| geneid | 4205 |
|---|---|
| ensemblid | ENSG00000068305.19 |
| hgncid | 6993 |
| symbol | MEF2A |
| name | myocyte enhancer factor 2A |
| refseq_nuc | NM_001319206.4 |
| refseq_prot | NP_001306135.1 |
| ensembl_nuc | ENST00000557942.6 |
| ensembl_prot | ENSP00000453095.1 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 99565984 |
| end | 99716488 |
| strand | + |
| ver | v1.2 |
| region | chr15:99565984-99716488 |
| region5000 | chr15:99560984-99721488 |
| regionname0 | MEF2A_chr15_99565984_99716488 |
| regionname5000 | MEF2A_chr15_99560984_99721488 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 505 | 182 | 61 | 32 | 64 | 9 | 14 | 51 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002 | 0/0 | 503 | 78 | 1 | 13 | 45 | 4 | 15 | 28 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003 | 0/0 | 504 | 71 | 14 | 18 | 34 | 2 | 3 | 23 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004 | 0/0 | 507 | 11 | 8 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0005 | 0/0 | 502 | 8 | 0 | 1 | 7 | 0 | 0 | 5 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0006 | 0/0 | 502 | 4 | 2 | 0 | 2 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0007 | 0/0 | 508 | 4 | 0 | 0 | 3 | 0 | 1 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0008 | 0/0 | 498 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0009 | 0/0 | 501 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0010 | 0/0 | 506 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0011 | 0/0 | 504 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0012 | 0/0 | 499 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0013 | 0/0 | 493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0014 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0015 | 0/0 | 465 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0016 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0017 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0018 | 0/0 | 510 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1518 | 91 | 10 | 14 | 50 | 8 | 9 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0002 | 0/0 | 1512 | 65 | 1 | 12 | 34 | 4 | 14 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0003 | 0/0 | 1515 | 55 | 3 | 15 | 32 | 2 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0004 | 0/0 | 1518 | 32 | 22 | 5 | 3 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0005 | 1/0 | 1518 | 25 | 23 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0006 | 0/0 | 1518 | 15 | 0 | 6 | 7 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0007 | 0/1 | 1518 | 9 | 1 | 5 | 0 | 1 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0008 | 0/0 | 1524 | 9 | 7 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0009 | 0/0 | 1509 | 8 | 0 | 1 | 7 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0010 | 0/0 | 1515 | 8 | 8 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0011 | 0/0 | 1512 | 7 | 0 | 1 | 6 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0012 | 0/0 | 1518 | 6 | 5 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0013 | 0/0 | 1515 | 5 | 3 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0014 | 0/0 | 1512 | 5 | 0 | 0 | 4 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0015 | 0/0 | 1509 | 4 | 2 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0016 | 0/0 | 1527 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0017 | 0/0 | 1518 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0018 | 0/0 | 1497 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0019 | 0/0 | 1524 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0020 | 0/0 | 1521 | 2 | 1 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0021 | 0/0 | 1506 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0022 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0023 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0024 | 0/0 | 1537 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0025 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0026 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0027 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0028 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0029 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0030 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0031 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0032 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0033 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0034 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0035 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0036 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| c0037 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4066 | 49 | 5 | 10 | 21 | 6 | 6 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0002 | 0/0 | 4065 | 41 | 3 | 11 | 25 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0003 | 0/0 | 4062 | 14 | 14 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0004 | 0/0 | 4065 | 14 | 3 | 3 | 7 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0005 | 0/0 | 4061 | 10 | 0 | 1 | 5 | 0 | 4 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0006 | 0/0 | 4066 | 9 | 5 | 0 | 4 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0007 | 0/0 | 4061 | 8 | 0 | 0 | 8 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0008 | 0/0 | 4061 | 8 | 0 | 4 | 0 | 1 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0009 | 0/0 | 4068 | 8 | 7 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0010 | 0/0 | 4066 | 8 | 0 | 6 | 1 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0011 | 0/0 | 4066 | 6 | 1 | 0 | 4 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0012 | 0/0 | 4061 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0013 | 0/0 | 4062 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0014 | 0/0 | 4062 | 5 | 0 | 2 | 0 | 2 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0015 | 0/0 | 4062 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0016 | 0/0 | 4065 | 5 | 0 | 0 | 4 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0017 | 0/0 | 4061 | 4 | 3 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0018 | 0/0 | 4062 | 4 | 0 | 2 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0019 | 0/0 | 4061 | 4 | 0 | 0 | 4 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0020 | 0/0 | 4062 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0021 | 0/0 | 4062 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0022 | 0/0 | 4061 | 3 | 0 | 0 | 0 | 1 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0023 | 0/0 | 4062 | 3 | 0 | 1 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0024 | 0/0 | 4066 | 3 | 0 | 0 | 2 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0025 | 0/0 | 4066 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0026 | 0/0 | 4067 | 3 | 0 | 1 | 1 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0027 | 0/0 | 4067 | 3 | 2 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0028 | 0/0 | 4065 | 3 | 2 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0029 | 0/0 | 4061 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0030 | 0/0 | 4061 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0031 | 0/0 | 4061 | 2 | 0 | 1 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0032 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0033 | 0/0 | 4063 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0034 | 0/0 | 4061 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0035 | 0/0 | 4061 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0036 | 0/0 | 4062 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0037 | 0/0 | 4062 | 2 | 0 | 0 | 1 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0038 | 0/0 | 4063 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0039 | 0/0 | 4066 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0040 | 0/0 | 4065 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0041 | 0/0 | 4066 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0042 | 0/0 | 4066 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0043 | 0/0 | 4067 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0044 | 0/0 | 4067 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0045 | 0/0 | 4065 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0046 | 0/0 | 4065 | 2 | 1 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0047 | 0/0 | 4065 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0048 | 0/0 | 4066 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0049 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0050 | 0/0 | 4067 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0051 | 0/0 | 4067 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0052 | 0/0 | 4066 | 2 | 1 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0053 | 0/0 | 4066 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0054 | 0/0 | 4067 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0055 | 0/0 | 4066 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0056 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0057 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0058 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0059 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0060 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0061 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0062 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0063 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0064 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0065 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0066 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0067 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0068 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0069 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0070 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0071 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0072 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0073 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0074 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0075 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0076 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0077 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0078 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0079 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0080 | 0/0 | 4063 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0081 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0082 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0083 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0084 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0085 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0086 | 1/0 | 4063 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0087 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0088 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0089 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0090 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0091 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0092 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0093 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0094 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0095 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0096 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0097 | 0/0 | 4066 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0098 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0099 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0100 | 0/0 | 4066 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0101 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0102 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0103 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0104 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0105 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0106 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0107 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0108 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0109 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0110 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0111 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0112 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0113 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0114 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0115 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0116 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0117 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0118 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0119 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0120 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0121 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0122 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0123 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0124 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0125 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0126 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0127 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0128 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0129 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0130 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0131 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0132 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0133 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0134 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0135 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0136 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0137 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| t0138 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1518 | 91 | 10 | 14 | 50 | 8 | 9 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004 | 0/0 | 1518 | 32 | 22 | 5 | 3 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005 | 1/0 | 1518 | 25 | 23 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006 | 0/0 | 1518 | 15 | 0 | 6 | 7 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0007 | 0/1 | 1518 | 9 | 1 | 5 | 0 | 1 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0012 | 0/0 | 1518 | 6 | 5 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0017 | 0/0 | 1518 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0028 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002 | 0/0 | 1512 | 65 | 1 | 12 | 34 | 4 | 14 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0011 | 0/0 | 1512 | 7 | 0 | 1 | 6 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0014 | 0/0 | 1512 | 5 | 0 | 0 | 4 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0036 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003 | 0/0 | 1515 | 55 | 3 | 15 | 32 | 2 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0010 | 0/0 | 1515 | 8 | 8 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0013 | 0/0 | 1515 | 5 | 3 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0022 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0031 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004c0008 | 0/0 | 1524 | 9 | 7 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004c0019 | 0/0 | 1524 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0005c0009 | 0/0 | 1509 | 8 | 0 | 1 | 7 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0006c0015 | 0/0 | 1509 | 4 | 2 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0007c0016 | 0/0 | 1527 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0007c0026 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0008c0018 | 0/0 | 1497 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0009c0021 | 0/0 | 1506 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0009c0037 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0010c0020 | 0/0 | 1521 | 2 | 1 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0010c0035 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0011c0023 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0011c0027 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0012c0033 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0013c0032 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0014c0030 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0015c0024 | 0/0 | 1537 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0016c0029 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0017c0034 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0018c0025 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5583 | 32 | 2 | 6 | 14 | 5 | 5 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0004 | 0/0 | 5582 | 11 | 1 | 3 | 6 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0006 | 0/0 | 5583 | 4 | 0 | 0 | 4 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0011 | 0/0 | 5583 | 4 | 0 | 0 | 3 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0020 | 0/0 | 5579 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0024 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0025 | 0/0 | 5583 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0026 | 0/0 | 5584 | 2 | 0 | 0 | 1 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0027 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0028 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0032 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0039 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0040 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0041 | 0/0 | 5583 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0043 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0044 | 0/0 | 5584 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0045 | 0/0 | 5582 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0046 | 0/0 | 5582 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0064 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0077 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0081 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0087 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0088 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0089 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0093 | 0/0 | 5582 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0096 | 0/0 | 5582 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0097 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0102 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0103 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0104 | 0/0 | 5584 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0105 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0106 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0113 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0120 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0121 | 0/0 | 5584 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0001t0124 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0001 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0002 | 0/0 | 5582 | 4 | 0 | 4 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0006 | 0/0 | 5583 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0010 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0011 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0026 | 0/0 | 5584 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0027 | 0/0 | 5584 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0046 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0047 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0048 | 0/0 | 5583 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0049 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0051 | 0/0 | 5584 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0052 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0053 | 0/0 | 5583 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0091 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0092 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0107 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0112 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0115 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0117 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0131 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0132 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0004t0137 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0003 | 0/0 | 5579 | 12 | 12 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0009 | 0/0 | 5585 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0015 | 0/0 | 5579 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0084 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0085 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0086 | 1/0 | 5580 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0125 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0005t0138 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0005 | 0/0 | 5578 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0007 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0008 | 0/0 | 5578 | 4 | 0 | 3 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0012 | 0/0 | 5578 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0018 | 0/0 | 5579 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0021 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0065 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0006t0071 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0007t0001 | 0/1 | 5583 | 7 | 1 | 3 | 0 | 1 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0007t0040 | 0/0 | 5582 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0007t0100 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0012t0017 | 0/0 | 5578 | 4 | 3 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0012t0063 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0012t0066 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0017t0001 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0017t0043 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0001c0028t0095 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0005 | 0/0 | 5572 | 6 | 0 | 0 | 3 | 0 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0007 | 0/0 | 5572 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0008 | 0/0 | 5572 | 4 | 0 | 1 | 0 | 1 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0012 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0013 | 0/0 | 5573 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0014 | 0/0 | 5573 | 5 | 0 | 2 | 0 | 2 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0021 | 0/0 | 5573 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0022 | 0/0 | 5572 | 3 | 0 | 0 | 0 | 1 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0023 | 0/0 | 5573 | 3 | 0 | 1 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0029 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0030 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0031 | 0/0 | 5572 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0033 | 0/0 | 5574 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0034 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0035 | 0/0 | 5572 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0036 | 0/0 | 5573 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0037 | 0/0 | 5573 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0038 | 0/0 | 5574 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0056 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0057 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0058 | 0/0 | 5573 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0060 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0062 | 0/0 | 5574 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0068 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0072 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0073 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0074 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0075 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0078 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0079 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0080 | 0/0 | 5574 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0082 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0002t0083 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0011t0001 | 0/0 | 5577 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0011t0011 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0011t0024 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0011t0042 | 0/0 | 5577 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0011t0044 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0011t0090 | 0/0 | 5576 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0014t0002 | 0/0 | 5576 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0014t0007 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0014t0016 | 0/0 | 5576 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0014t0109 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0002c0036t0005 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0002 | 0/0 | 5579 | 28 | 0 | 5 | 21 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0006 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0010 | 0/0 | 5580 | 6 | 0 | 5 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0016 | 0/0 | 5579 | 4 | 0 | 0 | 3 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0052 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0054 | 0/0 | 5581 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0098 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0108 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0110 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0116 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0118 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0119 | 0/0 | 5579 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0123 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0126 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0127 | 0/0 | 5581 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0128 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0133 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0134 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0003t0136 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0010t0002 | 0/0 | 5579 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0010t0003 | 0/0 | 5576 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0010t0055 | 0/0 | 5580 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0010t0130 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0010t0135 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0013t0001 | 0/0 | 5580 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0013t0002 | 0/0 | 5579 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0013t0032 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0022t0002 | 0/0 | 5579 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0022t0010 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0003c0031t0070 | 0/0 | 5576 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004c0008t0009 | 0/0 | 5591 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004c0008t0047 | 0/0 | 5588 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004c0008t0050 | 0/0 | 5590 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004c0008t0099 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0004c0019t0028 | 0/0 | 5588 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0005c0009t0019 | 0/0 | 5569 | 4 | 0 | 0 | 4 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0005c0009t0031 | 0/0 | 5569 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0005c0009t0037 | 0/0 | 5570 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0005c0009t0061 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0005c0009t0076 | 0/0 | 5570 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0006c0015t0004 | 0/0 | 5573 | 3 | 2 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0006c0015t0101 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0007c0016t0018 | 0/0 | 5588 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0007c0016t0067 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0007c0026t0024 | 0/0 | 5592 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0008c0018t0002 | 0/0 | 5561 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0008c0018t0129 | 0/0 | 5563 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0009c0021t0001 | 0/0 | 5571 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0009c0037t0003 | 0/0 | 5567 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0010c0020t0001 | 0/0 | 5586 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0010c0020t0049 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0010c0035t0122 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0011c0023t0006 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0011c0027t0059 | 0/0 | 5576 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0012c0033t0094 | 0/0 | 5564 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0013c0032t0005 | 0/0 | 5542 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0014c0030t0069 | 0/0 | 5576 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0015c0024t0038 | 0/0 | 5599 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0016c0029t0114 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0017c0034t0111 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| a0018c0025t0001 | 0/0 | 5598 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | copy fasta | chr15 | 99560984 | 99721488 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0011g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0011g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0011g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0020g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0020g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0020g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0024g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0025g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0025g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0025g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0026g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0026g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0027g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0028g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0032g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0039g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0039g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0040g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0041g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0041g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0043g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0044g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0045g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0045g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0046g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0064g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0077g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0081g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0087g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0088g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0089g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0093g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0096g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0097g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0102g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0103g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0104g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0105g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0106g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0113g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0120g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0121g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0124g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0006g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0010g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0011g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0026g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0027g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0027g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0046g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0047g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0048g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0048g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0049g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0051g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0051g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0052g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0053g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0053g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0091g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0092g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0107g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0112g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0115g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0117g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0131g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0132g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0137g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0084g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0085g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0086g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0125g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0138g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0008g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0012g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0018g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0018g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0021g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0065g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0071g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0040g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0100g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0012t0017g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0012t0017g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0012t0017g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0012t0017g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0012t0063g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0012t0066g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0017t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0017t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0017t0043g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0028t0095g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0012g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0013g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0013g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0013g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0013g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0021g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0021g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0022g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0022g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0022g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0023g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0023g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0023g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0029g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0029g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0030g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0030g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0031g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0033g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0033g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0034g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0034g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0035g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0035g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0036g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0036g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0037g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0038g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0056g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0057g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0058g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0060g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0062g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0068g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0072g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0073g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0074g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0075g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0078g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0079g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0080g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0082g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0083g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0011t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0011t0011g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0011t0024g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0011t0042g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0011t0042g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0011t0044g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0011t0090g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0014t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0014t0007g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0014t0007g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0014t0016g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0014t0109g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0036t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0010g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0010g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0010g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0010g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0010g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0010g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0052g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0054g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0054g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0098g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0108g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0110g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0116g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0118g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0119g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0123g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0126g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0127g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0128g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0133g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0134g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0136g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0055g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0055g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0130g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0010t0135g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0013t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0013t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0013t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0013t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0013t0032g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0022t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0022t0010g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0031t0070g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0047g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0050g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0050g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0099g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0019t0028g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0019t0028g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0019g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0019g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0031g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0037g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0061g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0009t0076g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0015t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0015t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0015t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0015t0101g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0007c0016t0018g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0007c0016t0018g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0007c0016t0067g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0007c0026t0024g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0008c0018t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0008c0018t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0008c0018t0129g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0009c0021t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0009c0021t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0009c0037t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0010c0020t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0010c0020t0049g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0010c0035t0122g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0011c0023t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0011c0027t0059g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0012c0033t0094g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0013c0032t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0014c0030t0069g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0015c0024t0038g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0016c0029t0114g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0017c0034t0111g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0018c0025t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0011 | c0027 | t0059 | g0099 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00140 | hp2 | a0002 | c0002 | t0014 | g0086 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00280 | hp1 | a0003 | c0003 | t0016 | g0053 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00323 | hp1 | a0002 | c0002 | t0022 | g0104 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00323 | hp2 | a0001 | c0001 | t0120 | g0244 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00408 | hp2 | a0003 | c0003 | t0016 | g0312 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00423 | hp1 | a0001 | c0001 | t0039 | g0265 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00423 | hp2 | a0003 | c0003 | t0002 | g0305 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00438 | hp1 | a0001 | c0006 | t0021 | g0164 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00438 | hp2 | a0003 | c0003 | t0016 | g0333 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00544 | hp1 | a0001 | c0001 | t0077 | g0206 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00544 | hp2 | a0001 | c0001 | t0106 | g0254 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00558 | hp1 | a0002 | c0014 | t0002 | g0326 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00558 | hp2 | a0002 | c0002 | t0060 | g0202 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00597 | hp1 | a0001 | c0001 | t0039 | g0268 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00597 | hp2 | a0005 | c0009 | t0037 | g0085 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00609 | hp1 | a0003 | c0003 | t0110 | g0194 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00609 | hp2 | a0006 | c0015 | t0101 | g0175 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00621 | hp1 | a0001 | c0001 | t0102 | g0163 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00621 | hp2 | a0003 | c0003 | t0002 | g0319 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00639 | hp1 | a0003 | c0003 | t0119 | g0287 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00639 | hp2 | a0001 | c0007 | t0100 | g0044 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00642 | hp2 | a0001 | c0006 | t0018 | g0233 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0358 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00673 | hp2 | a0002 | c0002 | t0007 | g0088 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00733 | hp1 | a0001 | c0007 | t0001 | g0169 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00733 | hp2 | a0004 | c0008 | t0009 | g0032 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00735 | hp1 | a0004 | c0019 | t0028 | g0121 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00738 | hp1 | a0003 | c0003 | t0002 | g0302 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01071 | hp1 | a0005 | c0009 | t0031 | g0080 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0228 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01074 | hp1 | a0002 | c0002 | t0014 | g0091 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01074 | hp2 | a0003 | c0003 | t0128 | g0303 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01081 | hp1 | a0002 | c0002 | t0068 | g0160 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01081 | hp2 | a0003 | c0022 | t0002 | g0345 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01099 | hp1 | a0001 | c0004 | t0002 | g0360 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01099 | hp2 | a0004 | c0008 | t0050 | g0215 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01109 | hp1 | a0001 | c0005 | t0015 | g0027 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01109 | hp2 | a0001 | c0001 | t0093 | g0042 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01167 | hp1 | a0002 | c0002 | t0014 | g0092 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01167 | hp2 | a0001 | c0004 | t0002 | g0363 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01168 | hp1 | a0003 | c0022 | t0010 | g0365 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01168 | hp2 | a0001 | c0006 | t0008 | g0111 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01169 | hp1 | a0001 | c0006 | t0008 | g0112 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01169 | hp2 | a0001 | c0004 | t0002 | g0357 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01175 | hp1 | a0002 | c0002 | t0038 | g0165 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01175 | hp2 | a0001 | c0001 | t0044 | g0240 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01192 | hp1 | a0001 | c0007 | t0001 | g0168 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01192 | hp2 | a0001 | c0006 | t0008 | g0115 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01255 | hp1 | a0001 | c0001 | t0097 | g0189 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01255 | hp2 | a0003 | c0003 | t0002 | g0294 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01257 | hp1 | a0001 | c0007 | t0040 | g0118 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01258 | hp2 | a0001 | c0006 | t0018 | g0231 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01261 | hp1 | a0001 | c0004 | t0026 | g0002 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01261 | hp2 | a0015 | c0024 | t0038 | g0114 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01346 | hp1 | a0001 | c0007 | t0001 | g0260 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01346 | hp2 | a0002 | c0002 | t0023 | g0116 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01358 | hp1 | a0002 | c0002 | t0008 | g0031 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01358 | hp2 | a0001 | c0001 | t0096 | g0029 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01361 | hp1 | a0001 | c0006 | t0005 | g0093 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01433 | hp1 | a0002 | c0002 | t0036 | g0140 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01496 | hp2 | a0001 | c0012 | t0017 | g0352 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01515 | hp1 | a0001 | c0001 | t0121 | g0190 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0370 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01517 | hp1 | a0002 | c0002 | t0014 | g0230 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0369 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01884 | hp1 | a0001 | c0004 | t0046 | g0343 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01884 | hp2 | a0011 | c0023 | t0006 | g0219 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01891 | hp1 | a0014 | c0030 | t0069 | g0276 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01891 | hp2 | a0001 | c0005 | t0003 | g0020 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01928 | hp1 | a0003 | c0003 | t0010 | g0258 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01928 | hp2 | a0001 | c0004 | t0002 | g0361 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01934 | hp1 | a0003 | c0003 | t0054 | g0007 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01934 | hp2 | a0002 | c0002 | t0082 | g0095 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01943 | hp1 | a0002 | c0011 | t0001 | g0172 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01943 | hp2 | a0003 | c0003 | t0010 | g0005 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01978 | hp1 | a0002 | c0002 | t0035 | g0142 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01978 | hp2 | a0003 | c0003 | t0010 | g0004 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0293 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01981 | hp2 | a0002 | c0002 | t0036 | g0041 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01993 | hp1 | a0001 | c0001 | t0041 | g0186 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01993 | hp2 | a0003 | c0003 | t0123 | g0008 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02015 | hp1 | a0003 | c0003 | t0002 | g0317 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02015 | hp2 | a0002 | c0002 | t0007 | g0221 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02027 | hp1 | a0002 | c0002 | t0007 | g0052 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02027 | hp2 | a0002 | c0011 | t0044 | g0171 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02040 | hp1 | a0005 | c0009 | t0061 | g0129 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02040 | hp2 | a0002 | c0002 | t0074 | g0252 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02055 | hp1 | a0001 | c0004 | t0049 | g0290 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02055 | hp2 | a0001 | c0004 | t0137 | g0283 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02056 | hp1 | a0002 | c0014 | t0016 | g0348 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02056 | hp2 | a0001 | c0001 | t0105 | g0255 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02074 | hp1 | a0001 | c0004 | t0001 | g0327 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02074 | hp2 | a0001 | c0001 | t0041 | g0170 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02080 | hp1 | a0003 | c0003 | t0134 | g0331 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02080 | hp2 | a0002 | c0002 | t0007 | g0087 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02083 | hp1 | a0002 | c0011 | t0042 | g0105 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02083 | hp2 | a0001 | c0001 | t0087 | g0270 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02129 | hp1 | a0002 | c0002 | t0007 | g0103 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02129 | hp2 | a0002 | c0011 | t0011 | g0159 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02132 | hp1 | a0002 | c0011 | t0042 | g0106 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02132 | hp2 | a0003 | c0003 | t0002 | g0306 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02135 | hp1 | a0001 | c0001 | t0088 | g0131 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02135 | hp2 | a0003 | c0003 | t0002 | g0315 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02145 | hp1 | a0010 | c0020 | t0049 | g0235 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02145 | hp2 | a0001 | c0004 | t0091 | g0289 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02148 | hp1 | a0002 | c0002 | t0083 | g0143 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02148 | hp2 | a0003 | c0003 | t0010 | g0009 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02155 | hp1 | a0002 | c0002 | t0021 | g0039 | EAS | CDX | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02155 | hp2 | a0003 | c0003 | t0126 | g0347 | EAS | CDX | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02257 | hp1 | a0004 | c0008 | t0050 | g0218 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02257 | hp2 | a0003 | c0010 | t0002 | g0199 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02280 | hp1 | a0001 | c0005 | t0003 | g0022 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02280 | hp2 | a0001 | c0004 | t0006 | g0285 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02293 | hp1 | a0002 | c0002 | t0035 | g0144 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02293 | hp2 | a0003 | c0003 | t0054 | g0010 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0054 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0346 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02451 | hp1 | a0003 | c0013 | t0032 | g0132 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02451 | hp2 | a0001 | c0005 | t0003 | g0012 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02523 | hp1 | a0002 | c0002 | t0021 | g0097 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02523 | hp2 | a0001 | c0001 | t0011 | g0281 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02572 | hp1 | a0017 | c0034 | t0111 | g0308 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0236 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02615 | hp1 | a0004 | c0008 | t0009 | g0253 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02615 | hp2 | a0001 | c0005 | t0125 | g0220 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02622 | hp1 | a0001 | c0005 | t0015 | g0021 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02622 | hp2 | a0001 | c0004 | t0131 | g0286 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02630 | hp2 | a0001 | c0005 | t0003 | g0019 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02647 | hp1 | a0003 | c0010 | t0135 | g0134 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02647 | hp2 | a0001 | c0004 | t0006 | g0342 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02698 | hp1 | a0002 | c0002 | t0005 | g0057 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02717 | hp1 | a0001 | c0005 | t0003 | g0018 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02723 | hp1 | a0003 | c0003 | t0006 | g0295 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0193 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02735 | hp1 | a0001 | c0007 | t0001 | g0184 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02735 | hp2 | a0002 | c0002 | t0005 | g0110 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02738 | hp1 | a0002 | c0002 | t0008 | g0055 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02738 | hp2 | a0001 | c0001 | t0011 | g0242 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02809 | hp1 | a0001 | c0004 | t0117 | g0311 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02809 | hp2 | a0004 | c0008 | t0009 | g0214 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02886 | hp1 | a0001 | c0001 | t0028 | g0162 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02886 | hp2 | a0003 | c0010 | t0003 | g0017 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02895 | hp1 | a0001 | c0004 | t0107 | g0350 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02895 | hp2 | a0006 | c0015 | t0004 | g0154 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02896 | hp1 | a0004 | c0008 | t0009 | g0034 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02896 | hp2 | a0003 | c0003 | t0098 | g0291 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02897 | hp1 | a0006 | c0015 | t0004 | g0155 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02897 | hp2 | a0004 | c0008 | t0009 | g0033 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02922 | hp1 | a0001 | c0005 | t0015 | g0023 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02922 | hp2 | a0001 | c0004 | t0047 | g0296 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02965 | hp1 | a0001 | c0005 | t0009 | g0213 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02965 | hp2 | a0003 | c0010 | t0002 | g0198 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02970 | hp1 | a0001 | c0012 | t0066 | g0284 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02970 | hp2 | a0001 | c0005 | t0138 | g0014 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02976 | hp1 | a0016 | c0029 | t0114 | g0040 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02976 | hp2 | a0001 | c0005 | t0085 | g0011 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03017 | hp1 | a0003 | c0003 | t0127 | g0314 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03017 | hp2 | a0002 | c0002 | t0005 | g0108 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03041 | hp1 | a0001 | c0004 | t0048 | g0292 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03041 | hp2 | a0003 | c0013 | t0001 | g0257 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03098 | hp1 | a0001 | c0001 | t0064 | g0278 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0279 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03130 | hp1 | a0001 | c0012 | t0063 | g0351 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03130 | hp2 | a0001 | c0004 | t0092 | g0288 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03139 | hp1 | a0001 | c0005 | t0003 | g0263 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03139 | hp2 | a0001 | c0005 | t0009 | g0212 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03195 | hp1 | a0001 | c0012 | t0017 | g0336 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03195 | hp2 | a0001 | c0005 | t0003 | g0264 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03209 | hp1 | a0001 | c0004 | t0048 | g0047 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03209 | hp2 | a0001 | c0004 | t0052 | g0373 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03225 | hp1 | a0003 | c0010 | t0130 | g0277 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03225 | hp2 | a0001 | c0004 | t0053 | g0374 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03453 | hp1 | a0001 | c0004 | t0006 | g0200 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03453 | hp2 | a0001 | c0005 | t0003 | g0016 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03486 | hp1 | a0001 | c0004 | t0027 | g0310 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03486 | hp2 | a0009 | c0037 | t0003 | g0015 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03490 | hp2 | a0002 | c0002 | t0014 | g0059 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03492 | hp2 | a0013 | c0032 | t0005 | g0166 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03516 | hp2 | a0001 | c0004 | t0011 | g0366 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03540 | hp1 | a0003 | c0003 | t0136 | g0282 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03540 | hp2 | a0001 | c0005 | t0015 | g0024 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03579 | hp1 | a0004 | c0008 | t0099 | g0216 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03579 | hp2 | a0003 | c0010 | t0002 | g0197 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03654 | hp1 | a0001 | c0001 | t0026 | g0146 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03654 | hp2 | a0002 | c0002 | t0058 | g0058 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03669 | hp1 | a0001 | c0006 | t0008 | g0113 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03669 | hp2 | a0002 | c0014 | t0109 | g0051 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03688 | hp1 | a0007 | c0026 | t0024 | g0161 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03688 | hp2 | a0002 | c0002 | t0033 | g0072 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03704 | hp1 | a0001 | c0006 | t0071 | g0089 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03704 | hp2 | a0001 | c0001 | t0046 | g0180 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03710 | hp2 | a0002 | c0002 | t0080 | g0211 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03831 | hp1 | a0002 | c0002 | t0033 | g0073 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03831 | hp2 | a0002 | c0002 | t0031 | g0241 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03834 | hp1 | a0002 | c0002 | t0022 | g0223 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0321 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03942 | hp1 | a0002 | c0002 | t0022 | g0232 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03942 | hp2 | a0002 | c0002 | t0008 | g0181 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04184 | hp1 | a0001 | c0001 | t0104 | g0030 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04184 | hp2 | a0001 | c0004 | t0051 | g0049 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0368 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04204 | hp1 | a0001 | c0004 | t0051 | g0050 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04204 | hp2 | a0002 | c0002 | t0037 | g0153 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18522 | hp1 | a0001 | c0005 | t0009 | g0133 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18522 | hp2 | a0001 | c0005 | t0015 | g0025 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18747 | hp1 | a0002 | c0036 | t0005 | g0313 | EAS | CHB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18747 | hp2 | a0002 | c0011 | t0024 | g0157 | EAS | CHB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18906 | hp1 | a0001 | c0004 | t0053 | g0375 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18906 | hp2 | a0001 | c0004 | t0027 | g0349 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18939 | hp1 | a0005 | c0009 | t0019 | g0003 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18939 | hp2 | a0003 | c0003 | t0002 | g0316 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18940 | hp1 | a0003 | c0031 | t0070 | g0204 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18940 | hp2 | a0002 | c0002 | t0005 | g0101 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18942 | hp1 | a0003 | c0003 | t0002 | g0318 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18942 | hp2 | a0007 | c0016 | t0018 | g0060 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18945 | hp1 | a0001 | c0001 | t0027 | g0151 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18945 | hp2 | a0010 | c0020 | t0001 | g0177 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18947 | hp1 | a0002 | c0002 | t0057 | g0038 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18947 | hp2 | a0009 | c0021 | t0001 | g0126 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18948 | hp2 | a0001 | c0006 | t0007 | g0098 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18949 | hp1 | a0002 | c0002 | t0030 | g0084 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18949 | hp2 | a0001 | c0001 | t0103 | g0210 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18950 | hp1 | a0002 | c0002 | t0005 | g0102 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18950 | hp2 | a0001 | c0001 | t0024 | g0274 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18957 | hp1 | a0003 | c0003 | t0002 | g0323 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18961 | hp1 | a0008 | c0018 | t0129 | g0329 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18962 | hp1 | a0005 | c0009 | t0019 | g0071 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18963 | hp1 | a0001 | c0001 | t0089 | g0273 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18963 | hp2 | a0002 | c0002 | t0023 | g0094 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18964 | hp1 | a0003 | c0003 | t0002 | g0300 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18964 | hp2 | a0002 | c0002 | t0075 | g0109 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18967 | hp2 | a0008 | c0018 | t0002 | g0338 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18968 | hp2 | a0002 | c0002 | t0079 | g0201 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18969 | hp1 | a0002 | c0002 | t0029 | g0069 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18969 | hp2 | a0006 | c0015 | t0004 | g0269 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18970 | hp1 | a0002 | c0002 | t0013 | g0066 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18971 | hp1 | a0003 | c0003 | t0002 | g0355 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18975 | hp1 | a0001 | c0001 | t0040 | g0141 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0301 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18977 | hp1 | a0005 | c0009 | t0019 | g0096 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0299 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18978 | hp2 | a0001 | c0004 | t0010 | g0309 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18980 | hp2 | a0001 | c0004 | t0115 | g0332 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18983 | hp1 | a0002 | c0002 | t0012 | g0082 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18983 | hp2 | a0001 | c0001 | t0011 | g0225 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18984 | hp1 | a0003 | c0003 | t0002 | g0307 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18984 | hp2 | a0001 | c0017 | t0001 | g0123 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18986 | hp1 | a0001 | c0001 | t0045 | g0226 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18986 | hp2 | a0001 | c0001 | t0113 | g0148 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18990 | hp1 | a0001 | c0006 | t0012 | g0079 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18990 | hp2 | a0001 | c0001 | t0025 | g0209 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18991 | hp1 | a0002 | c0002 | t0013 | g0063 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18991 | hp2 | a0003 | c0003 | t0108 | g0298 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18994 | hp1 | a0003 | c0003 | t0118 | g0344 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18994 | hp2 | a0002 | c0002 | t0078 | g0117 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18995 | hp1 | a0001 | c0006 | t0065 | g0062 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18998 | hp1 | a0002 | c0002 | t0072 | g0130 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18999 | hp1 | a0003 | c0013 | t0002 | g0205 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18999 | hp2 | a0003 | c0003 | t0133 | g0330 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19001 | hp2 | a0005 | c0009 | t0076 | g0158 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19002 | hp1 | a0018 | c0025 | t0001 | g0173 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19002 | hp2 | a0001 | c0001 | t0081 | g0078 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19003 | hp2 | a0001 | c0006 | t0012 | g0077 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19004 | hp1 | a0002 | c0002 | t0013 | g0068 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19004 | hp2 | a0002 | c0014 | t0007 | g0340 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19005 | hp1 | a0002 | c0014 | t0007 | g0341 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19005 | hp2 | a0002 | c0002 | t0013 | g0064 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19010 | hp1 | a0007 | c0016 | t0067 | g0074 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19043 | hp1 | a0001 | c0001 | t0032 | g0272 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19043 | hp2 | a0001 | c0005 | t0003 | g0335 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19056 | hp1 | a0001 | c0017 | t0001 | g0187 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19056 | hp2 | a0010 | c0035 | t0122 | g0334 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0356 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19057 | hp2 | a0002 | c0011 | t0090 | g0156 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19058 | hp1 | a0002 | c0002 | t0034 | g0261 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19058 | hp2 | a0012 | c0033 | t0094 | g0267 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19063 | hp2 | a0003 | c0003 | t0002 | g0324 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19064 | hp1 | a0008 | c0018 | t0002 | g0320 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19064 | hp2 | a0002 | c0002 | t0030 | g0083 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19065 | hp1 | a0003 | c0003 | t0016 | g0339 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19065 | hp2 | a0001 | c0001 | t0045 | g0227 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19066 | hp1 | a0005 | c0009 | t0019 | g0070 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19066 | hp2 | a0001 | c0001 | t0025 | g0208 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19068 | hp1 | a0001 | c0006 | t0005 | g0145 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19068 | hp2 | a0002 | c0002 | t0034 | g0251 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19070 | hp2 | a0002 | c0002 | t0029 | g0090 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19072 | hp1 | a0001 | c0006 | t0012 | g0076 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19072 | hp2 | a0001 | c0001 | t0025 | g0207 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19074 | hp1 | a0002 | c0002 | t0013 | g0065 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19075 | hp1 | a0003 | c0003 | t0002 | g0328 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19076 | hp1 | a0001 | c0028 | t0095 | g0203 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19076 | hp2 | a0002 | c0002 | t0023 | g0056 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19077 | hp1 | a0007 | c0016 | t0018 | g0081 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19077 | hp2 | a0001 | c0017 | t0043 | g0125 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19079 | hp1 | a0001 | c0001 | t0043 | g0149 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0325 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19081 | hp1 | a0002 | c0002 | t0073 | g0067 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19081 | hp2 | a0003 | c0003 | t0052 | g0297 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19082 | hp1 | a0003 | c0003 | t0002 | g0362 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19082 | hp2 | a0002 | c0002 | t0012 | g0107 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19083 | hp1 | a0009 | c0021 | t0001 | g0122 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19083 | hp2 | a0001 | c0001 | t0026 | g0147 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19084 | hp1 | a0002 | c0002 | t0056 | g0100 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0322 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19090 | hp1 | a0002 | c0002 | t0005 | g0196 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19090 | hp2 | a0003 | c0003 | t0116 | g0136 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19091 | hp1 | a0003 | c0003 | t0002 | g0304 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19091 | hp2 | a0001 | c0001 | t0011 | g0224 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20129 | hp1 | a0003 | c0013 | t0001 | g0256 | AFR | ASW | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20129 | hp2 | a0001 | c0012 | t0017 | g0367 | AFR | ASW | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20752 | hp1 | a0002 | c0002 | t0008 | g0075 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20752 | hp2 | a0003 | c0003 | t0010 | g0006 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0035 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20805 | hp2 | a0001 | c0007 | t0001 | g0191 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01123 | hp1 | a0003 | c0013 | t0002 | g0372 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01123 | hp2 | a0003 | c0003 | t0010 | g0364 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02109 | hp1 | a0004 | c0008 | t0047 | g0217 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02109 | hp2 | a0001 | c0005 | t0084 | g0262 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02486 | hp1 | a0001 | c0012 | t0017 | g0353 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02486 | hp2 | a0004 | c0019 | t0028 | g0120 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02559 | hp1 | a0003 | c0010 | t0055 | g0152 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02559 | hp2 | a0001 | c0005 | t0003 | g0028 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03471 | hp1 | a0003 | c0010 | t0055 | g0135 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03471 | hp2 | a0001 | c0004 | t0112 | g0354 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG06807 | hp1 | a0001 | c0005 | t0003 | g0026 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG06807 | hp2 | a0002 | c0002 | t0062 | g0061 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20300 | hp1 | a0001 | c0004 | t0132 | g0359 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20300 | hp2 | a0001 | c0005 | t0003 | g0013 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0259 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA21309 | hp2 | a0001 | c0001 | t0124 | g0371 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0007 | t0001 | g0185 | REF | REF | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0086 | g0337 | REF | REF | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99712504
|
C | CCAG | 1 | a0010 | 3 | HG02145.hp1 NA18945.hp2 NA19056.hp2 |
disruptive_inframe_insertion | MODERATE | c.1283_1285dupAGC | p.Gln428dup | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1631/5580 | 1286/1518 | 429/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
C | CCAGCAG | 1 | a0004 | 11 | HG00733.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
disruptive_inframe_insertion | MODERATE | c.1280_1285dupAGCAGC | p.Gln427_Gln428dup | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1631/5580 | 1286/1518 | 429/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
C | CCAGCAGC others(2): Show |
1 | a0007 | 4 | HG03688.hp1 NA18942.hp2 NA19010.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.1277_1285dupAGCAGC others(3): Show |
p.Gln426_Gln428dup | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1631/5580 | 1286/1518 | 429/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
C | CCAGCAGC others(8): Show |
1 | a0018 | 1 | NA19002.hp1 | disruptive_inframe_insertion | MODERATE | c.1271_1285dupAGCAGC others(9): Show |
p.Gln424_Gln428dup | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1631/5580 | 1286/1518 | 429/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
CCAG | C | 2 | a0003a0014 | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
disruptive_inframe_deletion | MODERATE | c.1283_1285delAGC | p.Gln428del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1628/5580 | 1283/1518 | 428/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
CCAGCAG | C | 2 | a0002a0005 | 86 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(83): Show |
disruptive_inframe_deletion | MODERATE | c.1280_1285delAGCAGC | p.Gln427_Gln428del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1625/5580 | 1280/1518 | 427/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
CCAGCAGC others(2): Show |
C | 1 | a0006 | 4 | HG00609.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.1277_1285delAGCAGC others(3): Show |
p.Gln426_Gln428del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1622/5580 | 1277/1518 | 426/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
CCAGCAGC others(5): Show |
C | 1 | a0009 | 3 | HG03486.hp2 NA18947.hp2 NA19083.hp1 |
disruptive_inframe_deletion | MODERATE | c.1274_1285delAGCAGC others(6): Show |
p.Gln425_Gln428del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1619/5580 | 1274/1518 | 425/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
CCAGCAGC others(11): Show |
C | 1 | a0012 | 1 | NA19058.hp2 | disruptive_inframe_deletion | MODERATE | c.1268_1285delAGCAGC others(12): Show |
p.Gln423_Gln428del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1613/5580 | 1268/1518 | 423/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712504
|
CCAGCAGC others(14): Show |
C | 1 | a0008 | 3 | NA18961.hp1 NA18967.hp2 NA19064.hp1 |
disruptive_inframe_deletion | MODERATE | c.1265_1285delAGCAGC others(15): Show |
p.Gln422_Gln428del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1610/5580 | 1265/1518 | 422/505 | INFO_REALIGN_3_PRIME | chr15 | 99712504 | |
| chr15:99712522
|
GCAGCAGC others(29): Show |
G | 1 | a0013 | 1 | HG03492.hp2 | disruptive_inframe_deletion | MODERATE | c.1274_1309delAGCAGC others(30): Show |
p.Gln425_Gln436del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1619/5580 | 1274/1518 | 425/505 | INFO_REALIGN_3_PRIME | chr15 | 99712522 | |
| chr15:99712533
|
A | AGCAGCAC others(12): Show |
1 | a0015 | 1 | HG01261.hp2 | frameshift_variant | HIGH | c.1285_1286insACAGCA others(13): Show |
p.Pro429fs | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1631/5580 | 1286/1518 | 429/505 | INFO_REALIGN_3_PRIME | chr15 | 99712533 | |
| chr15:99712536
|
AGCC | A | 2 | a0005a0011 | 10 | HG00099.hp1 HG00597.hp2 HG01071.hp1 others(7): Show |
disruptive_inframe_deletion | MODERATE | c.1290_1292delGCC | p.Pro431del | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1635/5580 | 1290/1518 | 430/505 | INFO_REALIGN_3_PRIME | chr15 | 99712536 | |
| chr15:99712539
|
C | A | 1 | a0017 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1286C>A | p.Pro429Gln | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1631/5580 | 1286/1518 | 429/505 | chr15 | 99712539 | ||
| chr15:99712545
|
C | G | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1292C>G | p.Pro431Arg | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1637/5580 | 1292/1518 | 431/505 | chr15 | 99712545 | ||
| chr15:99712560
|
A | C | 1 | a0013 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.1307A>C | p.Gln436Pro | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1652/5580 | 1307/1518 | 436/505 | chr15 | 99712560 | ||
| chr15:99712566
|
A | C | 1 | a0013 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.1313A>C | p.Gln438Pro | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1658/5580 | 1313/1518 | 438/505 | chr15 | 99712566 | ||
| chr15:99712572
|
C | T | 1 | a0016 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1319C>T | p.Pro440Leu | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1664/5580 | 1319/1518 | 440/505 | chr15 | 99712572 | ||
| chr15:99712624
|
C | A | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1371C>A | p.Ser457Arg | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1716/5580 | 1371/1518 | 457/505 | chr15 | 99712624 | ||
| chr15:99712664
|
C | A | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1411C>A | p.Pro471Thr | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1756/5580 | 1411/1518 | 471/505 | chr15 | 99712664 | ||
| chr15:99712665
|
C | G | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1412C>G | p.Pro471Arg | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1757/5580 | 1412/1518 | 471/505 | chr15 | 99712665 | ||
| chr15:99712670
|
G | A | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1417G>A | p.Gly473Ser | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1762/5580 | 1417/1518 | 473/505 | chr15 | 99712670 | ||
| chr15:99712683
|
C | A | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1430C>A | p.Ser477Tyr | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1775/5580 | 1430/1518 | 477/505 | chr15 | 99712683 | ||
| chr15:99712685
|
C | G | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1432C>G | p.Pro478Ala | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1777/5580 | 1432/1518 | 478/505 | chr15 | 99712685 | ||
| chr15:99712686
|
C | G | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1433C>G | p.Pro478Arg | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1778/5580 | 1433/1518 | 478/505 | chr15 | 99712686 | ||
| chr15:99712688
|
A | G | 1 | a0014 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1435A>G | p.Ile479Val | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1780/5580 | 1435/1518 | 479/505 | chr15 | 99712688 | ||
| chr15:99712689
|
T | C | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1436T>C | p.Ile479Thr | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1781/5580 | 1436/1518 | 479/505 | chr15 | 99712689 | ||
| chr15:99712690
|
T | G | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1437T>G | p.Ile479Met | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1782/5580 | 1437/1518 | 479/505 | chr15 | 99712690 | ||
| chr15:99712694
|
C | T | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1441C>T | p.Leu481Phe | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1786/5580 | 1441/1518 | 481/505 | chr15 | 99712694 | ||
| chr15:99712700
|
C | T | 1 | a0015 | 1 | HG01261.hp2 | stop_gained | HIGH | c.1447C>T | p.Arg483* | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1792/5580 | 1447/1518 | 483/505 | chr15 | 99712700 | ||
| chr15:99712707
|
C | G | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1454C>G | p.Pro485Arg | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1799/5580 | 1454/1518 | 485/505 | chr15 | 99712707 | ||
| chr15:99712711
|
C | A | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1458C>A | p.Asn486Lys | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1803/5580 | 1458/1518 | 486/505 | chr15 | 99712711 | ||
| chr15:99712712
|
A | T | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1459A>T | p.Thr487Ser | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1804/5580 | 1459/1518 | 487/505 | chr15 | 99712712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99703377
|
T | C | 1 | a0011c0023 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.874T>C | p.Leu292Leu | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/12 | 1219/5580 | 874/1518 | 292/505 | chr15 | 99703377 | ||
| chr15:99706731
|
T | C | 23 | a0001c0001a0001c0006a0001c0007others(20): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
splice_region_variant&synonymous_variant | LOW | c.885T>C | p.Asn295Asn | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/12 | 1230/5580 | 885/1518 | 295/505 | chr15 | 99706731 | ||
| chr15:99706737
|
G | A | 32 | a0001c0001a0001c0004a0001c0006others(29): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
synonymous_variant | LOW | c.891G>A | p.Gln297Gln | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/12 | 1236/5580 | 891/1518 | 297/505 | chr15 | 99706737 | ||
| chr15:99712498
|
G | A | 1 | a0003c0022 | 2 | HG01081.hp2 HG01168.hp1 |
synonymous_variant | LOW | c.1245G>A | p.Ser415Ser | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1590/5580 | 1245/1518 | 415/505 | chr15 | 99712498 | ||
| chr15:99712552
|
G | A | 2 | a0001c0017a0001c0028 | 4 | NA18984.hp2 NA19056.hp1 NA19076.hp1 others(1): Show |
synonymous_variant | LOW | c.1299G>A | p.Pro433Pro | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1644/5580 | 1299/1518 | 433/505 | chr15 | 99712552 | ||
| chr15:99712564
|
A | G | 1 | a0013c0032 | 1 | HG03492.hp2 | synonymous_variant | LOW | c.1311A>G | p.Pro437Pro | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1656/5580 | 1311/1518 | 437/505 | chr15 | 99712564 | ||
| chr15:99712570
|
C | A | 1 | a0013c0032 | 1 | HG03492.hp2 | synonymous_variant | LOW | c.1317C>A | p.Pro439Pro | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1662/5580 | 1317/1518 | 439/505 | chr15 | 99712570 | ||
| chr15:99712600
|
G | T | 10 | a0001c0006a0001c0012a0001c0028others(7): Show | 102 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
synonymous_variant | LOW | c.1347G>T | p.Gly449Gly | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1692/5580 | 1347/1518 | 449/505 | chr15 | 99712600 | ||
| chr15:99712657
|
G | A | 1 | a0015c0024 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1404G>A | p.Arg468Arg | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1749/5580 | 1404/1518 | 468/505 | chr15 | 99712657 | ||
| chr15:99712660
|
G | A | 1 | a0015c0024 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1407G>A | p.Glu469Glu | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1752/5580 | 1407/1518 | 469/505 | chr15 | 99712660 | ||
| chr15:99712667
|
C | A | 1 | a0015c0024 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1414C>A | p.Arg472Arg | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1759/5580 | 1414/1518 | 472/505 | chr15 | 99712667 | ||
| chr15:99712684
|
T | C | 1 | a0015c0024 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1431T>C | p.Ser477Ser | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1776/5580 | 1431/1518 | 477/505 | chr15 | 99712684 | ||
| chr15:99712687
|
A | G | 1 | a0001c0007 | 9 | HG00639.hp2 HG00733.hp1 HG01192.hp1 others(6): Show |
synonymous_variant | LOW | c.1434A>G | p.Pro478Pro | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1779/5580 | 1434/1518 | 478/505 | chr15 | 99712687 | ||
| chr15:99712687
|
A | T | 1 | a0015c0024 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1434A>T | p.Pro478Pro | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1779/5580 | 1434/1518 | 478/505 | chr15 | 99712687 | ||
| chr15:99712693
|
G | A | 1 | a0015c0024 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1440G>A | p.Val480Val | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1785/5580 | 1440/1518 | 480/505 | chr15 | 99712693 | ||
| chr15:99712699
|
C | G | 1 | a0015c0024 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1446C>G | p.Gly482Gly | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1791/5580 | 1446/1518 | 482/505 | chr15 | 99712699 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99566015
|
G | T | 1 | a0001c0005t0138 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-314G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/12 | 67105 | chr15 | 99566015 | |||||
| chr15:99598477
|
A | G | 2 | a0001c0004t0137a0003c0003t0136 | 2 | HG02055.hp2 HG03540.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-177A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/12 | chr15 | 99598477 | ||||||
| chr15:99712916
|
A | AGTGT | 117 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(114): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*148_*151dupGTGT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 152 | INFO_REALIGN_3_PRIME | chr15 | 99712916 | ||||
| chr15:99713345
|
AG | A | 14 | a0001c0001t0004a0001c0001t0024a0001c0001t0039others(11): Show | 27 | HG00423.hp1 HG00597.hp1 HG00642.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*575delG | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 575 | chr15 | 99713345 | |||||
| chr15:99713411
|
A | T | 1 | a0012c0033t0094 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 640 | chr15 | 99713411 | |||||
| chr15:99713423
|
T | G | 6 | a0001c0006t0007a0002c0002t0007a0002c0002t0029others(3): Show | 12 | HG00673.hp2 HG02015.hp2 HG02027.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*652T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 652 | chr15 | 99713423 | |||||
| chr15:99713636
|
C | T | 1 | a0001c0001t0093 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*865C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 865 | chr15 | 99713636 | |||||
| chr15:99713788
|
A | G | 2 | a0003c0010t0055a0003c0010t0135 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1017 | chr15 | 99713788 | |||||
| chr15:99713963
|
G | A | 1 | a0001c0001t0087 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1192G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1192 | chr15 | 99713963 | |||||
| chr15:99714239
|
G | A | 181 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(178): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*1468G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1468 | chr15 | 99714239 | |||||
| chr15:99714390
|
G | A | 1 | a0001c0028t0095 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1619G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1619 | chr15 | 99714390 | |||||
| chr15:99714429
|
G | A | 1 | a0002c0002t0029 | 2 | NA18969.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1658G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1658 | chr15 | 99714429 | |||||
| chr15:99714520
|
T | C | 90 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(87): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1749T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1749 | chr15 | 99714520 | |||||
| chr15:99714708
|
C | T | 1 | a0001c0001t0064 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1937C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 1937 | chr15 | 99714708 | |||||
| chr15:99714803
|
C | A | 2 | a0003c0010t0055a0003c0010t0135 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2032C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2032 | chr15 | 99714803 | |||||
| chr15:99714805
|
C | CA | 3 | a0001c0001t0032a0003c0013t0032a0016c0029t0114 | 3 | HG02451.hp1 HG02976.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2034_*2035insA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2035 | chr15 | 99714805 | |||||
| chr15:99714806
|
C | G | 11 | a0001c0001t0081a0001c0001t0113a0001c0004t0132others(8): Show | 17 | HG00673.hp2 HG01934.hp2 HG02015.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2035C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2035 | chr15 | 99714806 | |||||
| chr15:99714807
|
C | A | 2 | a0001c0001t0064a0002c0002t0033 | 3 | HG03098.hp1 HG03688.hp2 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2036C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2036 | chr15 | 99714807 | |||||
| chr15:99714807
|
C | G | 1 | a0002c0002t0057 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2036C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2036 | chr15 | 99714807 | |||||
| chr15:99714808
|
C | A | 97 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(94): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*2037C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2037 | chr15 | 99714808 | |||||
| chr15:99714808
|
C | CA | 3 | a0001c0005t0009a0001c0005t0125a0004c0008t0009 | 9 | HG00733.hp2 HG02615.hp1 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2037_*2038insA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2038 | chr15 | 99714808 | |||||
| chr15:99714809
|
C | A | 8 | a0001c0001t0024a0001c0001t0103a0001c0001t0104others(5): Show | 8 | HG01993.hp2 HG03688.hp1 HG04184.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2038C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2038 | chr15 | 99714809 | |||||
| chr15:99714809
|
CCA | C | 33 | a0001c0001t0045a0001c0001t0046a0001c0001t0064others(30): Show | 53 | HG00323.hp1 HG00558.hp2 HG00673.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2040_*2041delAC | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2040 | INFO_REALIGN_3_PRIME | chr15 | 99714809 | ||||
| chr15:99714811
|
A | C | 16 | a0001c0001t0024a0001c0001t0027a0001c0001t0103others(13): Show | 18 | HG01993.hp2 HG02572.hp1 HG02647.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2040A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2040 | chr15 | 99714811 | |||||
| chr15:99714811
|
AC | A | 76 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(73): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*2050delC | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2050 | INFO_REALIGN_3_PRIME | chr15 | 99714811 | ||||
| chr15:99714811
|
ACC | A | 30 | a0001c0001t0028a0001c0001t0040a0001c0001t0088others(27): Show | 81 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2049_*2050delCC | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2049 | INFO_REALIGN_3_PRIME | chr15 | 99714811 | ||||
| chr15:99714812
|
C | A | 51 | a0001c0001t0024a0001c0001t0027a0001c0001t0045others(48): Show | 73 | HG00323.hp1 HG00558.hp2 HG00673.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2041C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2041 | chr15 | 99714812 | |||||
| chr15:99714813
|
C | A | 3 | a0002c0002t0033a0003c0003t0128a0010c0035t0122 | 4 | HG01074.hp2 HG03688.hp2 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2042C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2042 | chr15 | 99714813 | |||||
| chr15:99714815
|
C | A | 1 | a0002c0002t0058 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2044C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2044 | chr15 | 99714815 | |||||
| chr15:99714816
|
C | A | 32 | a0001c0001t0040a0001c0001t0088a0001c0001t0096others(29): Show | 83 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2045C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2045 | chr15 | 99714816 | |||||
| chr15:99714829
|
G | C | 26 | a0001c0001t0004a0001c0001t0011a0001c0001t0024others(23): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2058G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2058 | chr15 | 99714829 | |||||
| chr15:99714841
|
A | G | 64 | a0001c0001t0006a0001c0001t0026a0001c0001t0027others(61): Show | 102 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2070A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2070 | chr15 | 99714841 | |||||
| chr15:99714841
|
A | T | 1 | a0001c0028t0095 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2070A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2070 | chr15 | 99714841 | |||||
| chr15:99714890
|
T | C | 1 | a0001c0001t0102 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2119T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2119 | chr15 | 99714890 | |||||
| chr15:99714899
|
G | C | 76 | a0001c0001t0006a0001c0001t0020a0001c0001t0025others(73): Show | 120 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2128G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2128 | chr15 | 99714899 | |||||
| chr15:99715004
|
G | T | 1 | a0001c0005t0138 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2233G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2233 | chr15 | 99715004 | |||||
| chr15:99715007
|
T | C | 1 | a0001c0005t0138 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2236T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2236 | chr15 | 99715007 | |||||
| chr15:99715090
|
G | T | 1 | a0001c0001t0124 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2319 | chr15 | 99715090 | |||||
| chr15:99715446
|
G | T | 3 | a0001c0004t0117a0001c0012t0017a0001c0012t0066 | 6 | HG01496.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2675G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2675 | chr15 | 99715446 | |||||
| chr15:99715609
|
A | T | 141 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(138): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*2838A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 2838 | chr15 | 99715609 | |||||
| chr15:99715834
|
G | A | 1 | a0001c0001t0102 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 3063 | chr15 | 99715834 | |||||
| chr15:99715860
|
C | T | 3 | a0002c0002t0035a0002c0002t0036a0002c0002t0083 | 5 | HG01433.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3089C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 3089 | chr15 | 99715860 | |||||
| chr15:99715867
|
C | T | 30 | a0001c0004t0002a0001c0004t0010a0001c0004t0115others(27): Show | 73 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3096C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 3096 | chr15 | 99715867 | |||||
| chr15:99715887
|
T | C | 7 | a0001c0004t0047a0001c0004t0048a0001c0005t0009others(4): Show | 15 | HG00733.hp2 HG01099.hp2 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3116T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 3116 | chr15 | 99715887 | |||||
| chr15:99716335
|
A | C | 11 | a0001c0001t0077a0001c0006t0021a0001c0028t0095others(8): Show | 13 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3564A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 3564 | chr15 | 99716335 | |||||
| chr15:99716413
|
A | C | 59 | a0001c0001t0077a0001c0001t0081a0001c0006t0005others(56): Show | 104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3642A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 3642 | chr15 | 99716413 | |||||
| chr15:99716470
|
C | T | 2 | a0001c0001t0032a0003c0013t0032 | 2 | HG02451.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3699C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 12/12 | 3699 | chr15 | 99716470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99566155
|
G | A | 1 | a0001c0004t0026g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-225+51G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566155 | ||||||
| chr15:99566180
|
C | G | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-225+76C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566180 | ||||||
| chr15:99566181
|
C | G | 1 | a0003c0013t0002g0372 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-225+77C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566181 | ||||||
| chr15:99566315
|
G | GGGCGGGT others(12): Show |
1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-225+236_-225+254d others(21): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99566315 | |||||
| chr15:99566441
|
T | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-225+337T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566441 | ||||||
| chr15:99566444
|
G | T | 1 | a0001c0001t0011g0281 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-225+340G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566444 | ||||||
| chr15:99566448
|
G | A | 1 | a0005c0009t0019g0003 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-225+344G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566448 | ||||||
| chr15:99566526
|
C | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-225+422C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566526 | ||||||
| chr15:99566558
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-225+454C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566558 | ||||||
| chr15:99566682
|
G | T | 1 | a0001c0001t0020g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-225+578G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566682 | ||||||
| chr15:99566695
|
T | C | 1 | a0001c0005t0085g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-225+591T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99566695 | ||||||
| chr15:99567143
|
A | G | 2 | a0001c0001t0064g0278a0003c0010t0130g0277 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-225+1039A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567143 | ||||||
| chr15:99567626
|
A | AATGTGTG others(1): Show |
3 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0138g0014 | 3 | HG02451.hp2 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-225+1522_-225+152 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567626 | ||||||
| chr15:99567626
|
A | AATGTGTG others(3): Show |
2 | a0001c0005t0085g0011a0009c0037t0003g0015 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-225+1522_-225+152 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567626 | ||||||
| chr15:99567626
|
A | AATGTGTG others(5): Show |
5 | a0001c0005t0003g0016a0001c0005t0003g0018a0001c0005t0003g0019others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-225+1522_-225+152 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567626 | ||||||
| chr15:99567626
|
A | AATGTGTG others(7): Show |
8 | a0001c0005t0003g0022a0001c0005t0003g0026a0001c0005t0003g0028others(5): Show | 8 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-225+1522_-225+152 others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567626 | ||||||
| chr15:99567627
|
C | CTG | 108 | a0001c0001t0001g0167a0001c0001t0001g0174a0001c0001t0001g0176others(105): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-225+1559_-225+156 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
C | CTGTG | 31 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238others(28): Show | 31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-225+1557_-225+156 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
C | CTGTGTG | 11 | a0001c0001t0001g0001a0001c0001t0001g0369a0001c0001t0001g0370others(8): Show | 12 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.-225+1555_-225+156 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
C | CTGTGTGT others(3): Show |
11 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0039g0265others(8): Show | 11 | HG00423.hp1 HG00597.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.-225+1551_-225+156 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
C | CTGTGTGT others(5): Show |
4 | a0001c0001t0004g0275a0001c0001t0024g0274a0001c0001t0032g0272others(1): Show | 4 | NA18950.hp2 NA18963.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-225+1549_-225+156 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
C | CTGTGTGT others(7): Show |
1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-225+1547_-225+156 others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
C | G | 18 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(15): Show | 18 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-225+1523C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567627 | ||||||
| chr15:99567627
|
CTG | C | 14 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(11): Show | 14 | HG00639.hp1 HG01981.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-225+1559_-225+156 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
CTGTGTGT others(1): Show |
C | 3 | a0004c0008t0009g0032a0004c0008t0009g0033a0004c0008t0009g0034 | 3 | HG00733.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-225+1553_-225+156 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
CTGTGTGT others(3): Show |
C | 3 | a0001c0004t0137g0283a0001c0012t0066g0284a0003c0003t0136g0282 | 3 | HG02055.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-225+1551_-225+156 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567627
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0096g0029a0001c0001t0104g0030 | 2 | HG01358.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-225+1549_-225+156 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99567627 | |||||
| chr15:99567653
|
GTGTGTGT others(4): Show |
G | 1 | a0002c0002t0008g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-225+1550_-225+156 others(15): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567653 | ||||||
| chr15:99567908
|
G | A | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-225+1804G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567908 | ||||||
| chr15:99567915
|
T | C | 1 | a0001c0005t0084g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-225+1811T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99567915 | ||||||
| chr15:99568215
|
T | C | 8 | a0001c0001t0004g0035a0001c0001t0004g0043a0001c0001t0004g0045others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-225+2111T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568215 | ||||||
| chr15:99568416
|
G | A | 21 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(18): Show | 21 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-225+2312G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568416 | ||||||
| chr15:99568428
|
C | G | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-225+2324C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568428 | ||||||
| chr15:99568477
|
C | G | 1 | a0002c0011t0011g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-225+2373C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568477 | ||||||
| chr15:99568628
|
G | C | 3 | a0001c0004t0048g0047a0001c0004t0048g0292a0001c0005t0015g0021 | 3 | HG02622.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-225+2524G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568628 | ||||||
| chr15:99568741
|
G | A | 2 | a0003c0003t0002g0293a0003c0003t0002g0294 | 2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-225+2637G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568741 | ||||||
| chr15:99568821
|
A | G | 23 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(20): Show | 23 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-225+2717A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568821 | ||||||
| chr15:99568882
|
G | A | 1 | a0008c0018t0002g0338 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-225+2778G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568882 | ||||||
| chr15:99568883
|
A | C | 1 | a0008c0018t0002g0338 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-225+2779A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99568883 | ||||||
| chr15:99569008
|
TAATAAGT others(3): Show |
T | 1 | a0003c0003t0054g0010 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-225+2909_-225+291 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99569008 | |||||
| chr15:99569180
|
T | A | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-225+3076T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569180 | ||||||
| chr15:99569193
|
A | G | 1 | a0001c0005t0138g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-225+3089A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569193 | ||||||
| chr15:99569260
|
C | T | 1 | a0005c0009t0076g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-225+3156C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569260 | ||||||
| chr15:99569279
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+3175A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569279 | ||||||
| chr15:99569314
|
G | A | 5 | a0001c0004t0006g0285a0001c0004t0011g0366a0001c0004t0047g0296others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-225+3210G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569314 | ||||||
| chr15:99569500
|
C | G | 1 | a0001c0005t0003g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-225+3396C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569500 | ||||||
| chr15:99569594
|
A | G | 1 | a0003c0022t0010g0365 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-225+3490A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569594 | ||||||
| chr15:99569643
|
G | A | 2 | a0001c0001t0004g0036a0001c0001t0004g0037 | 2 | NA18967.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-225+3539G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569643 | ||||||
| chr15:99569754
|
T | C | 21 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(18): Show | 21 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-225+3650T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569754 | ||||||
| chr15:99569846
|
A | G | 1 | a0001c0005t0003g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-225+3742A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569846 | ||||||
| chr15:99569856
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-225+3752C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569856 | ||||||
| chr15:99569905
|
T | C | 1 | a0001c0001t0028g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-225+3801T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569905 | ||||||
| chr15:99569931
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-225+3827A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569931 | ||||||
| chr15:99569939
|
A | G | 32 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(29): Show | 32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-225+3835A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99569939 | ||||||
| chr15:99570011
|
T | TTTTTTTA others(35): Show |
1 | a0002c0002t0037g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-225+3907_-225+390 others(46): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570011 | ||||||
| chr15:99570012
|
G | A | 1 | a0002c0002t0037g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-225+3908G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570012 | ||||||
| chr15:99570013
|
C | T | 1 | a0002c0002t0037g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-225+3909C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570013 | ||||||
| chr15:99570079
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-225+3975T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570079 | ||||||
| chr15:99570398
|
G | C | 374 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(371): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-225+4294G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570398 | ||||||
| chr15:99570578
|
G | A | 3 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051 | 3 | HG03669.hp2 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-225+4474G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570578 | ||||||
| chr15:99570809
|
G | GA | 7 | a0001c0001t0039g0265a0002c0002t0007g0052a0002c0002t0037g0153others(4): Show | 7 | HG00423.hp1 HG01978.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-225+4718dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99570809 | |||||
| chr15:99570809
|
GA | G | 47 | a0001c0001t0001g0222a0001c0001t0006g0137a0001c0001t0006g0138others(44): Show | 47 | HG01109.hp1 HG01123.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.-225+4718delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99570809 | |||||
| chr15:99570905
|
C | A | 20 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-225+4801C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570905 | ||||||
| chr15:99570965
|
A | G | 1 | a0003c0003t0002g0294 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-225+4861A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570965 | ||||||
| chr15:99571001
|
G | A | 1 | a0001c0001t0102g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-225+4897G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571001 | ||||||
| chr15:99571097
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+4993T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571097 | ||||||
| chr15:99571195
|
A | C | 25 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0124g0371others(22): Show | 25 | HG00733.hp2 HG01099.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.-225+5091A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571195 | ||||||
| chr15:99571365
|
G | C | 3 | a0002c0014t0007g0340a0002c0014t0007g0341a0003c0003t0016g0339 | 3 | NA19004.hp2 NA19005.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-225+5261G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571365 | ||||||
| chr15:99571411
|
C | T | 1 | a0002c0002t0080g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-225+5307C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571411 | ||||||
| chr15:99571430
|
A | G | 2 | a0001c0005t0003g0335a0001c0012t0017g0336 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-225+5326A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571430 | ||||||
| chr15:99571442
|
G | A | 2 | a0001c0004t0026g0002a0016c0029t0114g0040 | 2 | HG01261.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-225+5338G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571442 | ||||||
| chr15:99571569
|
C | A | 1 | a0003c0003t0052g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-225+5465C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571569 | ||||||
| chr15:99571616
|
A | G | 5 | a0001c0005t0003g0016a0001c0005t0003g0018a0001c0005t0003g0263others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-225+5512A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571616 | ||||||
| chr15:99571671
|
A | T | 15 | a0001c0001t0025g0207a0001c0001t0025g0208a0001c0001t0025g0209others(12): Show | 15 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.-225+5567A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571671 | ||||||
| chr15:99571676
|
C | T | 4 | a0001c0001t0004g0035a0001c0001t0004g0045a0001c0001t0004g0046others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.-225+5572C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571676 | ||||||
| chr15:99571722
|
CT | C | 349 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(346): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-225+5620delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99571722 | |||||
| chr15:99571744
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+5640C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571744 | ||||||
| chr15:99571757
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-225+5653T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571757 | ||||||
| chr15:99571808
|
A | G | 1 | a0003c0013t0032g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-225+5704A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571808 | ||||||
| chr15:99571969
|
A | C | 2 | a0001c0004t0026g0002a0016c0029t0114g0040 | 2 | HG01261.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-225+5865A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571969 | ||||||
| chr15:99571989
|
T | G | 3 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139 | 3 | NA18957.hp2 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-225+5885T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99571989 | ||||||
| chr15:99572013
|
GT | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-225+5928delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99572013 | |||||
| chr15:99572222
|
G | C | 32 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(29): Show | 32 | HG00733.hp2 HG01099.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-225+6118G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99572222 | ||||||
| chr15:99572263
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-225+6159C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99572263 | ||||||
| chr15:99572528
|
C | CAGAG | 101 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-225+6425_-225+642 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99572528 | |||||
| chr15:99572924
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+6820G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99572924 | ||||||
| chr15:99573007
|
G | A | 1 | a0001c0001t0104g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-225+6903G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573007 | ||||||
| chr15:99573010
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-225+6906C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573010 | ||||||
| chr15:99573059
|
C | T | 1 | a0001c0001t0004g0271 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-225+6955C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573059 | ||||||
| chr15:99573084
|
C | G | 4 | a0001c0001t0025g0207a0001c0001t0025g0208a0001c0001t0025g0209others(1): Show | 4 | NA18949.hp2 NA18990.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-225+6980C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573084 | ||||||
| chr15:99573088
|
A | G | 1 | a0002c0011t0024g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-225+6984A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573088 | ||||||
| chr15:99573116
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-225+7012A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573116 | ||||||
| chr15:99573142
|
G | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+7038G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573142 | ||||||
| chr15:99573205
|
G | A | 1 | a0002c0002t0079g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-225+7101G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573205 | ||||||
| chr15:99573286
|
C | CA | 10 | a0001c0001t0004g0035a0001c0001t0093g0042a0001c0004t0051g0049others(7): Show | 10 | HG01109.hp2 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-225+7203dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99573286 | |||||
| chr15:99573286
|
CA | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-225+7203delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99573286 | |||||
| chr15:99573332
|
A | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+7228A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573332 | ||||||
| chr15:99573764
|
T | G | 37 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(34): Show | 37 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.-225+7660T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573764 | ||||||
| chr15:99573944
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+7840C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99573944 | ||||||
| chr15:99574055
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-225+7951T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99574055 | ||||||
| chr15:99574077
|
C | G | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-225+7973C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99574077 | ||||||
| chr15:99574090
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-225+7986A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99574090 | ||||||
| chr15:99574169
|
T | C | 1 | a0002c0002t0005g0196 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-225+8065T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99574169 | ||||||
| chr15:99574592
|
GCATGTGT others(4): Show |
G | 1 | a0002c0002t0005g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-225+8491_-225+850 others(15): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99574592 | |||||
| chr15:99574687
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+8583C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99574687 | ||||||
| chr15:99574828
|
A | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-225+8724A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99574828 | ||||||
| chr15:99574831
|
G | A | 1 | a0002c0002t0058g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-225+8727G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99574831 | ||||||
| chr15:99575143
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-225+9039A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99575143 | ||||||
| chr15:99575384
|
G | C | 1 | a0001c0004t0053g0374 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-225+9280G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99575384 | ||||||
| chr15:99575444
|
G | A | 1 | a0001c0004t0006g0342 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-225+9340G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99575444 | ||||||
| chr15:99575673
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+9569G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99575673 | ||||||
| chr15:99575697
|
A | G | 1 | a0013c0032t0005g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-225+9593A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99575697 | ||||||
| chr15:99576184
|
C | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+10080C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576184 | ||||||
| chr15:99576216
|
G | A | 139 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(136): Show | 139 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-225+10112G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576216 | ||||||
| chr15:99576367
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0237 | 2 | NA18961.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-225+10263G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576367 | ||||||
| chr15:99576494
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+10390A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576494 | ||||||
| chr15:99576802
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.-225+10698G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576802 | ||||||
| chr15:99576927
|
G | A | 98 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-225+10823G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576927 | ||||||
| chr15:99576973
|
T | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+10869T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576973 | ||||||
| chr15:99577014
|
G | C | 1 | a0002c0002t0014g0059 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-225+10910G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99577014 | ||||||
| chr15:99577045
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+10941G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99577045 | ||||||
| chr15:99577053
|
G | A | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-225+10949G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99577053 | ||||||
| chr15:99577066
|
G | A | 1 | a0001c0001t0020g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-225+10962G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99577066 | ||||||
| chr15:99577110
|
A | C | 144 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(141): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-225+11006A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99577110 | ||||||
| chr15:99577152
|
A | G | 1 | a0004c0008t0050g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-225+11048A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99577152 | ||||||
| chr15:99577404
|
T | TGCGGAAT others(8): Show |
222 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-225+11302_-225+11 others(21): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99577404 | |||||
| chr15:99577645
|
T | C | 1 | a0001c0007t0001g0168 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-225+11541T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99577645 | ||||||
| chr15:99577673
|
TG | T | 20 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-225+11571delG | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99577673 | |||||
| chr15:99578011
|
A | T | 1 | a0001c0007t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-225+11907A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578011 | ||||||
| chr15:99578037
|
G | A | 1 | a0003c0010t0002g0197 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-225+11933G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578037 | ||||||
| chr15:99578059
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+11955T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578059 | ||||||
| chr15:99578072
|
A | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-225+11968A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578072 | ||||||
| chr15:99578096
|
T | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-225+11992T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578096 | ||||||
| chr15:99578370
|
G | T | 19 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(16): Show | 19 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-225+12266G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578370 | ||||||
| chr15:99578554
|
A | G | 35 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(32): Show | 35 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.-225+12450A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578554 | ||||||
| chr15:99578613
|
T | C | 1 | a0007c0016t0018g0060 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-225+12509T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578613 | ||||||
| chr15:99578648
|
C | T | 1 | a0001c0001t0004g0119 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-225+12544C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578648 | ||||||
| chr15:99578662
|
T | G | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-225+12558T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578662 | ||||||
| chr15:99578748
|
A | G | 1 | a0001c0001t0077g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-225+12644A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578748 | ||||||
| chr15:99578912
|
T | G | 143 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(140): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-225+12808T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99578912 | ||||||
| chr15:99579287
|
T | G | 1 | a0001c0004t0107g0350 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-225+13183T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99579287 | ||||||
| chr15:99579306
|
G | GT | 9 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(6): Show | 9 | HG01168.hp1 HG01257.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-225+13212dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99579306 | |||||
| chr15:99579335
|
G | A | 1 | a0002c0002t0036g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-225+13231G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99579335 | ||||||
| chr15:99579725
|
A | G | 8 | a0003c0003t0010g0004a0003c0003t0010g0005a0003c0003t0010g0006others(5): Show | 8 | HG01928.hp1 HG01934.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-225+13621A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99579725 | ||||||
| chr15:99579727
|
A | G | 1 | a0003c0003t0010g0009 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-225+13623A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99579727 | ||||||
| chr15:99579770
|
A | G | 1 | a0002c0002t0036g0041 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-225+13666A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99579770 | ||||||
| chr15:99579966
|
C | T | 137 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(134): Show | 137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-225+13862C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99579966 | ||||||
| chr15:99580015
|
C | A | 1 | a0003c0010t0003g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-225+13911C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580015 | ||||||
| chr15:99580082
|
T | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-225+13978T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580082 | ||||||
| chr15:99580313
|
A | T | 1 | a0001c0001t0004g0119 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-225+14209A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580313 | ||||||
| chr15:99580329
|
C | G | 1 | a0004c0008t0047g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-225+14225C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580329 | ||||||
| chr15:99580443
|
G | A | 3 | a0001c0004t0137g0283a0001c0012t0066g0284a0003c0003t0136g0282 | 3 | HG02055.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-225+14339G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580443 | ||||||
| chr15:99580477
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-225+14373G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580477 | ||||||
| chr15:99580511
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-225+14407G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580511 | ||||||
| chr15:99580638
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-225+14534G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580638 | ||||||
| chr15:99580720
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.-225+14616C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580720 | ||||||
| chr15:99580756
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-225+14652A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580756 | ||||||
| chr15:99580832
|
T | C | 1 | a0002c0011t0024g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-225+14728T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580832 | ||||||
| chr15:99580836
|
T | C | 1 | a0001c0004t0026g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-225+14732T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580836 | ||||||
| chr15:99580885
|
A | C | 3 | a0001c0004t0011g0366a0001c0004t0047g0296a0001c0004t0131g0286 | 3 | HG02622.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-225+14781A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99580885 | ||||||
| chr15:99581150
|
T | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-225+15046T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581150 | ||||||
| chr15:99581258
|
A | G | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-225+15154A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581258 | ||||||
| chr15:99581281
|
C | T | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-225+15177C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581281 | ||||||
| chr15:99581365
|
C | T | 2 | a0002c0011t0024g0157a0002c0011t0090g0156 | 2 | NA18747.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-225+15261C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581365 | ||||||
| chr15:99581373
|
A | G | 1 | a0003c0013t0032g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-225+15269A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581373 | ||||||
| chr15:99581414
|
CT | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-225+15322delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99581414 | |||||
| chr15:99581506
|
T | G | 1 | a0013c0032t0005g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-225+15402T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581506 | ||||||
| chr15:99581527
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-225+15423C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581527 | ||||||
| chr15:99581594
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-225+15490A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581594 | ||||||
| chr15:99581596
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-225+15492C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581596 | ||||||
| chr15:99581655
|
A | G | 1 | a0003c0010t0130g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-225+15551A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99581655 | ||||||
| chr15:99582175
|
CTTA | C | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-225+16078_-225+16 others(9): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99582175 | |||||
| chr15:99582185
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-225+16081A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582185 | ||||||
| chr15:99582342
|
C | A | 2 | a0003c0003t0002g0300a0003c0003t0002g0301 | 2 | NA18964.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.-224-16088C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582342 | ||||||
| chr15:99582396
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-16034T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582396 | ||||||
| chr15:99582453
|
C | T | 1 | a0002c0002t0078g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-224-15977C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582453 | ||||||
| chr15:99582663
|
G | A | 1 | a0009c0021t0001g0122 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-224-15767G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582663 | ||||||
| chr15:99582767
|
C | T | 1 | a0001c0004t0001g0327 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-224-15663C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582767 | ||||||
| chr15:99582865
|
A | G | 1 | a0002c0014t0016g0348 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-224-15565A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582865 | ||||||
| chr15:99582899
|
C | G | 146 | a0001c0001t0001g0195a0001c0001t0004g0035a0001c0001t0004g0036others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-224-15531C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582899 | ||||||
| chr15:99582917
|
T | C | 1 | a0002c0002t0062g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-224-15513T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582917 | ||||||
| chr15:99582965
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-224-15465G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99582965 | ||||||
| chr15:99583162
|
G | A | 1 | a0001c0006t0065g0062 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-224-15268G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99583162 | ||||||
| chr15:99583251
|
A | G | 1 | a0003c0003t0126g0347 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-224-15179A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99583251 | ||||||
| chr15:99583258
|
G | A | 32 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(29): Show | 32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-224-15172G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99583258 | ||||||
| chr15:99583291
|
G | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248 | 3 | HG00280.hp2 NA18962.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-224-15139G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99583291 | ||||||
| chr15:99583579
|
G | A | 10 | a0001c0001t0028g0162a0001c0005t0009g0133a0001c0005t0125g0220others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-224-14851G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99583579 | ||||||
| chr15:99583698
|
A | ATAATATG others(19): Show |
1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-14725_-224-14 others(32): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99583698 | |||||
| chr15:99583736
|
A | G | 2 | a0004c0019t0028g0120a0004c0019t0028g0121 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-224-14694A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99583736 | ||||||
| chr15:99583989
|
A | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-224-14441A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99583989 | ||||||
| chr15:99584036
|
G | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-224-14394G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584036 | ||||||
| chr15:99584346
|
A | G | 1 | a0002c0002t0023g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-224-14084A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584346 | ||||||
| chr15:99584429
|
C | G | 1 | a0002c0002t0037g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-224-14001C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584429 | ||||||
| chr15:99584457
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-224-13973C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584457 | ||||||
| chr15:99584547
|
G | C | 1 | a0003c0003t0136g0282 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-224-13883G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584547 | ||||||
| chr15:99584625
|
A | G | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-224-13805A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584625 | ||||||
| chr15:99584633
|
G | C | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-224-13797G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584633 | ||||||
| chr15:99584728
|
T | C | 1 | a0002c0002t0038g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-224-13702T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584728 | ||||||
| chr15:99584850
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-224-13580T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99584850 | ||||||
| chr15:99585287
|
C | A | 4 | a0003c0003t0002g0054a0003c0003t0002g0302a0003c0003t0016g0053others(1): Show | 4 | HG00280.hp1 HG00738.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-224-13143C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585287 | ||||||
| chr15:99585351
|
A | G | 97 | a0001c0001t0004g0119a0001c0001t0006g0137a0001c0001t0006g0138others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-224-13079A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585351 | ||||||
| chr15:99585482
|
T | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-12948T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585482 | ||||||
| chr15:99585551
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(84): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-224-12879T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585551 | ||||||
| chr15:99585679
|
CTG | C | 7 | a0001c0001t0006g0137a0002c0002t0013g0063a0002c0002t0013g0064others(4): Show | 7 | NA18970.hp1 NA18991.hp1 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-224-12748_-224-12 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99585679 | |||||
| chr15:99585686
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(127): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-224-12744G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585686 | ||||||
| chr15:99585686
|
G | T | 136 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(133): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-224-12744G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585686 | ||||||
| chr15:99585687
|
A | C | 136 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(133): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-224-12743A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585687 | ||||||
| chr15:99585699
|
GCTTA | G | 99 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-224-12726_-224-12 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99585699 | |||||
| chr15:99585743
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-224-12687C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585743 | ||||||
| chr15:99585856
|
G | A | 41 | a0001c0001t0028g0162a0001c0005t0003g0012a0001c0005t0003g0013others(38): Show | 41 | HG00733.hp2 HG01099.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-224-12574G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585856 | ||||||
| chr15:99586361
|
G | A | 1 | a0001c0001t0020g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-224-12069G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99586361 | ||||||
| chr15:99586469
|
T | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-224-11961T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99586469 | ||||||
| chr15:99586557
|
A | G | 11 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(8): Show | 11 | HG00733.hp2 HG01099.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-224-11873A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99586557 | ||||||
| chr15:99586621
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-11809A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99586621 | ||||||
| chr15:99586685
|
C | G | 1 | a0002c0002t0080g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-224-11745C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99586685 | ||||||
| chr15:99586938
|
G | A | 1 | a0001c0001t0040g0141 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-224-11492G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99586938 | ||||||
| chr15:99587138
|
A | G | 1 | a0001c0005t0003g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-224-11292A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99587138 | ||||||
| chr15:99587198
|
C | T | 5 | a0001c0006t0008g0111a0001c0006t0008g0112a0001c0006t0008g0113others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-224-11232C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99587198 | ||||||
| chr15:99587416
|
C | G | 1 | a0001c0001t0006g0139 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-224-11014C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99587416 | ||||||
| chr15:99587461
|
G | A | 6 | a0001c0004t0107g0350a0001c0004t0112g0354a0001c0012t0017g0352others(3): Show | 6 | HG01496.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-224-10969G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99587461 | ||||||
| chr15:99587670
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-224-10760T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99587670 | ||||||
| chr15:99587944
|
G | GGAC | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-224-10485_-224-10 others(9): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99587944 | |||||
| chr15:99588039
|
A | C | 4 | a0001c0001t0064g0278a0001c0004t0052g0373a0001c0004t0053g0374others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-224-10391A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588039 | ||||||
| chr15:99588046
|
T | A | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-224-10384T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588046 | ||||||
| chr15:99588076
|
TAGGTTGA others(28): Show |
T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-224-10349_-224-10 others(41): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99588076 | |||||
| chr15:99588085
|
G | A | 1 | a0004c0008t0047g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-224-10345G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588085 | ||||||
| chr15:99588230
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-224-10200C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588230 | ||||||
| chr15:99588253
|
A | G | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-224-10177A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588253 | ||||||
| chr15:99588278
|
A | C | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-224-10152A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588278 | ||||||
| chr15:99588342
|
C | T | 1 | a0001c0005t0003g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-224-10088C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588342 | ||||||
| chr15:99588719
|
A | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(77): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-224-9711A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588719 | ||||||
| chr15:99588723
|
G | T | 2 | a0001c0005t0003g0263a0001c0005t0003g0264 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-224-9707G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588723 | ||||||
| chr15:99588749
|
C | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-9681C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588749 | ||||||
| chr15:99588771
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-224-9659T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588771 | ||||||
| chr15:99588776
|
T | A | 4 | a0001c0007t0001g0169a0001c0007t0001g0260a0002c0002t0014g0230others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-224-9654T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588776 | ||||||
| chr15:99588813
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-224-9617A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588813 | ||||||
| chr15:99588822
|
G | A | 1 | a0003c0003t0016g0339 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-224-9608G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588822 | ||||||
| chr15:99588852
|
T | A | 1 | a0002c0002t0037g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-224-9578T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588852 | ||||||
| chr15:99588906
|
A | G | 1 | a0002c0014t0002g0326 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-224-9524A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588906 | ||||||
| chr15:99588989
|
C | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-9441C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99588989 | ||||||
| chr15:99589235
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-224-9195C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99589235 | ||||||
| chr15:99589315
|
T | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-9115T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99589315 | ||||||
| chr15:99589362
|
T | G | 1 | a0003c0003t0119g0287 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-224-9068T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99589362 | ||||||
| chr15:99589622
|
G | A | 2 | a0002c0002t0013g0063a0002c0002t0013g0064 | 2 | NA18991.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-224-8808G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99589622 | ||||||
| chr15:99589796
|
A | G | 1 | a0002c0002t0022g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-224-8634A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99589796 | ||||||
| chr15:99589807
|
C | A | 1 | a0002c0002t0062g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-224-8623C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99589807 | ||||||
| chr15:99590119
|
A | G | 1 | a0003c0003t0002g0325 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-224-8311A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590119 | ||||||
| chr15:99590318
|
T | C | 2 | a0001c0001t0041g0170a0002c0011t0044g0171 | 2 | HG02027.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-224-8112T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590318 | ||||||
| chr15:99590349
|
GTTAAT | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.-224-8076_-224-807 others(9): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99590349 | |||||
| chr15:99590371
|
T | C | 1 | a0002c0002t0029g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-224-8059T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590371 | ||||||
| chr15:99590502
|
T | C | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-224-7928T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590502 | ||||||
| chr15:99590760
|
C | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-224-7670C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590760 | ||||||
| chr15:99590781
|
T | G | 3 | a0001c0004t0048g0047a0001c0004t0048g0292a0001c0005t0015g0021 | 3 | HG02622.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-224-7649T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590781 | ||||||
| chr15:99590846
|
A | G | 6 | a0001c0004t0107g0350a0001c0004t0112g0354a0001c0012t0017g0352others(3): Show | 6 | HG01496.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-224-7584A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590846 | ||||||
| chr15:99590960
|
T | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0044g0240 | 3 | HG00140.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-224-7470T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99590960 | ||||||
| chr15:99591483
|
T | C | 1 | a0003c0010t0130g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-224-6947T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99591483 | ||||||
| chr15:99591599
|
G | A | 2 | a0005c0009t0019g0070a0005c0009t0019g0071 | 2 | NA18962.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-224-6831G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99591599 | ||||||
| chr15:99591602
|
A | T | 1 | a0001c0001t0087g0270 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-224-6828A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99591602 | ||||||
| chr15:99591721
|
T | C | 1 | a0017c0034t0111g0308 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-224-6709T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99591721 | ||||||
| chr15:99591874
|
G | A | 1 | a0001c0004t0010g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-224-6556G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99591874 | ||||||
| chr15:99591943
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-224-6487T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99591943 | ||||||
| chr15:99592124
|
A | G | 1 | a0001c0004t0027g0349 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-224-6306A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592124 | ||||||
| chr15:99592152
|
T | A | 1 | a0001c0007t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-224-6278T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592152 | ||||||
| chr15:99592201
|
C | A | 5 | a0001c0001t0006g0150a0001c0001t0026g0147a0001c0001t0040g0141others(2): Show | 5 | NA18968.hp1 NA18975.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-224-6229C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592201 | ||||||
| chr15:99592354
|
C | T | 2 | a0004c0019t0028g0120a0004c0019t0028g0121 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-224-6076C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592354 | ||||||
| chr15:99592368
|
A | G | 1 | a0001c0006t0018g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-224-6062A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592368 | ||||||
| chr15:99592535
|
A | T | 1 | a0001c0001t0004g0228 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-224-5895A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592535 | ||||||
| chr15:99592545
|
G | T | 1 | a0003c0003t0002g0294 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-224-5885G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592545 | ||||||
| chr15:99592559
|
C | T | 1 | a0008c0018t0002g0338 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-224-5871C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592559 | ||||||
| chr15:99592587
|
A | G | 1 | a0001c0001t0004g0119 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-224-5843A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592587 | ||||||
| chr15:99592712
|
C | T | 99 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-224-5718C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592712 | ||||||
| chr15:99592770
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-224-5660G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592770 | ||||||
| chr15:99592895
|
A | G | 1 | a0017c0034t0111g0308 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-224-5535A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592895 | ||||||
| chr15:99592913
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-5517G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99592913 | ||||||
| chr15:99593012
|
CAAT | C | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-224-5416_-224-541 others(7): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99593012 | |||||
| chr15:99593203
|
T | C | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-224-5227T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99593203 | ||||||
| chr15:99593301
|
A | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-224-5129A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99593301 | ||||||
| chr15:99593326
|
C | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-224-5104C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99593326 | ||||||
| chr15:99593349
|
C | T | 105 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-224-5081C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99593349 | ||||||
| chr15:99593965
|
C | T | 1 | a0001c0007t0001g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-224-4465C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99593965 | ||||||
| chr15:99594043
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-224-4387C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594043 | ||||||
| chr15:99594084
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-224-4346C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594084 | ||||||
| chr15:99594127
|
C | G | 5 | a0001c0005t0009g0133a0003c0010t0055g0135a0003c0010t0055g0152others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-224-4303C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594127 | ||||||
| chr15:99594166
|
C | T | 1 | a0002c0002t0005g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-224-4264C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594166 | ||||||
| chr15:99594302
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-224-4128A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594302 | ||||||
| chr15:99594397
|
A | G | 1 | a0002c0002t0074g0252 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-224-4033A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594397 | ||||||
| chr15:99594454
|
T | C | 2 | a0002c0002t0033g0072a0002c0002t0033g0073 | 2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-224-3976T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594454 | ||||||
| chr15:99594459
|
CT | C | 95 | a0001c0001t0001g0192a0001c0001t0028g0162a0001c0001t0097g0189others(92): Show | 95 | HG00323.hp2 HG00673.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.-224-3950delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99594459 | |||||
| chr15:99594459
|
CTT | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-224-3951_-224-395 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99594459 | |||||
| chr15:99594459
|
CTTTTTTT others(2): Show |
C | 101 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-224-3958_-224-395 others(13): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99594459 | |||||
| chr15:99594509
|
T | TTACA | 20 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-224-3915_-224-391 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99594509 | |||||
| chr15:99594538
|
A | G | 1 | a0001c0001t0020g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-224-3892A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594538 | ||||||
| chr15:99594543
|
A | G | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-224-3887A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594543 | ||||||
| chr15:99594746
|
A | G | 1 | a0003c0003t0108g0298 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-224-3684A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594746 | ||||||
| chr15:99594823
|
T | C | 23 | a0001c0001t0004g0036a0001c0001t0004g0037a0001c0001t0004g0119others(20): Show | 23 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-224-3607T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594823 | ||||||
| chr15:99594873
|
T | C | 141 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-224-3557T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594873 | ||||||
| chr15:99594874
|
G | A | 1 | a0007c0016t0067g0074 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-224-3556G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594874 | ||||||
| chr15:99594882
|
A | G | 3 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051 | 3 | HG03669.hp2 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-224-3548A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594882 | ||||||
| chr15:99594924
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-224-3506C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99594924 | ||||||
| chr15:99595023
|
C | G | 1 | a0002c0014t0016g0348 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-224-3407C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99595023 | ||||||
| chr15:99595153
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-3277G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99595153 | ||||||
| chr15:99595325
|
A | G | 6 | a0001c0004t0117g0311a0001c0004t0137g0283a0001c0005t0003g0335others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-224-3105A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99595325 | ||||||
| chr15:99595344
|
T | G | 1 | a0002c0014t0016g0348 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-224-3086T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99595344 | ||||||
| chr15:99595509
|
A | G | 1 | a0002c0002t0022g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-224-2921A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99595509 | ||||||
| chr15:99595652
|
G | A | 2 | a0001c0004t0091g0289a0001c0004t0092g0288 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-224-2778G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99595652 | ||||||
| chr15:99596033
|
T | C | 147 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-224-2397T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596033 | ||||||
| chr15:99596072
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-224-2358A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596072 | ||||||
| chr15:99596097
|
T | C | 9 | a0001c0001t0028g0162a0001c0005t0009g0133a0001c0005t0125g0220others(6): Show | 9 | HG02257.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-224-2333T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596097 | ||||||
| chr15:99596176
|
C | A | 102 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-224-2254C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596176 | ||||||
| chr15:99596241
|
C | T | 2 | a0004c0008t0050g0215a0004c0008t0099g0216 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-224-2189C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596241 | ||||||
| chr15:99596384
|
C | T | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-224-2046C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596384 | ||||||
| chr15:99596469
|
T | G | 1 | a0001c0004t0047g0296 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-224-1961T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596469 | ||||||
| chr15:99596471
|
A | G | 1 | a0002c0002t0034g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-224-1959A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596471 | ||||||
| chr15:99596564
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-224-1866G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596564 | ||||||
| chr15:99596714
|
C | T | 2 | a0002c0002t0058g0058a0016c0029t0114g0040 | 2 | HG02976.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-224-1716C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596714 | ||||||
| chr15:99596804
|
C | G | 1 | a0002c0011t0024g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-224-1626C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596804 | ||||||
| chr15:99596826
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-224-1604A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596826 | ||||||
| chr15:99596869
|
G | T | 2 | a0004c0019t0028g0120a0004c0019t0028g0121 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-224-1561G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596869 | ||||||
| chr15:99596982
|
C | A | 1 | a0002c0011t0001g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-224-1448C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99596982 | ||||||
| chr15:99597013
|
G | A | 1 | a0002c0002t0062g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-224-1417G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597013 | ||||||
| chr15:99597048
|
T | C | 41 | a0001c0001t0028g0162a0001c0005t0003g0012a0001c0005t0003g0013others(38): Show | 41 | HG00733.hp2 HG01099.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-224-1382T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597048 | ||||||
| chr15:99597155
|
G | T | 1 | a0003c0003t0006g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-224-1275G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597155 | ||||||
| chr15:99597206
|
G | A | 2 | a0001c0004t0107g0350a0001c0004t0112g0354 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-224-1224G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597206 | ||||||
| chr15:99597262
|
C | T | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.-224-1168C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597262 | ||||||
| chr15:99597295
|
C | T | 5 | a0001c0001t0004g0035a0001c0001t0004g0045a0001c0001t0004g0046others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-224-1135C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597295 | ||||||
| chr15:99597362
|
C | T | 1 | a0002c0002t0075g0109 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-224-1068C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597362 | ||||||
| chr15:99597500
|
CGGTCCTG others(1): Show |
C | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-224-912_-224-905d others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99597500 | |||||
| chr15:99597501
|
G | C | 1 | a0002c0002t0058g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-224-929G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597501 | ||||||
| chr15:99597647
|
A | T | 4 | a0001c0001t0032g0272a0003c0010t0003g0017a0003c0013t0032g0132others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-224-783A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597647 | ||||||
| chr15:99597680
|
C | T | 1 | a0013c0032t0005g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-224-750C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597680 | ||||||
| chr15:99597773
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-224-657C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597773 | ||||||
| chr15:99597786
|
T | C | 146 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-224-644T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597786 | ||||||
| chr15:99597831
|
A | G | 1 | a0003c0003t0123g0008 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-224-599A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597831 | ||||||
| chr15:99597856
|
TAGAC | T | 10 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(7): Show | 10 | HG03654.hp1 NA18945.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-224-571_-224-568d others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 99597856 | |||||
| chr15:99597945
|
A | G | 8 | a0003c0003t0010g0004a0003c0003t0010g0005a0003c0003t0010g0006others(5): Show | 8 | HG01928.hp1 HG01934.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-224-485A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597945 | ||||||
| chr15:99597955
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-224-475T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99597955 | ||||||
| chr15:99598072
|
G | T | 1 | a0002c0002t0005g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-224-358G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99598072 | ||||||
| chr15:99598145
|
GA | G | 4 | a0001c0001t0032g0272a0003c0010t0003g0017a0003c0013t0032g0132others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-224-284delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99598145 | ||||||
| chr15:99598174
|
G | T | 2 | a0002c0002t0012g0107a0002c0002t0075g0109 | 2 | NA18964.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-224-256G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99598174 | ||||||
| chr15:99598543
|
G | A | 4 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257others(1): Show | 4 | HG02976.hp1 HG03041.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+32G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99598543 | ||||||
| chr15:99598685
|
A | G | 1 | a0002c0002t0005g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-143+174A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99598685 | ||||||
| chr15:99598788
|
C | T | 139 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(136): Show | 139 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-143+277C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99598788 | ||||||
| chr15:99599034
|
T | A | 1 | a0001c0001t0097g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-143+523T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99599034 | ||||||
| chr15:99599241
|
T | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-143+730T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99599241 | ||||||
| chr15:99599351
|
A | C | 1 | a0001c0004t0026g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-143+840A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99599351 | ||||||
| chr15:99599643
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+1132T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99599643 | ||||||
| chr15:99600312
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+1801A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99600312 | ||||||
| chr15:99600422
|
G | A | 1 | a0002c0002t0078g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-143+1911G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99600422 | ||||||
| chr15:99600702
|
A | G | 1 | a0003c0003t0054g0010 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-143+2191A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99600702 | ||||||
| chr15:99600742
|
T | C | 1 | a0018c0025t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-143+2231T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99600742 | ||||||
| chr15:99600754
|
ATATATCC others(1): Show |
A | 81 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-143+2247_-143+225 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99600754 | |||||
| chr15:99600942
|
C | G | 1 | a0003c0003t0116g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-143+2431C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99600942 | ||||||
| chr15:99601097
|
G | A | 342 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-143+2586G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601097 | ||||||
| chr15:99601202
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+2691T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601202 | ||||||
| chr15:99601301
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+2790A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601301 | ||||||
| chr15:99601510
|
G | GT | 117 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-143+3018dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601510 | |||||
| chr15:99601510
|
G | GTT | 13 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0245others(10): Show | 13 | HG00423.hp1 HG00597.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-143+3017_-143+301 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601510 | |||||
| chr15:99601510
|
GT | G | 23 | a0001c0001t0124g0371a0001c0004t0002g0357a0001c0004t0002g0360others(20): Show | 23 | HG00438.hp2 HG00673.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-143+3018delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601510 | |||||
| chr15:99601667
|
A | G | 1 | a0008c0018t0129g0329 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-143+3156A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601667 | ||||||
| chr15:99601677
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+3166A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601677 | ||||||
| chr15:99601689
|
A | G | 2 | a0001c0004t0047g0296a0003c0010t0055g0152 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-143+3178A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601689 | ||||||
| chr15:99601697
|
A | G | 3 | a0003c0003t0002g0346a0003c0022t0002g0345a0003c0022t0010g0365 | 3 | HG01081.hp2 HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-143+3186A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601697 | ||||||
| chr15:99601806
|
TTTGTGTG others(4): Show |
T | 1 | a0001c0006t0018g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-143+3297_-143+330 others(15): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601806 | |||||
| chr15:99601807
|
T | TTG | 4 | a0001c0004t0091g0289a0001c0004t0092g0288a0001c0012t0066g0284others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+3346_-143+334 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTG | T | 15 | a0001c0005t0003g0012a0001c0005t0003g0016a0001c0005t0003g0018others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-143+3346_-143+334 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTG | T | 14 | a0001c0001t0028g0162a0001c0004t0006g0342a0001c0004t0049g0290others(11): Show | 14 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-143+3344_-143+334 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTG | T | 32 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0361others(29): Show | 32 | HG00438.hp2 HG00673.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.-143+3342_-143+334 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(1): Show |
T | 15 | a0001c0004t0048g0292a0002c0014t0002g0326a0003c0003t0002g0293others(12): Show | 15 | HG00558.hp1 HG01099.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.-143+3340_-143+334 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(3): Show |
T | 40 | a0001c0004t0001g0327a0001c0004t0010g0309a0001c0004t0026g0002others(37): Show | 40 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.-143+3338_-143+334 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(5): Show |
T | 5 | a0001c0004t0006g0200a0002c0014t0109g0051a0003c0003t0002g0300others(2): Show | 5 | HG01123.hp2 HG03453.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+3336_-143+334 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(7): Show |
T | 8 | a0001c0001t0001g0195a0001c0004t0051g0049a0001c0004t0051g0050others(5): Show | 8 | HG00408.hp2 HG00639.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-143+3334_-143+334 others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(9): Show |
T | 16 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(13): Show | 16 | HG00280.hp2 HG00733.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-143+3332_-143+334 others(20): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(11): Show |
T | 72 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-143+3330_-143+334 others(22): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(13): Show |
T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+3328_-143+334 others(24): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601807
|
TTGTGTGT others(17): Show |
T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+3324_-143+334 others(28): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601807 | |||||
| chr15:99601829
|
G | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+3318G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601829 | ||||||
| chr15:99601833
|
G | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+3322G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601833 | ||||||
| chr15:99601835
|
G | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+3324G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601835 | ||||||
| chr15:99601837
|
G | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+3326G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601837 | ||||||
| chr15:99601839
|
GTGTGTGT others(13): Show |
G | 2 | a0001c0001t0032g0272a0002c0011t0011g0159 | 2 | HG02129.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-143+3329_-143+334 others(24): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601839 | ||||||
| chr15:99601841
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-143+3331_-143+334 others(22): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601841 | ||||||
| chr15:99601843
|
GTGTGTGT others(9): Show |
G | 7 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375others(4): Show | 7 | HG01517.hp1 HG02145.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.-143+3333_-143+334 others(20): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601843 | ||||||
| chr15:99601844
|
TGTGTGTG others(9): Show |
T | 1 | a0001c0001t0105g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-143+3335_-143+335 others(20): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99601844 | |||||
| chr15:99601845
|
GTGTGTGT others(7): Show |
G | 43 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(40): Show | 43 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-143+3335_-143+334 others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601845 | ||||||
| chr15:99601847
|
GTGTGTGT others(5): Show |
G | 72 | a0001c0001t0006g0150a0001c0001t0020g0236a0001c0001t0020g0259others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.-143+3337_-143+334 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601847 | ||||||
| chr15:99601849
|
GTGTGTGT others(3): Show |
G | 12 | a0001c0006t0008g0115a0001c0006t0021g0164a0001c0007t0040g0118others(9): Show | 12 | HG00438.hp1 HG01192.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-143+3339_-143+334 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601849 | ||||||
| chr15:99601851
|
GTGTGTGT others(1): Show |
G | 3 | a0001c0007t0100g0044a0002c0002t0022g0232a0002c0002t0078g0117 | 3 | HG00639.hp2 HG03942.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-143+3341_-143+334 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601851 | ||||||
| chr15:99601853
|
GTGTGTC | G | 4 | a0002c0002t0022g0104a0002c0002t0062g0061a0003c0010t0055g0135others(1): Show | 4 | HG00323.hp1 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+3343_-143+334 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601853 | ||||||
| chr15:99601859
|
C | G | 1 | a0001c0006t0018g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-143+3348C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99601859 | ||||||
| chr15:99602026
|
G | C | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-143+3515G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602026 | ||||||
| chr15:99602037
|
C | T | 2 | a0001c0001t0032g0272a0003c0013t0032g0132 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-143+3526C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602037 | ||||||
| chr15:99602076
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+3565A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602076 | ||||||
| chr15:99602196
|
G | C | 1 | a0001c0007t0040g0118 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-143+3685G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602196 | ||||||
| chr15:99602220
|
G | A | 1 | a0001c0001t0028g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-143+3709G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602220 | ||||||
| chr15:99602239
|
A | G | 355 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(352): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-143+3728A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602239 | ||||||
| chr15:99602247
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+3736A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602247 | ||||||
| chr15:99602336
|
T | A | 1 | a0001c0004t0006g0342 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-143+3825T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602336 | ||||||
| chr15:99602375
|
A | G | 1 | a0002c0002t0005g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-143+3864A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602375 | ||||||
| chr15:99602623
|
C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0044g0240 | 3 | HG00140.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-143+4112C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602623 | ||||||
| chr15:99602653
|
G | GGGGTGTG others(3): Show |
1 | a0001c0001t0097g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-143+4143_-143+414 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGT | 31 | a0001c0001t0001g0124a0001c0001t0001g0280a0001c0001t0027g0151others(28): Show | 31 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-143+4187_-143+418 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGGGTG others(5): Show |
1 | a0001c0001t0020g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-143+4145_-143+414 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGGGTG others(5): Show |
1 | a0003c0013t0001g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-143+4145_-143+414 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGT | 42 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0222others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-143+4185_-143+418 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGTGT | 53 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0001g0192others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-143+4183_-143+418 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGTGTG others(1): Show |
44 | a0001c0001t0001g0195a0001c0001t0001g0234a0001c0001t0001g0237others(41): Show | 44 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-143+4181_-143+418 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGTGTG others(3): Show |
26 | a0001c0001t0001g0128a0001c0001t0004g0037a0001c0001t0039g0265others(23): Show | 26 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.-143+4179_-143+418 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGTGTG others(5): Show |
19 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0248others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.-143+4177_-143+418 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGTGTG others(7): Show |
8 | a0001c0001t0001g0167a0001c0001t0004g0275a0002c0014t0007g0340others(5): Show | 8 | NA18957.hp1 NA18964.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.-143+4175_-143+418 others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GGTGTGTG others(11): Show |
1 | a0003c0003t0116g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-143+4171_-143+418 others(22): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
G | GTGTGTGT | 3 | a0001c0001t0105g0255a0002c0002t0005g0057a0002c0002t0022g0232 | 3 | HG02056.hp2 HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-143+4142_-143+414 others(11): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602653 | ||||||
| chr15:99602653
|
G | GTGTGTGT others(4): Show |
3 | a0001c0001t0011g0242a0002c0011t0090g0156a0003c0003t0002g0362 | 3 | HG02738.hp2 NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-143+4142_-143+414 others(15): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602653 | ||||||
| chr15:99602653
|
G | GTGTGTGT others(6): Show |
3 | a0001c0006t0008g0115a0001c0007t0001g0168a0007c0026t0024g0161 | 3 | HG01192.hp1 HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-143+4142_-143+414 others(17): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602653 | ||||||
| chr15:99602653
|
GGT | G | 40 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0028g0162others(37): Show | 40 | HG01071.hp1 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.-143+4187_-143+418 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
GGTGT | G | 8 | a0001c0001t0001g0174a0001c0004t0117g0311a0002c0002t0075g0109others(5): Show | 8 | HG01496.hp1 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-143+4185_-143+418 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
GGTGTGT | G | 13 | a0001c0001t0081g0078a0001c0006t0012g0076a0001c0006t0012g0077others(10): Show | 13 | HG01123.hp2 HG01891.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-143+4183_-143+418 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
GGTGTGTG others(1): Show |
G | 6 | a0001c0001t0001g0243a0001c0005t0003g0019a0003c0003t0010g0004others(3): Show | 6 | HG01884.hp2 HG01978.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+4181_-143+418 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
GGTGTGTG others(3): Show |
G | 9 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(6): Show | 9 | HG00733.hp2 HG01099.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+4179_-143+418 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602653
|
GGTGTGTG others(119): Show |
G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-143+4163_-143+428 others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602653 | |||||
| chr15:99602655
|
T | G | 1 | a0002c0036t0005g0313 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-143+4144T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602655 | ||||||
| chr15:99602657
|
T | G | 4 | a0001c0001t0124g0371a0007c0016t0018g0060a0007c0016t0067g0074others(1): Show | 4 | NA18942.hp2 NA19002.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+4146T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602657 | ||||||
| chr15:99602665
|
T | G | 1 | a0004c0008t0009g0032 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-143+4154T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602665 | ||||||
| chr15:99602665
|
TGTGTGTG others(83): Show |
T | 1 | a0003c0003t0002g0324 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-143+4189_-143+427 others(94): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602665 | |||||
| chr15:99602673
|
TGTGTGTG others(75): Show |
T | 1 | a0002c0014t0002g0326 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-143+4189_-143+427 others(86): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602673 | |||||
| chr15:99602692
|
G | GTGTT | 3 | a0002c0002t0005g0101a0002c0002t0005g0102a0002c0002t0023g0056 | 3 | NA18940.hp2 NA18950.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-143+4184_-143+418 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602692 | |||||
| chr15:99602698
|
G | A | 1 | a0001c0001t0020g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-143+4187G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602698 | ||||||
| chr15:99602698
|
G | GTGTGTGT others(5): Show |
1 | a0010c0020t0049g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-143+4188_-143+418 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602698 | |||||
| chr15:99602716
|
T | TTG | 3 | a0001c0001t0004g0036a0001c0001t0004g0037a0001c0001t0032g0272 | 3 | NA18967.hp1 NA19000.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-143+4218_-143+421 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602716 | |||||
| chr15:99602721
|
T | G | 10 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(7): Show | 10 | HG03654.hp1 NA18945.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+4210T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602721 | ||||||
| chr15:99602723
|
T | G | 10 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(7): Show | 10 | HG03654.hp1 NA18945.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+4212T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602723 | ||||||
| chr15:99602725
|
T | TGGGG | 87 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-143+4215_-143+421 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602725 | |||||
| chr15:99602725
|
TGTGTGG | T | 5 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(2): Show | 5 | HG00558.hp2 HG03098.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+4216_-143+422 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602725 | |||||
| chr15:99602727
|
T | G | 9 | a0001c0001t0006g0150a0001c0001t0026g0146a0001c0001t0026g0147others(6): Show | 9 | HG02615.hp2 HG02698.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+4216T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602727 | ||||||
| chr15:99602729
|
T | G | 97 | a0001c0001t0006g0150a0001c0001t0026g0146a0001c0001t0026g0147others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-143+4218T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602729 | ||||||
| chr15:99602731
|
G | GGT | 87 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-143+4221_-143+422 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602731 | |||||
| chr15:99602731
|
G | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(205): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-143+4220G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602731 | ||||||
| chr15:99602755
|
C | CGT | 38 | a0001c0001t0020g0279a0001c0001t0081g0078a0001c0004t0006g0285others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.-143+4287_-143+428 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602755
|
C | CGTGT | 33 | a0001c0004t0001g0327a0001c0004t0010g0309a0001c0005t0003g0026others(30): Show | 33 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-143+4285_-143+428 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602755
|
C | CGTGTGT | 6 | a0001c0004t0048g0292a0002c0036t0005g0313a0003c0003t0002g0322others(3): Show | 6 | HG02559.hp1 HG03041.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+4283_-143+428 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602755
|
CGT | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0006g0139others(67): Show | 71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-143+4287_-143+428 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602755
|
CGTGT | C | 88 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0167others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-143+4285_-143+428 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602755
|
CGTGTGT | C | 49 | a0001c0001t0001g0048a0001c0001t0001g0182a0001c0001t0001g0183others(46): Show | 49 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-143+4283_-143+428 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602755
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0121g0190a0001c0001t0124g0371a0001c0006t0005g0145others(1): Show | 4 | HG01515.hp1 NA18963.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+4281_-143+428 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602755
|
CGTGTGTG others(5): Show |
C | 6 | a0001c0004t0107g0350a0001c0004t0112g0354a0001c0012t0017g0352others(3): Show | 6 | HG01496.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+4277_-143+428 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99602755 | |||||
| chr15:99602818
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+4307C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99602818 | ||||||
| chr15:99603013
|
C | A | 80 | a0001c0001t0001g0048a0001c0001t0001g0124a0001c0001t0001g0127others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-143+4502C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603013 | ||||||
| chr15:99603035
|
A | G | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.-143+4524A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603035 | ||||||
| chr15:99603212
|
C | T | 2 | a0003c0003t0002g0302a0003c0003t0128g0303 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-143+4701C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603212 | ||||||
| chr15:99603213
|
G | A | 104 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.-143+4702G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603213 | ||||||
| chr15:99603346
|
A | G | 5 | a0003c0010t0003g0017a0003c0010t0055g0135a0003c0010t0055g0152others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+4835A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603346 | ||||||
| chr15:99603373
|
A | T | 1 | a0017c0034t0111g0308 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-143+4862A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603373 | ||||||
| chr15:99603373
|
AT | A | 110 | a0001c0001t0001g0369a0001c0001t0025g0207a0001c0001t0041g0186others(107): Show | 110 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-143+4879delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603373 | |||||
| chr15:99603541
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-143+5031_-143+503 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603541 | |||||
| chr15:99603543
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-143+5032T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603543 | ||||||
| chr15:99603543
|
T | TGTGTGTG others(20): Show |
1 | a0009c0021t0001g0122 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-143+5032_-143+503 others(31): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603543 | ||||||
| chr15:99603543
|
T | TTG | 10 | a0001c0005t0009g0212a0001c0005t0009g0213a0001c0005t0138g0014others(7): Show | 10 | HG01099.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-143+5066_-143+506 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTG | 3 | a0001c0005t0003g0013a0003c0010t0002g0197a0003c0010t0002g0198 | 3 | HG02965.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-143+5064_-143+506 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(1): Show |
85 | a0001c0001t0001g0222a0001c0001t0004g0035a0001c0001t0004g0036others(82): Show | 85 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-143+5060_-143+506 others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(3): Show |
35 | a0001c0001t0020g0236a0001c0004t0006g0342a0001c0004t0027g0310others(32): Show | 35 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-143+5058_-143+506 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(5): Show |
73 | a0001c0001t0001g0128a0001c0001t0001g0174a0001c0001t0001g0192others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-143+5056_-143+506 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(7): Show |
55 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0183others(52): Show | 55 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-143+5054_-143+506 others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(9): Show |
34 | a0001c0001t0001g0048a0001c0001t0001g0124a0001c0001t0001g0127others(31): Show | 34 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-143+5052_-143+506 others(20): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(11): Show |
23 | a0001c0001t0001g0178a0001c0001t0001g0245a0001c0001t0011g0281others(20): Show | 23 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-143+5050_-143+506 others(22): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(13): Show |
12 | a0001c0001t0001g0176a0001c0001t0001g0229a0001c0001t0001g0239others(9): Show | 12 | HG00140.hp1 HG00609.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.-143+5048_-143+506 others(24): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(15): Show |
6 | a0001c0001t0001g0238a0001c0012t0066g0284a0002c0002t0034g0261others(3): Show | 6 | HG00738.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+5046_-143+506 others(26): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(17): Show |
1 | a0001c0004t0137g0283 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-143+5044_-143+506 others(28): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603543
|
T | TTGTGTGT others(19): Show |
1 | a0009c0021t0001g0126 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-143+5042_-143+506 others(30): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603543 | |||||
| chr15:99603562
|
T | TGTGTGTG others(12): Show |
1 | a0003c0003t0002g0362 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-143+5067_-143+506 others(23): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99603562 | |||||
| chr15:99603578
|
T | TGTGTGTG others(8): Show |
2 | a0001c0004t0049g0290a0003c0010t0135g0134 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-143+5067_-143+506 others(19): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603578 | ||||||
| chr15:99603660
|
C | G | 2 | a0001c0004t0091g0289a0001c0004t0092g0288 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-143+5149C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603660 | ||||||
| chr15:99603794
|
T | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(77): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-143+5283T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603794 | ||||||
| chr15:99603805
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-143+5294C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603805 | ||||||
| chr15:99603920
|
C | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-143+5409C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603920 | ||||||
| chr15:99603937
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+5426C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99603937 | ||||||
| chr15:99604193
|
T | C | 1 | a0001c0004t0010g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-143+5682T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604193 | ||||||
| chr15:99604267
|
C | T | 1 | a0001c0001t0102g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-143+5756C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604267 | ||||||
| chr15:99604639
|
C | T | 2 | a0003c0003t0002g0302a0003c0003t0128g0303 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-143+6128C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604639 | ||||||
| chr15:99604703
|
G | A | 10 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(7): Show | 10 | HG03654.hp1 NA18945.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+6192G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604703 | ||||||
| chr15:99604855
|
G | T | 14 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0128others(11): Show | 15 | HG00323.hp2 HG01255.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-143+6344G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604855 | ||||||
| chr15:99604860
|
A | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+6349A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604860 | ||||||
| chr15:99604923
|
A | T | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-143+6412A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604923 | ||||||
| chr15:99604949
|
T | C | 2 | a0001c0005t0015g0025a0001c0005t0015g0027 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143+6438T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604949 | ||||||
| chr15:99604988
|
C | T | 1 | a0003c0003t0002g0328 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-143+6477C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99604988 | ||||||
| chr15:99605019
|
C | A | 100 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(97): Show | 100 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-143+6508C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99605019 | ||||||
| chr15:99605046
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+6535A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99605046 | ||||||
| chr15:99605317
|
A | G | 1 | a0001c0004t0047g0296 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-143+6806A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99605317 | ||||||
| chr15:99605691
|
T | C | 1 | a0001c0001t0039g0268 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-143+7180T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99605691 | ||||||
| chr15:99605758
|
C | G | 6 | a0001c0004t0006g0342a0001c0004t0027g0310a0001c0004t0027g0349others(3): Show | 6 | HG02647.hp2 HG03209.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+7247C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99605758 | ||||||
| chr15:99606006
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+7495A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99606006 | ||||||
| chr15:99606268
|
C | T | 1 | a0008c0018t0002g0320 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-143+7757C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99606268 | ||||||
| chr15:99606564
|
G | A | 1 | a0001c0001t0004g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-143+8053G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99606564 | ||||||
| chr15:99606702
|
C | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+8191C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99606702 | ||||||
| chr15:99606798
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+8287C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99606798 | ||||||
| chr15:99606855
|
T | A | 1 | a0002c0002t0082g0095 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-143+8344T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99606855 | ||||||
| chr15:99607071
|
C | T | 2 | a0002c0014t0002g0326a0003c0003t0002g0324 | 2 | HG00558.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-143+8560C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99607071 | ||||||
| chr15:99607572
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-143+9061C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99607572 | ||||||
| chr15:99607582
|
C | A | 6 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051others(3): Show | 6 | HG00733.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+9071C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99607582 | ||||||
| chr15:99607583
|
C | T | 1 | a0004c0008t0009g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-143+9072C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99607583 | ||||||
| chr15:99607837
|
G | A | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-143+9326G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99607837 | ||||||
| chr15:99607871
|
C | T | 1 | a0010c0020t0049g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-143+9360C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99607871 | ||||||
| chr15:99607921
|
C | T | 1 | a0001c0001t0120g0244 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-143+9410C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99607921 | ||||||
| chr15:99608343
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+9832C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99608343 | ||||||
| chr15:99608705
|
G | A | 1 | a0003c0003t0052g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-143+10194G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99608705 | ||||||
| chr15:99608901
|
C | CA | 39 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(36): Show | 39 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-143+10402dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99608901 | |||||
| chr15:99608936
|
G | T | 1 | a0002c0002t0034g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-143+10425G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99608936 | ||||||
| chr15:99609194
|
G | T | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-143+10683G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609194 | ||||||
| chr15:99609295
|
A | T | 5 | a0002c0002t0012g0082a0002c0002t0012g0107a0002c0002t0030g0083others(2): Show | 5 | NA18949.hp1 NA18964.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+10784A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609295 | ||||||
| chr15:99609412
|
A | G | 1 | a0002c0002t0005g0196 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-143+10901A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609412 | ||||||
| chr15:99609425
|
T | G | 1 | a0003c0003t0133g0330 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-143+10914T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609425 | ||||||
| chr15:99609466
|
G | A | 2 | a0003c0003t0002g0302a0003c0003t0128g0303 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-143+10955G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609466 | ||||||
| chr15:99609523
|
C | T | 1 | a0002c0002t0007g0052 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-143+11012C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609523 | ||||||
| chr15:99609524
|
G | A | 1 | a0001c0005t0125g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-143+11013G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609524 | ||||||
| chr15:99609573
|
G | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-143+11062G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609573 | ||||||
| chr15:99609604
|
C | T | 1 | a0002c0002t0008g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-143+11093C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99609604 | ||||||
| chr15:99610124
|
G | A | 1 | a0002c0002t0080g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-143+11613G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610124 | ||||||
| chr15:99610163
|
A | G | 1 | a0001c0007t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-143+11652A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610163 | ||||||
| chr15:99610302
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+11791C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610302 | ||||||
| chr15:99610405
|
TCCCCCGC others(7): Show |
T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-143+11900_-143+11 others(20): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610405 | |||||
| chr15:99610411
|
GC | G | 72 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0006g0138others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-143+11915delC | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610411 | |||||
| chr15:99610411
|
GCC | G | 44 | a0001c0001t0006g0137a0001c0001t0028g0162a0001c0004t0027g0349others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-143+11914_-143+11 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610411 | |||||
| chr15:99610411
|
GCCC | G | 17 | a0001c0004t0011g0366a0001c0004t0092g0288a0001c0004t0107g0350others(14): Show | 17 | HG00609.hp1 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-143+11913_-143+11 others(9): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610411 | |||||
| chr15:99610411
|
GCCCC | G | 38 | a0001c0004t0002g0360a0001c0004t0002g0363a0001c0004t0006g0200others(35): Show | 38 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-143+11912_-143+11 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610411 | |||||
| chr15:99610414
|
CCCCCCCC others(6): Show |
C | 3 | a0001c0001t0045g0226a0006c0015t0004g0154a0006c0015t0004g0155 | 3 | HG02895.hp2 HG02897.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-143+11913_-143+11 others(19): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610414 | |||||
| chr15:99610415
|
CCCCCCCC others(5): Show |
C | 3 | a0001c0001t0004g0043a0001c0001t0045g0227a0012c0033t0094g0267 | 3 | HG02717.hp2 NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-143+11914_-143+11 others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610415 | |||||
| chr15:99610416
|
CCCCCCCC others(4): Show |
C | 23 | a0001c0001t0004g0036a0001c0001t0004g0037a0001c0001t0004g0045others(20): Show | 23 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-143+11915_-143+11 others(17): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610416 | |||||
| chr15:99610417
|
C | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(68): Show | 72 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-143+11906C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610417 | ||||||
| chr15:99610417
|
CCCCCCCC others(3): Show |
C | 4 | a0001c0001t0004g0035a0001c0001t0004g0119a0001c0001t0088g0131others(1): Show | 4 | HG02135.hp1 NA18969.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+11916_-143+11 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610417 | |||||
| chr15:99610418
|
C | G | 6 | a0001c0001t0001g0192a0001c0001t0077g0206a0001c0001t0103g0210others(3): Show | 6 | HG00544.hp1 HG01192.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+11907C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610418 | ||||||
| chr15:99610419
|
C | G | 4 | a0001c0001t0064g0278a0001c0005t0009g0133a0001c0006t0008g0115others(1): Show | 4 | HG01192.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+11908C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610419 | ||||||
| chr15:99610420
|
C | G | 12 | a0001c0001t0020g0259a0001c0001t0026g0146a0001c0006t0018g0233others(9): Show | 12 | HG00642.hp2 HG01175.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-143+11909C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610420 | ||||||
| chr15:99610421
|
C | G | 92 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0006g0137others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-143+11910C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610421 | ||||||
| chr15:99610422
|
C | A | 1 | a0001c0004t0010g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-143+11911C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610422 | ||||||
| chr15:99610423
|
C | A | 20 | a0001c0004t0002g0361a0001c0004t0048g0047a0001c0004t0049g0290others(17): Show | 20 | HG00408.hp2 HG00423.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-143+11912C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610423 | ||||||
| chr15:99610423
|
CCCCA | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0167others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-143+11916_-143+11 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610423 | |||||
| chr15:99610424
|
C | A | 17 | a0001c0004t0006g0342a0001c0004t0026g0002a0001c0004t0091g0289others(14): Show | 17 | HG00621.hp2 HG01261.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-143+11913C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610424 | ||||||
| chr15:99610424
|
CCCA | C | 44 | a0001c0001t0001g0048a0001c0001t0001g0176a0001c0001t0001g0178others(41): Show | 44 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-143+11916_-143+11 others(9): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610424 | |||||
| chr15:99610425
|
C | A | 2 | a0003c0003t0054g0007a0003c0003t0108g0298 | 2 | HG01934.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-143+11914C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610425 | ||||||
| chr15:99610425
|
C | G | 1 | a0001c0006t0008g0115 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-143+11914C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610425 | ||||||
| chr15:99610425
|
CCA | C | 31 | a0001c0001t0001g0124a0001c0001t0001g0192a0001c0001t0001g0237others(28): Show | 31 | HG00609.hp2 HG00621.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.-143+11916_-143+11 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99610425 | |||||
| chr15:99610426
|
C | A | 2 | a0001c0005t0003g0022a0004c0008t0047g0217 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-143+11915C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610426 | ||||||
| chr15:99610426
|
C | G | 6 | a0001c0006t0021g0164a0002c0002t0005g0101a0002c0002t0008g0055others(3): Show | 6 | HG00438.hp1 HG01175.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+11915C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610426 | ||||||
| chr15:99610426
|
C | T | 1 | a0001c0001t0026g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-143+11915C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610426 | ||||||
| chr15:99610426
|
CA | C | 7 | a0001c0001t0011g0242a0001c0001t0020g0236a0001c0006t0008g0115others(4): Show | 7 | HG01192.hp2 HG01934.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+11916delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610426 | ||||||
| chr15:99610427
|
A | C | 20 | a0001c0001t0020g0279a0001c0001t0026g0146a0001c0001t0064g0278others(17): Show | 20 | HG00438.hp1 HG00544.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.-143+11916A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610427 | ||||||
| chr15:99610427
|
A | G | 87 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0044g0240others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-143+11916A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610427 | ||||||
| chr15:99610427
|
A | T | 9 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(6): Show | 9 | NA18945.hp1 NA18957.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+11916A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610427 | ||||||
| chr15:99610432
|
C | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0128others(12): Show | 16 | HG00323.hp2 HG01255.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-143+11921C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610432 | ||||||
| chr15:99610436
|
C | T | 10 | a0003c0003t0002g0293a0003c0003t0002g0294a0003c0003t0010g0004others(7): Show | 10 | HG00639.hp1 HG01255.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-143+11925C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610436 | ||||||
| chr15:99610494
|
A | G | 1 | a0002c0002t0072g0130 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-143+11983A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610494 | ||||||
| chr15:99610566
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+12055G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610566 | ||||||
| chr15:99610998
|
T | G | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0010c0020t0049g0235 | 3 | HG02145.hp1 HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-143+12487T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99610998 | ||||||
| chr15:99611103
|
G | A | 2 | a0001c0001t0096g0029a0001c0001t0104g0030 | 2 | HG01358.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-143+12592G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99611103 | ||||||
| chr15:99611200
|
C | T | 1 | a0001c0001t0105g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-143+12689C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99611200 | ||||||
| chr15:99611293
|
A | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-143+12782A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99611293 | ||||||
| chr15:99611329
|
C | T | 1 | a0001c0005t0003g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-143+12818C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99611329 | ||||||
| chr15:99611526
|
T | C | 1 | a0003c0010t0130g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-143+13015T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99611526 | ||||||
| chr15:99611916
|
CAG | C | 7 | a0001c0001t0028g0162a0001c0005t0125g0220a0003c0003t0098g0291others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+13407_-143+13 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99611916 | |||||
| chr15:99611947
|
T | A | 1 | a0001c0005t0125g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-143+13436T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99611947 | ||||||
| chr15:99612065
|
A | G | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-143+13554A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612065 | ||||||
| chr15:99612137
|
C | T | 3 | a0002c0014t0016g0348a0003c0003t0002g0315a0003c0003t0118g0344 | 3 | HG02056.hp1 HG02135.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-143+13626C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612137 | ||||||
| chr15:99612206
|
G | C | 1 | a0001c0001t0045g0226 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-143+13695G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612206 | ||||||
| chr15:99612277
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-143+13766C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612277 | ||||||
| chr15:99612278
|
G | A | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0010c0020t0049g0235 | 3 | HG02145.hp1 HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-143+13767G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612278 | ||||||
| chr15:99612365
|
C | T | 1 | a0001c0004t0046g0343 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+13854C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612365 | ||||||
| chr15:99612433
|
A | G | 1 | a0001c0006t0007g0098 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-143+13922A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612433 | ||||||
| chr15:99612465
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(74): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-143+13954G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99612465 | ||||||
| chr15:99613156
|
G | A | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-143+14645G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99613156 | ||||||
| chr15:99613330
|
T | A | 4 | a0001c0001t0028g0162a0001c0005t0125g0220a0003c0010t0002g0197others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+14819T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99613330 | ||||||
| chr15:99613535
|
G | T | 1 | a0009c0021t0001g0126 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-143+15024G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99613535 | ||||||
| chr15:99613738
|
G | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-143+15227G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99613738 | ||||||
| chr15:99613798
|
G | A | 1 | a0001c0001t0096g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-143+15287G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99613798 | ||||||
| chr15:99613853
|
G | A | 2 | a0003c0003t0002g0302a0003c0003t0128g0303 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-143+15342G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99613853 | ||||||
| chr15:99613857
|
T | A | 2 | a0005c0009t0019g0003a0005c0009t0076g0158 | 2 | NA18939.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-143+15346T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99613857 | ||||||
| chr15:99614002
|
G | A | 1 | a0001c0001t0105g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-143+15491G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614002 | ||||||
| chr15:99614092
|
C | T | 2 | a0001c0004t0091g0289a0001c0004t0092g0288 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-143+15581C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614092 | ||||||
| chr15:99614140
|
G | C | 1 | a0002c0011t0011g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-143+15629G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614140 | ||||||
| chr15:99614193
|
T | C | 1 | a0001c0001t0011g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-143+15682T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614193 | ||||||
| chr15:99614275
|
A | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-143+15764A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614275 | ||||||
| chr15:99614343
|
C | T | 1 | a0003c0003t0002g0315 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-143+15832C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614343 | ||||||
| chr15:99614381
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0124 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-143+15870G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614381 | ||||||
| chr15:99614402
|
T | C | 1 | a0001c0004t0010g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-143+15891T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614402 | ||||||
| chr15:99614720
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-143+16209T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614720 | ||||||
| chr15:99614823
|
A | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-143+16312A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614823 | ||||||
| chr15:99614893
|
G | T | 2 | a0001c0001t0020g0236a0001c0001t0020g0259 | 2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-143+16382G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614893 | ||||||
| chr15:99614894
|
C | T | 1 | a0002c0002t0023g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-143+16383C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614894 | ||||||
| chr15:99614947
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-143+16436A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614947 | ||||||
| chr15:99614976
|
A | G | 1 | a0001c0012t0017g0353 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-143+16465A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99614976 | ||||||
| chr15:99615191
|
G | C | 11 | a0005c0009t0019g0003a0005c0009t0019g0070a0005c0009t0019g0071others(8): Show | 11 | HG00597.hp2 HG01071.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.-143+16680G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615191 | ||||||
| chr15:99615412
|
G | A | 353 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(350): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.-143+16901G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615412 | ||||||
| chr15:99615588
|
A | G | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-143+17077A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615588 | ||||||
| chr15:99615779
|
T | C | 1 | a0003c0003t0002g0323 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-142-17199T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615779 | ||||||
| chr15:99615837
|
T | C | 1 | a0001c0001t0077g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-142-17141T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615837 | ||||||
| chr15:99615905
|
G | A | 7 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(4): Show | 7 | HG00408.hp1 HG00609.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-17073G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615905 | ||||||
| chr15:99615969
|
T | C | 8 | a0001c0001t0028g0162a0001c0005t0009g0133a0001c0005t0125g0220others(5): Show | 8 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-142-17009T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615969 | ||||||
| chr15:99615971
|
G | T | 1 | a0002c0002t0033g0073 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-142-17007G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615971 | ||||||
| chr15:99615982
|
G | A | 1 | a0003c0003t0010g0258 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-142-16996G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99615982 | ||||||
| chr15:99616153
|
C | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-142-16825C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616153 | ||||||
| chr15:99616299
|
G | A | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-142-16679G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616299 | ||||||
| chr15:99616460
|
A | G | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-142-16518A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616460 | ||||||
| chr15:99616482
|
A | G | 1 | a0003c0013t0032g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-142-16496A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616482 | ||||||
| chr15:99616605
|
T | C | 2 | a0002c0002t0007g0087a0002c0002t0007g0088 | 2 | HG00673.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-142-16373T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616605 | ||||||
| chr15:99616662
|
G | A | 5 | a0001c0005t0003g0016a0001c0005t0003g0018a0001c0005t0003g0263others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-16316G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616662 | ||||||
| chr15:99616665
|
A | G | 2 | a0001c0004t0137g0283a0003c0003t0136g0282 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-142-16313A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616665 | ||||||
| chr15:99616678
|
A | AAT | 3 | a0001c0001t0026g0146a0001c0006t0071g0089a0002c0002t0005g0110 | 3 | HG02735.hp2 HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-142-16286_-142-16 others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99616678 | |||||
| chr15:99616897
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-16081A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616897 | ||||||
| chr15:99616914
|
T | A | 2 | a0001c0001t0001g0222a0002c0002t0022g0223 | 2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-142-16064T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616914 | ||||||
| chr15:99616931
|
C | T | 92 | a0001c0001t0026g0146a0001c0001t0081g0078a0001c0006t0005g0093others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-142-16047C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616931 | ||||||
| chr15:99616969
|
G | A | 1 | a0002c0002t0005g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-142-16009G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99616969 | ||||||
| chr15:99617093
|
A | G | 1 | a0001c0012t0066g0284 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-142-15885A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617093 | ||||||
| chr15:99617096
|
C | T | 1 | a0003c0003t0052g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-142-15882C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617096 | ||||||
| chr15:99617142
|
T | G | 1 | a0002c0002t0022g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-142-15836T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617142 | ||||||
| chr15:99617216
|
C | T | 1 | a0001c0001t0077g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-142-15762C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617216 | ||||||
| chr15:99617244
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-142-15734A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617244 | ||||||
| chr15:99617275
|
T | TG | 225 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-142-15702dupG | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99617275 | |||||
| chr15:99617569
|
G | C | 1 | a0003c0003t0002g0346 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-142-15409G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617569 | ||||||
| chr15:99617804
|
A | T | 143 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(140): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-142-15174A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617804 | ||||||
| chr15:99617822
|
A | C | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-142-15156A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99617822 | ||||||
| chr15:99618206
|
T | A | 1 | a0001c0005t0085g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-142-14772T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99618206 | ||||||
| chr15:99618239
|
T | C | 105 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-142-14739T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99618239 | ||||||
| chr15:99618255
|
G | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-14723G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99618255 | ||||||
| chr15:99618408
|
C | G | 5 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0253others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-14570C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99618408 | ||||||
| chr15:99618482
|
G | A | 4 | a0001c0001t0004g0035a0001c0001t0004g0045a0001c0001t0093g0042others(1): Show | 4 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-14496G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99618482 | ||||||
| chr15:99619038
|
G | A | 330 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.-142-13940G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619038 | ||||||
| chr15:99619047
|
C | T | 1 | a0003c0003t0002g0368 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-142-13931C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619047 | ||||||
| chr15:99619126
|
T | G | 334 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(331): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-142-13852T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619126 | ||||||
| chr15:99619148
|
C | T | 1 | a0003c0003t0116g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-142-13830C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619148 | ||||||
| chr15:99619269
|
A | C | 1 | a0003c0003t0002g0054 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-142-13709A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619269 | ||||||
| chr15:99619271
|
A | C | 2 | a0001c0001t0004g0035a0002c0002t0068g0160 | 2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-142-13707A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619271 | ||||||
| chr15:99619315
|
C | G | 1 | a0002c0002t0023g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-142-13663C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619315 | ||||||
| chr15:99619352
|
G | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-142-13626G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619352 | ||||||
| chr15:99619552
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-13426G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619552 | ||||||
| chr15:99619620
|
T | C | 1 | a0002c0002t0005g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-142-13358T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619620 | ||||||
| chr15:99619864
|
G | A | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-142-13114G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99619864 | ||||||
| chr15:99620359
|
A | G | 37 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(34): Show | 37 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.-142-12619A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99620359 | ||||||
| chr15:99620536
|
G | T | 1 | a0004c0019t0028g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-142-12442G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99620536 | ||||||
| chr15:99620798
|
C | T | 2 | a0001c0001t0032g0272a0003c0013t0032g0132 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-142-12180C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99620798 | ||||||
| chr15:99620843
|
C | CT | 24 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.-142-12117dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99620843 | |||||
| chr15:99620843
|
CT | C | 16 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(13): Show | 16 | HG01934.hp1 HG01943.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.-142-12117delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99620843 | |||||
| chr15:99621045
|
A | G | 1 | a0001c0001t0020g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-142-11933A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621045 | ||||||
| chr15:99621110
|
G | A | 3 | a0001c0001t0124g0371a0001c0004t0048g0047a0001c0004t0048g0292 | 3 | HG03041.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-142-11868G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621110 | ||||||
| chr15:99621181
|
C | G | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-142-11797C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621181 | ||||||
| chr15:99621271
|
T | C | 1 | a0002c0002t0022g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-142-11707T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621271 | ||||||
| chr15:99621299
|
A | G | 12 | a0001c0001t0001g0192a0001c0001t0028g0162a0001c0005t0009g0133others(9): Show | 12 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-142-11679A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621299 | ||||||
| chr15:99621308
|
C | G | 2 | a0001c0001t0020g0236a0001c0001t0020g0259 | 2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-142-11670C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621308 | ||||||
| chr15:99621326
|
CT | C | 7 | a0003c0003t0010g0004a0003c0003t0010g0005a0003c0003t0010g0006others(4): Show | 7 | HG01934.hp1 HG01943.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-11648delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99621326 | |||||
| chr15:99621427
|
C | G | 3 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051 | 3 | HG03669.hp2 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-142-11551C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621427 | ||||||
| chr15:99621635
|
C | T | 1 | a0002c0002t0034g0261 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-142-11343C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621635 | ||||||
| chr15:99621640
|
A | T | 3 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051 | 3 | HG03669.hp2 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-142-11338A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621640 | ||||||
| chr15:99621728
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-11250A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99621728 | ||||||
| chr15:99622222
|
G | A | 1 | a0002c0002t0056g0100 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-142-10756G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622222 | ||||||
| chr15:99622239
|
A | G | 1 | a0001c0004t0002g0360 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-142-10739A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622239 | ||||||
| chr15:99622542
|
G | C | 1 | a0001c0001t0004g0046 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-142-10436G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622542 | ||||||
| chr15:99622702
|
C | CTTTTCTT others(1): Show |
11 | a0001c0001t0081g0078a0001c0006t0012g0076a0001c0006t0012g0077others(8): Show | 11 | NA18949.hp1 NA18964.hp2 NA18983.hp1 others(8): Show |
intron_variant | MODIFIER | c.-142-10272_-142-10 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99622702 | |||||
| chr15:99622702
|
C | CTTTTTTT others(1): Show |
205 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-142-10272_-142-10 others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99622702 | |||||
| chr15:99622702
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0011g0224others(6): Show | 9 | HG00544.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.-142-10273_-142-10 others(15): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99622702 | |||||
| chr15:99622764
|
G | A | 1 | a0004c0008t0009g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-142-10214G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622764 | ||||||
| chr15:99622769
|
C | T | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-142-10209C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622769 | ||||||
| chr15:99622803
|
T | C | 2 | a0004c0019t0028g0120a0004c0019t0028g0121 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-142-10175T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622803 | ||||||
| chr15:99622848
|
G | A | 1 | a0003c0010t0002g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-142-10130G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622848 | ||||||
| chr15:99622851
|
G | A | 1 | a0001c0001t0097g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-142-10127G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622851 | ||||||
| chr15:99622905
|
C | T | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-10073C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99622905 | ||||||
| chr15:99623030
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-9948C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99623030 | ||||||
| chr15:99623095
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-9883A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99623095 | ||||||
| chr15:99623643
|
A | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-9335A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99623643 | ||||||
| chr15:99623805
|
G | GT | 6 | a0002c0002t0007g0052a0002c0002t0014g0230a0002c0002t0030g0084others(3): Show | 6 | HG01517.hp1 HG01891.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.-142-9158dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99623805 | |||||
| chr15:99623864
|
A | G | 92 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-142-9114A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99623864 | ||||||
| chr15:99623880
|
T | C | 102 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-142-9098T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99623880 | ||||||
| chr15:99623901
|
G | T | 105 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-142-9077G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99623901 | ||||||
| chr15:99624057
|
C | T | 3 | a0003c0010t0055g0135a0003c0010t0055g0152a0003c0010t0135g0134 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-142-8921C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99624057 | ||||||
| chr15:99624080
|
A | G | 1 | a0010c0020t0049g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-142-8898A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99624080 | ||||||
| chr15:99624096
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-8882C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99624096 | ||||||
| chr15:99624169
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-8809T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99624169 | ||||||
| chr15:99624444
|
G | A | 1 | a0003c0010t0130g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-142-8534G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99624444 | ||||||
| chr15:99624622
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-142-8356G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99624622 | ||||||
| chr15:99625051
|
A | G | 2 | a0001c0004t0006g0200a0001c0004t0026g0002 | 2 | HG01261.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-142-7927A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625051 | ||||||
| chr15:99625101
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-7877T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625101 | ||||||
| chr15:99625179
|
G | A | 2 | a0001c0004t0048g0047a0001c0004t0048g0292 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-142-7799G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625179 | ||||||
| chr15:99625285
|
G | A | 2 | a0002c0002t0013g0063a0002c0002t0013g0064 | 2 | NA18991.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-142-7693G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625285 | ||||||
| chr15:99625318
|
A | G | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-142-7660A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625318 | ||||||
| chr15:99625327
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-7651A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625327 | ||||||
| chr15:99625386
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-7592G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625386 | ||||||
| chr15:99625400
|
A | G | 1 | a0002c0002t0078g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-142-7578A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625400 | ||||||
| chr15:99625449
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-7529A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625449 | ||||||
| chr15:99625479
|
C | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-7499C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625479 | ||||||
| chr15:99625550
|
C | T | 1 | a0002c0002t0008g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-142-7428C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625550 | ||||||
| chr15:99625688
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-7290G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625688 | ||||||
| chr15:99625748
|
T | C | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-142-7230T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625748 | ||||||
| chr15:99625843
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-7135C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625843 | ||||||
| chr15:99625851
|
A | G | 1 | a0001c0004t0131g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-142-7127A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625851 | ||||||
| chr15:99625852
|
T | C | 1 | a0001c0004t0107g0350 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-142-7126T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625852 | ||||||
| chr15:99625893
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-7085C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625893 | ||||||
| chr15:99625921
|
A | G | 1 | a0009c0037t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-142-7057A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99625921 | ||||||
| chr15:99626095
|
T | C | 102 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-142-6883T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626095 | ||||||
| chr15:99626217
|
T | C | 148 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(145): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-142-6761T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626217 | ||||||
| chr15:99626400
|
C | G | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-142-6578C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626400 | ||||||
| chr15:99626492
|
A | G | 1 | a0003c0003t0016g0339 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-142-6486A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626492 | ||||||
| chr15:99626529
|
G | A | 1 | a0003c0003t0116g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-142-6449G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626529 | ||||||
| chr15:99626565
|
A | G | 1 | a0001c0001t0020g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-142-6413A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626565 | ||||||
| chr15:99626680
|
G | A | 1 | a0003c0003t0002g0325 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-142-6298G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626680 | ||||||
| chr15:99626854
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-6124C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99626854 | ||||||
| chr15:99627128
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-5850C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99627128 | ||||||
| chr15:99627228
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-142-5750C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99627228 | ||||||
| chr15:99627287
|
A | G | 354 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-142-5691A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99627287 | ||||||
| chr15:99627295
|
C | T | 2 | a0001c0004t0048g0047a0001c0004t0048g0292 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-142-5683C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99627295 | ||||||
| chr15:99627312
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-5666C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99627312 | ||||||
| chr15:99627419
|
C | CA | 35 | a0001c0001t0001g0176a0001c0001t0001g0195a0001c0001t0032g0272others(32): Show | 35 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-142-5528dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99627419 | |||||
| chr15:99627419
|
C | CAA | 25 | a0001c0001t0001g0250a0001c0004t0002g0357a0001c0004t0002g0360others(22): Show | 25 | HG00438.hp2 HG00673.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-142-5529_-142-552 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99627419 | |||||
| chr15:99627419
|
C | CAAA | 12 | a0001c0004t0002g0361a0001c0004t0051g0049a0001c0004t0091g0289others(9): Show | 12 | HG01496.hp2 HG01928.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-142-5530_-142-552 others(7): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99627419 | |||||
| chr15:99627419
|
C | CAAAAAAA others(5): Show |
2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-5539_-142-552 others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99627419 | |||||
| chr15:99627419
|
CA | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-142-5528delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99627419 | |||||
| chr15:99627419
|
CAA | C | 110 | a0001c0001t0004g0035a0001c0001t0004g0037a0001c0001t0004g0043others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-142-5529_-142-552 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99627419 | |||||
| chr15:99627419
|
CAAA | C | 8 | a0001c0001t0011g0224a0001c0006t0008g0112a0001c0006t0012g0079others(5): Show | 8 | HG01169.hp1 HG01884.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-142-5530_-142-552 others(7): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99627419 | |||||
| chr15:99627768
|
T | C | 1 | a0001c0001t0011g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-142-5210T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99627768 | ||||||
| chr15:99628007
|
C | T | 1 | a0001c0007t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-142-4971C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99628007 | ||||||
| chr15:99628178
|
GTA | G | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-142-4798_-142-479 others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99628178 | |||||
| chr15:99628264
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-4714A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99628264 | ||||||
| chr15:99628268
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-4710T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99628268 | ||||||
| chr15:99628273
|
T | C | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-4705T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99628273 | ||||||
| chr15:99628707
|
T | C | 3 | a0004c0008t0009g0032a0004c0008t0009g0033a0004c0008t0009g0034 | 3 | HG00733.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-142-4271T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99628707 | ||||||
| chr15:99628736
|
G | A | 2 | a0001c0004t0049g0290a0003c0003t0098g0291 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-142-4242G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99628736 | ||||||
| chr15:99628963
|
A | AT | 13 | a0001c0001t0028g0162a0001c0005t0003g0020a0001c0005t0125g0220others(10): Show | 13 | HG01169.hp1 HG01891.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.-142-3998dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99628963 | |||||
| chr15:99628963
|
A | ATTTTTT | 45 | a0001c0001t0004g0035a0001c0001t0004g0037a0001c0001t0004g0043others(42): Show | 45 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-142-4003_-142-399 others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99628963 | |||||
| chr15:99628963
|
A | ATTTTTTT | 8 | a0001c0001t0004g0036a0001c0001t0004g0045a0001c0001t0088g0131others(5): Show | 8 | HG00735.hp2 HG01891.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-142-4004_-142-399 others(11): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99628963 | |||||
| chr15:99628963
|
AT | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-142-3998delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99628963 | |||||
| chr15:99629096
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-142-3882G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629096 | ||||||
| chr15:99629129
|
G | A | 1 | a0005c0009t0076g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-142-3849G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629129 | ||||||
| chr15:99629150
|
G | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-142-3828G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629150 | ||||||
| chr15:99629286
|
G | A | 5 | a0001c0001t0004g0035a0001c0001t0004g0045a0001c0001t0004g0046others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-3692G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629286 | ||||||
| chr15:99629310
|
A | G | 1 | a0001c0012t0066g0284 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-142-3668A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629310 | ||||||
| chr15:99629517
|
C | T | 4 | a0001c0005t0003g0013a0001c0005t0003g0020a0001c0005t0003g0022others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-3461C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629517 | ||||||
| chr15:99629539
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-142-3439G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629539 | ||||||
| chr15:99629591
|
G | A | 40 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(37): Show | 40 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-142-3387G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629591 | ||||||
| chr15:99629623
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-3355G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629623 | ||||||
| chr15:99629667
|
G | A | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-142-3311G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629667 | ||||||
| chr15:99629745
|
C | T | 5 | a0002c0002t0035g0142a0002c0002t0035g0144a0002c0002t0036g0041others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-142-3233C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629745 | ||||||
| chr15:99629807
|
G | A | 93 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(90): Show | 93 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-142-3171G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629807 | ||||||
| chr15:99629820
|
G | A | 1 | a0001c0004t0046g0343 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-142-3158G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629820 | ||||||
| chr15:99629839
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-142-3139C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629839 | ||||||
| chr15:99629888
|
C | T | 1 | a0002c0011t0001g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-142-3090C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629888 | ||||||
| chr15:99629909
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-3069C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99629909 | ||||||
| chr15:99630003
|
G | A | 2 | a0001c0004t0137g0283a0003c0003t0136g0282 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-142-2975G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99630003 | ||||||
| chr15:99630041
|
C | G | 1 | a0001c0001t0004g0271 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-142-2937C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99630041 | ||||||
| chr15:99630114
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-142-2864T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99630114 | ||||||
| chr15:99630403
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-142-2575T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99630403 | ||||||
| chr15:99630493
|
C | CT | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-142-2479dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99630493 | |||||
| chr15:99630583
|
G | T | 1 | a0001c0001t0081g0078 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-142-2395G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99630583 | ||||||
| chr15:99630830
|
C | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-2148C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99630830 | ||||||
| chr15:99631008
|
T | G | 2 | a0001c0001t0020g0236a0001c0001t0020g0259 | 2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-142-1970T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631008 | ||||||
| chr15:99631025
|
C | T | 1 | a0007c0026t0024g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-142-1953C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631025 | ||||||
| chr15:99631289
|
G | T | 2 | a0004c0008t0050g0215a0004c0008t0099g0216 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-142-1689G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631289 | ||||||
| chr15:99631337
|
A | C | 1 | a0002c0002t0056g0100 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-142-1641A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631337 | ||||||
| chr15:99631458
|
T | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-142-1520T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631458 | ||||||
| chr15:99631479
|
G | A | 138 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(135): Show | 138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-142-1499G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631479 | ||||||
| chr15:99631554
|
A | G | 1 | a0003c0003t0002g0300 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-142-1424A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631554 | ||||||
| chr15:99631612
|
C | T | 1 | a0001c0005t0125g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-142-1366C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631612 | ||||||
| chr15:99631626
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-142-1352C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99631626 | ||||||
| chr15:99632190
|
T | TAC | 4 | a0002c0002t0014g0059a0002c0002t0014g0086a0002c0002t0014g0091others(1): Show | 4 | HG00140.hp2 HG01074.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-777_-142-776d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 99632190 | |||||
| chr15:99632355
|
G | A | 1 | a0002c0014t0016g0348 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-142-623G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | chr15 | 99632355 | ||||||
| chr15:99633587
|
A | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+414A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99633587 | ||||||
| chr15:99633765
|
A | AGAGGCCA others(1650): Show |
1 | a0001c0007t0100g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.54+607_54+608insTT others(1655): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99633765 | |||||
| chr15:99633765
|
A | AGAGGCCA others(1651): Show |
1 | a0001c0001t0004g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.54+607_54+608insTT others(1656): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99633765 | |||||
| chr15:99633808
|
A | G | 3 | a0003c0003t0002g0346a0003c0022t0002g0345a0003c0022t0010g0365 | 3 | HG01081.hp2 HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.54+635A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99633808 | ||||||
| chr15:99633815
|
A | G | 2 | a0004c0019t0028g0120a0004c0019t0028g0121 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.54+642A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99633815 | ||||||
| chr15:99633867
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.54+694C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99633867 | ||||||
| chr15:99633906
|
A | G | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+733A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99633906 | ||||||
| chr15:99634346
|
A | T | 1 | a0001c0006t0005g0093 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.54+1173A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99634346 | ||||||
| chr15:99634461
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+1288G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99634461 | ||||||
| chr15:99634480
|
C | T | 1 | a0002c0002t0078g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.54+1307C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99634480 | ||||||
| chr15:99634661
|
A | G | 3 | a0001c0004t0006g0342a0001c0004t0027g0310a0001c0004t0027g0349 | 3 | HG02647.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.54+1488A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99634661 | ||||||
| chr15:99634702
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.54+1529C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99634702 | ||||||
| chr15:99635093
|
CTG | C | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0010c0020t0049g0235 | 3 | HG02145.hp1 HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.54+1924_54+1925del others(2): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99635093 | |||||
| chr15:99635203
|
C | T | 1 | a0015c0024t0038g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.54+2030C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99635203 | ||||||
| chr15:99635234
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54+2061T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99635234 | ||||||
| chr15:99635570
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54+2397C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99635570 | ||||||
| chr15:99635615
|
A | G | 2 | a0004c0019t0028g0120a0004c0019t0028g0121 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.54+2442A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99635615 | ||||||
| chr15:99635621
|
G | T | 10 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(7): Show | 10 | HG03654.hp1 NA18945.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+2448G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99635621 | ||||||
| chr15:99635727
|
T | C | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.54+2554T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99635727 | ||||||
| chr15:99635910
|
G | A | 1 | a0003c0003t0010g0364 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.54+2737G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99635910 | ||||||
| chr15:99636004
|
G | A | 1 | a0002c0011t0090g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.54+2831G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636004 | ||||||
| chr15:99636017
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.54+2844T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636017 | ||||||
| chr15:99636018
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.54+2845G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636018 | ||||||
| chr15:99636037
|
A | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.54+2864A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636037 | ||||||
| chr15:99636367
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54+3194G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636367 | ||||||
| chr15:99636410
|
G | A | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0010c0020t0049g0235 | 3 | HG02145.hp1 HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.54+3237G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636410 | ||||||
| chr15:99636501
|
A | AG | 8 | a0001c0001t0004g0035a0001c0001t0004g0043a0001c0001t0004g0045others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+3331dupG | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99636501 | |||||
| chr15:99636619
|
A | G | 1 | a0002c0002t0021g0039 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.54+3446A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636619 | ||||||
| chr15:99636783
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.54+3610T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636783 | ||||||
| chr15:99636803
|
C | CT | 112 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(109): Show | 112 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.54+3639dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99636803 | |||||
| chr15:99636913
|
G | A | 1 | a0001c0001t0020g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54+3740G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636913 | ||||||
| chr15:99636951
|
C | G | 4 | a0001c0001t0039g0268a0002c0011t0011g0159a0002c0011t0024g0157others(1): Show | 4 | HG00597.hp1 HG02129.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+3778C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636951 | ||||||
| chr15:99636982
|
G | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+3809G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99636982 | ||||||
| chr15:99637310
|
A | G | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.54+4137A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637310 | ||||||
| chr15:99637318
|
G | T | 1 | a0002c0002t0035g0144 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.54+4145G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637318 | ||||||
| chr15:99637443
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+4270T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637443 | ||||||
| chr15:99637588
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+4415T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637588 | ||||||
| chr15:99637673
|
C | T | 2 | a0002c0011t0090g0156a0016c0029t0114g0040 | 2 | HG02976.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.54+4500C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637673 | ||||||
| chr15:99637691
|
GGAGTGCA others(32): Show |
G | 1 | a0001c0001t0001g0195 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.54+4519_54+4557del others(39): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637691 | ||||||
| chr15:99637728
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.54+4555C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637728 | ||||||
| chr15:99637742
|
G | A | 352 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(349): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.54+4569G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637742 | ||||||
| chr15:99637742
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.54+4569G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637742 | ||||||
| chr15:99637784
|
A | G | 8 | a0001c0001t0004g0035a0001c0001t0004g0043a0001c0001t0004g0045others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+4611A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637784 | ||||||
| chr15:99637804
|
G | A | 1 | a0001c0004t0027g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.54+4631G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637804 | ||||||
| chr15:99637834
|
G | A | 1 | a0003c0010t0002g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.54+4661G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637834 | ||||||
| chr15:99637889
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.54+4716C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637889 | ||||||
| chr15:99637890
|
G | A | 3 | a0001c0001t0011g0242a0001c0001t0041g0186a0001c0001t0046g0180 | 3 | HG01993.hp1 HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.54+4717G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637890 | ||||||
| chr15:99637914
|
A | C | 2 | a0001c0004t0006g0200a0001c0004t0026g0002 | 2 | HG01261.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.54+4741A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99637914 | ||||||
| chr15:99638201
|
C | T | 4 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0363others(1): Show | 4 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+5028C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638201 | ||||||
| chr15:99638387
|
T | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54+5214T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638387 | ||||||
| chr15:99638442
|
C | T | 1 | a0002c0002t0005g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.54+5269C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638442 | ||||||
| chr15:99638551
|
G | A | 2 | a0001c0001t0004g0036a0001c0001t0004g0037 | 2 | NA18967.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.54+5378G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638551 | ||||||
| chr15:99638597
|
G | T | 2 | a0001c0004t0049g0290a0003c0003t0098g0291 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.54+5424G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638597 | ||||||
| chr15:99638660
|
A | G | 110 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(107): Show | 110 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.54+5487A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638660 | ||||||
| chr15:99638705
|
T | A | 1 | a0002c0002t0031g0241 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.54+5532T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638705 | ||||||
| chr15:99638816
|
A | G | 1 | a0001c0001t0028g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.54+5643A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638816 | ||||||
| chr15:99638863
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54+5690A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638863 | ||||||
| chr15:99638871
|
G | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54+5698G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99638871 | ||||||
| chr15:99639024
|
A | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+5851A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639024 | ||||||
| chr15:99639035
|
T | A | 1 | a0001c0001t0045g0226 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.54+5862T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639035 | ||||||
| chr15:99639110
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+5937C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639110 | ||||||
| chr15:99639490
|
A | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-6071A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639490 | ||||||
| chr15:99639514
|
T | C | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-6047T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639514 | ||||||
| chr15:99639553
|
C | T | 1 | a0001c0012t0066g0284 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.55-6008C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639553 | ||||||
| chr15:99639642
|
C | G | 2 | a0001c0005t0015g0025a0001c0005t0015g0027 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.55-5919C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639642 | ||||||
| chr15:99639694
|
A | G | 88 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.55-5867A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99639694 | ||||||
| chr15:99640105
|
G | A | 1 | a0001c0005t0085g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.55-5456G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640105 | ||||||
| chr15:99640130
|
C | A | 1 | a0003c0003t0002g0293 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.55-5431C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640130 | ||||||
| chr15:99640198
|
C | G | 1 | a0003c0003t0002g0315 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.55-5363C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640198 | ||||||
| chr15:99640398
|
C | T | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-5163C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640398 | ||||||
| chr15:99640559
|
C | CT | 9 | a0001c0001t0105g0255a0001c0004t0107g0350a0001c0004t0112g0354others(6): Show | 9 | HG00609.hp2 HG01496.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.55-4987dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99640559 | |||||
| chr15:99640640
|
T | A | 8 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-4921T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640640 | ||||||
| chr15:99640754
|
G | T | 2 | a0004c0008t0050g0215a0004c0008t0099g0216 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.55-4807G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640754 | ||||||
| chr15:99640839
|
C | T | 1 | a0002c0011t0090g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55-4722C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640839 | ||||||
| chr15:99640983
|
C | T | 1 | a0002c0002t0074g0252 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.55-4578C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99640983 | ||||||
| chr15:99641082
|
C | T | 1 | a0002c0002t0008g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.55-4479C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641082 | ||||||
| chr15:99641083
|
G | A | 1 | a0002c0036t0005g0313 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.55-4478G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641083 | ||||||
| chr15:99641214
|
A | G | 2 | a0001c0006t0008g0115a0015c0024t0038g0114 | 2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.55-4347A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641214 | ||||||
| chr15:99641263
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-4298C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641263 | ||||||
| chr15:99641343
|
C | T | 1 | a0001c0005t0125g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.55-4218C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641343 | ||||||
| chr15:99641442
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55-4119G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641442 | ||||||
| chr15:99641450
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.55-4111G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641450 | ||||||
| chr15:99641556
|
A | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.55-4005A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641556 | ||||||
| chr15:99641584
|
G | C | 1 | a0018c0025t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.55-3977G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641584 | ||||||
| chr15:99641636
|
C | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3925C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641636 | ||||||
| chr15:99641640
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3921A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641640 | ||||||
| chr15:99641646
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3915T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641646 | ||||||
| chr15:99641654
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.55-3907C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641654 | ||||||
| chr15:99641660
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3901T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641660 | ||||||
| chr15:99641670
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.55-3891T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641670 | ||||||
| chr15:99641678
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3883G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641678 | ||||||
| chr15:99641679
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3882T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641679 | ||||||
| chr15:99641694
|
A | G | 11 | a0005c0009t0019g0003a0005c0009t0019g0070a0005c0009t0019g0071others(8): Show | 11 | HG00597.hp2 HG01071.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-3867A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641694 | ||||||
| chr15:99641703
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55-3858G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99641703 | ||||||
| chr15:99642111
|
C | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(1): Show | 4 | HG00280.hp2 NA18962.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-3450C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99642111 | ||||||
| chr15:99642116
|
C | G | 1 | a0003c0003t0002g0319 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.55-3445C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99642116 | ||||||
| chr15:99642241
|
T | G | 2 | a0001c0001t0001g0195a0003c0003t0002g0317 | 2 | HG02015.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.55-3320T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99642241 | ||||||
| chr15:99642406
|
G | C | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55-3155G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99642406 | ||||||
| chr15:99642600
|
G | C | 1 | a0003c0003t0002g0315 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.55-2961G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99642600 | ||||||
| chr15:99642926
|
TTATGTAT others(7): Show |
T | 1 | a0001c0004t0048g0292 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.55-2623_55-2610del others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99642926 | |||||
| chr15:99642932
|
A | G | 2 | a0001c0001t0001g0195a0003c0003t0002g0317 | 2 | HG02015.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.55-2629A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99642932 | ||||||
| chr15:99643179
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55-2382G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643179 | ||||||
| chr15:99643286
|
G | A | 2 | a0002c0011t0042g0105a0002c0011t0042g0106 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.55-2275G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643286 | ||||||
| chr15:99643394
|
C | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-2167C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643394 | ||||||
| chr15:99643401
|
T | C | 2 | a0006c0015t0004g0154a0006c0015t0004g0155 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.55-2160T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643401 | ||||||
| chr15:99643452
|
G | A | 1 | a0001c0005t0138g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.55-2109G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643452 | ||||||
| chr15:99643486
|
A | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-2075A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643486 | ||||||
| chr15:99643518
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55-2043A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643518 | ||||||
| chr15:99643549
|
A | T | 1 | a0001c0006t0005g0093 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.55-2012A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643549 | ||||||
| chr15:99643592
|
A | AT | 6 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(3): Show | 6 | HG02129.hp1 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-1952dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 99643592 | |||||
| chr15:99643616
|
G | T | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.55-1945G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643616 | ||||||
| chr15:99643833
|
C | T | 2 | a0009c0021t0001g0122a0009c0021t0001g0126 | 2 | NA18947.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.55-1728C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643833 | ||||||
| chr15:99643834
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-1727G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643834 | ||||||
| chr15:99643850
|
C | A | 2 | a0009c0021t0001g0122a0009c0021t0001g0126 | 2 | NA18947.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.55-1711C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643850 | ||||||
| chr15:99643871
|
G | A | 1 | a0001c0001t0004g0271 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.55-1690G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643871 | ||||||
| chr15:99643932
|
G | A | 9 | a0001c0006t0007g0098a0002c0002t0007g0052a0002c0002t0007g0087others(6): Show | 9 | HG00673.hp2 HG02015.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.55-1629G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643932 | ||||||
| chr15:99643971
|
A | G | 1 | a0001c0005t0003g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.55-1590A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99643971 | ||||||
| chr15:99644141
|
T | C | 1 | a0002c0002t0008g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.55-1420T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644141 | ||||||
| chr15:99644169
|
G | A | 2 | a0001c0004t0137g0283a0003c0003t0136g0282 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.55-1392G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644169 | ||||||
| chr15:99644268
|
A | G | 1 | a0002c0014t0109g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.55-1293A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644268 | ||||||
| chr15:99644602
|
T | A | 1 | a0002c0002t0036g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.55-959T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644602 | ||||||
| chr15:99644604
|
T | C | 1 | a0002c0002t0036g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.55-957T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644604 | ||||||
| chr15:99644607
|
A | T | 1 | a0002c0002t0036g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.55-954A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644607 | ||||||
| chr15:99644609
|
G | T | 1 | a0002c0002t0036g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.55-952G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644609 | ||||||
| chr15:99644618
|
T | G | 1 | a0002c0014t0016g0348 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.55-943T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644618 | ||||||
| chr15:99644634
|
G | A | 1 | a0011c0023t0006g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55-927G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644634 | ||||||
| chr15:99644668
|
T | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55-893T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644668 | ||||||
| chr15:99644676
|
A | G | 39 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(36): Show | 39 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.55-885A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644676 | ||||||
| chr15:99644700
|
C | T | 355 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(352): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.55-861C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644700 | ||||||
| chr15:99644783
|
T | C | 1 | a0003c0003t0002g0293 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.55-778T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644783 | ||||||
| chr15:99644839
|
G | A | 5 | a0001c0004t0006g0285a0001c0004t0011g0366a0001c0004t0047g0296others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-722G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644839 | ||||||
| chr15:99644972
|
A | G | 1 | a0002c0002t0079g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.55-589A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644972 | ||||||
| chr15:99644994
|
T | A | 1 | a0001c0004t0048g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55-567T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99644994 | ||||||
| chr15:99645168
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-393G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645168 | ||||||
| chr15:99645207
|
C | G | 1 | a0004c0019t0028g0121 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.55-354C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645207 | ||||||
| chr15:99645212
|
T | G | 1 | a0003c0003t0116g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.55-349T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645212 | ||||||
| chr15:99645216
|
C | G | 6 | a0001c0004t0117g0311a0001c0004t0137g0283a0001c0005t0003g0335others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-345C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645216 | ||||||
| chr15:99645259
|
A | G | 7 | a0001c0001t0032g0272a0001c0005t0009g0133a0003c0010t0055g0135others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-302A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645259 | ||||||
| chr15:99645323
|
G | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.55-238G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645323 | ||||||
| chr15:99645433
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55-128G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645433 | ||||||
| chr15:99645539
|
A | G | 1 | a0001c0004t0117g0311 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.55-22A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645539 | ||||||
| chr15:99645541
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-20A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 3/11 | chr15 | 99645541 | ||||||
| chr15:99645867
|
G | A | 1 | a0001c0001t0004g0119 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.258+103G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99645867 | ||||||
| chr15:99645922
|
G | A | 1 | a0002c0002t0062g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.258+158G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99645922 | ||||||
| chr15:99646041
|
T | A | 1 | a0002c0002t0074g0252 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.258+277T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646041 | ||||||
| chr15:99646103
|
C | G | 1 | a0008c0018t0002g0338 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.258+339C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646103 | ||||||
| chr15:99646103
|
CTT | C | 19 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(16): Show | 19 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.258+340_258+341del others(2): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646103 | ||||||
| chr15:99646285
|
A | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG00323.hp2 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+521A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646285 | ||||||
| chr15:99646367
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+603G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646367 | ||||||
| chr15:99646411
|
A | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+647A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646411 | ||||||
| chr15:99646558
|
G | A | 3 | a0001c0004t0117g0311a0001c0005t0003g0335a0001c0012t0017g0336 | 3 | HG02809.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.258+794G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646558 | ||||||
| chr15:99646661
|
T | C | 62 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.258+897T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646661 | ||||||
| chr15:99646668
|
A | G | 3 | a0002c0002t0014g0059a0002c0002t0014g0091a0002c0002t0014g0092 | 3 | HG01074.hp1 HG01167.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.258+904A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646668 | ||||||
| chr15:99646801
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.258+1037C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99646801 | ||||||
| chr15:99647024
|
G | T | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.258+1260G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647024 | ||||||
| chr15:99647340
|
C | T | 2 | a0002c0002t0030g0083a0002c0002t0030g0084 | 2 | NA18949.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.258+1576C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647340 | ||||||
| chr15:99647428
|
C | G | 1 | a0003c0003t0116g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.258+1664C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647428 | ||||||
| chr15:99647440
|
C | G | 2 | a0001c0001t0032g0272a0003c0013t0032g0132 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.258+1676C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647440 | ||||||
| chr15:99647473
|
C | G | 1 | a0001c0004t0131g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.258+1709C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647473 | ||||||
| chr15:99647518
|
C | T | 1 | a0002c0002t0008g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.258+1754C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647518 | ||||||
| chr15:99647520
|
T | G | 7 | a0001c0001t0041g0170a0001c0017t0001g0123a0001c0017t0001g0187others(4): Show | 7 | HG02027.hp2 HG02074.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+1756T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647520 | ||||||
| chr15:99647552
|
T | A | 1 | a0003c0003t0052g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.258+1788T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647552 | ||||||
| chr15:99647601
|
A | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+1837A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647601 | ||||||
| chr15:99647712
|
T | G | 1 | a0003c0003t0052g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.258+1948T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647712 | ||||||
| chr15:99647768
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.258+2004A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647768 | ||||||
| chr15:99647794
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258+2030T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647794 | ||||||
| chr15:99647819
|
A | G | 1 | a0003c0010t0055g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.258+2055A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647819 | ||||||
| chr15:99647866
|
C | T | 2 | a0001c0004t0137g0283a0003c0003t0136g0282 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.258+2102C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647866 | ||||||
| chr15:99647991
|
T | C | 1 | a0005c0009t0019g0003 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.258+2227T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99647991 | ||||||
| chr15:99648018
|
T | G | 1 | a0003c0003t0052g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.258+2254T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648018 | ||||||
| chr15:99648019
|
G | C | 1 | a0003c0003t0052g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.258+2255G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648019 | ||||||
| chr15:99648039
|
C | T | 6 | a0002c0002t0013g0063a0002c0002t0013g0064a0002c0002t0013g0065others(3): Show | 6 | NA18970.hp1 NA18991.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+2275C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648039 | ||||||
| chr15:99648086
|
G | A | 1 | a0001c0001t0097g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.258+2322G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648086 | ||||||
| chr15:99648157
|
C | T | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+2393C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648157 | ||||||
| chr15:99648350
|
C | T | 9 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0214others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+2586C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648350 | ||||||
| chr15:99648670
|
A | T | 1 | a0001c0001t0020g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258+2906A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648670 | ||||||
| chr15:99648739
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.258+2975G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648739 | ||||||
| chr15:99648742
|
G | A | 81 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.258+2978G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648742 | ||||||
| chr15:99648778
|
A | G | 1 | a0003c0003t0002g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.258+3014A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648778 | ||||||
| chr15:99648819
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.258+3055C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648819 | ||||||
| chr15:99648830
|
G | A | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258+3066G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648830 | ||||||
| chr15:99648898
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+3134G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648898 | ||||||
| chr15:99648938
|
T | C | 1 | a0001c0001t0105g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.258+3174T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648938 | ||||||
| chr15:99648970
|
T | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258+3206T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99648970 | ||||||
| chr15:99649009
|
A | G | 5 | a0002c0002t0035g0142a0002c0002t0035g0144a0002c0002t0036g0041others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+3245A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99649009 | ||||||
| chr15:99649032
|
C | T | 5 | a0001c0004t0006g0285a0001c0004t0011g0366a0001c0004t0047g0296others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+3268C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99649032 | ||||||
| chr15:99649476
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.258+3712A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99649476 | ||||||
| chr15:99649477
|
A | C | 1 | a0001c0028t0095g0203 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.258+3713A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99649477 | ||||||
| chr15:99649756
|
T | G | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+3992T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99649756 | ||||||
| chr15:99649951
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+4187C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99649951 | ||||||
| chr15:99650039
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.258+4275G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99650039 | ||||||
| chr15:99650065
|
G | A | 2 | a0004c0008t0050g0215a0004c0008t0099g0216 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.258+4301G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99650065 | ||||||
| chr15:99650365
|
G | A | 100 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(97): Show | 100 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.258+4601G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99650365 | ||||||
| chr15:99650385
|
G | A | 2 | a0003c0010t0002g0197a0003c0010t0002g0198 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.258+4621G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99650385 | ||||||
| chr15:99650641
|
A | G | 7 | a0001c0001t0032g0272a0001c0005t0009g0133a0003c0010t0055g0135others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+4877A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99650641 | ||||||
| chr15:99650716
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.258+4952T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99650716 | ||||||
| chr15:99650898
|
G | A | 3 | a0001c0006t0008g0113a0001c0006t0008g0115a0015c0024t0038g0114 | 3 | HG01192.hp2 HG01261.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.258+5134G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99650898 | ||||||
| chr15:99651366
|
T | C | 1 | a0001c0001t0011g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.258+5602T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99651366 | ||||||
| chr15:99651704
|
C | T | 2 | a0003c0003t0002g0302a0003c0003t0128g0303 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.258+5940C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99651704 | ||||||
| chr15:99651788
|
A | G | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+6024A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99651788 | ||||||
| chr15:99652052
|
A | G | 2 | a0001c0001t0032g0272a0003c0013t0032g0132 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.258+6288A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652052 | ||||||
| chr15:99652079
|
A | C | 3 | a0001c0006t0021g0164a0002c0002t0007g0103a0002c0002t0057g0038 | 3 | HG00438.hp1 HG02129.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.258+6315A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652079 | ||||||
| chr15:99652193
|
T | C | 6 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0045g0226others(3): Show | 6 | HG00544.hp2 HG02056.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+6429T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652193 | ||||||
| chr15:99652198
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258+6434G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652198 | ||||||
| chr15:99652310
|
G | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(1): Show | 4 | HG00280.hp2 NA18962.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+6546G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652310 | ||||||
| chr15:99652314
|
G | A | 1 | a0002c0002t0036g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.258+6550G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652314 | ||||||
| chr15:99652335
|
C | T | 99 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(96): Show | 99 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.258+6571C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652335 | ||||||
| chr15:99652451
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+6687G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652451 | ||||||
| chr15:99652477
|
G | A | 3 | a0002c0002t0005g0101a0002c0002t0005g0102a0002c0002t0023g0056 | 3 | NA18940.hp2 NA18950.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.258+6713G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652477 | ||||||
| chr15:99652505
|
C | G | 1 | a0002c0002t0034g0261 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.258+6741C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652505 | ||||||
| chr15:99652505
|
C | T | 1 | a0001c0005t0003g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.258+6741C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652505 | ||||||
| chr15:99652563
|
C | T | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+6799C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652563 | ||||||
| chr15:99652865
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+7101G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652865 | ||||||
| chr15:99652971
|
T | C | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.258+7207T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99652971 | ||||||
| chr15:99653002
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+7238A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653002 | ||||||
| chr15:99653007
|
G | A | 5 | a0005c0009t0019g0070a0005c0009t0019g0071a0005c0009t0019g0096others(2): Show | 5 | HG00597.hp2 NA18962.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+7243G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653007 | ||||||
| chr15:99653072
|
A | G | 20 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(17): Show | 20 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.258+7308A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653072 | ||||||
| chr15:99653116
|
T | C | 4 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257others(1): Show | 4 | HG02976.hp1 HG03041.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+7352T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653116 | ||||||
| chr15:99653136
|
C | A | 1 | a0001c0007t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.258+7372C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653136 | ||||||
| chr15:99653212
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258+7448G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653212 | ||||||
| chr15:99653232
|
G | C | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+7468G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653232 | ||||||
| chr15:99653271
|
A | G | 1 | a0001c0001t0020g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258+7507A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653271 | ||||||
| chr15:99653305
|
A | G | 2 | a0001c0004t0091g0289a0001c0004t0092g0288 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.258+7541A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653305 | ||||||
| chr15:99653349
|
A | G | 1 | a0001c0004t0051g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.258+7585A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653349 | ||||||
| chr15:99653564
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.258+7800A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653564 | ||||||
| chr15:99653608
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+7844T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653608 | ||||||
| chr15:99653662
|
A | G | 1 | a0003c0003t0002g0293 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.258+7898A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653662 | ||||||
| chr15:99653784
|
T | C | 92 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.258+8020T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99653784 | ||||||
| chr15:99654003
|
T | C | 1 | a0003c0003t0002g0328 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.258+8239T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654003 | ||||||
| chr15:99654019
|
C | T | 1 | a0001c0004t0053g0374 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+8255C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654019 | ||||||
| chr15:99654028
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.258+8264C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654028 | ||||||
| chr15:99654263
|
T | C | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.258+8499T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654263 | ||||||
| chr15:99654491
|
T | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258+8727T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654491 | ||||||
| chr15:99654561
|
T | A | 4 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+8797T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654561 | ||||||
| chr15:99654577
|
A | G | 1 | a0001c0007t0001g0168 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.258+8813A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654577 | ||||||
| chr15:99654581
|
A | AG | 105 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(102): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.258+8825dupG | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99654581 | |||||
| chr15:99654581
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.258+8817A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654581 | ||||||
| chr15:99654582
|
G | C | 1 | a0001c0001t0044g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.258+8818G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654582 | ||||||
| chr15:99654583
|
G | C | 1 | a0003c0013t0002g0372 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.258+8819G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654583 | ||||||
| chr15:99654711
|
C | T | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+8947C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99654711 | ||||||
| chr15:99655078
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+9314A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655078 | ||||||
| chr15:99655247
|
G | A | 89 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.258+9483G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655247 | ||||||
| chr15:99655315
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.258+9551A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655315 | ||||||
| chr15:99655315
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.258+9551A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655315 | ||||||
| chr15:99655323
|
A | G | 1 | a0003c0003t0134g0331 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.258+9559A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655323 | ||||||
| chr15:99655389
|
G | C | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+9625G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655389 | ||||||
| chr15:99655501
|
G | T | 3 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139 | 3 | NA18957.hp2 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.258+9737G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655501 | ||||||
| chr15:99655624
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+9860C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655624 | ||||||
| chr15:99655786
|
A | C | 1 | a0002c0002t0007g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.258+10022A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99655786 | ||||||
| chr15:99656287
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+10523C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99656287 | ||||||
| chr15:99656290
|
G | A | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+10526G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99656290 | ||||||
| chr15:99656452
|
A | G | 354 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.258+10688A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99656452 | ||||||
| chr15:99656554
|
G | A | 9 | a0003c0003t0002g0304a0003c0003t0002g0305a0003c0003t0002g0306others(6): Show | 9 | HG00408.hp2 HG00423.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+10790G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99656554 | ||||||
| chr15:99656670
|
A | T | 1 | a0003c0003t0002g0368 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.258+10906A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99656670 | ||||||
| chr15:99656893
|
G | A | 1 | a0002c0002t0034g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.258+11129G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99656893 | ||||||
| chr15:99656992
|
C | T | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.258+11228C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99656992 | ||||||
| chr15:99657068
|
T | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.258+11304T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657068 | ||||||
| chr15:99657110
|
C | T | 1 | a0018c0025t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.258+11346C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657110 | ||||||
| chr15:99657130
|
C | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+11366C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657130 | ||||||
| chr15:99657144
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.258+11380C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657144 | ||||||
| chr15:99657181
|
A | C | 1 | a0001c0001t0045g0226 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.258+11417A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657181 | ||||||
| chr15:99657224
|
C | G | 1 | a0001c0001t0089g0273 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.258+11460C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657224 | ||||||
| chr15:99657312
|
T | TA | 110 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(107): Show | 110 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.258+11559dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99657312 | |||||
| chr15:99657312
|
TA | T | 7 | a0001c0001t0077g0206a0002c0002t0034g0251a0002c0002t0034g0261others(4): Show | 7 | HG00544.hp1 HG00558.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+11559delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99657312 | |||||
| chr15:99657472
|
G | A | 3 | a0001c0001t0124g0371a0003c0013t0001g0256a0003c0013t0001g0257 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+11708G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657472 | ||||||
| chr15:99657775
|
C | T | 1 | a0002c0002t0080g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.258+12011C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99657775 | ||||||
| chr15:99658044
|
A | G | 2 | a0001c0005t0015g0025a0001c0005t0015g0027 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.258+12280A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658044 | ||||||
| chr15:99658104
|
C | T | 2 | a0001c0005t0015g0025a0001c0005t0015g0027 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.258+12340C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658104 | ||||||
| chr15:99658175
|
T | C | 1 | a0003c0003t0126g0347 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.258+12411T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658175 | ||||||
| chr15:99658184
|
T | G | 1 | a0001c0004t0053g0375 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+12420T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658184 | ||||||
| chr15:99658359
|
G | A | 2 | a0002c0011t0042g0105a0002c0011t0042g0106 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.258+12595G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658359 | ||||||
| chr15:99658472
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.258+12708A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658472 | ||||||
| chr15:99658541
|
G | A | 1 | a0003c0003t0002g0324 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.258+12777G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658541 | ||||||
| chr15:99658543
|
T | G | 1 | a0001c0006t0012g0079 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.258+12779T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658543 | ||||||
| chr15:99658822
|
A | G | 5 | a0001c0001t0004g0035a0001c0001t0004g0045a0001c0001t0004g0046others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-12501A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658822 | ||||||
| chr15:99658894
|
C | T | 1 | a0002c0002t0008g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.259-12429C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99658894 | ||||||
| chr15:99659138
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-12185G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659138 | ||||||
| chr15:99659139
|
C | G | 1 | a0002c0002t0029g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.259-12184C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659139 | ||||||
| chr15:99659225
|
A | G | 144 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(141): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.259-12098A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659225 | ||||||
| chr15:99659270
|
G | A | 2 | a0002c0002t0062g0061a0016c0029t0114g0040 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.259-12053G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659270 | ||||||
| chr15:99659377
|
G | C | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259-11946G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659377 | ||||||
| chr15:99659516
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.259-11807C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659516 | ||||||
| chr15:99659933
|
A | C | 1 | a0001c0001t0020g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259-11390A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659933 | ||||||
| chr15:99659936
|
A | G | 11 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(8): Show | 11 | HG00733.hp2 HG01099.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-11387A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659936 | ||||||
| chr15:99659956
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.259-11367A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99659956 | ||||||
| chr15:99660287
|
C | T | 1 | a0001c0001t0113g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.259-11036C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660287 | ||||||
| chr15:99660437
|
C | T | 1 | a0003c0010t0002g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.259-10886C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660437 | ||||||
| chr15:99660478
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-10845G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660478 | ||||||
| chr15:99660478
|
G | C | 55 | a0001c0004t0001g0327a0001c0004t0010g0309a0001c0004t0115g0332others(52): Show | 55 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.259-10845G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660478 | ||||||
| chr15:99660553
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.259-10770G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660553 | ||||||
| chr15:99660615
|
G | T | 1 | a0001c0001t0006g0137 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.259-10708G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660615 | ||||||
| chr15:99660831
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259-10492C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660831 | ||||||
| chr15:99660852
|
T | C | 141 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.259-10471T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660852 | ||||||
| chr15:99660907
|
C | T | 1 | a0002c0002t0060g0202 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.259-10416C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99660907 | ||||||
| chr15:99661053
|
C | T | 1 | a0011c0023t0006g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.259-10270C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661053 | ||||||
| chr15:99661191
|
C | T | 2 | a0002c0002t0014g0230a0002c0002t0038g0165 | 2 | HG01175.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.259-10132C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661191 | ||||||
| chr15:99661222
|
A | G | 1 | a0001c0005t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.259-10101A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661222 | ||||||
| chr15:99661343
|
T | C | 1 | a0001c0001t0104g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.259-9980T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661343 | ||||||
| chr15:99661413
|
G | GT | 27 | a0001c0001t0001g0195a0001c0001t0001g0246a0001c0001t0020g0279others(24): Show | 27 | HG00597.hp1 HG00673.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.259-9895dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99661413 | |||||
| chr15:99661413
|
GT | G | 26 | a0001c0001t0001g0188a0001c0001t0004g0036a0001c0001t0004g0037others(23): Show | 26 | HG00323.hp1 HG00423.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-9895delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99661413 | |||||
| chr15:99661492
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-9831A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661492 | ||||||
| chr15:99661620
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259-9703T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661620 | ||||||
| chr15:99661706
|
T | A | 5 | a0002c0002t0035g0142a0002c0002t0035g0144a0002c0002t0036g0041others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-9617T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661706 | ||||||
| chr15:99661770
|
TCTATTC | T | 4 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0253others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-9549_259-9544d others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99661770 | |||||
| chr15:99661964
|
T | C | 354 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.259-9359T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661964 | ||||||
| chr15:99661982
|
C | T | 2 | a0006c0015t0004g0154a0006c0015t0004g0155 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.259-9341C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99661982 | ||||||
| chr15:99662006
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.259-9317G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662006 | ||||||
| chr15:99662021
|
G | A | 16 | a0002c0002t0013g0063a0002c0002t0013g0064a0002c0002t0013g0065others(13): Show | 16 | HG00597.hp2 HG01071.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-9302G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662021 | ||||||
| chr15:99662084
|
T | C | 4 | a0002c0002t0014g0059a0002c0002t0014g0086a0002c0002t0014g0091others(1): Show | 4 | HG00140.hp2 HG01074.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-9239T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662084 | ||||||
| chr15:99662171
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.259-9152G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662171 | ||||||
| chr15:99662264
|
G | T | 6 | a0001c0004t0117g0311a0001c0004t0137g0283a0001c0005t0003g0335others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-9059G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662264 | ||||||
| chr15:99662297
|
A | G | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-9026A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662297 | ||||||
| chr15:99662461
|
A | G | 1 | a0002c0002t0023g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.259-8862A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662461 | ||||||
| chr15:99662474
|
T | A | 1 | a0002c0002t0021g0039 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.259-8849T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662474 | ||||||
| chr15:99662506
|
G | T | 1 | a0001c0012t0063g0351 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259-8817G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662506 | ||||||
| chr15:99662527
|
T | C | 1 | a0013c0032t0005g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.259-8796T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662527 | ||||||
| chr15:99662770
|
G | A | 1 | a0002c0002t0062g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259-8553G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662770 | ||||||
| chr15:99662773
|
C | T | 2 | a0001c0007t0001g0169a0001c0007t0001g0260 | 2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.259-8550C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662773 | ||||||
| chr15:99662812
|
T | C | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-8511T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662812 | ||||||
| chr15:99662880
|
A | G | 2 | a0003c0003t0002g0321a0003c0003t0002g0368 | 2 | HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.259-8443A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99662880 | ||||||
| chr15:99663079
|
A | T | 2 | a0002c0002t0007g0103a0002c0002t0057g0038 | 2 | HG02129.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.259-8244A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663079 | ||||||
| chr15:99663162
|
G | A | 1 | a0003c0003t0118g0344 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.259-8161G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663162 | ||||||
| chr15:99663275
|
G | T | 6 | a0001c0004t0117g0311a0001c0004t0137g0283a0001c0005t0003g0335others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-8048G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663275 | ||||||
| chr15:99663316
|
A | G | 6 | a0001c0004t0117g0311a0001c0004t0137g0283a0001c0005t0003g0335others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-8007A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663316 | ||||||
| chr15:99663387
|
T | C | 2 | a0002c0002t0013g0065a0002c0002t0013g0066 | 2 | NA18970.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.259-7936T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663387 | ||||||
| chr15:99663598
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.259-7725C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663598 | ||||||
| chr15:99663814
|
T | G | 3 | a0004c0008t0009g0032a0004c0008t0009g0033a0004c0008t0009g0034 | 3 | HG00733.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-7509T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663814 | ||||||
| chr15:99663958
|
C | T | 1 | a0001c0004t0006g0200 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.259-7365C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663958 | ||||||
| chr15:99663977
|
G | C | 1 | a0002c0002t0021g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.259-7346G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99663977 | ||||||
| chr15:99664150
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-7173T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99664150 | ||||||
| chr15:99664313
|
C | G | 1 | a0001c0005t0138g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.259-7010C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99664313 | ||||||
| chr15:99664435
|
C | T | 1 | a0002c0002t0036g0041 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.259-6888C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99664435 | ||||||
| chr15:99664713
|
C | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.259-6610C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99664713 | ||||||
| chr15:99664835
|
T | A | 1 | a0002c0002t0005g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.259-6488T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99664835 | ||||||
| chr15:99664936
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-6387G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99664936 | ||||||
| chr15:99665168
|
C | T | 1 | a0002c0002t0005g0196 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.259-6155C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665168 | ||||||
| chr15:99665181
|
A | C | 1 | a0002c0011t0044g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.259-6142A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665181 | ||||||
| chr15:99665192
|
A | G | 1 | a0003c0003t0133g0330 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.259-6131A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665192 | ||||||
| chr15:99665255
|
A | G | 3 | a0001c0006t0005g0093a0001c0006t0008g0111a0001c0006t0008g0112 | 3 | HG01168.hp2 HG01169.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.259-6068A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665255 | ||||||
| chr15:99665334
|
G | A | 1 | a0001c0004t0006g0342 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-5989G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665334 | ||||||
| chr15:99665400
|
CTG | C | 106 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(103): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.259-5922_259-5921d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665400 | ||||||
| chr15:99665470
|
A | G | 3 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051 | 3 | HG03669.hp2 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.259-5853A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665470 | ||||||
| chr15:99665480
|
T | C | 91 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.259-5843T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665480 | ||||||
| chr15:99665496
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.259-5827T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665496 | ||||||
| chr15:99665503
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.259-5820G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665503 | ||||||
| chr15:99665630
|
C | T | 127 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(124): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.259-5693C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665630 | ||||||
| chr15:99665731
|
C | CA | 47 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0020g0259others(44): Show | 47 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.259-5568dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99665731 | |||||
| chr15:99665731
|
C | CAA | 7 | a0001c0001t0020g0236a0001c0004t0051g0049a0001c0004t0053g0375others(4): Show | 7 | HG00438.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-5569_259-5568d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99665731 | |||||
| chr15:99665731
|
CA | C | 49 | a0001c0001t0001g0174a0001c0001t0001g0234a0001c0001t0001g0370others(46): Show | 49 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.259-5568delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99665731 | |||||
| chr15:99665755
|
AG | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0044g0240 | 3 | HG00140.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.259-5567delG | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665755 | ||||||
| chr15:99665794
|
C | G | 2 | a0002c0002t0022g0104a0002c0002t0022g0232 | 2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.259-5529C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665794 | ||||||
| chr15:99665825
|
CAT | C | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279 | 3 | HG02572.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.259-5495_259-5494d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99665825 | |||||
| chr15:99665874
|
A | C | 3 | a0001c0001t0032g0272a0003c0013t0032g0132a0016c0029t0114g0040 | 3 | HG02451.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.259-5449A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665874 | ||||||
| chr15:99665888
|
T | TA | 8 | a0001c0001t0032g0272a0002c0002t0037g0153a0003c0010t0055g0135others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-5434dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99665888 | |||||
| chr15:99665977
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-5346A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665977 | ||||||
| chr15:99666053
|
G | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-5270G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666053 | ||||||
| chr15:99666439
|
G | A | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.259-4884G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666439 | ||||||
| chr15:99666451
|
AG | A | 10 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0361others(7): Show | 10 | HG00673.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-4871delG | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666451 | ||||||
| chr15:99666536
|
A | G | 1 | a0009c0037t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.259-4787A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666536 | ||||||
| chr15:99666548
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.259-4775C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666548 | ||||||
| chr15:99666578
|
T | TATA | 65 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0004g0035others(62): Show | 65 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.259-4713_259-4711d others(5): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99666578 | |||||
| chr15:99666578
|
T | TATAATA | 73 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0167others(70): Show | 73 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.259-4716_259-4711d others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99666578 | |||||
| chr15:99666578
|
T | TATAATAA others(2): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0064g0278others(21): Show | 25 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-4719_259-4711d others(11): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99666578 | |||||
| chr15:99666578
|
T | TATAATAA others(5): Show |
72 | a0001c0001t0001g0128a0001c0001t0011g0281a0001c0001t0039g0268others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.259-4722_259-4711d others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99666578 | |||||
| chr15:99666578
|
T | TATAATAA others(8): Show |
6 | a0001c0006t0012g0077a0002c0002t0007g0087a0002c0002t0007g0088others(3): Show | 6 | HG00673.hp2 HG02015.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-4725_259-4711d others(17): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99666578 | |||||
| chr15:99666578
|
TATA | T | 8 | a0001c0001t0001g0247a0001c0001t0041g0186a0001c0004t0052g0373others(5): Show | 8 | HG01884.hp2 HG01993.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-4713_259-4711d others(5): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99666578 | |||||
| chr15:99666578
|
TATAATA | T | 3 | a0003c0003t0002g0321a0006c0015t0004g0154a0006c0015t0004g0155 | 3 | HG02895.hp2 HG02897.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.259-4716_259-4711d others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99666578 | |||||
| chr15:99666607
|
T | C | 2 | a0004c0008t0050g0215a0004c0008t0099g0216 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.259-4716T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666607 | ||||||
| chr15:99666610
|
T | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-4713T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666610 | ||||||
| chr15:99666665
|
G | A | 6 | a0001c0004t0117g0311a0001c0004t0137g0283a0001c0005t0003g0335others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-4658G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666665 | ||||||
| chr15:99666684
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-4639T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666684 | ||||||
| chr15:99666771
|
C | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259-4552C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666771 | ||||||
| chr15:99666814
|
A | T | 1 | a0002c0002t0023g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.259-4509A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666814 | ||||||
| chr15:99666839
|
T | A | 2 | a0004c0008t0050g0215a0004c0008t0099g0216 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.259-4484T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99666839 | ||||||
| chr15:99667015
|
G | A | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279 | 3 | HG02572.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.259-4308G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667015 | ||||||
| chr15:99667086
|
A | G | 8 | a0001c0001t0032g0272a0001c0005t0009g0133a0003c0010t0055g0135others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-4237A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667086 | ||||||
| chr15:99667254
|
C | T | 2 | a0004c0008t0009g0033a0004c0008t0009g0034 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-4069C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667254 | ||||||
| chr15:99667307
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-4016G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667307 | ||||||
| chr15:99667345
|
C | T | 1 | a0001c0006t0071g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.259-3978C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667345 | ||||||
| chr15:99667569
|
C | T | 87 | a0001c0001t0081g0078a0001c0006t0005g0093a0001c0006t0005g0145others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.259-3754C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667569 | ||||||
| chr15:99667645
|
G | A | 374 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(371): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.259-3678G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667645 | ||||||
| chr15:99667679
|
T | A | 1 | a0015c0024t0038g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259-3644T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667679 | ||||||
| chr15:99667755
|
G | A | 2 | a0003c0003t0002g0300a0003c0003t0002g0301 | 2 | NA18964.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.259-3568G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667755 | ||||||
| chr15:99667868
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259-3455A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667868 | ||||||
| chr15:99667956
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-3367A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667956 | ||||||
| chr15:99667977
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259-3346A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99667977 | ||||||
| chr15:99668001
|
A | G | 6 | a0001c0004t0117g0311a0001c0004t0137g0283a0001c0005t0003g0335others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-3322A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668001 | ||||||
| chr15:99668030
|
G | A | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279 | 3 | HG02572.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.259-3293G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668030 | ||||||
| chr15:99668059
|
C | CA | 18 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(15): Show | 18 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.259-3254dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99668059 | |||||
| chr15:99668111
|
A | G | 1 | a0001c0005t0003g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259-3212A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668111 | ||||||
| chr15:99668182
|
G | A | 8 | a0001c0001t0004g0035a0001c0001t0004g0043a0001c0001t0004g0045others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-3141G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668182 | ||||||
| chr15:99668356
|
G | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-2967G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668356 | ||||||
| chr15:99668410
|
C | T | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.259-2913C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668410 | ||||||
| chr15:99668660
|
CTG | C | 102 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(99): Show | 102 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.259-2659_259-2658d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 99668660 | |||||
| chr15:99668681
|
A | G | 3 | a0001c0001t0011g0242a0001c0001t0041g0186a0001c0001t0046g0180 | 3 | HG01993.hp1 HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.259-2642A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668681 | ||||||
| chr15:99668701
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-2622C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668701 | ||||||
| chr15:99668746
|
G | A | 3 | a0003c0010t0055g0135a0003c0010t0055g0152a0003c0010t0135g0134 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.259-2577G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99668746 | ||||||
| chr15:99669221
|
G | A | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.259-2102G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669221 | ||||||
| chr15:99669225
|
G | C | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279 | 3 | HG02572.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.259-2098G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669225 | ||||||
| chr15:99669641
|
C | T | 1 | a0003c0003t0002g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.259-1682C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669641 | ||||||
| chr15:99669642
|
G | A | 16 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(13): Show | 16 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-1681G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669642 | ||||||
| chr15:99669750
|
T | G | 49 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(46): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.259-1573T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669750 | ||||||
| chr15:99669848
|
T | C | 3 | a0001c0006t0071g0089a0002c0002t0005g0057a0002c0002t0005g0110 | 3 | HG02698.hp1 HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.259-1475T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669848 | ||||||
| chr15:99669891
|
T | G | 2 | a0001c0006t0018g0231a0001c0006t0018g0233 | 2 | HG00642.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.259-1432T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669891 | ||||||
| chr15:99669898
|
T | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-1425T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669898 | ||||||
| chr15:99669986
|
A | G | 1 | a0001c0005t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.259-1337A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99669986 | ||||||
| chr15:99670102
|
G | C | 2 | a0002c0002t0033g0072a0002c0002t0033g0073 | 2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.259-1221G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99670102 | ||||||
| chr15:99670285
|
C | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259-1038C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99670285 | ||||||
| chr15:99670421
|
A | T | 1 | a0001c0005t0009g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.259-902A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99670421 | ||||||
| chr15:99670443
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.259-880C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99670443 | ||||||
| chr15:99670728
|
C | T | 1 | a0001c0005t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.259-595C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99670728 | ||||||
| chr15:99670757
|
G | T | 1 | a0001c0001t0004g0228 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.259-566G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99670757 | ||||||
| chr15:99671101
|
A | G | 5 | a0001c0001t0081g0078a0001c0006t0012g0076a0001c0006t0012g0077others(2): Show | 5 | NA18990.hp1 NA18995.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-222A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99671101 | ||||||
| chr15:99671201
|
A | G | 2 | a0001c0001t0020g0236a0001c0001t0020g0259 | 2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.259-122A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99671201 | ||||||
| chr15:99671621
|
G | A | 1 | a0001c0004t0006g0285 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.390+167G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99671621 | ||||||
| chr15:99671759
|
G | A | 20 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0361others(17): Show | 20 | HG00673.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.390+305G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99671759 | ||||||
| chr15:99671772
|
G | A | 9 | a0005c0009t0019g0070a0005c0009t0019g0071a0005c0009t0019g0096others(6): Show | 9 | HG00597.hp2 HG01071.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+318G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99671772 | ||||||
| chr15:99671839
|
C | T | 2 | a0003c0003t0002g0302a0003c0003t0128g0303 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.390+385C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99671839 | ||||||
| chr15:99671907
|
G | A | 2 | a0003c0003t0002g0054a0003c0003t0016g0053 | 2 | HG00280.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.390+453G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99671907 | ||||||
| chr15:99671913
|
G | A | 13 | a0001c0001t0025g0207a0001c0001t0025g0208a0001c0001t0025g0209others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.390+459G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99671913 | ||||||
| chr15:99672539
|
A | G | 7 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG00323.hp2 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+1085A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99672539 | ||||||
| chr15:99672598
|
C | G | 1 | a0003c0003t0116g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.390+1144C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99672598 | ||||||
| chr15:99672777
|
A | G | 1 | a0002c0002t0078g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.390+1323A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99672777 | ||||||
| chr15:99673276
|
C | A | 1 | a0003c0003t0127g0314 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.391-1117C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99673276 | ||||||
| chr15:99673343
|
G | A | 3 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279 | 3 | HG02572.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.391-1050G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99673343 | ||||||
| chr15:99673511
|
A | G | 20 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(17): Show | 20 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.391-882A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99673511 | ||||||
| chr15:99673693
|
G | T | 1 | a0001c0004t0010g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.391-700G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99673693 | ||||||
| chr15:99673858
|
CT | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.391-524delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr15 | 99673858 | |||||
| chr15:99674130
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-263G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | chr15 | 99674130 | ||||||
| chr15:99674214
|
C | CAT | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.391-176_391-175dup others(2): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr15 | 99674214 | |||||
| chr15:99674675
|
C | G | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.610+63C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674675 | ||||||
| chr15:99674706
|
A | G | 1 | a0001c0004t0048g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.610+94A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674706 | ||||||
| chr15:99674730
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.610+118T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674730 | ||||||
| chr15:99674732
|
A | C | 1 | a0001c0004t0001g0327 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.610+120A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674732 | ||||||
| chr15:99674753
|
A | T | 134 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(131): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.610+141A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674753 | ||||||
| chr15:99674802
|
A | C | 1 | a0001c0001t0105g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.610+190A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674802 | ||||||
| chr15:99674812
|
T | C | 1 | a0002c0011t0011g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.610+200T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674812 | ||||||
| chr15:99674831
|
A | G | 1 | a0001c0001t0077g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.610+219A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674831 | ||||||
| chr15:99674962
|
A | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.610+350A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99674962 | ||||||
| chr15:99675391
|
G | A | 1 | a0002c0002t0080g0211 | 1 | HG03710.hp2 | splice_region_variant&intron_variant | LOW | c.611-8G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 6/11 | chr15 | 99675391 | ||||||
| chr15:99675473
|
A | G | 1 | a0001c0001t0046g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.670+15A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99675473 | ||||||
| chr15:99675510
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.670+52C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99675510 | ||||||
| chr15:99675763
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.670+305C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99675763 | ||||||
| chr15:99675764
|
G | A | 4 | a0003c0003t0002g0304a0003c0003t0002g0306a0003c0003t0002g0307others(1): Show | 4 | HG02132.hp2 NA18984.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+306G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99675764 | ||||||
| chr15:99675856
|
T | C | 374 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(371): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.670+398T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99675856 | ||||||
| chr15:99676018
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.670+560C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676018 | ||||||
| chr15:99676098
|
TAAAC | T | 5 | a0001c0004t0011g0366a0003c0010t0055g0135a0003c0010t0055g0152others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+646_670+649del others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99676098 | |||||
| chr15:99676372
|
C | T | 1 | a0001c0005t0125g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.670+914C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676372 | ||||||
| chr15:99676437
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.670+979C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676437 | ||||||
| chr15:99676501
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670+1043C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676501 | ||||||
| chr15:99676576
|
GT | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.670+1131delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99676576 | |||||
| chr15:99676581
|
T | G | 1 | a0003c0003t0002g0301 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.670+1123T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676581 | ||||||
| chr15:99676665
|
C | T | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.670+1207C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676665 | ||||||
| chr15:99676682
|
G | A | 2 | a0009c0021t0001g0122a0009c0021t0001g0126 | 2 | NA18947.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.670+1224G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676682 | ||||||
| chr15:99676695
|
G | A | 1 | a0003c0010t0002g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+1237G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676695 | ||||||
| chr15:99676719
|
G | T | 3 | a0002c0002t0005g0101a0002c0002t0005g0102a0002c0002t0023g0056 | 3 | NA18940.hp2 NA18950.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.670+1261G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676719 | ||||||
| chr15:99676772
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.670+1314G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676772 | ||||||
| chr15:99676816
|
T | C | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.670+1358T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676816 | ||||||
| chr15:99676951
|
T | C | 1 | a0002c0002t0037g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.670+1493T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676951 | ||||||
| chr15:99676981
|
C | A | 141 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.670+1523C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99676981 | ||||||
| chr15:99677121
|
C | G | 33 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.670+1663C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99677121 | ||||||
| chr15:99677143
|
T | TA | 79 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.670+1688dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99677143 | |||||
| chr15:99677212
|
A | C | 18 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0025g0207others(15): Show | 18 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.670+1754A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99677212 | ||||||
| chr15:99677323
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670+1865G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99677323 | ||||||
| chr15:99677783
|
CAA | C | 16 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(13): Show | 16 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.670+2328_670+2329d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99677783 | |||||
| chr15:99678075
|
G | A | 3 | a0003c0010t0055g0135a0003c0010t0055g0152a0003c0010t0135g0134 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.670+2617G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678075 | ||||||
| chr15:99678260
|
T | C | 1 | a0002c0002t0034g0261 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.670+2802T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678260 | ||||||
| chr15:99678518
|
A | G | 1 | a0001c0007t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.670+3060A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678518 | ||||||
| chr15:99678568
|
G | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670+3110G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678568 | ||||||
| chr15:99678569
|
C | T | 1 | a0010c0020t0049g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.670+3111C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678569 | ||||||
| chr15:99678616
|
C | T | 1 | a0002c0002t0023g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.670+3158C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678616 | ||||||
| chr15:99678662
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.670+3204A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678662 | ||||||
| chr15:99678765
|
T | C | 3 | a0001c0001t0032g0272a0003c0013t0032g0132a0016c0029t0114g0040 | 3 | HG02451.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.670+3307T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678765 | ||||||
| chr15:99678784
|
T | C | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.670+3326T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99678784 | ||||||
| chr15:99679153
|
A | G | 106 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(103): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.670+3695A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99679153 | ||||||
| chr15:99679180
|
C | T | 5 | a0001c0005t0003g0028a0001c0005t0015g0021a0001c0005t0015g0023others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3722C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99679180 | ||||||
| chr15:99679233
|
A | G | 5 | a0001c0005t0009g0133a0003c0010t0055g0135a0003c0010t0055g0152others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3775A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99679233 | ||||||
| chr15:99679245
|
G | A | 5 | a0001c0005t0003g0028a0001c0005t0015g0021a0001c0005t0015g0023others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3787G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99679245 | ||||||
| chr15:99679922
|
A | G | 106 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(103): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.670+4464A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99679922 | ||||||
| chr15:99680100
|
T | A | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670+4642T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680100 | ||||||
| chr15:99680128
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.670+4670C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680128 | ||||||
| chr15:99680215
|
T | G | 2 | a0001c0004t0053g0374a0001c0004t0053g0375 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.670+4757T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680215 | ||||||
| chr15:99680225
|
T | G | 1 | a0002c0002t0030g0084 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.670+4767T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680225 | ||||||
| chr15:99680236
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.670+4778G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680236 | ||||||
| chr15:99680303
|
G | T | 1 | a0002c0014t0002g0326 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.670+4845G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680303 | ||||||
| chr15:99680347
|
C | CA | 5 | a0001c0001t0032g0272a0002c0002t0030g0084a0003c0003t0002g0368others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+4898dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99680347 | |||||
| chr15:99680415
|
T | C | 1 | a0003c0013t0032g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.670+4957T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680415 | ||||||
| chr15:99680458
|
T | C | 3 | a0001c0001t0032g0272a0003c0013t0032g0132a0016c0029t0114g0040 | 3 | HG02451.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.670+5000T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680458 | ||||||
| chr15:99680603
|
T | C | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.670+5145T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680603 | ||||||
| chr15:99680877
|
A | G | 1 | a0001c0005t0085g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.670+5419A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680877 | ||||||
| chr15:99680917
|
C | G | 1 | a0001c0001t0102g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.670+5459C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99680917 | ||||||
| chr15:99681130
|
A | G | 1 | a0001c0004t0131g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.670+5672A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681130 | ||||||
| chr15:99681213
|
A | G | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.670+5755A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681213 | ||||||
| chr15:99681216
|
T | A | 1 | a0002c0002t0030g0084 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.670+5758T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681216 | ||||||
| chr15:99681217
|
A | T | 1 | a0002c0002t0030g0084 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.670+5759A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681217 | ||||||
| chr15:99681518
|
A | G | 354 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.670+6060A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681518 | ||||||
| chr15:99681581
|
C | T | 142 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(139): Show | 142 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.670+6123C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681581 | ||||||
| chr15:99681585
|
T | G | 1 | a0002c0002t0014g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.670+6127T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681585 | ||||||
| chr15:99681682
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.670+6224A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681682 | ||||||
| chr15:99681716
|
C | A | 103 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+6258C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681716 | ||||||
| chr15:99682013
|
G | A | 1 | a0015c0024t0038g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.670+6555G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682013 | ||||||
| chr15:99682111
|
A | G | 4 | a0001c0001t0032g0272a0001c0005t0009g0133a0003c0013t0032g0132others(1): Show | 4 | HG01891.hp1 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+6653A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682111 | ||||||
| chr15:99682465
|
G | A | 11 | a0001c0004t0006g0285a0001c0004t0006g0342a0001c0004t0011g0366others(8): Show | 11 | HG02280.hp2 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+7007G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682465 | ||||||
| chr15:99682496
|
A | C | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.670+7038A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682496 | ||||||
| chr15:99682497
|
A | G | 2 | a0001c0006t0071g0089a0002c0002t0005g0110 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.670+7039A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682497 | ||||||
| chr15:99682586
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.670+7128G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682586 | ||||||
| chr15:99682611
|
A | C | 4 | a0001c0001t0032g0272a0001c0005t0009g0133a0003c0013t0032g0132others(1): Show | 4 | HG01891.hp1 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+7153A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682611 | ||||||
| chr15:99682692
|
G | A | 1 | a0011c0023t0006g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.670+7234G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682692 | ||||||
| chr15:99682746
|
T | G | 1 | a0002c0002t0030g0084 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.670+7288T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682746 | ||||||
| chr15:99682815
|
G | A | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.670+7357G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682815 | ||||||
| chr15:99682829
|
T | A | 2 | a0002c0002t0031g0241a0002c0002t0062g0061 | 2 | HG03831.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.670+7371T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682829 | ||||||
| chr15:99682917
|
T | C | 4 | a0001c0001t0032g0272a0001c0005t0009g0133a0003c0013t0032g0132others(1): Show | 4 | HG01891.hp1 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-7324T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682917 | ||||||
| chr15:99682950
|
A | G | 6 | a0001c0001t0006g0150a0001c0001t0026g0147a0001c0001t0027g0151others(3): Show | 6 | NA18945.hp1 NA18968.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-7291A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682950 | ||||||
| chr15:99682984
|
G | A | 105 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(102): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.671-7257G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99682984 | ||||||
| chr15:99683220
|
A | G | 1 | a0001c0007t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.671-7021A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683220 | ||||||
| chr15:99683336
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.671-6905G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683336 | ||||||
| chr15:99683389
|
T | C | 2 | a0002c0014t0007g0340a0002c0014t0007g0341 | 2 | NA19004.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.671-6852T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683389 | ||||||
| chr15:99683520
|
C | T | 1 | a0001c0007t0001g0260 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.671-6721C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683520 | ||||||
| chr15:99683580
|
A | AT | 12 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0361others(9): Show | 12 | HG00673.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.671-6652dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99683580 | |||||
| chr15:99683590
|
A | G | 1 | a0001c0001t0004g0266 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.671-6651A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683590 | ||||||
| chr15:99683686
|
G | A | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-6555G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683686 | ||||||
| chr15:99683687
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-6554A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683687 | ||||||
| chr15:99683711
|
T | TA | 61 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(58): Show | 61 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.671-6510dupA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99683711 | |||||
| chr15:99683711
|
TA | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.671-6510delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99683711 | |||||
| chr15:99683711
|
TAA | T | 9 | a0001c0001t0097g0189a0001c0007t0001g0191a0002c0002t0007g0221others(6): Show | 9 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-6511_671-6510d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99683711 | |||||
| chr15:99683910
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.671-6331G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683910 | ||||||
| chr15:99683940
|
T | C | 1 | a0002c0002t0029g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.671-6301T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99683940 | ||||||
| chr15:99684189
|
G | A | 2 | a0001c0005t0015g0025a0001c0005t0015g0027 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.671-6052G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684189 | ||||||
| chr15:99684214
|
C | A | 1 | a0002c0002t0007g0103 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.671-6027C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684214 | ||||||
| chr15:99684240
|
T | A | 1 | a0003c0010t0002g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.671-6001T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684240 | ||||||
| chr15:99684468
|
T | C | 1 | a0001c0004t0027g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671-5773T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684468 | ||||||
| chr15:99684483
|
G | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.671-5758G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684483 | ||||||
| chr15:99684499
|
T | G | 1 | a0001c0001t0120g0244 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.671-5742T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684499 | ||||||
| chr15:99684565
|
T | C | 1 | a0003c0003t0002g0322 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.671-5676T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684565 | ||||||
| chr15:99684585
|
C | T | 1 | a0001c0005t0138g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.671-5656C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684585 | ||||||
| chr15:99684714
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-5527A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684714 | ||||||
| chr15:99684735
|
A | G | 1 | a0002c0002t0062g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671-5506A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684735 | ||||||
| chr15:99684763
|
C | T | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.671-5478C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684763 | ||||||
| chr15:99684805
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671-5436T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684805 | ||||||
| chr15:99684827
|
C | G | 2 | a0003c0003t0002g0293a0003c0003t0002g0294 | 2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.671-5414C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684827 | ||||||
| chr15:99684928
|
G | A | 4 | a0002c0002t0008g0031a0002c0002t0008g0075a0002c0002t0014g0230others(1): Show | 4 | HG01175.hp1 HG01358.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-5313G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684928 | ||||||
| chr15:99684959
|
T | C | 352 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(349): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.671-5282T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99684959 | ||||||
| chr15:99685004
|
G | A | 4 | a0001c0006t0021g0164a0002c0002t0021g0097a0002c0002t0072g0130others(1): Show | 4 | HG00438.hp1 HG01934.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-5237G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99685004 | ||||||
| chr15:99685142
|
G | A | 1 | a0005c0009t0061g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.671-5099G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99685142 | ||||||
| chr15:99685421
|
G | T | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-4820G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99685421 | ||||||
| chr15:99685436
|
A | AT | 45 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(42): Show | 45 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-4793dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99685436 | |||||
| chr15:99685592
|
A | G | 1 | a0001c0001t0039g0265 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.671-4649A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99685592 | ||||||
| chr15:99685630
|
A | G | 1 | a0003c0003t0016g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.671-4611A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99685630 | ||||||
| chr15:99685764
|
C | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671-4477C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99685764 | ||||||
| chr15:99685933
|
T | C | 1 | a0004c0008t0009g0032 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.671-4308T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99685933 | ||||||
| chr15:99686041
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.671-4200G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686041 | ||||||
| chr15:99686290
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.671-3951T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686290 | ||||||
| chr15:99686373
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.671-3868A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686373 | ||||||
| chr15:99686508
|
C | T | 1 | a0011c0023t0006g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.671-3733C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686508 | ||||||
| chr15:99686620
|
C | T | 18 | a0001c0005t0003g0013a0001c0005t0003g0016a0001c0005t0003g0018others(15): Show | 18 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.671-3621C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686620 | ||||||
| chr15:99686737
|
C | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671-3504C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686737 | ||||||
| chr15:99686872
|
T | A | 1 | a0003c0003t0098g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.671-3369T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686872 | ||||||
| chr15:99686873
|
A | G | 1 | a0003c0003t0098g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.671-3368A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686873 | ||||||
| chr15:99686920
|
A | AT | 100 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.671-3311dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99686920 | |||||
| chr15:99687025
|
C | T | 1 | a0001c0017t0001g0123 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.671-3216C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687025 | ||||||
| chr15:99687049
|
C | CT | 80 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(77): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.671-3191dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99687049 | |||||
| chr15:99687084
|
C | CT | 175 | a0001c0001t0032g0272a0001c0001t0039g0265a0001c0001t0039g0268others(172): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.671-3132dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99687084 | |||||
| chr15:99687084
|
C | CTT | 26 | a0001c0001t0105g0255a0001c0004t0011g0366a0001c0004t0049g0290others(23): Show | 26 | HG00408.hp2 HG00438.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.671-3133_671-3132d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99687084 | |||||
| chr15:99687084
|
CT | C | 6 | a0001c0001t0001g0370a0001c0001t0004g0035a0001c0001t0064g0278others(3): Show | 6 | HG00621.hp1 HG01515.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-3132delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 99687084 | |||||
| chr15:99687090
|
T | TC | 3 | a0001c0001t0011g0242a0002c0002t0008g0181a0003c0013t0002g0372 | 3 | HG01123.hp1 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671-3151_671-3150i others(3): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687090 | ||||||
| chr15:99687091
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.671-3150T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687091 | ||||||
| chr15:99687092
|
T | C | 4 | a0001c0001t0001g0370a0001c0001t0102g0163a0002c0002t0068g0160others(1): Show | 4 | HG00621.hp1 HG01081.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-3149T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687092 | ||||||
| chr15:99687093
|
T | C | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671-3148T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687093 | ||||||
| chr15:99687109
|
T | G | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.671-3132T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687109 | ||||||
| chr15:99687342
|
C | T | 1 | a0001c0006t0018g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.671-2899C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687342 | ||||||
| chr15:99687604
|
C | G | 1 | a0003c0013t0002g0372 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.671-2637C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687604 | ||||||
| chr15:99687608
|
T | C | 2 | a0002c0011t0042g0105a0002c0011t0042g0106 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.671-2633T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687608 | ||||||
| chr15:99687630
|
A | G | 100 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.671-2611A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687630 | ||||||
| chr15:99687887
|
A | G | 1 | a0004c0008t0009g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-2354A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687887 | ||||||
| chr15:99687902
|
T | A | 1 | a0003c0013t0001g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.671-2339T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687902 | ||||||
| chr15:99687955
|
A | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671-2286A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99687955 | ||||||
| chr15:99688138
|
T | C | 1 | a0001c0001t0089g0273 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.671-2103T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688138 | ||||||
| chr15:99688254
|
A | G | 1 | a0016c0029t0114g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-1987A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688254 | ||||||
| chr15:99688434
|
T | C | 1 | a0001c0001t0004g0271 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.671-1807T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688434 | ||||||
| chr15:99688486
|
G | C | 2 | a0001c0004t0091g0289a0001c0004t0092g0288 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.671-1755G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688486 | ||||||
| chr15:99688493
|
C | G | 5 | a0002c0002t0035g0142a0002c0002t0035g0144a0002c0002t0036g0041others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1748C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688493 | ||||||
| chr15:99688614
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.671-1627G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688614 | ||||||
| chr15:99688711
|
C | G | 3 | a0003c0010t0055g0135a0003c0010t0055g0152a0003c0010t0135g0134 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.671-1530C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688711 | ||||||
| chr15:99688735
|
C | T | 141 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.671-1506C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688735 | ||||||
| chr15:99688736
|
A | G | 150 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.671-1505A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688736 | ||||||
| chr15:99688761
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.671-1480G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688761 | ||||||
| chr15:99688856
|
G | A | 20 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0361others(17): Show | 20 | HG00673.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.671-1385G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688856 | ||||||
| chr15:99689025
|
A | G | 109 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(106): Show | 109 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.671-1216A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689025 | ||||||
| chr15:99689055
|
G | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.671-1186G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689055 | ||||||
| chr15:99689095
|
A | G | 1 | a0001c0006t0018g0231 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.671-1146A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689095 | ||||||
| chr15:99689317
|
A | C | 1 | a0002c0002t0023g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.671-924A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689317 | ||||||
| chr15:99689526
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.671-715G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689526 | ||||||
| chr15:99689556
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.671-685C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689556 | ||||||
| chr15:99689669
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.671-572C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689669 | ||||||
| chr15:99689696
|
G | T | 2 | a0001c0001t0032g0272a0003c0013t0032g0132 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.671-545G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689696 | ||||||
| chr15:99689733
|
G | C | 9 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0214others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-508G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689733 | ||||||
| chr15:99689859
|
A | G | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671-382A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689859 | ||||||
| chr15:99689878
|
C | T | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.671-363C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689878 | ||||||
| chr15:99689940
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.671-301G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689940 | ||||||
| chr15:99689964
|
A | T | 1 | a0002c0002t0008g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.671-277A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99689964 | ||||||
| chr15:99690103
|
G | A | 1 | a0003c0003t0002g0318 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.671-138G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99690103 | ||||||
| chr15:99690585
|
A | G | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.858+157A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99690585 | ||||||
| chr15:99690703
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(330): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.858+275T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99690703 | ||||||
| chr15:99690828
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.858+400G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99690828 | ||||||
| chr15:99690837
|
G | A | 4 | a0002c0002t0014g0059a0002c0002t0014g0086a0002c0002t0014g0091others(1): Show | 4 | HG00140.hp2 HG01074.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+409G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99690837 | ||||||
| chr15:99690862
|
C | A | 3 | a0001c0005t0003g0013a0001c0005t0003g0022a0001c0005t0003g0026 | 3 | HG02280.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.858+434C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99690862 | ||||||
| chr15:99690968
|
C | T | 1 | a0002c0002t0082g0095 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.858+540C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99690968 | ||||||
| chr15:99691100
|
G | GT | 56 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.858+689dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99691100 | |||||
| chr15:99691100
|
G | GTT | 19 | a0001c0001t0089g0273a0001c0004t0002g0357a0001c0004t0002g0360others(16): Show | 19 | HG00673.hp1 HG01099.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.858+688_858+689dup others(2): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99691100 | |||||
| chr15:99691100
|
G | GTTT | 154 | a0001c0001t0001g0048a0001c0001t0001g0124a0001c0001t0001g0127others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.858+687_858+689dup others(3): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99691100 | |||||
| chr15:99691100
|
G | GTTTT | 13 | a0001c0001t0001g0001a0001c0001t0001g0249a0001c0004t0091g0289others(10): Show | 14 | HG00733.hp2 HG02015.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.858+686_858+689dup others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99691100 | |||||
| chr15:99691100
|
GT | G | 11 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0020g0279others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.858+689delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99691100 | |||||
| chr15:99691225
|
G | A | 333 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(330): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.858+797G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691225 | ||||||
| chr15:99691233
|
T | C | 1 | a0001c0001t0011g0281 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.858+805T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691233 | ||||||
| chr15:99691339
|
A | G | 1 | a0003c0010t0002g0197 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.858+911A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691339 | ||||||
| chr15:99691404
|
T | C | 4 | a0001c0012t0017g0352a0001c0012t0017g0353a0001c0012t0017g0367others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+976T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691404 | ||||||
| chr15:99691458
|
G | A | 1 | a0001c0006t0018g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.858+1030G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691458 | ||||||
| chr15:99691472
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.858+1044C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691472 | ||||||
| chr15:99691487
|
C | T | 10 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(7): Show | 10 | HG03654.hp1 NA18945.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.858+1059C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691487 | ||||||
| chr15:99691555
|
G | A | 2 | a0001c0004t0091g0289a0001c0004t0092g0288 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.858+1127G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691555 | ||||||
| chr15:99691567
|
G | A | 1 | a0003c0010t0003g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.858+1139G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691567 | ||||||
| chr15:99691628
|
G | T | 59 | a0001c0004t0001g0327a0001c0004t0010g0309a0001c0004t0115g0332others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.858+1200G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691628 | ||||||
| chr15:99691711
|
G | A | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.858+1283G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691711 | ||||||
| chr15:99691815
|
A | G | 1 | a0001c0005t0009g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.858+1387A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691815 | ||||||
| chr15:99691959
|
G | A | 1 | a0001c0004t0026g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.858+1531G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99691959 | ||||||
| chr15:99692026
|
A | G | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.858+1598A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99692026 | ||||||
| chr15:99692032
|
C | A | 112 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(109): Show | 112 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.858+1604C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99692032 | ||||||
| chr15:99692033
|
T | A | 112 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(109): Show | 112 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.858+1605T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99692033 | ||||||
| chr15:99692287
|
C | G | 2 | a0001c0001t0028g0162a0004c0019t0028g0121 | 2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.858+1859C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99692287 | ||||||
| chr15:99692341
|
T | G | 1 | a0003c0003t0002g0317 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.858+1913T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99692341 | ||||||
| chr15:99693083
|
G | C | 2 | a0003c0010t0055g0135a0003c0010t0135g0134 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.858+2655G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693083 | ||||||
| chr15:99693189
|
G | A | 1 | a0003c0003t0002g0299 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.858+2761G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693189 | ||||||
| chr15:99693301
|
G | A | 3 | a0003c0010t0055g0135a0003c0010t0055g0152a0003c0010t0135g0134 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.858+2873G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693301 | ||||||
| chr15:99693340
|
G | C | 2 | a0002c0002t0012g0107a0002c0002t0075g0109 | 2 | NA18964.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.858+2912G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693340 | ||||||
| chr15:99693399
|
C | T | 1 | a0002c0002t0013g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.858+2971C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693399 | ||||||
| chr15:99693425
|
ACACACAC others(13): Show |
A | 1 | a0003c0003t0002g0294 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.858+3001_858+3020d others(22): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99693425 | |||||
| chr15:99693517
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.858+3089C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693517 | ||||||
| chr15:99693931
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.858+3503C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693931 | ||||||
| chr15:99693953
|
A | G | 1 | a0003c0010t0130g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.858+3525A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99693953 | ||||||
| chr15:99694052
|
A | G | 1 | a0002c0002t0023g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.858+3624A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99694052 | ||||||
| chr15:99694470
|
A | G | 146 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.858+4042A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99694470 | ||||||
| chr15:99694701
|
T | A | 143 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(140): Show | 143 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.858+4273T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99694701 | ||||||
| chr15:99694917
|
G | C | 1 | a0011c0023t0006g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.858+4489G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99694917 | ||||||
| chr15:99694982
|
G | GT | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.858+4566dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99694982 | |||||
| chr15:99694982
|
GT | G | 115 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0006g0150others(112): Show | 115 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.858+4566delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99694982 | |||||
| chr15:99694982
|
GTT | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.858+4565_858+4566d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99694982 | |||||
| chr15:99694994
|
T | C | 1 | a0001c0005t0003g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.858+4566T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99694994 | ||||||
| chr15:99695008
|
C | T | 1 | a0001c0004t0052g0373 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.858+4580C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695008 | ||||||
| chr15:99695023
|
C | T | 5 | a0002c0002t0035g0142a0002c0002t0035g0144a0002c0002t0036g0041others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.858+4595C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695023 | ||||||
| chr15:99695072
|
C | T | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.858+4644C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695072 | ||||||
| chr15:99695149
|
T | A | 2 | a0014c0030t0069g0276a0016c0029t0114g0040 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.858+4721T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695149 | ||||||
| chr15:99695150
|
T | G | 2 | a0014c0030t0069g0276a0016c0029t0114g0040 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.858+4722T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695150 | ||||||
| chr15:99695151
|
T | A | 2 | a0014c0030t0069g0276a0016c0029t0114g0040 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.858+4723T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695151 | ||||||
| chr15:99695160
|
T | A | 2 | a0014c0030t0069g0276a0016c0029t0114g0040 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.858+4732T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695160 | ||||||
| chr15:99695301
|
A | T | 2 | a0001c0001t0032g0272a0003c0013t0032g0132 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.858+4873A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695301 | ||||||
| chr15:99695387
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.858+4959G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695387 | ||||||
| chr15:99695519
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.858+5091G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695519 | ||||||
| chr15:99695541
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0024g0274 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.858+5113_858+5114i others(17): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695541 | ||||||
| chr15:99695541
|
T | TGTGTGTG others(16): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0178a0001c0001t0103g0210 | 3 | HG01433.hp2 NA18949.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.858+5113_858+5114i others(25): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695541 | ||||||
| chr15:99695541
|
T | TTG | 18 | a0001c0001t0020g0279a0001c0004t0002g0357a0001c0004t0002g0360others(15): Show | 18 | HG00673.hp1 HG01081.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.858+5141_858+5142d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTG | 6 | a0001c0001t0020g0236a0001c0001t0020g0259a0001c0001t0124g0371others(3): Show | 6 | HG00099.hp1 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+5139_858+5142d others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(1): Show |
81 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.858+5135_858+5142d others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(3): Show |
11 | a0001c0001t0028g0162a0001c0001t0032g0272a0001c0005t0125g0220others(8): Show | 11 | HG00735.hp1 HG01175.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.858+5133_858+5142d others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(5): Show |
6 | a0001c0006t0018g0231a0001c0028t0095g0203a0002c0002t0013g0064others(3): Show | 6 | HG01258.hp2 HG02451.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.858+5131_858+5142d others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(7): Show |
14 | a0001c0001t0004g0271a0001c0001t0046g0180a0001c0001t0077g0206others(11): Show | 14 | HG00544.hp1 HG00609.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.858+5129_858+5142d others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(9): Show |
23 | a0001c0001t0001g0192a0001c0001t0004g0036a0001c0001t0004g0037others(20): Show | 23 | HG00544.hp2 HG00733.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.858+5127_858+5142d others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(11): Show |
12 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0004g0035others(9): Show | 12 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.858+5125_858+5142d others(20): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(13): Show |
10 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0238others(7): Show | 10 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.858+5123_858+5142d others(22): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(15): Show |
31 | a0001c0001t0001g0048a0001c0001t0001g0167a0001c0001t0001g0174others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.858+5121_858+5142d others(24): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(17): Show |
7 | a0001c0001t0001g0245a0001c0001t0011g0281a0001c0001t0102g0163others(4): Show | 7 | HG00621.hp1 HG01515.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.858+5119_858+5142d others(26): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(19): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0128others(7): Show | 11 | HG02738.hp2 HG03490.hp1 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.858+5117_858+5142d others(28): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(21): Show |
4 | a0001c0001t0001g0179a0001c0001t0001g0247a0001c0017t0001g0123others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+5115_858+5142d others(30): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
T | TTGTGTGT others(52): Show |
1 | a0001c0001t0025g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.858+5142_858+5143i others(61): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695541
|
TTG | T | 4 | a0001c0004t0051g0050a0002c0011t0042g0105a0002c0011t0042g0106others(1): Show | 4 | HG02083.hp1 HG02132.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+5141_858+5142d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695541 | |||||
| chr15:99695784
|
G | A | 1 | a0001c0001t0006g0150 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.858+5356G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695784 | ||||||
| chr15:99695855
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.858+5427G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695855 | ||||||
| chr15:99695859
|
CAA | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.858+5444_858+5445d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99695859 | |||||
| chr15:99696046
|
G | C | 140 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.858+5618G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696046 | ||||||
| chr15:99696111
|
A | G | 2 | a0001c0006t0071g0089a0002c0002t0005g0110 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.858+5683A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696111 | ||||||
| chr15:99696175
|
A | G | 1 | a0001c0007t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.858+5747A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696175 | ||||||
| chr15:99696259
|
A | T | 7 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG00323.hp2 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.858+5831A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696259 | ||||||
| chr15:99696389
|
A | G | 1 | a0001c0001t0011g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.858+5961A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696389 | ||||||
| chr15:99696517
|
A | C | 2 | a0006c0015t0004g0154a0006c0015t0004g0155 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.858+6089A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696517 | ||||||
| chr15:99696581
|
G | C | 1 | a0003c0003t0002g0305 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.858+6153G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696581 | ||||||
| chr15:99696754
|
A | G | 1 | a0001c0001t0020g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.858+6326A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696754 | ||||||
| chr15:99696822
|
C | G | 12 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0361others(9): Show | 12 | HG00673.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.858+6394C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696822 | ||||||
| chr15:99696823
|
C | T | 1 | a0001c0004t0052g0373 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.858+6395C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696823 | ||||||
| chr15:99696825
|
C | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(349): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.858+6397C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696825 | ||||||
| chr15:99696980
|
T | G | 1 | a0003c0003t0054g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.859-6382T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99696980 | ||||||
| chr15:99697008
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.859-6354C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697008 | ||||||
| chr15:99697054
|
TA | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.859-6297delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99697054 | |||||
| chr15:99697207
|
A | G | 1 | a0013c0032t0005g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.859-6155A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697207 | ||||||
| chr15:99697351
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.859-6011C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697351 | ||||||
| chr15:99697437
|
G | A | 1 | a0001c0004t0047g0296 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.859-5925G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697437 | ||||||
| chr15:99697457
|
AT | A | 3 | a0001c0001t0001g0280a0014c0030t0069g0276a0016c0029t0114g0040 | 3 | HG01891.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.859-5902delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99697457 | |||||
| chr15:99697459
|
T | TA | 3 | a0002c0002t0005g0108a0002c0002t0013g0065a0002c0002t0013g0066 | 3 | HG03017.hp2 NA18970.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.859-5903_859-5902i others(3): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697459 | ||||||
| chr15:99697460
|
T | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.859-5902T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697460 | ||||||
| chr15:99697477
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.859-5885A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697477 | ||||||
| chr15:99697487
|
TAAAG | T | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.859-5874_859-5871d others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697487 | ||||||
| chr15:99697571
|
AGAAAT | A | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-5786_859-5782d others(7): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99697571 | |||||
| chr15:99697644
|
A | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859-5718A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697644 | ||||||
| chr15:99697665
|
A | G | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-5697A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697665 | ||||||
| chr15:99697720
|
C | A | 1 | a0003c0003t0002g0323 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.859-5642C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697720 | ||||||
| chr15:99697806
|
C | T | 5 | a0002c0002t0035g0142a0002c0002t0035g0144a0002c0002t0036g0041others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.859-5556C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697806 | ||||||
| chr15:99697814
|
C | T | 272 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(269): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.859-5548C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697814 | ||||||
| chr15:99697904
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.859-5458C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697904 | ||||||
| chr15:99698160
|
C | T | 108 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(105): Show | 108 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.859-5202C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698160 | ||||||
| chr15:99698177
|
T | C | 1 | a0001c0005t0015g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.859-5185T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698177 | ||||||
| chr15:99698187
|
G | A | 6 | a0001c0001t0041g0170a0001c0017t0001g0123a0001c0017t0001g0187others(3): Show | 6 | HG02027.hp2 HG02074.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-5175G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698187 | ||||||
| chr15:99698366
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.859-4996C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698366 | ||||||
| chr15:99698413
|
T | C | 1 | a0003c0003t0136g0282 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.859-4949T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698413 | ||||||
| chr15:99698514
|
T | C | 108 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(105): Show | 108 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.859-4848T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698514 | ||||||
| chr15:99698517
|
G | T | 108 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(105): Show | 108 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.859-4845G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698517 | ||||||
| chr15:99698519
|
G | C | 1 | a0001c0005t0138g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.859-4843G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698519 | ||||||
| chr15:99698521
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.859-4841G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698521 | ||||||
| chr15:99698595
|
C | G | 2 | a0001c0004t0049g0290a0003c0003t0098g0291 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.859-4767C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698595 | ||||||
| chr15:99698605
|
C | G | 1 | a0001c0004t0132g0359 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.859-4757C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698605 | ||||||
| chr15:99698906
|
G | A | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-4456G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698906 | ||||||
| chr15:99698974
|
T | C | 1 | a0011c0023t0006g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.859-4388T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99698974 | ||||||
| chr15:99699068
|
A | C | 2 | a0001c0004t0091g0289a0001c0004t0092g0288 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.859-4294A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699068 | ||||||
| chr15:99699094
|
C | T | 1 | a0001c0007t0040g0118 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.859-4268C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699094 | ||||||
| chr15:99699146
|
T | C | 2 | a0001c0004t0046g0343a0017c0034t0111g0308 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.859-4216T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699146 | ||||||
| chr15:99699153
|
C | T | 1 | a0003c0010t0130g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.859-4209C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699153 | ||||||
| chr15:99699159
|
T | C | 1 | a0001c0004t0027g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.859-4203T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699159 | ||||||
| chr15:99699171
|
G | T | 1 | a0003c0003t0126g0347 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.859-4191G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699171 | ||||||
| chr15:99699204
|
A | G | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-4158A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699204 | ||||||
| chr15:99699269
|
A | G | 2 | a0006c0015t0004g0154a0006c0015t0004g0155 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.859-4093A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699269 | ||||||
| chr15:99699341
|
T | C | 276 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0004g0035others(273): Show | 276 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.859-4021T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699341 | ||||||
| chr15:99699343
|
A | G | 1 | a0001c0004t0001g0327 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.859-4019A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699343 | ||||||
| chr15:99699454
|
G | A | 1 | a0003c0003t0119g0287 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.859-3908G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699454 | ||||||
| chr15:99699461
|
G | GCTGTTTT others(15): Show |
1 | a0001c0001t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.859-3896_859-3875d others(24): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699461 | |||||
| chr15:99699508
|
CTG | C | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.859-3852_859-3851d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699508 | |||||
| chr15:99699712
|
G | T | 1 | a0004c0019t0028g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.859-3650G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699712 | ||||||
| chr15:99699813
|
A | G | 1 | a0001c0004t0006g0200 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.859-3549A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699813 | ||||||
| chr15:99699888
|
G | C | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-3474G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699888 | ||||||
| chr15:99699905
|
G | A | 10 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(7): Show | 10 | HG03654.hp1 NA18945.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.859-3457G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699905 | ||||||
| chr15:99699952
|
A | ATG | 5 | a0001c0001t0032g0272a0001c0006t0008g0111a0001c0006t0008g0112others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.859-3378_859-3377d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699952 | |||||
| chr15:99699952
|
A | ATGTG | 18 | a0001c0001t0004g0228a0001c0001t0004g0266a0001c0001t0004g0275others(15): Show | 18 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.859-3380_859-3377d others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699952 | |||||
| chr15:99699952
|
A | ATGTGTG | 12 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(9): Show | 12 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.859-3382_859-3377d others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699952 | |||||
| chr15:99699952
|
A | ATGTGTGT others(3): Show |
1 | a0007c0026t0024g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.859-3386_859-3377d others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699952 | |||||
| chr15:99699952
|
A | ATGTGTGT others(7): Show |
2 | a0006c0015t0004g0154a0006c0015t0004g0155 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.859-3390_859-3377d others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699952 | |||||
| chr15:99699952
|
ATGTG | A | 20 | a0001c0005t0003g0012a0001c0005t0003g0013a0001c0005t0003g0016others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.859-3380_859-3377d others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699952 | |||||
| chr15:99699956
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.859-3397_859-3396i others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699956 | |||||
| chr15:99699960
|
G | GTGTGTGT others(1): Show |
4 | a0001c0004t0006g0200a0001c0004t0026g0002a0001c0004t0091g0289others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-3395_859-3394i others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699960 | |||||
| chr15:99699962
|
G | GTGTGTT | 3 | a0001c0004t0048g0047a0001c0004t0048g0292a0001c0004t0137g0283 | 3 | HG02055.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.859-3395_859-3394i others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699962 | |||||
| chr15:99699964
|
G | GTGTT | 12 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(9): Show | 12 | HG00733.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.859-3395_859-3394i others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699964 | |||||
| chr15:99699966
|
G | GTT | 9 | a0001c0004t0010g0309a0003c0003t0002g0299a0003c0003t0002g0300others(6): Show | 9 | HG00609.hp1 HG00639.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.859-3395_859-3394i others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699966 | |||||
| chr15:99699966
|
G | T | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-3396G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699966 | ||||||
| chr15:99699968
|
G | T | 102 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0028g0162others(99): Show | 102 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.859-3394G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699968 | ||||||
| chr15:99699980
|
GTGTGTA | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0247 | 3 | NA18961.hp2 NA18995.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.859-3380_859-3375d others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699980 | |||||
| chr15:99699982
|
GTGTA | G | 60 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0167others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.859-3378_859-3375d others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699982 | |||||
| chr15:99699984
|
GTA | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0006g0137others(73): Show | 77 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.859-3363_859-3362d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699984 | |||||
| chr15:99699984
|
GTATA | G | 26 | a0001c0001t0001g0048a0001c0001t0001g0192a0001c0001t0020g0236others(23): Show | 26 | HG00099.hp2 HG00735.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.859-3365_859-3362d others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699984 | |||||
| chr15:99699984
|
GTATATA | G | 11 | a0001c0001t0011g0224a0001c0001t0064g0278a0001c0006t0005g0145others(8): Show | 11 | HG01934.hp2 HG02523.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.859-3367_859-3362d others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99699984 | |||||
| chr15:99699986
|
A | G | 176 | a0001c0001t0001g0222a0001c0001t0001g0369a0001c0001t0001g0370others(173): Show | 176 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.859-3376A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699986 | ||||||
| chr15:99699988
|
A | G | 242 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0004g0035others(239): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.859-3374A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699988 | ||||||
| chr15:99699990
|
A | G | 128 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(125): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.859-3372A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699990 | ||||||
| chr15:99699992
|
A | G | 8 | a0001c0001t0024g0274a0001c0001t0089g0273a0001c0001t0113g0148others(5): Show | 8 | HG01071.hp1 HG02015.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.859-3370A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699992 | ||||||
| chr15:99699994
|
A | G | 1 | a0002c0002t0033g0073 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.859-3368A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99699994 | ||||||
| chr15:99700007
|
G | A | 130 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0028g0162others(127): Show | 130 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.859-3355G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700007 | ||||||
| chr15:99700022
|
ACTAATTT others(7): Show |
A | 1 | a0001c0005t0138g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.859-3339_859-3326d others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700022 | ||||||
| chr15:99700040
|
AGTAGAGA others(132): Show |
A | 1 | a0003c0003t0002g0323 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.859-3318_859-3180d others(2): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700040 | |||||
| chr15:99700057
|
G | A | 1 | a0001c0005t0003g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.859-3305G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700057 | ||||||
| chr15:99700091
|
C | G | 133 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0028g0162others(130): Show | 133 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.859-3271C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700091 | ||||||
| chr15:99700096
|
C | T | 132 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0028g0162others(129): Show | 132 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.859-3266C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700096 | ||||||
| chr15:99700139
|
T | C | 12 | a0001c0001t0001g0188a0001c0001t0001g0243a0002c0002t0014g0091others(9): Show | 12 | HG01074.hp1 HG01167.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.859-3223T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700139 | ||||||
| chr15:99700168
|
G | A | 1 | a0004c0008t0009g0253 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.859-3194G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700168 | ||||||
| chr15:99700180
|
GTA | G | 15 | a0001c0004t0107g0350a0001c0004t0112g0354a0001c0005t0009g0212others(12): Show | 15 | HG01099.hp2 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.859-3175_859-3174d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700180 | |||||
| chr15:99700183
|
T | TACACAC | 6 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG00323.hp2 HG01255.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-3178_859-3177i others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700183 | |||||
| chr15:99700183
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0128a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG00140.hp1 HG00738.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-3178_859-3177i others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700183 | |||||
| chr15:99700183
|
T | TACACACA others(7): Show |
1 | a0001c0001t0044g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.859-3178_859-3177i others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700183 | |||||
| chr15:99700185
|
T | C | 15 | a0001c0001t0001g0128a0001c0001t0001g0174a0001c0001t0001g0182others(12): Show | 15 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.859-3177T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700185 | ||||||
| chr15:99700185
|
T | TAC | 105 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0004g0043others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.859-3176_859-3175i others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700185
|
T | TACAC | 13 | a0001c0001t0004g0036a0001c0001t0004g0037a0001c0001t0124g0371others(10): Show | 13 | HG01123.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.859-3176_859-3175i others(6): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700185
|
T | TACACAC | 8 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(5): Show | 9 | HG00099.hp2 HG01109.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.859-3176_859-3175i others(8): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700185
|
T | TACACACA others(1): Show |
24 | a0001c0001t0001g0167a0001c0001t0001g0247a0001c0001t0004g0045others(21): Show | 24 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.859-3176_859-3175i others(10): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700185
|
T | TACACACA others(3): Show |
51 | a0001c0001t0001g0127a0001c0001t0001g0176a0001c0001t0001g0178others(48): Show | 51 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.859-3176_859-3175i others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700185
|
T | TACACACA others(5): Show |
9 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0222others(6): Show | 9 | HG00733.hp1 HG02630.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.859-3176_859-3175i others(14): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700185
|
T | TACACACA others(7): Show |
1 | a0001c0007t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.859-3176_859-3175i others(16): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700185
|
T | TACACACA others(9): Show |
2 | a0001c0001t0105g0255a0004c0019t0028g0120 | 2 | HG02056.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.859-3176_859-3175i others(18): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700185 | |||||
| chr15:99700187
|
T | C | 331 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.859-3175T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700187 | ||||||
| chr15:99700204
|
A | ACACACAC others(3): Show |
1 | a0007c0026t0024g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.859-3149_859-3148i others(12): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700204 | |||||
| chr15:99700215
|
T | C | 3 | a0001c0001t0032g0272a0001c0001t0093g0042a0003c0013t0032g0132 | 3 | HG01109.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.859-3147T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700215 | ||||||
| chr15:99700221
|
C | T | 105 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(102): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.859-3141C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700221 | ||||||
| chr15:99700254
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859-3108C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700254 | ||||||
| chr15:99700340
|
C | T | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.859-3022C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700340 | ||||||
| chr15:99700381
|
A | G | 2 | a0014c0030t0069g0276a0016c0029t0114g0040 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.859-2981A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700381 | ||||||
| chr15:99700519
|
C | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.859-2843C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700519 | ||||||
| chr15:99700547
|
G | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.859-2815G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700547 | ||||||
| chr15:99700563
|
T | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859-2799T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700563 | ||||||
| chr15:99700705
|
G | A | 140 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.859-2657G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700705 | ||||||
| chr15:99700733
|
G | C | 1 | a0001c0001t0025g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.859-2629G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700733 | ||||||
| chr15:99700734
|
C | G | 1 | a0001c0001t0025g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.859-2628C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700734 | ||||||
| chr15:99700742
|
G | A | 1 | a0001c0005t0009g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.859-2620G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700742 | ||||||
| chr15:99700842
|
A | G | 1 | a0003c0003t0002g0355 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.859-2520A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700842 | ||||||
| chr15:99700863
|
G | A | 1 | a0001c0001t0025g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.859-2499G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700863 | ||||||
| chr15:99700887
|
T | G | 3 | a0001c0004t0006g0342a0001c0004t0027g0310a0001c0004t0027g0349 | 3 | HG02647.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.859-2475T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700887 | ||||||
| chr15:99700921
|
GAA | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.859-2437_859-2436d others(4): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99700921 | |||||
| chr15:99700952
|
C | T | 105 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(102): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.859-2410C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99700952 | ||||||
| chr15:99701005
|
A | G | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859-2357A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701005 | ||||||
| chr15:99701058
|
G | A | 3 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051 | 3 | HG03669.hp2 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.859-2304G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701058 | ||||||
| chr15:99701094
|
T | C | 1 | a0001c0001t0004g0275 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.859-2268T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701094 | ||||||
| chr15:99701101
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.859-2261G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701101 | ||||||
| chr15:99701107
|
C | G | 1 | a0001c0004t0052g0373 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.859-2255C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701107 | ||||||
| chr15:99701213
|
G | A | 1 | a0001c0006t0008g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.859-2149G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701213 | ||||||
| chr15:99701252
|
C | T | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859-2110C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701252 | ||||||
| chr15:99701332
|
C | T | 1 | a0002c0002t0005g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.859-2030C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701332 | ||||||
| chr15:99701376
|
TCAAAACA others(16): Show |
T | 1 | a0003c0003t0002g0323 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.859-1962_859-1940d others(25): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99701376 | |||||
| chr15:99701438
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.859-1924G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701438 | ||||||
| chr15:99701466
|
G | A | 1 | a0003c0003t0010g0364 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.859-1896G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701466 | ||||||
| chr15:99701706
|
T | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.859-1656T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701706 | ||||||
| chr15:99701752
|
A | C | 11 | a0001c0005t0009g0212a0001c0005t0009g0213a0004c0008t0009g0032others(8): Show | 11 | HG00733.hp2 HG01099.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.859-1610A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701752 | ||||||
| chr15:99701778
|
T | C | 1 | a0004c0019t0028g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.859-1584T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701778 | ||||||
| chr15:99701794
|
C | G | 1 | a0004c0019t0028g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.859-1568C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701794 | ||||||
| chr15:99701798
|
C | T | 2 | a0006c0015t0004g0154a0006c0015t0004g0155 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.859-1564C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701798 | ||||||
| chr15:99701832
|
G | A | 2 | a0001c0004t0006g0285a0003c0003t0006g0295 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.859-1530G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701832 | ||||||
| chr15:99702050
|
T | G | 1 | a0003c0003t0002g0317 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.859-1312T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702050 | ||||||
| chr15:99702117
|
G | T | 1 | a0001c0006t0018g0231 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.859-1245G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702117 | ||||||
| chr15:99702261
|
C | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859-1101C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702261 | ||||||
| chr15:99702263
|
T | G | 2 | a0001c0004t0049g0290a0003c0003t0098g0291 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.859-1099T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702263 | ||||||
| chr15:99702355
|
G | A | 1 | a0001c0006t0005g0145 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.859-1007G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702355 | ||||||
| chr15:99702384
|
G | A | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-978G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702384 | ||||||
| chr15:99702408
|
A | T | 6 | a0003c0003t0002g0299a0003c0003t0002g0300a0003c0003t0002g0301others(3): Show | 6 | NA18939.hp2 NA18964.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-954A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702408 | ||||||
| chr15:99702422
|
A | G | 1 | a0002c0002t0072g0130 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.859-940A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702422 | ||||||
| chr15:99702429
|
C | CT | 140 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.859-916dupT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99702429 | |||||
| chr15:99702429
|
C | CTT | 8 | a0001c0001t0004g0045a0001c0001t0004g0119a0001c0001t0093g0042others(5): Show | 8 | HG00735.hp2 HG01109.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.859-917_859-916dup others(2): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99702429 | |||||
| chr15:99702429
|
C | T | 1 | a0001c0001t0025g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.859-933C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702429 | ||||||
| chr15:99702430
|
T | C | 1 | a0001c0001t0025g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.859-932T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702430 | ||||||
| chr15:99702489
|
G | A | 3 | a0001c0004t0137g0283a0002c0002t0033g0072a0002c0002t0033g0073 | 3 | HG02055.hp2 HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.859-873G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702489 | ||||||
| chr15:99702658
|
C | T | 1 | a0001c0001t0024g0274 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.859-704C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702658 | ||||||
| chr15:99702669
|
G | A | 1 | a0001c0001t0064g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.859-693G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99702669 | ||||||
| chr15:99703100
|
C | G | 2 | a0001c0001t0032g0272a0003c0013t0032g0132 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.859-262C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99703100 | ||||||
| chr15:99703282
|
GT | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.859-74delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 99703282 | |||||
| chr15:99703414
|
T | G | 1 | a0001c0001t0025g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.882+29T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99703414 | ||||||
| chr15:99703467
|
G | A | 105 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0004t0001g0327others(102): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.882+82G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99703467 | ||||||
| chr15:99703566
|
A | G | 1 | a0001c0004t0137g0283 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+181A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99703566 | ||||||
| chr15:99703654
|
AT | A | 107 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.882+279delT | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr15 | 99703654 | |||||
| chr15:99703714
|
T | C | 1 | a0003c0013t0002g0372 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.882+329T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99703714 | ||||||
| chr15:99703837
|
C | T | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+452C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99703837 | ||||||
| chr15:99704029
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.882+644G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704029 | ||||||
| chr15:99704111
|
A | C | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.882+726A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704111 | ||||||
| chr15:99704129
|
G | A | 2 | a0002c0002t0014g0230a0002c0002t0038g0165 | 2 | HG01175.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.882+744G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704129 | ||||||
| chr15:99704271
|
G | A | 1 | a0001c0004t0011g0366 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.882+886G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704271 | ||||||
| chr15:99704388
|
G | T | 108 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.882+1003G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704388 | ||||||
| chr15:99704577
|
A | G | 2 | a0001c0004t0107g0350a0001c0004t0112g0354 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.882+1192A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704577 | ||||||
| chr15:99704711
|
A | G | 3 | a0001c0004t0006g0342a0001c0004t0027g0310a0001c0004t0027g0349 | 3 | HG02647.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.882+1326A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704711 | ||||||
| chr15:99704813
|
C | G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+1428C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704813 | ||||||
| chr15:99704912
|
T | C | 1 | a0001c0007t0100g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.882+1527T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99704912 | ||||||
| chr15:99705005
|
T | G | 10 | a0001c0006t0007g0098a0001c0006t0021g0164a0002c0002t0007g0052others(7): Show | 10 | HG00438.hp1 HG00673.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+1620T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705005 | ||||||
| chr15:99705022
|
C | T | 2 | a0004c0008t0050g0215a0004c0008t0099g0216 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+1637C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705022 | ||||||
| chr15:99705091
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.883-1638G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705091 | ||||||
| chr15:99705262
|
G | C | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1467G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705262 | ||||||
| chr15:99705310
|
A | G | 3 | a0001c0004t0051g0049a0001c0004t0051g0050a0002c0014t0109g0051 | 3 | HG03669.hp2 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.883-1419A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705310 | ||||||
| chr15:99705339
|
A | G | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.883-1390A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705339 | ||||||
| chr15:99705478
|
A | G | 1 | a0014c0030t0069g0276 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.883-1251A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705478 | ||||||
| chr15:99705513
|
A | G | 1 | a0001c0004t0048g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.883-1216A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705513 | ||||||
| chr15:99705578
|
C | T | 1 | a0001c0005t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-1151C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705578 | ||||||
| chr15:99705654
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.883-1075T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705654 | ||||||
| chr15:99705869
|
A | G | 2 | a0001c0006t0005g0093a0001c0007t0040g0118 | 2 | HG01257.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.883-860A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705869 | ||||||
| chr15:99705939
|
G | A | 1 | a0001c0004t0011g0366 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.883-790G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705939 | ||||||
| chr15:99705984
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.883-745G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705984 | ||||||
| chr15:99706247
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.883-482C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706247 | ||||||
| chr15:99706334
|
C | T | 2 | a0014c0030t0069g0276a0016c0029t0114g0040 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.883-395C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706334 | ||||||
| chr15:99706413
|
T | C | 34 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0037others(31): Show | 34 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.883-316T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706413 | ||||||
| chr15:99706467
|
T | G | 1 | a0001c0028t0095g0203 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.883-262T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706467 | ||||||
| chr15:99706477
|
A | G | 3 | a0003c0010t0055g0135a0003c0010t0055g0152a0003c0010t0135g0134 | 3 | HG02559.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883-252A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706477 | ||||||
| chr15:99706498
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.883-231G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706498 | ||||||
| chr15:99706513
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.883-216C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706513 | ||||||
| chr15:99706629
|
T | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.883-100T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706629 | ||||||
| chr15:99706879
|
G | A | 1 | a0004c0008t0050g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1009+24G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99706879 | ||||||
| chr15:99707094
|
C | A | 1 | a0003c0013t0032g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1009+239C>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707094 | ||||||
| chr15:99707102
|
C | T | 1 | a0001c0012t0066g0284 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1009+247C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707102 | ||||||
| chr15:99707325
|
G | C | 1 | a0005c0009t0061g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1009+470G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707325 | ||||||
| chr15:99707357
|
C | G | 2 | a0004c0008t0009g0033a0004c0008t0009g0034 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1009+502C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707357 | ||||||
| chr15:99707472
|
A | G | 1 | a0001c0006t0071g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1009+617A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707472 | ||||||
| chr15:99707479
|
C | T | 1 | a0001c0006t0008g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1009+624C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707479 | ||||||
| chr15:99707535
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1009+680C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707535 | ||||||
| chr15:99707658
|
A | G | 1 | a0002c0002t0029g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1009+803A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707658 | ||||||
| chr15:99707840
|
C | T | 2 | a0002c0011t0011g0159a0002c0011t0090g0156 | 2 | HG02129.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1009+985C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707840 | ||||||
| chr15:99707863
|
C | T | 1 | a0001c0001t0043g0149 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1009+1008C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707863 | ||||||
| chr15:99707938
|
GA | G | 107 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0360others(104): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1009+1094delA | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 99707938 | |||||
| chr15:99707951
|
T | C | 331 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1009+1096T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707951 | ||||||
| chr15:99707989
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1009+1134A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707989 | ||||||
| chr15:99708015
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1009+1160A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708015 | ||||||
| chr15:99708018
|
G | T | 3 | a0001c0004t0052g0373a0001c0004t0053g0374a0001c0004t0053g0375 | 3 | HG03209.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1009+1163G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708018 | ||||||
| chr15:99708057
|
A | T | 123 | a0001c0004t0001g0327a0001c0004t0002g0357a0001c0004t0002g0361others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1009+1202A>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708057 | ||||||
| chr15:99708250
|
G | A | 1 | a0001c0001t0039g0268 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1009+1395G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708250 | ||||||
| chr15:99708601
|
G | A | 1 | a0004c0008t0047g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1009+1746G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708601 | ||||||
| chr15:99708712
|
G | T | 1 | a0003c0003t0002g0315 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1009+1857G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708712 | ||||||
| chr15:99708783
|
C | T | 1 | a0002c0002t0005g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1010-1851C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708783 | ||||||
| chr15:99708852
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1010-1782T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708852 | ||||||
| chr15:99708928
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1010-1706C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99708928 | ||||||
| chr15:99709068
|
A | G | 4 | a0003c0013t0001g0256a0003c0013t0001g0257a0014c0030t0069g0276others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-1566A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709068 | ||||||
| chr15:99709088
|
G | A | 1 | a0002c0002t0058g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1010-1546G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709088 | ||||||
| chr15:99709286
|
G | A | 1 | a0001c0005t0015g0025 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1010-1348G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709286 | ||||||
| chr15:99709415
|
T | C | 10 | a0001c0004t0002g0357a0001c0004t0002g0360a0001c0004t0002g0361others(7): Show | 10 | HG00673.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1010-1219T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709415 | ||||||
| chr15:99709419
|
A | G | 1 | a0001c0001t0004g0046 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1010-1215A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709419 | ||||||
| chr15:99709456
|
G | A | 1 | a0001c0012t0066g0284 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1010-1178G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709456 | ||||||
| chr15:99709465
|
G | A | 106 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1010-1169G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709465 | ||||||
| chr15:99709495
|
C | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1010-1139C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709495 | ||||||
| chr15:99709894
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1010-740G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709894 | ||||||
| chr15:99709927
|
G | A | 2 | a0001c0004t0006g0285a0003c0003t0006g0295 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1010-707G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709927 | ||||||
| chr15:99709928
|
G | C | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1010-706G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709928 | ||||||
| chr15:99709964
|
A | G | 2 | a0001c0004t0053g0374a0001c0004t0053g0375 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1010-670A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709964 | ||||||
| chr15:99709973
|
C | T | 1 | a0001c0004t0027g0349 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1010-661C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99709973 | ||||||
| chr15:99710016
|
C | T | 2 | a0002c0002t0007g0087a0002c0002t0007g0088 | 2 | HG00673.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1010-618C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99710016 | ||||||
| chr15:99710367
|
C | T | 4 | a0002c0002t0014g0059a0002c0002t0014g0086a0002c0002t0014g0091others(1): Show | 4 | HG00140.hp2 HG01074.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-267C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99710367 | ||||||
| chr15:99710435
|
G | A | 1 | a0002c0002t0008g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1010-199G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99710435 | ||||||
| chr15:99710570
|
C | T | 2 | a0001c0012t0017g0336a0002c0002t0005g0196 | 2 | HG03195.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1010-64C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99710570 | ||||||
| chr15:99710571
|
G | A | 2 | a0002c0002t0056g0100a0003c0003t0002g0305 | 2 | HG00423.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1010-63G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99710571 | ||||||
| chr15:99710586
|
C | T | 1 | a0018c0025t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1010-48C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99710586 | ||||||
| chr15:99710810
|
C | G | 209 | a0001c0001t0004g0035a0001c0001t0004g0045a0001c0001t0004g0046others(206): Show | 209 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1136+50C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99710810 | ||||||
| chr15:99710850
|
T | C | 1 | a0004c0019t0028g0121 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1136+90T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99710850 | ||||||
| chr15:99710899
|
G | A | 1 | a0017c0034t0111g0308 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1136+139G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99710899 | ||||||
| chr15:99710902
|
A | C | 1 | a0001c0001t0011g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1136+142A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99710902 | ||||||
| chr15:99710902
|
A | G | 1 | a0002c0002t0012g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1136+142A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99710902 | ||||||
| chr15:99711106
|
A | C | 25 | a0001c0001t0001g0280a0001c0001t0004g0043a0001c0001t0020g0259others(22): Show | 25 | HG00597.hp1 HG00639.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1136+346A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711106 | ||||||
| chr15:99711156
|
C | T | 1 | a0001c0007t0040g0118 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1136+396C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711156 | ||||||
| chr15:99711177
|
T | C | 141 | a0001c0001t0004g0036a0001c0001t0004g0037a0001c0001t0004g0043others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1136+417T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711177 | ||||||
| chr15:99711205
|
T | C | 15 | a0001c0001t0020g0236a0001c0001t0020g0279a0001c0004t0027g0310others(12): Show | 15 | HG00735.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1136+445T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711205 | ||||||
| chr15:99711245
|
G | C | 346 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1136+485G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711245 | ||||||
| chr15:99711438
|
G | A | 2 | a0003c0013t0001g0256a0003c0013t0001g0257 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1136+678G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711438 | ||||||
| chr15:99711457
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(94): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1136+697A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711457 | ||||||
| chr15:99711461
|
G | A | 8 | a0003c0003t0010g0004a0003c0003t0010g0005a0003c0003t0010g0006others(5): Show | 8 | HG01928.hp1 HG01934.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136+701G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711461 | ||||||
| chr15:99711500
|
C | T | 1 | a0001c0004t0026g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1136+740C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711500 | ||||||
| chr15:99711704
|
G | A | 2 | a0001c0005t0003g0019a0001c0005t0003g0335 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1137-686G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711704 | ||||||
| chr15:99711723
|
C | G | 5 | a0001c0007t0001g0168a0003c0003t0002g0054a0003c0003t0002g0346others(2): Show | 5 | HG00280.hp1 HG01123.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-667C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711723 | ||||||
| chr15:99711724
|
T | G | 5 | a0001c0007t0001g0168a0003c0003t0002g0054a0003c0003t0002g0346others(2): Show | 5 | HG00280.hp1 HG01123.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-666T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711724 | ||||||
| chr15:99711746
|
AAAAGCAG others(10): Show |
A | 1 | a0001c0028t0095g0203 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1137-643_1137-627d others(19): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711746 | ||||||
| chr15:99711949
|
G | A | 1 | a0002c0011t0001g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1137-441G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711949 | ||||||
| chr15:99711959
|
C | T | 2 | a0001c0004t0053g0374a0001c0004t0053g0375 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1137-431C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711959 | ||||||
| chr15:99711969
|
A | C | 51 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(48): Show | 51 | HG00733.hp2 HG00735.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.1137-421A>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711969 | ||||||
| chr15:99711972
|
G | C | 3 | a0002c0002t0080g0211a0003c0003t0002g0321a0003c0003t0002g0368 | 3 | HG03710.hp2 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1137-418G>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711972 | ||||||
| chr15:99711980
|
G | A | 4 | a0001c0001t0011g0242a0001c0001t0046g0180a0002c0002t0062g0061others(1): Show | 4 | HG00735.hp1 HG02738.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-410G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99711980 | ||||||
| chr15:99712025
|
GGAGCAGA others(21): Show |
G | 1 | a0001c0001t0124g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1137-355_1137-328d others(30): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 99712025 | |||||
| chr15:99712103
|
T | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0124others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1137-287T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99712103 | ||||||
| chr15:99712122
|
T | G | 1 | a0002c0002t0005g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1137-268T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99712122 | ||||||
| chr15:99712131
|
T | A | 2 | a0001c0004t0048g0047a0001c0004t0048g0292 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1137-259T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99712131 | ||||||
| chr15:99712311
|
G | T | 6 | a0001c0001t0011g0224a0001c0001t0011g0225a0001c0001t0045g0226others(3): Show | 6 | HG00544.hp2 HG02056.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-79G>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99712311 | ||||||
| chr15:99712355
|
C | G | 1 | a0001c0001t0001g0245 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1137-35C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99712355 |