Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 505 | 185 | 63 | 32 | 64 | 10 | 14 | 51 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(500): Show |
chr15 | 99560984 | 99721488 |
| a0002 | 0/0 | 503 | 86 | 1 | 14 | 52 | 4 | 15 | 33 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(498): Show |
chr15 | 99560984 | 99721488 |
| a0003 | 0/0 | 504 | 72 | 15 | 18 | 34 | 2 | 3 | 23 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(499): Show |
chr15 | 99560984 | 99721488 |
| a0004 | 0/0 | 507 | 11 | 8 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(502): Show |
chr15 | 99560984 | 99721488 |
| a0005 | 0/0 | 502 | 4 | 2 | 0 | 2 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(497): Show |
chr15 | 99560984 | 99721488 |
| a0006 | 0/0 | 508 | 4 | 0 | 0 | 3 | 0 | 1 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(503): Show |
chr15 | 99560984 | 99721488 |
| a0007 | 0/0 | 506 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(501): Show |
chr15 | 99560984 | 99721488 |
| a0008 | 0/0 | 501 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(496): Show |
chr15 | 99560984 | 99721488 |
| a0009 | 0/0 | 498 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(493): Show |
chr15 | 99560984 | 99721488 |
| a0010 | 0/0 | 482 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(477): Show |
chr15 | 99560984 | 99721488 |
| a0011 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(500): Show |
chr15 | 99560984 | 99721488 |
| a0012 | 0/0 | 493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(488): Show |
chr15 | 99560984 | 99721488 |
| a0013 | 0/0 | 510 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(505): Show |
chr15 | 99560984 | 99721488 |
| a0014 | 0/0 | 499 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | MGRKK others(494): Show |
chr15 | 99560984 | 99721488 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1515 | 94 | 10 | 14 | 53 | 8 | 9 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0001c0004 | 0/0 | 1515 | 33 | 23 | 5 | 3 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0001c0005 | 1/0 | 1515 | 25 | 23 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0001c0006 | 0/0 | 1515 | 17 | 0 | 6 | 8 | 1 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0001c0007 | 0/1 | 1515 | 9 | 1 | 5 | 0 | 1 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0001c0011 | 0/0 | 1515 | 6 | 5 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0001c0021 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0002c0002 | 0/0 | 1509 | 73 | 1 | 13 | 41 | 4 | 14 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1504): Show |
chr15 | 99560984 | 99721488 | ||
| a0002c0010 | 0/0 | 1509 | 7 | 0 | 1 | 6 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1504): Show |
chr15 | 99560984 | 99721488 | ||
| a0002c0013 | 0/0 | 1509 | 5 | 0 | 0 | 4 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1504): Show |
chr15 | 99560984 | 99721488 | ||
| a0002c0031 | 0/0 | 1509 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1504): Show |
chr15 | 99560984 | 99721488 | ||
| a0003c0003 | 0/0 | 1512 | 55 | 3 | 15 | 32 | 2 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1507): Show |
chr15 | 99560984 | 99721488 | ||
| a0003c0009 | 0/0 | 1512 | 8 | 8 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1507): Show |
chr15 | 99560984 | 99721488 | ||
| a0003c0012 | 0/0 | 1512 | 5 | 3 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1507): Show |
chr15 | 99560984 | 99721488 | ||
| a0003c0020 | 0/0 | 1512 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1507): Show |
chr15 | 99560984 | 99721488 | ||
| a0003c0026 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1507): Show |
chr15 | 99560984 | 99721488 | ||
| a0003c0027 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1507): Show |
chr15 | 99560984 | 99721488 | ||
| a0004c0008 | 0/0 | 1521 | 9 | 7 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1516): Show |
chr15 | 99560984 | 99721488 | ||
| a0004c0017 | 0/0 | 1521 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1516): Show |
chr15 | 99560984 | 99721488 | ||
| a0005c0014 | 0/0 | 1506 | 4 | 2 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1501): Show |
chr15 | 99560984 | 99721488 | ||
| a0006c0015 | 0/0 | 1524 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1519): Show |
chr15 | 99560984 | 99721488 | ||
| a0006c0023 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1519): Show |
chr15 | 99560984 | 99721488 | ||
| a0007c0018 | 0/0 | 1518 | 2 | 1 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1513): Show |
chr15 | 99560984 | 99721488 | ||
| a0007c0030 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1513): Show |
chr15 | 99560984 | 99721488 | ||
| a0008c0019 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1498): Show |
chr15 | 99560984 | 99721488 | ||
| a0008c0032 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1498): Show |
chr15 | 99560984 | 99721488 | ||
| a0009c0016 | 0/0 | 1494 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1489): Show |
chr15 | 99560984 | 99721488 | ||
| a0010c0024 | 0/0 | 1515 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0011c0025 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1510): Show |
chr15 | 99560984 | 99721488 | ||
| a0012c0028 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1474): Show |
chr15 | 99560984 | 99721488 | ||
| a0013c0022 | 0/0 | 1530 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1525): Show |
chr15 | 99560984 | 99721488 | ||
| a0014c0029 | 0/0 | 1497 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATGGG others(1492): Show |
chr15 | 99560984 | 99721488 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5584 | 36 | 2 | 6 | 18 | 5 | 5 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0003 | 0/0 | 5583 | 13 | 1 | 3 | 8 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0005 | 0/0 | 5584 | 6 | 0 | 0 | 5 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0012 | 0/0 | 5584 | 4 | 0 | 0 | 3 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0017 | 0/0 | 5584 | 3 | 1 | 0 | 0 | 2 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0022 | 0/0 | 5584 | 3 | 0 | 2 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0023 | 0/0 | 5580 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0027 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0028 | 0/0 | 5584 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0029 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0034 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0040 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0042 | 0/0 | 5582 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5577): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0043 | 0/0 | 5582 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5577): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0059 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0074 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0075 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0078 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0079 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0080 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0084 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0087 | 0/0 | 5584 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0089 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0090 | 0/0 | 5584 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0095 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0096 | 0/0 | 5584 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0097 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5577): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0100 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0104 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5577): Show |
chr15 | 99560984 | 99721488 |
| a0001c0001t0112 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0001 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0002 | 0/0 | 5584 | 4 | 0 | 4 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0005 | 0/0 | 5584 | 4 | 3 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0007 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0012 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0029 | 0/0 | 5584 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0030 | 0/0 | 5584 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0043 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5577): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0044 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5577): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0045 | 0/0 | 5584 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0047 | 0/0 | 5584 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0048 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0049 | 0/0 | 5584 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0082 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0083 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0098 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0099 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0106 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0108 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0120 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0121 | 0/0 | 5582 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5577): Show |
chr15 | 99560984 | 99721488 |
| a0001c0004t0126 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0005t0004 | 0/0 | 5580 | 13 | 13 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0005t0010 | 0/0 | 5585 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5580): Show |
chr15 | 99560984 | 99721488 |
| a0001c0005t0015 | 0/0 | 5580 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0005t0039 | 1/0 | 5580 | 2 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0005t0114 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5580): Show |
chr15 | 99560984 | 99721488 |
| a0001c0005t0127 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0006 | 0/0 | 5578 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0008 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0009 | 0/0 | 5580 | 4 | 0 | 3 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0013 | 0/0 | 5580 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0019 | 0/0 | 5580 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0024 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0054 | 0/0 | 5580 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0060 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0066 | 0/0 | 5580 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0006t0086 | 0/0 | 5584 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0007t0001 | 0/0 | 5584 | 6 | 1 | 3 | 0 | 1 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0007t0040 | 0/0 | 5584 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0007t0088 | 0/1 | 5583 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5578): Show |
chr15 | 99560984 | 99721488 |
| a0001c0007t0093 | 0/0 | 5584 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0001c0011t0018 | 0/0 | 5580 | 4 | 3 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0011t0057 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0011t0061 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0001c0021t0005 | 0/0 | 5584 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5579): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0006 | 0/0 | 5572 | 6 | 0 | 0 | 3 | 0 | 3 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0008 | 0/0 | 5572 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0009 | 0/0 | 5574 | 4 | 0 | 1 | 0 | 1 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0011 | 0/0 | 5574 | 6 | 0 | 0 | 6 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0013 | 0/0 | 5574 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0014 | 0/0 | 5574 | 5 | 0 | 2 | 0 | 2 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0020 | 0/0 | 5572 | 4 | 0 | 0 | 4 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0021 | 0/0 | 5574 | 3 | 0 | 1 | 1 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0024 | 0/0 | 5574 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0025 | 0/0 | 5572 | 3 | 0 | 0 | 0 | 1 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0026 | 0/0 | 5574 | 3 | 0 | 1 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0031 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0032 | 0/0 | 5574 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0033 | 0/0 | 5572 | 2 | 0 | 1 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0035 | 0/0 | 5574 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0036 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0037 | 0/0 | 5572 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0038 | 0/0 | 5574 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0051 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0052 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0053 | 0/0 | 5574 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0055 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0056 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0058 | 0/0 | 5574 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0063 | 0/0 | 5574 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0067 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0068 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0069 | 0/0 | 5574 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0070 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0071 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0072 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0073 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0076 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0002t0077 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0010t0001 | 0/0 | 5578 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0002c0010t0012 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0002c0010t0022 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0002c0010t0027 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5572): Show |
chr15 | 99560984 | 99721488 |
| a0002c0010t0041 | 0/0 | 5578 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0002c0010t0081 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5572): Show |
chr15 | 99560984 | 99721488 |
| a0002c0013t0002 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0002c0013t0008 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0002c0013t0016 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0002c0013t0102 | 0/0 | 5578 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0002c0031t0006 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0002 | 0/0 | 5581 | 28 | 0 | 5 | 21 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0005 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0007 | 0/0 | 5581 | 8 | 0 | 7 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0016 | 0/0 | 5581 | 4 | 0 | 0 | 3 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0048 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0091 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0101 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0103 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0107 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0109 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0110 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0111 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0115 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5574): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0116 | 0/0 | 5581 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0117 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0122 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5574): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0123 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5574): Show |
chr15 | 99560984 | 99721488 |
| a0003c0003t0125 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5574): Show |
chr15 | 99560984 | 99721488 |
| a0003c0009t0002 | 0/0 | 5581 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0009t0004 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5572): Show |
chr15 | 99560984 | 99721488 |
| a0003c0009t0050 | 0/0 | 5581 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0009t0119 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0009t0124 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0012t0001 | 0/0 | 5581 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0012t0002 | 0/0 | 5581 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0012t0034 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5573): Show |
chr15 | 99560984 | 99721488 |
| a0003c0020t0002 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0020t0007 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5576): Show |
chr15 | 99560984 | 99721488 |
| a0003c0026t0064 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5572): Show |
chr15 | 99560984 | 99721488 |
| a0003c0027t0065 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5572): Show |
chr15 | 99560984 | 99721488 |
| a0004c0008t0010 | 0/0 | 5591 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5586): Show |
chr15 | 99560984 | 99721488 |
| a0004c0008t0044 | 0/0 | 5588 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5583): Show |
chr15 | 99560984 | 99721488 |
| a0004c0008t0046 | 0/0 | 5590 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5585): Show |
chr15 | 99560984 | 99721488 |
| a0004c0008t0092 | 0/0 | 5590 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5585): Show |
chr15 | 99560984 | 99721488 |
| a0004c0017t0017 | 0/0 | 5590 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5585): Show |
chr15 | 99560984 | 99721488 |
| a0005c0014t0003 | 0/0 | 5574 | 3 | 2 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5569): Show |
chr15 | 99560984 | 99721488 |
| a0005c0014t0094 | 0/0 | 5575 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5570): Show |
chr15 | 99560984 | 99721488 |
| a0006c0015t0019 | 0/0 | 5589 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5584): Show |
chr15 | 99560984 | 99721488 |
| a0006c0015t0062 | 0/0 | 5589 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5584): Show |
chr15 | 99560984 | 99721488 |
| a0006c0023t0027 | 0/0 | 5592 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5587): Show |
chr15 | 99560984 | 99721488 |
| a0007c0018t0001 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5582): Show |
chr15 | 99560984 | 99721488 |
| a0007c0018t0030 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5582): Show |
chr15 | 99560984 | 99721488 |
| a0007c0030t0113 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5582): Show |
chr15 | 99560984 | 99721488 |
| a0008c0019t0001 | 0/0 | 5572 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5567): Show |
chr15 | 99560984 | 99721488 |
| a0008c0032t0004 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5563): Show |
chr15 | 99560984 | 99721488 |
| a0009c0016t0002 | 0/0 | 5563 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5558): Show |
chr15 | 99560984 | 99721488 |
| a0009c0016t0118 | 0/0 | 5563 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5558): Show |
chr15 | 99560984 | 99721488 |
| a0010c0024t0021 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5575): Show |
chr15 | 99560984 | 99721488 |
| a0011c0025t0105 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5580): Show |
chr15 | 99560984 | 99721488 |
| a0012c0028t0006 | 0/0 | 5542 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5537): Show |
chr15 | 99560984 | 99721488 |
| a0013c0022t0001 | 0/0 | 5599 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5594): Show |
chr15 | 99560984 | 99721488 |
| a0014c0029t0085 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | ATCCG others(5560): Show |
chr15 | 99560984 | 99721488 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0175 | 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 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0012g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0012g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0017g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0017g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0022g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0022g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0022g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0023g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0023g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0023g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0027g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0028g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0028g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0028g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0029g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0034g0270 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0042g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0042g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0043g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0059g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0074g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0075g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0078g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0079g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0080g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0084g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0087g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0089g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0090g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0095g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0096g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0097g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0100g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0104g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0001t0112g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0004t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0012g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0029g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0029g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0030g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0030g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0043g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0044g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0045g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0045g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0047g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0047g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0048g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0049g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0049g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0082g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0083g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0098g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0099g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0106g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0108g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0120g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0121g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0004t0126g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0010g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0010g0211 | 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 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0015g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0039g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0039g0333 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0114g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0005t0127g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0009g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0009g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0009g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0013g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0019g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0019g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0024g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0054g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0060g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0066g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0006t0086g0200 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0007t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0001g0258 | 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 |
| a0001c0007t0088g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0007t0093g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0011t0018g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0011t0018g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0011t0018g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0011t0018g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0011t0057g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0011t0061g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0001c0021t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0006g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0009g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0009g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0009g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0011g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0014g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0020g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0020g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0020g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0021g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0021g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0021g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0024g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0024g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0025g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0025g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0025g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0026g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0026g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0026g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0031g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0031g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0032g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0032g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0033g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0033g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0035g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0035g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0036g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0036g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0037g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0037g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0038g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0038g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0051g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0052g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0053g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0055g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0056g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0058g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0063g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0067g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0068g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0069g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0070g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0071g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0072g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0073g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0076g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0002t0077g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0010t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0010t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0010t0022g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0010t0027g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0010t0041g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0010t0081g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0013t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0013t0008g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0013t0016g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0013t0102g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0002c0031t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0003c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0314 | 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 |
| a0003c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0003c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0002g0354 | 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 |
| a0003c0003t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0007g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0016g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0048g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0091g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0101g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0103g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0107g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0109g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0110g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0111g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0115g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0116g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0117g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0122g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0123g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0003t0125g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0050g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0050g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0119g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0009t0124g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0012t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0012t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0012t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0012t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0012t0034g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0020t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0020t0007g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0026t0064g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0003c0027t0065g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0010g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0010g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0044g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0046g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0046g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0008t0092g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0017t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0004c0017t0017g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0014t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0014t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0014t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0005c0014t0094g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0015t0019g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0015t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0015t0062g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0006c0023t0027g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0007c0018t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0007c0018t0030g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0007c0030t0113g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0008c0019t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0008c0019t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0008c0032t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0009c0016t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0009c0016t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0009c0016t0118g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0010c0024t0021g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0011c0025t0105g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0012c0028t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0013c0022t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| a0014c0029t0085g0265 | 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 | a0001 | c0006 | t0054 | g0105 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00140 | hp2 | a0002 | c0002 | t0014 | g0090 | EUR | GBR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00280 | hp1 | a0003 | c0003 | t0016 | g0055 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00323 | hp1 | a0002 | c0002 | t0025 | g0102 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00323 | hp2 | a0001 | c0001 | t0017 | g0242 | EUR | FIN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00408 | hp2 | a0003 | c0003 | t0016 | g0321 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00423 | hp2 | a0003 | c0003 | t0002 | g0303 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00438 | hp1 | a0001 | c0006 | t0024 | g0165 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00438 | hp2 | a0003 | c0003 | t0016 | g0331 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00544 | hp1 | a0001 | c0001 | t0074 | g0204 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00544 | hp2 | a0001 | c0001 | t0100 | g0252 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00558 | hp1 | a0002 | c0013 | t0002 | g0324 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00558 | hp2 | a0002 | c0002 | t0055 | g0201 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00597 | hp2 | a0002 | c0002 | t0021 | g0087 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00609 | hp1 | a0003 | c0003 | t0103 | g0192 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00609 | hp2 | a0005 | c0014 | t0094 | g0177 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00621 | hp1 | a0001 | c0001 | t0089 | g0164 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00621 | hp2 | a0003 | c0003 | t0002 | g0315 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00639 | hp1 | a0003 | c0003 | t0110 | g0285 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00639 | hp2 | a0001 | c0007 | t0093 | g0045 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00642 | hp2 | a0001 | c0006 | t0019 | g0231 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0353 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00673 | hp2 | a0002 | c0002 | t0008 | g0093 | EAS | CHS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00733 | hp1 | a0001 | c0007 | t0001 | g0170 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00733 | hp2 | a0004 | c0008 | t0010 | g0036 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00735 | hp1 | a0004 | c0017 | t0017 | g0121 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00738 | hp1 | a0003 | c0003 | t0002 | g0300 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01071 | hp1 | a0002 | c0002 | t0033 | g0082 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01074 | hp1 | a0002 | c0002 | t0014 | g0095 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01074 | hp2 | a0003 | c0003 | t0117 | g0301 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01081 | hp1 | a0002 | c0002 | t0063 | g0160 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01081 | hp2 | a0003 | c0020 | t0002 | g0342 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01099 | hp1 | a0001 | c0004 | t0002 | g0356 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01099 | hp2 | a0004 | c0008 | t0046 | g0213 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01109 | hp1 | a0001 | c0005 | t0015 | g0031 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01109 | hp2 | a0001 | c0001 | t0084 | g0044 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01167 | hp1 | a0002 | c0002 | t0014 | g0096 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01167 | hp2 | a0001 | c0004 | t0002 | g0359 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01168 | hp1 | a0003 | c0020 | t0007 | g0361 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01168 | hp2 | a0001 | c0006 | t0009 | g0111 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01169 | hp1 | a0001 | c0006 | t0009 | g0112 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01169 | hp2 | a0001 | c0004 | t0002 | g0352 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01175 | hp1 | a0002 | c0002 | t0021 | g0166 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01175 | hp2 | a0001 | c0001 | t0022 | g0238 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01192 | hp1 | a0001 | c0007 | t0001 | g0169 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01192 | hp2 | a0001 | c0006 | t0009 | g0115 | AMR | PUR | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01255 | hp1 | a0001 | c0001 | t0090 | g0187 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01255 | hp2 | a0003 | c0003 | t0002 | g0292 | 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 | g0003 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01258 | hp2 | a0001 | c0006 | t0019 | g0229 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01261 | hp1 | a0001 | c0004 | t0005 | g0006 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01261 | hp2 | a0010 | c0024 | t0021 | g0114 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01346 | hp1 | a0001 | c0007 | t0001 | g0258 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01346 | hp2 | a0002 | c0002 | t0026 | g0116 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01358 | hp1 | a0002 | c0002 | t0009 | g0035 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01358 | hp2 | a0001 | c0001 | t0087 | g0033 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01361 | hp1 | a0001 | c0006 | t0006 | g0091 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01433 | hp1 | a0002 | c0002 | t0038 | g0140 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01496 | hp2 | a0001 | c0011 | t0018 | g0347 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01515 | hp1 | a0001 | c0001 | t0017 | g0188 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0366 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01517 | hp1 | a0002 | c0002 | t0014 | g0228 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0365 | EUR | IBS | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01884 | hp1 | a0001 | c0004 | t0043 | g0339 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01884 | hp2 | a0001 | c0021 | t0005 | g0217 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01891 | hp1 | a0003 | c0026 | t0064 | g0274 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01891 | hp2 | a0001 | c0005 | t0004 | g0024 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01928 | hp1 | a0003 | c0003 | t0007 | g0256 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01928 | hp2 | a0001 | c0004 | t0002 | g0357 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01934 | hp1 | a0003 | c0003 | t0007 | g0010 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01934 | hp2 | a0002 | c0002 | t0076 | g0098 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01943 | hp1 | a0002 | c0010 | t0001 | g0173 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01943 | hp2 | a0003 | c0003 | t0007 | g0009 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01978 | hp1 | a0002 | c0002 | t0037 | g0142 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01978 | hp2 | a0003 | c0003 | t0007 | g0008 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0291 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01981 | hp2 | a0002 | c0002 | t0038 | g0043 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01993 | hp1 | a0001 | c0001 | t0022 | g0184 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01993 | hp2 | a0003 | c0003 | t0111 | g0012 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02015 | hp1 | a0003 | c0003 | t0002 | g0313 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02015 | hp2 | a0002 | c0002 | t0008 | g0219 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02027 | hp1 | a0002 | c0002 | t0008 | g0054 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02027 | hp2 | a0002 | c0010 | t0022 | g0172 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02040 | hp1 | a0002 | c0002 | t0056 | g0129 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02040 | hp2 | a0002 | c0002 | t0068 | g0250 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02055 | hp1 | a0001 | c0004 | t0030 | g0288 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02055 | hp2 | a0001 | c0004 | t0126 | g0281 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02056 | hp1 | a0002 | c0013 | t0016 | g0344 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02056 | hp2 | a0001 | c0001 | t0097 | g0253 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02074 | hp1 | a0001 | c0004 | t0001 | g0325 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02074 | hp2 | a0001 | c0001 | t0022 | g0171 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02080 | hp1 | a0003 | c0003 | t0123 | g0329 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02080 | hp2 | a0002 | c0002 | t0008 | g0092 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02083 | hp1 | a0002 | c0010 | t0041 | g0002 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02083 | hp2 | a0001 | c0001 | t0078 | g0268 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02129 | hp1 | a0002 | c0002 | t0008 | g0094 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02129 | hp2 | a0002 | c0010 | t0012 | g0159 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02132 | hp1 | a0002 | c0010 | t0041 | g0002 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02132 | hp2 | a0003 | c0003 | t0002 | g0304 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02135 | hp1 | a0001 | c0001 | t0079 | g0131 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02135 | hp2 | a0003 | c0003 | t0002 | g0316 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02145 | hp1 | a0007 | c0018 | t0030 | g0233 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02145 | hp2 | a0001 | c0004 | t0083 | g0287 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02148 | hp1 | a0002 | c0002 | t0077 | g0143 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02148 | hp2 | a0003 | c0003 | t0007 | g0013 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02155 | hp1 | a0002 | c0002 | t0024 | g0041 | EAS | CDX | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02155 | hp2 | a0003 | c0003 | t0115 | g0343 | EAS | CDX | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02257 | hp1 | a0004 | c0008 | t0046 | g0216 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02257 | hp2 | a0003 | c0009 | t0002 | g0196 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02280 | hp1 | a0001 | c0005 | t0004 | g0026 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02280 | hp2 | a0001 | c0004 | t0005 | g0283 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02293 | hp1 | a0002 | c0002 | t0037 | g0144 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02293 | hp2 | a0003 | c0003 | t0007 | g0014 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0056 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0341 | AMR | PEL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02451 | hp1 | a0003 | c0012 | t0034 | g0132 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02451 | hp2 | a0001 | c0005 | t0004 | g0016 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02523 | hp1 | a0002 | c0002 | t0024 | g0100 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02523 | hp2 | a0001 | c0001 | t0012 | g0279 | EAS | KHV | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02572 | hp1 | a0001 | c0004 | t0098 | g0306 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02572 | hp2 | a0001 | c0001 | t0023 | g0234 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02615 | hp1 | a0004 | c0008 | t0010 | g0251 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02615 | hp2 | a0001 | c0005 | t0114 | g0218 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02622 | hp1 | a0001 | c0005 | t0015 | g0025 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02622 | hp2 | a0001 | c0004 | t0120 | g0284 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02630 | hp2 | a0001 | c0005 | t0004 | g0023 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02647 | hp1 | a0003 | c0009 | t0124 | g0134 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02647 | hp2 | a0001 | c0004 | t0005 | g0338 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02698 | hp1 | a0002 | c0002 | t0006 | g0059 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02717 | hp1 | a0001 | c0005 | t0004 | g0022 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02723 | hp1 | a0003 | c0003 | t0005 | g0293 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0191 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02735 | hp1 | a0001 | c0007 | t0001 | g0183 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02735 | hp2 | a0002 | c0002 | t0006 | g0110 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02738 | hp1 | a0002 | c0002 | t0009 | g0058 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0240 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02809 | hp1 | a0001 | c0004 | t0108 | g0309 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02809 | hp2 | a0004 | c0008 | t0010 | g0212 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02886 | hp1 | a0001 | c0001 | t0017 | g0162 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02886 | hp2 | a0003 | c0009 | t0004 | g0021 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02895 | hp1 | a0001 | c0004 | t0030 | g0346 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02895 | hp2 | a0005 | c0014 | t0003 | g0154 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02896 | hp1 | a0004 | c0008 | t0010 | g0001 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02896 | hp2 | a0003 | c0003 | t0091 | g0289 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02897 | hp1 | a0005 | c0014 | t0003 | g0155 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02897 | hp2 | a0004 | c0008 | t0010 | g0001 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02922 | hp1 | a0001 | c0005 | t0015 | g0028 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02922 | hp2 | a0001 | c0004 | t0044 | g0294 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02965 | hp1 | a0001 | c0005 | t0010 | g0211 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02965 | hp2 | a0003 | c0009 | t0002 | g0197 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02970 | hp1 | a0001 | c0011 | t0061 | g0282 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02970 | hp2 | a0001 | c0005 | t0127 | g0018 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02976 | hp1 | a0011 | c0025 | t0105 | g0042 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02976 | hp2 | a0001 | c0005 | t0039 | g0015 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03017 | hp1 | a0003 | c0003 | t0116 | g0311 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03017 | hp2 | a0002 | c0002 | t0006 | g0108 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03041 | hp1 | a0001 | c0004 | t0047 | g0290 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03041 | hp2 | a0003 | c0012 | t0001 | g0255 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03098 | hp1 | a0001 | c0001 | t0059 | g0276 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03098 | hp2 | a0001 | c0001 | t0023 | g0277 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03130 | hp1 | a0001 | c0011 | t0057 | g0348 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03130 | hp2 | a0001 | c0004 | t0082 | g0286 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03139 | hp1 | a0001 | c0005 | t0004 | g0261 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03139 | hp2 | a0001 | c0005 | t0010 | g0210 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03195 | hp1 | a0001 | c0011 | t0018 | g0335 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03195 | hp2 | a0001 | c0005 | t0004 | g0262 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03209 | hp1 | a0001 | c0004 | t0047 | g0049 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03209 | hp2 | a0001 | c0004 | t0048 | g0369 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03225 | hp1 | a0003 | c0009 | t0119 | g0275 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03225 | hp2 | a0001 | c0004 | t0049 | g0370 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03453 | hp1 | a0001 | c0004 | t0005 | g0198 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0020 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03486 | hp1 | a0001 | c0004 | t0029 | g0308 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03486 | hp2 | a0008 | c0032 | t0004 | g0019 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03490 | hp2 | a0002 | c0002 | t0014 | g0061 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03492 | hp2 | a0012 | c0028 | t0006 | g0167 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03516 | hp2 | a0001 | c0004 | t0012 | g0362 | AFR | ESN | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03540 | hp1 | a0003 | c0003 | t0125 | g0280 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03540 | hp2 | a0001 | c0005 | t0015 | g0027 | AFR | GWD | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03579 | hp1 | a0004 | c0008 | t0092 | g0214 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03579 | hp2 | a0003 | c0009 | t0002 | g0195 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0146 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03654 | hp2 | a0002 | c0002 | t0053 | g0060 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03669 | hp1 | a0001 | c0006 | t0009 | g0113 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03669 | hp2 | a0002 | c0013 | t0102 | g0052 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03688 | hp1 | a0006 | c0023 | t0027 | g0161 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03688 | hp2 | a0002 | c0002 | t0035 | g0074 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03704 | hp1 | a0001 | c0006 | t0066 | g0097 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03704 | hp2 | a0001 | c0001 | t0043 | g0181 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03710 | hp2 | a0002 | c0002 | t0069 | g0209 | SAS | PJL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03831 | hp1 | a0002 | c0002 | t0035 | g0075 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03831 | hp2 | a0002 | c0002 | t0033 | g0239 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03834 | hp1 | a0002 | c0002 | t0025 | g0221 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0319 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03942 | hp1 | a0002 | c0002 | t0025 | g0230 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03942 | hp2 | a0002 | c0002 | t0009 | g0182 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04184 | hp1 | a0001 | c0001 | t0096 | g0034 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04184 | hp2 | a0001 | c0004 | t0045 | g0051 | SAS | BEB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0364 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04204 | hp1 | a0001 | c0004 | t0045 | g0053 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG04204 | hp2 | a0002 | c0002 | t0021 | g0153 | SAS | STU | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18522 | hp1 | a0001 | c0005 | t0010 | g0133 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18522 | hp2 | a0001 | c0005 | t0015 | g0029 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18747 | hp1 | a0002 | c0031 | t0006 | g0310 | EAS | CHB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18747 | hp2 | a0002 | c0010 | t0027 | g0157 | EAS | CHB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18906 | hp1 | a0001 | c0004 | t0049 | g0371 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18906 | hp2 | a0001 | c0004 | t0029 | g0345 | AFR | YRI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18939 | hp1 | a0002 | c0002 | t0020 | g0007 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18939 | hp2 | a0003 | c0003 | t0002 | g0312 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18940 | hp1 | a0003 | c0027 | t0065 | g0202 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18940 | hp2 | a0002 | c0002 | t0006 | g0086 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18942 | hp1 | a0003 | c0003 | t0002 | g0314 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18942 | hp2 | a0006 | c0015 | t0019 | g0062 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18945 | hp1 | a0001 | c0001 | t0029 | g0151 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18945 | hp2 | a0007 | c0018 | t0001 | g0179 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18947 | hp1 | a0002 | c0002 | t0052 | g0040 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18947 | hp2 | a0008 | c0019 | t0001 | g0123 | 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 | t0008 | g0104 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18949 | hp1 | a0002 | c0002 | t0032 | g0085 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18949 | hp2 | a0001 | c0001 | t0095 | g0208 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18950 | hp1 | a0002 | c0002 | t0006 | g0088 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18950 | hp2 | a0001 | c0001 | t0027 | g0272 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18957 | hp1 | a0003 | c0003 | t0002 | g0322 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18961 | hp1 | a0009 | c0016 | t0118 | g0327 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18962 | hp1 | a0002 | c0002 | t0020 | g0073 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18963 | hp1 | a0001 | c0001 | t0080 | g0271 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18963 | hp2 | a0002 | c0002 | t0026 | g0101 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18964 | hp1 | a0003 | c0003 | t0002 | g0299 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18964 | hp2 | a0002 | c0002 | t0070 | g0109 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18967 | hp2 | a0009 | c0016 | t0002 | g0336 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18968 | hp2 | a0002 | c0002 | t0073 | g0199 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18969 | hp1 | a0002 | c0002 | t0031 | g0071 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18969 | hp2 | a0005 | c0014 | t0003 | g0267 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18970 | hp1 | a0002 | c0002 | t0011 | g0068 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18971 | hp1 | a0003 | c0003 | t0002 | g0354 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | 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 | g0298 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18977 | hp1 | a0002 | c0002 | t0020 | g0099 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0297 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18978 | hp2 | a0001 | c0004 | t0007 | g0307 | 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 | t0106 | g0330 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18983 | hp1 | a0002 | c0002 | t0013 | g0083 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18983 | hp2 | a0001 | c0001 | t0012 | g0223 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18984 | hp1 | a0003 | c0003 | t0002 | g0305 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18986 | hp1 | a0001 | c0001 | t0042 | g0224 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18986 | hp2 | a0001 | c0001 | t0104 | g0149 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18990 | hp1 | a0001 | c0006 | t0013 | g0080 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18990 | hp2 | a0001 | c0001 | t0028 | g0207 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18991 | hp1 | a0002 | c0002 | t0011 | g0066 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18991 | hp2 | a0003 | c0003 | t0101 | g0296 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18994 | hp1 | a0003 | c0003 | t0109 | g0340 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18994 | hp2 | a0002 | c0002 | t0071 | g0117 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18995 | hp1 | a0001 | c0006 | t0060 | g0064 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18998 | hp1 | a0002 | c0002 | t0067 | g0130 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18999 | hp1 | a0003 | c0012 | t0002 | g0203 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA18999 | hp2 | a0003 | c0003 | t0122 | g0328 | 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 | t0003 | g0038 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19001 | hp2 | a0002 | c0002 | t0072 | g0158 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19002 | hp1 | a0013 | c0022 | t0001 | g0174 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19002 | hp2 | a0001 | c0001 | t0075 | g0079 | 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 | t0013 | g0078 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19004 | hp1 | a0002 | c0002 | t0011 | g0070 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19004 | hp2 | a0002 | c0013 | t0008 | g0005 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19005 | hp1 | a0002 | c0013 | t0008 | g0005 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19005 | hp2 | a0002 | c0002 | t0011 | g0065 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19010 | hp1 | a0006 | c0015 | t0062 | g0076 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19043 | hp1 | a0001 | c0001 | t0034 | g0270 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19043 | hp2 | a0001 | c0005 | t0004 | g0334 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19056 | hp2 | a0007 | c0030 | t0113 | g0332 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0351 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19057 | hp2 | a0002 | c0010 | t0081 | g0156 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19058 | hp1 | a0002 | c0002 | t0036 | g0259 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19058 | hp2 | a0014 | c0029 | t0085 | g0265 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19063 | hp2 | a0003 | c0003 | t0002 | g0318 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19064 | hp1 | a0009 | c0016 | t0002 | g0317 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19064 | hp2 | a0002 | c0002 | t0032 | g0084 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19065 | hp1 | a0003 | c0003 | t0016 | g0337 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19065 | hp2 | a0001 | c0001 | t0042 | g0225 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19066 | hp1 | a0002 | c0002 | t0020 | g0072 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19066 | hp2 | a0001 | c0001 | t0028 | g0206 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19068 | hp1 | a0001 | c0006 | t0006 | g0145 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19068 | hp2 | a0002 | c0002 | t0036 | g0249 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19070 | hp2 | a0002 | c0002 | t0031 | g0089 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19072 | hp1 | a0001 | c0006 | t0013 | g0077 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19072 | hp2 | a0001 | c0001 | t0028 | g0205 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19074 | hp1 | a0002 | c0002 | t0011 | g0067 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19075 | hp1 | a0003 | c0003 | t0002 | g0326 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19076 | hp1 | a0001 | c0006 | t0086 | g0200 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19076 | hp2 | a0002 | c0002 | t0026 | g0057 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19077 | hp1 | a0006 | c0015 | t0019 | g0081 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0323 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19081 | hp1 | a0002 | c0002 | t0011 | g0069 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19081 | hp2 | a0003 | c0003 | t0048 | g0295 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19082 | hp1 | a0003 | c0003 | t0002 | g0358 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19082 | hp2 | a0002 | c0002 | t0013 | g0107 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19083 | hp1 | a0008 | c0019 | t0001 | g0122 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19084 | hp1 | a0002 | c0002 | t0051 | g0106 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0320 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19090 | hp1 | a0002 | c0002 | t0006 | g0194 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19090 | hp2 | a0003 | c0003 | t0107 | g0136 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19091 | hp1 | a0003 | c0003 | t0002 | g0302 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA19091 | hp2 | a0001 | c0001 | t0012 | g0222 | EAS | JPT | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20129 | hp1 | a0003 | c0012 | t0001 | g0254 | AFR | ASW | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20129 | hp2 | a0001 | c0011 | t0018 | g0363 | AFR | ASW | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20752 | hp1 | a0002 | c0002 | t0009 | g0103 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20752 | hp2 | a0003 | c0003 | t0007 | g0011 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0037 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20805 | hp2 | a0001 | c0007 | t0001 | g0189 | EUR | TSI | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01123 | hp1 | a0003 | c0012 | t0002 | g0368 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG01123 | hp2 | a0003 | c0003 | t0007 | g0360 | AMR | CLM | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02109 | hp1 | a0004 | c0008 | t0044 | g0215 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02109 | hp2 | a0001 | c0005 | t0004 | g0260 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02486 | hp1 | a0001 | c0011 | t0018 | g0349 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02486 | hp2 | a0004 | c0017 | t0017 | g0120 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02559 | hp1 | a0003 | c0009 | t0050 | g0152 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG02559 | hp2 | a0001 | c0005 | t0004 | g0032 | AFR | ACB | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03471 | hp1 | a0003 | c0009 | t0050 | g0135 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG03471 | hp2 | a0001 | c0004 | t0099 | g0350 | AFR | MSL | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG06807 | hp1 | a0001 | c0005 | t0004 | g0030 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| HG06807 | hp2 | a0002 | c0002 | t0058 | g0063 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20300 | hp1 | a0001 | c0004 | t0121 | g0355 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA20300 | hp2 | a0001 | c0005 | t0004 | g0017 | AFR | USA | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA21309 | hp1 | a0001 | c0001 | t0023 | g0257 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| NA21309 | hp2 | a0001 | c0001 | t0112 | g0367 | AFR | LWK | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| homoSapiens | chm13v2 | a0001 | c0007 | t0088 | g0163 | REF | REF | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0039 | g0333 | REF | REF | MEF2A_chr15_99560984_99721488 | MEF2A | chr15 | 99560984 | 99721488 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99712504 | C | CCAG | 1 | a0007 | 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 | a0006 | 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 | a0013 | 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 | 1 | a0003 | 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 | 1 | a0002 | 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 | a0005 | 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 | a0008 | 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 | a0014 | 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 | a0009 | 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 | a0012 | 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 | a0010 | 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 | a0001 a0002 |
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 | a0001 | 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 | a0010 | 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 | a0012 | 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 | a0012 | 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 | a0011 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0003 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 | a0010 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99703377 | T | C | 1 | a0001c0021 | 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 | 19 | a0001c0001 a0001c0006 a0001c0007 others(16): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | 27 | a0001c0001 a0001c0004 a0001c0006 others(24): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0003c0020 | 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 | a0001c0001 a0001c0006 |
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 | a0012c0028 | 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 | a0012c0028 | 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 | 7 | a0001c0006 a0001c0011 a0002c0002 others(4): 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 | a0010c0024 | 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 | a0010c0024 | 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 | a0010c0024 | 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 | a0010c0024 | 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 | 8 | HG00639.hp2 HG00733.hp1 HG01192.hp1 others(5): 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 | a0010c0024 | 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 | a0010c0024 | 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 | a0010c0024 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99566015 | G | T | 1 | a0001c0005t0127 | 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 | a0001c0004t0126 a0003c0003t0125 |
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 | 106 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(103): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): 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 | 13 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0078 others(10): 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 | a0014c0029t0085 | 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 | a0001c0006t0008 a0002c0002t0008 a0002c0002t0031 others(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 | a0001c0001t0084 | 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 | a0003c0009t0050 a0003c0009t0124 |
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 | a0001c0001t0078 | 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 | 166 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(163): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): 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 | a0001c0006t0086 | 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 | a0002c0002t0031 | 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 | 81 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(78): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): 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 | a0001c0001t0059 | 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 | a0003c0009t0050 a0003c0009t0124 |
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 | a0001c0001t0034 a0003c0012t0034 a0011c0025t0105 |
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 | a0001c0001t0075 a0001c0001t0104 a0001c0004t0121 others(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 | a0001c0001t0059 a0002c0002t0035 |
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 | a0002c0002t0052 | 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 | 87 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(84): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): 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 | a0001c0005t0010 a0001c0005t0114 a0004c0008t0010 |
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 | a0001c0001t0027 a0001c0001t0095 a0001c0001t0096 others(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 | 32 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0059 others(29): 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 | a0001c0001t0027 a0001c0001t0029 a0001c0001t0095 others(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 | 74 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(71): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): 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 | a0001c0001t0017 a0001c0001t0040 a0001c0001t0079 others(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 | 50 | a0001c0001t0027 a0001c0001t0029 a0001c0001t0042 others(47): 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 | a0002c0002t0035 a0003c0003t0117 a0007c0030t0113 |
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 | a0002c0002t0053 | 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 | a0001c0001t0040 a0001c0001t0079 a0001c0001t0087 others(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 | 24 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0027 others(21): 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 | 58 | a0001c0001t0005 a0001c0001t0022 a0001c0001t0029 others(55): 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 | a0001c0006t0086 | 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 | a0001c0001t0089 | 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 | 71 | a0001c0001t0005 a0001c0001t0023 a0001c0001t0028 others(68): 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 | a0001c0005t0127 | 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 | a0001c0005t0127 | 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 | a0001c0001t0112 | 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 | a0001c0004t0108 a0001c0011t0018 a0001c0011t0061 |
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 | 127 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(124): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0001t0089 | 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 | a0002c0002t0037 a0002c0002t0038 a0002c0002t0077 |
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 | 29 | a0001c0004t0002 a0001c0004t0007 a0001c0004t0106 others(26): 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 | a0001c0004t0044 a0001c0004t0047 a0001c0005t0010 others(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 | a0001c0001t0074 a0001c0006t0024 a0001c0006t0086 others(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 | 55 | a0001c0001t0074 a0001c0001t0075 a0001c0006t0006 others(52): 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 | a0001c0001t0034 a0003c0012t0034 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:99566155 | G | A | 1 | a0001c0004t0005g0006 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0003c0012t0002g0368 | 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 | a0001c0001t0112g0367 | 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 | 278 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(275): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): 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 | a0001c0001t0012g0279 | 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 | a0002c0002t0020g0007 | 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 | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(268): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0023g0277 | 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 | a0001c0005t0039g0015 | 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 | a0001c0001t0059g0276 a0003c0009t0119g0275 |
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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0127g0018 |
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 | a0001c0005t0039g0015 a0008c0032t0004g0019 |
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 | a0001c0005t0004g0020 a0001c0005t0004g0022 a0001c0005t0004g0023 others(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 | a0001c0005t0004g0026 a0001c0005t0004g0030 a0001c0005t0004g0032 others(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 | 105 | a0001c0001t0001g0003 a0001c0001t0001g0168 a0001c0001t0001g0175 others(102): Show |
107 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(104): 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 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0365 a0001c0001t0001g0366 others(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 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0266 others(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 | a0001c0001t0003g0273 a0001c0001t0027g0272 a0001c0001t0034g0270 others(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 | a0003c0026t0064g0274 | 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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 2 | a0004c0008t0010g0001 a0004c0008t0010g0036 |
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 | a0001c0004t0126g0281 a0001c0011t0061g0282 a0003c0003t0125g0280 |
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 | a0001c0001t0087g0033 a0001c0001t0096g0034 |
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 | a0002c0002t0009g0035 | 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 | a0003c0026t0064g0274 | 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 | a0001c0005t0004g0260 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0046 a0001c0001t0003g0047 others(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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0003c0026t0064g0274 | 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 | a0002c0010t0012g0159 | 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 | a0001c0004t0047g0049 a0001c0004t0047g0290 a0001c0005t0015g0025 |
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 | a0003c0003t0002g0291 a0003c0003t0002g0292 |
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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0009c0016t0002g0336 | 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 | a0009c0016t0002g0336 | 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 | a0003c0003t0007g0014 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0001c0005t0127g0018 | 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 | a0002c0002t0072g0158 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0005g0283 a0001c0004t0012g0362 a0001c0004t0044g0294 others(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 | a0001c0005t0004g0024 | 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 | a0003c0020t0007g0361 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0001c0005t0004g0023 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0017g0162 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0002c0002t0021g0153 | 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 | a0002c0002t0021g0153 | 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 | a0002c0002t0021g0153 | 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 | a0001c0001t0001g0050 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-225+3975T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99570079 | |||||||
| chr15:99570578 | G | A | 3 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 |
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 | a0001c0001t0003g0263 a0002c0002t0008g0054 a0002c0002t0021g0153 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0220 a0001c0001t0005g0137 others(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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0003c0003t0002g0292 | 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 | a0001c0001t0089g0164 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 24 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0112g0367 others(21): 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 | 2 | a0002c0013t0008g0005 a0003c0003t0016g0337 |
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 | a0002c0002t0069g0209 | 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 | a0001c0005t0004g0334 a0001c0011t0018g0335 |
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 | a0001c0004t0005g0006 a0011c0025t0105g0042 |
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 | a0003c0003t0048g0295 | 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 | a0001c0005t0004g0020 a0001c0005t0004g0022 a0001c0005t0004g0260 others(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 | a0001c0001t0028g0205 a0001c0001t0028g0206 a0001c0001t0028g0207 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0047 a0001c0001t0003g0048 others(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 | 345 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(342): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | a0003c0012t0034g0132 | 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 | a0001c0004t0005g0006 a0011c0025t0105g0042 |
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 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 |
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 | 217 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(214): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | 31 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(28): 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 | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-225+6159C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99572263 | |||||||
| chr15:99572528 | C | CAGAG | 100 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(97): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0096g0034 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0003g0269 | 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 | a0001c0001t0028g0205 a0001c0001t0028g0206 a0001c0001t0028g0207 others(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 | a0002c0010t0027g0157 | 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 | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0073g0199 | 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 | a0001c0001t0003g0037 a0001c0001t0084g0044 a0001c0004t0045g0051 others(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 | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0001g0168 | 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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0006g0194 | 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 | a0002c0002t0006g0059 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0059g0276 | 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 | a0002c0002t0053g0060 | 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 | a0001c0001t0001g0246 | 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 | a0001c0004t0049g0370 | 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 | a0001c0004t0005g0338 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0012c0028t0006g0167 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 138 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(135): 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 | a0001c0001t0001g0232 a0001c0001t0001g0235 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(72): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-225+10698G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99576802 | |||||||
| chr15:99576927 | G | A | 97 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(94): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0014g0061 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0059g0276 | 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 | a0001c0001t0023g0257 | 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 | 143 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(140): 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 | a0004c0008t0046g0216 | 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 |
219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): 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 | a0001c0007t0001g0169 | 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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0001c0007t0001g0191 | 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 | a0003c0009t0002g0195 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0011c0025t0105g0042 | 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 | a0001c0001t0059g0276 | 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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0006c0015t0019g0062 | 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 | a0001c0001t0003g0119 | 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 | a0003c0026t0064g0274 | 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 | a0001c0001t0074g0204 | 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 | 142 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(139): 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 | a0001c0004t0030g0346 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0002c0002t0038g0140 | 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 | a0003c0003t0007g0008 a0003c0003t0007g0009 a0003c0003t0007g0010 others(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 | a0003c0003t0007g0013 | 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 | a0002c0002t0038g0043 | 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 | 136 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(133): 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 | a0003c0009t0004g0021 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0003g0119 | 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 | a0004c0008t0044g0215 | 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 | a0001c0004t0126g0281 a0001c0011t0061g0282 a0003c0003t0125g0280 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(72): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): 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 | a0001c0001t0001g0245 | 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 | a0002c0010t0027g0157 | 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 | a0001c0004t0005g0006 | 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 | a0001c0004t0012g0362 a0001c0004t0044g0294 a0001c0004t0120g0284 |
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 | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0010t0027g0157 a0002c0010t0081g0156 |
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 | a0003c0012t0034g0132 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0012c0028t0006g0167 | 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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): 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 | a0011c0025t0105g0042 | 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 | a0011c0025t0105g0042 | 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 | a0003c0009t0119g0275 | 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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | a0001c0001t0001g0278 | 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 | a0003c0003t0002g0298 a0003c0003t0002g0299 |
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 | a0001c0001t0112g0367 | 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 | a0002c0002t0071g0117 | 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 | a0008c0019t0001g0122 | 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 | a0001c0004t0001g0325 | 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 | a0002c0013t0016g0344 | 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 | 145 | a0001c0001t0001g0150 a0001c0001t0001g0193 a0001c0001t0003g0037 others(142): 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 | a0002c0002t0058g0063 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0006t0060g0064 | 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 | a0003c0003t0115g0343 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0246 |
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 | a0001c0001t0017g0162 a0001c0005t0010g0133 a0001c0005t0114g0218 others(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 | a0001c0001t0112g0367 | 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 | a0004c0017t0017g0120 a0004c0017t0017g0121 |
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 | a0001c0001t0059g0276 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0026g0116 | 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 | a0002c0002t0021g0153 | 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 | a0001c0001t0059g0276 | 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 | a0003c0003t0125g0280 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0021g0166 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0003t0002g0056 a0003c0003t0002g0300 a0003c0003t0016g0055 others(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 | 96 | a0001c0001t0001g0150 a0001c0001t0003g0119 a0001c0001t0005g0137 others(93): 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 | a0001c0001t0112g0367 | 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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): 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 | a0001c0001t0005g0137 a0002c0002t0011g0065 a0002c0002t0011g0066 others(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 | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.-224-12744G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585686 | |||||||
| chr15:99585686 | G | T | 135 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(132): 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 | 135 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(132): 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 | 98 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(95): 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 | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-224-12687C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99585743 | |||||||
| chr15:99585856 | G | A | 40 | a0001c0001t0017g0162 a0001c0005t0004g0016 a0001c0005t0004g0017 others(37): 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 | a0001c0001t0023g0277 | 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 | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(76): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-224-11961T>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99586469 | |||||||
| chr15:99586557 | A | G | 10 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0004c0008t0010g0001 others(7): 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0069g0209 | 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 | a0001c0005t0004g0024 | 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 | a0001c0006t0009g0111 a0001c0006t0009g0112 a0001c0006t0009g0113 others(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 | a0001c0001t0005g0139 | 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 | a0001c0004t0030g0346 a0001c0004t0099g0350 a0001c0011t0018g0347 others(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 | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-224-10760T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 1/11 | chr15 | 99587670 | |||||||
| chr15:99587944 | G | GGAC | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0001c0001t0059g0276 a0001c0004t0048g0369 a0001c0004t0049g0370 others(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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0004c0008t0044g0215 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0005t0004g0020 | 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 | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(75): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): 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 | a0001c0005t0004g0261 a0001c0005t0004g0262 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0001g0278 | 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 | a0001c0007t0001g0170 a0001c0007t0001g0258 a0002c0002t0014g0228 others(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 | a0001c0001t0001g0190 | 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 | a0003c0003t0016g0337 | 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 | a0002c0002t0021g0153 | 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 | a0002c0013t0002g0324 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0112g0367 | 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 | a0003c0003t0110g0285 | 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 | a0002c0002t0011g0065 a0002c0002t0011g0066 |
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 | a0002c0002t0025g0221 | 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 | a0002c0002t0058g0063 | 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 | a0003c0003t0002g0323 | 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 | a0001c0001t0022g0171 a0002c0010t0022g0172 |
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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(72): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): 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 | a0002c0002t0031g0071 | 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 | a0001c0005t0010g0133 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0047g0049 a0001c0004t0047g0290 a0001c0005t0015g0025 |
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 | a0001c0004t0030g0346 a0001c0004t0099g0350 a0001c0011t0018g0347 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0022g0238 |
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 | a0003c0009t0119g0275 | 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 | a0002c0002t0020g0072 a0002c0002t0020g0073 |
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 | a0001c0001t0078g0268 | 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 | a0001c0004t0098g0306 | 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 | a0001c0004t0007g0307 | 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 | a0001c0001t0001g0227 | 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 | a0001c0004t0029g0345 | 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 | a0001c0007t0001g0170 | 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 | a0001c0001t0001g0150 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0004c0017t0017g0120 a0004c0017t0017g0121 |
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 | a0001c0006t0019g0231 | 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 | a0001c0001t0003g0226 | 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 | a0003c0003t0002g0292 | 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 | a0009c0016t0002g0336 | 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 | a0001c0001t0003g0119 | 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 | 98 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(95): 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 | a0011c0025t0105g0042 | 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 | a0001c0004t0098g0306 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0059g0276 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 104 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(101): 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 | a0001c0007t0001g0189 | 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0059g0276 | 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 | a0001c0005t0010g0133 a0003c0009t0050g0135 a0003c0009t0050g0152 others(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 | a0002c0002t0006g0110 | 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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): 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 | a0002c0002t0068g0250 | 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 | a0002c0002t0035g0074 a0002c0002t0035g0075 |
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 | 93 | a0001c0001t0001g0190 a0001c0001t0017g0162 a0001c0001t0017g0188 others(90): 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 | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(109): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): 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 | 100 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(97): 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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0001c0001t0023g0257 | 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 | a0001c0005t0010g0133 | 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 | a0003c0003t0101g0296 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0119 others(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 | 140 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(137): 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 | a0006c0015t0062g0076 | 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 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 |
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 | a0011c0025t0105g0042 | 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 | a0002c0013t0016g0344 | 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 | a0001c0001t0112g0367 | 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 | a0001c0004t0108g0309 a0001c0004t0126g0281 a0001c0005t0004g0334 others(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 | a0002c0013t0016g0344 | 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 | a0002c0002t0025g0230 | 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 | a0001c0004t0082g0286 a0001c0004t0083g0287 |
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 | 146 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(143): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0017g0162 a0001c0005t0010g0133 a0001c0005t0114g0218 others(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 | 101 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(98): 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 | a0004c0008t0046g0213 a0004c0008t0092g0214 |
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 | a0001c0005t0010g0133 | 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 | a0001c0004t0044g0294 | 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 | a0002c0002t0036g0249 | 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 | a0011c0025t0105g0042 | 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 | a0002c0002t0053g0060 a0011c0025t0105g0042 |
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 | a0002c0010t0027g0157 | 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 | a0001c0001t0001g0241 | 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 | a0004c0017t0017g0120 a0004c0017t0017g0121 |
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 | a0002c0010t0001g0173 | 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 | a0002c0002t0058g0063 | 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 | 40 | a0001c0001t0017g0162 a0001c0005t0004g0016 a0001c0005t0004g0017 others(37): 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 | a0003c0003t0005g0293 | 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 | a0001c0004t0030g0346 a0001c0004t0099g0350 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0047 a0001c0001t0003g0048 others(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 | a0002c0002t0070g0109 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0002c0002t0053g0060 | 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 | a0001c0001t0034g0270 a0003c0009t0004g0021 a0003c0012t0034g0132 others(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 | a0012c0028t0006g0167 | 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 | a0001c0001t0112g0367 | 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 | 145 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(142): 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 | a0003c0003t0111g0012 | 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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0003c0003t0007g0008 a0003c0003t0007g0009 a0003c0003t0007g0010 others(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 | a0011c0025t0105g0042 | 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 | a0002c0002t0006g0108 | 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 | a0001c0001t0034g0270 a0003c0009t0004g0021 a0003c0012t0034g0132 others(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 | a0002c0002t0013g0107 a0002c0002t0070g0109 |
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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 others(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 | a0002c0002t0006g0108 | 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 | 138 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(135): 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 | a0001c0001t0090g0187 | 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 | a0011c0025t0105g0042 | 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 | a0001c0004t0005g0006 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0071g0117 | 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 | a0003c0003t0007g0014 | 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 | a0013c0022t0001g0174 | 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 | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(76): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): 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 | a0003c0003t0107g0136 | 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 | 338 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(335): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(111): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): 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 | a0001c0001t0001g0127 a0001c0001t0001g0186 a0001c0001t0001g0243 others(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 | 22 | a0001c0001t0112g0367 a0001c0004t0002g0352 a0001c0004t0002g0356 others(19): 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 | a0009c0016t0118g0327 | 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 | a0001c0001t0112g0367 | 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 | a0001c0004t0044g0294 a0003c0009t0050g0152 |
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 | a0003c0003t0002g0341 a0003c0020t0002g0342 a0003c0020t0007g0361 |
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 | a0001c0006t0019g0231 | 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 | a0001c0004t0082g0286 a0001c0004t0083g0287 a0001c0011t0061g0282 others(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 | a0001c0005t0004g0016 a0001c0005t0004g0020 a0001c0005t0004g0022 others(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 | a0001c0001t0017g0162 a0001c0004t0005g0338 a0001c0004t0030g0288 others(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 | 31 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0357 others(28): 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 | 14 | a0001c0004t0047g0290 a0002c0013t0002g0324 a0003c0003t0002g0291 others(11): 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 | a0001c0004t0001g0325 a0001c0004t0005g0006 a0001c0004t0007g0307 others(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 | a0001c0004t0005g0198 a0002c0013t0102g0052 a0003c0003t0002g0299 others(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 | a0001c0001t0001g0193 a0001c0004t0045g0051 a0001c0004t0045g0053 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0246 others(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 | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(67): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0034g0270 a0002c0010t0012g0159 |
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 | a0001c0001t0059g0276 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 others(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 | a0001c0001t0097g0253 | 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 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(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 | 71 | a0001c0001t0005g0148 a0001c0001t0023g0234 a0001c0001t0023g0257 others(68): 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 | a0001c0006t0009g0115 a0001c0006t0024g0165 a0001c0007t0040g0118 others(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 | a0001c0007t0093g0045 a0002c0002t0025g0230 a0002c0002t0071g0117 |
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 | a0002c0002t0025g0102 a0002c0002t0058g0063 a0003c0009t0050g0135 others(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 | a0001c0006t0019g0231 | 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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | a0001c0001t0034g0270 a0003c0012t0034g0132 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0017g0162 | 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 | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(347): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0005g0338 | 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 | a0002c0002t0006g0059 | 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 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0022g0238 |
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 | a0001c0001t0090g0187 | 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 | 30 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0278 others(27): 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 | a0001c0001t0023g0277 | 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 | a0003c0012t0001g0254 | 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 | 41 | a0001c0001t0001g0003 a0001c0001t0001g0220 a0001c0001t0001g0248 others(38): 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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0232 a0001c0001t0001g0235 others(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 |
25 | a0001c0001t0001g0128 a0001c0001t0001g0185 a0001c0001t0003g0039 others(22): Show |
25 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(22): 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 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0246 others(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 |
7 | a0001c0001t0001g0168 a0001c0001t0003g0273 a0002c0013t0008g0005 others(4): 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 | a0003c0003t0107g0136 | 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 | a0001c0001t0097g0253 a0002c0002t0006g0059 a0002c0002t0025g0230 |
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 | a0001c0001t0012g0240 a0002c0010t0081g0156 a0003c0003t0002g0358 |
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 | a0001c0006t0009g0115 a0001c0007t0001g0169 a0006c0023t0027g0161 |
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 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0017g0162 others(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 | a0001c0001t0001g0175 a0001c0004t0108g0309 a0002c0002t0070g0109 others(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 | a0001c0001t0075g0079 a0001c0006t0013g0077 a0001c0006t0013g0078 others(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 | 5 | a0001c0001t0001g0241 a0001c0005t0004g0023 a0001c0021t0005g0217 others(2): 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 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0004c0008t0010g0036 others(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 | a0011c0025t0105g0042 | 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 | a0002c0031t0006g0310 | 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 | a0001c0001t0112g0367 a0006c0015t0019g0062 a0006c0015t0062g0076 others(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 | a0004c0008t0010g0036 | 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 | a0003c0003t0002g0318 | 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 | a0002c0013t0002g0324 | 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 | a0002c0002t0006g0086 a0002c0002t0006g0088 a0002c0002t0026g0057 |
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 | a0001c0001t0023g0234 | 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 | a0007c0018t0030g0233 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0034g0270 |
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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | 86 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(83): 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 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(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 | a0001c0001t0001g0150 a0001c0001t0005g0146 a0001c0001t0005g0147 others(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 | 96 | a0001c0001t0001g0150 a0001c0001t0005g0146 a0001c0001t0005g0147 others(93): 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 | 86 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(83): 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 | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(203): 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 | a0001c0001t0023g0277 a0001c0001t0075g0079 a0001c0004t0005g0283 others(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 | a0001c0004t0001g0325 a0001c0004t0007g0307 a0001c0005t0004g0030 others(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 | a0001c0004t0047g0290 a0002c0031t0006g0310 a0003c0003t0002g0320 others(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 | 69 | a0001c0001t0001g0004 a0001c0001t0001g0127 a0001c0001t0001g0150 others(66): 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 | 87 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(84): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): 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 | 47 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0193 others(44): 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 | a0001c0001t0017g0188 a0001c0001t0112g0367 a0001c0006t0006g0145 others(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 | a0001c0004t0030g0346 a0001c0004t0099g0350 a0001c0011t0018g0347 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 78 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0124 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0003c0003t0002g0300 a0003c0003t0117g0301 |
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 | 103 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(100): 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 | a0003c0009t0004g0021 a0003c0009t0050g0135 a0003c0009t0050g0152 others(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 | a0001c0004t0098g0306 | 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 | 109 | a0001c0001t0001g0365 a0001c0001t0022g0184 a0001c0001t0028g0205 others(106): 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0004 | 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 | a0008c0019t0001g0122 | 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 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0005t0127g0018 others(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 | a0001c0005t0004g0017 a0003c0009t0002g0195 a0003c0009t0002g0197 |
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 | a0001c0001t0001g0220 a0001c0001t0003g0037 a0001c0001t0003g0038 others(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 | a0001c0001t0023g0234 a0001c0004t0005g0338 a0001c0004t0029g0308 others(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 |
71 | a0001c0001t0001g0128 a0001c0001t0001g0175 a0001c0001t0001g0190 others(68): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(69): 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 |
54 | a0001c0001t0001g0003 a0001c0001t0001g0150 a0001c0001t0001g0180 others(51): 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 | a0001c0001t0001g0050 a0001c0001t0001g0125 a0001c0001t0001g0127 others(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 |
22 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0178 others(19): 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 | a0001c0001t0001g0176 a0001c0001t0001g0227 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0236 a0001c0011t0061g0282 a0002c0002t0036g0259 others(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 | a0001c0004t0126g0281 | 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 | a0008c0019t0001g0123 | 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 | a0003c0003t0002g0358 | 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 | a0001c0004t0030g0288 a0003c0009t0124g0134 |
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 | a0001c0004t0082g0286 a0001c0004t0083g0287 |
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 | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(75): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): 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 | a0001c0001t0001g0232 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0112g0367 | 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 | a0001c0004t0007g0307 | 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 | a0001c0001t0089g0164 | 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 | a0003c0003t0002g0300 a0003c0003t0117g0301 |
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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0127 others(10): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0005t0015g0029 a0001c0005t0015g0031 |
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 | a0003c0003t0002g0326 | 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 | 99 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(96): 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 | a0001c0001t0112g0367 | 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 | a0001c0004t0044g0294 | 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 | a0001c0001t0003g0266 | 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 | a0001c0004t0005g0338 a0001c0004t0029g0308 a0001c0004t0029g0345 others(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 | a0001c0001t0112g0367 | 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 | a0009c0016t0002g0317 | 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 | a0001c0001t0003g0047 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0002c0002t0076g0098 | 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 | a0002c0013t0002g0324 a0003c0003t0002g0318 |
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 | a0011c0025t0105g0042 | 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 | 5 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 others(2): 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 | a0004c0008t0010g0212 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0007c0018t0030g0233 | 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 | a0001c0001t0017g0242 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0003t0048g0295 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0002c0002t0036g0249 | 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 | a0001c0005t0010g0133 | 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 | a0002c0002t0013g0083 a0002c0002t0013g0107 a0002c0002t0032g0084 others(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 | a0002c0002t0006g0194 | 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 | a0003c0003t0122g0328 | 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 | a0003c0003t0002g0300 a0003c0003t0117g0301 |
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 | a0002c0002t0008g0054 | 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 | a0001c0005t0114g0218 | 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 | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(76): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): 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 | a0002c0002t0009g0182 | 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 | a0002c0002t0069g0209 | 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 | a0001c0007t0001g0170 | 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 | a0001c0001t0112g0367 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0005g0137 a0001c0001t0017g0162 a0001c0004t0029g0345 others(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 | a0001c0004t0012g0362 a0001c0004t0030g0346 a0001c0004t0082g0286 others(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 | a0001c0004t0002g0356 a0001c0004t0002g0359 a0001c0004t0005g0198 others(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 | a0001c0001t0042g0224 a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | a0001c0001t0003g0046 a0001c0001t0042g0225 a0014c0029t0085g0265 |
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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0047 others(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 | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(66): Show |
71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): 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 | a0001c0001t0003g0037 a0001c0001t0003g0119 a0001c0001t0079g0131 others(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 | a0001c0001t0001g0190 a0001c0001t0074g0204 a0001c0001t0095g0208 others(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 | a0001c0001t0059g0276 a0001c0005t0010g0133 a0001c0006t0009g0115 others(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 | a0001c0001t0005g0146 a0001c0001t0023g0257 a0001c0006t0019g0231 others(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 | 91 | a0001c0001t0001g0150 a0001c0001t0001g0236 a0001c0001t0001g0237 others(88): 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 | a0001c0004t0007g0307 | 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 | a0001c0004t0002g0357 a0001c0004t0030g0288 a0001c0004t0045g0051 others(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 | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0127 others(28): Show |
32 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(29): 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 | a0001c0004t0005g0006 a0001c0004t0005g0338 a0001c0004t0083g0287 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0126 a0001c0001t0001g0176 others(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 | a0003c0003t0007g0010 a0003c0003t0101g0296 |
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 | a0001c0006t0009g0115 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0190 a0001c0001t0001g0235 others(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 | a0001c0005t0004g0026 a0004c0008t0044g0215 |
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 | a0001c0006t0024g0165 a0002c0002t0006g0086 a0002c0002t0009g0058 others(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 | a0001c0001t0005g0146 | 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 | a0001c0001t0001g0124 a0001c0001t0012g0240 a0001c0001t0023g0234 others(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 | a0001c0001t0005g0146 a0001c0001t0023g0277 a0001c0001t0059g0276 others(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 | 86 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0022g0238 others(83): 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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | 14 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0127 others(11): 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 | a0003c0003t0002g0291 a0003c0003t0002g0292 a0003c0003t0007g0008 others(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 | a0002c0002t0067g0130 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0007c0018t0030g0233 |
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 | a0001c0001t0087g0033 a0001c0001t0096g0034 |
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 | a0001c0001t0097g0253 | 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 | a0001c0001t0112g0367 | 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 | a0001c0005t0004g0030 | 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 | a0003c0009t0119g0275 | 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 | a0001c0001t0017g0162 a0001c0005t0114g0218 a0003c0003t0091g0289 others(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 | a0001c0005t0114g0218 | 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 | a0001c0005t0010g0133 | 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 | a0002c0013t0016g0344 a0003c0003t0002g0316 a0003c0003t0109g0340 |
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 | a0001c0001t0042g0224 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0007c0018t0030g0233 |
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 | a0001c0004t0043g0339 | 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 | a0001c0006t0008g0104 | 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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(72): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(74): 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0017g0162 a0001c0005t0114g0218 a0003c0009t0002g0195 others(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 | a0008c0019t0001g0123 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0087g0033 | 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 | a0003c0003t0002g0300 a0003c0003t0117g0301 |
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 | a0002c0002t0020g0007 a0002c0002t0072g0158 |
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 | a0001c0001t0097g0253 | 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 | a0001c0004t0082g0286 a0001c0004t0083g0287 |
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 | a0002c0010t0012g0159 | 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 | a0001c0001t0012g0240 | 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 | a0001c0001t0059g0276 | 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 | a0003c0003t0002g0316 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0125 |
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 | a0001c0004t0007g0307 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 |
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 | a0002c0002t0026g0116 | 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 | a0001c0011t0018g0349 | 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 | a0002c0002t0020g0007 a0002c0002t0020g0072 a0002c0002t0020g0073 others(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 | 348 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): 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 | a0001c0005t0010g0133 | 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 | a0003c0003t0002g0322 | 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 | a0001c0001t0074g0204 | 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 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0180 others(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 | a0001c0001t0017g0162 a0001c0005t0010g0133 a0001c0005t0114g0218 others(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 | a0002c0002t0035g0075 | 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 | a0003c0003t0007g0256 | 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 | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(73): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): 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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0003c0012t0034g0132 | 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 | a0002c0002t0008g0092 a0002c0002t0008g0093 |
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 | a0001c0005t0004g0020 a0001c0005t0004g0022 a0001c0005t0004g0260 others(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 | a0001c0004t0126g0281 a0003c0003t0125g0280 |
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 | a0001c0001t0005g0146 a0001c0006t0066g0097 a0002c0002t0006g0110 |
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 | a0011c0025t0105g0042 | 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 | a0001c0001t0001g0220 a0002c0002t0025g0221 |
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 | 91 | a0001c0001t0005g0146 a0001c0001t0075g0079 a0001c0006t0006g0091 others(88): 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 | a0002c0002t0006g0108 | 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 | a0001c0011t0061g0282 | 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 | a0003c0003t0048g0295 | 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 | a0002c0002t0025g0221 | 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 | a0001c0001t0074g0204 | 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 | a0001c0001t0001g0190 | 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 | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | a0003c0003t0002g0341 | 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 | 142 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(139): 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 | a0003c0026t0064g0274 | 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 | a0001c0005t0039g0015 | 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 | 103 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(100): 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 | a0001c0001t0112g0367 | 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 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0004c0008t0010g0251 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0047 a0001c0001t0084g0044 others(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 | 326 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(323): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | a0003c0003t0002g0364 | 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 | 329 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(326): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0003c0003t0107g0136 | 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 | a0003c0003t0002g0056 | 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 | a0001c0001t0003g0037 a0002c0002t0063g0160 |
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 | a0002c0002t0026g0116 | 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(223): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): 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 | a0011c0025t0105g0042 | 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 | a0002c0002t0006g0110 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0004c0017t0017g0120 | 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 | a0001c0001t0034g0270 a0003c0012t0034g0132 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0246 others(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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0001t0023g0277 | 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 | a0001c0001t0112g0367 a0001c0004t0047g0049 a0001c0004t0047g0290 |
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 | a0001c0001t0001g0235 | 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 | a0002c0002t0025g0230 | 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 | a0001c0001t0001g0190 a0001c0001t0017g0162 a0001c0005t0010g0133 others(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 | a0001c0001t0023g0234 a0001c0001t0023g0257 |
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 | a0003c0003t0007g0008 a0003c0003t0007g0009 a0003c0003t0007g0010 others(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 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 |
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 | a0002c0002t0036g0259 | 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 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 |
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 | a0001c0001t0112g0367 | 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 | a0002c0002t0051g0106 | 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 | a0001c0004t0002g0356 | 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 | a0001c0001t0003g0048 | 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 | a0001c0001t0075g0079 a0001c0006t0013g0077 a0001c0006t0013g0078 others(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 |
202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): 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 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0012g0222 others(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 | a0004c0008t0010g0212 | 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 | a0003c0026t0064g0274 | 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 | a0004c0017t0017g0120 a0004c0017t0017g0121 |
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 | a0003c0009t0002g0196 | 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 | a0001c0001t0090g0187 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0008g0054 a0002c0002t0014g0228 a0002c0002t0020g0007 others(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 | 91 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(88): 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 | 101 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(98): 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 | 104 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(101): 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 | a0003c0009t0050g0135 a0003c0009t0050g0152 a0003c0009t0124g0134 |
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 | a0007c0018t0030g0233 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0112g0367 | 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 | a0003c0009t0119g0275 | 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 | a0001c0001t0001g0190 | 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 | a0001c0004t0005g0006 a0001c0004t0005g0198 |
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 | a0011c0025t0105g0042 | 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 | a0001c0004t0047g0049 a0001c0004t0047g0290 |
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 | a0002c0002t0011g0065 a0002c0002t0011g0066 |
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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0071g0117 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0009g0058 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0120g0284 | 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 | a0001c0004t0030g0346 | 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 | a0011c0025t0105g0042 | 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 | a0008c0032t0004g0019 | 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 | 101 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(98): 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 | 147 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(144): 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 | a0003c0026t0064g0274 | 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 | a0003c0003t0016g0337 | 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 | a0003c0003t0107g0136 | 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 | a0001c0001t0023g0234 | 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 | a0003c0003t0002g0323 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): 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 | a0001c0004t0047g0049 a0001c0004t0047g0290 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0001g0176 a0001c0001t0001g0193 a0001c0001t0022g0238 others(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 | 24 | a0001c0001t0001g0248 a0001c0004t0002g0352 a0001c0004t0002g0356 others(21): 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 | a0001c0004t0002g0357 a0001c0004t0030g0346 a0001c0004t0045g0051 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(78): 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 | a0001c0001t0003g0037 a0001c0001t0003g0039 a0001c0001t0003g0046 others(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 | 7 | a0001c0001t0012g0222 a0001c0006t0009g0112 a0001c0006t0013g0080 others(4): 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 | a0001c0001t0012g0240 | 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 | a0001c0007t0001g0191 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | 2 | a0004c0008t0010g0001 a0004c0008t0010g0036 |
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 | a0001c0004t0030g0288 a0003c0003t0091g0289 |
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 | a0001c0001t0017g0162 a0001c0005t0004g0024 a0001c0005t0114g0218 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0039 a0001c0001t0003g0046 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0047 a0001c0001t0079g0131 others(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 | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(73): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): 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 | a0001c0001t0001g0186 | 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 | a0002c0002t0072g0158 | 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 | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): 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 | a0001c0001t0003g0037 a0001c0001t0003g0047 a0001c0001t0003g0048 others(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 | a0001c0011t0061g0282 | 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 | a0001c0005t0004g0017 a0001c0005t0004g0024 a0001c0005t0004g0026 others(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 | 1 | a0001c0001t0001g0003 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0011c0025t0105g0042 | 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 | a0001c0001t0059g0276 | 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 | a0002c0002t0037g0142 a0002c0002t0037g0144 a0002c0002t0038g0043 others(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 | 92 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(89): 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 | a0001c0004t0043g0339 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0010t0001g0173 | 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 | a0011c0025t0105g0042 | 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 | a0001c0004t0126g0281 a0003c0003t0125g0280 |
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 | a0001c0001t0003g0269 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0112g0367 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0001c0001t0075g0079 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 |
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 | a0006c0023t0027g0161 | 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 | a0004c0008t0046g0213 a0004c0008t0092g0214 |
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 | a0002c0002t0051g0106 | 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 | a0011c0025t0105g0042 | 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 | 137 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(134): 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 | a0003c0003t0002g0299 | 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 | a0001c0005t0114g0218 | 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 | a0001c0001t0001g0246 | 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 | a0002c0002t0014g0061 a0002c0002t0014g0090 a0002c0002t0014g0095 others(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 | a0002c0013t0016g0344 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0007t0093g0045 | 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 | a0001c0001t0003g0046 | 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 | a0003c0003t0002g0341 a0003c0020t0002g0342 a0003c0020t0007g0361 |
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 | a0004c0017t0017g0120 a0004c0017t0017g0121 |
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 | a0001c0001t0059g0276 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0006t0006g0091 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0071g0117 | 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 | a0001c0004t0005g0338 a0001c0004t0029g0308 a0001c0004t0029g0345 |
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 | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0007c0018t0030g0233 |
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 | a0010c0024t0021g0114 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 | 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 | a0004c0017t0017g0120 a0004c0017t0017g0121 |
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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | a0003c0003t0007g0360 | 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 | a0002c0010t0081g0156 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0004 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0007c0018t0030g0233 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0046 a0001c0001t0003g0047 others(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 | a0002c0002t0024g0041 | 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 | a0011c0025t0105g0042 | 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 | 110 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(107): 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 | a0001c0001t0023g0277 | 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 | a0001c0001t0003g0266 a0002c0010t0012g0159 a0002c0010t0027g0157 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0005t0010g0133 | 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 | a0002c0002t0037g0144 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0010t0081g0156 a0011c0025t0105g0042 |
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 | a0001c0001t0001g0193 | 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 | a0011c0025t0105g0042 | 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 | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(344): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0046 a0001c0001t0003g0047 others(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 | a0001c0004t0029g0308 | 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 | a0003c0009t0002g0196 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0012g0240 a0001c0001t0022g0184 a0001c0001t0043g0181 |
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 | a0001c0004t0005g0006 a0001c0004t0005g0198 |
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 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0359 others(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 | a0001c0001t0112g0367 | 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 | a0002c0002t0006g0088 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
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 | a0001c0004t0030g0288 a0003c0003t0091g0289 |
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 | 108 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(105): 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 | a0002c0002t0033g0239 | 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 | a0001c0001t0017g0162 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0042g0224 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0011t0061g0282 | 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 | a0001c0005t0015g0029 a0001c0005t0015g0031 |
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 | 87 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(84): 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 | a0001c0005t0039g0015 | 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 | a0003c0003t0002g0291 | 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 | a0003c0003t0002g0316 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0001t0097g0253 a0001c0004t0030g0346 a0001c0004t0099g0350 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0180 others(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 | a0004c0008t0046g0213 a0004c0008t0092g0214 |
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 | a0002c0010t0081g0156 | 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 | a0002c0002t0068g0250 | 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 | a0002c0002t0009g0058 | 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 | a0002c0031t0006g0310 | 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 | a0001c0006t0009g0115 a0010c0024t0021g0114 |
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 | a0001c0001t0112g0367 | 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 | a0001c0005t0114g0218 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0001g0190 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0013c0022t0001g0174 | 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 | a0011c0025t0105g0042 | 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 | a0011c0025t0105g0042 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0001g0190 | 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 | a0011c0025t0105g0042 | 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 | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0011c0025t0105g0042 | 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 | a0011c0025t0105g0042 | 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 | a0002c0002t0020g0007 a0002c0002t0020g0072 a0002c0002t0020g0073 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0246 others(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 | a0003c0003t0002g0315 | 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 | a0001c0001t0001g0193 a0003c0003t0002g0313 |
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 | a0001c0005t0010g0133 | 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 | a0003c0003t0002g0316 | 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 | a0001c0004t0047g0290 | 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 | a0001c0001t0001g0193 a0003c0003t0002g0313 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 1 | a0002c0010t0041g0002 | 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 | a0001c0001t0112g0367 | 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 | a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | a0001c0005t0127g0018 | 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 | a0011c0025t0105g0042 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0006t0006g0091 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0008c0019t0001g0122 a0008c0019t0001g0123 |
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 | a0001c0001t0112g0367 | 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 | a0008c0019t0001g0122 a0008c0019t0001g0123 |
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 | a0001c0001t0003g0269 | 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 | a0001c0006t0008g0104 a0002c0002t0008g0054 a0002c0002t0008g0092 others(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 | a0001c0005t0004g0023 | 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 | a0002c0002t0009g0182 | 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 | a0001c0004t0126g0281 a0003c0003t0125g0280 |
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 | a0002c0013t0102g0052 | 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 | a0002c0002t0038g0140 | 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 | a0002c0002t0038g0140 | 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 | a0002c0002t0038g0140 | 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 | a0002c0002t0038g0140 | 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 | a0002c0013t0016g0344 | 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 | a0001c0021t0005g0217 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(347): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): 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 | a0003c0003t0002g0291 | 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 | a0001c0004t0005g0283 a0001c0004t0012g0362 a0001c0004t0044g0294 others(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 | a0002c0002t0073g0199 | 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 | a0001c0004t0047g0049 | 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 | a0001c0001t0112g0367 | 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 | a0004c0017t0017g0121 | 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 | a0003c0003t0107g0136 | 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 | a0001c0004t0108g0309 a0001c0004t0126g0281 a0001c0005t0004g0334 others(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 | a0001c0001t0034g0270 a0001c0005t0010g0133 a0003c0009t0050g0135 others(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 | a0001c0001t0059g0276 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0108g0309 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0003g0119 | 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 | a0002c0002t0058g0063 | 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 | a0002c0002t0068g0250 | 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 | a0009c0016t0002g0336 | 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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | 6 | a0001c0001t0001g0003 a0001c0001t0001g0175 a0001c0001t0017g0188 others(3): 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 | 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 | a0001c0004t0108g0309 a0001c0005t0004g0334 a0001c0011t0018g0335 |
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 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(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 | a0002c0002t0014g0061 a0002c0002t0014g0095 a0002c0002t0014g0096 |
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 | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(208): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): 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 | a0001c0001t0001g0004 | 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 | a0002c0002t0032g0084 a0002c0002t0032g0085 |
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 | a0003c0003t0107g0136 | 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 | a0001c0001t0034g0270 a0003c0012t0034g0132 |
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 | a0001c0004t0120g0284 | 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 | a0002c0002t0009g0035 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0185 others(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 | a0003c0003t0048g0295 | 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 | a0001c0001t0112g0367 | 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 | a0003c0003t0048g0295 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0011c0025t0105g0042 | 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 | a0003c0009t0050g0152 | 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 | a0001c0004t0126g0281 a0003c0003t0125g0280 |
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 | a0002c0002t0020g0007 | 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 | a0003c0003t0048g0295 | 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 | a0003c0003t0048g0295 | 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 | a0002c0002t0011g0065 a0002c0002t0011g0066 a0002c0002t0011g0067 others(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 | a0001c0001t0090g0187 | 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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(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 | a0001c0001t0023g0277 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 80 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(77): 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 | a0003c0003t0002g0312 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0097g0253 | 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 | a0011c0025t0105g0042 | 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 | a0002c0002t0037g0142 a0002c0002t0037g0144 a0002c0002t0038g0043 others(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 | a0001c0004t0005g0283 a0001c0004t0012g0362 a0001c0004t0044g0294 others(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 | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0001c0006t0086g0200 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0001t0112g0367 | 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 | a0001c0001t0001g0168 | 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 | a0004c0008t0046g0213 a0004c0008t0092g0214 |
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 | 99 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(96): 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 | a0003c0009t0002g0195 a0003c0009t0002g0197 |
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 | a0001c0001t0034g0270 a0001c0005t0010g0133 a0003c0009t0050g0135 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0006t0009g0113 a0001c0006t0009g0115 a0010c0024t0021g0114 |
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 | a0001c0001t0012g0240 | 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 | a0003c0003t0002g0300 a0003c0003t0117g0301 |
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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0034g0270 a0003c0012t0034g0132 |
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 | a0001c0006t0024g0165 a0002c0002t0008g0094 a0002c0002t0052g0040 |
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 | a0001c0001t0012g0222 a0001c0001t0012g0223 a0001c0001t0042g0224 others(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 | a0011c0025t0105g0042 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0246 others(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 | a0002c0002t0038g0140 | 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 | 98 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(95): 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0006g0086 a0002c0002t0006g0088 a0002c0002t0026g0057 |
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 | a0002c0002t0036g0259 | 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 | a0001c0005t0004g0023 | 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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0112g0367 | 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 | a0002c0002t0020g0072 a0002c0002t0020g0073 a0002c0002t0020g0099 others(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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 others(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 | a0001c0007t0001g0170 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0023g0234 | 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 | a0001c0004t0082g0286 a0001c0004t0083g0287 |
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 | a0001c0004t0045g0051 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | a0003c0003t0002g0291 | 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 | 91 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(88): 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 | a0003c0003t0002g0326 | 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 | a0001c0004t0049g0370 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0011c0025t0105g0042 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | a0001c0007t0001g0169 | 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 | 103 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(100): 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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): 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 | a0001c0001t0022g0238 | 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 | a0003c0012t0002g0368 | 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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0112g0367 | 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 | 88 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(85): 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0241 | 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 | a0003c0003t0123g0329 | 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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 |
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 | a0001c0001t0112g0367 | 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 | a0002c0002t0008g0219 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): 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 | a0003c0003t0002g0302 a0003c0003t0002g0303 a0003c0003t0002g0304 others(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 | a0003c0003t0002g0364 | 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 | a0002c0002t0036g0249 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0013c0022t0001g0174 | 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 | a0001c0001t0112g0367 | 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 | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(76): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): 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 | a0001c0001t0042g0224 | 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 | a0001c0001t0080g0271 | 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 | 108 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(105): 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 | a0001c0001t0074g0204 a0002c0002t0036g0249 a0002c0002t0036g0259 others(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 | a0001c0001t0112g0367 a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0069g0209 | 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 | a0001c0005t0015g0029 a0001c0005t0015g0031 |
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 | a0001c0005t0015g0029 a0001c0005t0015g0031 |
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 | a0003c0003t0115g0343 | 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 | a0001c0004t0049g0371 | 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 | 1 | a0002c0010t0041g0002 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0003t0002g0318 | 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 | a0001c0006t0013g0080 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0047 a0001c0001t0003g0048 others(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 | a0002c0002t0009g0058 | 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0031g0071 | 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 | 143 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(140): 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 | a0002c0002t0058g0063 a0011c0025t0105g0042 |
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 | a0001c0001t0059g0276 | 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 | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(73): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): 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 | a0001c0001t0023g0257 | 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 | 10 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0004c0008t0010g0001 others(7): 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 | a0001c0001t0104g0149 | 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 | a0003c0009t0002g0196 | 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 | a0001c0001t0112g0367 | 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 | a0001c0004t0001g0325 a0001c0004t0007g0307 a0001c0004t0106g0330 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0005g0137 | 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 | a0011c0025t0105g0042 | 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 | 140 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(137): 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 | a0002c0002t0055g0201 | 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 | a0001c0021t0005g0217 | 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 | a0002c0002t0014g0228 a0002c0002t0021g0166 |
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 | a0001c0005t0004g0016 | 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 | a0001c0001t0096g0034 | 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 | 26 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0003g0266 others(23): Show |
26 | HG00597.hp1 HG00673.hp2 HG00733.hp1 others(23): 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 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0003g0038 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0011c0025t0105g0042 | 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 | a0002c0002t0037g0142 a0002c0002t0037g0144 a0002c0002t0038g0043 others(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 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0004c0008t0010g0251 others(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 | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): 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 | a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): 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 | a0002c0002t0011g0065 a0002c0002t0011g0066 a0002c0002t0011g0067 others(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 | a0002c0002t0014g0061 a0002c0002t0014g0090 a0002c0002t0014g0095 others(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 | a0001c0001t0001g0278 | 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 | a0001c0004t0108g0309 a0001c0004t0126g0281 a0001c0005t0004g0334 others(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 | a0003c0026t0064g0274 | 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 | a0002c0002t0026g0116 | 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 | a0002c0002t0024g0041 | 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 | a0001c0011t0057g0348 | 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 | a0012c0028t0006g0167 | 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 | a0002c0002t0058g0063 | 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 | a0001c0007t0001g0170 a0001c0007t0001g0258 |
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 | a0003c0026t0064g0274 | 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 | a0003c0003t0002g0319 a0003c0003t0002g0364 |
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 | a0002c0002t0008g0094 a0002c0002t0052g0040 |
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 | a0003c0003t0109g0340 | 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 | a0001c0004t0108g0309 a0001c0004t0126g0281 a0001c0005t0004g0334 others(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 | a0001c0004t0108g0309 a0001c0004t0126g0281 a0001c0005t0004g0334 others(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 | a0002c0002t0011g0067 a0002c0002t0011g0068 |
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 | 2 | a0004c0008t0010g0001 a0004c0008t0010g0036 |
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 | a0001c0004t0005g0198 | 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 | a0002c0002t0024g0100 | 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 | a0001c0001t0112g0367 | 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 | a0001c0005t0127g0018 | 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 | a0002c0002t0038g0043 | 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 | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): 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 | a0002c0002t0006g0110 | 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0006g0194 | 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 | a0002c0010t0022g0172 | 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 | a0003c0003t0122g0328 | 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 | a0001c0006t0006g0091 a0001c0006t0009g0111 a0001c0006t0009g0112 |
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 | a0001c0004t0005g0338 | 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 | 105 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(102): 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 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 |
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 | 90 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(87): 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 | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(213): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.259-5827T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665496 | |||||||
| chr15:99665503 | G | A | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.259-5820G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 4/11 | chr15 | 99665503 | |||||||
| chr15:99665630 | C | T | 126 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(123): 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 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0178 others(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 | a0001c0001t0023g0234 a0001c0004t0045g0051 a0001c0004t0049g0371 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0232 a0001c0001t0001g0366 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0022g0238 |
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 | a0002c0002t0025g0102 a0002c0002t0025g0230 |
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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 |
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 | a0001c0001t0034g0270 a0003c0012t0034g0132 a0011c0025t0105g0042 |
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 | a0001c0001t0034g0270 a0002c0002t0021g0153 a0003c0009t0050g0135 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 9 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0357 others(6): 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 | a0008c0032t0004g0019 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0001c0001t0001g0150 a0001c0001t0001g0365 a0001c0001t0001g0366 others(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 | 70 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0125 others(67): Show |
72 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(69): 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 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0185 others(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 |
71 | a0001c0001t0001g0128 a0001c0001t0003g0266 a0001c0001t0012g0279 others(68): 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 | a0001c0006t0013g0078 a0002c0002t0008g0092 a0002c0002t0008g0093 others(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 | a0001c0001t0001g0245 a0001c0001t0022g0184 a0001c0004t0048g0369 others(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 | a0003c0003t0002g0319 a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | a0004c0008t0046g0213 a0004c0008t0092g0214 |
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 | a0001c0001t0112g0367 | 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 | a0001c0004t0108g0309 a0001c0004t0126g0281 a0001c0005t0004g0334 others(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 | a0001c0001t0112g0367 | 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 | a0011c0025t0105g0042 | 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 | a0002c0002t0026g0116 | 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 | a0004c0008t0046g0213 a0004c0008t0092g0214 |
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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 |
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 | a0001c0001t0034g0270 a0001c0005t0010g0133 a0003c0009t0050g0135 others(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 | 1 | a0004c0008t0010g0001 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0006t0066g0097 | 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 | 86 | a0001c0001t0075g0079 a0001c0006t0006g0091 a0001c0006t0006g0145 others(83): 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 | |||||||
| chr15:99667679 | T | A | 1 | a0010c0024t0021g0114 | 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 | a0003c0003t0002g0298 a0003c0003t0002g0299 |
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 | a0011c0025t0105g0042 | 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 | a0001c0001t0112g0367 | 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 | a0011c0025t0105g0042 | 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 | a0001c0004t0108g0309 a0001c0004t0126g0281 a0001c0005t0004g0334 others(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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 |
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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0005t0004g0020 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0046 a0001c0001t0003g0047 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 101 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(98): 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 | a0001c0001t0012g0240 a0001c0001t0022g0184 a0001c0001t0043g0181 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0009t0050g0135 a0003c0009t0050g0152 a0003c0009t0124g0134 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 |
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 | a0003c0003t0002g0312 | 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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0006t0066g0097 a0002c0002t0006g0059 a0002c0002t0006g0110 |
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 | a0001c0006t0019g0229 a0001c0006t0019g0231 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0005t0004g0016 | 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 | a0002c0002t0035g0074 a0002c0002t0035g0075 |
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 | a0011c0025t0105g0042 | 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 | a0001c0005t0010g0211 | 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 | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): 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 | a0001c0005t0004g0016 | 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 | a0001c0001t0003g0226 | 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 | a0001c0001t0075g0079 a0001c0006t0013g0077 a0001c0006t0013g0078 others(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 | a0001c0001t0023g0234 a0001c0001t0023g0257 |
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 | a0001c0004t0005g0283 | 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 | 19 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0357 others(16): 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 | a0002c0002t0020g0072 a0002c0002t0020g0073 a0002c0002t0020g0099 others(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 | a0003c0003t0002g0300 a0003c0003t0117g0301 |
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 | a0003c0003t0002g0056 a0003c0003t0016g0055 |
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 | a0001c0001t0028g0205 a0001c0001t0028g0206 a0001c0001t0028g0207 others(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 | 6 | a0001c0001t0001g0003 a0001c0001t0001g0175 a0001c0001t0017g0188 others(3): 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 | a0003c0003t0107g0136 | 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 | a0002c0002t0071g0117 | 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 | a0003c0003t0116g0311 | 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 |
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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0004t0007g0307 | 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 | 208 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0001c0005t0010g0133 | 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 | a0001c0004t0047g0049 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): 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 | a0001c0004t0001g0325 | 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 | 133 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(130): 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 | a0001c0001t0097g0253 | 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 | a0002c0010t0012g0159 | 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 | a0001c0001t0074g0204 | 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 | a0001c0001t0112g0367 | 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 | a0002c0002t0069g0209 | 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 | a0001c0001t0043g0181 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0003t0002g0302 a0003c0003t0002g0304 a0003c0003t0002g0305 others(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 | |||||||
| chr15:99676018 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(76): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): 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 | a0001c0004t0012g0362 a0003c0009t0050g0135 a0003c0009t0050g0152 others(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 | a0001c0005t0114g0218 | 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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): 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 | a0001c0001t0112g0367 | 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 | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): 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 | a0003c0003t0002g0298 | 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 | a0003c0026t0064g0274 | 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 | a0008c0019t0001g0122 a0008c0019t0001g0123 |
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 | a0003c0009t0002g0196 | 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 | a0002c0002t0006g0086 a0002c0002t0006g0088 a0002c0002t0026g0057 |
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 | a0011c0025t0105g0042 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0002c0002t0021g0153 | 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 | 140 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(137): 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): 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 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0028g0205 others(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 | a0001c0001t0112g0367 | 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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0003c0009t0050g0135 a0003c0009t0050g0152 a0003c0009t0124g0134 |
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 | a0002c0002t0036g0259 | 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 | a0001c0007t0001g0170 | 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 | a0001c0001t0112g0367 | 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 | a0007c0018t0030g0233 | 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 | a0002c0002t0026g0116 | 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 | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): 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 | a0001c0001t0034g0270 a0003c0012t0034g0132 a0011c0025t0105g0042 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 105 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(102): 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 | a0001c0005t0004g0032 a0001c0005t0015g0025 a0001c0005t0015g0028 others(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 | a0001c0005t0010g0133 a0003c0009t0050g0135 a0003c0009t0050g0152 others(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 | a0001c0005t0004g0032 a0001c0005t0015g0025 a0001c0005t0015g0028 others(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 | 105 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(102): 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0001g0004 | 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 | a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0002c0002t0032g0085 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): 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 | a0002c0013t0002g0324 | 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 | a0001c0001t0034g0270 a0002c0002t0032g0085 a0003c0003t0002g0364 others(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 | a0003c0012t0034g0132 | 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 | a0001c0001t0034g0270 a0003c0012t0034g0132 a0011c0025t0105g0042 |
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 | a0011c0025t0105g0042 | 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 | a0001c0005t0039g0015 | 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 | a0001c0001t0089g0164 | 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 | a0001c0004t0120g0284 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0002c0002t0032g0085 | 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 | a0002c0002t0032g0085 | 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 | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.670+6060A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681518 | |||||||
| chr15:99681581 | C | T | 141 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(138): 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 | a0002c0002t0014g0090 | 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 | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(73): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.670+6224A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99681682 | |||||||
| chr15:99681716 | C | A | 102 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(99): 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 | a0010c0024t0021g0114 | 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 | a0001c0001t0034g0270 a0001c0005t0010g0133 a0003c0012t0034g0132 others(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 | a0001c0004t0005g0283 a0001c0004t0005g0338 a0001c0004t0012g0362 others(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 | a0001c0001t0059g0276 | 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 | a0001c0006t0066g0097 a0002c0002t0006g0110 |
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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(72): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): 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 | a0001c0001t0034g0270 a0001c0005t0010g0133 a0003c0012t0034g0132 others(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 | a0001c0021t0005g0217 | 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 | a0002c0002t0032g0085 | 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 | a0003c0026t0064g0274 | 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 | a0002c0002t0033g0239 a0002c0002t0058g0063 |
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 | a0001c0001t0034g0270 a0001c0005t0010g0133 a0003c0012t0034g0132 others(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 | a0001c0001t0001g0150 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | 104 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(101): 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 | a0001c0007t0001g0170 | 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 | 1 | a0002c0013t0008g0005 | 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 | a0001c0007t0001g0258 | 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 | 11 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0357 others(8): 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 | a0001c0001t0003g0264 | 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 | a0011c0025t0105g0042 | 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 | a0011c0025t0105g0042 | 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 | 60 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(57): 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 | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0001c0001t0090g0187 a0001c0007t0001g0189 a0002c0002t0008g0219 others(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 | a0001c0001t0001g0193 | 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 | a0002c0002t0031g0071 | 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 | a0001c0005t0015g0029 a0001c0005t0015g0031 |
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 | a0002c0002t0008g0094 | 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 | a0003c0009t0002g0196 | 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 | a0001c0004t0029g0308 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0017g0242 | 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 | a0003c0003t0002g0320 | 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 | a0001c0005t0127g0018 | 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 | a0011c0025t0105g0042 | 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 | a0002c0002t0058g0063 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0001c0001t0112g0367 | 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 | a0003c0003t0002g0291 a0003c0003t0002g0292 |
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 | a0002c0002t0009g0035 a0002c0002t0009g0103 a0002c0002t0014g0228 others(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 | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(344): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): 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 | a0001c0006t0024g0165 a0002c0002t0024g0100 a0002c0002t0067g0130 others(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 | a0002c0002t0056g0129 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0003g0263 | 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 | a0003c0003t0016g0055 | 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 | a0001c0001t0112g0367 | 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 | a0004c0008t0010g0036 | 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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(72): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.671-4200G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99686041 | |||||||
| chr15:99686290 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(73): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): 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 | a0001c0001t0001g0248 | 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 | a0001c0021t0005g0217 | 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 | a0001c0005t0004g0017 a0001c0005t0004g0020 a0001c0005t0004g0022 others(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 | a0001c0001t0059g0276 | 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 | a0003c0003t0091g0289 | 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 | a0003c0003t0091g0289 | 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 | 99 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(96): 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 | a0001c0001t0001g0124 | 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 | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(75): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): 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 | 172 | a0001c0001t0003g0263 a0001c0001t0003g0266 a0001c0001t0034g0270 others(169): 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 | a0001c0001t0097g0253 a0001c0004t0012g0362 a0001c0004t0030g0288 others(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 | a0001c0001t0001g0366 a0001c0001t0003g0037 a0001c0001t0059g0276 others(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 | a0001c0001t0012g0240 a0002c0002t0009g0182 a0003c0012t0002g0368 |
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 | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(70): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): 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 | a0001c0001t0001g0366 a0001c0001t0089g0164 a0002c0002t0063g0160 others(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 | a0001c0001t0112g0367 | 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 | a0001c0006t0019g0231 | 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 | a0003c0012t0002g0368 | 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 | 1 | a0002c0010t0041g0002 | 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 | 99 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(96): 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 | a0004c0008t0010g0212 | 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 | a0003c0012t0001g0254 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0080g0271 | 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 | a0011c0025t0105g0042 | 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 | a0001c0001t0003g0269 | 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 | a0001c0004t0082g0286 a0001c0004t0083g0287 |
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 | a0002c0002t0037g0142 a0002c0002t0037g0144 a0002c0002t0038g0043 others(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 | a0001c0001t0001g0190 | 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 | a0003c0009t0050g0135 a0003c0009t0050g0152 a0003c0009t0124g0134 |
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 | 140 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(137): 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 | 149 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(146): 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 | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(222): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.671-1480G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 7/11 | chr15 | 99688761 | |||||||
| chr15:99688856 | G | A | 19 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0357 others(16): 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 | 107 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(104): 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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): 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 | a0001c0006t0019g0229 | 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 | a0002c0002t0026g0101 | 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 | a0001c0001t0001g0168 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0034g0270 a0003c0012t0034g0132 |
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 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(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 | a0001c0001t0059g0276 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0001c0001t0001g0190 | 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 | a0002c0002t0009g0058 | 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 | a0003c0003t0002g0314 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 328 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(325): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.858+275T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99690703 | |||||||
| chr15:99690828 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): 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 | a0002c0002t0014g0061 a0002c0002t0014g0090 a0002c0002t0014g0095 others(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 | a0001c0005t0004g0017 a0001c0005t0004g0026 a0001c0005t0004g0030 |
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 | a0002c0002t0076g0098 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | 18 | a0001c0001t0080g0271 a0001c0004t0002g0352 a0001c0004t0002g0356 others(15): 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 | 152 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0124 others(149): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): 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 | 12 | a0001c0001t0001g0004 a0001c0001t0001g0247 a0001c0004t0082g0286 others(9): 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0023g0277 others(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 | 328 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(325): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0001c0001t0012g0279 | 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 | a0003c0009t0002g0195 | 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 | a0001c0011t0018g0347 a0001c0011t0018g0349 a0001c0011t0018g0363 others(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 | a0001c0006t0019g0231 | 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 | a0001c0001t0112g0367 | 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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0004t0082g0286 a0001c0004t0083g0287 |
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 | a0003c0009t0004g0021 | 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 | a0001c0004t0001g0325 a0001c0004t0007g0307 a0001c0004t0106g0330 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0005t0010g0210 | 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 | a0001c0004t0005g0006 | 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 | a0001c0005t0010g0133 | 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 | 110 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(107): 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 | 110 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(107): 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 | a0001c0001t0017g0162 a0004c0017t0017g0121 |
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 | a0003c0003t0002g0313 | 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 | a0003c0009t0050g0135 a0003c0009t0124g0134 |
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 | a0003c0003t0002g0297 | 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 | a0003c0009t0050g0135 a0003c0009t0050g0152 a0003c0009t0124g0134 |
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 | a0002c0002t0013g0107 a0002c0002t0070g0109 |
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 | a0002c0002t0011g0066 | 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 | a0003c0003t0002g0292 | 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 | a0001c0001t0003g0047 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0009t0119g0275 | 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 | a0002c0002t0026g0101 | 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 | 145 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(142): 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 | 142 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(139): 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 | a0001c0021t0005g0217 | 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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | 114 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0005g0148 others(111): 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 | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): 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 | a0001c0005t0004g0022 | 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 | a0001c0004t0048g0369 | 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 | a0002c0002t0037g0142 a0002c0002t0037g0144 a0002c0002t0038g0043 others(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 | a0003c0026t0064g0274 | 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 | a0003c0026t0064g0274 a0011c0025t0105g0042 |
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 | a0003c0026t0064g0274 a0011c0025t0105g0042 |
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 | a0003c0026t0064g0274 a0011c0025t0105g0042 |
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 | a0003c0026t0064g0274 a0011c0025t0105g0042 |
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 | a0001c0001t0034g0270 a0003c0012t0034g0132 |
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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(72): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0027g0272 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0178 a0001c0001t0095g0208 |
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 | 17 | a0001c0001t0023g0277 a0001c0004t0002g0352 a0001c0004t0002g0356 others(14): 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 | a0001c0001t0023g0234 a0001c0001t0023g0257 a0001c0001t0112g0367 others(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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0001t0017g0162 a0001c0001t0034g0270 a0001c0005t0114g0218 others(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 | a0001c0006t0019g0229 a0001c0006t0086g0200 a0002c0002t0011g0065 others(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 | a0001c0001t0003g0269 a0001c0001t0043g0181 a0001c0001t0074g0204 others(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 |
22 | a0001c0001t0001g0190 a0001c0001t0003g0038 a0001c0001t0003g0039 others(19): Show |
22 | HG00544.hp2 HG00733.hp1 HG01071.hp2 others(19): 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 | a0001c0001t0001g0220 a0001c0001t0001g0247 a0001c0001t0003g0037 others(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 |
9 | a0001c0001t0001g0003 a0001c0001t0001g0236 a0001c0001t0001g0248 others(6): 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 | a0001c0001t0001g0050 a0001c0001t0001g0126 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0243 a0001c0001t0012g0279 a0001c0001t0017g0188 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0180 a0001c0001t0001g0245 others(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 | a0001c0001t0028g0205 | 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 | 3 | a0001c0004t0045g0053 a0002c0010t0041g0002 a0003c0003t0116g0311 |
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 | a0001c0001t0005g0148 | 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 | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.858+5427G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99695855 | |||||||
| chr15:99695859 | CAA | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): 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 | 139 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(136): 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 | a0001c0006t0066g0097 a0002c0002t0006g0110 |
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 | a0001c0007t0001g0191 | 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 | 6 | a0001c0001t0001g0003 a0001c0001t0001g0175 a0001c0001t0017g0188 others(3): 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 | a0001c0001t0012g0240 | 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 | a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | a0003c0003t0002g0303 | 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 | a0001c0001t0023g0277 | 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 | 11 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0357 others(8): 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 | a0001c0004t0048g0369 | 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 | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(344): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): 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 | a0003c0003t0007g0010 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.859-6354C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697008 | |||||||
| chr15:99697054 | TA | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): 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 | a0012c0028t0006g0167 | 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 | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): 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 | a0001c0004t0044g0294 | 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 | a0001c0001t0001g0278 a0003c0026t0064g0274 a0011c0025t0105g0042 |
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 | a0002c0002t0006g0108 a0002c0002t0011g0067 a0002c0002t0011g0068 |
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 | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.859-5902T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99697460 | |||||||
| chr15:99697477 | A | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0003c0003t0002g0322 | 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 | a0002c0002t0037g0142 a0002c0002t0037g0144 a0002c0002t0038g0043 others(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 | 269 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(266): 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 | a0001c0001t0001g0175 | 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 | 106 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(103): 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 | a0001c0005t0015g0031 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0185 others(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 | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0003c0003t0125g0280 | 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 | 106 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(103): 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 | 106 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(103): 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 | a0001c0005t0127g0018 | 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 | a0001c0001t0001g0004 | 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 | a0001c0004t0030g0288 a0003c0003t0091g0289 |
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 | a0001c0004t0121g0355 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0001c0021t0005g0217 | 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 | a0001c0004t0082g0286 a0001c0004t0083g0287 |
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 | a0001c0004t0043g0339 a0001c0004t0098g0306 |
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 | a0003c0009t0119g0275 | 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 | a0001c0004t0029g0308 | 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 | a0003c0003t0115g0343 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | 273 | a0001c0001t0001g0150 a0001c0001t0001g0365 a0001c0001t0001g0366 others(270): 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 | a0001c0004t0001g0325 | 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 | a0003c0003t0110g0285 | 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 | a0001c0001t0001g0186 | 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0004c0017t0017g0120 | 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 | a0001c0004t0005g0198 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0001c0001t0034g0270 a0001c0006t0009g0111 a0001c0006t0009g0112 others(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 | a0001c0001t0003g0226 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0006c0023t0027g0161 | 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 | a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | a0001c0005t0004g0016 a0001c0005t0004g0017 a0001c0005t0004g0020 others(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 | a0001c0001t0112g0367 | 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 | a0001c0004t0005g0006 a0001c0004t0005g0198 a0001c0004t0082g0286 others(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 | a0001c0004t0047g0049 a0001c0004t0047g0290 a0001c0004t0126g0281 |
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 | 11 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0001c0021t0005g0217 others(8): 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 | a0001c0004t0007g0307 a0003c0003t0002g0297 a0003c0003t0002g0298 others(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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | 101 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0017g0162 others(98): 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 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0245 |
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 | 58 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0125 others(55): Show |
59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): 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 | 75 | a0001c0001t0001g0004 a0001c0001t0001g0127 a0001c0001t0001g0150 others(72): 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 | a0001c0001t0001g0050 a0001c0001t0001g0190 a0001c0001t0017g0162 others(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 | a0001c0001t0012g0222 a0001c0001t0059g0276 a0001c0006t0006g0145 others(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 | 174 | a0001c0001t0001g0220 a0001c0001t0001g0365 a0001c0001t0001g0366 others(171): 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 | 239 | a0001c0001t0001g0150 a0001c0001t0001g0365 a0001c0001t0001g0366 others(236): 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 | 127 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(124): 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 | a0001c0001t0027g0272 a0001c0001t0080g0271 a0001c0001t0104g0149 others(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 | a0002c0002t0035g0075 | 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 | 128 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0017g0162 others(125): 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 | a0001c0005t0127g0018 | 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 | a0003c0003t0002g0322 | 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 | a0001c0005t0004g0024 | 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 | 131 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0017g0162 others(128): 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 | 130 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0017g0162 others(127): 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 | a0001c0001t0001g0186 a0001c0001t0001g0241 a0002c0002t0014g0095 others(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 | a0004c0008t0010g0251 | 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 | a0001c0004t0030g0346 a0001c0004t0099g0350 a0001c0005t0010g0210 others(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 | 5 | a0001c0001t0001g0003 a0001c0001t0001g0175 a0001c0001t0017g0188 others(2): 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 | a0001c0001t0001g0128 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0022g0238 | 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 | 14 | a0001c0001t0001g0003 a0001c0001t0001g0128 a0001c0001t0001g0175 others(11): 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 | 104 | a0001c0001t0001g0150 a0001c0001t0001g0365 a0001c0001t0001g0366 others(101): 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0112g0367 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0003g0047 others(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 |
50 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(47): Show |
50 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0220 others(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 | a0001c0007t0001g0183 | 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 | a0001c0001t0097g0253 a0004c0017t0017g0120 |
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 | 326 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(323): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0006c0023t0027g0161 | 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 | a0001c0001t0034g0270 a0001c0001t0084g0044 a0003c0012t0034g0132 |
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 | 104 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(101): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0001t0059g0276 | 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 | a0003c0026t0064g0274 a0011c0025t0105g0042 |
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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0112g0367 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 139 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(136): 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 | a0001c0001t0028g0205 | 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 | a0001c0001t0028g0205 | 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 | a0001c0005t0010g0133 | 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 | a0003c0003t0002g0354 | 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 | a0001c0001t0028g0205 | 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 | a0001c0004t0005g0338 a0001c0004t0029g0308 a0001c0004t0029g0345 |
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 | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): 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 | 104 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(101): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 |
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 | a0001c0001t0003g0273 | 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 | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): 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 | a0001c0004t0048g0369 | 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 | a0001c0006t0009g0113 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0002c0002t0006g0059 | 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 | a0003c0003t0002g0322 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): 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 | a0003c0003t0007g0360 | 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 | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.859-1656T>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 8/11 | chr15 | 99701706 | |||||||
| chr15:99701752 | A | C | 10 | a0001c0005t0010g0210 a0001c0005t0010g0211 a0004c0008t0010g0001 others(7): 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 | a0004c0017t0017g0120 | 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 | a0004c0017t0017g0120 | 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 | a0005c0014t0003g0154 a0005c0014t0003g0155 |
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 | a0001c0004t0005g0283 a0003c0003t0005g0293 |
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 | a0003c0003t0002g0313 | 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 | a0001c0006t0019g0229 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0030g0288 a0003c0003t0091g0289 |
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 | a0001c0006t0006g0145 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0003c0003t0002g0297 a0003c0003t0002g0298 a0003c0003t0002g0299 others(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 | a0002c0002t0067g0130 | 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 | 139 | a0001c0001t0001g0150 a0001c0001t0003g0037 a0001c0001t0003g0038 others(136): 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 | a0001c0001t0003g0047 a0001c0001t0003g0119 a0001c0001t0084g0044 others(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 | a0001c0001t0028g0205 | 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 | a0001c0001t0028g0205 | 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 | a0001c0004t0126g0281 a0002c0002t0035g0074 a0002c0002t0035g0075 |
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 | a0001c0001t0027g0272 | 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 | a0001c0001t0059g0276 | 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 | a0001c0001t0034g0270 a0003c0012t0034g0132 |
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 | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): 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 | a0001c0001t0028g0205 | 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 | 104 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0004t0001g0325 others(101): 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 | a0001c0004t0126g0281 | 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 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(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 | a0003c0012t0002g0368 | 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 | a0001c0001t0112g0367 | 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 | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): 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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0002c0002t0014g0228 a0002c0002t0021g0166 |
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 | a0001c0004t0012g0362 | 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 | 107 | a0001c0001t0001g0150 a0001c0001t0005g0137 a0001c0001t0005g0138 others(104): 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 | a0001c0004t0030g0346 a0001c0004t0099g0350 |
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 | a0001c0004t0005g0338 a0001c0004t0029g0308 a0001c0004t0029g0345 |
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 | a0001c0001t0112g0367 | 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 | a0001c0007t0093g0045 | 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 | a0001c0006t0008g0104 a0001c0006t0024g0165 a0002c0002t0008g0054 others(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 | a0004c0008t0046g0213 a0004c0008t0092g0214 |
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 | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0001c0004t0045g0051 a0001c0004t0045g0053 a0002c0013t0102g0052 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0003c0026t0064g0274 | 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 | a0001c0004t0047g0049 | 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 | a0001c0005t0004g0016 | 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 | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(73): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): 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 | a0001c0006t0006g0091 a0001c0007t0040g0118 |
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 | a0001c0004t0012g0362 | 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 | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.883-745G>A | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99705984 | |||||||
| chr15:99706247 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): 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 | a0003c0026t0064g0274 a0011c0025t0105g0042 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0006t0086g0200 | 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 | a0003c0009t0050g0135 a0003c0009t0050g0152 a0003c0009t0124g0134 |
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 | a0001c0001t0001g0168 | 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 | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.883-216C>T | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 9/11 | chr15 | 99706513 | |||||||
| chr15:99706629 | T | G | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | a0004c0008t0046g0213 | 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 | a0003c0012t0034g0132 | 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 | a0001c0011t0061g0282 | 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 | a0002c0002t0056g0129 | 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 | 1 | a0004c0008t0010g0001 | 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 | a0001c0006t0066g0097 | 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 | a0001c0006t0009g0113 | 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 | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): 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 | a0002c0002t0031g0071 | 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 | a0002c0010t0012g0159 a0002c0010t0081g0156 |
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 | a0001c0001t0001g0150 | 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 | 106 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0356 others(103): 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 | 327 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(324): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1009+1096T>C | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707951 | |||||||
| chr15:99707989 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(227): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1009+1134A>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 10/11 | chr15 | 99707989 | |||||||
| chr15:99708015 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): 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 | a0001c0004t0048g0369 a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | 121 | a0001c0004t0001g0325 a0001c0004t0002g0352 a0001c0004t0002g0357 others(118): 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 | a0001c0001t0003g0266 | 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 | a0004c0008t0044g0215 | 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 | a0003c0003t0002g0316 | 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 | a0002c0002t0006g0059 | 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(223): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0193 | 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 a0003c0026t0064g0274 others(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 | a0002c0002t0053g0060 | 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 | a0001c0005t0015g0029 | 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 | a0001c0004t0002g0352 a0001c0004t0002g0356 a0001c0004t0002g0357 others(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 | a0001c0001t0003g0048 | 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 | a0001c0011t0061g0282 | 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 | 105 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(102): 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 | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(224): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): 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 | a0001c0001t0001g0190 | 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 | a0001c0004t0005g0283 a0003c0003t0005g0293 |
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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | a0001c0004t0029g0345 | 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 | a0002c0002t0008g0092 a0002c0002t0008g0093 |
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 | a0002c0002t0014g0061 a0002c0002t0014g0090 a0002c0002t0014g0095 others(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 | a0002c0002t0009g0182 | 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 | a0001c0011t0018g0335 a0002c0002t0006g0194 |
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 | a0002c0002t0051g0106 a0003c0003t0002g0303 |
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 | a0013c0022t0001g0174 | 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 | 207 | a0001c0001t0003g0037 a0001c0001t0003g0047 a0001c0001t0003g0048 others(204): 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 | a0004c0017t0017g0121 | 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 | a0001c0004t0098g0306 | 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 | a0001c0001t0012g0240 | 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 | a0002c0002t0013g0083 | 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 | a0001c0001t0001g0278 a0001c0001t0003g0046 a0001c0001t0003g0266 others(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 | 140 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0046 others(137): 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 | a0001c0001t0023g0234 a0001c0001t0023g0277 a0001c0004t0029g0308 others(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 | 341 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(338): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0003c0012t0001g0254 a0003c0012t0001g0255 |
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 | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(91): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): 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 | a0003c0003t0007g0008 a0003c0003t0007g0009 a0003c0003t0007g0010 others(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 | a0001c0004t0005g0006 | 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 | a0001c0005t0004g0023 a0001c0005t0004g0334 |
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 | a0001c0007t0001g0169 a0003c0003t0002g0056 a0003c0003t0002g0341 others(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 | a0001c0007t0001g0169 a0003c0003t0002g0056 a0003c0003t0002g0341 others(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 | a0001c0006t0086g0200 | 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 | a0002c0010t0001g0173 | 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 | a0001c0004t0049g0370 a0001c0004t0049g0371 |
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 | 50 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(47): 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 | a0002c0002t0069g0209 a0003c0003t0002g0319 a0003c0003t0002g0364 |
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 | a0001c0001t0012g0240 a0001c0001t0043g0181 a0002c0002t0058g0063 others(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 | a0001c0001t0112g0367 | 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 | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(68): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): 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 | a0002c0002t0006g0059 | 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 | a0001c0004t0047g0049 a0001c0004t0047g0290 |
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 | a0001c0001t0012g0222 a0001c0001t0012g0223 a0001c0001t0042g0224 others(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 | a0001c0001t0001g0243 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1137-35C>G | MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 11/11 | chr15 | 99712355 |