Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MASNS others(516): Show |
chr6 | 45323330 | 45556082 |
| a0002 | 0/0 | 515 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | MASNS others(510): Show |
chr6 | 45323330 | 45556082 |
| a0003 | 0/0 | 521 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | MASNS others(516): Show |
chr6 | 45323330 | 45556082 |
| a0004 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | MASNS others(516): Show |
chr6 | 45323330 | 45556082 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1563 | 158 | 73 | 28 | 36 | 6 | 13 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATGGC others(1558): Show |
chr6 | 45323330 | 45556082 | ||
| a0001c0002 | 0/0 | 1563 | 14 | 0 | 5 | 5 | 1 | 3 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATGGC others(1558): Show |
chr6 | 45323330 | 45556082 | ||
| a0001c0006 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATGGC others(1558): Show |
chr6 | 45323330 | 45556082 | ||
| a0001c0007 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATGGC others(1558): Show |
chr6 | 45323330 | 45556082 | ||
| a0002c0003 | 0/0 | 1545 | 2 | 0 | 2 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATGGC others(1540): Show |
chr6 | 45323330 | 45556082 | ||
| a0003c0004 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATGGC others(1558): Show |
chr6 | 45323330 | 45556082 | ||
| a0004c0005 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATGGC others(1558): Show |
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 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0002 | 0/0 | 5539 | 24 | 23 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0003 | 0/0 | 5538 | 16 | 2 | 4 | 7 | 1 | 2 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5533): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0004 | 0/0 | 5538 | 8 | 0 | 2 | 2 | 1 | 3 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5533): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0005 | 0/0 | 5539 | 7 | 0 | 5 | 1 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0006 | 0/0 | 5540 | 4 | 0 | 3 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0007 | 0/0 | 5539 | 4 | 4 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0008 | 0/0 | 5539 | 3 | 2 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0009 | 0/0 | 5539 | 3 | 3 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0010 | 0/0 | 5540 | 2 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0011 | 0/0 | 5540 | 2 | 2 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0012 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0013 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0014 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0016 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0017 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0018 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5534): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0019 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0020 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0001t0021 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0002t0001 | 0/0 | 5540 | 6 | 0 | 2 | 3 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0002t0003 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5533): Show |
chr6 | 45323330 | 45556082 |
| a0001c0002t0004 | 0/0 | 5538 | 4 | 0 | 1 | 1 | 0 | 2 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5533): Show |
chr6 | 45323330 | 45556082 |
| a0001c0002t0006 | 0/0 | 5540 | 2 | 0 | 2 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0002t0015 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5533): Show |
chr6 | 45323330 | 45556082 |
| a0001c0006t0001 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0001c0007t0001 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0002c0003t0001 | 0/0 | 5522 | 2 | 0 | 2 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5517): Show |
chr6 | 45323330 | 45556082 |
| a0003c0004t0001 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| a0004c0005t0001 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | ATTCG others(5535): Show |
chr6 | 45323330 | 45556082 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 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 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0055 | 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 |
| a0001c0001t0001g0063 | 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 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0093 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0133 | 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 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0001g0145 | 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 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0002g0120 | 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 |
| a0001c0001t0002g0127 | 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 |
| a0001c0001t0002g0137 | 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 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0003g0146 | 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 |
| a0001c0001t0004g0054 | 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 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0004g0121 | 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 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0005g0109 | 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 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0006g0084 | 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 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0008g0161 | 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 |
| a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0001t0014g0033 | 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 |
| a0001c0001t0017g0138 | 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 |
| a0001c0001t0019g0118 | 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 |
| a0001c0001t0021g0104 | 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 |
| 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 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0002t0001g0143 | 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 |
| a0001c0002t0004g0040 | 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 |
| a0001c0002t0015g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0001c0006t0001g0065 | 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 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| a0004c0005t0001g0007 | 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 | g0044 | EUR | GBR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00099 | hp2 | a0003 | c0004 | t0001 | g0081 | 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 | g0108 | EUR | FIN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | 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 | g0115 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0144 | 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 | g0056 | 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 | g0063 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0112 | 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 | g0082 | 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 | g0105 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01106 | hp2 | a0004 | c0005 | t0001 | g0007 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0038 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0122 | 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 | g0148 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0036 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0160 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0084 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0109 | 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 | g0083 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | CLM | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0099 | 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 | g0067 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0075 | 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 | g0113 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0101 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0049 | 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 | g0142 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02056 | hp1 | a0001 | c0001 | t0021 | g0104 | EAS | KHV | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0050 | 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 | g0116 | 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 | g0033 | 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 | g0111 | 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 | g0098 | 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 | g0068 | 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 | g0119 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0138 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0135 | 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 | g0139 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0161 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0071 | 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 | g0120 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0077 | 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 | g0110 | 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 | g0127 | 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 | g0073 | 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 | g0133 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0019 | 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 | g0126 | 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 | g0145 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0146 | 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 | g0078 | AFR | GWD | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0121 | 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 | g0118 | 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 | g0090 | 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 | g0087 | EAS | CHB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0091 | 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 | g0141 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0140 | 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 | g0128 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0086 | 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 | g0039 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0147 | AFR | LWK | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0124 | AFR | LWK | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0117 | 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 | g0043 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0095 | 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 | g0047 | 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 | g0129 | 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 | g0125 | AFR | YRI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20129 | hp1 | a0001 | c0006 | t0001 | g0065 | AFR | ASW | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0080 | EUR | TSI | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0097 | 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 | g0069 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | USA | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | USA | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0123 | 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 | g0072 | 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 | a0001 | c0001 | t0001 | g0006 | REF | REF | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0100 | REF | REF | RUNX2_chr6_45323330_45556082 | RUNX2 | chr6 | 45323330 | 45556082 |
| view | 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 |
| view | 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 |
| view | 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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(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 | a0001c0001t0003 a0001c0001t0012 a0001c0002t0003 |
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 | a0001c0001t0009 a0001c0001t0020 |
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 | a0001c0001t0007 a0001c0001t0017 |
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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0004 others(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 | a0001c0001t0006 a0001c0002t0006 |
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 |
| view | 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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0007t0001g0028 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | 59 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+1961G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45330745 | |||||||
| chr6:45330794 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0167 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(13): 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 | a0001c0001t0001g0022 a0001c0001t0007g0023 a0001c0001t0010g0002 |
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 | a0001c0001t0002g0035 a0001c0001t0011g0019 |
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 | a0001c0001t0003g0113 a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | 19 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(16): 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 | a0002c0003t0001g0148 a0002c0003t0001g0160 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0003g0076 | 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 | a0001c0001t0001g0057 a0001c0001t0004g0059 a0001c0001t0005g0056 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0131 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0037 a0001c0001t0002g0132 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0145 others(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 | 34 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(31): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 54 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(51): 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 | a0001c0001t0008g0161 | 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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | 51 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(48): Show |
51 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(48): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0167 a0001c0001t0002g0166 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | 47 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(44): Show |
47 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(44): 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 58 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): 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 | 19 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.58+11161C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45339945 | |||||||
| chr6:45340169 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0003g0146 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0003g0146 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0002c0003t0001g0148 a0002c0003t0001g0160 |
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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.58+13744C>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45342528 | |||||||
| chr6:45342548 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0135 a0001c0001t0003g0083 others(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 | a0001c0001t0002g0032 a0001c0001t0010g0002 |
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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0002g0120 | 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 | a0001c0001t0002g0137 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0139 a0001c0001t0002g0068 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | 58 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): 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 | a0001c0001t0001g0119 | 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 | 68 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(65): Show |
68 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(65): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0055 a0001c0001t0002g0094 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0055 a0001c0001t0004g0054 a0001c0001t0006g0038 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | 54 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(51): 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0053 a0001c0001t0001g0062 others(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 |
80 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): 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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0011g0019 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0002t0006g0015 a0001c0002t0006g0016 |
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 | a0001c0001t0001g0069 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0078 a0001c0001t0002g0120 a0001c0001t0007g0077 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0125 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0142 | 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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0003g0052 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 128 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.58+23979A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45352763 | |||||||
| chr6:45352783 | T | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(18): Show |
21 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(18): 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 | a0001c0001t0003g0129 | 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 | a0001c0001t0002g0035 a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0072 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0003g0129 | 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 | a0001c0001t0001g0069 | 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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.58+24684C>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45353468 | |||||||
| chr6:45353718 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0020 a0001c0001t0004g0021 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0002t0004g0040 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | 24 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(21): Show |
24 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(21): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0051 a0001c0001t0002g0068 a0001c0001t0002g0173 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0002t0001g0143 | 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 | a0001c0001t0001g0145 a0001c0001t0003g0146 |
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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0074 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0145 a0001c0001t0003g0146 |
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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | a0001c0001t0007g0034 | 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 | a0001c0001t0003g0130 | 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 | 54 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(51): 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 | a0001c0001t0012g0147 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | 58 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.58+28630G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45357414 | |||||||
| chr6:45357449 | GC | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | |||||||
| chr6:45357884 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0116 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0035 | 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 | a0001c0001t0014g0033 | 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 | a0001c0001t0007g0034 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0078 a0001c0001t0002g0120 a0001c0001t0007g0077 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0115 | 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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): 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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0002g0035 a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0078 a0001c0001t0002g0120 a0001c0001t0007g0077 |
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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0002g0064 a0001c0001t0002g0137 |
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 | a0001c0002t0006g0015 a0001c0002t0006g0016 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | 58 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+32855G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45361639 | |||||||
| chr6:45361752 | C | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0004g0054 a0001c0001t0006g0038 |
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 | a0001c0001t0001g0095 | 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0002c0003t0001g0148 a0002c0003t0001g0160 |
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 | a0001c0001t0003g0083 a0001c0001t0006g0084 |
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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | 105 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): 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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0003g0050 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 58 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0002g0074 | 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 | a0001c0001t0005g0080 | 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 | a0001c0001t0003g0130 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0011g0019 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0004c0005t0001g0007 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0130 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0114 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0002g0126 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0003g0113 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0097 | 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 | a0001c0001t0002g0137 | 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | 12 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(9): Show |
12 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(9): 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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0098 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0002g0126 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0020 a0001c0001t0004g0021 a0001c0001t0005g0018 |
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 | 58 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 |
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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0013g0090 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0037 a0001c0001t0002g0132 |
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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0002g0072 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0003g0050 | 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 | a0002c0003t0001g0148 a0002c0003t0001g0160 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | 56 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | 19 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(16): 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0013 |
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 | a0001c0001t0004g0014 a0004c0005t0001g0007 |
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 | a0001c0001t0001g0082 a0003c0004t0001g0081 |
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 | a0001c0001t0011g0019 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0003g0154 a0001c0001t0016g0153 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0002g0035 a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0069 | 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 | a0001c0001t0002g0017 a0001c0001t0009g0025 a0001c0002t0001g0026 others(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 | a0001c0001t0001g0037 a0001c0001t0002g0132 |
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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | a0001c0001t0001g0078 a0001c0001t0007g0077 |
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 | a0001c0001t0011g0019 | 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | 133 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(130): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): 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 | a0001c0001t0001g0020 a0001c0001t0004g0021 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0002t0001g0143 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0005g0018 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0003g0076 | 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0062 others(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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | 3 | a0001c0001t0005g0011 a0001c0001t0006g0001 a0001c0001t0006g0003 |
3 | HG00280.hp1 HG00733.hp2 HG01928.hp2 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(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 | a0001c0001t0003g0050 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(17): 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0003g0129 | 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 | a0001c0001t0001g0022 a0001c0001t0007g0023 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0001g0078 a0001c0001t0001g0089 a0001c0001t0001g0091 others(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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): 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 | a0001c0001t0001g0078 a0001c0001t0002g0120 a0001c0001t0007g0077 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0131 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.59-41142G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45381451 | |||||||
| chr6:45381760 | G | A | 28 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0002t0001g0099 | 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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.59-40453A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45382140 | |||||||
| chr6:45382370 | A | G | 104 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): 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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0116 | 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 | a0001c0001t0002g0035 a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0008g0036 | 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 | a0002c0003t0001g0148 | 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 | a0001c0001t0001g0125 a0001c0001t0002g0126 a0001c0001t0010g0124 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0011g0110 | 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 | a0001c0001t0004g0014 a0004c0005t0001g0007 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | 67 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(64): Show |
67 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(64): 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0002g0035 a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0037 a0001c0001t0002g0132 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0003g0141 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0096 a0001c0001t0001g0125 others(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 | 37 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0063 others(34): Show |
37 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(34): 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 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0158 a0001c0001t0002g0132 others(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 | a0001c0001t0008g0036 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0004g0014 a0004c0005t0001g0007 |
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 | 57 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(54): 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 | a0001c0001t0001g0070 a0001c0001t0002g0072 |
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 | 57 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(54): 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 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | 109 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(106): 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | 3 | a0001c0001t0005g0011 a0001c0001t0006g0001 a0001c0001t0006g0003 |
3 | HG00280.hp1 HG00733.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.59-34437A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45388156 | |||||||
| chr6:45388266 | T | C | 1 | a0001c0001t0002g0126 | 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 | a0001c0001t0004g0014 a0004c0005t0001g0007 |
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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0004g0027 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0108 | 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 | 109 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.59-32631A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45389962 | |||||||
| chr6:45390005 | CA | C | 121 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(118): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): 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 | a0001c0001t0008g0036 a0001c0001t0010g0002 |
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 | 29 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(26): Show |
29 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-32349delG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390243 | |||||||
| chr6:45390370 | G | A | 64 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0156 others(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 | 19 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.59-32007G>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45390586 | |||||||
| chr6:45390666 | T | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(16): 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0002t0006g0015 a0001c0002t0006g0016 |
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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(12): 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0079 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | 121 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): 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 | a0001c0001t0002g0074 a0001c0001t0007g0075 a0001c0001t0016g0153 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | 25 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(22): 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0002t0006g0015 a0001c0002t0006g0016 |
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 | a0001c0001t0001g0020 a0001c0001t0004g0021 a0001c0001t0005g0018 |
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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0017g0138 | 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 | a0001c0002t0004g0040 | 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 | a0001c0001t0003g0050 | 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0115 | 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 | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(12): 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 | a0001c0001t0009g0025 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | 25 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(22): 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | 57 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(54): 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0095 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(12): 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | a0001c0001t0001g0093 a0001c0002t0001g0026 a0001c0002t0001g0045 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-25390A>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45397203 | |||||||
| chr6:45397369 | A | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(12): 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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0116 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0003g0076 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0078 others(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 | a0001c0001t0003g0083 | 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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0135 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0122 a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0063 others(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 | 7 | a0001c0001t0001g0089 a0001c0001t0002g0004 a0001c0001t0002g0012 others(4): Show |
7 | HG00733.hp2 HG02055.hp1 HG02895.hp2 others(4): 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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0003g0150 others(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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0143 |
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 | a0001c0002t0004g0040 a0001c0002t0006g0015 a0001c0002t0006g0016 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0134 a0001c0001t0002g0072 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0164 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0078 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0012 |
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 | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): 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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | 47 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(44): Show |
47 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(44): 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 | a0001c0001t0005g0080 | 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 | a0001c0001t0005g0018 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-22408A>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400185 | |||||||
| chr6:45400186 | T | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-22407T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45400186 | |||||||
| chr6:45400189 | G | GGGAA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0164 others(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 | a0001c0001t0003g0154 a0001c0001t0016g0153 |
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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0136 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | 30 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(27): Show |
30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): 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 | a0001c0001t0001g0063 a0001c0006t0001g0065 |
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 | a0001c0001t0001g0070 | 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 | a0001c0001t0011g0019 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 19 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0020 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(16): 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0078 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0047 others(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 | a0001c0001t0019g0118 | 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 | 61 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(58): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.59-19164C>T | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45403429 | |||||||
| chr6:45403485 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0079 others(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 | a0001c0001t0003g0129 | 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 | 61 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(58): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(58): 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 | a0001c0001t0001g0013 a0001c0001t0003g0150 |
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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0133 a0001c0001t0001g0169 others(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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | 17 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(14): Show |
17 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-18318delG | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45404274 | |||||||
| chr6:45404275 | G | A | 136 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0096 a0001c0001t0002g0032 a0001c0001t0002g0120 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | 59 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(56): 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 | a0003c0004t0001g0081 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0005g0018 | 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 | a0001c0001t0001g0095 | 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 | a0004c0005t0001g0007 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0095 | 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 | a0001c0001t0004g0121 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0017g0138 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0008g0036 | 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 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0007t0001g0028 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | 61 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(58): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(58): 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 | a0001c0001t0004g0121 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0128 a0001c0001t0002g0049 a0001c0001t0003g0130 |
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 | 61 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(58): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(58): 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 | a0001c0001t0001g0067 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0089 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0086 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0003g0130 | 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 | 173 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0135 | 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 | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-14461delA | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45408131 | |||||||
| chr6:45408484 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0003g0150 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 156 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0003g0076 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0167 others(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 | a0001c0001t0002g0066 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0011g0019 | 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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0067 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0055 | 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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | 124 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): 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 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0125 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0078 a0001c0001t0007g0077 a0001c0001t0010g0002 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0003g0052 | 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 | 29 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(26): Show |
29 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(26): 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 | a0001c0001t0001g0082 a0001c0001t0001g0135 a0001c0001t0005g0080 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0086 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 67 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0020 others(64): Show |
67 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(64): 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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0003g0113 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0003g0058 a0001c0002t0004g0040 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 44 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0051 others(41): Show |
44 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(41): 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 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0067 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0145 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0078 a0001c0001t0010g0002 |
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 | a0001c0001t0002g0072 | 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 | 154 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): 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 | a0001c0001t0012g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-7243G>A | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | chr6 | 45415350 | |||||||
| chr6:45415709 | A | G | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0107 | 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 | 47 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(44): Show |
47 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(44): 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0098 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0053 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0037 a0001c0001t0002g0132 |
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 | a0001c0001t0001g0122 a0001c0001t0004g0014 a0004c0005t0001g0007 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0139 a0001c0001t0002g0068 |
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 | a0001c0001t0017g0138 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 143 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0019g0118 | 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 | a0001c0001t0003g0050 | 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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0011g0110 | 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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0001t0004g0105 a0001c0001t0005g0109 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0156 others(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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0001g0169 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0003g0083 | 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 | a0001c0001t0001g0013 a0001c0001t0003g0150 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | |||||||
| chr6:45423212 | G | C | 14 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0079 others(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 | a0001c0002t0004g0040 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0089 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0089 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0086 others(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 | 143 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): 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 | a0001c0001t0001g0091 | 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 | 143 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0002c0003t0001g0148 a0002c0003t0001g0160 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0002g0074 a0001c0001t0007g0075 |
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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | |||||||
| chr6:45427725 | A | G | 1 | a0001c0001t0002g0066 | 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 | a0001c0001t0017g0138 | 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 | a0001c0002t0001g0045 | 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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | 143 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.424-3811A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 3/8 | chr6 | 45428052 | |||||||
| chr6:45428055 | A | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | 141 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): 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 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0007g0034 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | 173 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): 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 | a0001c0001t0001g0122 a0001c0001t0002g0035 a0001c0001t0002g0127 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0095 others(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 | a0002c0003t0001g0148 a0002c0003t0001g0160 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0002t0004g0060 a0001c0002t0004g0061 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0108 a0001c0001t0003g0076 a0001c0001t0003g0083 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0002c0003t0001g0148 a0002c0003t0001g0160 |
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 | a0001c0001t0006g0084 | 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0001g0145 a0001c0001t0003g0146 |
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 | a0001c0002t0015g0044 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0126 a0001c0001t0008g0123 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0051 a0001c0001t0003g0043 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0035 a0001c0001t0002g0127 others(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 | a0001c0001t0002g0126 | 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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0037 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(13): 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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0007g0023 others(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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0003g0150 |
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 | a0001c0001t0001g0020 a0001c0001t0004g0021 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0007g0077 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0125 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0003g0141 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0062 a0001c0001t0002g0074 a0001c0001t0002g0127 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0155 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0114 others(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 | a0001c0001t0008g0123 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0007g0023 a0001c0001t0007g0075 |
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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0145 a0001c0001t0003g0146 |
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 | a0001c0001t0002g0126 | 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 | a0001c0001t0001g0136 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0078 a0001c0001t0001g0089 |
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 | a0001c0001t0001g0062 a0001c0006t0001g0065 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | 127 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(124): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(124): 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 | 84 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(81): 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 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0139 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0057 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0003g0050 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0062 a0001c0001t0002g0004 others(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 | a0001c0001t0002g0126 | 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 | 148 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(145): Show |
148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): 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 | a0001c0001t0006g0084 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0004g0105 a0001c0001t0004g0178 a0001c0001t0005g0018 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0051 others(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 | 108 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(105): Show |
108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | |||||||
| chr6:45444085 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0062 a0001c0006t0001g0065 |
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 | a0001c0001t0007g0023 a0001c0001t0007g0075 a0001c0001t0007g0077 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0176 a0001c0001t0010g0124 |
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 | a0001c0001t0005g0056 | 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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0007g0023 a0001c0001t0007g0075 a0001c0001t0007g0077 |
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 | a0001c0001t0010g0002 a0001c0001t0011g0110 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0062 others(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 | a0001c0001t0002g0032 a0001c0001t0002g0126 |
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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | a0001c0001t0003g0043 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0125 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0097 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0005g0109 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0005g0109 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0176 a0001c0001t0010g0124 |
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 | a0001c0001t0004g0021 a0001c0001t0004g0105 a0001c0002t0015g0044 |
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 | 149 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(146): Show |
149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): 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 | a0004c0005t0001g0007 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0134 a0001c0001t0009g0025 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0088 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): 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 | a0001c0001t0006g0038 | 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 | a0001c0001t0001g0097 | 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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.685+13640A>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45451691 | |||||||
| chr6:45452185 | T | C | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0001g0031 a0001c0001t0001g0115 a0001c0001t0001g0128 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | 147 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(144): Show |
147 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(144): 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 | a0001c0006t0001g0065 | 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 | 172 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.685+15260G>C | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 5/8 | chr6 | 45453311 | |||||||
| chr6:45453893 | C | T | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0007g0023 a0001c0001t0007g0075 |
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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0002t0001g0047 | 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 | a0001c0002t0001g0047 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0112 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0079 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0073 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0069 a0001c0001t0002g0064 a0001c0001t0002g0068 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0002g0024 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0003g0129 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0003g0130 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0007g0077 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0162 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0003g0129 | 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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0010g0002 a0001c0001t0011g0110 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0135 a0001c0001t0002g0127 others(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 | a0001c0001t0007g0075 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0135 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0019g0118 | 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 | a0001c0001t0021g0104 | 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 | a0001c0001t0013g0090 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0051 a0001c0001t0003g0009 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0062 a0001c0006t0001g0065 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0041 | 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 | 171 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | |||||||
| chr6:45464191 | TA | T | 24 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0097 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0021g0104 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0176 a0001c0001t0002g0132 others(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 | a0001c0001t0005g0039 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0135 a0001c0001t0002g0127 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0012g0147 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0006t0001g0065 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0135 a0001c0001t0002g0127 others(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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | a0001c0001t0008g0123 | 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 | a0001c0001t0010g0002 a0001c0001t0011g0110 |
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 | a0001c0001t0001g0162 | 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 | a0001c0001t0021g0104 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0002g0064 others(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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0017g0138 | 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 | a0001c0001t0005g0109 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0017g0138 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0125 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0079 a0001c0001t0002g0049 a0001c0002t0001g0143 |
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 | a0001c0001t0001g0062 a0001c0006t0001g0065 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0097 a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0005g0056 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0005g0039 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0006t0001g0065 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0089 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0006t0001g0065 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | 152 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(149): 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0003g0050 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0007g0034 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0019g0118 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0003g0113 a0001c0001t0005g0080 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0097 a0001c0001t0004g0014 a0001c0001t0004g0054 others(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 | a0001c0006t0001g0065 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | a0001c0001t0002g0126 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0168 |
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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0007g0023 a0001c0001t0007g0034 a0001c0001t0007g0075 others(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 | a0001c0001t0005g0101 | 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 | a0001c0001t0014g0033 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0014g0033 | 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 | a0001c0001t0010g0124 | 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 | a0001c0001t0001g0097 a0001c0001t0002g0120 |
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 | a0001c0001t0001g0070 a0001c0001t0002g0072 |
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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0111 others(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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0097 a0001c0001t0002g0120 |
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 | a0001c0001t0014g0033 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0097 a0001c0001t0001g0111 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0088 | 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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0108 a0003c0004t0001g0081 |
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 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0074 |
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 | a0001c0001t0001g0139 a0001c0001t0008g0036 |
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 | a0001c0001t0014g0033 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0096 | 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 | a0001c0001t0003g0129 a0001c0001t0003g0150 |
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 | a0001c0001t0003g0050 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0053 a0001c0001t0003g0029 a0001c0001t0005g0011 |
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 | a0001c0001t0006g0084 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0002g0120 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0140 a0001c0001t0003g0076 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0085 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0009g0025 a0001c0001t0012g0147 |
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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0164 others(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 | a0001c0001t0002g0137 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0128 |
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 | a0001c0001t0001g0136 a0001c0001t0002g0049 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0162 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0114 a0001c0001t0002g0171 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0158 a0001c0001t0010g0124 |
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 | a0001c0001t0001g0078 | 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 | a0001c0001t0007g0023 a0001c0001t0007g0075 |
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 | a0001c0001t0007g0034 | 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 | a0001c0001t0002g0032 a0001c0001t0003g0141 a0001c0001t0009g0152 others(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 | a0001c0001t0008g0123 | 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 | a0001c0001t0001g0169 a0001c0001t0007g0077 |
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 | a0001c0001t0001g0125 a0001c0001t0008g0161 |
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 | a0001c0001t0013g0090 | 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 | a0001c0001t0004g0014 a0001c0001t0004g0054 a0001c0001t0006g0038 |
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 | a0001c0001t0005g0101 a0001c0001t0018g0157 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0003g0113 others(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 | a0001c0001t0002g0172 a0001c0001t0004g0021 a0001c0001t0004g0105 others(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 | a0001c0002t0015g0044 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0014g0033 | 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 | a0002c0003t0001g0160 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0006t0001g0065 | 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 | a0001c0001t0003g0083 a0001c0001t0003g0150 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0115 |
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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0062 a0001c0001t0010g0124 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0079 others(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 | a0001c0001t0012g0147 | 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 | a0001c0002t0004g0040 | 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 | a0001c0001t0001g0097 a0001c0001t0002g0120 |
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 | a0001c0001t0001g0097 a0001c0001t0002g0120 |
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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0116 a0001c0001t0021g0104 |
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 | a0001c0001t0002g0127 a0001c0001t0002g0172 a0001c0001t0008g0123 others(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 | a0001c0001t0008g0161 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0086 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0133 others(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 | a0001c0001t0012g0147 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0002g0064 others(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 | a0001c0001t0001g0037 a0001c0001t0016g0153 a0002c0003t0001g0148 |
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 | a0001c0001t0002g0127 a0001c0001t0002g0172 a0001c0001t0018g0157 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0134 a0001c0001t0009g0025 |
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 | a0001c0001t0012g0147 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0067 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0177 a0001c0001t0010g0124 |
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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0067 a0001c0001t0011g0110 |
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 | a0001c0001t0012g0147 | 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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0014g0033 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0134 a0001c0001t0002g0064 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0016g0153 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0069 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
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 | a0001c0001t0001g0169 a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0005g0080 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0002g0127 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0085 others(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 | a0002c0003t0001g0160 | 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 | a0001c0001t0014g0033 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0008g0123 a0001c0001t0008g0161 a0001c0001t0014g0033 |
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 | a0001c0001t0005g0011 a0001c0001t0006g0084 |
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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0014g0033 | 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 | a0001c0001t0014g0033 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0134 a0001c0001t0002g0064 others(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 | ||||||
| chr6:45499510 | T | C | 1 | a0001c0001t0001g0133 | 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 | a0001c0001t0014g0033 | 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 | a0001c0001t0001g0062 a0001c0001t0010g0124 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0037 a0001c0001t0016g0153 |
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 | a0001c0002t0015g0044 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0003g0103 a0001c0001t0003g0146 |
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 | a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0135 a0001c0001t0003g0113 a0001c0001t0004g0005 others(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 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0009g0152 others(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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0002g0120 | 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 | a0001c0001t0005g0039 | 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 | a0001c0001t0017g0138 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.860-8761T>G | RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 6/8 | chr6 | 45503485 | |||||||
| chr6:45504154 | C | T | 1 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0012 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0134 a0001c0001t0002g0064 others(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 | a0001c0001t0001g0134 a0001c0001t0009g0025 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 a0001c0001t0014g0033 |
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 | a0002c0003t0001g0148 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0134 a0001c0001t0002g0064 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0069 a0001c0001t0016g0153 |
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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0062 a0001c0001t0010g0124 |
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 | a0001c0001t0014g0033 | 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 | a0001c0001t0021g0104 | 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 | a0001c0001t0001g0167 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0168 |
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 | a0001c0001t0014g0033 | 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 | a0001c0001t0007g0023 a0001c0001t0007g0034 a0001c0001t0007g0075 others(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 | a0001c0001t0001g0062 a0001c0001t0010g0124 |
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 | a0001c0001t0002g0074 a0001c0001t0017g0138 |
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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0158 others(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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0127 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0009g0152 others(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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0069 a0001c0001t0016g0153 |
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 | a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0134 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0114 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0022 a0001c0001t0002g0004 a0001c0001t0002g0012 others(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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0073 a0001c0001t0014g0033 |
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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(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 | a0001c0001t0001g0069 a0001c0001t0016g0153 |
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 | a0001c0001t0001g0134 a0001c0001t0002g0120 a0001c0001t0005g0011 others(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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0134 a0001c0001t0002g0064 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0134 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0114 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0135 a0001c0001t0003g0113 a0001c0001t0004g0005 others(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 | a0001c0001t0017g0138 | 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 | a0001c0001t0001g0062 a0001c0001t0010g0124 |
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 | a0001c0001t0003g0052 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(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 | a0001c0001t0002g0017 a0001c0001t0008g0036 a0001c0001t0011g0110 others(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 | a0001c0001t0001g0022 a0001c0001t0002g0174 |
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 | a0001c0001t0001g0114 a0001c0001t0001g0125 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0009 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0169 a0001c0001t0002g0035 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0175 others(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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(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 | a0001c0001t0003g0141 | 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 | a0001c0001t0008g0036 a0001c0001t0011g0110 a0001c0001t0020g0170 |
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 | a0001c0001t0001g0073 | 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 | a0001c0001t0002g0074 a0001c0001t0009g0152 a0001c0001t0009g0168 others(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 | a0001c0002t0006g0015 a0001c0002t0006g0016 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0012 |
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 | a0001c0001t0001g0155 a0001c0001t0002g0017 a0001c0001t0002g0120 others(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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0155 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0155 a0001c0001t0002g0017 a0001c0001t0002g0120 others(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 | a0001c0001t0003g0103 a0001c0001t0003g0146 |
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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | a0001c0001t0002g0035 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0069 a0001c0001t0002g0094 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0008g0036 a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0002g0126 |
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 | a0001c0001t0002g0035 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0135 |
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 | a0001c0001t0001g0067 a0001c0001t0005g0039 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0098 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0116 a0001c0001t0004g0021 a0001c0001t0004g0059 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0095 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0115 |
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 | a0001c0001t0001g0069 a0001c0001t0002g0094 a0001c0001t0002g0127 others(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 | a0001c0001t0003g0043 a0001c0001t0012g0147 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0093 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0069 a0001c0001t0002g0094 a0001c0001t0002g0127 others(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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0127 | 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 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 |
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 | a0001c0001t0002g0074 a0001c0001t0002g0126 a0001c0001t0009g0025 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0004g0105 a0001c0001t0004g0121 a0001c0001t0005g0080 others(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 | a0001c0001t0001g0114 a0001c0001t0004g0005 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0178 a0001c0001t0005g0018 |
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 | a0001c0001t0005g0101 | 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 | a0001c0001t0005g0056 | 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 | a0001c0001t0001g0175 a0001c0002t0001g0099 |
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 | a0001c0001t0001g0155 a0001c0001t0006g0003 a0001c0001t0013g0090 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0008g0036 a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0116 a0001c0001t0021g0104 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | 128 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0031 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): 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 | a0001c0001t0008g0161 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0003g0103 a0001c0001t0003g0146 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0004g0005 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0085 a0001c0001t0001g0087 others(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 | a0001c0001t0005g0011 a0001c0001t0006g0001 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0003g0103 a0001c0001t0003g0146 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0125 others(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 | a0001c0001t0006g0084 | 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 | a0001c0001t0001g0069 a0001c0001t0002g0094 a0001c0001t0011g0019 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0140 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0004g0005 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0017 |
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 | a0001c0001t0002g0035 a0001c0001t0002g0126 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0004g0005 others(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 | a0001c0001t0003g0141 | 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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0125 others(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 | 175 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(172): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): 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 | a0001c0001t0003g0083 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0164 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0004g0005 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0004g0005 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0074 a0001c0001t0009g0025 a0001c0001t0009g0152 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0176 a0001c0001t0010g0002 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0008g0036 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0074 a0001c0001t0009g0025 a0001c0001t0009g0152 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0002g0126 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(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 | a0001c0001t0002g0074 a0001c0001t0009g0025 a0001c0001t0009g0152 others(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 | a0001c0001t0003g0103 a0001c0001t0003g0146 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0008g0036 a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0008g0036 a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0002g0049 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0005g0080 | 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 | a0001c0001t0010g0124 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0003g0141 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0093 others(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 | 19 | a0001c0001t0001g0010 a0001c0001t0001g0112 a0001c0001t0001g0136 others(16): Show |
19 | HG01069.hp1 HG01243.hp2 HG01884.hp1 others(16): 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0070 a0001c0001t0002g0072 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0128 |
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 | a0001c0001t0002g0035 a0001c0001t0002g0126 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0004g0005 others(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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0155 a0001c0001t0003g0050 a0001c0001t0005g0011 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0067 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0002g0064 a0001c0001t0002g0137 |
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 | a0001c0001t0008g0036 a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0001g0069 a0001c0001t0002g0094 a0001c0001t0011g0019 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0167 a0001c0001t0002g0126 a0001c0001t0005g0018 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0035 a0001c0001t0002g0171 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0006g0084 | 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 | 13 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG00423.hp2 HG00733.hp1 HG00741.hp1 others(10): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0002g0035 a0001c0001t0014g0033 |
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 | a0001c0001t0002g0126 | 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 | a0001c0001t0005g0039 | 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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0114 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0069 a0001c0001t0002g0094 a0001c0001t0011g0019 others(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 | a0001c0001t0010g0124 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0004g0059 a0001c0001t0004g0178 |
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 | a0001c0001t0002g0024 a0001c0001t0002g0171 a0001c0001t0002g0173 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0067 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0067 a0001c0001t0004g0005 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0069 a0001c0001t0002g0094 a0001c0001t0011g0019 others(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 | a0001c0001t0003g0113 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0002g0132 a0001c0001t0005g0039 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0140 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0067 | 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 | 14 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0041 others(11): Show |
14 | HG00423.hp2 HG00733.hp1 HG00741.hp1 others(11): 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0017 others(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 | a0001c0001t0008g0036 a0001c0001t0008g0123 a0001c0001t0008g0161 |
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 | a0001c0001t0002g0127 | 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 | a0001c0001t0003g0129 | 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 | a0001c0001t0001g0155 a0001c0001t0005g0011 a0001c0001t0006g0001 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0004g0121 a0001c0002t0004g0060 |
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 | a0001c0001t0001g0069 a0001c0001t0002g0094 a0001c0001t0011g0019 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0062 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0002g0035 a0001c0001t0014g0033 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0114 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0017 others(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 | a0001c0001t0021g0104 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0115 |
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 | a0001c0001t0002g0074 a0001c0001t0009g0025 a0001c0001t0009g0152 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0114 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0029 a0001c0001t0003g0030 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0125 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0067 others(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 | |||||||
| chr6:45544886 | T | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0069 a0001c0001t0002g0074 a0001c0001t0002g0094 others(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 | a0001c0001t0001g0069 a0001c0001t0002g0094 |
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 | a0001c0001t0012g0147 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0017 others(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 |