chr10:96899301
|
C | T | 1 | a0002c0002t0145g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-329-7964C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96899301 | ||||||
| chr10:96899752
|
C | T | 1 | a0001c0001t0118g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-329-7513C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96899752 | ||||||
| chr10:96899777
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-7488G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96899777 | ||||||
| chr10:96899853
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-329-7412C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96899853 | ||||||
| chr10:96899958
|
T | C | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-329-7307T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96899958 | ||||||
| chr10:96900003
|
T | A | 8 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(5): Show | 8 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-329-7262T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900003 | ||||||
| chr10:96900063
|
G | A | 59 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0002g0058others(56): Show | 59 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.-329-7202G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900063 | ||||||
| chr10:96900163
|
A | G | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-7102A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900163 | ||||||
| chr10:96900352
|
CT | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-6906delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96900352 | |||||
| chr10:96900455
|
T | G | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-329-6810T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900455 | ||||||
| chr10:96900751
|
A | AT | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-6513dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96900751 | |||||
| chr10:96900824
|
C | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-329-6441C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900824 | ||||||
| chr10:96900838
|
T | A | 16 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-329-6427T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900838 | ||||||
| chr10:96900866
|
CT | C | 19 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0106g0286others(16): Show | 19 | HG01109.hp1 HG01243.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-329-6385delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96900866 | |||||
| chr10:96900886
|
T | C | 2 | a0003c0003t0004g0028a0003c0003t0004g0052 | 2 | NA18989.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-329-6379T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900886 | ||||||
| chr10:96900890
|
G | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-6375G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900890 | ||||||
| chr10:96900907
|
C | A | 1 | a0001c0001t0005g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-329-6358C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900907 | ||||||
| chr10:96900908
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-6357G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900908 | ||||||
| chr10:96900965
|
G | A | 1 | a0001c0001t0143g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-329-6300G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96900965 | ||||||
| chr10:96901192
|
A | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-329-6073A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901192 | ||||||
| chr10:96901195
|
T | A | 1 | a0001c0001t0027g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-329-6070T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901195 | ||||||
| chr10:96901389
|
C | G | 3 | a0002c0002t0033g0112a0002c0002t0128g0087a0012c0017t0127g0077 | 3 | NA19005.hp1 NA19060.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-329-5876C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901389 | ||||||
| chr10:96901606
|
G | C | 1 | a0001c0004t0088g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-329-5659G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901606 | ||||||
| chr10:96901615
|
T | C | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-5650T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901615 | ||||||
| chr10:96901648
|
A | G | 1 | a0001c0001t0107g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-329-5617A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901648 | ||||||
| chr10:96901793
|
A | G | 2 | a0001c0001t0005g0261a0002c0002t0126g0160 | 2 | HG04184.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-329-5472A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901793 | ||||||
| chr10:96901851
|
C | G | 1 | a0008c0011t0002g0203 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-329-5414C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901851 | ||||||
| chr10:96901994
|
G | C | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-329-5271G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96901994 | ||||||
| chr10:96902115
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-5150C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96902115 | ||||||
| chr10:96902131
|
T | TA | 62 | a0001c0001t0056g0284a0001c0001t0097g0008a0001c0001t0098g0010others(59): Show | 62 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-329-5122dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96902131 | |||||
| chr10:96902131
|
TA | T | 40 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(37): Show | 40 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-329-5122delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96902131 | |||||
| chr10:96902148
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-5117A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96902148 | ||||||
| chr10:96902245
|
G | A | 1 | a0001c0001t0023g0159 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-329-5020G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96902245 | ||||||
| chr10:96902543
|
A | T | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-4722A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96902543 | ||||||
| chr10:96902586
|
G | T | 1 | a0002c0002t0055g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-329-4679G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96902586 | ||||||
| chr10:96902818
|
A | G | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-329-4447A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96902818 | ||||||
| chr10:96902901
|
G | A | 4 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0047g0172others(1): Show | 4 | HG03453.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-4364G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96902901 | ||||||
| chr10:96903117
|
G | A | 1 | a0003c0003t0002g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-329-4148G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96903117 | ||||||
| chr10:96903191
|
G | T | 15 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-4074G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96903191 | ||||||
| chr10:96903338
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-3927C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96903338 | ||||||
| chr10:96903544
|
A | T | 1 | a0001c0001t0016g0176 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-329-3721A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96903544 | ||||||
| chr10:96903557
|
G | C | 1 | a0007c0013t0141g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-329-3708G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96903557 | ||||||
| chr10:96904123
|
A | T | 1 | a0001c0001t0143g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-329-3142A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904123 | ||||||
| chr10:96904211
|
G | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-329-3054G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904211 | ||||||
| chr10:96904249
|
A | G | 1 | a0001c0001t0101g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-329-3016A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904249 | ||||||
| chr10:96904250
|
C | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0005g0262 | 3 | HG01070.hp1 HG01074.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-329-3015C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904250 | ||||||
| chr10:96904416
|
T | C | 2 | a0001c0004t0109g0027a0001c0004t0110g0043 | 2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-329-2849T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904416 | ||||||
| chr10:96904544
|
A | G | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-2721A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904544 | ||||||
| chr10:96904819
|
G | T | 1 | a0001c0001t0012g0252 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-329-2446G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904819 | ||||||
| chr10:96904821
|
A | G | 2 | a0004c0009t0021g0187a0004c0009t0044g0186 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-329-2444A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904821 | ||||||
| chr10:96904822
|
C | T | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-2443C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904822 | ||||||
| chr10:96904989
|
A | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-2276A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96904989 | ||||||
| chr10:96905143
|
A | T | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-329-2122A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96905143 | ||||||
| chr10:96905228
|
C | A | 1 | a0001c0001t0029g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-329-2037C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96905228 | ||||||
| chr10:96905605
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-329-1660C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96905605 | ||||||
| chr10:96905681
|
G | A | 1 | a0016c0022t0028g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-329-1584G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96905681 | ||||||
| chr10:96905709
|
C | T | 61 | a0001c0001t0100g0226a0002c0002t0001g0078a0002c0002t0009g0073others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-329-1556C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96905709 | ||||||
| chr10:96905763
|
T | A | 1 | a0002c0002t0055g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-329-1502T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96905763 | ||||||
| chr10:96905810
|
A | C | 1 | a0001c0001t0115g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-329-1455A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96905810 | ||||||
| chr10:96906035
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-329-1230A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96906035 | ||||||
| chr10:96906106
|
G | A | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-329-1159G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96906106 | ||||||
| chr10:96906124
|
G | T | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-329-1141G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96906124 | ||||||
| chr10:96906497
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-329-768G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96906497 | ||||||
| chr10:96906657
|
C | CT | 5 | a0001c0001t0106g0286a0004c0009t0044g0186a0005c0006t0040g0288others(2): Show | 5 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-600dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96906657 | |||||
| chr10:96906724
|
A | G | 1 | a0001c0007t0147g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-329-541A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96906724 | ||||||
| chr10:96906794
|
T | G | 1 | a0002c0002t0136g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-329-471T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96906794 | ||||||
| chr10:96906820
|
T | G | 38 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(35): Show | 38 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-329-445T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | chr10 | 96906820 | ||||||
| chr10:96907186
|
C | CT | 62 | a0001c0004t0002g0009a0002c0002t0001g0078a0002c0002t0009g0073others(59): Show | 62 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-329-68dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96907186 | |||||
| chr10:96907186
|
CT | C | 36 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(33): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-329-68delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 96907186 | |||||
| chr10:96907367
|
G | A | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-264+37G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 3/7 | chr10 | 96907367 | ||||||
| chr10:96907658
|
A | G | 2 | a0002c0002t0058g0107a0002c0002t0059g0120 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-263-10A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 3/7 | chr10 | 96907658 | ||||||
| chr10:96907772
|
T | C | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-184+25T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96907772 | ||||||
| chr10:96907893
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+146C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96907893 | ||||||
| chr10:96907896
|
G | C | 4 | a0001c0004t0002g0058a0001c0004t0007g0126a0001c0004t0109g0027others(1): Show | 4 | HG01928.hp2 HG02257.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+149G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96907896 | ||||||
| chr10:96907949
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+202A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96907949 | ||||||
| chr10:96907980
|
TG | T | 3 | a0004c0005t0045g0168a0004c0005t0048g0167a0004c0005t0049g0169 | 3 | HG01109.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-184+234delG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96907980 | ||||||
| chr10:96907997
|
G | T | 2 | a0001c0004t0084g0025a0001c0004t0089g0055 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-184+250G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96907997 | ||||||
| chr10:96908105
|
C | T | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-184+358C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908105 | ||||||
| chr10:96908117
|
C | T | 1 | a0001c0007t0147g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-184+370C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908117 | ||||||
| chr10:96908367
|
G | A | 19 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0197others(16): Show | 19 | HG02027.hp1 HG02074.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-184+620G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908367 | ||||||
| chr10:96908521
|
A | G | 1 | a0003c0003t0004g0156 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-184+774A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908521 | ||||||
| chr10:96908723
|
C | CT | 55 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0205others(52): Show | 55 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.-184+986dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96908723 | |||||
| chr10:96908725
|
T | C | 1 | a0002c0002t0061g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-184+978T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908725 | ||||||
| chr10:96908804
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+1057C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908804 | ||||||
| chr10:96908817
|
G | A | 1 | a0001c0001t0030g0228 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-184+1070G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908817 | ||||||
| chr10:96908860
|
C | T | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-184+1113C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908860 | ||||||
| chr10:96908864
|
C | T | 11 | a0002c0002t0001g0078a0002c0002t0013g0083a0002c0002t0019g0086others(8): Show | 11 | NA18942.hp1 NA18944.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.-184+1117C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908864 | ||||||
| chr10:96908866
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+1119C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908866 | ||||||
| chr10:96908905
|
C | T | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-184+1158C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908905 | ||||||
| chr10:96908936
|
C | T | 1 | a0001c0001t0100g0226 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-184+1189C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96908936 | ||||||
| chr10:96909107
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-184+1360A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96909107 | ||||||
| chr10:96909321
|
G | T | 1 | a0011c0014t0125g0081 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-184+1574G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96909321 | ||||||
| chr10:96909337
|
T | C | 1 | a0008c0011t0002g0203 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-184+1590T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96909337 | ||||||
| chr10:96909400
|
G | C | 54 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(51): Show | 54 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.-184+1653G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96909400 | ||||||
| chr10:96909406
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+1659C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96909406 | ||||||
| chr10:96909677
|
T | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+1930T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96909677 | ||||||
| chr10:96910042
|
T | C | 9 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-184+2295T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96910042 | ||||||
| chr10:96910071
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-184+2324A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96910071 | ||||||
| chr10:96910235
|
A | G | 1 | a0001c0001t0005g0262 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-184+2488A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96910235 | ||||||
| chr10:96910257
|
TAAAAC | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+2513_-184+251 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96910257 | |||||
| chr10:96910530
|
C | A | 1 | a0003c0003t0085g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-184+2783C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96910530 | ||||||
| chr10:96911093
|
C | CT | 40 | a0001c0001t0001g0230a0001c0001t0001g0248a0001c0001t0003g0193others(37): Show | 40 | HG00621.hp1 HG00733.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.-184+3368dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96911093 | |||||
| chr10:96911093
|
C | CTT | 12 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0002g0058others(9): Show | 12 | HG00558.hp2 HG01928.hp2 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.-184+3367_-184+336 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96911093 | |||||
| chr10:96911093
|
CT | C | 47 | a0001c0001t0016g0004a0001c0001t0016g0176a0001c0001t0017g0145others(44): Show | 47 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.-184+3368delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96911093 | |||||
| chr10:96911132
|
C | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+3385C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96911132 | ||||||
| chr10:96911216
|
G | A | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-184+3469G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96911216 | ||||||
| chr10:96911217
|
C | T | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-184+3470C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96911217 | ||||||
| chr10:96911345
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-184+3598G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96911345 | ||||||
| chr10:96911391
|
C | T | 3 | a0003c0003t0002g0046a0003c0003t0004g0038a0003c0003t0095g0053 | 3 | HG01361.hp1 NA18971.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-184+3644C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96911391 | ||||||
| chr10:96911908
|
G | T | 1 | a0001c0001t0115g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-184+4161G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96911908 | ||||||
| chr10:96911941
|
T | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+4194T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96911941 | ||||||
| chr10:96911984
|
TAC | T | 6 | a0001c0001t0001g0263a0001c0001t0005g0222a0001c0001t0006g0241others(3): Show | 6 | HG00741.hp1 HG01081.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-184+4239_-184+424 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96911984 | |||||
| chr10:96912304
|
A | G | 4 | a0002c0002t0014g0101a0002c0002t0137g0097a0002c0002t0138g0075others(1): Show | 4 | HG00558.hp1 NA18943.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+4557A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96912304 | ||||||
| chr10:96912323
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+4576T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96912323 | ||||||
| chr10:96912531
|
A | G | 2 | a0004c0009t0021g0187a0004c0009t0044g0186 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-184+4784A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96912531 | ||||||
| chr10:96912590
|
A | ATCTTCCT others(1): Show |
3 | a0004c0009t0021g0187a0004c0009t0044g0186a0004c0009t0064g0166 | 3 | HG02486.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-184+4860_-184+486 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912590 | |||||
| chr10:96912599
|
T | TCTTC | 6 | a0002c0002t0015g0122a0002c0002t0015g0123a0002c0002t0057g0119others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-184+4856_-184+485 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912599 | |||||
| chr10:96912599
|
T | TCTTCCTT others(9): Show |
2 | a0003c0003t0001g0036a0003c0003t0004g0026 | 2 | NA18612.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-184+4859_-184+486 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912599 | |||||
| chr10:96912599
|
T | TCTTCCTT others(5): Show |
43 | a0002c0002t0001g0078a0002c0002t0009g0076a0002c0002t0009g0092others(40): Show | 43 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-184+4860_-184+487 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912599 | |||||
| chr10:96912599
|
TCTTCCTT others(5): Show |
T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+4860_-184+487 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912599 | |||||
| chr10:96912607
|
T | C | 3 | a0002c0002t0015g0102a0003c0003t0001g0036a0003c0003t0004g0026 | 3 | HG03041.hp2 NA18612.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-184+4860T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96912607 | ||||||
| chr10:96912607
|
T | TCTTC | 16 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0250others(13): Show | 16 | HG01167.hp2 HG01168.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+4896_-184+489 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(1): Show |
9 | a0001c0001t0001g0259a0001c0001t0005g0235a0001c0001t0032g0012others(6): Show | 9 | HG01243.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-184+4892_-184+489 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(5): Show |
18 | a0001c0001t0016g0004a0001c0001t0017g0145a0001c0001t0017g0146others(15): Show | 18 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+4888_-184+489 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(9): Show |
22 | a0001c0001t0016g0136a0001c0001t0016g0176a0001c0001t0065g0148others(19): Show | 22 | HG00558.hp2 HG01081.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-184+4884_-184+489 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(13): Show |
28 | a0001c0001t0023g0130a0001c0001t0023g0159a0001c0001t0026g0223others(25): Show | 28 | HG00673.hp1 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-184+4880_-184+489 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(17): Show |
26 | a0001c0001t0018g0150a0001c0001t0018g0152a0001c0001t0051g0133others(23): Show | 26 | HG00733.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-184+4876_-184+489 others(28): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(21): Show |
6 | a0001c0001t0018g0151a0001c0001t0038g0059a0001c0001t0076g0149others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-184+4872_-184+489 others(32): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(25): Show |
1 | a0001c0001t0038g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-184+4868_-184+489 others(36): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(9): Show |
6 | a0002c0002t0034g0104a0002c0002t0037g0071a0002c0002t0058g0107others(3): Show | 6 | HG00544.hp2 HG01167.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-184+4871_-184+487 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
T | TCTTCCTT others(13): Show |
2 | a0002c0002t0009g0073a0002c0002t0036g0072 | 2 | NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-184+4871_-184+487 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912607
|
TCTTC | T | 10 | a0001c0001t0027g0188a0004c0005t0021g0171a0004c0005t0042g0170others(7): Show | 10 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-184+4896_-184+489 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912607 | |||||
| chr10:96912611
|
C | CCTTCCTT others(1): Show |
3 | a0002c0002t0014g0089a0002c0002t0035g0098a0002c0002t0145g0115 | 3 | NA18978.hp1 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-184+4871_-184+487 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912611 | |||||
| chr10:96912611
|
C | T | 1 | a0002c0002t0015g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-184+4864C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96912611 | ||||||
| chr10:96912619
|
C | T | 9 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-184+4872C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96912619 | ||||||
| chr10:96912887
|
C | CTGTT | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+5141_-184+514 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96912887 | |||||
| chr10:96913004
|
G | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+5257G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96913004 | ||||||
| chr10:96913013
|
G | A | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(282): Show | 285 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(282): Show |
intron_variant | MODIFIER | c.-184+5266G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96913013 | ||||||
| chr10:96913370
|
C | T | 1 | a0004c0005t0021g0171 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-184+5623C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96913370 | ||||||
| chr10:96913396
|
T | C | 2 | a0002c0002t0058g0107a0002c0002t0059g0120 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-184+5649T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96913396 | ||||||
| chr10:96913793
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-184+6046C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96913793 | ||||||
| chr10:96913822
|
G | A | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-184+6075G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96913822 | ||||||
| chr10:96913902
|
GA | G | 16 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+6169delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96913902 | |||||
| chr10:96914050
|
A | C | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+6303A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914050 | ||||||
| chr10:96914154
|
A | G | 1 | a0001c0001t0093g0204 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-184+6407A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914154 | ||||||
| chr10:96914174
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+6427C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914174 | ||||||
| chr10:96914268
|
G | C | 54 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(51): Show | 54 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.-184+6521G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914268 | ||||||
| chr10:96914440
|
G | A | 5 | a0001c0001t0001g0274a0001c0001t0003g0265a0001c0001t0031g0267others(2): Show | 5 | HG00323.hp2 HG01168.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-184+6693G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914440 | ||||||
| chr10:96914558
|
T | G | 1 | a0002c0002t0126g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-184+6811T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914558 | ||||||
| chr10:96914712
|
A | C | 1 | a0002c0002t0132g0088 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-184+6965A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914712 | ||||||
| chr10:96914820
|
T | A | 54 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(51): Show | 54 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.-184+7073T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96914820 | ||||||
| chr10:96914865
|
T | TG | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+7119dupG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96914865 | |||||
| chr10:96915068
|
C | A | 1 | a0002c0002t0129g0070 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-184+7321C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915068 | ||||||
| chr10:96915121
|
C | A | 1 | a0002c0002t0135g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-184+7374C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915121 | ||||||
| chr10:96915139
|
C | T | 1 | a0002c0002t0015g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-184+7392C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915139 | ||||||
| chr10:96915182
|
G | T | 65 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0097g0008others(62): Show | 65 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-184+7435G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915182 | ||||||
| chr10:96915187
|
T | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+7440T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915187 | ||||||
| chr10:96915196
|
C | T | 3 | a0002c0002t0055g0109a0002c0002t0058g0107a0002c0002t0059g0120 | 3 | HG02809.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-184+7449C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915196 | ||||||
| chr10:96915214
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-184+7467G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915214 | ||||||
| chr10:96915249
|
G | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-184+7502G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915249 | ||||||
| chr10:96915258
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+7511C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915258 | ||||||
| chr10:96915351
|
T | G | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+7604T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915351 | ||||||
| chr10:96915381
|
C | T | 16 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+7634C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915381 | ||||||
| chr10:96915390
|
G | A | 19 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-184+7643G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915390 | ||||||
| chr10:96915394
|
G | A | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+7647G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915394 | ||||||
| chr10:96915588
|
T | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+7841T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915588 | ||||||
| chr10:96915875
|
G | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+8128G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915875 | ||||||
| chr10:96915918
|
G | A | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+8171G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915918 | ||||||
| chr10:96915939
|
G | A | 5 | a0001c0001t0106g0286a0001c0004t0002g0029a0005c0006t0040g0288others(2): Show | 5 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-184+8192G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96915939 | ||||||
| chr10:96916093
|
G | A | 1 | a0005c0006t0054g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-184+8346G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916093 | ||||||
| chr10:96916435
|
A | G | 6 | a0001c0001t0001g0192a0001c0001t0001g0275a0001c0001t0001g0276others(3): Show | 6 | HG02074.hp2 HG02132.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-184+8688A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916435 | ||||||
| chr10:96916470
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+8723C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916470 | ||||||
| chr10:96916480
|
C | T | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-184+8733C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916480 | ||||||
| chr10:96916487
|
A | G | 57 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(54): Show | 57 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-184+8740A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916487 | ||||||
| chr10:96916517
|
T | C | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-184+8770T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916517 | ||||||
| chr10:96916587
|
C | CCATATAT others(5): Show |
1 | a0005c0006t0040g0288 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-184+8840_-184+884 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916587 | ||||||
| chr10:96916587
|
C | CCATATAT others(7): Show |
1 | a0005c0006t0060g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-184+8840_-184+884 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916587 | ||||||
| chr10:96916587
|
C | CCATATAT others(11): Show |
1 | a0001c0001t0106g0286 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-184+8840_-184+884 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916587 | ||||||
| chr10:96916587
|
C | CTA | 4 | a0001c0001t0026g0223a0001c0001t0026g0242a0001c0001t0068g0134others(1): Show | 4 | HG00741.hp1 HG01081.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-184+8858_-184+885 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATA | 4 | a0001c0004t0007g0041a0001c0004t0084g0025a0003c0003t0010g0162others(1): Show | 4 | HG01106.hp2 HG02735.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+8854_-184+885 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(1): Show |
11 | a0001c0004t0002g0058a0001c0004t0010g0049a0001c0004t0089g0055others(8): Show | 11 | HG00673.hp1 HG01099.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-184+8852_-184+885 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(3): Show |
20 | a0001c0001t0056g0284a0001c0004t0007g0126a0001c0004t0010g0044others(17): Show | 20 | HG00733.hp2 HG02074.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-184+8850_-184+885 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(5): Show |
13 | a0001c0004t0094g0017a0001c0004t0109g0027a0003c0003t0002g0005others(10): Show | 13 | HG01361.hp1 HG01993.hp1 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.-184+8848_-184+885 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(7): Show |
12 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0007g0019others(9): Show | 12 | HG00558.hp2 HG01109.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-184+8846_-184+885 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(9): Show |
5 | a0001c0004t0091g0018a0001c0004t0122g0011a0003c0003t0008g0280others(2): Show | 5 | HG03239.hp1 NA18968.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-184+8844_-184+885 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(11): Show |
1 | a0003c0003t0004g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-184+8842_-184+885 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(13): Show |
2 | a0003c0003t0004g0047a0003c0003t0085g0056 | 2 | HG02738.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-184+8859_-184+886 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(19): Show |
1 | a0003c0003t0002g0048 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-184+8859_-184+886 others(30): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916587
|
C | CTATATAT others(27): Show |
1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+8859_-184+886 others(38): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96916587 | |||||
| chr10:96916595
|
ATATATAT others(15): Show |
A | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+8849_-184+887 others(26): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916595 | ||||||
| chr10:96916607
|
C | A | 77 | a0001c0001t0056g0284a0001c0001t0106g0286a0001c0004t0002g0009others(74): Show | 77 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.-184+8860C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916607 | ||||||
| chr10:96916617
|
G | A | 15 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(12): Show | 15 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-184+8870G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916617 | ||||||
| chr10:96916675
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+8928C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916675 | ||||||
| chr10:96916716
|
G | A | 1 | a0007c0013t0141g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-184+8969G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916716 | ||||||
| chr10:96916771
|
C | T | 6 | a0001c0004t0002g0154a0001c0004t0002g0157a0001c0004t0007g0158others(3): Show | 6 | NA18943.hp2 NA18960.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-184+9024C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916771 | ||||||
| chr10:96916894
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0005g0262 | 3 | HG01070.hp1 HG01074.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-184+9147C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916894 | ||||||
| chr10:96916895
|
G | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+9148G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916895 | ||||||
| chr10:96916994
|
T | C | 1 | a0001c0001t0016g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-184+9247T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96916994 | ||||||
| chr10:96917142
|
G | A | 2 | a0003c0003t0001g0036a0003c0003t0004g0026 | 2 | NA18612.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-184+9395G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917142 | ||||||
| chr10:96917398
|
G | C | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+9651G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917398 | ||||||
| chr10:96917432
|
A | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+9685A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917432 | ||||||
| chr10:96917478
|
T | C | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+9731T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917478 | ||||||
| chr10:96917556
|
C | T | 1 | a0003c0003t0086g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-184+9809C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917556 | ||||||
| chr10:96917744
|
A | G | 1 | a0006c0008t0011g0032 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-184+9997A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917744 | ||||||
| chr10:96917790
|
T | C | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+10043T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917790 | ||||||
| chr10:96917882
|
A | G | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-184+10135A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96917882 | ||||||
| chr10:96918006
|
G | A | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-184+10259G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96918006 | ||||||
| chr10:96918049
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-184+10302A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96918049 | ||||||
| chr10:96918050
|
T | C | 1 | a0002c0002t0136g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-184+10303T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96918050 | ||||||
| chr10:96918095
|
C | T | 1 | a0001c0004t0109g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-184+10348C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96918095 | ||||||
| chr10:96918344
|
A | G | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-184+10597A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96918344 | ||||||
| chr10:96918464
|
C | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+10717C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96918464 | ||||||
| chr10:96919220
|
T | C | 16 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(13): Show | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+11473T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96919220 | ||||||
| chr10:96919434
|
T | C | 2 | a0001c0001t0032g0012a0001c0001t0120g0003 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-184+11687T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96919434 | ||||||
| chr10:96919787
|
T | C | 1 | a0002c0002t0015g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-184+12040T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96919787 | ||||||
| chr10:96919798
|
T | C | 2 | a0001c0001t0026g0223a0001c0001t0026g0242 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-184+12051T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96919798 | ||||||
| chr10:96920244
|
C | T | 1 | a0001c0001t0028g0233 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-184+12497C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920244 | ||||||
| chr10:96920392
|
G | A | 1 | a0001c0001t0017g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-184+12645G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920392 | ||||||
| chr10:96920402
|
G | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+12655G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920402 | ||||||
| chr10:96920403
|
T | TATATATA others(3): Show |
1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+12656_-184+12 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920403 | ||||||
| chr10:96920404
|
G | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+12657G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920404 | ||||||
| chr10:96920404
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0012g0225 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-184+12664_-184+12 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920404 | |||||
| chr10:96920414
|
A | G | 2 | a0001c0001t0012g0225a0001c0001t0056g0284 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-184+12667A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920414 | ||||||
| chr10:96920422
|
T | G | 2 | a0001c0001t0012g0225a0001c0001t0056g0284 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-184+12675T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920422 | ||||||
| chr10:96920423
|
C | T | 2 | a0001c0001t0012g0225a0001c0001t0056g0284 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-184+12676C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920423 | ||||||
| chr10:96920424
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0003g0240a0001c0007t0147g0183a0002c0002t0036g0072 | 3 | NA18906.hp2 NA18953.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-184+12695_-184+12 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920424 | |||||
| chr10:96920432
|
G | T | 2 | a0001c0001t0012g0225a0001c0001t0056g0284 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-184+12685G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920432 | ||||||
| chr10:96920433
|
T | C | 2 | a0001c0001t0012g0225a0001c0001t0056g0284 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-184+12686T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920433 | ||||||
| chr10:96920434
|
G | A | 2 | a0001c0001t0012g0225a0001c0001t0056g0284 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-184+12687G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920434 | ||||||
| chr10:96920434
|
G | GTATATAT others(11): Show |
13 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(10): Show | 13 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-184+12694_-184+12 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920434 | |||||
| chr10:96920434
|
G | GTATATAT others(13): Show |
220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(217): Show | 220 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-184+12696_-184+12 others(26): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920434 | |||||
| chr10:96920434
|
G | GTATATAT others(41): Show |
1 | a0001c0001t0032g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-184+12696_-184+12 others(54): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920434 | |||||
| chr10:96920434
|
G | GTATATAT others(39): Show |
2 | a0001c0001t0032g0012a0001c0001t0120g0003 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-184+12696_-184+12 others(52): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920434 | |||||
| chr10:96920440
|
ATG | A | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+12697_-184+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920440 | |||||
| chr10:96920442
|
G | GTATATAT others(11): Show |
30 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(27): Show | 30 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-184+12696_-184+12 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920442 | |||||
| chr10:96920442
|
G | GTATATAT others(39): Show |
3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-184+12696_-184+12 others(52): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920442 | |||||
| chr10:96920446
|
A | G | 30 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(27): Show | 30 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-184+12699A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920446 | ||||||
| chr10:96920454
|
G | A | 1 | a0001c0001t0069g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-184+12707G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920454 | ||||||
| chr10:96920454
|
G | T | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+12707G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920454 | ||||||
| chr10:96920455
|
T | C | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+12708T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920455 | ||||||
| chr10:96920457
|
TATTC | T | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+12713_-184+12 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920457 | |||||
| chr10:96920461
|
C | CATATATG others(21): Show |
2 | a0001c0001t0081g0231a0001c0001t0144g0257 | 2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-184+12731_-184+12 others(34): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920461 | |||||
| chr10:96920461
|
CAT | C | 30 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(27): Show | 30 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-184+12719_-184+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920461 | |||||
| chr10:96920468
|
G | A | 5 | a0001c0001t0069g0129a0001c0001t0106g0286a0005c0006t0040g0288others(2): Show | 5 | HG02622.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-184+12721G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920468 | ||||||
| chr10:96920472
|
A | G | 4 | a0001c0001t0069g0129a0001c0001t0106g0286a0005c0006t0040g0288others(1): Show | 4 | HG02622.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+12725A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920472 | ||||||
| chr10:96920474
|
A | G | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-184+12727A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920474 | ||||||
| chr10:96920476
|
A | ATATGTAT others(83): Show |
1 | a0002c0002t0014g0065 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-184+12771_-184+12 others(96): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920476 | |||||
| chr10:96920487
|
CAT | C | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+12747_-184+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920487 | |||||
| chr10:96920489
|
T | TATATATG others(23): Show |
1 | a0002c0002t0036g0072 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-184+12772_-184+12 others(36): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920489 | |||||
| chr10:96920489
|
TATATATG others(23): Show |
T | 27 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(24): Show | 27 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-184+12772_-184+12 others(36): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920489 | |||||
| chr10:96920504
|
ATG | A | 10 | a0001c0004t0010g0044a0003c0003t0004g0023a0003c0003t0004g0028others(7): Show | 10 | NA18747.hp1 NA18939.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+12759_-184+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920504 | |||||
| chr10:96920519
|
G | GATATATG others(23): Show |
2 | a0001c0001t0056g0284a0001c0004t0122g0011 | 2 | HG02647.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-184+12837_-184+12 others(36): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920519 | |||||
| chr10:96920519
|
G | T | 16 | a0001c0001t0003g0240a0001c0001t0017g0145a0001c0001t0017g0146others(13): Show | 16 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.-184+12772G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920519 | ||||||
| chr10:96920544
|
A | ATTCAGAT others(23): Show |
11 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(8): Show | 11 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-184+12801_-184+12 others(36): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920544 | |||||
| chr10:96920544
|
A | ATTCAGAT others(53): Show |
1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12801_-184+12 others(66): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920544 | |||||
| chr10:96920547
|
C | CAT | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-184+12807_-184+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920547 | |||||
| chr10:96920549
|
T | G | 16 | a0001c0001t0003g0265a0001c0001t0106g0286a0001c0004t0010g0044others(13): Show | 16 | HG02602.hp1 HG02922.hp2 HG02976.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+12802T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920549 | ||||||
| chr10:96920549
|
T | TATATATG others(21): Show |
2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+12809_-184+12 others(34): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920549 | |||||
| chr10:96920574
|
A | G | 11 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(8): Show | 11 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-184+12827A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920574 | ||||||
| chr10:96920592
|
A | G | 2 | a0001c0001t0005g0221a0001c0001t0005g0261 | 2 | NA18998.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-184+12845A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920592 | ||||||
| chr10:96920603
|
T | C | 4 | a0001c0001t0017g0145a0001c0001t0017g0146a0001c0001t0030g0228others(1): Show | 4 | HG01258.hp1 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+12856T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920603 | ||||||
| chr10:96920617
|
TATATATG others(11): Show |
T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12879_-184+12 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920617 | |||||
| chr10:96920626
|
A | G | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12879A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920626 | ||||||
| chr10:96920628
|
G | A | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12881G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920628 | ||||||
| chr10:96920631
|
C | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+12884C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920631 | ||||||
| chr10:96920634
|
T | G | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12887T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920634 | ||||||
| chr10:96920635
|
C | T | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12888C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920635 | ||||||
| chr10:96920644
|
G | A | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12897G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920644 | ||||||
| chr10:96920652
|
G | T | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12905G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920652 | ||||||
| chr10:96920653
|
T | C | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12906T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920653 | ||||||
| chr10:96920654
|
G | A | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12907G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920654 | ||||||
| chr10:96920660
|
A | G | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+12913A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920660 | ||||||
| chr10:96920670
|
G | GTA | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-184+12929_-184+12 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920670 | |||||
| chr10:96920670
|
G | GTATATAT others(23): Show |
11 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(8): Show | 11 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-184+12930_-184+12 others(36): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920670 | |||||
| chr10:96920672
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12925A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920672 | ||||||
| chr10:96920678
|
T | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12931T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920678 | ||||||
| chr10:96920679
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12932C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920679 | ||||||
| chr10:96920680
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12933A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920680 | ||||||
| chr10:96920686
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12939G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920686 | ||||||
| chr10:96920686
|
G | GTGTATAT others(1): Show |
14 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-184+12943_-184+12 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920686 | |||||
| chr10:96920686
|
G | GTGTATAT others(29): Show |
1 | a0001c0001t0106g0286 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-184+12949_-184+12 others(42): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920686 | |||||
| chr10:96920686
|
G | GTGTATAT others(59): Show |
1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-184+12949_-184+12 others(72): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920686 | |||||
| chr10:96920687
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12940T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920687 | ||||||
| chr10:96920706
|
G | A | 16 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(13): Show | 16 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+12959G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920706 | ||||||
| chr10:96920711
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12964T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920711 | ||||||
| chr10:96920730
|
A | ATATATAT others(3): Show |
21 | a0001c0001t0056g0284a0001c0001t0106g0286a0001c0001t0142g0061others(18): Show | 21 | HG00558.hp2 HG01884.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-184+12993_-184+13 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920730 | |||||
| chr10:96920730
|
A | ATATATGT others(3): Show |
1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-184+12988_-184+12 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920730 | |||||
| chr10:96920736
|
A | G | 2 | a0001c0001t0070g0139a0002c0002t0061g0118 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-184+12989A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920736 | ||||||
| chr10:96920746
|
A | ATG | 15 | a0001c0001t0016g0004a0001c0001t0017g0145a0001c0001t0022g0143others(12): Show | 15 | HG00733.hp1 HG00741.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-184+13001_-184+13 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920746 | |||||
| chr10:96920748
|
G | GTGTA | 53 | a0001c0001t0016g0136a0001c0001t0016g0176a0001c0001t0066g0137others(50): Show | 53 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-184+13002_-184+13 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920748 | |||||
| chr10:96920748
|
G | GTGTATA | 16 | a0001c0001t0017g0146a0001c0001t0075g0140a0001c0004t0002g0029others(13): Show | 16 | HG00544.hp2 HG00642.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+13002_-184+13 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920748 | |||||
| chr10:96920748
|
G | GTGTATAT others(1): Show |
10 | a0001c0001t0038g0060a0001c0001t0143g0006a0001c0004t0011g0155others(7): Show | 10 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+13002_-184+13 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920748 | |||||
| chr10:96920748
|
G | GTGTATAT others(5): Show |
31 | a0001c0001t0032g0012a0001c0004t0002g0058a0001c0004t0002g0154others(28): Show | 31 | HG00673.hp1 HG00733.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-184+13002_-184+13 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920748 | |||||
| chr10:96920749
|
T | TGTATATA others(7): Show |
13 | a0001c0001t0032g0013a0001c0004t0010g0044a0001c0004t0084g0025others(10): Show | 13 | HG01106.hp2 HG01361.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-184+13002_-184+13 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920749 | ||||||
| chr10:96920749
|
T | TGTATATA others(9): Show |
8 | a0001c0001t0098g0010a0001c0001t0120g0003a0001c0004t0089g0055others(5): Show | 8 | HG01099.hp2 HG01243.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-184+13002_-184+13 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920749 | ||||||
| chr10:96920749
|
T | TGTATATA others(11): Show |
2 | a0009c0012t0007g0063a0009c0012t0008g0020 | 2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-184+13002_-184+13 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920749 | ||||||
| chr10:96920749
|
T | TGTATATA others(17): Show |
1 | a0007c0013t0141g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-184+13002_-184+13 others(30): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920749 | ||||||
| chr10:96920749
|
T | TGTATATA others(35): Show |
1 | a0001c0001t0097g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-184+13002_-184+13 others(48): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920749 | ||||||
| chr10:96920750
|
A | G | 23 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(20): Show | 23 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-184+13003A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920750 | ||||||
| chr10:96920751
|
T | C | 57 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0056g0284others(54): Show | 57 | HG00673.hp1 HG00733.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-184+13004T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920751 | ||||||
| chr10:96920751
|
T | TAC | 33 | a0001c0001t0001g0001a0001c0001t0001g0192a0001c0001t0001g0236others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-184+13043_-184+13 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920751 | |||||
| chr10:96920751
|
T | TACAC | 16 | a0001c0001t0001g0198a0001c0001t0001g0250a0001c0001t0001g0259others(13): Show | 16 | HG00639.hp2 HG01099.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+13041_-184+13 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920751 | |||||
| chr10:96920751
|
T | TACACAC | 11 | a0001c0001t0001g0196a0001c0001t0001g0215a0001c0001t0001g0232others(8): Show | 11 | HG01168.hp1 HG01993.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.-184+13039_-184+13 others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920751 | |||||
| chr10:96920751
|
T | TATATGTT others(37): Show |
2 | a0005c0006t0040g0288a0005c0006t0060g0287 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-184+13005_-184+13 others(50): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920751 | |||||
| chr10:96920752
|
A | ATATGTTC others(29): Show |
1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-184+13005_-184+13 others(42): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920752 | ||||||
| chr10:96920752
|
A | G | 16 | a0001c0001t0017g0146a0001c0001t0075g0140a0001c0004t0002g0029others(13): Show | 16 | HG00544.hp2 HG00642.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-184+13005A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920752 | ||||||
| chr10:96920753
|
C | T | 108 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(105): Show | 108 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-184+13006C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920753 | ||||||
| chr10:96920754
|
A | G | 53 | a0001c0001t0016g0136a0001c0001t0016g0176a0001c0001t0066g0137others(50): Show | 53 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-184+13007A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920754 | ||||||
| chr10:96920755
|
C | T | 98 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(95): Show | 98 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.-184+13008C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920755 | ||||||
| chr10:96920756
|
A | G | 15 | a0001c0001t0016g0004a0001c0001t0017g0145a0001c0001t0022g0143others(12): Show | 15 | HG00733.hp1 HG00741.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-184+13009A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920756 | ||||||
| chr10:96920757
|
C | T | 81 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(78): Show | 81 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-184+13010C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920757 | ||||||
| chr10:96920758
|
A | G | 13 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-184+13011A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920758 | ||||||
| chr10:96920759
|
C | T | 28 | a0001c0001t0016g0004a0001c0001t0017g0145a0001c0001t0018g0150others(25): Show | 28 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-184+13012C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920759 | ||||||
| chr10:96920761
|
C | T | 11 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-184+13014C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920761 | ||||||
| chr10:96920780
|
ACACACAC others(5): Show |
A | 4 | a0001c0001t0001g0253a0001c0001t0001g0268a0001c0001t0006g0244others(1): Show | 4 | HG02027.hp1 NA18980.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+13035_-184+13 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920780 | |||||
| chr10:96920782
|
ACACACAC others(3): Show |
A | 1 | a0001c0001t0001g0197 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-184+13037_-184+13 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920782 | |||||
| chr10:96920788
|
ACACG | A | 3 | a0001c0001t0003g0194a0001c0001t0005g0222a0001c0019t0003g0195 | 3 | NA18942.hp2 NA18957.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-184+13043_-184+13 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920788 | |||||
| chr10:96920790
|
ACG | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0189a0001c0001t0001g0234others(10): Show | 13 | HG00621.hp2 HG01106.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-184+13048_-184+13 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920790 | |||||
| chr10:96920792
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0192a0001c0001t0001g0196others(256): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.-184+13045G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920792 | ||||||
| chr10:96920794
|
G | A | 184 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(181): Show | 184 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.-184+13047G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920794 | ||||||
| chr10:96920797
|
G | T | 2 | a0004c0005t0043g0124a0004c0005t0046g0125 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-184+13050G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920797 | ||||||
| chr10:96920798
|
T | G | 2 | a0004c0005t0043g0124a0004c0005t0046g0125 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-184+13051T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920798 | ||||||
| chr10:96920798
|
T | TG | 10 | a0001c0001t0118g0249a0004c0005t0021g0171a0004c0005t0042g0170others(7): Show | 10 | HG02257.hp1 HG02486.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-184+13058dupG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96920798 | |||||
| chr10:96920853
|
A | C | 1 | a0001c0001t0051g0133 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-184+13106A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920853 | ||||||
| chr10:96920925
|
G | A | 1 | a0001c0001t0016g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-184+13178G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920925 | ||||||
| chr10:96920926
|
C | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-184+13179C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920926 | ||||||
| chr10:96920963
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-184+13216A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920963 | ||||||
| chr10:96920990
|
G | A | 1 | a0001c0001t0118g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-184+13243G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96920990 | ||||||
| chr10:96921329
|
G | A | 1 | a0002c0002t0055g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-184+13582G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96921329 | ||||||
| chr10:96921525
|
A | G | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-184+13778A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96921525 | ||||||
| chr10:96921543
|
C | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+13796C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96921543 | ||||||
| chr10:96922069
|
G | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+14322G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96922069 | ||||||
| chr10:96922187
|
A | G | 1 | a0001c0001t0031g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-184+14440A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96922187 | ||||||
| chr10:96922188
|
T | C | 1 | a0002c0002t0053g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-184+14441T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96922188 | ||||||
| chr10:96922235
|
A | C | 1 | a0001c0001t0005g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-184+14488A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96922235 | ||||||
| chr10:96922306
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+14559A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96922306 | ||||||
| chr10:96922327
|
T | C | 7 | a0002c0002t0015g0102a0002c0002t0015g0122a0002c0002t0015g0123others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-184+14580T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96922327 | ||||||
| chr10:96922990
|
A | G | 65 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0002g0058others(62): Show | 65 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-184+15243A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96922990 | ||||||
| chr10:96923273
|
A | C | 1 | a0001c0001t0093g0204 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-184+15526A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96923273 | ||||||
| chr10:96923461
|
C | T | 4 | a0002c0002t0034g0104a0002c0002t0035g0100a0002c0002t0036g0093others(1): Show | 4 | HG00642.hp1 HG01123.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+15714C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96923461 | ||||||
| chr10:96923870
|
A | G | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+16123A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96923870 | ||||||
| chr10:96923926
|
G | A | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-184+16179G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96923926 | ||||||
| chr10:96924315
|
G | C | 1 | a0002c0002t0055g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-184+16568G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96924315 | ||||||
| chr10:96924367
|
C | T | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-184+16620C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96924367 | ||||||
| chr10:96924375
|
TTTTG | T | 187 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0197others(184): Show | 187 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.-184+16660_-184+16 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96924375 | |||||
| chr10:96924375
|
TTTTGTTT others(1): Show |
T | 8 | a0001c0001t0001g0198a0001c0001t0001g0270a0001c0001t0143g0006others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-184+16656_-184+16 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96924375 | |||||
| chr10:96924453
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-184+16706G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96924453 | ||||||
| chr10:96924553
|
T | A | 3 | a0003c0003t0010g0162a0003c0003t0024g0161a0003c0003t0024g0283 | 3 | NA18952.hp1 NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-184+16806T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96924553 | ||||||
| chr10:96924893
|
T | C | 67 | a0001c0001t0097g0008a0001c0001t0098g0010a0001c0004t0002g0009others(64): Show | 67 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.-184+17146T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96924893 | ||||||
| chr10:96925163
|
C | T | 5 | a0001c0007t0102g0181a0001c0007t0103g0179a0001c0007t0105g0182others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-184+17416C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96925163 | ||||||
| chr10:96925280
|
T | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-184+17533T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96925280 | ||||||
| chr10:96925492
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-184+17745A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96925492 | ||||||
| chr10:96925511
|
A | G | 1 | a0002c0002t0145g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-184+17764A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96925511 | ||||||
| chr10:96925639
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-184+17892C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96925639 | ||||||
| chr10:96925825
|
G | C | 1 | a0001c0001t0003g0265 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-184+18078G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96925825 | ||||||
| chr10:96926421
|
T | A | 35 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-183-17692T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96926421 | ||||||
| chr10:96926490
|
C | G | 1 | a0002c0002t0034g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-183-17623C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96926490 | ||||||
| chr10:96926728
|
AG | A | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-183-17384delG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96926728 | ||||||
| chr10:96926834
|
T | G | 9 | a0002c0002t0014g0089a0002c0002t0014g0101a0002c0002t0014g0113others(6): Show | 9 | HG00558.hp1 NA18943.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.-183-17279T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96926834 | ||||||
| chr10:96927122
|
G | A | 5 | a0001c0001t0016g0176a0001c0001t0017g0145a0001c0001t0017g0146others(2): Show | 5 | HG00639.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-183-16991G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96927122 | ||||||
| chr10:96927284
|
C | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-183-16829C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96927284 | ||||||
| chr10:96927348
|
TAA | T | 9 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-183-16764_-183-16 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96927348 | ||||||
| chr10:96927424
|
T | G | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-183-16689T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96927424 | ||||||
| chr10:96927485
|
A | G | 1 | a0002c0002t0037g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-183-16628A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96927485 | ||||||
| chr10:96927800
|
C | T | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-183-16313C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96927800 | ||||||
| chr10:96927873
|
A | G | 1 | a0001c0001t0113g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-183-16240A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96927873 | ||||||
| chr10:96928344
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-15769C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928344 | ||||||
| chr10:96928353
|
A | G | 1 | a0002c0015t0009g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-183-15760A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928353 | ||||||
| chr10:96928357
|
C | T | 2 | a0008c0011t0004g0202a0008c0011t0008g0201 | 2 | HG00639.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-183-15756C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928357 | ||||||
| chr10:96928473
|
C | T | 10 | a0002c0002t0014g0065a0002c0002t0014g0089a0002c0002t0014g0101others(7): Show | 10 | HG00558.hp1 HG02132.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.-183-15640C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928473 | ||||||
| chr10:96928657
|
G | A | 5 | a0002c0002t0013g0096a0002c0002t0020g0090a0002c0002t0020g0091others(2): Show | 5 | HG03017.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-183-15456G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928657 | ||||||
| chr10:96928686
|
A | G | 45 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(42): Show | 45 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-183-15427A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928686 | ||||||
| chr10:96928696
|
G | A | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-183-15417G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928696 | ||||||
| chr10:96928975
|
A | C | 6 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-183-15138A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96928975 | ||||||
| chr10:96929206
|
G | A | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-183-14907G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96929206 | ||||||
| chr10:96929378
|
G | A | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-183-14735G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96929378 | ||||||
| chr10:96929633
|
C | G | 3 | a0007c0013t0080g0174a0007c0013t0141g0175a0007c0016t0146g0007 | 3 | HG01884.hp1 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-14480C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96929633 | ||||||
| chr10:96929696
|
A | G | 1 | a0001c0007t0105g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-183-14417A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96929696 | ||||||
| chr10:96929817
|
A | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-183-14296A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96929817 | ||||||
| chr10:96930021
|
A | G | 50 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(47): Show | 50 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.-183-14092A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930021 | ||||||
| chr10:96930066
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-183-14047A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930066 | ||||||
| chr10:96930145
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-13968C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930145 | ||||||
| chr10:96930186
|
G | A | 19 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-183-13927G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930186 | ||||||
| chr10:96930233
|
A | G | 1 | a0002c0002t0037g0094 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-183-13880A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930233 | ||||||
| chr10:96930320
|
GT | G | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-183-13787delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96930320 | |||||
| chr10:96930430
|
T | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-13683T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930430 | ||||||
| chr10:96930629
|
T | C | 1 | a0002c0002t0014g0089 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-183-13484T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930629 | ||||||
| chr10:96930694
|
C | T | 1 | a0001c0001t0078g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-183-13419C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930694 | ||||||
| chr10:96930866
|
C | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-183-13247C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930866 | ||||||
| chr10:96930954
|
A | G | 4 | a0001c0001t0001g0189a0001c0001t0099g0216a0001c0001t0100g0226others(1): Show | 4 | NA18939.hp2 NA18982.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-13159A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96930954 | ||||||
| chr10:96931131
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-183-12982T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96931131 | ||||||
| chr10:96931230
|
AT | A | 62 | a0001c0001t0074g0131a0001c0001t0113g0191a0002c0002t0001g0078others(59): Show | 62 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-183-12866delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96931230 | |||||
| chr10:96931320
|
G | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-183-12793G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96931320 | ||||||
| chr10:96931334
|
A | G | 1 | a0007c0013t0141g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-183-12779A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96931334 | ||||||
| chr10:96931487
|
G | A | 1 | a0002c0002t0034g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-183-12626G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96931487 | ||||||
| chr10:96931579
|
C | T | 50 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(47): Show | 50 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-183-12534C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96931579 | ||||||
| chr10:96931712
|
A | G | 2 | a0001c0001t0077g0127a0001c0001t0078g0128 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-183-12401A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96931712 | ||||||
| chr10:96931993
|
G | A | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-183-12120G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96931993 | ||||||
| chr10:96932123
|
A | C | 14 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-183-11990A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932123 | ||||||
| chr10:96932165
|
A | T | 3 | a0003c0003t0092g0042a0005c0006t0052g0165a0005c0006t0054g0164 | 3 | HG03453.hp2 HG04199.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-183-11948A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932165 | ||||||
| chr10:96932181
|
C | T | 1 | a0002c0002t0053g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-183-11932C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932181 | ||||||
| chr10:96932424
|
A | G | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-183-11689A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932424 | ||||||
| chr10:96932441
|
TTTTTA | T | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-183-11648_-183-11 others(11): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96932441 | |||||
| chr10:96932451
|
A | T | 1 | a0002c0002t0034g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-183-11662A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932451 | ||||||
| chr10:96932526
|
C | T | 1 | a0004c0009t0044g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-183-11587C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932526 | ||||||
| chr10:96932588
|
C | T | 1 | a0002c0002t0135g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-183-11525C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932588 | ||||||
| chr10:96932742
|
A | G | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-183-11371A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932742 | ||||||
| chr10:96932773
|
T | C | 1 | a0002c0002t0009g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-183-11340T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932773 | ||||||
| chr10:96932968
|
A | G | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-183-11145A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932968 | ||||||
| chr10:96932999
|
C | A | 37 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(34): Show | 37 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-183-11114C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96932999 | ||||||
| chr10:96933494
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-183-10619C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96933494 | ||||||
| chr10:96933545
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-183-10568G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96933545 | ||||||
| chr10:96933629
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-10484C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96933629 | ||||||
| chr10:96933696
|
T | C | 1 | a0002c0002t0034g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-183-10417T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96933696 | ||||||
| chr10:96933882
|
C | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-10231C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96933882 | ||||||
| chr10:96933962
|
C | T | 2 | a0001c0001t0081g0231a0001c0001t0144g0257 | 2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-183-10151C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96933962 | ||||||
| chr10:96934188
|
A | G | 4 | a0001c0001t0001g0189a0001c0001t0099g0216a0001c0001t0100g0226others(1): Show | 4 | NA18939.hp2 NA18982.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-9925A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934188 | ||||||
| chr10:96934244
|
A | G | 2 | a0001c0001t0032g0012a0001c0001t0120g0003 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-183-9869A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934244 | ||||||
| chr10:96934249
|
C | T | 1 | a0002c0002t0013g0067 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-183-9864C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934249 | ||||||
| chr10:96934274
|
T | G | 1 | a0001c0001t0001g0236 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-183-9839T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934274 | ||||||
| chr10:96934538
|
T | C | 2 | a0002c0002t0058g0107a0002c0002t0059g0120 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-183-9575T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934538 | ||||||
| chr10:96934613
|
T | C | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-9500T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934613 | ||||||
| chr10:96934687
|
C | T | 1 | a0009c0012t0007g0063 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-183-9426C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934687 | ||||||
| chr10:96934711
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-9402C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934711 | ||||||
| chr10:96934724
|
C | T | 2 | a0002c0002t0013g0096a0002c0002t0020g0090 | 2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-183-9389C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934724 | ||||||
| chr10:96934854
|
G | A | 1 | a0002c0002t0132g0088 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-183-9259G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934854 | ||||||
| chr10:96934889
|
A | C | 1 | a0001c0004t0002g0154 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-183-9224A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96934889 | ||||||
| chr10:96935072
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-9041G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935072 | ||||||
| chr10:96935090
|
A | G | 9 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-183-9023A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935090 | ||||||
| chr10:96935136
|
T | A | 2 | a0001c0001t0005g0221a0001c0001t0005g0261 | 2 | NA18998.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-183-8977T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935136 | ||||||
| chr10:96935139
|
C | CT | 13 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0230others(10): Show | 13 | HG00741.hp2 HG01167.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-183-8947dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96935139 | |||||
| chr10:96935139
|
CT | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0189a0001c0001t0001g0197others(76): Show | 79 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.-183-8947delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96935139 | |||||
| chr10:96935139
|
CTT | C | 53 | a0001c0001t0032g0012a0001c0001t0038g0059a0001c0001t0142g0061others(50): Show | 53 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-183-8948_-183-894 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96935139 | |||||
| chr10:96935139
|
CTTT | C | 7 | a0002c0002t0037g0071a0004c0005t0021g0171a0004c0005t0042g0170others(4): Show | 7 | HG00544.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-183-8949_-183-894 others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96935139 | |||||
| chr10:96935139
|
CTTTT | C | 14 | a0001c0001t0106g0286a0004c0005t0043g0124a0004c0005t0046g0125others(11): Show | 14 | HG01109.hp1 HG02486.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-183-8950_-183-894 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96935139 | |||||
| chr10:96935194
|
T | C | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-183-8919T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935194 | ||||||
| chr10:96935200
|
A | G | 186 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(183): Show | 186 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-183-8913A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935200 | ||||||
| chr10:96935222
|
C | T | 1 | a0001c0001t0116g0255 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-183-8891C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935222 | ||||||
| chr10:96935284
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-8829A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935284 | ||||||
| chr10:96935331
|
C | T | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-183-8782C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935331 | ||||||
| chr10:96935544
|
CAG | C | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-183-8567_-183-856 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96935544 | |||||
| chr10:96935618
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(88): Show | 91 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-183-8495G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935618 | ||||||
| chr10:96935771
|
C | T | 1 | a0002c0015t0009g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-183-8342C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935771 | ||||||
| chr10:96935851
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0104g0206 | 2 | HG00544.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-183-8262A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935851 | ||||||
| chr10:96935897
|
C | G | 1 | a0002c0002t0001g0078 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-183-8216C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96935897 | ||||||
| chr10:96936189
|
C | A | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-183-7924C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96936189 | ||||||
| chr10:96936224
|
T | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-183-7889T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96936224 | ||||||
| chr10:96936285
|
A | G | 1 | a0001c0001t0101g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-183-7828A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96936285 | ||||||
| chr10:96936454
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-7659G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96936454 | ||||||
| chr10:96936461
|
T | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-7652T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96936461 | ||||||
| chr10:96936727
|
CCACCCCT others(68): Show |
C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-183-7384_-183-731 others(79): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96936727 | |||||
| chr10:96936953
|
T | C | 1 | a0002c0002t0035g0098 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-183-7160T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96936953 | ||||||
| chr10:96937010
|
G | C | 1 | a0014c0020t0012g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-183-7103G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96937010 | ||||||
| chr10:96937069
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-7044A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96937069 | ||||||
| chr10:96937955
|
T | A | 2 | a0001c0001t0027g0285a0001c0001t0111g0184 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-183-6158T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96937955 | ||||||
| chr10:96938085
|
C | G | 51 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(48): Show | 51 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.-183-6028C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96938085 | ||||||
| chr10:96938147
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-5966G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96938147 | ||||||
| chr10:96938248
|
GTT | G | 50 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(47): Show | 50 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.-183-5861_-183-586 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96938248 | |||||
| chr10:96938320
|
C | T | 5 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-183-5793C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96938320 | ||||||
| chr10:96938398
|
A | G | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-183-5715A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96938398 | ||||||
| chr10:96938622
|
T | C | 1 | a0006c0008t0002g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-183-5491T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96938622 | ||||||
| chr10:96938681
|
A | T | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-183-5432A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96938681 | ||||||
| chr10:96939031
|
T | A | 1 | a0016c0022t0028g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-183-5082T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939031 | ||||||
| chr10:96939122
|
A | T | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-183-4991A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939122 | ||||||
| chr10:96939161
|
A | T | 3 | a0001c0001t0017g0145a0001c0001t0017g0146a0015c0021t0017g0147 | 3 | HG02818.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-183-4952A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939161 | ||||||
| chr10:96939243
|
C | T | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-183-4870C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939243 | ||||||
| chr10:96939244
|
G | A | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-183-4869G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939244 | ||||||
| chr10:96939260
|
G | A | 1 | a0005c0006t0052g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-183-4853G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939260 | ||||||
| chr10:96939379
|
C | A | 196 | a0001c0001t0006g0273a0001c0001t0016g0004a0001c0001t0016g0136others(193): Show | 196 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.-183-4734C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939379 | ||||||
| chr10:96939846
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-4267T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939846 | ||||||
| chr10:96939894
|
C | T | 1 | a0001c0001t0006g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-183-4219C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96939894 | ||||||
| chr10:96940014
|
T | A | 1 | a0002c0002t0134g0095 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-183-4099T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940014 | ||||||
| chr10:96940267
|
A | G | 1 | a0001c0004t0002g0058 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-183-3846A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940267 | ||||||
| chr10:96940279
|
A | G | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-183-3834A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940279 | ||||||
| chr10:96940284
|
T | C | 5 | a0002c0002t0013g0096a0002c0002t0020g0090a0002c0002t0020g0091others(2): Show | 5 | HG03017.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-183-3829T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940284 | ||||||
| chr10:96940303
|
A | AT | 16 | a0001c0001t0001g0001a0001c0001t0001g0196a0001c0001t0001g0197others(13): Show | 16 | HG00621.hp2 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-183-3779dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
AT | A | 36 | a0001c0001t0001g0248a0001c0001t0003g0193a0001c0001t0003g0210others(33): Show | 36 | HG01071.hp2 HG01106.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-183-3779delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATT | A | 67 | a0001c0001t0016g0004a0001c0001t0016g0176a0001c0001t0017g0145others(64): Show | 67 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.-183-3780_-183-377 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATTT | A | 20 | a0001c0001t0016g0136a0001c0001t0066g0137a0001c0001t0067g0138others(17): Show | 20 | HG00639.hp1 HG01081.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-183-3781_-183-377 others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATTTT | A | 59 | a0002c0002t0009g0073a0002c0002t0009g0076a0002c0002t0009g0092others(56): Show | 59 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-183-3782_-183-377 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATTTTT | A | 10 | a0002c0002t0001g0078a0002c0002t0033g0080a0002c0002t0033g0112others(7): Show | 10 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-183-3783_-183-377 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0230a0001c0007t0103g0179 | 2 | HG01928.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-183-3790_-183-377 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0099g0216a0001c0001t0100g0226 | 2 | NA18982.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-183-3792_-183-377 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATTTTTTT others(9): Show |
A | 3 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-183-3794_-183-377 others(20): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940303
|
ATTTTTTT others(10): Show |
A | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-183-3795_-183-377 others(21): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940303 | |||||
| chr10:96940307
|
T | A | 1 | a0002c0002t0126g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-183-3806T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940307 | ||||||
| chr10:96940334
|
T | A | 70 | a0001c0001t0001g0215a0001c0001t0005g0218a0001c0001t0016g0136others(67): Show | 70 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.-183-3779T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940334 | ||||||
| chr10:96940338
|
G | A | 1 | a0006c0008t0002g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-183-3775G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940338 | ||||||
| chr10:96940358
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-3755C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940358 | ||||||
| chr10:96940523
|
G | A | 71 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0097g0008others(68): Show | 71 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.-183-3590G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940523 | ||||||
| chr10:96940536
|
T | C | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-183-3577T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940536 | ||||||
| chr10:96940601
|
A | C | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-183-3512A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940601 | ||||||
| chr10:96940688
|
A | G | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-183-3425A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940688 | ||||||
| chr10:96940771
|
G | T | 1 | a0001c0001t0081g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-183-3342G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940771 | ||||||
| chr10:96940824
|
C | T | 6 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-183-3289C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940824 | ||||||
| chr10:96940934
|
C | G | 1 | a0001c0001t0079g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-183-3179C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96940934 | ||||||
| chr10:96940965
|
GCGGCCGG others(34): Show |
G | 1 | a0001c0001t0003g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-183-3138_-183-309 others(45): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96940965 | |||||
| chr10:96941007
|
C | T | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-183-3106C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941007 | ||||||
| chr10:96941012
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-183-3101G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941012 | ||||||
| chr10:96941012
|
GGGCGGGG others(160): Show |
G | 6 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0215others(3): Show | 6 | HG00544.hp1 HG03688.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.-183-3065_-183-289 others(4): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941012 | |||||
| chr10:96941025
|
A | AC | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-183-3081dupC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941025 | |||||
| chr10:96941056
|
TGGCCGAC others(29): Show |
T | 2 | a0002c0002t0019g0110a0002c0002t0039g0084 | 2 | NA18944.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-183-3053_-183-301 others(40): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941056 | |||||
| chr10:96941060
|
C | CG | 41 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(38): Show | 41 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-183-3052dupG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941060 | |||||
| chr10:96941062
|
A | AC | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(140): Show | 143 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-183-3041dupC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941062 | |||||
| chr10:96941062
|
A | ACC | 13 | a0001c0001t0003g0193a0001c0001t0026g0242a0001c0004t0002g0058others(10): Show | 13 | HG01081.hp2 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.-183-3042_-183-304 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941062 | |||||
| chr10:96941062
|
A | C | 41 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(38): Show | 41 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-183-3051A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941062 | ||||||
| chr10:96941062
|
A | G | 18 | a0002c0002t0009g0111a0002c0002t0013g0067a0002c0002t0013g0068others(15): Show | 18 | HG00323.hp1 HG01167.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-183-3051A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941062 | ||||||
| chr10:96941066
|
CCCCCCCG others(168): Show |
C | 1 | a0001c0001t0118g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-183-3040_-183-286 others(4): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941066 | |||||
| chr10:96941068
|
C | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0248 | 2 | NA18959.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-183-3045C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941068 | ||||||
| chr10:96941068
|
C | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-183-3045C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941068 | ||||||
| chr10:96941103
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-3010G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941103 | ||||||
| chr10:96941133
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0099g0216a0001c0001t0100g0226 | 3 | NA18939.hp2 NA18982.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-183-2980C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941133 | ||||||
| chr10:96941170
|
C | T | 1 | a0001c0001t0023g0130 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-183-2943C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941170 | ||||||
| chr10:96941179
|
AGGCGGGG others(42): Show |
A | 10 | a0001c0007t0102g0181a0004c0005t0021g0171a0004c0005t0042g0170others(7): Show | 10 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-183-2885_-183-283 others(53): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941179 | |||||
| chr10:96941192
|
A | AC | 28 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(25): Show | 28 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-183-2914dupC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941192 | |||||
| chr10:96941213
|
A | G | 2 | a0001c0001t0027g0285a0001c0001t0111g0184 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-183-2900A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941213 | ||||||
| chr10:96941228
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0217 | 2 | HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-183-2885G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941228 | ||||||
| chr10:96941241
|
A | AC | 32 | a0001c0001t0005g0261a0001c0001t0016g0004a0001c0001t0016g0136others(29): Show | 32 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-183-2865dupC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941241 | |||||
| chr10:96941242
|
CCCCCCCA others(42): Show |
C | 1 | a0001c0001t0006g0241 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-183-2836_-183-278 others(53): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941242 | |||||
| chr10:96941249
|
A | G | 1 | a0001c0001t0118g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-183-2864A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941249 | ||||||
| chr10:96941265
|
G | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-2848G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941265 | ||||||
| chr10:96941280
|
C | T | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-183-2833C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941280 | ||||||
| chr10:96941291
|
T | C | 1 | a0001c0001t0032g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-183-2822T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941291 | ||||||
| chr10:96941335
|
A | G | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-183-2778A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941335 | ||||||
| chr10:96941370
|
GCGCCCCT others(366): Show |
G | 6 | a0003c0003t0002g0005a0003c0003t0002g0048a0003c0003t0002g0057others(3): Show | 6 | HG00673.hp1 NA18945.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.-183-2739_-183-236 others(4): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941370 | |||||
| chr10:96941379
|
A | G | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-183-2734A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941379 | ||||||
| chr10:96941542
|
A | AC | 32 | a0001c0001t0001g0274a0001c0001t0016g0004a0001c0001t0016g0136others(29): Show | 32 | HG00639.hp1 HG00741.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-183-2563dupC | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941542 | |||||
| chr10:96941577
|
C | T | 1 | a0002c0002t0015g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-183-2536C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941577 | ||||||
| chr10:96941585
|
G | A | 1 | a0002c0002t0035g0098 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-183-2528G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941585 | ||||||
| chr10:96941604
|
A | C | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-2509A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941604 | ||||||
| chr10:96941618
|
A | G | 1 | a0001c0001t0115g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-183-2495A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941618 | ||||||
| chr10:96941620
|
G | A | 1 | a0001c0001t0115g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-183-2493G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941620 | ||||||
| chr10:96941628
|
G | A | 2 | a0001c0001t0003g0194a0001c0019t0003g0195 | 2 | NA18942.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-183-2485G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941628 | ||||||
| chr10:96941637
|
T | G | 1 | a0008c0011t0008g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-183-2476T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941637 | ||||||
| chr10:96941645
|
C | T | 1 | a0002c0002t0034g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-183-2468C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941645 | ||||||
| chr10:96941771
|
G | A | 57 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(54): Show | 57 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-183-2342G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96941771 | ||||||
| chr10:96941977
|
GGCTCCTC others(32): Show |
G | 1 | a0006c0008t0011g0032 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-183-2127_-183-208 others(43): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96941977 | |||||
| chr10:96942000
|
G | C | 1 | a0001c0004t0002g0009 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-183-2113G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942000 | ||||||
| chr10:96942000
|
G | T | 1 | a0003c0003t0004g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-183-2113G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942000 | ||||||
| chr10:96942001
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-2112G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942001 | ||||||
| chr10:96942034
|
C | CG | 4 | a0001c0001t0001g0197a0001c0001t0001g0259a0001c0001t0032g0013others(1): Show | 4 | HG00438.hp2 HG03516.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-2075dupG | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96942034 | |||||
| chr10:96942061
|
A | G | 2 | a0004c0009t0021g0187a0004c0009t0044g0186 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-183-2052A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942061 | ||||||
| chr10:96942075
|
G | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-183-2038G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942075 | ||||||
| chr10:96942153
|
T | C | 61 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(58): Show | 61 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-183-1960T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942153 | ||||||
| chr10:96942240
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-1873G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942240 | ||||||
| chr10:96942249
|
G | C | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-183-1864G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942249 | ||||||
| chr10:96942277
|
C | CA | 21 | a0001c0001t0001g0250a0001c0001t0001g0277a0001c0001t0003g0243others(18): Show | 21 | HG00558.hp1 HG02615.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.-183-1826dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96942277 | |||||
| chr10:96942326
|
G | A | 2 | a0002c0002t0058g0107a0002c0002t0059g0120 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-183-1787G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942326 | ||||||
| chr10:96942435
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-183-1678A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942435 | ||||||
| chr10:96942436
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-183-1677G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942436 | ||||||
| chr10:96942442
|
C | A | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-183-1671C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942442 | ||||||
| chr10:96942458
|
G | GGAGGGA | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(233): Show | 236 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(233): Show |
intron_variant | MODIFIER | c.-183-1641_-183-163 others(10): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96942458 | |||||
| chr10:96942458
|
G | GGAGGGAG others(5): Show |
14 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(11): Show | 14 | HG02486.hp1 HG02895.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.-183-1647_-183-163 others(16): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96942458 | |||||
| chr10:96942458
|
G | GGAGGGAG others(11): Show |
2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-183-1653_-183-163 others(22): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96942458 | |||||
| chr10:96942541
|
T | G | 2 | a0001c0001t0027g0285a0001c0001t0111g0184 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-183-1572T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942541 | ||||||
| chr10:96942610
|
A | G | 1 | a0014c0020t0012g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-183-1503A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942610 | ||||||
| chr10:96942729
|
A | T | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-183-1384A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96942729 | ||||||
| chr10:96943104
|
T | TTTTG | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(262): Show | 265 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(262): Show |
intron_variant | MODIFIER | c.-183-1001_-183-998 others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96943104 | |||||
| chr10:96943142
|
C | G | 1 | a0001c0001t0005g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-183-971C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96943142 | ||||||
| chr10:96943460
|
A | G | 187 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(184): Show | 187 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.-183-653A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96943460 | ||||||
| chr10:96943497
|
C | T | 1 | a0002c0002t0013g0083 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-183-616C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96943497 | ||||||
| chr10:96943531
|
A | T | 1 | a0002c0002t0013g0083 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-183-582A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96943531 | ||||||
| chr10:96943735
|
T | A | 7 | a0003c0003t0002g0046a0003c0003t0004g0038a0003c0003t0010g0162others(4): Show | 7 | HG01361.hp1 HG04199.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-183-378T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96943735 | ||||||
| chr10:96943752
|
TA | T | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-183-349delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96943752 | |||||
| chr10:96943797
|
ATAAC | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-183-313_-183-310d others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 96943797 | |||||
| chr10:96943885
|
G | A | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-183-228G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96943885 | ||||||
| chr10:96944026
|
T | C | 1 | a0001c0004t0109g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-183-87T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96944026 | ||||||
| chr10:96944051
|
A | G | 67 | a0001c0001t0097g0008a0001c0001t0098g0010a0001c0004t0002g0009others(64): Show | 67 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.-183-62A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 4/7 | chr10 | 96944051 | ||||||
| chr10:96944412
|
G | A | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+167G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96944412 | ||||||
| chr10:96944592
|
A | AT | 33 | a0001c0001t0001g0197a0001c0001t0001g0230a0001c0001t0001g0236others(30): Show | 33 | HG00642.hp2 HG00673.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.-51+363dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 96944592 | |||||
| chr10:96944592
|
AT | A | 21 | a0001c0001t0056g0284a0001c0001t0076g0149a0001c0001t0106g0286others(18): Show | 21 | HG01070.hp2 HG01109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-51+363delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 96944592 | |||||
| chr10:96944900
|
C | A | 188 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(185): Show | 188 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.-51+655C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96944900 | ||||||
| chr10:96945323
|
C | T | 1 | a0006c0008t0002g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-51+1078C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96945323 | ||||||
| chr10:96945480
|
A | G | 3 | a0001c0001t0005g0221a0001c0001t0005g0261a0001c0001t0027g0188 | 3 | NA18971.hp2 NA18998.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-51+1235A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96945480 | ||||||
| chr10:96945924
|
CT | C | 6 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(3): Show | 6 | HG01167.hp1 HG01993.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+1692delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 96945924 | |||||
| chr10:96946137
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-51+1892G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946137 | ||||||
| chr10:96946155
|
C | T | 2 | a0001c0001t0022g0143a0001c0001t0022g0144 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-51+1910C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946155 | ||||||
| chr10:96946278
|
T | G | 1 | a0001c0001t0005g0261 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-51+2033T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946278 | ||||||
| chr10:96946482
|
A | G | 1 | a0001c0004t0091g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-51+2237A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946482 | ||||||
| chr10:96946561
|
C | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-51+2316C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946561 | ||||||
| chr10:96946638
|
G | A | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-50-2370G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946638 | ||||||
| chr10:96946705
|
T | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-50-2303T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946705 | ||||||
| chr10:96946837
|
C | T | 1 | a0001c0004t0091g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-50-2171C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946837 | ||||||
| chr10:96946979
|
A | G | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-50-2029A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96946979 | ||||||
| chr10:96947263
|
G | T | 1 | a0004c0005t0042g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-50-1745G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96947263 | ||||||
| chr10:96947430
|
T | G | 2 | a0001c0004t0002g0058a0001c0004t0007g0126 | 2 | HG01928.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-50-1578T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96947430 | ||||||
| chr10:96947504
|
C | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-50-1504C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96947504 | ||||||
| chr10:96947681
|
T | C | 4 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-1327T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96947681 | ||||||
| chr10:96947732
|
T | C | 1 | a0005c0006t0054g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-50-1276T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96947732 | ||||||
| chr10:96947924
|
A | G | 1 | a0016c0022t0028g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-50-1084A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96947924 | ||||||
| chr10:96948349
|
A | C | 2 | a0011c0014t0123g0079a0011c0014t0125g0081 | 2 | NA18990.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-50-659A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96948349 | ||||||
| chr10:96948879
|
C | T | 1 | a0002c0002t0014g0089 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-50-129C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96948879 | ||||||
| chr10:96948959
|
T | G | 1 | a0001c0001t0027g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-50-49T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96948959 | ||||||
| chr10:96949000
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.-50-8A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 5/7 | chr10 | 96949000 | ||||||
| chr10:96949895
|
G | A | 67 | a0001c0001t0097g0008a0001c0001t0098g0010a0001c0004t0002g0009others(64): Show | 67 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.238+600G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96949895 | ||||||
| chr10:96950060
|
C | A | 4 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0047g0172others(1): Show | 4 | HG03453.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+765C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96950060 | ||||||
| chr10:96950717
|
T | C | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.239-1386T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96950717 | ||||||
| chr10:96950820
|
C | T | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.239-1283C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96950820 | ||||||
| chr10:96951132
|
C | A | 60 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(57): Show | 60 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.239-971C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951132 | ||||||
| chr10:96951201
|
T | G | 1 | a0001c0001t0118g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.239-902T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951201 | ||||||
| chr10:96951202
|
T | A | 1 | a0001c0001t0118g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.239-901T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951202 | ||||||
| chr10:96951234
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.239-869G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951234 | ||||||
| chr10:96951378
|
T | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.239-725T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951378 | ||||||
| chr10:96951585
|
A | ATATACTA others(47): Show |
1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.239-518_239-517ins others(54): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951585 | ||||||
| chr10:96951586
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.239-517C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951586 | ||||||
| chr10:96951657
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.239-446A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951657 | ||||||
| chr10:96951702
|
G | T | 1 | a0002c0002t0145g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.239-401G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96951702 | ||||||
| chr10:96952024
|
C | A | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.239-79C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 6/7 | chr10 | 96952024 | ||||||
| chr10:96952233
|
A | G | 2 | a0001c0001t0077g0127a0001c0001t0078g0128 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.332+37A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96952233 | ||||||
| chr10:96952251
|
G | A | 2 | a0001c0001t0113g0191a0013c0018t0006g0190 | 2 | HG01099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.332+55G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96952251 | ||||||
| chr10:96952350
|
A | G | 1 | a0002c0002t0009g0092 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.332+154A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96952350 | ||||||
| chr10:96952431
|
T | G | 31 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(28): Show | 31 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.332+235T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96952431 | ||||||
| chr10:96952565
|
TTG | T | 188 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(185): Show | 188 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.332+387_332+388del others(2): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96952565 | |||||
| chr10:96952584
|
T | C | 3 | a0010c0010t0002g0014a0010c0010t0011g0015a0010c0010t0011g0062 | 3 | NA18947.hp1 NA18968.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.332+388T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96952584 | ||||||
| chr10:96952843
|
A | T | 1 | a0001c0004t0109g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.332+647A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96952843 | ||||||
| chr10:96952916
|
A | G | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.332+720A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96952916 | ||||||
| chr10:96953057
|
A | G | 1 | a0014c0020t0012g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.332+861A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96953057 | ||||||
| chr10:96953198
|
A | G | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.332+1002A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96953198 | ||||||
| chr10:96953334
|
T | C | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+1138T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96953334 | ||||||
| chr10:96953457
|
G | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.332+1261G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96953457 | ||||||
| chr10:96953550
|
C | CCAAAA | 94 | a0001c0001t0001g0253a0001c0001t0016g0004a0001c0001t0016g0136others(91): Show | 94 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.332+1375_332+1379d others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96953550 | |||||
| chr10:96953550
|
C | CCAAAACA others(3): Show |
2 | a0001c0001t0022g0143a0001c0001t0022g0144 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.332+1370_332+1379d others(12): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96953550 | |||||
| chr10:96953626
|
T | G | 1 | a0001c0001t0006g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.332+1430T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96953626 | ||||||
| chr10:96953863
|
T | A | 1 | a0001c0001t0069g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.332+1667T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96953863 | ||||||
| chr10:96954025
|
T | G | 1 | a0001c0001t0051g0133 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.332+1829T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96954025 | ||||||
| chr10:96954081
|
GT | G | 5 | a0004c0005t0043g0124a0004c0005t0045g0168a0004c0005t0046g0125others(2): Show | 5 | HG01109.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.332+1893delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96954081 | |||||
| chr10:96954257
|
G | A | 18 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.332+2061G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96954257 | ||||||
| chr10:96954362
|
C | T | 1 | a0001c0001t0098g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332+2166C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96954362 | ||||||
| chr10:96954702
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(284): Show | 287 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(284): Show |
intron_variant | MODIFIER | c.332+2506G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96954702 | ||||||
| chr10:96955486
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+3290G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96955486 | ||||||
| chr10:96955941
|
A | T | 4 | a0001c0001t0023g0130a0001c0001t0023g0159a0001c0001t0071g0132others(1): Show | 4 | HG00733.hp1 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+3745A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96955941 | ||||||
| chr10:96955986
|
A | G | 1 | a0001c0001t0143g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332+3790A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96955986 | ||||||
| chr10:96956330
|
A | G | 7 | a0002c0002t0015g0102a0002c0002t0015g0122a0002c0002t0015g0123others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.332+4134A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96956330 | ||||||
| chr10:96956369
|
T | TATA | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+4174_332+4176d others(5): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96956369 | |||||
| chr10:96956553
|
G | A | 4 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0142g0061others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+4357G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96956553 | ||||||
| chr10:96956596
|
G | A | 2 | a0001c0001t0006g0273a0001c0001t0031g0272 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.332+4400G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96956596 | ||||||
| chr10:96957039
|
C | A | 1 | a0002c0002t0145g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.332+4843C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957039 | ||||||
| chr10:96957123
|
A | G | 1 | a0001c0001t0072g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.332+4927A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957123 | ||||||
| chr10:96957146
|
G | T | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.332+4950G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957146 | ||||||
| chr10:96957185
|
A | G | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.332+4989A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957185 | ||||||
| chr10:96957370
|
A | C | 1 | a0001c0001t0101g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.332+5174A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957370 | ||||||
| chr10:96957418
|
C | T | 1 | a0003c0003t0085g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.332+5222C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957418 | ||||||
| chr10:96957952
|
T | C | 14 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0003g0194others(11): Show | 14 | HG00438.hp1 HG00673.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.332+5756T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957952 | ||||||
| chr10:96957967
|
A | G | 1 | a0001c0004t0007g0041 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.332+5771A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96957967 | ||||||
| chr10:96958237
|
A | G | 1 | a0002c0002t0015g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.332+6041A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96958237 | ||||||
| chr10:96958836
|
T | C | 1 | a0004c0009t0064g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.332+6640T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96958836 | ||||||
| chr10:96958906
|
T | TA | 12 | a0001c0001t0001g0234a0001c0001t0001g0248a0001c0001t0001g0256others(9): Show | 12 | HG00639.hp2 HG01070.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.332+6731dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96958906 | |||||
| chr10:96958906
|
T | TAA | 25 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(22): Show | 25 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.332+6730_332+6731d others(4): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96958906 | |||||
| chr10:96958906
|
TA | T | 42 | a0001c0001t0001g0196a0001c0001t0001g0207a0001c0001t0001g0215others(39): Show | 42 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.332+6731delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96958906 | |||||
| chr10:96958906
|
TAA | T | 110 | a0001c0001t0001g0253a0001c0001t0001g0259a0001c0001t0006g0244others(107): Show | 110 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.332+6730_332+6731d others(4): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96958906 | |||||
| chr10:96958906
|
TAAA | T | 15 | a0001c0001t0097g0008a0001c0001t0098g0010a0001c0004t0007g0019others(12): Show | 15 | HG00558.hp2 HG02559.hp2 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.332+6729_332+6731d others(5): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96958906 | |||||
| chr10:96959050
|
C | T | 2 | a0004c0009t0021g0187a0004c0009t0044g0186 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332+6854C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96959050 | ||||||
| chr10:96959078
|
C | T | 1 | a0001c0001t0101g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.332+6882C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96959078 | ||||||
| chr10:96959226
|
A | G | 1 | a0003c0003t0004g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.332+7030A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96959226 | ||||||
| chr10:96959404
|
A | T | 2 | a0001c0004t0007g0041a0001c0004t0083g0024 | 2 | HG02602.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.332+7208A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96959404 | ||||||
| chr10:96959946
|
C | T | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.332+7750C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96959946 | ||||||
| chr10:96960154
|
C | T | 1 | a0001c0001t0079g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.332+7958C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96960154 | ||||||
| chr10:96960717
|
A | G | 2 | a0004c0005t0043g0124a0004c0005t0046g0125 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.332+8521A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96960717 | ||||||
| chr10:96961252
|
C | T | 7 | a0001c0004t0007g0019a0001c0004t0088g0016a0001c0004t0091g0018others(4): Show | 7 | HG00558.hp2 NA18947.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+9056C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96961252 | ||||||
| chr10:96961845
|
C | T | 65 | a0001c0004t0002g0009a0001c0004t0002g0029a0001c0004t0002g0058others(62): Show | 65 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.332+9649C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96961845 | ||||||
| chr10:96962315
|
A | G | 20 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+10119A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96962315 | ||||||
| chr10:96962461
|
A | C | 1 | a0001c0001t0143g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332+10265A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96962461 | ||||||
| chr10:96962638
|
A | C | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.332+10442A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96962638 | ||||||
| chr10:96963112
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+10916A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96963112 | ||||||
| chr10:96963219
|
TA | T | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.332+11030delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96963219 | |||||
| chr10:96963228
|
C | T | 19 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.332+11032C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96963228 | ||||||
| chr10:96963808
|
A | G | 1 | a0001c0004t0122g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.332+11612A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96963808 | ||||||
| chr10:96963880
|
T | C | 19 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.332+11684T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96963880 | ||||||
| chr10:96964082
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.332+11886A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96964082 | ||||||
| chr10:96964241
|
CT | C | 49 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(46): Show | 49 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.332+12059delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96964241 | |||||
| chr10:96964242
|
T | C | 1 | a0001c0001t0114g0246 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.332+12046T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96964242 | ||||||
| chr10:96964573
|
C | T | 10 | a0001c0001t0016g0136a0001c0001t0016g0176a0001c0001t0017g0145others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+12377C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96964573 | ||||||
| chr10:96964591
|
A | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+12395A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96964591 | ||||||
| chr10:96964627
|
A | C | 1 | a0002c0002t0034g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.332+12431A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96964627 | ||||||
| chr10:96964873
|
G | T | 185 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(182): Show | 185 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.332+12677G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96964873 | ||||||
| chr10:96964875
|
C | T | 1 | a0001c0001t0099g0216 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.332+12679C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96964875 | ||||||
| chr10:96964902
|
TGTCA | T | 19 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.332+12713_332+1271 others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96964902 | |||||
| chr10:96965014
|
A | T | 91 | a0001c0001t0001g0259a0001c0001t0016g0004a0001c0001t0016g0136others(88): Show | 91 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.332+12818A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965014 | ||||||
| chr10:96965015
|
T | A | 2 | a0001c0001t0001g0253a0001c0001t0006g0244 | 2 | NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.332+12819T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965015 | ||||||
| chr10:96965211
|
A | G | 1 | a0001c0001t0003g0199 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.332+13015A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965211 | ||||||
| chr10:96965366
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+13170T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965366 | ||||||
| chr10:96965392
|
A | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.332+13196A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965392 | ||||||
| chr10:96965522
|
C | T | 3 | a0001c0001t0017g0145a0001c0001t0017g0146a0015c0021t0017g0147 | 3 | HG02818.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.332+13326C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965522 | ||||||
| chr10:96965616
|
C | T | 3 | a0002c0002t0055g0109a0002c0002t0058g0107a0002c0002t0059g0120 | 3 | HG02809.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.332+13420C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965616 | ||||||
| chr10:96965618
|
C | T | 3 | a0002c0002t0055g0109a0002c0002t0058g0107a0002c0002t0059g0120 | 3 | HG02809.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.332+13422C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965618 | ||||||
| chr10:96965628
|
C | T | 1 | a0001c0001t0107g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.332+13432C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965628 | ||||||
| chr10:96965661
|
C | CA | 15 | a0001c0001t0001g0002a0001c0001t0001g0197a0001c0001t0001g0217others(12): Show | 15 | HG00642.hp2 HG00741.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.332+13488dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96965661 | |||||
| chr10:96965661
|
C | CAA | 6 | a0001c0001t0097g0008a0001c0001t0098g0010a0003c0003t0004g0023others(3): Show | 6 | HG02071.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.332+13487_332+1348 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96965661 | |||||
| chr10:96965661
|
C | CAAA | 8 | a0003c0003t0004g0028a0003c0003t0004g0034a0003c0003t0004g0039others(5): Show | 8 | HG01884.hp1 HG02027.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.332+13486_332+1348 others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96965661 | |||||
| chr10:96965661
|
CA | C | 138 | a0001c0001t0001g0207a0001c0001t0001g0232a0001c0001t0001g0278others(135): Show | 138 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.332+13488delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96965661 | |||||
| chr10:96965687
|
C | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+13491C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965687 | ||||||
| chr10:96965690
|
G | A | 3 | a0005c0006t0040g0288a0005c0006t0041g0163a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.332+13494G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965690 | ||||||
| chr10:96965765
|
T | C | 1 | a0003c0003t0096g0279 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.332+13569T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965765 | ||||||
| chr10:96965793
|
C | T | 1 | a0001c0001t0027g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.332+13597C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965793 | ||||||
| chr10:96965797
|
A | G | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.332+13601A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96965797 | ||||||
| chr10:96966056
|
C | A | 31 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(28): Show | 31 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.332+13860C>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96966056 | ||||||
| chr10:96966158
|
G | T | 16 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(13): Show | 16 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.332+13962G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96966158 | ||||||
| chr10:96966163
|
C | CT | 14 | a0001c0001t0001g0230a0001c0001t0056g0284a0004c0005t0021g0171others(11): Show | 14 | HG01109.hp1 HG01928.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.332+13984dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966163 | |||||
| chr10:96966163
|
C | CTT | 8 | a0001c0001t0106g0286a0005c0006t0040g0288a0005c0006t0041g0163others(5): Show | 8 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.332+13983_332+1398 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966163 | |||||
| chr10:96966163
|
CT | C | 85 | a0001c0001t0001g0189a0001c0001t0006g0251a0001c0001t0006g0273others(82): Show | 85 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.332+13984delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966163 | |||||
| chr10:96966220
|
C | CT | 53 | a0001c0001t0001g0207a0001c0001t0001g0236a0001c0001t0001g0260others(50): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.332+14050dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966220 | |||||
| chr10:96966220
|
C | CTT | 10 | a0001c0001t0001g0269a0001c0001t0016g0004a0001c0001t0066g0137others(7): Show | 10 | HG01081.hp1 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+14049_332+1405 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966220 | |||||
| chr10:96966220
|
CT | C | 29 | a0001c0001t0005g0218a0001c0001t0032g0013a0001c0001t0056g0284others(26): Show | 29 | HG00642.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.332+14050delT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966220 | |||||
| chr10:96966220
|
CTT | C | 50 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(47): Show | 50 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.332+14049_332+1405 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966220 | |||||
| chr10:96966220
|
CTTTTTTT others(4): Show |
C | 1 | a0006c0008t0011g0032 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.332+14040_332+1405 others(15): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966220 | |||||
| chr10:96966220
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0006g0241 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.332+14037_332+1405 others(18): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96966220 | |||||
| chr10:96966252
|
G | A | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.332+14056G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96966252 | ||||||
| chr10:96966570
|
C | T | 1 | a0003c0003t0096g0279 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.333-14223C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96966570 | ||||||
| chr10:96966621
|
A | C | 31 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(28): Show | 31 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.333-14172A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96966621 | ||||||
| chr10:96966913
|
T | G | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.333-13880T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96966913 | ||||||
| chr10:96966915
|
T | C | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.333-13878T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96966915 | ||||||
| chr10:96967017
|
A | C | 1 | a0002c0002t0037g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.333-13776A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967017 | ||||||
| chr10:96967200
|
G | A | 2 | a0001c0001t0077g0127a0001c0001t0078g0128 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.333-13593G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967200 | ||||||
| chr10:96967243
|
T | C | 1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333-13550T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967243 | ||||||
| chr10:96967671
|
G | A | 14 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.333-13122G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967671 | ||||||
| chr10:96967724
|
T | A | 1 | a0009c0012t0007g0063 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.333-13069T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967724 | ||||||
| chr10:96967835
|
A | G | 2 | a0005c0006t0052g0165a0005c0006t0054g0164 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.333-12958A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967835 | ||||||
| chr10:96967885
|
G | T | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.333-12908G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967885 | ||||||
| chr10:96967888
|
C | G | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.333-12905C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96967888 | ||||||
| chr10:96968030
|
G | A | 19 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.333-12763G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96968030 | ||||||
| chr10:96968227
|
A | C | 1 | a0001c0001t0118g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.333-12566A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96968227 | ||||||
| chr10:96968367
|
C | T | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-12426C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96968367 | ||||||
| chr10:96968491
|
A | C | 1 | a0005c0006t0060g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.333-12302A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96968491 | ||||||
| chr10:96968780
|
C | T | 1 | a0002c0002t0055g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.333-12013C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96968780 | ||||||
| chr10:96968937
|
C | CA | 73 | a0001c0001t0006g0251a0001c0001t0038g0059a0001c0001t0038g0060others(70): Show | 73 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.333-11843dupA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96968937 | |||||
| chr10:96969092
|
C | T | 45 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(42): Show | 45 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.333-11701C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969092 | ||||||
| chr10:96969164
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0189others(32): Show | 35 | HG00438.hp1 HG00673.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.333-11629T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969164 | ||||||
| chr10:96969564
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.333-11229G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969564 | ||||||
| chr10:96969583
|
C | T | 1 | a0001c0001t0005g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.333-11210C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969583 | ||||||
| chr10:96969684
|
G | A | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.333-11109G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969684 | ||||||
| chr10:96969729
|
T | G | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-11064T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969729 | ||||||
| chr10:96969770
|
T | TTTC | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-11021_333-1102 others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96969770 | |||||
| chr10:96969774
|
C | CT | 65 | a0001c0001t0001g0234a0001c0001t0016g0004a0001c0001t0016g0136others(62): Show | 65 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.333-11004dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96969774 | |||||
| chr10:96969774
|
C | T | 3 | a0007c0013t0080g0174a0007c0013t0141g0175a0007c0016t0146g0007 | 3 | HG01884.hp1 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.333-11019C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969774 | ||||||
| chr10:96969801
|
CAA | C | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.333-10991_333-1099 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969801 | ||||||
| chr10:96969911
|
C | G | 3 | a0005c0006t0040g0288a0005c0006t0041g0163a0005c0006t0060g0287 | 3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.333-10882C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96969911 | ||||||
| chr10:96969946
|
A | AT | 160 | a0001c0001t0001g0001a0001c0001t0001g0192a0001c0001t0001g0196others(157): Show | 160 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.333-10821dupT | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96969946 | |||||
| chr10:96969946
|
A | ATT | 67 | a0001c0001t0001g0002a0001c0001t0001g0234a0001c0001t0003g0193others(64): Show | 67 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.333-10822_333-1082 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96969946 | |||||
| chr10:96969946
|
A | ATTT | 12 | a0001c0001t0001g0263a0001c0004t0002g0157a0001c0004t0007g0019others(9): Show | 12 | HG00558.hp2 HG01361.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.333-10823_333-1082 others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96969946 | |||||
| chr10:96969946
|
ATT | A | 6 | a0005c0006t0040g0288a0005c0006t0041g0163a0005c0006t0052g0165others(3): Show | 6 | HG01884.hp1 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.333-10822_333-1082 others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96969946 | |||||
| chr10:96969946
|
ATTT | A | 13 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(10): Show | 13 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.333-10823_333-1082 others(7): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96969946 | |||||
| chr10:96970037
|
C | T | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-10756C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970037 | ||||||
| chr10:96970125
|
C | T | 1 | a0004c0005t0021g0171 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333-10668C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970125 | ||||||
| chr10:96970126
|
G | A | 2 | a0001c0004t0084g0025a0001c0004t0089g0055 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.333-10667G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970126 | ||||||
| chr10:96970360
|
T | A | 1 | a0002c0002t0001g0078 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.333-10433T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970360 | ||||||
| chr10:96970388
|
C | T | 2 | a0002c0002t0009g0076a0002c0002t0135g0082 | 2 | HG00438.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.333-10405C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970388 | ||||||
| chr10:96970435
|
G | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.333-10358G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970435 | ||||||
| chr10:96970598
|
C | CATTTT | 44 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(41): Show | 44 | HG00558.hp2 HG00733.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.333-10170_333-1016 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970598 | |||||
| chr10:96970598
|
C | CATTTTAT others(3): Show |
50 | a0002c0002t0009g0073a0002c0002t0009g0076a0002c0002t0013g0067others(47): Show | 50 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.333-10175_333-1016 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970598 | |||||
| chr10:96970598
|
C | CATTTTAT others(8): Show |
23 | a0002c0002t0001g0078a0002c0002t0009g0111a0002c0002t0014g0065others(20): Show | 23 | HG00323.hp1 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.333-10180_333-1016 others(19): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970598 | |||||
| chr10:96970598
|
C | CATTTTAT others(13): Show |
2 | a0002c0002t0009g0092a0005c0006t0060g0287 | 2 | HG02300.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.333-10185_333-1016 others(24): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970598 | |||||
| chr10:96970598
|
C | CATTTTAT others(18): Show |
1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.333-10190_333-1016 others(29): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970598 | |||||
| chr10:96970598
|
CATTTT | C | 4 | a0001c0001t0067g0138a0004c0005t0021g0171a0004c0005t0042g0170others(1): Show | 4 | HG00639.hp1 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-10170_333-1016 others(9): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970598 | |||||
| chr10:96970652
|
T | A | 18 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.333-10141T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970652 | ||||||
| chr10:96970653
|
A | ATTTATTT others(12): Show |
1 | a0007c0013t0080g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333-10123_333-1012 others(23): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970653 | |||||
| chr10:96970653
|
A | ATTTTATT others(17): Show |
1 | a0007c0013t0141g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.333-10137_333-1013 others(28): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970653 | |||||
| chr10:96970653
|
A | T | 18 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(15): Show | 18 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.333-10140A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970653 | ||||||
| chr10:96970653
|
ATTTATTT others(3): Show |
A | 1 | a0001c0001t0003g0265 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.333-10125_333-1011 others(14): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96970653 | |||||
| chr10:96970715
|
A | C | 1 | a0001c0007t0105g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.333-10078A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96970715 | ||||||
| chr10:96971111
|
A | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.333-9682A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96971111 | ||||||
| chr10:96971234
|
G | A | 2 | a0005c0006t0040g0288a0005c0006t0060g0287 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.333-9559G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96971234 | ||||||
| chr10:96971560
|
T | G | 21 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.333-9233T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96971560 | ||||||
| chr10:96971623
|
G | T | 1 | a0001c0001t0068g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333-9170G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96971623 | ||||||
| chr10:96971983
|
T | G | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.333-8810T>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96971983 | ||||||
| chr10:96972294
|
T | A | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-8499T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96972294 | ||||||
| chr10:96972751
|
G | A | 29 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.333-8042G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96972751 | ||||||
| chr10:96972760
|
T | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.333-8033T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96972760 | ||||||
| chr10:96972883
|
A | G | 45 | a0002c0002t0001g0078a0002c0002t0009g0073a0002c0002t0009g0076others(42): Show | 45 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.333-7910A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96972883 | ||||||
| chr10:96973115
|
A | G | 1 | a0001c0001t0114g0246 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.333-7678A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96973115 | ||||||
| chr10:96973444
|
A | G | 2 | a0002c0002t0058g0107a0002c0002t0059g0120 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.333-7349A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96973444 | ||||||
| chr10:96973934
|
A | T | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.333-6859A>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96973934 | ||||||
| chr10:96974139
|
A | G | 1 | a0001c0001t0056g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.333-6654A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96974139 | ||||||
| chr10:96974212
|
C | G | 2 | a0001c0001t0038g0059a0001c0001t0142g0061 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.333-6581C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96974212 | ||||||
| chr10:96974263
|
C | G | 1 | a0003c0003t0004g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.333-6530C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96974263 | ||||||
| chr10:96974549
|
G | A | 1 | a0004c0005t0046g0125 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.333-6244G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96974549 | ||||||
| chr10:96975058
|
G | C | 21 | a0001c0001t0106g0286a0004c0005t0021g0171a0004c0005t0042g0170others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.333-5735G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975058 | ||||||
| chr10:96975098
|
G | T | 1 | a0012c0017t0127g0077 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.333-5695G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975098 | ||||||
| chr10:96975190
|
AATACTT | A | 5 | a0002c0002t0013g0096a0002c0002t0020g0090a0002c0002t0020g0091others(2): Show | 5 | HG03017.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-5600_333-5595d others(8): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96975190 | |||||
| chr10:96975197
|
A | G | 5 | a0002c0002t0013g0096a0002c0002t0020g0090a0002c0002t0020g0091others(2): Show | 5 | HG03017.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-5596A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975197 | ||||||
| chr10:96975198
|
T | C | 1 | a0012c0017t0127g0077 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.333-5595T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975198 | ||||||
| chr10:96975280
|
A | G | 1 | a0001c0001t0003g0238 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.333-5513A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975280 | ||||||
| chr10:96975420
|
C | T | 31 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(28): Show | 31 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.333-5373C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975420 | ||||||
| chr10:96975450
|
T | C | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-5343T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975450 | ||||||
| chr10:96975483
|
G | C | 51 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(48): Show | 51 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.333-5310G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975483 | ||||||
| chr10:96975567
|
A | C | 1 | a0005c0006t0041g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.333-5226A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975567 | ||||||
| chr10:96975643
|
C | T | 1 | a0001c0001t0032g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.333-5150C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975643 | ||||||
| chr10:96975783
|
G | T | 1 | a0016c0022t0028g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.333-5010G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975783 | ||||||
| chr10:96975792
|
A | C | 3 | a0001c0001t0005g0221a0001c0001t0005g0261a0001c0001t0027g0188 | 3 | NA18971.hp2 NA18998.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.333-5001A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975792 | ||||||
| chr10:96975804
|
C | G | 2 | a0001c0001t0038g0059a0001c0001t0142g0061 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.333-4989C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975804 | ||||||
| chr10:96975913
|
G | A | 4 | a0001c0004t0002g0058a0001c0004t0007g0126a0001c0004t0109g0027others(1): Show | 4 | HG01928.hp2 HG02257.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-4880G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96975913 | ||||||
| chr10:96976015
|
A | G | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-4778A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96976015 | ||||||
| chr10:96976128
|
C | T | 2 | a0001c0001t0026g0223a0001c0001t0026g0242 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.333-4665C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96976128 | ||||||
| chr10:96976372
|
A | G | 1 | a0001c0004t0091g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.333-4421A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96976372 | ||||||
| chr10:96976389
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.333-4404T>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96976389 | ||||||
| chr10:96976686
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333-4107C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96976686 | ||||||
| chr10:96976885
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.333-3908G>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96976885 | ||||||
| chr10:96976927
|
C | T | 1 | a0001c0004t0002g0058 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.333-3866C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96976927 | ||||||
| chr10:96977058
|
A | AT | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-3735_333-3734i others(3): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96977058 | ||||||
| chr10:96977263
|
T | C | 1 | a0007c0016t0146g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.333-3530T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96977263 | ||||||
| chr10:96977451
|
T | C | 5 | a0002c0002t0013g0096a0002c0002t0020g0090a0002c0002t0020g0091others(2): Show | 5 | HG03017.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-3342T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96977451 | ||||||
| chr10:96977519
|
A | G | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-3274A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96977519 | ||||||
| chr10:96977662
|
AGTTT | A | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-3110_333-3107d others(6): Show |
LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96977662 | |||||
| chr10:96977917
|
A | G | 17 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(14): Show | 17 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-2876A>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96977917 | ||||||
| chr10:96978234
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.333-2559G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96978234 | ||||||
| chr10:96978240
|
T | C | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-2553T>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96978240 | ||||||
| chr10:96978429
|
G | A | 2 | a0001c0001t0018g0151a0001c0001t0076g0149 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.333-2364G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96978429 | ||||||
| chr10:96978459
|
C | G | 1 | a0003c0003t0008g0280 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.333-2334C>G | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96978459 | ||||||
| chr10:96978671
|
C | T | 31 | a0001c0001t0016g0004a0001c0001t0016g0136a0001c0001t0016g0176others(28): Show | 31 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.333-2122C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96978671 | ||||||
| chr10:96979064
|
G | C | 1 | a0001c0001t0003g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.333-1729G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96979064 | ||||||
| chr10:96979128
|
C | T | 1 | a0001c0001t0066g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.333-1665C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96979128 | ||||||
| chr10:96979356
|
G | A | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-1437G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96979356 | ||||||
| chr10:96979577
|
G | A | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.333-1216G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96979577 | ||||||
| chr10:96979851
|
G | C | 12 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.333-942G>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96979851 | ||||||
| chr10:96979861
|
C | T | 1 | a0001c0007t0108g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.333-932C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96979861 | ||||||
| chr10:96979919
|
G | A | 3 | a0001c0001t0032g0012a0001c0001t0032g0013a0001c0001t0120g0003 | 3 | HG01243.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.333-874G>A | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96979919 | ||||||
| chr10:96980009
|
C | T | 5 | a0001c0001t0038g0059a0001c0001t0038g0060a0001c0001t0098g0010others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-784C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96980009 | ||||||
| chr10:96980162
|
CA | C | 190 | a0001c0001t0006g0273a0001c0001t0016g0004a0001c0001t0016g0136others(187): Show | 190 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.333-619delA | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 96980162 | |||||
| chr10:96980168
|
A | C | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-625A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96980168 | ||||||
| chr10:96980410
|
C | T | 2 | a0001c0001t0071g0132a0001c0001t0074g0131 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.333-383C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96980410 | ||||||
| chr10:96980431
|
C | T | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-362C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96980431 | ||||||
| chr10:96980456
|
A | C | 2 | a0007c0013t0080g0174a0007c0013t0141g0175 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.333-337A>C | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96980456 | ||||||
| chr10:96980644
|
C | T | 20 | a0004c0005t0021g0171a0004c0005t0042g0170a0004c0005t0043g0124others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-149C>T | LCOR | ENSG00000196233.14 | transcript | ENST00000421806.4 | protein_coding | 7/7 | chr10 | 96980644 |