Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 860 |
|---|---|
| ensemblid | ENSG00000124813.23 |
| hgncid | 10472 |
| symbol | RUNX2 |
| name | RUNX family transcription factor 2 |
| refseq_nuc | NM_001024630.4 |
| refseq_prot | NP_001019801.3 |
| ensembl_nuc | ENST00000647337.2 |
| ensembl_prot | ENSP00000495497.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 45328330 |
| end | 45551082 |
| strand | + |
| ver | v1.2 |
| region | chr6:45328330-45551082 |
| region5000 | chr6:45323330-45556082 |
| regionname0 | RUNX2_chr6_45328330_45551082 |
| regionname5000 | RUNX2_chr6_45323330_45556082 |
| 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 | 521 | 174 | 74 | 33 | 42 | 7 | 16 | 28 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0002 | 0/0 | 515 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0003 | 0/0 | 521 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0004 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| 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 | 1566 | 158 | 73 | 28 | 36 | 6 | 13 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| c0002 | 0/0 | 1566 | 14 | 0 | 5 | 5 | 1 | 3 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| c0003 | 0/0 | 1548 | 2 | 0 | 2 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| c0004 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| c0005 | 0/0 | 1566 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| c0006 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| c0007 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3975 | 88 | 30 | 17 | 29 | 3 | 7 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0002 | 0/0 | 3974 | 24 | 23 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0003 | 0/0 | 3973 | 17 | 2 | 4 | 8 | 1 | 2 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0004 | 0/0 | 3973 | 12 | 0 | 3 | 3 | 1 | 5 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0005 | 0/0 | 3974 | 7 | 0 | 5 | 1 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0006 | 0/0 | 3975 | 6 | 0 | 5 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0007 | 0/0 | 3974 | 4 | 4 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0008 | 0/0 | 3974 | 3 | 2 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0009 | 0/0 | 3974 | 3 | 3 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0010 | 0/0 | 3975 | 2 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0011 | 0/0 | 3975 | 2 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0012 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0013 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0014 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0015 | 0/0 | 3973 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0016 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0017 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0018 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0019 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0020 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| t0021 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| 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 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| 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 | 1566 | 158 | 73 | 28 | 36 | 6 | 13 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0002 | 0/0 | 1566 | 14 | 0 | 5 | 5 | 1 | 3 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0006 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0007 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0002c0003 | 0/0 | 1548 | 2 | 0 | 2 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0003c0004 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0004c0005 | 0/0 | 1566 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5540 | 76 | 29 | 12 | 25 | 2 | 6 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0002 | 0/0 | 5539 | 24 | 23 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0003 | 0/0 | 5538 | 16 | 2 | 4 | 7 | 1 | 2 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0004 | 0/0 | 5538 | 8 | 0 | 2 | 2 | 1 | 3 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0005 | 0/0 | 5539 | 7 | 0 | 5 | 1 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0006 | 0/0 | 5540 | 4 | 0 | 3 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0007 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0008 | 0/0 | 5539 | 3 | 2 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0009 | 0/0 | 5539 | 3 | 3 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0010 | 0/0 | 5540 | 2 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0011 | 0/0 | 5540 | 2 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0012 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0013 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0014 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0016 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0017 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0018 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0019 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0020 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0001t0021 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0002t0001 | 0/0 | 5540 | 6 | 0 | 2 | 3 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0002t0003 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0002t0004 | 0/0 | 5538 | 4 | 0 | 1 | 1 | 0 | 2 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0002t0006 | 0/0 | 5540 | 2 | 0 | 2 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0002t0015 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0006t0001 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0001c0007t0001 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0002c0003t0001 | 0/0 | 5522 | 2 | 0 | 2 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0003c0004t0001 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| a0004c0005t0001 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | copy fasta | chr6 | 45323330 | 45556082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0013g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0017g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0018g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0019g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0020g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0021g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0015g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0003c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0004c0005t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0015 | g0043 | EUR | GBR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00099 | hp2 | a0003 | c0004 | t0001 | g0072 | EUR | GBR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0001 | EUR | FIN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0014 | EUR | FIN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0150 | EUR | FIN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0039 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00597 | hp1 | a0001 | c0007 | t0001 | g0028 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0055 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0061 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01069 | hp2 | a0001 | c0002 | t0006 | g0016 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01071 | hp2 | a0001 | c0002 | t0006 | g0015 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0089 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01106 | hp2 | a0004 | c0005 | t0001 | g0006 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0037 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0161 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0034 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0162 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0075 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0093 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02056 | hp1 | a0001 | c0001 | t0021 | g0088 | EAS | KHV | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0035 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02451 | hp2 | a0001 | c0001 | t0018 | g0157 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0027 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0144 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0060 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0168 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02818 | hp2 | a0001 | c0001 | t0020 | g0170 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0118 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0064 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0153 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0053 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0099 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03710 | hp2 | a0001 | c0001 | t0019 | g0098 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0021 | SAS | STU | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG04115 | hp2 | a0001 | c0001 | t0013 | g0121 | SAS | STU | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | YRI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0148 | AFR | LWK | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0129 | AFR | LWK | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0058 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20129 | hp1 | a0001 | c0006 | t0001 | g0108 | AFR | ASW | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0071 | EUR | TSI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0025 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | USA | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | USA | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | USA | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | USA | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | LWK | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0096 | REF | REF | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:45422749
|
AGGCGGCG others(11): Show |
A | 1 | a0002 | 2 | HG01192.hp2 HG01255.hp1 |
disruptive_inframe_deletion | MODERATE | c.243_260delGGCGGCTG others(10): Show |
p.Ala82_Ala87del | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/9 | 440/5540 | 243/1566 | 81/521 | INFO_REALIGN_3_PRIME | chr6 | 45422749 | |
| chr6:45431974
|
G | C | 1 | a0003 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.535G>C | p.Val179Leu | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/9 | 732/5540 | 535/1566 | 179/521 | chr6 | 45431974 | ||
| chr6:45547270
|
G | A | 1 | a0004 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1531G>A | p.Gly511Ser | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 1728/5540 | 1531/1566 | 511/521 | chr6 | 45547270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:45422693
|
A | G | 1 | a0001c0007 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.159A>G | p.Gln53Gln | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/9 | 356/5540 | 159/1566 | 53/521 | chr6 | 45422693 | ||
| chr6:45422774
|
G | A | 1 | a0001c0002 | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
synonymous_variant | LOW | c.240G>A | p.Ala80Ala | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/9 | 437/5540 | 240/1566 | 80/521 | chr6 | 45422774 | ||
| chr6:45438029
|
A | G | 1 | a0001c0006 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.663A>G | p.Val221Val | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/9 | 860/5540 | 663/1566 | 221/521 | chr6 | 45438029 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:45547583
|
G | A | 1 | a0001c0001t0010 | 2 | HG01884.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*278G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 278 | chr6 | 45547583 | |||||
| chr6:45547896
|
GT | G | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(5): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*608delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 608 | INFO_REALIGN_3_PRIME | chr6 | 45547896 | ||||
| chr6:45547904
|
T | G | 3 | a0001c0001t0003a0001c0001t0012a0001c0002t0003 | 18 | HG00323.hp1 HG01243.hp2 HG01346.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*599T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 599 | chr6 | 45547904 | |||||
| chr6:45547913
|
T | C | 1 | a0001c0001t0013 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*608T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 608 | chr6 | 45547913 | |||||
| chr6:45548389
|
C | A | 1 | a0001c0001t0014 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1084C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 1084 | chr6 | 45548389 | |||||
| chr6:45548609
|
A | G | 1 | a0001c0001t0021 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1304A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 1304 | chr6 | 45548609 | |||||
| chr6:45548753
|
C | T | 2 | a0001c0001t0009a0001c0001t0020 | 4 | HG02109.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1448C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 1448 | chr6 | 45548753 | |||||
| chr6:45549067
|
G | C | 2 | a0001c0001t0007a0001c0001t0017 | 5 | HG01891.hp1 HG02647.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1762G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 1762 | chr6 | 45549067 | |||||
| chr6:45549164
|
A | G | 1 | a0001c0001t0009 | 3 | HG02109.hp1 HG02717.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1859A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 1859 | chr6 | 45549164 | |||||
| chr6:45549224
|
C | T | 1 | a0001c0001t0008 | 3 | HG01243.hp1 HG02723.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1919C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 1919 | chr6 | 45549224 | |||||
| chr6:45549306
|
G | A | 1 | a0001c0002t0015 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2001G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 2001 | chr6 | 45549306 | |||||
| chr6:45550002
|
CT | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2712delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 2712 | INFO_REALIGN_3_PRIME | chr6 | 45550002 | ||||
| chr6:45550143
|
G | C | 1 | a0001c0001t0011 | 2 | HG02922.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2838G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 2838 | chr6 | 45550143 | |||||
| chr6:45550343
|
C | G | 1 | a0001c0001t0018 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3038C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 3038 | chr6 | 45550343 | |||||
| chr6:45550464
|
C | T | 1 | a0001c0001t0016 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3159C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 3159 | chr6 | 45550464 | |||||
| chr6:45550465
|
G | T | 4 | a0001c0001t0004a0001c0001t0005a0001c0002t0004others(1): Show | 20 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3160G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 3160 | chr6 | 45550465 | |||||
| chr6:45550650
|
G | A | 1 | a0001c0001t0019 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3345G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 3345 | chr6 | 45550650 | |||||
| chr6:45550897
|
A | G | 2 | a0001c0001t0006a0001c0002t0006 | 6 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3592A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 9/9 | 3592 | chr6 | 45550897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:45328881
|
T | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+97T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45328881 | ||||||
| chr6:45329246
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.58+462T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45329246 | ||||||
| chr6:45329250
|
T | C | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+466T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45329250 | ||||||
| chr6:45329572
|
G | A | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0007t0001g0028 | 3 | HG00597.hp1 HG01928.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58+788G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45329572 | ||||||
| chr6:45329917
|
T | C | 1 | a0001c0001t0006g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.58+1133T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45329917 | ||||||
| chr6:45330062
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.58+1278G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330062 | ||||||
| chr6:45330070
|
A | G | 1 | a0001c0001t0004g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.58+1286A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330070 | ||||||
| chr6:45330105
|
C | G | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+1321C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330105 | ||||||
| chr6:45330343
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+1559C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330343 | ||||||
| chr6:45330467
|
C | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+1683C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330467 | ||||||
| chr6:45330711
|
T | G | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58+1927T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330711 | ||||||
| chr6:45330745
|
G | A | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.58+1961G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330745 | ||||||
| chr6:45330794
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+2010C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330794 | ||||||
| chr6:45330911
|
T | A | 33 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(30): Show | 33 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+2127T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330911 | ||||||
| chr6:45330912
|
C | T | 33 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(30): Show | 33 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+2128C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330912 | ||||||
| chr6:45331104
|
G | GGT | 55 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.58+2342_58+2343dup others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45331104 | |||||
| chr6:45331104
|
G | GGTGT | 8 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+2340_58+2343dup others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45331104 | |||||
| chr6:45331104
|
GGT | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.58+2342_58+2343del others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45331104 | |||||
| chr6:45331124
|
TGTGC | T | 3 | a0001c0001t0001g0022a0001c0001t0007g0023a0001c0001t0010g0002 | 3 | HG01884.hp1 HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+2342_58+2345del others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45331124 | |||||
| chr6:45331126
|
T | C | 2 | a0001c0001t0002g0033a0001c0001t0011g0018 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.58+2342T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331126 | ||||||
| chr6:45331126
|
T | TGC | 3 | a0001c0001t0003g0105a0001c0001t0007g0036a0001c0001t0014g0035 | 3 | HG01934.hp2 HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.58+2355_58+2356dup others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45331126 | |||||
| chr6:45331126
|
TGC | T | 8 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG01069.hp1 HG01891.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+2355_58+2356del others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45331126 | |||||
| chr6:45331128
|
C | T | 70 | a0001c0001t0001g0057a0001c0001t0001g0106a0001c0001t0001g0110others(67): Show | 70 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.58+2344C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331128 | ||||||
| chr6:45331129
|
G | T | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+2345G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331129 | ||||||
| chr6:45331160
|
T | C | 10 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(7): Show | 10 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+2376T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331160 | ||||||
| chr6:45331437
|
G | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+2653G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331437 | ||||||
| chr6:45331711
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+2927G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331711 | ||||||
| chr6:45331890
|
A | C | 1 | a0001c0001t0001g0136 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.58+3106A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331890 | ||||||
| chr6:45331900
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.58+3116C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45331900 | ||||||
| chr6:45332087
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.58+3303C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332087 | ||||||
| chr6:45332088
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3304G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332088 | ||||||
| chr6:45332244
|
C | T | 31 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(28): Show | 31 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.58+3460C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332244 | ||||||
| chr6:45332346
|
G | GTA | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(17): Show | 20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+3572_58+3573dup others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45332346 | |||||
| chr6:45332360
|
A | T | 2 | a0002c0003t0001g0161a0002c0003t0001g0162 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.58+3576A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332360 | ||||||
| chr6:45332542
|
T | A | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+3758T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332542 | ||||||
| chr6:45332659
|
T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+3875T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332659 | ||||||
| chr6:45332698
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.58+3914T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332698 | ||||||
| chr6:45332843
|
T | G | 1 | a0001c0001t0003g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58+4059T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332843 | ||||||
| chr6:45332862
|
A | T | 3 | a0001c0001t0001g0056a0001c0001t0004g0059a0001c0001t0005g0055 | 3 | HG00735.hp1 HG01952.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.58+4078A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332862 | ||||||
| chr6:45332891
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0103 | 2 | NA18965.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.58+4107C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332891 | ||||||
| chr6:45332934
|
T | C | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+4150T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45332934 | ||||||
| chr6:45333214
|
T | A | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+4430T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45333214 | ||||||
| chr6:45333273
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0002g0133 | 2 | HG01255.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.58+4489G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45333273 | ||||||
| chr6:45333333
|
A | G | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+4549A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45333333 | ||||||
| chr6:45334051
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+5267T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334051 | ||||||
| chr6:45334068
|
A | G | 43 | a0001c0001t0001g0057a0001c0001t0001g0106a0001c0001t0001g0110others(40): Show | 43 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.58+5284A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334068 | ||||||
| chr6:45334114
|
C | A | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+5330C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334114 | ||||||
| chr6:45334180
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+5396T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334180 | ||||||
| chr6:45334449
|
C | CA | 7 | a0001c0001t0001g0070a0001c0001t0001g0119a0001c0001t0001g0146others(4): Show | 7 | HG01192.hp2 HG01978.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+5685dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45334449 | |||||
| chr6:45334449
|
CA | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.58+5685delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45334449 | |||||
| chr6:45334449
|
CAA | C | 30 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(27): Show | 30 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.58+5684_58+5685del others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45334449 | |||||
| chr6:45334567
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+5783G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334567 | ||||||
| chr6:45334791
|
AC | A | 44 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(41): Show | 44 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.58+6008delC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334791 | ||||||
| chr6:45334811
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+6027T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334811 | ||||||
| chr6:45334822
|
T | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58+6038T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334822 | ||||||
| chr6:45334871
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58+6087G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334871 | ||||||
| chr6:45334898
|
G | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+6114G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334898 | ||||||
| chr6:45334917
|
A | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.58+6133A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45334917 | ||||||
| chr6:45335637
|
A | G | 1 | a0001c0001t0008g0160 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.58+6853A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45335637 | ||||||
| chr6:45335756
|
T | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+6972T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45335756 | ||||||
| chr6:45335976
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.58+7192A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45335976 | ||||||
| chr6:45336116
|
C | A | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(49): Show | 52 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.58+7332C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45336116 | ||||||
| chr6:45336183
|
C | CT | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+7401dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45336183 | |||||
| chr6:45336317
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58+7533A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45336317 | ||||||
| chr6:45336323
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.58+7539C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45336323 | ||||||
| chr6:45336738
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+7954T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45336738 | ||||||
| chr6:45336829
|
C | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+8045C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45336829 | ||||||
| chr6:45337060
|
A | T | 2 | a0001c0001t0001g0167a0001c0001t0002g0166 | 2 | HG02145.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.58+8276A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45337060 | ||||||
| chr6:45337468
|
G | A | 1 | a0001c0007t0001g0028 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.58+8684G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45337468 | ||||||
| chr6:45337730
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+8946G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45337730 | ||||||
| chr6:45337857
|
T | C | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+9073T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45337857 | ||||||
| chr6:45338344
|
TA | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.58+9572delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45338344 | |||||
| chr6:45338356
|
A | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+9572A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45338356 | ||||||
| chr6:45338370
|
C | G | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+9586C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45338370 | ||||||
| chr6:45338495
|
T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+9711T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45338495 | ||||||
| chr6:45338634
|
A | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+9850A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45338634 | ||||||
| chr6:45338734
|
C | T | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+9950C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45338734 | ||||||
| chr6:45338796
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+10012T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45338796 | ||||||
| chr6:45338825
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+10041C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45338825 | ||||||
| chr6:45339368
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+10584A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339368 | ||||||
| chr6:45339397
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58+10613A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339397 | ||||||
| chr6:45339617
|
TAC | T | 7 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG01255.hp2 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+10835_58+10836d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45339617 | |||||
| chr6:45339642
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+10858T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339642 | ||||||
| chr6:45339646
|
C | G | 5 | a0001c0001t0001g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02965.hp2 HG03225.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+10862C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339646 | ||||||
| chr6:45339706
|
C | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.58+10922C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339706 | ||||||
| chr6:45339801
|
A | G | 1 | a0001c0002t0004g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.58+11017A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339801 | ||||||
| chr6:45339802
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+11018T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339802 | ||||||
| chr6:45339945
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(17): Show | 20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+11161C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339945 | ||||||
| chr6:45340169
|
A | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+11385A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45340169 | ||||||
| chr6:45340298
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.58+11514A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45340298 | ||||||
| chr6:45340338
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+11554C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45340338 | ||||||
| chr6:45340570
|
C | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+11786C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45340570 | ||||||
| chr6:45340709
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+11925A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45340709 | ||||||
| chr6:45340785
|
C | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+12001C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45340785 | ||||||
| chr6:45341446
|
C | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0003g0147others(1): Show | 4 | HG00323.hp1 HG01934.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+12662C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341446 | ||||||
| chr6:45341469
|
T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+12685T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341469 | ||||||
| chr6:45341504
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+12720A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341504 | ||||||
| chr6:45341824
|
A | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+13040A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341824 | ||||||
| chr6:45341880
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.58+13096G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341880 | ||||||
| chr6:45341895
|
T | G | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+13111T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341895 | ||||||
| chr6:45341984
|
A | C | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG01928.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58+13200A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341984 | ||||||
| chr6:45341998
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+13214C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45341998 | ||||||
| chr6:45342007
|
A | C | 4 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0003g0147others(1): Show | 4 | HG00323.hp1 HG01934.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+13223A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342007 | ||||||
| chr6:45342065
|
AC | A | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+13282delC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342065 | ||||||
| chr6:45342418
|
C | T | 2 | a0002c0003t0001g0161a0002c0003t0001g0162 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.58+13634C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342418 | ||||||
| chr6:45342528
|
C | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.58+13744C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342528 | ||||||
| chr6:45342548
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+13764G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342548 | ||||||
| chr6:45342740
|
TTAA | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+13958_58+13960d others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45342740 | |||||
| chr6:45342788
|
T | C | 6 | a0001c0001t0001g0073a0001c0001t0001g0104a0001c0001t0003g0074others(3): Show | 6 | HG00099.hp2 HG01071.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+14004T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342788 | ||||||
| chr6:45342896
|
T | C | 2 | a0001c0001t0002g0032a0001c0001t0010g0002 | 2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.58+14112T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342896 | ||||||
| chr6:45343413
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.58+14629C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45343413 | ||||||
| chr6:45343552
|
GAGA | G | 10 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(7): Show | 10 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+14771_58+14773d others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45343552 | |||||
| chr6:45343569
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58+14785A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45343569 | ||||||
| chr6:45343906
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.58+15122T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45343906 | ||||||
| chr6:45344068
|
A | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58+15284A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344068 | ||||||
| chr6:45344091
|
G | A | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+15307G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344091 | ||||||
| chr6:45344190
|
G | A | 1 | a0001c0001t0006g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.58+15406G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344190 | ||||||
| chr6:45344307
|
T | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00423.hp2 NA18747.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+15523T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344307 | ||||||
| chr6:45344436
|
G | GT | 7 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG01255.hp2 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+15662dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45344436 | |||||
| chr6:45344493
|
G | T | 1 | a0001c0001t0009g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58+15709G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344493 | ||||||
| chr6:45344495
|
G | A | 8 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 8 | HG00438.hp2 HG03704.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+15711G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344495 | ||||||
| chr6:45344499
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+15715C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344499 | ||||||
| chr6:45344504
|
T | C | 1 | a0001c0001t0009g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58+15720T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344504 | ||||||
| chr6:45344525
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+15741G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344525 | ||||||
| chr6:45344951
|
A | G | 7 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG01255.hp2 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+16167A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45344951 | ||||||
| chr6:45345105
|
A | G | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+16321A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45345105 | ||||||
| chr6:45345106
|
T | G | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58+16322T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45345106 | ||||||
| chr6:45345351
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58+16567C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45345351 | ||||||
| chr6:45345412
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.58+16628C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45345412 | ||||||
| chr6:45345791
|
T | C | 1 | a0001c0002t0004g0060 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.58+17007T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45345791 | ||||||
| chr6:45345939
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0002g0111 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.58+17155C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45345939 | ||||||
| chr6:45345986
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+17202C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45345986 | ||||||
| chr6:45346007
|
T | C | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+17223T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346007 | ||||||
| chr6:45346054
|
G | A | 1 | a0001c0001t0010g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+17270G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346054 | ||||||
| chr6:45346172
|
ATT | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+17389_58+17390d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346172 | ||||||
| chr6:45346210
|
CTT | C | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+17427_58+17428d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346210 | ||||||
| chr6:45346215
|
G | A | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+17431G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346215 | ||||||
| chr6:45346229
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.58+17445A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346229 | ||||||
| chr6:45346567
|
C | CT | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.58+17798dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45346567 | |||||
| chr6:45346567
|
C | CTTTT | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+17795_58+17798d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45346567 | |||||
| chr6:45346807
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.58+18023C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346807 | ||||||
| chr6:45346948
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.58+18164G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45346948 | ||||||
| chr6:45347156
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.58+18372A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347156 | ||||||
| chr6:45347591
|
T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+18807T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347591 | ||||||
| chr6:45347613
|
G | C | 43 | a0001c0001t0001g0057a0001c0001t0001g0106a0001c0001t0001g0110others(40): Show | 43 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.58+18829G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347613 | ||||||
| chr6:45347767
|
A | T | 2 | a0001c0001t0001g0054a0001c0001t0002g0125 | 2 | HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58+18983A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347767 | ||||||
| chr6:45347798
|
CTGTT | C | 44 | a0001c0001t0001g0057a0001c0001t0001g0100a0001c0001t0001g0106others(41): Show | 44 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.58+19018_58+19021d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45347798 | |||||
| chr6:45347816
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.58+19032G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347816 | ||||||
| chr6:45347836
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0004g0053a0001c0001t0006g0037 | 3 | HG01167.hp1 HG01258.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58+19052A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347836 | ||||||
| chr6:45347864
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+19080A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347864 | ||||||
| chr6:45347888
|
A | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+19104A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45347888 | ||||||
| chr6:45348008
|
T | C | 31 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(28): Show | 31 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.58+19224T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45348008 | ||||||
| chr6:45348030
|
CAT | C | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+19247_58+19248d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45348030 | ||||||
| chr6:45348445
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.58+19661T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45348445 | ||||||
| chr6:45348465
|
C | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.58+19681C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45348465 | ||||||
| chr6:45348512
|
C | CA | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+19740dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45348512 | |||||
| chr6:45348512
|
C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+19730_58+19740d others(13): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45348512 | |||||
| chr6:45348512
|
C | CAAAAAAA others(5): Show |
81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.58+19729_58+19740d others(14): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45348512 | |||||
| chr6:45348512
|
C | CAAAAAAA others(6): Show |
11 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0003g0029others(8): Show | 11 | HG00735.hp2 HG01928.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+19740_58+19741i others(15): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45348512 | |||||
| chr6:45348512
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+19740_58+19741i others(18): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45348512 | |||||
| chr6:45348544
|
G | A | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+19760G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45348544 | ||||||
| chr6:45348674
|
C | CA | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+19908dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45348674 | |||||
| chr6:45348931
|
C | A | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+20147C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45348931 | ||||||
| chr6:45348984
|
A | T | 31 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(28): Show | 31 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.58+20200A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45348984 | ||||||
| chr6:45349174
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+20390A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45349174 | ||||||
| chr6:45349426
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+20642T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45349426 | ||||||
| chr6:45349485
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.58+20701G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45349485 | ||||||
| chr6:45349492
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.58+20708T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45349492 | ||||||
| chr6:45349719
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+20935A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45349719 | ||||||
| chr6:45349843
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.58+21059A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45349843 | ||||||
| chr6:45349848
|
C | T | 1 | a0001c0001t0018g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58+21064C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45349848 | ||||||
| chr6:45350144
|
T | G | 1 | a0001c0001t0004g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.58+21360T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350144 | ||||||
| chr6:45350258
|
C | G | 1 | a0001c0001t0011g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.58+21474C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350258 | ||||||
| chr6:45350265
|
A | T | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+21481A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350265 | ||||||
| chr6:45350284
|
A | G | 2 | a0001c0002t0006g0015a0001c0002t0006g0016 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.58+21500A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350284 | ||||||
| chr6:45350512
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+21728T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350512 | ||||||
| chr6:45350688
|
C | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+21904C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350688 | ||||||
| chr6:45350906
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+22122G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350906 | ||||||
| chr6:45350984
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+22200A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45350984 | ||||||
| chr6:45351013
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0002g0126a0001c0001t0007g0118 | 3 | HG02886.hp2 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.58+22229G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351013 | ||||||
| chr6:45351028
|
C | A | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+22244C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351028 | ||||||
| chr6:45351127
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.58+22343C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351127 | ||||||
| chr6:45351133
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58+22349T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351133 | ||||||
| chr6:45351226
|
A | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0001g0175others(14): Show | 17 | HG01891.hp2 HG02622.hp2 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.58+22442A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351226 | ||||||
| chr6:45351320
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0169a0001c0001t0009g0168 | 3 | HG02630.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+22536A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351320 | ||||||
| chr6:45351814
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+23030T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351814 | ||||||
| chr6:45351933
|
C | T | 1 | a0001c0001t0010g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+23149C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45351933 | ||||||
| chr6:45352002
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58+23218T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352002 | ||||||
| chr6:45352067
|
T | A | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.58+23283T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352067 | ||||||
| chr6:45352139
|
C | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.58+23355C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352139 | ||||||
| chr6:45352257
|
A | G | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+23473A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352257 | ||||||
| chr6:45352354
|
G | A | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+23570G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352354 | ||||||
| chr6:45352420
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+23636T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352420 | ||||||
| chr6:45352659
|
T | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+23875T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352659 | ||||||
| chr6:45352731
|
G | T | 1 | a0001c0001t0003g0051 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.58+23947G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352731 | ||||||
| chr6:45352755
|
GTA | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+23973_58+23974d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45352755 | |||||
| chr6:45352763
|
A | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.58+23979A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352763 | ||||||
| chr6:45352783
|
T | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(19): Show | 22 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.58+23999T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352783 | ||||||
| chr6:45353057
|
T | C | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.58+24273T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353057 | ||||||
| chr6:45353079
|
CATT | C | 3 | a0001c0001t0002g0033a0001c0001t0007g0036a0001c0001t0014g0035 | 3 | HG02145.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58+24297_58+24299d others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45353079 | |||||
| chr6:45353316
|
T | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0002g0115 | 3 | HG02647.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.58+24532T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353316 | ||||||
| chr6:45353340
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+24556T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353340 | ||||||
| chr6:45353391
|
T | C | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.58+24607T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353391 | ||||||
| chr6:45353453
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+24669C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353453 | ||||||
| chr6:45353468
|
C | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+24684C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353468 | ||||||
| chr6:45353718
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+24934G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353718 | ||||||
| chr6:45353725
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0004g0021 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.58+24941A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353725 | ||||||
| chr6:45353809
|
T | C | 44 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(41): Show | 44 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.58+25025T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353809 | ||||||
| chr6:45353842
|
G | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+25058G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353842 | ||||||
| chr6:45353997
|
A | G | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+25213A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353997 | ||||||
| chr6:45354043
|
T | C | 1 | a0001c0002t0004g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.58+25259T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45354043 | ||||||
| chr6:45354276
|
T | C | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+25492T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45354276 | ||||||
| chr6:45354380
|
A | G | 4 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0173others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+25596A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45354380 | ||||||
| chr6:45354486
|
C | T | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+25702C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45354486 | ||||||
| chr6:45354544
|
TCA | T | 24 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0146others(21): Show | 24 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.58+25761_58+25762d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45354544 | ||||||
| chr6:45354630
|
TAC | T | 45 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(42): Show | 45 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.58+25868_58+25869d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45354630 | |||||
| chr6:45354630
|
TACAC | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(22): Show | 25 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.58+25866_58+25869d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45354630 | |||||
| chr6:45354630
|
TACACAC | T | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+25864_58+25869d others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45354630 | |||||
| chr6:45354646
|
C | T | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+25862C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45354646 | ||||||
| chr6:45354955
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+26171A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45354955 | ||||||
| chr6:45355138
|
C | CT | 5 | a0001c0001t0001g0050a0001c0001t0002g0111a0001c0001t0002g0173others(2): Show | 5 | HG00609.hp2 HG01891.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+26370dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45355138 | |||||
| chr6:45355154
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.58+26370T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45355154 | ||||||
| chr6:45355417
|
AT | A | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+26634delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45355417 | ||||||
| chr6:45355429
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.58+26645C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45355429 | ||||||
| chr6:45355590
|
T | C | 1 | a0001c0002t0001g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.58+26806T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45355590 | ||||||
| chr6:45355782
|
C | G | 2 | a0001c0001t0001g0146a0001c0001t0003g0147 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.58+26998C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45355782 | ||||||
| chr6:45355863
|
T | A | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+27079T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45355863 | ||||||
| chr6:45356157
|
G | T | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+27373G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45356157 | ||||||
| chr6:45356201
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+27417T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45356201 | ||||||
| chr6:45356388
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0003g0147 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.58+27604A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45356388 | ||||||
| chr6:45356599
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58+27815C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45356599 | ||||||
| chr6:45356607
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+27823G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45356607 | ||||||
| chr6:45357107
|
C | T | 44 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(41): Show | 44 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.58+28323C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357107 | ||||||
| chr6:45357156
|
G | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+28372G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357156 | ||||||
| chr6:45357210
|
T | A | 1 | a0001c0001t0007g0036 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.58+28426T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357210 | ||||||
| chr6:45357220
|
G | C | 1 | a0001c0001t0003g0102 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.58+28436G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357220 | ||||||
| chr6:45357254
|
A | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.58+28470A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357254 | ||||||
| chr6:45357272
|
G | T | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.58+28488G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357272 | ||||||
| chr6:45357302
|
C | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+28518C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357302 | ||||||
| chr6:45357414
|
G | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+28630G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357414 | ||||||
| chr6:45357449
|
GC | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+28667delC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45357449 | |||||
| chr6:45357535
|
G | A | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+28751G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357535 | ||||||
| chr6:45357840
|
G | C | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.58+29056G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357840 | ||||||
| chr6:45357884
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+29100A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357884 | ||||||
| chr6:45357895
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.58+29111A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357895 | ||||||
| chr6:45357991
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.58+29207A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357991 | ||||||
| chr6:45358082
|
T | TAAAAAAG others(6094): Show |
1 | a0001c0001t0002g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.58+29315_58+29316i others(6103): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45358082 | |||||
| chr6:45358082
|
T | TAAAAAAG others(6094): Show |
1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.58+29315_58+29316i others(6103): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45358082 | |||||
| chr6:45358082
|
T | TAAAAAAG others(6093): Show |
1 | a0001c0001t0007g0036 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.58+29315_58+29316i others(6102): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45358082 | |||||
| chr6:45358314
|
T | C | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+29530T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45358314 | ||||||
| chr6:45358377
|
C | T | 24 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0146others(21): Show | 24 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.58+29593C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45358377 | ||||||
| chr6:45358477
|
A | T | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.58+29693A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45358477 | ||||||
| chr6:45358748
|
C | G | 3 | a0001c0001t0001g0119a0001c0001t0002g0126a0001c0001t0007g0118 | 3 | HG02886.hp2 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.58+29964C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45358748 | ||||||
| chr6:45358807
|
G | A | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+30023G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45358807 | ||||||
| chr6:45358954
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0103 | 2 | NA18965.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.58+30170G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45358954 | ||||||
| chr6:45359125
|
T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+30341T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45359125 | ||||||
| chr6:45359492
|
T | C | 5 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+30708T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45359492 | ||||||
| chr6:45359499
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58+30715T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45359499 | ||||||
| chr6:45359541
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.58+30757A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45359541 | ||||||
| chr6:45359664
|
G | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.58+30880G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45359664 | ||||||
| chr6:45359730
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+30946G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45359730 | ||||||
| chr6:45359955
|
A | G | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+31171A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45359955 | ||||||
| chr6:45360382
|
C | A | 3 | a0001c0001t0002g0033a0001c0001t0007g0036a0001c0001t0014g0035 | 3 | HG02145.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58+31598C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360382 | ||||||
| chr6:45360420
|
G | C | 28 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.58+31636G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360420 | ||||||
| chr6:45360528
|
A | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+31744A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360528 | ||||||
| chr6:45360670
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+31886T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360670 | ||||||
| chr6:45360676
|
T | C | 3 | a0001c0001t0001g0119a0001c0001t0002g0126a0001c0001t0007g0118 | 3 | HG02886.hp2 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.58+31892T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360676 | ||||||
| chr6:45360829
|
C | T | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.58+32045C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360829 | ||||||
| chr6:45360887
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+32103C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360887 | ||||||
| chr6:45360889
|
T | G | 1 | a0001c0001t0010g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+32105T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45360889 | ||||||
| chr6:45361004
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0143 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.58+32220G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361004 | ||||||
| chr6:45361010
|
T | C | 2 | a0001c0002t0006g0015a0001c0002t0006g0016 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.58+32226T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361010 | ||||||
| chr6:45361210
|
T | C | 31 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(28): Show | 31 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.58+32426T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361210 | ||||||
| chr6:45361311
|
C | A | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+32527C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361311 | ||||||
| chr6:45361456
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+32672A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361456 | ||||||
| chr6:45361639
|
G | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+32855G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361639 | ||||||
| chr6:45361752
|
C | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+32968C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361752 | ||||||
| chr6:45361878
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+33094C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361878 | ||||||
| chr6:45361919
|
C | T | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(33): Show | 36 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.58+33135C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361919 | ||||||
| chr6:45362274
|
T | C | 1 | a0001c0001t0010g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+33490T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45362274 | ||||||
| chr6:45362526
|
T | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+33742T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45362526 | ||||||
| chr6:45362843
|
G | GT | 44 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(41): Show | 44 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.58+34066dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45362843 | |||||
| chr6:45362883
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58+34099T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45362883 | ||||||
| chr6:45363001
|
G | C | 2 | a0001c0001t0004g0053a0001c0001t0006g0037 | 2 | HG01167.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58+34217G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363001 | ||||||
| chr6:45363017
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.58+34233A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363017 | ||||||
| chr6:45363051
|
A | C | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+34267A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363051 | ||||||
| chr6:45363084
|
A | C | 2 | a0002c0003t0001g0161a0002c0003t0001g0162 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.58+34300A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363084 | ||||||
| chr6:45363134
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58+34350C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363134 | ||||||
| chr6:45363155
|
A | G | 2 | a0001c0001t0003g0074a0001c0001t0006g0075 | 2 | HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.58+34371A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363155 | ||||||
| chr6:45363237
|
T | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+34453T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363237 | ||||||
| chr6:45363566
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.58+34782T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363566 | ||||||
| chr6:45363732
|
T | A | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+34948T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363732 | ||||||
| chr6:45363829
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+35045T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363829 | ||||||
| chr6:45363960
|
C | T | 1 | a0001c0001t0003g0150 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.58+35176C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45363960 | ||||||
| chr6:45364028
|
T | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+35244T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45364028 | ||||||
| chr6:45364036
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+35252A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45364036 | ||||||
| chr6:45364114
|
CA | C | 106 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(103): Show | 106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.58+35343delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45364114 | |||||
| chr6:45364186
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.58+35402T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45364186 | ||||||
| chr6:45364208
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+35424A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45364208 | ||||||
| chr6:45364522
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58+35738T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45364522 | ||||||
| chr6:45364545
|
CTATG | C | 44 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(41): Show | 44 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.58+35763_58+35766d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45364545 | |||||
| chr6:45364568
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+35784A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45364568 | ||||||
| chr6:45365048
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+36264G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45365048 | ||||||
| chr6:45365447
|
C | T | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+36663C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45365447 | ||||||
| chr6:45365884
|
T | TATG | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+37102_58+37103i others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45365884 | |||||
| chr6:45365915
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.58+37131A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45365915 | ||||||
| chr6:45365990
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58+37206T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45365990 | ||||||
| chr6:45366155
|
A | C | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58+37371A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45366155 | ||||||
| chr6:45366237
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+37453T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45366237 | ||||||
| chr6:45366244
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+37460G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45366244 | ||||||
| chr6:45366370
|
TA | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.58+37589delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45366370 | |||||
| chr6:45366519
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.58+37735G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45366519 | ||||||
| chr6:45366629
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.58+37845A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45366629 | ||||||
| chr6:45366800
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+38016G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45366800 | ||||||
| chr6:45367237
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+38453C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367237 | ||||||
| chr6:45367334
|
G | A | 1 | a0001c0001t0005g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.58+38550G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367334 | ||||||
| chr6:45367357
|
T | G | 1 | a0001c0001t0003g0102 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.58+38573T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367357 | ||||||
| chr6:45367601
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+38817T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367601 | ||||||
| chr6:45367645
|
G | A | 1 | a0001c0001t0011g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.58+38861G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367645 | ||||||
| chr6:45367673
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+38889A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367673 | ||||||
| chr6:45367768
|
T | C | 1 | a0004c0005t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.58+38984T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367768 | ||||||
| chr6:45367894
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.58+39110A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367894 | ||||||
| chr6:45367964
|
T | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+39180T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45367964 | ||||||
| chr6:45368089
|
TAC | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+39307_58+39308d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45368089 | |||||
| chr6:45368221
|
G | C | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.58+39437G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45368221 | ||||||
| chr6:45368410
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.58+39626C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45368410 | ||||||
| chr6:45368886
|
C | A | 1 | a0001c0001t0003g0102 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.58+40102C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45368886 | ||||||
| chr6:45368986
|
GTCAA | G | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+40206_58+40209d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45368986 | |||||
| chr6:45369017
|
T | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+40233T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369017 | ||||||
| chr6:45369284
|
T | G | 1 | a0001c0001t0001g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.58+40500T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369284 | ||||||
| chr6:45369334
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+40550C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369334 | ||||||
| chr6:45369439
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.58+40655T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369439 | ||||||
| chr6:45369691
|
C | T | 3 | a0001c0002t0001g0044a0001c0002t0001g0045a0001c0002t0001g0046 | 3 | NA18955.hp1 NA18995.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.58+40907C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369691 | ||||||
| chr6:45369713
|
C | G | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+40929C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369713 | ||||||
| chr6:45369781
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58+40997C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369781 | ||||||
| chr6:45369895
|
C | A | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+41111C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369895 | ||||||
| chr6:45369912
|
C | G | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.58+41128C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45369912 | ||||||
| chr6:45370007
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+41223G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45370007 | ||||||
| chr6:45370047
|
G | T | 1 | a0001c0001t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.58+41263G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45370047 | ||||||
| chr6:45370199
|
G | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+41415G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45370199 | ||||||
| chr6:45370347
|
T | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+41563T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45370347 | ||||||
| chr6:45370419
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.58+41635T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45370419 | ||||||
| chr6:45370895
|
C | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+42111C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45370895 | ||||||
| chr6:45370966
|
T | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(10): Show | 13 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+42182T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45370966 | ||||||
| chr6:45371318
|
T | G | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58+42534T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45371318 | ||||||
| chr6:45371330
|
T | C | 24 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0146others(21): Show | 24 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.58+42546T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45371330 | ||||||
| chr6:45371394
|
C | CT | 31 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.58+42626dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45371394 | |||||
| chr6:45371394
|
CT | C | 9 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0169others(6): Show | 9 | HG01934.hp2 HG02109.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+42626delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45371394 | |||||
| chr6:45371961
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+43177G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45371961 | ||||||
| chr6:45371988
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.58+43204G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45371988 | ||||||
| chr6:45372114
|
T | C | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.58+43330T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372114 | ||||||
| chr6:45372206
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0004g0021a0001c0001t0005g0019 | 3 | HG01346.hp2 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.58+43422C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372206 | ||||||
| chr6:45372333
|
T | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+43549T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372333 | ||||||
| chr6:45372336
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.58+43552T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372336 | ||||||
| chr6:45372346
|
T | G | 3 | a0001c0002t0001g0044a0001c0002t0001g0045a0001c0002t0001g0046 | 3 | NA18955.hp1 NA18995.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.58+43562T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372346 | ||||||
| chr6:45372448
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.58+43664G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372448 | ||||||
| chr6:45372458
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+43674A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372458 | ||||||
| chr6:45372464
|
G | A | 1 | a0001c0001t0013g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.58+43680G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372464 | ||||||
| chr6:45372663
|
A | G | 44 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(41): Show | 44 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.58+43879A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372663 | ||||||
| chr6:45372747
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0002g0133 | 2 | HG01255.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.58+43963C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372747 | ||||||
| chr6:45372774
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+43990T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372774 | ||||||
| chr6:45372894
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+44110T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372894 | ||||||
| chr6:45372955
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+44171C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45372955 | ||||||
| chr6:45373008
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+44224T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45373008 | ||||||
| chr6:45373008
|
T | G | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.58+44224T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45373008 | ||||||
| chr6:45373460
|
TTAGCAG | T | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+44680_58+44685d others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45373460 | |||||
| chr6:45373547
|
G | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.58+44763G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45373547 | ||||||
| chr6:45373597
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58+44813G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45373597 | ||||||
| chr6:45373654
|
G | A | 2 | a0002c0003t0001g0161a0002c0003t0001g0162 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.58+44870G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45373654 | ||||||
| chr6:45373819
|
CT | C | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+45036delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45373819 | ||||||
| chr6:45373942
|
A | G | 1 | a0001c0001t0018g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58+45158A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45373942 | ||||||
| chr6:45374314
|
C | T | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.58+45530C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374314 | ||||||
| chr6:45374480
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.58+45696G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374480 | ||||||
| chr6:45374495
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+45711G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374495 | ||||||
| chr6:45374568
|
T | G | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(17): Show | 20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+45784T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374568 | ||||||
| chr6:45374617
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.58+45833C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374617 | ||||||
| chr6:45374657
|
CATAA | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0013 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.58+45875_58+45878d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45374657 | |||||
| chr6:45374717
|
A | G | 2 | a0001c0001t0004g0014a0004c0005t0001g0006 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.58+45933A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374717 | ||||||
| chr6:45374929
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+46145G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374929 | ||||||
| chr6:45374935
|
G | A | 2 | a0001c0001t0001g0073a0003c0004t0001g0072 | 2 | HG00099.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.58+46151G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45374935 | ||||||
| chr6:45375001
|
G | A | 1 | a0001c0001t0011g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.58+46217G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45375001 | ||||||
| chr6:45375122
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.58+46338G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45375122 | ||||||
| chr6:45375130
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.58+46346C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45375130 | ||||||
| chr6:45375549
|
A | AT | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+46776dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45375549 | |||||
| chr6:45375598
|
G | GC | 24 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0146others(21): Show | 24 | HG00323.hp1 HG01192.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.58+46816dupC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45375598 | |||||
| chr6:45375780
|
GTTCT | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-46810_59-46807d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45375780 | |||||
| chr6:45375826
|
T | TA | 10 | a0001c0001t0001g0106a0001c0001t0001g0122a0001c0001t0001g0164others(7): Show | 10 | HG00741.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-46755dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45375826 | |||||
| chr6:45375911
|
A | T | 1 | a0001c0001t0010g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-46682A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45375911 | ||||||
| chr6:45376096
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-46497T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45376096 | ||||||
| chr6:45376134
|
T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.59-46459T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45376134 | ||||||
| chr6:45376180
|
CTTTAA | C | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.59-46409_59-46405d others(7): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45376180 | |||||
| chr6:45376198
|
T | A | 2 | a0001c0001t0003g0154a0001c0001t0016g0153 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.59-46395T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45376198 | ||||||
| chr6:45376267
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-46326T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45376267 | ||||||
| chr6:45376864
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0007g0036a0001c0001t0014g0035 | 3 | HG02145.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.59-45729T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45376864 | ||||||
| chr6:45376870
|
T | TACATATA others(39): Show |
1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-45718_59-45673d others(48): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45376870 | |||||
| chr6:45376910
|
T | C | 4 | a0001c0001t0002g0017a0001c0001t0009g0025a0001c0002t0001g0026others(1): Show | 4 | HG02109.hp1 HG02602.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-45683T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45376910 | ||||||
| chr6:45376923
|
C | G | 2 | a0001c0001t0001g0057a0001c0001t0002g0133 | 2 | HG01255.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.59-45670C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45376923 | ||||||
| chr6:45377100
|
TCA | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-45490_59-45489d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45377100 | |||||
| chr6:45377117
|
T | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-45476T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377117 | ||||||
| chr6:45377402
|
A | C | 2 | a0001c0001t0001g0119a0001c0001t0007g0118 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.59-45191A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377402 | ||||||
| chr6:45377443
|
C | A | 1 | a0001c0001t0011g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-45150C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377443 | ||||||
| chr6:45377470
|
C | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-45123C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377470 | ||||||
| chr6:45377511
|
A | C | 134 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(131): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.59-45082A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377511 | ||||||
| chr6:45377620
|
A | T | 2 | a0001c0001t0001g0020a0001c0001t0004g0021 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.59-44973A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377620 | ||||||
| chr6:45377640
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-44953C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377640 | ||||||
| chr6:45377660
|
G | A | 1 | a0001c0002t0001g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-44933G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377660 | ||||||
| chr6:45377688
|
A | G | 7 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG01255.hp2 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-44905A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377688 | ||||||
| chr6:45377743
|
C | T | 43 | a0001c0001t0001g0057a0001c0001t0001g0106a0001c0001t0001g0110others(40): Show | 43 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.59-44850C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377743 | ||||||
| chr6:45377837
|
C | T | 1 | a0001c0001t0005g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.59-44756C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377837 | ||||||
| chr6:45377908
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-44685G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377908 | ||||||
| chr6:45377922
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.59-44671G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377922 | ||||||
| chr6:45377952
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-44641G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377952 | ||||||
| chr6:45377994
|
T | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-44599T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45377994 | ||||||
| chr6:45378007
|
G | C | 1 | a0001c0001t0003g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.59-44586G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45378007 | ||||||
| chr6:45378225
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-44368C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45378225 | ||||||
| chr6:45378419
|
G | A | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-44174G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45378419 | ||||||
| chr6:45378530
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-44063A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45378530 | ||||||
| chr6:45378661
|
C | CT | 7 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0062others(4): Show | 7 | HG01261.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-43918dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45378661 | |||||
| chr6:45378828
|
C | A | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-43765C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45378828 | ||||||
| chr6:45379098
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0005g0011a0001c0001t0006g0001others(1): Show | 4 | HG00280.hp1 HG00733.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-43495C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45379098 | ||||||
| chr6:45379446
|
G | C | 1 | a0001c0001t0002g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.59-43147G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45379446 | ||||||
| chr6:45379616
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-42977C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45379616 | ||||||
| chr6:45379759
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.59-42834G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45379759 | ||||||
| chr6:45379907
|
G | A | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-42686G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45379907 | ||||||
| chr6:45380045
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-42548G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380045 | ||||||
| chr6:45380237
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-42356G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380237 | ||||||
| chr6:45380579
|
T | G | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59-42014T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380579 | ||||||
| chr6:45380582
|
A | G | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-42011A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380582 | ||||||
| chr6:45380680
|
G | A | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.59-41913G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380680 | ||||||
| chr6:45380724
|
G | T | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.59-41869G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380724 | ||||||
| chr6:45380738
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0007g0023 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.59-41855G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380738 | ||||||
| chr6:45380800
|
C | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-41793C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380800 | ||||||
| chr6:45380827
|
G | A | 25 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(22): Show | 25 | HG00438.hp2 HG01891.hp2 HG02622.hp2 others(22): Show |
intron_variant | MODIFIER | c.59-41766G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380827 | ||||||
| chr6:45380896
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-41697G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45380896 | ||||||
| chr6:45381184
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0002g0126a0001c0001t0007g0118 | 3 | HG02886.hp2 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.59-41409G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381184 | ||||||
| chr6:45381191
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-41402T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381191 | ||||||
| chr6:45381451
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.59-41142G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381451 | ||||||
| chr6:45381662
|
T | C | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.59-40931T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381662 | ||||||
| chr6:45381760
|
G | A | 28 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-40833G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381760 | ||||||
| chr6:45381761
|
T | A | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-40832T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381761 | ||||||
| chr6:45381772
|
A | G | 21 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(18): Show | 21 | HG01192.hp2 HG01255.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-40821A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381772 | ||||||
| chr6:45382125
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.59-40468G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45382125 | ||||||
| chr6:45382140
|
A | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-40453A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45382140 | ||||||
| chr6:45382370
|
A | G | 105 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.59-40223A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45382370 | ||||||
| chr6:45382738
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59-39855C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45382738 | ||||||
| chr6:45382741
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-39852A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45382741 | ||||||
| chr6:45382809
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.59-39784A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45382809 | ||||||
| chr6:45383008
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0007g0036a0001c0001t0014g0035 | 3 | HG02145.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.59-39585C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383008 | ||||||
| chr6:45383013
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-39580G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383013 | ||||||
| chr6:45383101
|
A | C | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.59-39492A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383101 | ||||||
| chr6:45383153
|
G | A | 1 | a0002c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.59-39440G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383153 | ||||||
| chr6:45383162
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0002g0131a0001c0001t0010g0129 | 3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.59-39431C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383162 | ||||||
| chr6:45383226
|
G | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-39367G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383226 | ||||||
| chr6:45383276
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.59-39317A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383276 | ||||||
| chr6:45383400
|
G | A | 1 | a0001c0001t0011g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59-39193G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383400 | ||||||
| chr6:45383632
|
A | G | 2 | a0001c0001t0004g0014a0004c0005t0001g0006 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.59-38961A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383632 | ||||||
| chr6:45383634
|
A | AT | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38953dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45383634 | |||||
| chr6:45383654
|
A | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.59-38939A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383654 | ||||||
| chr6:45383790
|
C | CATGTA | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38802_59-38801i others(7): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45383790 | |||||
| chr6:45383792
|
A | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38801A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383792 | ||||||
| chr6:45383794
|
A | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38799A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383794 | ||||||
| chr6:45383795
|
G | T | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38798G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383795 | ||||||
| chr6:45383869
|
T | G | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38724T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45383869 | ||||||
| chr6:45384014
|
T | C | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38579T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384014 | ||||||
| chr6:45384159
|
T | C | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38434T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384159 | ||||||
| chr6:45384206
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0007g0036a0001c0001t0014g0035 | 3 | HG02145.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.59-38387C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384206 | ||||||
| chr6:45384258
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0002g0133 | 2 | HG01255.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.59-38335G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384258 | ||||||
| chr6:45384274
|
T | G | 34 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0106others(31): Show | 34 | HG00741.hp1 HG01192.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.59-38319T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384274 | ||||||
| chr6:45384278
|
G | T | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0050others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-38315G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384278 | ||||||
| chr6:45384294
|
C | G | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-38299C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384294 | ||||||
| chr6:45384367
|
C | T | 1 | a0001c0001t0003g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.59-38226C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384367 | ||||||
| chr6:45384377
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-38216G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384377 | ||||||
| chr6:45384706
|
C | CT | 8 | a0001c0001t0001g0081a0001c0001t0001g0119a0001c0001t0001g0130others(5): Show | 8 | HG02895.hp1 HG02965.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-37859dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45384706 | |||||
| chr6:45384706
|
CT | C | 38 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0020others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.59-37859delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45384706 | |||||
| chr6:45384706
|
CTT | C | 62 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0022others(59): Show | 62 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.59-37860_59-37859d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45384706 | |||||
| chr6:45384706
|
CTTT | C | 5 | a0001c0001t0001g0057a0001c0001t0001g0158a0001c0001t0002g0133others(2): Show | 5 | HG01167.hp1 HG01255.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-37861_59-37859d others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45384706 | |||||
| chr6:45384940
|
G | A | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.59-37653G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45384940 | ||||||
| chr6:45385262
|
C | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-37331C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45385262 | ||||||
| chr6:45385295
|
C | T | 2 | a0001c0001t0004g0014a0004c0005t0001g0006 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.59-37298C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45385295 | ||||||
| chr6:45385363
|
C | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.59-37230C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45385363 | ||||||
| chr6:45385692
|
G | C | 2 | a0001c0001t0001g0113a0001c0001t0002g0115 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.59-36901G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45385692 | ||||||
| chr6:45385693
|
T | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.59-36900T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45385693 | ||||||
| chr6:45386068
|
C | CT | 16 | a0001c0001t0001g0057a0001c0001t0001g0113a0001c0001t0001g0114others(13): Show | 16 | HG01255.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-36509dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45386068 | |||||
| chr6:45386294
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-36299C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45386294 | ||||||
| chr6:45386747
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.59-35846G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45386747 | ||||||
| chr6:45387077
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-35516A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387077 | ||||||
| chr6:45387109
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-35484C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387109 | ||||||
| chr6:45387485
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.59-35108G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387485 | ||||||
| chr6:45387648
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.59-34945C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387648 | ||||||
| chr6:45387761
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-34832A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387761 | ||||||
| chr6:45387807
|
G | A | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-34786G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387807 | ||||||
| chr6:45387872
|
T | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.59-34721T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387872 | ||||||
| chr6:45387881
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.59-34712A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45387881 | ||||||
| chr6:45388087
|
T | C | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-34506T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45388087 | ||||||
| chr6:45388156
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0005g0011a0001c0001t0006g0001others(1): Show | 4 | HG00280.hp1 HG00733.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-34437A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45388156 | ||||||
| chr6:45388266
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.59-34327T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45388266 | ||||||
| chr6:45388289
|
G | A | 2 | a0001c0001t0004g0014a0004c0005t0001g0006 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.59-34304G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45388289 | ||||||
| chr6:45388563
|
G | A | 3 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0004g0027 | 3 | HG02109.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-34030G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45388563 | ||||||
| chr6:45388828
|
T | TA | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-33757dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45388828 | |||||
| chr6:45389007
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(7): Show | 10 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-33586G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45389007 | ||||||
| chr6:45389246
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-33347A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45389246 | ||||||
| chr6:45389732
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.59-32861C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45389732 | ||||||
| chr6:45389962
|
A | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.59-32631A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45389962 | ||||||
| chr6:45390005
|
CA | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.59-32574delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45390005 | |||||
| chr6:45390067
|
G | A | 2 | a0001c0001t0008g0034a0001c0001t0010g0002 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.59-32526G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390067 | ||||||
| chr6:45390243
|
TG | T | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.59-32349delG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390243 | ||||||
| chr6:45390370
|
G | A | 64 | a0001c0001t0001g0031a0001c0001t0001g0065a0001c0001t0001g0066others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.59-32223G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390370 | ||||||
| chr6:45390396
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.59-32197T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390396 | ||||||
| chr6:45390478
|
T | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0001t0001g0156others(2): Show | 5 | HG02886.hp1 HG02976.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-32115T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390478 | ||||||
| chr6:45390586
|
G | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.59-32007G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390586 | ||||||
| chr6:45390666
|
T | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.59-31927T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390666 | ||||||
| chr6:45390676
|
A | G | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-31917A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390676 | ||||||
| chr6:45390692
|
G | T | 12 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01192.hp2 HG01255.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-31901G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390692 | ||||||
| chr6:45390761
|
A | C | 1 | a0001c0001t0005g0011 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.59-31832A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390761 | ||||||
| chr6:45390828
|
A | T | 2 | a0001c0002t0006g0015a0001c0002t0006g0016 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.59-31765A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390828 | ||||||
| chr6:45390852
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59-31741G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390852 | ||||||
| chr6:45390867
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.59-31726G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390867 | ||||||
| chr6:45390945
|
A | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-31648A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390945 | ||||||
| chr6:45391657
|
T | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-30936T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45391657 | ||||||
| chr6:45391687
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-30906G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45391687 | ||||||
| chr6:45391794
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-30799A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45391794 | ||||||
| chr6:45392139
|
A | C | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-30454A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45392139 | ||||||
| chr6:45392457
|
C | T | 42 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0070others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.59-30136C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45392457 | ||||||
| chr6:45392580
|
T | C | 1 | a0001c0007t0001g0028 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.59-30013T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45392580 | ||||||
| chr6:45392696
|
T | C | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-29897T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45392696 | ||||||
| chr6:45392707
|
AT | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.59-29872delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45392707 | |||||
| chr6:45392720
|
T | A | 3 | a0001c0001t0002g0117a0001c0001t0007g0063a0001c0001t0016g0153 | 3 | HG01891.hp1 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.59-29873T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45392720 | ||||||
| chr6:45392764
|
G | T | 5 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-29829G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45392764 | ||||||
| chr6:45393076
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.59-29517A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393076 | ||||||
| chr6:45393376
|
C | T | 10 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0119others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-29217C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393376 | ||||||
| chr6:45393431
|
AT | A | 16 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(13): Show | 16 | HG01255.hp1 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-29149delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45393431 | |||||
| chr6:45393452
|
A | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.59-29141A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393452 | ||||||
| chr6:45393473
|
C | T | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-29120C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393473 | ||||||
| chr6:45393523
|
A | G | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-29070A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393523 | ||||||
| chr6:45393554
|
C | T | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-29039C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393554 | ||||||
| chr6:45393561
|
C | T | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-29032C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393561 | ||||||
| chr6:45393567
|
C | T | 2 | a0001c0002t0006g0015a0001c0002t0006g0016 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.59-29026C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393567 | ||||||
| chr6:45393575
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0004g0021a0001c0001t0005g0019 | 3 | HG01346.hp2 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.59-29018G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393575 | ||||||
| chr6:45393581
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-29012C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393581 | ||||||
| chr6:45393657
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-28936T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393657 | ||||||
| chr6:45393710
|
G | A | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.59-28883G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393710 | ||||||
| chr6:45393767
|
C | T | 1 | a0001c0002t0004g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.59-28826C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393767 | ||||||
| chr6:45393892
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.59-28701G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393892 | ||||||
| chr6:45393927
|
C | CT | 13 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-28652dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45393927 | |||||
| chr6:45393937
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.59-28656T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45393937 | ||||||
| chr6:45394058
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.59-28535G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394058 | ||||||
| chr6:45394101
|
C | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-28492C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394101 | ||||||
| chr6:45394137
|
C | T | 14 | a0001c0001t0009g0025a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-28456C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394137 | ||||||
| chr6:45394146
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.59-28447C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394146 | ||||||
| chr6:45394153
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-28440C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394153 | ||||||
| chr6:45394188
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG02818.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-28405G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394188 | ||||||
| chr6:45394318
|
T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.59-28275T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394318 | ||||||
| chr6:45394951
|
G | T | 1 | a0001c0001t0004g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.59-27642G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45394951 | ||||||
| chr6:45395357
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-27236C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395357 | ||||||
| chr6:45395417
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-27176C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395417 | ||||||
| chr6:45395575
|
T | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-27018T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395575 | ||||||
| chr6:45395616
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-26977C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395616 | ||||||
| chr6:45395670
|
A | G | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-26923A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395670 | ||||||
| chr6:45395819
|
G | C | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-26774G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395819 | ||||||
| chr6:45395886
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0097 | 2 | HG00609.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.59-26707A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395886 | ||||||
| chr6:45395909
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.59-26684A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395909 | ||||||
| chr6:45395997
|
A | G | 1 | a0001c0001t0003g0009 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.59-26596A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45395997 | ||||||
| chr6:45396027
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.59-26566A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45396027 | ||||||
| chr6:45396059
|
C | A | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-26534C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45396059 | ||||||
| chr6:45396359
|
A | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-26234A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45396359 | ||||||
| chr6:45396380
|
T | C | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-26213T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45396380 | ||||||
| chr6:45396533
|
A | G | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-26060A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45396533 | ||||||
| chr6:45396595
|
A | G | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-25998A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45396595 | ||||||
| chr6:45397107
|
C | CT | 14 | a0001c0001t0001g0124a0001c0002t0001g0026a0001c0002t0001g0044others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-25472dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45397107 | |||||
| chr6:45397107
|
CT | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-25472delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45397107 | |||||
| chr6:45397142
|
C | T | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-25451C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397142 | ||||||
| chr6:45397165
|
G | A | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-25428G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397165 | ||||||
| chr6:45397203
|
A | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-25390A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397203 | ||||||
| chr6:45397369
|
A | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-25224A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397369 | ||||||
| chr6:45397863
|
A | C | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.59-24730A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397863 | ||||||
| chr6:45397868
|
A | G | 8 | a0001c0001t0001g0095a0001c0001t0001g0120a0001c0001t0001g0123others(5): Show | 8 | HG00438.hp2 HG02074.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-24725A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397868 | ||||||
| chr6:45397950
|
T | C | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-24643T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397950 | ||||||
| chr6:45398102
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-24491A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398102 | ||||||
| chr6:45398191
|
G | A | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-24402G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398191 | ||||||
| chr6:45398201
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-24392C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398201 | ||||||
| chr6:45398395
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-24198G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398395 | ||||||
| chr6:45398413
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.59-24180C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398413 | ||||||
| chr6:45398430
|
A | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG00423.hp2 HG00597.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-24163A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398430 | ||||||
| chr6:45398470
|
T | C | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-24123T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398470 | ||||||
| chr6:45398530
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-24063C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398530 | ||||||
| chr6:45398688
|
C | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0119others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-23905C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398688 | ||||||
| chr6:45398785
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.59-23808T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398785 | ||||||
| chr6:45398804
|
T | C | 1 | a0001c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.59-23789T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398804 | ||||||
| chr6:45398862
|
T | G | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.59-23731T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45398862 | ||||||
| chr6:45398991
|
GTTTACAA others(8): Show |
G | 12 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01192.hp2 HG01255.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-23600_59-23586d others(17): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45398991 | |||||
| chr6:45399002
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-23591C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399002 | ||||||
| chr6:45399209
|
A | G | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-23384A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399209 | ||||||
| chr6:45399288
|
C | T | 3 | a0001c0001t0001g0127a0001c0002t0004g0060a0001c0002t0004g0061 | 3 | HG00735.hp2 HG01167.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-23305C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399288 | ||||||
| chr6:45399349
|
C | CT | 39 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0077others(36): Show | 39 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.59-23216dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
C | CTT | 8 | a0001c0001t0001g0007a0001c0001t0001g0120a0001c0001t0002g0004others(5): Show | 8 | HG00733.hp2 HG02055.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-23217_59-23216d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
C | CTTT | 5 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0003g0150others(2): Show | 5 | HG00280.hp1 HG00323.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-23218_59-23216d others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
C | CTTTTTTT others(3): Show |
3 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0140 | 3 | HG00741.hp2 NA18995.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.59-23225_59-23216d others(12): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
C | CTTTTTTT others(4): Show |
3 | a0001c0002t0004g0039a0001c0002t0006g0015a0001c0002t0006g0016 | 3 | HG00423.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.59-23226_59-23216d others(13): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
CT | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0062others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-23216delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0002g0115others(2): Show | 5 | HG01255.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-23223_59-23216d others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
CTTTTTTT others(2): Show |
C | 11 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0164others(8): Show | 11 | HG00735.hp2 HG01192.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-23224_59-23216d others(11): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.59-23225_59-23216d others(12): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399349
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-23228_59-23216d others(15): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399349 | |||||
| chr6:45399391
|
G | A | 13 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(10): Show | 13 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-23202G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399391 | ||||||
| chr6:45399505
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(7): Show | 10 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-23088G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399505 | ||||||
| chr6:45399575
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0119others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-23018G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399575 | ||||||
| chr6:45399692
|
C | CAAAG | 2 | a0001c0001t0002g0004a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.59-22886_59-22883d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399692 | |||||
| chr6:45399759
|
A | AAAGG | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-22824_59-22821d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399759 | |||||
| chr6:45399769
|
AGGAG | A | 10 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0164others(7): Show | 10 | HG01192.hp2 HG01255.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-22810_59-22807d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399769 | |||||
| chr6:45399799
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.59-22794G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399799 | ||||||
| chr6:45399819
|
TAAGG | T | 13 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(10): Show | 13 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-22751_59-22748d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45399819 | |||||
| chr6:45399880
|
T | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.59-22713T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399880 | ||||||
| chr6:45399902
|
C | T | 1 | a0001c0001t0005g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.59-22691C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399902 | ||||||
| chr6:45399947
|
T | C | 1 | a0001c0001t0005g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.59-22646T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399947 | ||||||
| chr6:45399993
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG02818.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-22600G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45399993 | ||||||
| chr6:45400032
|
GGGAAGGA others(22): Show |
G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-22545_59-22517d others(31): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45400032 | |||||
| chr6:45400043
|
A | G | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59-22550A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400043 | ||||||
| chr6:45400057
|
G | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-22536G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400057 | ||||||
| chr6:45400185
|
A | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-22408A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400185 | ||||||
| chr6:45400186
|
T | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-22407T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400186 | ||||||
| chr6:45400189
|
G | GGGAA | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-22388_59-22385d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45400189 | |||||
| chr6:45400189
|
G | GGGAAGGA others(1): Show |
14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-22392_59-22385d others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45400189 | |||||
| chr6:45400256
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0164others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-22337G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400256 | ||||||
| chr6:45400262
|
G | A | 2 | a0001c0001t0003g0154a0001c0001t0016g0153 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.59-22331G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400262 | ||||||
| chr6:45400477
|
G | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-22116G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400477 | ||||||
| chr6:45400485
|
C | T | 6 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0001g0136others(3): Show | 6 | HG00438.hp2 HG03704.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-22108C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400485 | ||||||
| chr6:45400719
|
T | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-21874T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400719 | ||||||
| chr6:45400820
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-21773C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400820 | ||||||
| chr6:45401060
|
G | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.59-21533G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45401060 | ||||||
| chr6:45401613
|
G | A | 2 | a0001c0001t0001g0106a0001c0006t0001g0108 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.59-20980G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45401613 | ||||||
| chr6:45401772
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.59-20821G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45401772 | ||||||
| chr6:45402088
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-20505T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45402088 | ||||||
| chr6:45402092
|
A | G | 1 | a0001c0001t0004g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.59-20501A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45402092 | ||||||
| chr6:45402746
|
C | T | 1 | a0001c0001t0011g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-19847C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45402746 | ||||||
| chr6:45402787
|
G | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-19806G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45402787 | ||||||
| chr6:45402865
|
T | C | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-19728T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45402865 | ||||||
| chr6:45403147
|
GA | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01192.hp2 HG01255.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-19445delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403147 | ||||||
| chr6:45403160
|
A | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-19433A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403160 | ||||||
| chr6:45403229
|
CT | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-19343delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45403229 | |||||
| chr6:45403229
|
CTTTTTTT others(4): Show |
C | 14 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0113others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-19353_59-19343d others(13): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45403229 | |||||
| chr6:45403248
|
T | TTTG | 12 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0046others(9): Show | 12 | HG00099.hp1 HG00423.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-19344_59-19342d others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45403248 | |||||
| chr6:45403319
|
C | T | 1 | a0001c0001t0019g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.59-19274C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403319 | ||||||
| chr6:45403429
|
C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.59-19164C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403429 | ||||||
| chr6:45403485
|
A | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-19108A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403485 | ||||||
| chr6:45403629
|
G | T | 41 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0070others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.59-18964G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403629 | ||||||
| chr6:45403720
|
T | A | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.59-18873T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403720 | ||||||
| chr6:45403816
|
T | A | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.59-18777T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403816 | ||||||
| chr6:45403922
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0003g0150 | 2 | HG00323.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.59-18671C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403922 | ||||||
| chr6:45404058
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.59-18535G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404058 | ||||||
| chr6:45404111
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.59-18482T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404111 | ||||||
| chr6:45404259
|
C | CA | 20 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0113others(17): Show | 20 | HG01192.hp2 HG01255.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.59-18319dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45404259 | |||||
| chr6:45404259
|
C | CAA | 15 | a0001c0001t0001g0022a0001c0001t0001g0134a0001c0001t0001g0169others(12): Show | 15 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-18320_59-18319d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45404259 | |||||
| chr6:45404268
|
AAAAAAAG others(25): Show |
A | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.59-18318_59-18287d others(34): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45404268 | |||||
| chr6:45404274
|
A | G | 10 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(7): Show | 10 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-18319A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404274 | ||||||
| chr6:45404274
|
AG | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(15): Show | 18 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-18318delG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404274 | ||||||
| chr6:45404275
|
G | A | 136 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0031others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.59-18318G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404275 | ||||||
| chr6:45404288
|
G | GA | 17 | a0001c0001t0001g0081a0001c0001t0002g0032a0001c0001t0002g0126others(14): Show | 17 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-18295dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45404288 | |||||
| chr6:45404289
|
AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.59-18295_59-18269d others(29): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45404289 | |||||
| chr6:45404316
|
G | GA | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.59-18269dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45404316 | |||||
| chr6:45404480
|
C | A | 1 | a0003c0004t0001g0072 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.59-18113C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404480 | ||||||
| chr6:45404481
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-18112G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404481 | ||||||
| chr6:45404568
|
A | C | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-18025A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404568 | ||||||
| chr6:45404583
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-18010A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404583 | ||||||
| chr6:45404622
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-17971G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404622 | ||||||
| chr6:45404644
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.59-17949A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404644 | ||||||
| chr6:45404652
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.59-17941A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404652 | ||||||
| chr6:45404769
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.59-17824T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404769 | ||||||
| chr6:45404820
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.59-17773G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404820 | ||||||
| chr6:45404843
|
G | A | 1 | a0001c0001t0005g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.59-17750G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404843 | ||||||
| chr6:45405009
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.59-17584C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405009 | ||||||
| chr6:45405066
|
A | G | 1 | a0004c0005t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.59-17527A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405066 | ||||||
| chr6:45405105
|
G | A | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-17488G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405105 | ||||||
| chr6:45405134
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.59-17459A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405134 | ||||||
| chr6:45405272
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.59-17321G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405272 | ||||||
| chr6:45405659
|
C | T | 1 | a0001c0001t0004g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.59-16934C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405659 | ||||||
| chr6:45405694
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.59-16899G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405694 | ||||||
| chr6:45405703
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59-16890C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405703 | ||||||
| chr6:45405727
|
C | T | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.59-16866C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405727 | ||||||
| chr6:45405795
|
A | AT | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-16798_59-16797i others(3): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405795 | ||||||
| chr6:45405980
|
G | T | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.59-16613G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45405980 | ||||||
| chr6:45406010
|
C | A | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0007t0001g0028 | 3 | HG00597.hp1 HG01928.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.59-16583C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406010 | ||||||
| chr6:45406033
|
A | G | 1 | a0001c0007t0001g0028 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.59-16560A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406033 | ||||||
| chr6:45406106
|
T | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-16487T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406106 | ||||||
| chr6:45406170
|
G | A | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-16423G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406170 | ||||||
| chr6:45406178
|
A | G | 13 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(10): Show | 13 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-16415A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406178 | ||||||
| chr6:45406236
|
AC | A | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-16356delC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406236 | ||||||
| chr6:45406267
|
G | C | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.59-16326G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406267 | ||||||
| chr6:45406277
|
A | G | 18 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0001g0100others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-16316A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406277 | ||||||
| chr6:45406446
|
A | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.59-16147A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406446 | ||||||
| chr6:45406640
|
A | C | 1 | a0001c0001t0004g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.59-15953A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406640 | ||||||
| chr6:45406660
|
C | A | 13 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(10): Show | 13 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-15933C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406660 | ||||||
| chr6:45406677
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.59-15916G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406677 | ||||||
| chr6:45406681
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-15912G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406681 | ||||||
| chr6:45406795
|
A | T | 3 | a0001c0001t0001g0100a0001c0001t0002g0048a0001c0001t0003g0102 | 3 | HG01978.hp2 NA18965.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.59-15798A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406795 | ||||||
| chr6:45406871
|
T | A | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.59-15722T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406871 | ||||||
| chr6:45406943
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0002g0107a0001c0001t0002g0109others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-15650A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406943 | ||||||
| chr6:45406962
|
A | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-15631A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45406962 | ||||||
| chr6:45407196
|
C | T | 32 | a0001c0001t0001g0057a0001c0001t0001g0120a0001c0001t0001g0123others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.59-15397C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45407196 | ||||||
| chr6:45407269
|
C | T | 9 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0113others(6): Show | 9 | HG01978.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-15324C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45407269 | ||||||
| chr6:45407294
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-15299C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45407294 | ||||||
| chr6:45407487
|
A | G | 12 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(9): Show | 12 | HG00099.hp1 HG00423.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-15106A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45407487 | ||||||
| chr6:45407755
|
C | A | 1 | a0001c0001t0004g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.59-14838C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45407755 | ||||||
| chr6:45407824
|
T | A | 1 | a0001c0001t0003g0102 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.59-14769T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45407824 | ||||||
| chr6:45407920
|
A | T | 174 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.59-14673A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45407920 | ||||||
| chr6:45408014
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-14579A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45408014 | ||||||
| chr6:45408015
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-14578C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45408015 | ||||||
| chr6:45408131
|
GA | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-14461delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45408131 | ||||||
| chr6:45408484
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0003g0150 | 3 | HG00323.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.59-14109G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45408484 | ||||||
| chr6:45408649
|
C | T | 1 | a0001c0001t0009g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59-13944C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45408649 | ||||||
| chr6:45409027
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-13566T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409027 | ||||||
| chr6:45409119
|
G | C | 78 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.59-13474G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409119 | ||||||
| chr6:45409122
|
T | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-13471T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409122 | ||||||
| chr6:45409301
|
G | A | 157 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.59-13292G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409301 | ||||||
| chr6:45409318
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-13275G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409318 | ||||||
| chr6:45409343
|
A | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-13250A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409343 | ||||||
| chr6:45409499
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.59-13094A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409499 | ||||||
| chr6:45409524
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.59-13069G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409524 | ||||||
| chr6:45409527
|
C | T | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.59-13066C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409527 | ||||||
| chr6:45409682
|
A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-12911A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409682 | ||||||
| chr6:45409829
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.59-12764G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45409829 | ||||||
| chr6:45410040
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-12553A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45410040 | ||||||
| chr6:45410111
|
C | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-12482C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45410111 | ||||||
| chr6:45410355
|
A | G | 12 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(9): Show | 12 | HG00099.hp1 HG00423.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-12238A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45410355 | ||||||
| chr6:45410365
|
A | C | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.59-12228A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45410365 | ||||||
| chr6:45410623
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-11970G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45410623 | ||||||
| chr6:45410734
|
G | A | 1 | a0001c0001t0011g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-11859G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45410734 | ||||||
| chr6:45411072
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-11521C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45411072 | ||||||
| chr6:45411236
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-11357A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45411236 | ||||||
| chr6:45411810
|
T | C | 4 | a0001c0001t0001g0110a0001c0001t0002g0107a0001c0001t0002g0109others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-10783T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45411810 | ||||||
| chr6:45411904
|
T | C | 14 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0113others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-10689T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45411904 | ||||||
| chr6:45412072
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.59-10521G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412072 | ||||||
| chr6:45412102
|
C | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.59-10491C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412102 | ||||||
| chr6:45412187
|
C | CA | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.59-10387dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45412187 | |||||
| chr6:45412187
|
C | CAA | 23 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(20): Show | 23 | HG00438.hp1 HG00741.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-10388_59-10387d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45412187 | |||||
| chr6:45412217
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-10376A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412217 | ||||||
| chr6:45412386
|
CA | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-10199delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45412386 | |||||
| chr6:45412387
|
A | C | 21 | a0001c0001t0001g0091a0001c0001t0001g0130a0001c0001t0001g0156others(18): Show | 21 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-10206A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412387 | ||||||
| chr6:45412543
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0007g0118a0001c0001t0010g0002 | 3 | HG01884.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.59-10050G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412543 | ||||||
| chr6:45412674
|
C | CT | 12 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01192.hp2 HG01255.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-9907dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45412674 | |||||
| chr6:45412733
|
C | T | 1 | a0001c0001t0003g0051 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.59-9860C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412733 | ||||||
| chr6:45412794
|
T | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(27): Show | 30 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-9799T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412794 | ||||||
| chr6:45412821
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0104a0001c0001t0005g0071others(2): Show | 5 | HG00099.hp2 HG01071.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-9772T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412821 | ||||||
| chr6:45412902
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.59-9691C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412902 | ||||||
| chr6:45412910
|
T | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-9683T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45412910 | ||||||
| chr6:45413058
|
C | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-9535C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413058 | ||||||
| chr6:45413331
|
GAC | G | 10 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0113others(7): Show | 10 | HG01978.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-9250_59-9249del others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45413331 | |||||
| chr6:45413345
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-9248A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413345 | ||||||
| chr6:45413429
|
CT | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.59-9137delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45413429 | |||||
| chr6:45413429
|
CTT | C | 71 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.59-9138_59-9137del others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45413429 | |||||
| chr6:45413575
|
T | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-9018T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413575 | ||||||
| chr6:45413579
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.59-9014C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413579 | ||||||
| chr6:45413591
|
T | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-9002T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413591 | ||||||
| chr6:45413662
|
C | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-8931C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413662 | ||||||
| chr6:45413687
|
C | T | 2 | a0001c0002t0003g0058a0001c0002t0004g0039 | 2 | HG00423.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.59-8906C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413687 | ||||||
| chr6:45413847
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-8746G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45413847 | ||||||
| chr6:45414033
|
T | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-8560T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45414033 | ||||||
| chr6:45414064
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-8529C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45414064 | ||||||
| chr6:45414356
|
C | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-8237C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45414356 | ||||||
| chr6:45414754
|
CT | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0041others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.59-7809delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45414754 | |||||
| chr6:45414754
|
CTT | C | 47 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0020others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.59-7810_59-7809del others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45414754 | |||||
| chr6:45414754
|
CTTT | C | 33 | a0001c0001t0001g0031a0001c0001t0001g0066a0001c0001t0001g0078others(30): Show | 33 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.59-7811_59-7809del others(3): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45414754 | |||||
| chr6:45414754
|
CTTTT | C | 17 | a0001c0001t0001g0057a0001c0001t0001g0146a0001c0001t0001g0151others(14): Show | 17 | HG01255.hp2 HG01891.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-7812_59-7809del others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45414754 | |||||
| chr6:45414754
|
CTTTTTTT others(2): Show |
C | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0004others(2): Show | 5 | HG02895.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-7817_59-7809del others(9): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45414754 | |||||
| chr6:45414754
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0119a0001c0001t0010g0002 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.59-7818_59-7809del others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45414754 | |||||
| chr6:45415029
|
T | A | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-7564T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45415029 | ||||||
| chr6:45415039
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-7554G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45415039 | ||||||
| chr6:45415341
|
A | C | 155 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.59-7252A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45415341 | ||||||
| chr6:45415350
|
G | A | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-7243G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45415350 | ||||||
| chr6:45415684
|
A | AC | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.59-6908dupC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45415684 | |||||
| chr6:45415709
|
A | G | 9 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0113others(6): Show | 9 | HG01978.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-6884A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45415709 | ||||||
| chr6:45415796
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-6797A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45415796 | ||||||
| chr6:45416192
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.59-6401T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45416192 | ||||||
| chr6:45416281
|
T | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.59-6312T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45416281 | ||||||
| chr6:45416730
|
C | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-5863C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45416730 | ||||||
| chr6:45417153
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.59-5440G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417153 | ||||||
| chr6:45417322
|
AT | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-5267delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45417322 | |||||
| chr6:45417363
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.59-5230A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417363 | ||||||
| chr6:45417657
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.59-4936A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417657 | ||||||
| chr6:45417702
|
C | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-4891C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417702 | ||||||
| chr6:45417741
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0002g0133 | 2 | HG01255.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.59-4852C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417741 | ||||||
| chr6:45417775
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0004g0014a0004c0005t0001g0006 | 3 | HG00280.hp2 HG01106.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.59-4818G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417775 | ||||||
| chr6:45417870
|
A | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-4723A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417870 | ||||||
| chr6:45417882
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0002g0111 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.59-4711A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45417882 | ||||||
| chr6:45418004
|
C | T | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.59-4589C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45418004 | ||||||
| chr6:45418005
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-4588G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45418005 | ||||||
| chr6:45418173
|
T | TAAC | 144 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.59-4418_59-4417ins others(3): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 45418173 | |||||
| chr6:45418176
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.59-4417G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45418176 | ||||||
| chr6:45418268
|
T | C | 1 | a0001c0001t0004g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.59-4325T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45418268 | ||||||
| chr6:45418359
|
C | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-4234C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45418359 | ||||||
| chr6:45418465
|
T | C | 13 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 13 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-4128T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45418465 | ||||||
| chr6:45418516
|
C | T | 13 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(10): Show | 13 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-4077C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45418516 | ||||||
| chr6:45419112
|
C | T | 1 | a0001c0001t0004g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.59-3481C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45419112 | ||||||
| chr6:45419258
|
C | A | 1 | a0001c0001t0019g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.59-3335C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45419258 | ||||||
| chr6:45419533
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.59-3060G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45419533 | ||||||
| chr6:45419758
|
T | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-2835T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45419758 | ||||||
| chr6:45419829
|
G | A | 1 | a0001c0001t0011g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59-2764G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45419829 | ||||||
| chr6:45419922
|
G | A | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-2671G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45419922 | ||||||
| chr6:45419926
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-2667G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45419926 | ||||||
| chr6:45420162
|
G | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-2431G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420162 | ||||||
| chr6:45420342
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.59-2251C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420342 | ||||||
| chr6:45420352
|
G | A | 2 | a0001c0001t0004g0089a0001c0001t0005g0093 | 2 | HG01106.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.59-2241G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420352 | ||||||
| chr6:45420398
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-2195T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420398 | ||||||
| chr6:45420493
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-2100C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420493 | ||||||
| chr6:45420607
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-1986C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420607 | ||||||
| chr6:45420621
|
C | T | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-1972C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420621 | ||||||
| chr6:45420791
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.59-1802A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45420791 | ||||||
| chr6:45421085
|
A | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0001t0001g0156others(2): Show | 5 | HG02886.hp1 HG02976.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1508A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421085 | ||||||
| chr6:45421116
|
G | C | 1 | a0001c0001t0002g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-1477G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421116 | ||||||
| chr6:45421405
|
CT | C | 21 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(18): Show | 21 | HG00099.hp1 HG00423.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-1187delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421405 | ||||||
| chr6:45421406
|
T | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0169others(5): Show | 8 | HG00735.hp2 HG02258.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1187T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421406 | ||||||
| chr6:45421497
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-1096A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421497 | ||||||
| chr6:45421552
|
T | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-1041T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421552 | ||||||
| chr6:45421606
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-987G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421606 | ||||||
| chr6:45421798
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.59-795C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421798 | ||||||
| chr6:45421921
|
T | A | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-672T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421921 | ||||||
| chr6:45421963
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59-630C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45421963 | ||||||
| chr6:45422104
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.59-489G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45422104 | ||||||
| chr6:45422351
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0003g0150 | 2 | HG00323.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.59-242G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45422351 | ||||||
| chr6:45422996
|
G | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+39G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45422996 | ||||||
| chr6:45423101
|
C | CCT | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.423+146_423+147dup others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45423101 | |||||
| chr6:45423212
|
G | C | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+255G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423212 | ||||||
| chr6:45423225
|
C | T | 41 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0070others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.423+268C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423225 | ||||||
| chr6:45423345
|
C | A | 1 | a0001c0002t0004g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.423+388C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423345 | ||||||
| chr6:45423454
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+497G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423454 | ||||||
| chr6:45423547
|
C | G | 33 | a0001c0001t0001g0057a0001c0001t0001g0120a0001c0001t0001g0123others(30): Show | 33 | HG00280.hp2 HG00438.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.423+590C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423547 | ||||||
| chr6:45423563
|
G | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(9): Show | 12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.423+606G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423563 | ||||||
| chr6:45423599
|
C | CG | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+646dupG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45423599 | |||||
| chr6:45423688
|
AG | A | 33 | a0001c0001t0001g0057a0001c0001t0001g0120a0001c0001t0001g0123others(30): Show | 33 | HG00280.hp2 HG00438.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.423+736delG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45423688 | |||||
| chr6:45423698
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+741A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423698 | ||||||
| chr6:45423745
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+788A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423745 | ||||||
| chr6:45423917
|
G | C | 19 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.423+960G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423917 | ||||||
| chr6:45423954
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.423+997C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45423954 | ||||||
| chr6:45424011
|
C | T | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+1054C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424011 | ||||||
| chr6:45424025
|
A | G | 9 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0113others(6): Show | 9 | HG01978.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+1068A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424025 | ||||||
| chr6:45424123
|
A | G | 144 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.423+1166A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424123 | ||||||
| chr6:45424163
|
T | TGGCAGCC others(12): Show |
1 | a0001c0001t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.423+1212_423+1230d others(21): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45424163 | |||||
| chr6:45424206
|
T | G | 144 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.423+1249T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424206 | ||||||
| chr6:45424234
|
C | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+1277C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424234 | ||||||
| chr6:45424554
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423+1597T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424554 | ||||||
| chr6:45424559
|
G | T | 2 | a0002c0003t0001g0161a0002c0003t0001g0162 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.423+1602G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424559 | ||||||
| chr6:45424590
|
C | A | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.423+1633C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424590 | ||||||
| chr6:45424682
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.423+1725A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424682 | ||||||
| chr6:45424728
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0007g0063 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.423+1771T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424728 | ||||||
| chr6:45424841
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423+1884A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45424841 | ||||||
| chr6:45425245
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+2288A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425245 | ||||||
| chr6:45425273
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+2316A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425273 | ||||||
| chr6:45425437
|
A | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+2480A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425437 | ||||||
| chr6:45425457
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.423+2500C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425457 | ||||||
| chr6:45425503
|
A | G | 5 | a0001c0002t0001g0044a0001c0002t0001g0045a0001c0002t0001g0046others(2): Show | 5 | HG00741.hp2 HG01496.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.423+2546A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425503 | ||||||
| chr6:45425625
|
G | A | 83 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0047others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.423+2668G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425625 | ||||||
| chr6:45425626
|
T | C | 78 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.423+2669T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425626 | ||||||
| chr6:45425893
|
T | TAC | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+2952_423+2953d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45425893 | |||||
| chr6:45425893
|
TAC | T | 15 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0076others(12): Show | 15 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.423+2952_423+2953d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45425893 | |||||
| chr6:45425993
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+3036C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45425993 | ||||||
| chr6:45426050
|
C | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+3093C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426050 | ||||||
| chr6:45426112
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.423+3155T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426112 | ||||||
| chr6:45426158
|
A | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01192.hp2 HG01255.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.423+3201A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426158 | ||||||
| chr6:45426515
|
C | T | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+3558C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426515 | ||||||
| chr6:45426592
|
T | C | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+3635T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426592 | ||||||
| chr6:45426837
|
T | G | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.423+3880T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426837 | ||||||
| chr6:45426847
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(7): Show | 10 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.423+3890G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426847 | ||||||
| chr6:45426948
|
G | A | 23 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0106others(20): Show | 23 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.423+3991G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45426948 | ||||||
| chr6:45427004
|
T | C | 13 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 13 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.423+4047T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45427004 | ||||||
| chr6:45427401
|
T | G | 78 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.423+4444T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45427401 | ||||||
| chr6:45427453
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-4410C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45427453 | ||||||
| chr6:45427682
|
G | A | 1 | a0001c0001t0001g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.424-4181G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45427682 | ||||||
| chr6:45427725
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424-4138A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45427725 | ||||||
| chr6:45427794
|
A | C | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424-4069A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45427794 | ||||||
| chr6:45427946
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.424-3917C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45427946 | ||||||
| chr6:45428005
|
C | T | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-3858C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428005 | ||||||
| chr6:45428052
|
A | C | 144 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.424-3811A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428052 | ||||||
| chr6:45428055
|
A | C | 144 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.424-3808A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428055 | ||||||
| chr6:45428132
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-3731A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428132 | ||||||
| chr6:45428136
|
C | T | 142 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.424-3727C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428136 | ||||||
| chr6:45428169
|
C | A | 4 | a0001c0001t0002g0033a0001c0001t0002g0132a0001c0001t0007g0036others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-3694C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428169 | ||||||
| chr6:45428183
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.424-3680A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428183 | ||||||
| chr6:45428445
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.424-3418G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428445 | ||||||
| chr6:45428517
|
T | C | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424-3346T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428517 | ||||||
| chr6:45428560
|
A | C | 75 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(72): Show | 75 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.424-3303A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428560 | ||||||
| chr6:45428582
|
A | T | 75 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(72): Show | 75 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.424-3281A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428582 | ||||||
| chr6:45428618
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424-3245C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428618 | ||||||
| chr6:45428678
|
A | G | 1 | a0001c0001t0006g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.424-3185A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428678 | ||||||
| chr6:45428807
|
T | C | 174 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.424-3056T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428807 | ||||||
| chr6:45428837
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0002g0033a0001c0001t0002g0132others(4): Show | 7 | HG00280.hp2 HG01106.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-3026G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428837 | ||||||
| chr6:45428838
|
C | CT | 124 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0047others(121): Show | 124 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.424-3008dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45428838 | |||||
| chr6:45428838
|
C | CTT | 9 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0080others(6): Show | 9 | HG00099.hp2 HG00597.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.424-3009_424-3008d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45428838 | |||||
| chr6:45428855
|
T | TC | 2 | a0002c0003t0001g0161a0002c0003t0001g0162 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.424-3007dupC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45428855 | |||||
| chr6:45429037
|
C | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.424-2826C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429037 | ||||||
| chr6:45429164
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424-2699G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429164 | ||||||
| chr6:45429259
|
C | T | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.424-2604C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429259 | ||||||
| chr6:45429313
|
C | T | 75 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(72): Show | 75 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.424-2550C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429313 | ||||||
| chr6:45429569
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0003g0069a0001c0001t0003g0074 | 3 | HG00323.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.424-2294C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429569 | ||||||
| chr6:45429723
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424-2140G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429723 | ||||||
| chr6:45429821
|
C | T | 75 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(72): Show | 75 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.424-2042C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429821 | ||||||
| chr6:45429868
|
C | T | 2 | a0002c0003t0001g0161a0002c0003t0001g0162 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.424-1995C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429868 | ||||||
| chr6:45429909
|
C | T | 1 | a0001c0001t0006g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.424-1954C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429909 | ||||||
| chr6:45429958
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.424-1905G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45429958 | ||||||
| chr6:45430042
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-1821C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430042 | ||||||
| chr6:45430049
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424-1814G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430049 | ||||||
| chr6:45430093
|
CA | C | 102 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(99): Show | 102 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.424-1755delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45430093 | |||||
| chr6:45430093
|
CAA | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG00280.hp2 HG01106.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-1756_424-1755d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 45430093 | |||||
| chr6:45430113
|
T | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-1750T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430113 | ||||||
| chr6:45430157
|
T | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424-1706T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430157 | ||||||
| chr6:45430173
|
CAGAT | C | 2 | a0001c0001t0001g0146a0001c0001t0003g0147 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.424-1689_424-1686d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430173 | ||||||
| chr6:45430302
|
C | T | 1 | a0001c0002t0015g0043 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.424-1561C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430302 | ||||||
| chr6:45430420
|
C | T | 75 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(72): Show | 75 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.424-1443C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430420 | ||||||
| chr6:45430434
|
A | G | 2 | a0001c0001t0002g0131a0001c0001t0008g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.424-1429A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430434 | ||||||
| chr6:45430518
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0003g0042others(1): Show | 4 | HG00609.hp2 NA19000.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-1345G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430518 | ||||||
| chr6:45430660
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424-1203A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430660 | ||||||
| chr6:45430794
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0002g0033a0001c0001t0002g0132others(4): Show | 7 | HG00280.hp2 HG01106.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-1069C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430794 | ||||||
| chr6:45430918
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.424-945T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430918 | ||||||
| chr6:45430934
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424-929G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45430934 | ||||||
| chr6:45431221
|
C | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.424-642C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45431221 | ||||||
| chr6:45431280
|
G | A | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.424-583G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45431280 | ||||||
| chr6:45431769
|
C | G | 1 | a0001c0002t0004g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.424-94C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45431769 | ||||||
| chr6:45432031
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.580+12A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45432031 | ||||||
| chr6:45432222
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.580+203A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45432222 | ||||||
| chr6:45432325
|
A | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+306A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45432325 | ||||||
| chr6:45432409
|
A | G | 14 | a0001c0002t0001g0026a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.580+390A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45432409 | ||||||
| chr6:45432657
|
A | G | 98 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0047others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.580+638A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45432657 | ||||||
| chr6:45433007
|
T | G | 1 | a0001c0001t0009g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.580+988T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45433007 | ||||||
| chr6:45433203
|
T | A | 83 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0047others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.580+1184T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45433203 | ||||||
| chr6:45433490
|
CT | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.580+1482delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 45433490 | |||||
| chr6:45433684
|
A | G | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.580+1665A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45433684 | ||||||
| chr6:45433961
|
G | A | 15 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.580+1942G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45433961 | ||||||
| chr6:45434032
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.580+2013C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45434032 | ||||||
| chr6:45434542
|
A | G | 4 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00423.hp2 NA18747.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+2523A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45434542 | ||||||
| chr6:45434704
|
A | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.580+2685A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45434704 | ||||||
| chr6:45434708
|
T | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.580+2689T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45434708 | ||||||
| chr6:45434957
|
T | C | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.580+2938T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45434957 | ||||||
| chr6:45435025
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0007g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-2922G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45435025 | ||||||
| chr6:45435185
|
A | C | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.581-2762A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45435185 | ||||||
| chr6:45435524
|
A | C | 6 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0001g0136others(3): Show | 6 | HG00438.hp2 HG03704.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-2423A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45435524 | ||||||
| chr6:45435633
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-2314C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45435633 | ||||||
| chr6:45435637
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0003g0150 | 3 | HG00323.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.581-2310C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45435637 | ||||||
| chr6:45435825
|
C | G | 2 | a0001c0001t0001g0020a0001c0001t0004g0021 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.581-2122C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45435825 | ||||||
| chr6:45436037
|
C | T | 92 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.581-1910C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45436037 | ||||||
| chr6:45436330
|
GA | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0119a0001c0001t0007g0118others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-1612delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 45436330 | |||||
| chr6:45436352
|
A | AT | 13 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 13 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.581-1589dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 45436352 | |||||
| chr6:45436365
|
T | C | 12 | a0001c0001t0001g0057a0001c0001t0001g0130a0001c0001t0001g0146others(9): Show | 12 | HG01255.hp2 HG02055.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.581-1582T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45436365 | ||||||
| chr6:45436433
|
G | A | 13 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 13 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.581-1514G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45436433 | ||||||
| chr6:45436493
|
C | T | 78 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.581-1454C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45436493 | ||||||
| chr6:45436545
|
C | T | 1 | a0001c0001t0003g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.581-1402C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45436545 | ||||||
| chr6:45436638
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.581-1309G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45436638 | ||||||
| chr6:45436791
|
A | G | 79 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0057others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.581-1156A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45436791 | ||||||
| chr6:45437313
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0002g0117a0001c0001t0002g0132others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-634G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45437313 | ||||||
| chr6:45437342
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0002g0004others(5): Show | 8 | HG02258.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-605G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45437342 | ||||||
| chr6:45437397
|
C | A | 8 | a0001c0001t0001g0073a0001c0001t0001g0155a0001c0001t0004g0014others(5): Show | 8 | HG00280.hp2 HG00735.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.581-550C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45437397 | ||||||
| chr6:45437853
|
A | T | 12 | a0001c0001t0001g0067a0001c0001t0001g0112a0001c0001t0001g0119others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.581-94A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 4/8 | chr6 | 45437853 | ||||||
| chr6:45438556
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.685+505T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45438556 | ||||||
| chr6:45438702
|
C | T | 1 | a0001c0001t0008g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.685+651C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45438702 | ||||||
| chr6:45438716
|
T | C | 13 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(10): Show | 13 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.685+665T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45438716 | ||||||
| chr6:45438811
|
C | T | 13 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(10): Show | 13 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.685+760C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45438811 | ||||||
| chr6:45439030
|
C | T | 2 | a0001c0001t0007g0023a0001c0001t0007g0063 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.685+979C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439030 | ||||||
| chr6:45439031
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.685+980A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439031 | ||||||
| chr6:45439177
|
G | C | 1 | a0001c0001t0005g0011 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.685+1126G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439177 | ||||||
| chr6:45439324
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0003g0147 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.685+1273G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439324 | ||||||
| chr6:45439461
|
C | A | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.685+1410C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439461 | ||||||
| chr6:45439483
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0142 | 2 | NA18990.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.685+1432T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439483 | ||||||
| chr6:45439668
|
C | CGT | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03540.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.685+1632_685+1633d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45439668 | |||||
| chr6:45439701
|
T | TTG | 2 | a0001c0001t0001g0062a0001c0006t0001g0108 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.685+1658_685+1659d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45439701 | |||||
| chr6:45439780
|
G | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0062others(21): Show | 24 | HG01255.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.685+1729G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439780 | ||||||
| chr6:45439861
|
A | G | 13 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(10): Show | 13 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.685+1810A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439861 | ||||||
| chr6:45439917
|
A | G | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(125): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.685+1866A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45439917 | ||||||
| chr6:45440154
|
C | T | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.685+2103C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45440154 | ||||||
| chr6:45440579
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.685+2528T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45440579 | ||||||
| chr6:45440652
|
A | AT | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.685+2612dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45440652 | |||||
| chr6:45440652
|
AT | A | 28 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0052others(25): Show | 28 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.685+2612delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45440652 | |||||
| chr6:45440682
|
G | A | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG01928.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.685+2631G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45440682 | ||||||
| chr6:45440703
|
T | G | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+2652T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45440703 | ||||||
| chr6:45440758
|
C | T | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685+2707C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45440758 | ||||||
| chr6:45440788
|
T | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+2737T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45440788 | ||||||
| chr6:45440833
|
T | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0145a0001c0001t0002g0017others(2): Show | 5 | HG01243.hp1 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.685+2782T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45440833 | ||||||
| chr6:45441020
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0041a0001c0001t0001g0056others(5): Show | 8 | HG00733.hp1 HG00741.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.685+2969C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45441020 | ||||||
| chr6:45441094
|
G | A | 1 | a0001c0001t0006g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.685+3043G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45441094 | ||||||
| chr6:45441374
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+3323T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45441374 | ||||||
| chr6:45441645
|
C | A | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685+3594C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45441645 | ||||||
| chr6:45442144
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.685+4093T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442144 | ||||||
| chr6:45442180
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.685+4129C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442180 | ||||||
| chr6:45442272
|
C | A | 13 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(10): Show | 13 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.685+4221C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442272 | ||||||
| chr6:45442378
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0002g0004others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.685+4327A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442378 | ||||||
| chr6:45442477
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.685+4426A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442477 | ||||||
| chr6:45442575
|
T | C | 149 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(146): Show | 149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.685+4524T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442575 | ||||||
| chr6:45442586
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.685+4535G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442586 | ||||||
| chr6:45442813
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.685+4762C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442813 | ||||||
| chr6:45442963
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+4912G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45442963 | ||||||
| chr6:45443036
|
C | CT | 7 | a0001c0001t0004g0089a0001c0001t0004g0178a0001c0001t0005g0019others(4): Show | 7 | HG00423.hp1 HG00735.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.685+5013dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45443036 | |||||
| chr6:45443036
|
CT | C | 34 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0056others(31): Show | 34 | HG00609.hp2 HG01106.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.685+5013delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45443036 | |||||
| chr6:45443036
|
CTT | C | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.685+5012_685+5013d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45443036 | |||||
| chr6:45443196
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.685+5145A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443196 | ||||||
| chr6:45443386
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.685+5335G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443386 | ||||||
| chr6:45443472
|
T | G | 1 | a0001c0001t0003g0009 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.685+5421T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443472 | ||||||
| chr6:45443664
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.685+5613A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443664 | ||||||
| chr6:45443732
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.685+5681T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443732 | ||||||
| chr6:45443843
|
T | C | 13 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(10): Show | 13 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.685+5792T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443843 | ||||||
| chr6:45443884
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.685+5833T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443884 | ||||||
| chr6:45443892
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.685+5841C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45443892 | ||||||
| chr6:45444043
|
A | G | 1 | a0001c0001t0001g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.685+5992A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444043 | ||||||
| chr6:45444085
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+6034G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444085 | ||||||
| chr6:45444102
|
G | C | 2 | a0001c0001t0001g0062a0001c0006t0001g0108 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.685+6051G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444102 | ||||||
| chr6:45444242
|
G | T | 3 | a0001c0001t0007g0023a0001c0001t0007g0063a0001c0001t0007g0118 | 3 | HG01891.hp1 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.685+6191G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444242 | ||||||
| chr6:45444368
|
A | C | 23 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.685+6317A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444368 | ||||||
| chr6:45444494
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.685+6443A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444494 | ||||||
| chr6:45444807
|
C | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0176a0001c0001t0010g0129 | 3 | HG01884.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.685+6756C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444807 | ||||||
| chr6:45444911
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.685+6860C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444911 | ||||||
| chr6:45444920
|
G | A | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+6869G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45444920 | ||||||
| chr6:45445086
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.685+7035G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445086 | ||||||
| chr6:45445094
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+7043G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445094 | ||||||
| chr6:45445147
|
C | T | 3 | a0001c0001t0007g0023a0001c0001t0007g0063a0001c0001t0007g0118 | 3 | HG01891.hp1 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.685+7096C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445147 | ||||||
| chr6:45445172
|
G | A | 2 | a0001c0001t0010g0002a0001c0001t0011g0064 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.685+7121G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445172 | ||||||
| chr6:45445314
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+7263G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445314 | ||||||
| chr6:45445689
|
G | A | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685+7638G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445689 | ||||||
| chr6:45445703
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.685+7652A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445703 | ||||||
| chr6:45445742
|
G | A | 33 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0062others(30): Show | 33 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.685+7691G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445742 | ||||||
| chr6:45445830
|
G | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0131 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.685+7779G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445830 | ||||||
| chr6:45445849
|
G | A | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.685+7798G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45445849 | ||||||
| chr6:45446121
|
G | C | 1 | a0001c0001t0003g0042 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.685+8070G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446121 | ||||||
| chr6:45446170
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0130 | 2 | NA19240.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.685+8119G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446170 | ||||||
| chr6:45446213
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+8162A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446213 | ||||||
| chr6:45446350
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.685+8299T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446350 | ||||||
| chr6:45446485
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.685+8434C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446485 | ||||||
| chr6:45446501
|
C | CT | 7 | a0001c0001t0001g0022a0001c0001t0001g0082a0001c0001t0002g0004others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.685+8464dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45446501 | |||||
| chr6:45446515
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.685+8464T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446515 | ||||||
| chr6:45446633
|
G | A | 9 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0159others(6): Show | 9 | HG01884.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+8582G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446633 | ||||||
| chr6:45446737
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.685+8686T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45446737 | ||||||
| chr6:45447032
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.685+8981G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45447032 | ||||||
| chr6:45447148
|
G | C | 1 | a0001c0001t0001g0137 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.685+9097G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45447148 | ||||||
| chr6:45447323
|
C | G | 1 | a0001c0001t0005g0011 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.685+9272C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45447323 | ||||||
| chr6:45447454
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.685+9403C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45447454 | ||||||
| chr6:45447463
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685+9412T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45447463 | ||||||
| chr6:45447622
|
G | A | 1 | a0001c0002t0003g0058 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.685+9571G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45447622 | ||||||
| chr6:45447639
|
T | C | 1 | a0001c0001t0005g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.685+9588T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45447639 | ||||||
| chr6:45448012
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.685+9961A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45448012 | ||||||
| chr6:45448434
|
C | T | 1 | a0001c0001t0005g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.685+10383C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45448434 | ||||||
| chr6:45448773
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.685+10722G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45448773 | ||||||
| chr6:45449183
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0176a0001c0001t0010g0129 | 3 | HG01884.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.685+11132G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449183 | ||||||
| chr6:45449284
|
T | C | 3 | a0001c0001t0004g0021a0001c0001t0004g0089a0001c0002t0015g0043 | 3 | HG00099.hp1 HG01106.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.685+11233T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449284 | ||||||
| chr6:45449357
|
A | G | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.685+11306A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449357 | ||||||
| chr6:45449381
|
T | C | 150 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(147): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.685+11330T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449381 | ||||||
| chr6:45449621
|
A | G | 1 | a0004c0005t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.685+11570A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449621 | ||||||
| chr6:45449706
|
G | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+11655G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449706 | ||||||
| chr6:45449926
|
C | A | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+11875C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449926 | ||||||
| chr6:45449990
|
T | A | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685+11939T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45449990 | ||||||
| chr6:45450024
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685+11973C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450024 | ||||||
| chr6:45450166
|
C | G | 2 | a0001c0001t0001g0135a0001c0001t0009g0025 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.685+12115C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450166 | ||||||
| chr6:45450269
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.685+12218T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450269 | ||||||
| chr6:45450349
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.685+12298A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450349 | ||||||
| chr6:45450360
|
T | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+12309T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450360 | ||||||
| chr6:45450436
|
AG | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0079 | 2 | HG00423.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.685+12386delG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450436 | ||||||
| chr6:45450635
|
C | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+12584C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450635 | ||||||
| chr6:45450665
|
C | T | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+12614C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450665 | ||||||
| chr6:45450697
|
A | G | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685+12646A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450697 | ||||||
| chr6:45450970
|
T | G | 1 | a0001c0001t0001g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.685+12919T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45450970 | ||||||
| chr6:45451019
|
C | T | 9 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(6): Show | 9 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+12968C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451019 | ||||||
| chr6:45451362
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.685+13311A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451362 | ||||||
| chr6:45451373
|
C | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.685+13322C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451373 | ||||||
| chr6:45451435
|
G | A | 1 | a0001c0001t0006g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.685+13384G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451435 | ||||||
| chr6:45451452
|
C | G | 1 | a0001c0002t0004g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.685+13401C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451452 | ||||||
| chr6:45451563
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.685+13512G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451563 | ||||||
| chr6:45451691
|
A | C | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+13640A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451691 | ||||||
| chr6:45452185
|
T | C | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+14134T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45452185 | ||||||
| chr6:45452593
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0094a0001c0001t0001g0100 | 3 | HG00597.hp2 NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.685+14542A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45452593 | ||||||
| chr6:45452894
|
T | C | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.685+14843T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45452894 | ||||||
| chr6:45452955
|
C | T | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.685+14904C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45452955 | ||||||
| chr6:45453110
|
C | T | 148 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.685+15059C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45453110 | ||||||
| chr6:45453120
|
A | G | 1 | a0001c0006t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.685+15069A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45453120 | ||||||
| chr6:45453311
|
G | C | 173 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.685+15260G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45453311 | ||||||
| chr6:45453893
|
C | T | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+15842C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45453893 | ||||||
| chr6:45454024
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+15973A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454024 | ||||||
| chr6:45454038
|
GA | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+15988delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454038 | ||||||
| chr6:45454255
|
G | A | 2 | a0001c0001t0007g0023a0001c0001t0007g0063 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.685+16204G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454255 | ||||||
| chr6:45454260
|
G | A | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685+16209G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454260 | ||||||
| chr6:45454274
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+16223T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454274 | ||||||
| chr6:45454580
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685+16529C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454580 | ||||||
| chr6:45454586
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.685+16535A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454586 | ||||||
| chr6:45454720
|
G | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+16669G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454720 | ||||||
| chr6:45454759
|
C | T | 18 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.685+16708C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454759 | ||||||
| chr6:45454835
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+16784C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45454835 | ||||||
| chr6:45455036
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.685+16985C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45455036 | ||||||
| chr6:45455066
|
A | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+17015A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45455066 | ||||||
| chr6:45455302
|
T | C | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685+17251T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45455302 | ||||||
| chr6:45455624
|
G | A | 1 | a0001c0002t0001g0046 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.685+17573G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45455624 | ||||||
| chr6:45455625
|
C | A | 1 | a0001c0002t0001g0046 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.685+17574C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45455625 | ||||||
| chr6:45455829
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.685+17778C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45455829 | ||||||
| chr6:45456182
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+18131A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45456182 | ||||||
| chr6:45456240
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.685+18189T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45456240 | ||||||
| chr6:45456576
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+18525T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45456576 | ||||||
| chr6:45456761
|
G | A | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+18710G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45456761 | ||||||
| chr6:45457152
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.685+19101A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45457152 | ||||||
| chr6:45457203
|
A | G | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.685+19152A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45457203 | ||||||
| chr6:45457501
|
G | A | 9 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(6): Show | 9 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+19450G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45457501 | ||||||
| chr6:45457513
|
ACT | A | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.685+19465_685+1946 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45457513 | |||||
| chr6:45458022
|
A | ATTTTT | 7 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG01069.hp1 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.685+19983_685+1998 others(9): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45458022 | |||||
| chr6:45458022
|
A | ATTTTTT | 36 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0076others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.685+19982_685+1998 others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45458022 | |||||
| chr6:45458022
|
A | ATTTTTTT | 23 | a0001c0001t0001g0040a0001c0001t0001g0065a0001c0001t0001g0068others(20): Show | 23 | HG00735.hp1 HG00735.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.685+19981_685+1998 others(11): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45458022 | |||||
| chr6:45458022
|
A | ATTTTTTT others(2): Show |
6 | a0001c0001t0001g0112a0001c0001t0002g0107a0001c0001t0002g0111others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.685+19979_685+1998 others(13): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45458022 | |||||
| chr6:45458022
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0057a0001c0001t0001g0119a0001c0001t0002g0024others(1): Show | 4 | HG01255.hp2 HG02630.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+19978_685+1998 others(14): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45458022 | |||||
| chr6:45458049
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.685+19998C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458049 | ||||||
| chr6:45458185
|
C | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+20134C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458185 | ||||||
| chr6:45458331
|
G | A | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.685+20280G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458331 | ||||||
| chr6:45458384
|
G | GT | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.685+20335dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45458384 | |||||
| chr6:45458457
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.685+20406A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458457 | ||||||
| chr6:45458672
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+20621C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458672 | ||||||
| chr6:45458680
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+20629A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458680 | ||||||
| chr6:45458942
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+20891A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458942 | ||||||
| chr6:45458974
|
A | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+20923A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45458974 | ||||||
| chr6:45459411
|
C | G | 1 | a0001c0001t0003g0102 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.685+21360C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459411 | ||||||
| chr6:45459445
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.685+21394C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459445 | ||||||
| chr6:45459468
|
A | T | 9 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(6): Show | 9 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+21417A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459468 | ||||||
| chr6:45459532
|
A | G | 1 | a0001c0001t0007g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.685+21481A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459532 | ||||||
| chr6:45459680
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+21629T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459680 | ||||||
| chr6:45459844
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.685+21793G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459844 | ||||||
| chr6:45459859
|
A | G | 9 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(6): Show | 9 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+21808A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459859 | ||||||
| chr6:45459941
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.685+21890C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45459941 | ||||||
| chr6:45460109
|
G | T | 9 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0159others(6): Show | 9 | HG01884.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+22058G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45460109 | ||||||
| chr6:45460379
|
G | A | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685+22328G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45460379 | ||||||
| chr6:45460442
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.685+22391C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45460442 | ||||||
| chr6:45460534
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+22483G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45460534 | ||||||
| chr6:45460552
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.685+22501G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45460552 | ||||||
| chr6:45460771
|
T | TA | 69 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0057others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.685+22730dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45460771 | |||||
| chr6:45460893
|
A | G | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.685+22842A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45460893 | ||||||
| chr6:45461115
|
G | A | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.685+23064G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461115 | ||||||
| chr6:45461120
|
T | C | 18 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.685+23069T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461120 | ||||||
| chr6:45461187
|
A | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+23136A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461187 | ||||||
| chr6:45461282
|
C | T | 2 | a0001c0001t0010g0002a0001c0001t0011g0064 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.685+23231C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461282 | ||||||
| chr6:45461402
|
C | A | 29 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0002g0132others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.685+23351C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461402 | ||||||
| chr6:45461567
|
G | A | 1 | a0001c0001t0007g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.685+23516G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461567 | ||||||
| chr6:45461600
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.685+23549A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461600 | ||||||
| chr6:45461752
|
AT | A | 28 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0002g0004others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.685+23713delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45461752 | |||||
| chr6:45461865
|
A | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0122others(1): Show | 4 | HG00438.hp1 NA18747.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+23814A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461865 | ||||||
| chr6:45461884
|
T | C | 9 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(6): Show | 9 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+23833T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45461884 | ||||||
| chr6:45462098
|
T | G | 1 | a0001c0001t0019g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.685+24047T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462098 | ||||||
| chr6:45462259
|
T | G | 1 | a0001c0001t0021g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.685+24208T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462259 | ||||||
| chr6:45462265
|
G | T | 1 | a0001c0001t0013g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.685+24214G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462265 | ||||||
| chr6:45462311
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+24260G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462311 | ||||||
| chr6:45462371
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.685+24320G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462371 | ||||||
| chr6:45462410
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0003g0009 | 2 | HG00609.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.685+24359G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462410 | ||||||
| chr6:45462599
|
C | A | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.685+24548C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462599 | ||||||
| chr6:45462626
|
T | A | 2 | a0001c0001t0001g0062a0001c0006t0001g0108 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.685+24575T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45462626 | ||||||
| chr6:45463077
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.685+25026G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45463077 | ||||||
| chr6:45463121
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.685+25070A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45463121 | ||||||
| chr6:45463635
|
T | A | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.685+25584T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45463635 | ||||||
| chr6:45463921
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.685+25870C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45463921 | ||||||
| chr6:45463931
|
C | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+25880C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45463931 | ||||||
| chr6:45463975
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0002g0107a0001c0001t0002g0109others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.685+25924C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45463975 | ||||||
| chr6:45464054
|
G | A | 1 | a0001c0001t0001g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.685+26003G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464054 | ||||||
| chr6:45464191
|
TA | T | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.685+26155delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45464191 | |||||
| chr6:45464269
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685+26218G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464269 | ||||||
| chr6:45464395
|
C | A | 1 | a0001c0001t0003g0029 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.685+26344C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464395 | ||||||
| chr6:45464477
|
G | A | 76 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0057others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.685+26426G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464477 | ||||||
| chr6:45464528
|
C | T | 28 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.685+26477C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464528 | ||||||
| chr6:45464719
|
C | T | 18 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0145others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.685+26668C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464719 | ||||||
| chr6:45464742
|
A | C | 6 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.685+26691A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464742 | ||||||
| chr6:45464882
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.685+26831A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45464882 | ||||||
| chr6:45465385
|
T | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-26556T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465385 | ||||||
| chr6:45465411
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-26530G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465411 | ||||||
| chr6:45465521
|
C | T | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.686-26420C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465521 | ||||||
| chr6:45465547
|
G | A | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686-26394G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465547 | ||||||
| chr6:45465600
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-26341T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465600 | ||||||
| chr6:45465877
|
C | T | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.686-26064C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465877 | ||||||
| chr6:45465932
|
G | A | 1 | a0001c0001t0021g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.686-26009G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465932 | ||||||
| chr6:45465940
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.686-26001C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45465940 | ||||||
| chr6:45466036
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0176a0001c0001t0002g0133others(1): Show | 4 | HG01884.hp2 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-25905G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466036 | ||||||
| chr6:45466042
|
A | G | 1 | a0001c0001t0005g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.686-25899A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466042 | ||||||
| chr6:45466067
|
A | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-25874A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466067 | ||||||
| chr6:45466102
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.686-25839C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466102 | ||||||
| chr6:45466205
|
C | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-25736C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466205 | ||||||
| chr6:45466309
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.686-25632G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466309 | ||||||
| chr6:45466475
|
C | T | 29 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0002g0132others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.686-25466C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466475 | ||||||
| chr6:45466560
|
T | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-25381T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466560 | ||||||
| chr6:45466728
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-25213T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466728 | ||||||
| chr6:45466822
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-25119G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466822 | ||||||
| chr6:45466947
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-24994A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45466947 | ||||||
| chr6:45467127
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.686-24814T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467127 | ||||||
| chr6:45467133
|
C | T | 1 | a0001c0002t0004g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.686-24808C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467133 | ||||||
| chr6:45467464
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.686-24477T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467464 | ||||||
| chr6:45467601
|
G | A | 18 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.686-24340G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467601 | ||||||
| chr6:45467613
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-24328G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467613 | ||||||
| chr6:45467764
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.686-24177C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467764 | ||||||
| chr6:45467967
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-23974T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467967 | ||||||
| chr6:45467969
|
A | G | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.686-23972A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45467969 | ||||||
| chr6:45468157
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-23784C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468157 | ||||||
| chr6:45468219
|
C | T | 1 | a0001c0006t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.686-23722C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468219 | ||||||
| chr6:45468234
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-23707T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468234 | ||||||
| chr6:45468512
|
C | T | 29 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0002g0132others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.686-23429C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468512 | ||||||
| chr6:45468564
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.686-23377A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468564 | ||||||
| chr6:45468570
|
G | C | 1 | a0001c0001t0008g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.686-23371G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468570 | ||||||
| chr6:45468673
|
C | A | 2 | a0001c0001t0010g0002a0001c0001t0011g0064 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.686-23268C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468673 | ||||||
| chr6:45468707
|
C | T | 1 | a0001c0002t0004g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.686-23234C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468707 | ||||||
| chr6:45468708
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.686-23233T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468708 | ||||||
| chr6:45468710
|
G | T | 1 | a0001c0001t0021g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.686-23231G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45468710 | ||||||
| chr6:45469099
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.686-22842G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45469099 | ||||||
| chr6:45469747
|
A | G | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.686-22194A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45469747 | ||||||
| chr6:45469767
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-22174G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45469767 | ||||||
| chr6:45469991
|
T | G | 6 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0002g0107others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.686-21950T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45469991 | ||||||
| chr6:45470031
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.686-21910G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470031 | ||||||
| chr6:45470093
|
T | A | 5 | a0001c0001t0001g0119a0001c0001t0002g0107a0001c0001t0002g0109others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.686-21848T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470093 | ||||||
| chr6:45470430
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.686-21511G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470430 | ||||||
| chr6:45470431
|
A | G | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.686-21510A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470431 | ||||||
| chr6:45470465
|
C | T | 1 | a0001c0001t0005g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.686-21476C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470465 | ||||||
| chr6:45470735
|
A | G | 28 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.686-21206A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470735 | ||||||
| chr6:45470940
|
A | G | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.686-21001A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470940 | ||||||
| chr6:45470992
|
C | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-20949C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45470992 | ||||||
| chr6:45471137
|
T | C | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.686-20804T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471137 | ||||||
| chr6:45471262
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-20679G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471262 | ||||||
| chr6:45471323
|
A | C | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686-20618A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471323 | ||||||
| chr6:45471339
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.686-20602T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471339 | ||||||
| chr6:45471351
|
GT | G | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-20588delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45471351 | |||||
| chr6:45471408
|
T | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-20533T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471408 | ||||||
| chr6:45471424
|
C | CA | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-20517_686-2051 others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471424 | ||||||
| chr6:45471425
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-20516G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471425 | ||||||
| chr6:45471513
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.686-20428C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471513 | ||||||
| chr6:45471549
|
A | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-20392A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471549 | ||||||
| chr6:45471570
|
C | G | 28 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.686-20371C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471570 | ||||||
| chr6:45471594
|
A | G | 3 | a0001c0001t0001g0070a0001c0001t0002g0048a0001c0002t0001g0140 | 3 | HG00741.hp2 HG01978.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.686-20347A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471594 | ||||||
| chr6:45471686
|
C | T | 2 | a0001c0001t0001g0062a0001c0006t0001g0108 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.686-20255C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471686 | ||||||
| chr6:45471949
|
A | G | 28 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.686-19992A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45471949 | ||||||
| chr6:45472079
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0002g0117a0001c0001t0017g0144 | 3 | HG02559.hp1 HG02647.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.686-19862T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45472079 | ||||||
| chr6:45472386
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-19555A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45472386 | ||||||
| chr6:45472404
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.686-19537A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45472404 | ||||||
| chr6:45472405
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-19536A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45472405 | ||||||
| chr6:45472571
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.686-19370T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45472571 | ||||||
| chr6:45472700
|
C | A | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686-19241C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45472700 | ||||||
| chr6:45473151
|
C | A | 1 | a0001c0002t0003g0058 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.686-18790C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473151 | ||||||
| chr6:45473319
|
C | A | 1 | a0001c0001t0006g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.686-18622C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473319 | ||||||
| chr6:45473429
|
G | GTC | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-18512_686-1851 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473429 | ||||||
| chr6:45473432
|
GGA | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-18508_686-1850 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473432 | ||||||
| chr6:45473435
|
C | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-18506C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473435 | ||||||
| chr6:45473436
|
A | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-18505A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473436 | ||||||
| chr6:45473500
|
C | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-18441C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473500 | ||||||
| chr6:45473501
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.686-18440G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473501 | ||||||
| chr6:45473586
|
T | C | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.686-18355T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473586 | ||||||
| chr6:45473662
|
A | C | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-18279A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473662 | ||||||
| chr6:45473755
|
A | G | 1 | a0001c0001t0005g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.686-18186A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473755 | ||||||
| chr6:45473806
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-18135A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473806 | ||||||
| chr6:45473820
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.686-18121A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473820 | ||||||
| chr6:45473872
|
G | A | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.686-18069G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473872 | ||||||
| chr6:45473906
|
G | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-18035G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45473906 | ||||||
| chr6:45474129
|
A | T | 1 | a0001c0002t0003g0058 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.686-17812A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474129 | ||||||
| chr6:45474158
|
CT | C | 10 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(7): Show | 10 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.686-17770delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45474158 | |||||
| chr6:45474171
|
T | C | 8 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(5): Show | 8 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.686-17770T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474171 | ||||||
| chr6:45474192
|
G | A | 18 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.686-17749G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474192 | ||||||
| chr6:45474314
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-17627A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474314 | ||||||
| chr6:45474326
|
T | A | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.686-17615T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474326 | ||||||
| chr6:45474373
|
ATG | A | 42 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0092others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.686-17536_686-1753 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45474373 | |||||
| chr6:45474373
|
ATGTG | A | 30 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0052others(27): Show | 30 | HG00423.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.686-17538_686-1753 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45474373 | |||||
| chr6:45474373
|
ATGTGTG | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0094a0001c0001t0001g0100others(3): Show | 6 | HG00438.hp2 HG00597.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-17540_686-1753 others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45474373 | |||||
| chr6:45474373
|
ATGTGTGT others(1): Show |
A | 14 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(11): Show | 14 | HG01255.hp2 HG02109.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.686-17542_686-1753 others(12): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45474373 | |||||
| chr6:45474373
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686-17544_686-1753 others(14): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45474373 | |||||
| chr6:45474373
|
ATGTGTGT others(7): Show |
A | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.686-17548_686-1753 others(18): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45474373 | |||||
| chr6:45474646
|
G | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-17295G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474646 | ||||||
| chr6:45474713
|
T | C | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-17228T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474713 | ||||||
| chr6:45474806
|
T | C | 1 | a0001c0006t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.686-17135T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45474806 | ||||||
| chr6:45475057
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-16884G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475057 | ||||||
| chr6:45475083
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.686-16858C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475083 | ||||||
| chr6:45475109
|
G | GT | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-16831dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45475109 | |||||
| chr6:45475123
|
TA | T | 29 | a0001c0001t0001g0104a0001c0001t0002g0004a0001c0001t0002g0012others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.686-16800delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45475123 | |||||
| chr6:45475268
|
A | G | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686-16673A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475268 | ||||||
| chr6:45475298
|
G | A | 1 | a0001c0006t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.686-16643G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475298 | ||||||
| chr6:45475318
|
G | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-16623G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475318 | ||||||
| chr6:45475397
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.686-16544A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475397 | ||||||
| chr6:45475439
|
A | G | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.686-16502A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475439 | ||||||
| chr6:45475476
|
A | G | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.686-16465A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475476 | ||||||
| chr6:45475612
|
T | C | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-16329T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475612 | ||||||
| chr6:45475875
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.686-16066T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45475875 | ||||||
| chr6:45476146
|
C | T | 7 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-15795C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476146 | ||||||
| chr6:45476315
|
C | T | 1 | a0001c0007t0001g0028 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.686-15626C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476315 | ||||||
| chr6:45476324
|
C | T | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-15617C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476324 | ||||||
| chr6:45476346
|
G | GA | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-15594dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45476346 | |||||
| chr6:45476391
|
AT | A | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-15545delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45476391 | |||||
| chr6:45476521
|
A | G | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-15420A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476521 | ||||||
| chr6:45476705
|
C | G | 2 | a0001c0001t0007g0036a0001c0001t0014g0035 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686-15236C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476705 | ||||||
| chr6:45476852
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.686-15089C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476852 | ||||||
| chr6:45476872
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.686-15069A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476872 | ||||||
| chr6:45476887
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-15054G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45476887 | ||||||
| chr6:45477230
|
A | T | 28 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.686-14711A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45477230 | ||||||
| chr6:45477275
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-14666G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45477275 | ||||||
| chr6:45477718
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-14223A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45477718 | ||||||
| chr6:45477720
|
C | T | 1 | a0001c0001t0019g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.686-14221C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45477720 | ||||||
| chr6:45478065
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-13876C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45478065 | ||||||
| chr6:45478098
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.686-13843C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45478098 | ||||||
| chr6:45478210
|
G | A | 2 | a0001c0001t0003g0105a0001c0001t0005g0071 | 2 | HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.686-13731G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45478210 | ||||||
| chr6:45478284
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-13657A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45478284 | ||||||
| chr6:45478314
|
G | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-13627G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45478314 | ||||||
| chr6:45478638
|
A | ATG | 20 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0112others(17): Show | 20 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.686-13279_686-1327 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45478638 | |||||
| chr6:45478638
|
ATG | A | 25 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0123others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.686-13279_686-1327 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45478638 | |||||
| chr6:45478638
|
ATGTG | A | 4 | a0001c0001t0001g0082a0001c0001t0004g0014a0001c0001t0004g0053others(1): Show | 4 | HG00280.hp2 HG01167.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-13281_686-1327 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45478638 | |||||
| chr6:45478835
|
A | G | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686-13106A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45478835 | ||||||
| chr6:45478862
|
A | G | 1 | a0001c0006t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.686-13079A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45478862 | ||||||
| chr6:45479059
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-12882T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479059 | ||||||
| chr6:45479174
|
G | A | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.686-12767G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479174 | ||||||
| chr6:45479459
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.686-12482C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479459 | ||||||
| chr6:45479465
|
C | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-12476C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479465 | ||||||
| chr6:45479467
|
C | A | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686-12474C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479467 | ||||||
| chr6:45479509
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.686-12432C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479509 | ||||||
| chr6:45479545
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-12396C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479545 | ||||||
| chr6:45479821
|
A | G | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-12120A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45479821 | ||||||
| chr6:45480129
|
T | C | 26 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(23): Show | 26 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.686-11812T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45480129 | ||||||
| chr6:45480136
|
T | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-11805T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45480136 | ||||||
| chr6:45480197
|
A | T | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-11744A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45480197 | ||||||
| chr6:45480468
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.686-11473G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45480468 | ||||||
| chr6:45480839
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-11102G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45480839 | ||||||
| chr6:45480878
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.686-11063G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45480878 | ||||||
| chr6:45481123
|
C | G | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-10818C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481123 | ||||||
| chr6:45481132
|
A | C | 1 | a0001c0001t0004g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.686-10809A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481132 | ||||||
| chr6:45481275
|
C | G | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.686-10666C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481275 | ||||||
| chr6:45481425
|
A | T | 4 | a0001c0001t0007g0023a0001c0001t0007g0036a0001c0001t0007g0063others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-10516A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481425 | ||||||
| chr6:45481435
|
A | G | 1 | a0001c0001t0005g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.686-10506A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481435 | ||||||
| chr6:45481541
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.686-10400C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481541 | ||||||
| chr6:45481624
|
A | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0001g0119others(5): Show | 8 | HG01255.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.686-10317A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481624 | ||||||
| chr6:45481781
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.686-10160A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481781 | ||||||
| chr6:45481993
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.686-9948A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45481993 | ||||||
| chr6:45482061
|
G | A | 29 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.686-9880G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482061 | ||||||
| chr6:45482197
|
T | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-9744T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482197 | ||||||
| chr6:45482226
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.686-9715C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482226 | ||||||
| chr6:45482242
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.686-9699T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482242 | ||||||
| chr6:45482473
|
T | C | 85 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0052others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.686-9468T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482473 | ||||||
| chr6:45482549
|
A | C | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.686-9392A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482549 | ||||||
| chr6:45482757
|
T | C | 1 | a0001c0001t0010g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.686-9184T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482757 | ||||||
| chr6:45482767
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0002g0126 | 2 | HG02886.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.686-9174G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482767 | ||||||
| chr6:45482937
|
T | A | 2 | a0001c0001t0001g0113a0001c0001t0002g0115 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.686-9004T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45482937 | ||||||
| chr6:45483174
|
C | T | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.686-8767C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45483174 | ||||||
| chr6:45483230
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.686-8711A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45483230 | ||||||
| chr6:45483351
|
CT | C | 34 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.686-8579delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45483351 | |||||
| chr6:45483506
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.686-8435A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45483506 | ||||||
| chr6:45483635
|
C | T | 20 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(17): Show | 20 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.686-8306C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45483635 | ||||||
| chr6:45483831
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.686-8110G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45483831 | ||||||
| chr6:45483855
|
C | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0116others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-8086C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45483855 | ||||||
| chr6:45483885
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0002g0126 | 2 | HG02886.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.686-8056G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45483885 | ||||||
| chr6:45484016
|
C | A | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686-7925C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484016 | ||||||
| chr6:45484054
|
A | C | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.686-7887A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484054 | ||||||
| chr6:45484099
|
C | T | 36 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.686-7842C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484099 | ||||||
| chr6:45484267
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-7674G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484267 | ||||||
| chr6:45484372
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.686-7569G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484372 | ||||||
| chr6:45484416
|
A | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.686-7525A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484416 | ||||||
| chr6:45484561
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-7380T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484561 | ||||||
| chr6:45484760
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.686-7181A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45484760 | ||||||
| chr6:45485064
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-6877G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485064 | ||||||
| chr6:45485132
|
CTGCCAAA others(38): Show |
C | 1 | a0001c0002t0003g0058 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.686-6807_686-6763d others(47): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485132 | |||||
| chr6:45485192
|
CT | C | 26 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0127others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.686-6734delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485192 | |||||
| chr6:45485220
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.686-6721G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485220 | ||||||
| chr6:45485350
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.686-6591G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485350 | ||||||
| chr6:45485390
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.686-6551C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485390 | ||||||
| chr6:45485583
|
T | C | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.686-6358T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485583 | ||||||
| chr6:45485607
|
C | T | 2 | a0001c0001t0001g0092a0003c0004t0001g0072 | 2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.686-6334C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485607 | ||||||
| chr6:45485608
|
G | A | 26 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0127others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.686-6333G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485608 | ||||||
| chr6:45485646
|
C | T | 84 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0052others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.686-6295C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485646 | ||||||
| chr6:45485669
|
A | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(12): Show | 15 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.686-6272A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485669 | ||||||
| chr6:45485673
|
A | ATG | 12 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0134others(9): Show | 12 | HG01884.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.686-6244_686-6243d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485673 | |||||
| chr6:45485673
|
A | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0052others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.686-6268A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485673 | ||||||
| chr6:45485673
|
ATG | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0117 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.686-6244_686-6243d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485673 | |||||
| chr6:45485673
|
ATGTG | A | 2 | a0001c0001t0001g0145a0001c0001t0008g0034 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.686-6246_686-6243d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485673 | |||||
| chr6:45485691
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.686-6249_686-6248i others(22): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485691 | |||||
| chr6:45485693
|
G | A | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.686-6248G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485693 | ||||||
| chr6:45485693
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.686-6247_686-6246i others(22): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485693 | |||||
| chr6:45485693
|
G | GTATATAT others(15): Show |
2 | a0001c0001t0003g0101a0001c0001t0003g0150 | 2 | HG00323.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.686-6247_686-6246i others(24): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485693 | |||||
| chr6:45485693
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0003g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.686-6247_686-6246i others(26): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485693 | |||||
| chr6:45485693
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0006g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.686-6247_686-6246i others(30): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485693 | |||||
| chr6:45485695
|
G | A | 32 | a0001c0001t0001g0057a0001c0001t0001g0081a0001c0001t0001g0104others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.686-6246G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485695 | ||||||
| chr6:45485695
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0052a0001c0001t0003g0029a0001c0001t0005g0011 | 3 | HG01928.hp1 HG01928.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.686-6245_686-6244i others(20): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485695
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0006g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.686-6245_686-6244i others(22): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485695
|
G | GTATATAT others(15): Show |
7 | a0001c0001t0001g0097a0001c0001t0001g0135a0001c0001t0002g0126others(4): Show | 7 | HG01346.hp1 HG01496.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-6245_686-6244i others(24): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485695
|
G | GTATATAT others(17): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0003g0069others(3): Show | 6 | HG01167.hp2 HG01243.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.686-6245_686-6244i others(26): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485695
|
G | GTATATAT others(19): Show |
10 | a0001c0001t0001g0040a0001c0001t0001g0076a0001c0001t0001g0080others(7): Show | 10 | HG00280.hp1 HG00609.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.686-6245_686-6244i others(28): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485695
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.686-6245_686-6244i others(30): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485695
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0009g0025a0001c0001t0012g0148 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.686-6245_686-6244i others(32): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485695
|
G | GTATGTAT others(23): Show |
1 | a0001c0001t0001g0079 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.686-6245_686-6244i others(32): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485695 | |||||
| chr6:45485697
|
G | A | 68 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0057others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.686-6244G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485697 | ||||||
| chr6:45485697
|
G | GTA | 8 | a0001c0001t0001g0020a0001c0001t0001g0151a0001c0001t0001g0164others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.686-6225_686-6224d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0002g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.686-6235_686-6224d others(14): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTATATAT others(7): Show |
3 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0111 | 3 | HG02622.hp1 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.686-6237_686-6224d others(16): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTATATAT others(15): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0100 | 2 | HG00438.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.686-6224_686-6223i others(24): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0001g0136a0001c0001t0002g0048 | 2 | HG01978.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.686-6224_686-6223i others(26): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTATATAT others(19): Show |
3 | a0001c0001t0001g0070a0001c0001t0001g0142a0001c0001t0002g0173 | 3 | HG01891.hp2 HG01978.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.686-6224_686-6223i others(28): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTATATAT others(21): Show |
4 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0002g0171others(1): Show | 4 | HG00741.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-6224_686-6223i others(30): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTA | 3 | a0001c0001t0001g0062a0001c0001t0001g0158a0001c0001t0010g0129 | 3 | HG02717.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.686-6243_686-6242i others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTATAT others(7): Show |
1 | a0001c0001t0001g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.686-6243_686-6242i others(16): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTATAT others(9): Show |
2 | a0001c0001t0007g0023a0001c0001t0007g0063 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.686-6243_686-6242i others(18): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0007g0036 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.686-6243_686-6242i others(20): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTATAT others(15): Show |
4 | a0001c0001t0002g0032a0001c0001t0003g0138a0001c0001t0009g0152others(1): Show | 4 | HG02717.hp2 HG02976.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-6243_686-6242i others(24): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTGTAT others(11): Show |
1 | a0001c0001t0008g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.686-6243_686-6242i others(20): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTGTAT others(17): Show |
2 | a0001c0001t0001g0169a0001c0001t0007g0118 | 2 | HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.686-6243_686-6242i others(26): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485697
|
G | GTGTGTAT others(19): Show |
2 | a0001c0001t0001g0130a0001c0001t0008g0160 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.686-6243_686-6242i others(28): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485697 | |||||
| chr6:45485699
|
A | G | 1 | a0001c0001t0013g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.686-6242A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485699 | ||||||
| chr6:45485716
|
T | TATATATA others(1): Show |
3 | a0001c0001t0004g0014a0001c0001t0004g0053a0001c0001t0006g0037 | 3 | HG00280.hp2 HG01167.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.686-6224_686-6223i others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485716 | |||||
| chr6:45485716
|
T | TATATATA others(3): Show |
2 | a0001c0001t0005g0085a0001c0001t0018g0157 | 2 | HG01952.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.686-6224_686-6223i others(12): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485716 | |||||
| chr6:45485716
|
T | TATATATA others(5): Show |
13 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0003g0105others(10): Show | 13 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.686-6224_686-6223i others(14): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485716 | |||||
| chr6:45485716
|
T | TATATATA others(9): Show |
4 | a0001c0001t0002g0172a0001c0001t0004g0021a0001c0001t0004g0089others(1): Show | 4 | HG01106.hp1 HG01346.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-6224_686-6223i others(18): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485716 | |||||
| chr6:45485716
|
T | TATATATA others(11): Show |
1 | a0001c0002t0015g0043 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.686-6224_686-6223i others(20): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45485716 | |||||
| chr6:45485968
|
A | G | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.686-5973A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45485968 | ||||||
| chr6:45486118
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.686-5823A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45486118 | ||||||
| chr6:45486226
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.686-5715T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45486226 | ||||||
| chr6:45486957
|
T | C | 1 | a0002c0003t0001g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.686-4984T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45486957 | ||||||
| chr6:45487052
|
T | A | 1 | a0001c0007t0001g0028 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.686-4889T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45487052 | ||||||
| chr6:45487107
|
A | G | 24 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.686-4834A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45487107 | ||||||
| chr6:45487180
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.686-4761A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45487180 | ||||||
| chr6:45487416
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-4525T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45487416 | ||||||
| chr6:45487663
|
A | T | 1 | a0001c0006t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.686-4278A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45487663 | ||||||
| chr6:45488354
|
T | A | 2 | a0001c0001t0003g0074a0001c0001t0003g0150 | 2 | HG00323.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.686-3587T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45488354 | ||||||
| chr6:45488716
|
G | GA | 68 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0057others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.686-3223dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45488716 | |||||
| chr6:45488827
|
G | T | 26 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.686-3114G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45488827 | ||||||
| chr6:45488863
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0094a0001c0001t0001g0123 | 3 | HG00438.hp2 HG00597.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.686-3078T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45488863 | ||||||
| chr6:45489084
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.686-2857A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45489084 | ||||||
| chr6:45489244
|
T | C | 27 | a0001c0001t0001g0104a0001c0001t0002g0132a0001c0001t0002g0172others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.686-2697T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45489244 | ||||||
| chr6:45489637
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.686-2304C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45489637 | ||||||
| chr6:45489638
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0010g0129 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.686-2303G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45489638 | ||||||
| chr6:45489704
|
GTGTC | G | 28 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(25): Show | 28 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.686-2233_686-2230d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45489704 | |||||
| chr6:45490037
|
C | T | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.686-1904C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45490037 | ||||||
| chr6:45490325
|
T | C | 1 | a0001c0002t0004g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.686-1616T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45490325 | ||||||
| chr6:45490617
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0002g0126 | 2 | HG02886.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.686-1324T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45490617 | ||||||
| chr6:45490628
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0002g0126 | 2 | HG02886.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.686-1313A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45490628 | ||||||
| chr6:45490643
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-1298C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45490643 | ||||||
| chr6:45491161
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0095a0001c0001t0021g0088 | 3 | HG02056.hp1 HG02074.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.686-780C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491161 | ||||||
| chr6:45491166
|
C | T | 5 | a0001c0001t0002g0132a0001c0001t0002g0172a0001c0001t0008g0128others(2): Show | 5 | HG02451.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.686-775C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491166 | ||||||
| chr6:45491267
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.686-674C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491267 | ||||||
| chr6:45491502
|
C | T | 1 | a0001c0001t0008g0160 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.686-439C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491502 | ||||||
| chr6:45491622
|
G | GT | 30 | a0001c0001t0001g0041a0001c0001t0001g0077a0001c0001t0001g0081others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.686-296dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45491622 | |||||
| chr6:45491622
|
G | GTT | 10 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0116others(7): Show | 10 | HG01069.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.686-297_686-296dup others(2): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45491622 | |||||
| chr6:45491622
|
GT | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0056a0001c0001t0001g0134others(3): Show | 6 | HG01952.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-296delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 45491622 | |||||
| chr6:45491624
|
T | G | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.686-317T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491624 | ||||||
| chr6:45491625
|
T | TG | 6 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0002g0107others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.686-316_686-315ins others(1): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491625 | ||||||
| chr6:45491626
|
T | G | 3 | a0001c0001t0001g0057a0001c0001t0016g0153a0002c0003t0001g0161 | 3 | HG01192.hp2 HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.686-315T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491626 | ||||||
| chr6:45491677
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0172a0001c0001t0018g0157 | 3 | HG02451.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.686-264C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491677 | ||||||
| chr6:45491763
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.686-178C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491763 | ||||||
| chr6:45491771
|
G | A | 1 | a0001c0001t0010g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.686-170G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45491771 | ||||||
| chr6:45492148
|
C | G | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.859+34C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45492148 | ||||||
| chr6:45492366
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.859+252G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45492366 | ||||||
| chr6:45492448
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.859+334C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45492448 | ||||||
| chr6:45492587
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0009g0025 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.859+473T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45492587 | ||||||
| chr6:45492760
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.859+646C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45492760 | ||||||
| chr6:45493510
|
G | A | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.859+1396G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45493510 | ||||||
| chr6:45493516
|
G | A | 26 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0110others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.859+1402G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45493516 | ||||||
| chr6:45493730
|
C | CTG | 68 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0094others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.859+1642_859+1643d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45493730 | |||||
| chr6:45493730
|
C | CTGTG | 3 | a0001c0001t0001g0062a0001c0001t0001g0177a0001c0001t0010g0129 | 3 | HG02717.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.859+1640_859+1643d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45493730 | |||||
| chr6:45493730
|
CTG | C | 5 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(2): Show | 5 | HG01255.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+1642_859+1643d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45493730 | |||||
| chr6:45493851
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.859+1737A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45493851 | ||||||
| chr6:45493901
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.859+1787T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45493901 | ||||||
| chr6:45494017
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0011g0064 | 2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.859+1903G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494017 | ||||||
| chr6:45494038
|
A | T | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.859+1924A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494038 | ||||||
| chr6:45494082
|
T | TG | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+1968_859+1969i others(3): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494082 | ||||||
| chr6:45494089
|
T | C | 10 | a0001c0001t0001g0119a0001c0001t0002g0107a0001c0001t0002g0109others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.859+1975T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494089 | ||||||
| chr6:45494198
|
A | G | 11 | a0001c0001t0001g0119a0001c0001t0002g0107a0001c0001t0002g0109others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.859+2084A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494198 | ||||||
| chr6:45494427
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+2313G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494427 | ||||||
| chr6:45494727
|
G | A | 1 | a0001c0002t0004g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.859+2613G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494727 | ||||||
| chr6:45494750
|
C | T | 20 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0002g0107others(17): Show | 20 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.859+2636C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494750 | ||||||
| chr6:45494823
|
G | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0016g0153 | 3 | HG01255.hp2 HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.859+2709G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45494823 | ||||||
| chr6:45495117
|
C | T | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.859+3003C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45495117 | ||||||
| chr6:45495188
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.859+3074A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45495188 | ||||||
| chr6:45495516
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.859+3402T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45495516 | ||||||
| chr6:45495670
|
T | G | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG01928.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.859+3556T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45495670 | ||||||
| chr6:45495725
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0009g0152a0001c0001t0009g0168 | 3 | HG02717.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.859+3611T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45495725 | ||||||
| chr6:45496013
|
C | T | 1 | a0001c0001t0005g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.859+3899C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45496013 | ||||||
| chr6:45496020
|
A | G | 1 | a0001c0002t0004g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.859+3906A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45496020 | ||||||
| chr6:45496048
|
C | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0076others(2): Show | 5 | HG00423.hp2 NA18747.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+3934C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45496048 | ||||||
| chr6:45496287
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.859+4173G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45496287 | ||||||
| chr6:45496317
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.859+4203C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45496317 | ||||||
| chr6:45496705
|
G | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.859+4591G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45496705 | ||||||
| chr6:45496803
|
A | C | 8 | a0001c0001t0001g0119a0001c0001t0002g0107a0001c0001t0002g0109others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.859+4689A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45496803 | ||||||
| chr6:45496899
|
CTT | C | 8 | a0001c0001t0001g0119a0001c0001t0002g0107a0001c0001t0002g0109others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.859+4792_859+4793d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45496899 | |||||
| chr6:45497020
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.859+4906G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45497020 | ||||||
| chr6:45497174
|
T | G | 27 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0067others(24): Show | 27 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.859+5060T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45497174 | ||||||
| chr6:45497695
|
A | G | 1 | a0002c0003t0001g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.859+5581A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45497695 | ||||||
| chr6:45497843
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.859+5729G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45497843 | ||||||
| chr6:45497873
|
C | G | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+5759C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45497873 | ||||||
| chr6:45498016
|
A | T | 84 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0052others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.859+5902A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498016 | ||||||
| chr6:45498222
|
T | C | 3 | a0001c0001t0008g0128a0001c0001t0008g0160a0001c0001t0014g0035 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.859+6108T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498222 | ||||||
| chr6:45498273
|
T | C | 2 | a0001c0001t0005g0011a0001c0001t0006g0075 | 2 | HG01258.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.859+6159T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498273 | ||||||
| chr6:45498281
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.859+6167T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498281 | ||||||
| chr6:45498355
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.859+6241G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498355 | ||||||
| chr6:45498444
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.859+6330G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498444 | ||||||
| chr6:45498476
|
T | G | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.859+6362T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498476 | ||||||
| chr6:45498597
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.859+6483G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498597 | ||||||
| chr6:45498964
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+6850G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45498964 | ||||||
| chr6:45499166
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+7052T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45499166 | ||||||
| chr6:45499316
|
A | ATC | 21 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0002g0107others(18): Show | 21 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.859+7204_859+7205d others(4): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45499316 | |||||
| chr6:45499370
|
C | A | 1 | a0001c0001t0001g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.859+7256C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45499370 | ||||||
| chr6:45499510
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.859+7396T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45499510 | ||||||
| chr6:45499623
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+7509C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45499623 | ||||||
| chr6:45499679
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0010g0129 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.859+7565A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45499679 | ||||||
| chr6:45500028
|
A | G | 85 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0052others(82): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.859+7914A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45500028 | ||||||
| chr6:45500049
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0016g0153 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.859+7935G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45500049 | ||||||
| chr6:45500115
|
G | T | 1 | a0001c0002t0015g0043 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.859+8001G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45500115 | ||||||
| chr6:45500337
|
T | G | 53 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0057others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.859+8223T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45500337 | ||||||
| chr6:45500494
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.859+8380A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45500494 | ||||||
| chr6:45500807
|
G | A | 2 | a0001c0001t0003g0087a0001c0001t0003g0147 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.859+8693G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45500807 | ||||||
| chr6:45500842
|
A | G | 2 | a0001c0001t0009g0152a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.859+8728A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45500842 | ||||||
| chr6:45501152
|
C | G | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.859+9038C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45501152 | ||||||
| chr6:45501179
|
C | T | 1 | a0001c0002t0003g0058 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.859+9065C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45501179 | ||||||
| chr6:45501434
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.859+9320T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45501434 | ||||||
| chr6:45501609
|
A | G | 1 | a0001c0002t0003g0058 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.859+9495A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45501609 | ||||||
| chr6:45501889
|
C | A | 18 | a0001c0001t0001g0104a0001c0001t0003g0105a0001c0001t0004g0005others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.859+9775C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45501889 | ||||||
| chr6:45501921
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.859+9807G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45501921 | ||||||
| chr6:45502024
|
G | C | 8 | a0001c0001t0001g0119a0001c0001t0002g0107a0001c0001t0002g0109others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.859+9910G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502024 | ||||||
| chr6:45502060
|
T | A | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.859+9946T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502060 | ||||||
| chr6:45502173
|
G | T | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.859+10059G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502173 | ||||||
| chr6:45502485
|
C | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0009g0152others(2): Show | 5 | HG01255.hp2 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-9761C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502485 | ||||||
| chr6:45502486
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.860-9760G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502486 | ||||||
| chr6:45502621
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.860-9625G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502621 | ||||||
| chr6:45502717
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.860-9529G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502717 | ||||||
| chr6:45502960
|
G | A | 1 | a0001c0001t0020g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.860-9286G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45502960 | ||||||
| chr6:45503123
|
A | G | 1 | a0001c0001t0005g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.860-9123A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45503123 | ||||||
| chr6:45503485
|
T | G | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.860-8761T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45503485 | ||||||
| chr6:45503692
|
G | A | 1 | a0001c0001t0001g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.860-8554G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45503692 | ||||||
| chr6:45504154
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.860-8092C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45504154 | ||||||
| chr6:45504198
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-8048G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45504198 | ||||||
| chr6:45504407
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.860-7839T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45504407 | ||||||
| chr6:45504561
|
T | C | 52 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0057others(49): Show | 52 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.860-7685T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45504561 | ||||||
| chr6:45505000
|
C | T | 21 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0002g0107others(18): Show | 21 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.860-7246C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45505000 | ||||||
| chr6:45505033
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0009g0025 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.860-7213C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45505033 | ||||||
| chr6:45505056
|
T | C | 3 | a0001c0001t0008g0128a0001c0001t0008g0160a0001c0001t0014g0035 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.860-7190T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45505056 | ||||||
| chr6:45505249
|
C | T | 1 | a0002c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.860-6997C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45505249 | ||||||
| chr6:45505352
|
T | C | 21 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0002g0107others(18): Show | 21 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.860-6894T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45505352 | ||||||
| chr6:45505519
|
T | C | 53 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0057others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.860-6727T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45505519 | ||||||
| chr6:45505832
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0016g0153 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.860-6414G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45505832 | ||||||
| chr6:45506200
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.860-6046C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506200 | ||||||
| chr6:45506240
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-6006C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506240 | ||||||
| chr6:45506243
|
A | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.860-6003A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506243 | ||||||
| chr6:45506318
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.860-5928C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506318 | ||||||
| chr6:45506729
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0010g0129 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.860-5517C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506729 | ||||||
| chr6:45506795
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.860-5451T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506795 | ||||||
| chr6:45506953
|
G | T | 1 | a0001c0001t0021g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.860-5293G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506953 | ||||||
| chr6:45506969
|
C | CT | 9 | a0001c0001t0001g0167a0001c0001t0002g0107a0001c0001t0002g0109others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-5264dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45506969 | |||||
| chr6:45506999
|
A | G | 2 | a0001c0001t0009g0152a0001c0001t0009g0168 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.860-5247A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45506999 | ||||||
| chr6:45507037
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.860-5209C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45507037 | ||||||
| chr6:45507226
|
G | A | 4 | a0001c0001t0007g0023a0001c0001t0007g0036a0001c0001t0007g0063others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-5020G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45507226 | ||||||
| chr6:45507473
|
G | T | 2 | a0001c0001t0001g0062a0001c0001t0010g0129 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.860-4773G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45507473 | ||||||
| chr6:45507607
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0017g0144 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.860-4639T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45507607 | ||||||
| chr6:45507609
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.860-4637T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45507609 | ||||||
| chr6:45507949
|
A | C | 1 | a0001c0002t0004g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.860-4297A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45507949 | ||||||
| chr6:45507961
|
C | A | 1 | a0001c0002t0004g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.860-4285C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45507961 | ||||||
| chr6:45508057
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.860-4189G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45508057 | ||||||
| chr6:45508220
|
C | CT | 46 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0054others(43): Show | 46 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.860-4001dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45508220 | |||||
| chr6:45508220
|
CT | C | 16 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0158others(13): Show | 16 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.860-4001delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45508220 | |||||
| chr6:45508220
|
CTTTTTTT | C | 5 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0132others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-4007_860-4001d others(9): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45508220 | |||||
| chr6:45508319
|
C | T | 5 | a0001c0001t0001g0057a0001c0001t0001g0112a0001c0001t0009g0152others(2): Show | 5 | HG01255.hp2 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-3927C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45508319 | ||||||
| chr6:45508324
|
G | A | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.860-3922G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45508324 | ||||||
| chr6:45508506
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-3740G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45508506 | ||||||
| chr6:45508716
|
C | A | 1 | a0001c0001t0001g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.860-3530C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45508716 | ||||||
| chr6:45508847
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.860-3399G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45508847 | ||||||
| chr6:45508891
|
G | GGTTC | 2 | a0001c0001t0001g0112a0001c0001t0016g0153 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.860-3354_860-3351d others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45508891 | |||||
| chr6:45509242
|
AG | A | 2 | a0001c0001t0008g0128a0001c0001t0008g0160 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.860-3003delG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45509242 | ||||||
| chr6:45509322
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.860-2924A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45509322 | ||||||
| chr6:45509423
|
A | G | 8 | a0001c0001t0001g0135a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.860-2823A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45509423 | ||||||
| chr6:45509501
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.860-2745A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45509501 | ||||||
| chr6:45510077
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0169 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.860-2169G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45510077 | ||||||
| chr6:45510380
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.860-1866G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45510380 | ||||||
| chr6:45510748
|
A | T | 4 | a0001c0001t0001g0022a0001c0001t0002g0004a0001c0001t0002g0012others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-1498A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45510748 | ||||||
| chr6:45510761
|
A | G | 7 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0111others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.860-1485A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45510761 | ||||||
| chr6:45510803
|
T | G | 1 | a0001c0001t0002g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.860-1443T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45510803 | ||||||
| chr6:45510889
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0014g0035 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.860-1357G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45510889 | ||||||
| chr6:45510930
|
G | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.860-1316G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45510930 | ||||||
| chr6:45511078
|
C | T | 7 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0111others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.860-1168C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45511078 | ||||||
| chr6:45511289
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.860-957G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45511289 | ||||||
| chr6:45511578
|
ATGAGAGT others(8): Show |
A | 1 | a0001c0001t0018g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.860-665_860-651del others(15): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 45511578 | |||||
| chr6:45512020
|
T | G | 9 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0111others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.860-226T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45512020 | ||||||
| chr6:45512052
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0016g0153 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.860-194C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45512052 | ||||||
| chr6:45512453
|
G | A | 9 | a0001c0001t0001g0135a0001c0001t0002g0126a0001c0001t0005g0011others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021+46G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45512453 | ||||||
| chr6:45512607
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1021+200C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45512607 | ||||||
| chr6:45512762
|
G | C | 19 | a0001c0001t0001g0135a0001c0001t0002g0107a0001c0001t0002g0109others(16): Show | 19 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1021+355G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45512762 | ||||||
| chr6:45512779
|
A | T | 8 | a0001c0001t0001g0135a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021+372A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45512779 | ||||||
| chr6:45512799
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1021+392C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45512799 | ||||||
| chr6:45512800
|
T | G | 3 | a0001c0001t0001g0067a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1021+393T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45512800 | ||||||
| chr6:45513243
|
AC | A | 20 | a0001c0001t0001g0104a0001c0001t0003g0105a0001c0001t0004g0005others(17): Show | 20 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1021+839delC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45513243 | |||||
| chr6:45513289
|
G | A | 1 | a0001c0007t0001g0028 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1021+882G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513289 | ||||||
| chr6:45513322
|
G | A | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1021+915G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513322 | ||||||
| chr6:45513345
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0010g0129 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1021+938G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513345 | ||||||
| chr6:45513452
|
C | T | 1 | a0001c0001t0003g0051 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1021+1045C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513452 | ||||||
| chr6:45513516
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1021+1109C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513516 | ||||||
| chr6:45513529
|
G | A | 8 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0111others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+1122G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513529 | ||||||
| chr6:45513667
|
GAA | G | 4 | a0001c0001t0002g0017a0001c0001t0008g0034a0001c0001t0011g0064others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1261_1021+126 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513667 | ||||||
| chr6:45513857
|
G | C | 2 | a0001c0001t0001g0022a0001c0001t0002g0174 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1021+1450G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513857 | ||||||
| chr6:45513900
|
G | A | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1021+1493G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45513900 | ||||||
| chr6:45514136
|
A | G | 21 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0001t0001g0135others(18): Show | 21 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1021+1729A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45514136 | ||||||
| chr6:45514151
|
C | A | 1 | a0001c0001t0001g0020 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1021+1744C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45514151 | ||||||
| chr6:45514721
|
A | G | 16 | a0001c0001t0001g0020a0001c0001t0003g0009a0001c0001t0003g0029others(13): Show | 16 | HG00323.hp1 HG01243.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1021+2314A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45514721 | ||||||
| chr6:45514937
|
G | GT | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0100others(5): Show | 8 | HG02074.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+2544dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45514937 | |||||
| chr6:45514937
|
GT | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0169a0001c0001t0002g0033others(9): Show | 12 | HG01255.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021+2544delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45514937 | |||||
| chr6:45514948
|
T | G | 6 | a0001c0001t0001g0047a0001c0001t0001g0112a0001c0001t0001g0155others(3): Show | 6 | HG00423.hp1 HG02109.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+2541T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45514948 | ||||||
| chr6:45515188
|
A | G | 1 | a0001c0001t0018g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1021+2781A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45515188 | ||||||
| chr6:45515256
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1021+2849G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45515256 | ||||||
| chr6:45515375
|
T | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0175others(1): Show | 4 | HG02965.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021+2968T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45515375 | ||||||
| chr6:45515400
|
G | A | 8 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0111others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+2993G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45515400 | ||||||
| chr6:45515692
|
A | G | 1 | a0001c0001t0003g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1021+3285A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45515692 | ||||||
| chr6:45515821
|
A | C | 3 | a0001c0001t0008g0034a0001c0001t0011g0064a0001c0001t0020g0170 | 3 | HG01243.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1021+3414A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45515821 | ||||||
| chr6:45516235
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1021+3828T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45516235 | ||||||
| chr6:45516627
|
G | A | 4 | a0001c0001t0002g0117a0001c0001t0009g0152a0001c0001t0009g0168others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+4220G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45516627 | ||||||
| chr6:45516689
|
T | C | 2 | a0001c0002t0006g0015a0001c0002t0006g0016 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1021+4282T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45516689 | ||||||
| chr6:45516837
|
G | T | 1 | a0001c0001t0018g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1021+4430G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45516837 | ||||||
| chr6:45516911
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1021+4504G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45516911 | ||||||
| chr6:45516947
|
GT | G | 11 | a0001c0001t0001g0155a0001c0001t0002g0017a0001c0001t0002g0126others(8): Show | 11 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021+4550delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45516947 | |||||
| chr6:45517527
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1021+5120T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45517527 | ||||||
| chr6:45517809
|
AACCCC | A | 16 | a0001c0001t0001g0112a0001c0001t0001g0155a0001c0001t0002g0017others(13): Show | 16 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1021+5409_1021+541 others(9): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45517809 | |||||
| chr6:45518277
|
AC | A | 10 | a0001c0001t0001g0155a0001c0001t0002g0017a0001c0001t0002g0126others(7): Show | 10 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1021+5871delC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518277 | ||||||
| chr6:45518288
|
C | A | 2 | a0001c0001t0003g0087a0001c0001t0003g0147 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1021+5881C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518288 | ||||||
| chr6:45518311
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1021+5904C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518311 | ||||||
| chr6:45518366
|
G | A | 14 | a0001c0001t0001g0081a0001c0001t0001g0090a0001c0001t0001g0091others(11): Show | 14 | HG00438.hp1 HG00609.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+5959G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518366 | ||||||
| chr6:45518380
|
T | C | 2 | a0001c0001t0002g0033a0001c0001t0014g0035 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1021+5973T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518380 | ||||||
| chr6:45518470
|
C | G | 78 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1021+6063C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518470 | ||||||
| chr6:45518646
|
T | A | 77 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1021+6239T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518646 | ||||||
| chr6:45518694
|
T | G | 2 | a0001c0001t0001g0112a0001c0001t0002g0125 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1021+6287T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518694 | ||||||
| chr6:45518736
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1021+6329G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518736 | ||||||
| chr6:45518759
|
G | A | 64 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+6352G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45518759 | ||||||
| chr6:45519360
|
G | A | 3 | a0001c0001t0008g0034a0001c0001t0008g0128a0001c0001t0008g0160 | 3 | HG01243.hp1 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1021+6953G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519360 | ||||||
| chr6:45519386
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1021+6979T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519386 | ||||||
| chr6:45519513
|
A | T | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021+7106A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519513 | ||||||
| chr6:45519746
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1021+7339C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519746 | ||||||
| chr6:45519774
|
T | TTA | 3 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0001t0002g0131 | 3 | HG03225.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1021+7383_1021+738 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519774 | |||||
| chr6:45519774
|
T | TTATATAT others(1): Show |
2 | a0001c0001t0002g0033a0001c0001t0014g0035 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1021+7377_1021+738 others(12): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519774 | |||||
| chr6:45519774
|
TTA | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0104 | 2 | HG02683.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1021+7383_1021+738 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519774 | |||||
| chr6:45519790
|
A | ATATGTG | 2 | a0001c0001t0001g0110a0001c0001t0005g0038 | 2 | HG01884.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1021+7384_1021+738 others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519790
|
A | ATG | 6 | a0001c0001t0001g0056a0001c0001t0001g0083a0001c0001t0001g0136others(3): Show | 6 | HG00597.hp1 HG01192.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+7429_1021+743 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519790
|
A | G | 6 | a0001c0001t0001g0095a0001c0001t0004g0021a0001c0001t0004g0059others(3): Show | 6 | HG00423.hp1 HG01346.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+7383A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519790 | ||||||
| chr6:45519790
|
ATG | A | 28 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0065others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1021+7429_1021+743 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519790
|
ATGTG | A | 17 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0068others(14): Show | 17 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1021+7427_1021+743 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519790
|
ATGTGTG | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0094a0001c0001t0001g0123 | 3 | HG00438.hp2 HG00597.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1021+7425_1021+743 others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519790
|
ATGTGTGT others(5): Show |
A | 6 | a0001c0001t0001g0112a0001c0001t0002g0125a0001c0001t0002g0132others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+7419_1021+743 others(16): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519790
|
ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0003g0042a0001c0001t0012g0148 | 2 | NA19030.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1021+7415_1021+743 others(20): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519790
|
ATGTGTGT others(11): Show |
A | 19 | a0001c0001t0001g0020a0001c0001t0001g0124a0001c0001t0001g0137others(16): Show | 19 | HG00323.hp1 HG01243.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1021+7413_1021+743 others(22): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519790 | |||||
| chr6:45519792
|
G | A | 28 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0001t0001g0155others(25): Show | 28 | HG00733.hp2 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1021+7385G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519792 | ||||||
| chr6:45519794
|
G | A | 33 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0130others(30): Show | 33 | HG00280.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1021+7387G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519794 | ||||||
| chr6:45519796
|
G | A | 38 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0135others(35): Show | 38 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1021+7389G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519796 | ||||||
| chr6:45519798
|
G | A | 23 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0135others(20): Show | 23 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+7391G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519798 | ||||||
| chr6:45519800
|
G | A | 16 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0151others(13): Show | 16 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1021+7393G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519800 | ||||||
| chr6:45519802
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1021+7395G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519802 | ||||||
| chr6:45519804
|
G | A | 6 | a0001c0001t0001g0112a0001c0001t0002g0125a0001c0001t0002g0132others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+7397G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519804 | ||||||
| chr6:45519806
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021+7399G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519806 | ||||||
| chr6:45519808
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021+7401G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519808 | ||||||
| chr6:45519810
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021+7403G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519810 | ||||||
| chr6:45519812
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021+7405G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519812 | ||||||
| chr6:45519832
|
GTGTGTA | G | 3 | a0001c0002t0001g0044a0001c0002t0001g0045a0001c0002t0001g0046 | 3 | NA18955.hp1 NA18995.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1021+7427_1021+743 others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519832 | |||||
| chr6:45519834
|
G | A | 6 | a0001c0001t0002g0117a0001c0001t0002g0131a0001c0001t0009g0025others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+7427G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519834 | ||||||
| chr6:45519836
|
G | A | 36 | a0001c0001t0001g0022a0001c0001t0001g0082a0001c0001t0001g0104others(33): Show | 36 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1021+7429G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519836 | ||||||
| chr6:45519836
|
G | GTA | 6 | a0001c0001t0004g0089a0001c0001t0004g0099a0001c0001t0005g0071others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+7435_1021+743 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519836 | |||||
| chr6:45519836
|
G | GTGTA | 7 | a0001c0001t0001g0067a0001c0001t0004g0005a0001c0001t0004g0014others(4): Show | 7 | HG00280.hp2 HG00423.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1021+7430_1021+743 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519836 | |||||
| chr6:45519836
|
G | GTGTGTA | 2 | a0001c0001t0004g0178a0001c0001t0005g0019 | 2 | HG01346.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1021+7430_1021+743 others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519836 | |||||
| chr6:45519836
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0005g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1021+7430_1021+743 others(14): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519836 | |||||
| chr6:45519836
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0005g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1021+7430_1021+743 others(18): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519836 | |||||
| chr6:45519836
|
GTA | G | 2 | a0001c0001t0001g0175a0001c0002t0001g0084 | 2 | HG01496.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1021+7435_1021+743 others(6): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45519836 | |||||
| chr6:45519838
|
A | G | 3 | a0001c0001t0001g0155a0001c0001t0006g0003a0001c0001t0013g0121 | 3 | HG00733.hp2 HG02922.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1021+7431A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519838 | ||||||
| chr6:45519849
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1021+7442A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519849 | ||||||
| chr6:45519952
|
C | T | 3 | a0001c0001t0008g0034a0001c0001t0008g0128a0001c0001t0008g0160 | 3 | HG01243.hp1 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1021+7545C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519952 | ||||||
| chr6:45519969
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0021g0088 | 2 | HG02056.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1021+7562T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519969 | ||||||
| chr6:45519977
|
C | T | 1 | a0001c0001t0006g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1021+7570C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45519977 | ||||||
| chr6:45520170
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1021+7763A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45520170 | ||||||
| chr6:45520207
|
C | A | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+7800C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45520207 | ||||||
| chr6:45520738
|
T | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0151others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+8331T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45520738 | ||||||
| chr6:45521021
|
T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0022others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1021+8614T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521021 | ||||||
| chr6:45521047
|
C | G | 1 | a0001c0001t0008g0160 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1021+8640C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521047 | ||||||
| chr6:45521192
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1021+8785T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521192 | ||||||
| chr6:45521193
|
A | T | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+8786A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521193 | ||||||
| chr6:45521309
|
G | T | 2 | a0001c0001t0003g0087a0001c0001t0003g0147 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1021+8902G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521309 | ||||||
| chr6:45521455
|
T | A | 21 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0004g0005others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1021+9048T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521455 | ||||||
| chr6:45521709
|
C | T | 1 | a0001c0002t0004g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1021+9302C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521709 | ||||||
| chr6:45521808
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0078others(1): Show | 4 | HG00423.hp2 NA18747.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+9401C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45521808 | ||||||
| chr6:45522160
|
A | G | 7 | a0001c0001t0005g0011a0001c0001t0006g0001a0001c0001t0006g0003others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021+9753A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522160 | ||||||
| chr6:45522289
|
G | T | 1 | a0001c0002t0004g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1021+9882G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522289 | ||||||
| chr6:45522378
|
G | T | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021+9971G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522378 | ||||||
| chr6:45522444
|
AC | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0151others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+10038delC | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522444 | ||||||
| chr6:45522445
|
C | A | 50 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0110others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1021+10038C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522445 | ||||||
| chr6:45522448
|
C | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0151others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+10041C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522448 | ||||||
| chr6:45522481
|
C | T | 63 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1021+10074C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522481 | ||||||
| chr6:45522500
|
C | T | 2 | a0001c0001t0003g0087a0001c0001t0003g0147 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1021+10093C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522500 | ||||||
| chr6:45522555
|
A | G | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+10148A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522555 | ||||||
| chr6:45522725
|
C | A | 20 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0130others(17): Show | 20 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1021+10318C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522725 | ||||||
| chr6:45522800
|
T | C | 1 | a0001c0001t0006g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1021+10393T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522800 | ||||||
| chr6:45522953
|
C | T | 5 | a0001c0001t0001g0112a0001c0001t0002g0125a0001c0001t0011g0018others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021+10546C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522953 | ||||||
| chr6:45522975
|
C | T | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+10568C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45522975 | ||||||
| chr6:45523006
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0137 | 2 | NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1021+10599G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523006 | ||||||
| chr6:45523016
|
C | T | 21 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0004g0005others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1021+10609C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523016 | ||||||
| chr6:45523178
|
AT | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0017 | 3 | HG02895.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1021+10773delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45523178 | |||||
| chr6:45523225
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0131a0001c0001t0014g0035 | 3 | HG02145.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1021+10818G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523225 | ||||||
| chr6:45523302
|
A | G | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+10895A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523302 | ||||||
| chr6:45523522
|
C | T | 21 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0004g0005others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1021+11115C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523522 | ||||||
| chr6:45523523
|
G | A | 1 | a0001c0001t0003g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1021+11116G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523523 | ||||||
| chr6:45523937
|
A | T | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021+11530A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523937 | ||||||
| chr6:45523947
|
C | T | 1 | a0001c0001t0018g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1021+11540C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45523947 | ||||||
| chr6:45524340
|
G | A | 20 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0130others(17): Show | 20 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1021+11933G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45524340 | ||||||
| chr6:45524348
|
C | T | 176 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1021+11941C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45524348 | ||||||
| chr6:45524404
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1021+11997G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45524404 | ||||||
| chr6:45525055
|
G | A | 60 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1021+12648G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525055 | ||||||
| chr6:45525226
|
C | T | 14 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0151others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+12819C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525226 | ||||||
| chr6:45525346
|
C | T | 77 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1021+12939C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525346 | ||||||
| chr6:45525360
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1021+12953T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525360 | ||||||
| chr6:45525370
|
C | A | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1021+12963C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525370 | ||||||
| chr6:45525500
|
T | C | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021+13093T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525500 | ||||||
| chr6:45525610
|
T | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0164 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1021+13203T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525610 | ||||||
| chr6:45525936
|
A | T | 21 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0004g0005others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1021+13529A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525936 | ||||||
| chr6:45525938
|
G | A | 21 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0004g0005others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1021+13531G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525938 | ||||||
| chr6:45525945
|
T | C | 63 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1021+13538T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45525945 | ||||||
| chr6:45527018
|
A | C | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1021+14611A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45527018 | ||||||
| chr6:45527353
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1021+14946T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45527353 | ||||||
| chr6:45527759
|
G | A | 5 | a0001c0001t0002g0117a0001c0001t0009g0025a0001c0001t0009g0152others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021+15352G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45527759 | ||||||
| chr6:45527999
|
A | G | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+15592A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45527999 | ||||||
| chr6:45528011
|
C | G | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+15604C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45528011 | ||||||
| chr6:45528078
|
A | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0176a0001c0001t0010g0002others(1): Show | 4 | HG01884.hp1 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+15671A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45528078 | ||||||
| chr6:45528311
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1021+15904C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45528311 | ||||||
| chr6:45528590
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1021+16183C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45528590 | ||||||
| chr6:45528719
|
C | T | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+16312C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45528719 | ||||||
| chr6:45528968
|
G | A | 1 | a0001c0001t0008g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1022-16249G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45528968 | ||||||
| chr6:45529070
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1022-16147G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45529070 | ||||||
| chr6:45529705
|
A | G | 4 | a0001c0001t0002g0117a0001c0001t0009g0025a0001c0001t0009g0152others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-15512A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45529705 | ||||||
| chr6:45529789
|
C | T | 3 | a0001c0001t0002g0024a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1022-15428C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45529789 | ||||||
| chr6:45529790
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1022-15427G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45529790 | ||||||
| chr6:45529815
|
G | A | 6 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0111others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-15402G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45529815 | ||||||
| chr6:45529954
|
G | C | 4 | a0001c0001t0002g0117a0001c0001t0009g0025a0001c0001t0009g0152others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-15263G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45529954 | ||||||
| chr6:45530087
|
A | C | 2 | a0001c0001t0003g0087a0001c0001t0003g0147 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1022-15130A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45530087 | ||||||
| chr6:45530331
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1022-14886T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45530331 | ||||||
| chr6:45530475
|
G | T | 3 | a0001c0001t0008g0034a0001c0001t0008g0128a0001c0001t0008g0160 | 3 | HG01243.hp1 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1022-14742G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45530475 | ||||||
| chr6:45530600
|
C | T | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-14617C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45530600 | ||||||
| chr6:45531000
|
T | C | 72 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1022-14217T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531000 | ||||||
| chr6:45531138
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1022-14079G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531138 | ||||||
| chr6:45531169
|
G | A | 3 | a0001c0001t0008g0034a0001c0001t0008g0128a0001c0001t0008g0160 | 3 | HG01243.hp1 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1022-14048G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531169 | ||||||
| chr6:45531263
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1022-13954C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531263 | ||||||
| chr6:45531750
|
T | TA | 8 | a0001c0001t0002g0048a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-13457dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45531750 | |||||
| chr6:45531760
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1022-13457A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531760 | ||||||
| chr6:45531774
|
A | G | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-13443A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531774 | ||||||
| chr6:45531827
|
A | G | 1 | a0001c0001t0005g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1022-13390A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531827 | ||||||
| chr6:45531840
|
T | C | 1 | a0001c0001t0010g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1022-13377T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531840 | ||||||
| chr6:45531876
|
A | AT | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1022-13338dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45531876 | |||||
| chr6:45531884
|
T | C | 1 | a0001c0001t0003g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1022-13333T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45531884 | ||||||
| chr6:45532162
|
A | AT | 24 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0077others(21): Show | 24 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1022-13030dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45532162 | |||||
| chr6:45532162
|
A | ATT | 11 | a0001c0001t0001g0041a0001c0001t0001g0081a0001c0001t0001g0112others(8): Show | 11 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1022-13031_1022-13 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45532162 | |||||
| chr6:45532162
|
AT | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0066others(17): Show | 20 | HG01069.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1022-13030delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45532162 | |||||
| chr6:45532162
|
ATT | A | 48 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1022-13031_1022-13 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45532162 | |||||
| chr6:45532263
|
G | A | 77 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1022-12954G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532263 | ||||||
| chr6:45532367
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0002g0115 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1022-12850G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532367 | ||||||
| chr6:45532382
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0100 | 2 | HG00438.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1022-12835G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532382 | ||||||
| chr6:45532396
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0131a0001c0001t0014g0035 | 3 | HG02145.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1022-12821T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532396 | ||||||
| chr6:45532529
|
C | T | 21 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0004g0005others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1022-12688C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532529 | ||||||
| chr6:45532683
|
T | C | 1 | a0001c0001t0018g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1022-12534T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532683 | ||||||
| chr6:45532721
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1022-12496T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532721 | ||||||
| chr6:45532733
|
G | A | 64 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1022-12484G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532733 | ||||||
| chr6:45532876
|
G | A | 77 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1022-12341G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532876 | ||||||
| chr6:45532905
|
C | CT | 12 | a0001c0001t0001g0155a0001c0001t0003g0049a0001c0001t0005g0011others(9): Show | 12 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1022-12292dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45532905 | |||||
| chr6:45532905
|
CT | C | 33 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0110others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1022-12292delT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45532905 | |||||
| chr6:45532905
|
CTT | C | 27 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0151others(24): Show | 27 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1022-12293_1022-12 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45532905 | |||||
| chr6:45532929
|
G | A | 60 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1022-12288G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45532929 | ||||||
| chr6:45533033
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0002g0143 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1022-12184C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45533033 | ||||||
| chr6:45533034
|
G | A | 3 | a0001c0001t0008g0034a0001c0001t0008g0128a0001c0001t0008g0160 | 3 | HG01243.hp1 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1022-12183G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45533034 | ||||||
| chr6:45533135
|
G | GGTGTGT | 5 | a0001c0001t0001g0112a0001c0001t0002g0125a0001c0001t0011g0018others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1022-12063_1022-12 others(12): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45533135 | |||||
| chr6:45533135
|
GGT | G | 61 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1022-12059_1022-12 others(8): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45533135 | |||||
| chr6:45533426
|
TA | T | 128 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0057others(125): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1022-11786delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45533426 | |||||
| chr6:45533548
|
A | C | 1 | a0001c0001t0003g0154 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1022-11669A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45533548 | ||||||
| chr6:45533815
|
A | G | 72 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1022-11402A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45533815 | ||||||
| chr6:45533888
|
C | CT | 19 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0070others(16): Show | 19 | HG00438.hp2 HG01496.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022-11306dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45533888 | |||||
| chr6:45533888
|
CTTTT | C | 6 | a0001c0001t0001g0167a0001c0001t0002g0131a0001c0001t0005g0019others(3): Show | 6 | HG01243.hp1 HG01346.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-11309_1022-11 others(10): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45533888 | |||||
| chr6:45533888
|
CTTTTT | C | 52 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1022-11310_1022-11 others(11): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45533888 | |||||
| chr6:45533888
|
CTTTTTT | C | 5 | a0001c0001t0002g0024a0001c0001t0002g0033a0001c0001t0002g0171others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-11311_1022-11 others(12): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45533888 | |||||
| chr6:45534001
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1022-11216T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534001 | ||||||
| chr6:45534044
|
G | A | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1022-11173G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534044 | ||||||
| chr6:45534048
|
T | C | 77 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1022-11169T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534048 | ||||||
| chr6:45534052
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1022-11165G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534052 | ||||||
| chr6:45534200
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0040others(11): Show | 14 | HG00423.hp2 HG00733.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1022-11017G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534200 | ||||||
| chr6:45534252
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1022-10965T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534252 | ||||||
| chr6:45534358
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1022-10859T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534358 | ||||||
| chr6:45534520
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1022-10697C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45534520 | ||||||
| chr6:45535162
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0014g0035 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1022-10055G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45535162 | ||||||
| chr6:45535236
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1022-9981A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45535236 | ||||||
| chr6:45535251
|
T | A | 1 | a0001c0001t0005g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1022-9966T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45535251 | ||||||
| chr6:45535251
|
T | TA | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-9957dupA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45535251 | |||||
| chr6:45535279
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1022-9938G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45535279 | ||||||
| chr6:45535561
|
G | A | 6 | a0001c0001t0001g0067a0001c0002t0001g0044a0001c0002t0001g0045others(3): Show | 6 | HG01496.hp1 HG03579.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-9656G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45535561 | ||||||
| chr6:45535603
|
CA | C | 62 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1022-9601delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45535603 | |||||
| chr6:45535698
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1022-9519T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45535698 | ||||||
| chr6:45536432
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0002g0125a0001c0001t0011g0018others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-8785C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45536432 | ||||||
| chr6:45536455
|
A | G | 1 | a0001c0001t0010g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1022-8762A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45536455 | ||||||
| chr6:45536608
|
G | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1022-8609G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45536608 | ||||||
| chr6:45536714
|
G | A | 2 | a0001c0001t0004g0059a0001c0001t0004g0178 | 2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1022-8503G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45536714 | ||||||
| chr6:45536900
|
C | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0171a0001c0001t0002g0173others(1): Show | 4 | HG01891.hp2 HG02451.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-8317C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45536900 | ||||||
| chr6:45536975
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0130 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1022-8242A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45536975 | ||||||
| chr6:45536978
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1022-8239C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45536978 | ||||||
| chr6:45537438
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1022-7779C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45537438 | ||||||
| chr6:45537685
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1022-7532C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45537685 | ||||||
| chr6:45537714
|
G | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01891.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1022-7503G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45537714 | ||||||
| chr6:45537828
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1022-7389G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45537828 | ||||||
| chr6:45538183
|
G | C | 8 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-7034G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45538183 | ||||||
| chr6:45538385
|
A | G | 19 | a0001c0001t0001g0110a0001c0001t0004g0005a0001c0001t0004g0014others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022-6832A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45538385 | ||||||
| chr6:45538676
|
T | C | 4 | a0001c0001t0001g0112a0001c0001t0002g0125a0001c0001t0011g0018others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-6541T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45538676 | ||||||
| chr6:45538968
|
G | C | 1 | a0001c0001t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1022-6249G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45538968 | ||||||
| chr6:45539141
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1022-6076T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539141 | ||||||
| chr6:45539211
|
G | GT | 75 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1022-5997dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45539211 | |||||
| chr6:45539213
|
T | G | 1 | a0001c0001t0001g0137 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1022-6004T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539213 | ||||||
| chr6:45539219
|
T | TC | 2 | a0001c0001t0002g0133a0001c0001t0005g0038 | 2 | HG02809.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1022-5998_1022-599 others(5): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539219 | ||||||
| chr6:45539221
|
C | T | 19 | a0001c0001t0001g0124a0001c0001t0001g0137a0001c0001t0003g0009others(16): Show | 19 | HG00323.hp1 HG01243.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022-5996C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539221 | ||||||
| chr6:45539346
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1022-5871T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539346 | ||||||
| chr6:45539364
|
G | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(12): Show | 15 | HG00423.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1022-5853G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539364 | ||||||
| chr6:45539557
|
G | A | 74 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1022-5660G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539557 | ||||||
| chr6:45539676
|
A | G | 1 | a0001c0002t0003g0058 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1022-5541A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45539676 | ||||||
| chr6:45540018
|
G | A | 9 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-5199G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540018 | ||||||
| chr6:45540063
|
G | A | 6 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0017others(3): Show | 6 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-5154G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540063 | ||||||
| chr6:45540086
|
C | T | 1 | a0001c0001t0016g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1022-5131C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540086 | ||||||
| chr6:45540209
|
C | T | 3 | a0001c0001t0008g0034a0001c0001t0008g0128a0001c0001t0008g0160 | 3 | HG01243.hp1 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1022-5008C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540209 | ||||||
| chr6:45540379
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1022-4838G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540379 | ||||||
| chr6:45540476
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1022-4741A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540476 | ||||||
| chr6:45540712
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1022-4505C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540712 | ||||||
| chr6:45540872
|
G | A | 9 | a0001c0001t0001g0155a0001c0001t0005g0011a0001c0001t0006g0001others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-4345G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45540872 | ||||||
| chr6:45541060
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1022-4157T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45541060 | ||||||
| chr6:45541093
|
A | G | 2 | a0001c0001t0004g0099a0001c0002t0004g0060 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1022-4124A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45541093 | ||||||
| chr6:45541124
|
A | T | 4 | a0001c0001t0001g0112a0001c0001t0002g0125a0001c0001t0011g0018others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-4093A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45541124 | ||||||
| chr6:45541166
|
A | AT | 31 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0083others(28): Show | 31 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1022-4041dupT | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 45541166 | |||||
| chr6:45541310
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1022-3907G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45541310 | ||||||
| chr6:45541893
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0014g0035 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1022-3324G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45541893 | ||||||
| chr6:45542087
|
A | G | 78 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1022-3130A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45542087 | ||||||
| chr6:45542120
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0135a0001c0001t0001g0151others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-3097C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45542120 | ||||||
| chr6:45542370
|
C | T | 55 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0110others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1022-2847C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45542370 | ||||||
| chr6:45543077
|
A | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0017others(5): Show | 8 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-2140A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45543077 | ||||||
| chr6:45543124
|
T | C | 1 | a0001c0001t0021g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1022-2093T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45543124 | ||||||
| chr6:45543804
|
C | T | 81 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0067others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1022-1413C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45543804 | ||||||
| chr6:45544123
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0123 | 2 | HG00438.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1022-1094C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544123 | ||||||
| chr6:45544140
|
G | A | 5 | a0001c0001t0002g0117a0001c0001t0009g0025a0001c0001t0009g0152others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1022-1077G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544140 | ||||||
| chr6:45544208
|
G | A | 54 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0112others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1022-1009G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544208 | ||||||
| chr6:45544478
|
C | T | 20 | a0001c0001t0003g0009a0001c0001t0003g0029a0001c0001t0003g0030others(17): Show | 20 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1022-739C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544478 | ||||||
| chr6:45544589
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0169 | 3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1022-628G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544589 | ||||||
| chr6:45544595
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1022-622G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544595 | ||||||
| chr6:45544605
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0110others(6): Show | 9 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1022-612C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544605 | ||||||
| chr6:45544621
|
C | G | 1 | a0001c0001t0001g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1022-596C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544621 | ||||||
| chr6:45544886
|
T | A | 9 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0017others(6): Show | 9 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-331T>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544886 | ||||||
| chr6:45544918
|
G | C | 8 | a0001c0001t0001g0112a0001c0001t0002g0117a0001c0001t0002g0125others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022-299G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 7/8 | chr6 | 45544918 | ||||||
| chr6:45545299
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0002g0125 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1087+17T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 8/8 | chr6 | 45545299 | ||||||
| chr6:45545441
|
T | C | 1 | a0001c0001t0012g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1087+159T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 8/8 | chr6 | 45545441 | ||||||
| chr6:45545842
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1087+560C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 8/8 | chr6 | 45545842 | ||||||
| chr6:45545926
|
G | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0012a0001c0001t0002g0017others(6): Show | 9 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1087+644G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 8/8 | chr6 | 45545926 | ||||||
| chr6:45546043
|
T | C | 1 | a0001c0002t0004g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1087+761T>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 8/8 | chr6 | 45546043 | ||||||
| chr6:45546618
|
G | A | 1 | a0001c0002t0004g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1088-209G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 8/8 | chr6 | 45546618 |