Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4209 |
| ensemblid | ENSG00000116604.19 |
| hgncid | 6997 |
| symbol | MEF2D |
| name | myocyte enhancer factor 2D |
| refseq_nuc | NM_005920.4 |
| refseq_prot | NP_005911.1 |
| ensembl_nuc | ENST00000348159.9 |
| ensembl_prot | ENSP00000271555.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 156463727 |
| end | 156500775 |
| strand | - |
| ver | v1.2 |
| region | chr1:156463727-156500775 |
| region5000 | chr1:156458727-156505775 |
| regionname0 | MEF2D_chr1_156463727_156500775 |
| regionname5000 | MEF2D_chr1_156458727_156505775 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 521 | 280 | 97 | 58 | 87 | 12 | 24 | 75 | MEF2D_chr1_156458727_156505775 | MEF2D | MGRKK others(516): Show |
chr1 | 156458727 | 156505775 |
| a0002 | 0/0 | 521 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | MGRKK others(516): Show |
chr1 | 156458727 | 156505775 |
| a0003 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | MGRKK others(516): Show |
chr1 | 156458727 | 156505775 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1563 | 119 | 28 | 26 | 43 | 7 | 14 | MEF2D_chr1_156458727_156505775 | MEF2D | ATGGG others(1558): Show |
chr1 | 156458727 | 156505775 | ||
| a0001c0002 | 0/0 | 1563 | 96 | 16 | 25 | 44 | 3 | 8 | MEF2D_chr1_156458727_156505775 | MEF2D | ATGGG others(1558): Show |
chr1 | 156458727 | 156505775 | ||
| a0001c0003 | 1/0 | 1563 | 64 | 52 | 7 | 0 | 2 | 2 | MEF2D_chr1_156458727_156505775 | MEF2D | ATGGG others(1558): Show |
chr1 | 156458727 | 156505775 | ||
| a0001c0005 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | ATGGG others(1558): Show |
chr1 | 156458727 | 156505775 | ||
| a0002c0004 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | ATGGG others(1558): Show |
chr1 | 156458727 | 156505775 | ||
| a0003c0006 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | ATGGG others(1558): Show |
chr1 | 156458727 | 156505775 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5912 | 106 | 25 | 26 | 35 | 6 | 13 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0011 | 0/0 | 5913 | 3 | 1 | 0 | 2 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5908): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0021 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0022 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0024 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0025 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0028 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0029 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0030 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0033 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0037 | 0/0 | 5913 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5908): Show |
chr1 | 156458727 | 156505775 |
| a0001c0001t0041 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0001 | 0/0 | 5912 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0002 | 0/0 | 5912 | 41 | 4 | 17 | 18 | 0 | 2 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0003 | 0/0 | 5914 | 9 | 0 | 0 | 9 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5909): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0004 | 0/0 | 5912 | 12 | 0 | 1 | 11 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0005 | 0/0 | 5912 | 9 | 3 | 2 | 0 | 2 | 2 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0009 | 0/0 | 5912 | 4 | 0 | 1 | 1 | 0 | 2 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0012 | 0/0 | 5913 | 3 | 0 | 3 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5908): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0015 | 0/0 | 5912 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0016 | 0/0 | 5912 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0018 | 0/0 | 5915 | 2 | 1 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5910): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0019 | 0/0 | 5912 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0020 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0023 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0027 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0032 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0034 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0035 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0036 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0002t0039 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0002 | 1/0 | 5912 | 19 | 10 | 4 | 0 | 2 | 2 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0003 | 0/0 | 5914 | 8 | 7 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5909): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0006 | 0/0 | 5913 | 8 | 6 | 2 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5908): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0007 | 0/0 | 5914 | 7 | 7 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5909): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0008 | 0/0 | 5913 | 5 | 5 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5908): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0010 | 0/0 | 5914 | 4 | 4 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5909): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0013 | 0/0 | 5913 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5908): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0014 | 0/0 | 5915 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5910): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0017 | 0/0 | 5915 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5910): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0026 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0031 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0038 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0040 | 0/0 | 5913 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5908): Show |
chr1 | 156458727 | 156505775 |
| a0001c0003t0042 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5910): Show |
chr1 | 156458727 | 156505775 |
| a0001c0005t0002 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| a0002c0004t0007 | 0/0 | 5914 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5909): Show |
chr1 | 156458727 | 156505775 |
| a0003c0006t0002 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | GAGTT others(5907): Show |
chr1 | 156458727 | 156505775 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 0 | 7 | 10 | 2 | 3 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0011g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0021g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0022g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0024g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0025g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0028g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0029g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0030g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0033g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0037g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0001t0041g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0005g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0009g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0009g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0012g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0012g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0012g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0015g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0015g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0016g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0016g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0018g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0018g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0019g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0019g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0020g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0027g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0032g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0034g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0035g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0036g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0002t0039g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0002 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0015 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0003g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0007g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0008g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0010g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0013g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0014g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0017g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0026g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0031g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0038g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0040g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0003t0042g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0001c0005t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0002c0004t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| a0003c0006t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0005 | g0048 | EUR | GBR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0002 | EUR | FIN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0007 | EUR | FIN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0002 | EUR | FIN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00673 | hp1 | a0001 | c0002 | t0004 | g0195 | EAS | CHS | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00733 | hp1 | a0001 | c0002 | t0009 | g0152 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00735 | hp2 | a0001 | c0003 | t0006 | g0076 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0043 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00741 | hp1 | a0001 | c0002 | t0012 | g0188 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01070 | hp1 | a0001 | c0002 | t0004 | g0179 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0005 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01168 | hp2 | a0001 | c0002 | t0005 | g0047 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0007 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01175 | hp1 | a0001 | c0002 | t0012 | g0191 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01175 | hp2 | a0001 | c0003 | t0006 | g0041 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01433 | hp2 | a0001 | c0002 | t0012 | g0151 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01516 | hp2 | a0001 | c0002 | t0020 | g0029 | EUR | IBS | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01884 | hp2 | a0001 | c0003 | t0006 | g0075 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0085 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0180 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01975 | hp2 | a0001 | c0002 | t0019 | g0171 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02004 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0161 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0200 | EAS | KHV | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | KHV | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02145 | hp1 | a0001 | c0003 | t0013 | g0081 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | CDX | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02257 | hp2 | a0001 | c0003 | t0008 | g0070 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02258 | hp2 | a0001 | c0003 | t0026 | g0063 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02280 | hp1 | a0001 | c0002 | t0015 | g0143 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0205 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0207 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0209 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02572 | hp2 | a0001 | c0003 | t0006 | g0008 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02615 | hp1 | a0001 | c0003 | t0010 | g0013 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0015 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02622 | hp2 | a0001 | c0003 | t0006 | g0008 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02630 | hp1 | a0001 | c0003 | t0006 | g0074 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02647 | hp2 | a0002 | c0004 | t0007 | g0073 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02683 | hp1 | a0001 | c0001 | t0021 | g0030 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0208 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02723 | hp1 | a0001 | c0003 | t0040 | g0077 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02723 | hp2 | a0001 | c0003 | t0007 | g0082 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0170 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02809 | hp2 | a0001 | c0003 | t0007 | g0078 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02895 | hp1 | a0001 | c0003 | t0010 | g0013 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02896 | hp1 | a0001 | c0003 | t0014 | g0028 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02896 | hp2 | a0001 | c0003 | t0010 | g0035 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02897 | hp1 | a0001 | c0003 | t0010 | g0036 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02897 | hp2 | a0001 | c0003 | t0014 | g0028 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02922 | hp1 | a0001 | c0001 | t0028 | g0055 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02922 | hp2 | a0001 | c0005 | t0002 | g0071 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02965 | hp1 | a0001 | c0002 | t0035 | g0160 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0206 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02976 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03017 | hp2 | a0001 | c0002 | t0005 | g0050 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03041 | hp1 | a0001 | c0003 | t0013 | g0068 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03098 | hp1 | a0001 | c0003 | t0017 | g0039 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03098 | hp2 | a0001 | c0003 | t0006 | g0087 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03130 | hp1 | a0001 | c0003 | t0007 | g0009 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03139 | hp1 | a0001 | c0002 | t0034 | g0173 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0052 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0008 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0145 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03453 | hp2 | a0001 | c0003 | t0031 | g0079 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03486 | hp1 | a0001 | c0002 | t0005 | g0046 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03486 | hp2 | a0001 | c0003 | t0008 | g0019 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03490 | hp2 | a0001 | c0002 | t0039 | g0049 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0038 | AFR | ESN | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03540 | hp1 | a0001 | c0003 | t0014 | g0213 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03540 | hp2 | a0001 | c0002 | t0019 | g0184 | AFR | GWD | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03579 | hp2 | a0001 | c0003 | t0007 | g0009 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0044 | SAS | BEB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0182 | SAS | BEB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03942 | hp1 | a0001 | c0002 | t0009 | g0142 | SAS | BEB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG04115 | hp1 | a0001 | c0002 | t0005 | g0007 | SAS | STU | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG04204 | hp1 | a0001 | c0002 | t0032 | g0168 | SAS | STU | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0037 | AFR | YRI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | CHB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18906 | hp1 | a0001 | c0003 | t0008 | g0019 | AFR | YRI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18906 | hp2 | a0001 | c0003 | t0038 | g0064 | AFR | YRI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18939 | hp1 | a0003 | c0006 | t0002 | g0194 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18949 | hp1 | a0001 | c0001 | t0011 | g0204 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18950 | hp1 | a0001 | c0002 | t0018 | g0175 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18950 | hp2 | a0001 | c0001 | t0037 | g0112 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18957 | hp1 | a0001 | c0002 | t0004 | g0159 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18961 | hp1 | a0001 | c0001 | t0030 | g0101 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18961 | hp2 | a0001 | c0002 | t0004 | g0192 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18963 | hp1 | a0001 | c0002 | t0016 | g0148 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18967 | hp1 | a0001 | c0002 | t0004 | g0189 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18974 | hp1 | a0001 | c0002 | t0009 | g0146 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18977 | hp2 | a0001 | c0002 | t0004 | g0201 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18982 | hp2 | a0001 | c0002 | t0004 | g0158 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19005 | hp1 | a0001 | c0001 | t0025 | g0111 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19030 | hp1 | a0001 | c0003 | t0007 | g0086 | AFR | LWK | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19043 | hp1 | a0001 | c0002 | t0036 | g0174 | AFR | LWK | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19043 | hp2 | a0001 | c0003 | t0017 | g0040 | AFR | LWK | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19056 | hp2 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19063 | hp1 | a0001 | c0001 | t0041 | g0115 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19067 | hp1 | a0001 | c0002 | t0004 | g0199 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19070 | hp1 | a0001 | c0002 | t0016 | g0147 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19070 | hp2 | a0001 | c0001 | t0033 | g0135 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0198 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19084 | hp1 | a0001 | c0001 | t0029 | g0108 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0140 | EAS | JPT | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19240 | hp1 | a0001 | c0002 | t0015 | g0149 | AFR | YRI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA19240 | hp2 | a0001 | c0003 | t0008 | g0067 | AFR | YRI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20129 | hp1 | a0001 | c0002 | t0018 | g0178 | AFR | ASW | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ASW | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20752 | hp1 | a0001 | c0001 | t0022 | g0097 | EUR | TSI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20905 | hp2 | a0001 | c0002 | t0009 | g0150 | SAS | GIH | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02109 | hp2 | a0001 | c0003 | t0013 | g0072 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02486 | hp1 | a0001 | c0001 | t0024 | g0058 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0084 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02559 | hp1 | a0001 | c0003 | t0042 | g0212 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03471 | hp1 | a0001 | c0003 | t0007 | g0083 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | MSL | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0069 | AFR | USA | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0057 | AFR | USA | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20300 | hp1 | a0001 | c0003 | t0007 | g0009 | AFR | USA | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA21309 | hp1 | a0001 | c0002 | t0027 | g0181 | AFR | LWK | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| NA21309 | hp2 | a0001 | c0002 | t0023 | g0045 | AFR | LWK | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0098 | REF | REF | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0015 | REF | REF | MEF2D_chr1_156458727_156505775 | MEF2D | chr1 | 156458727 | 156505775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156475200 | T | A | 1 | a0003 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.914A>T | p.His305Leu | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/12 | 1342/5912 | 914/1566 | 305/521 | chr1 | 156475200 | |||
| chr1:156479613 | C | T | 1 | a0002 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.580G>A | p.Gly194Ser | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 5/12 | 1008/5912 | 580/1566 | 194/521 | chr1 | 156479613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156475214 | G | A | 1 | a0001c0005 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.900C>T | p.Val300Val | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/12 | 1328/5912 | 900/1566 | 300/521 | chr1 | 156475214 | |||
| chr1:156477111 | T | C | 1 | a0001c0001 | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
synonymous_variant | LOW | c.756A>G | p.Pro252Pro | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 7/12 | 1184/5912 | 756/1566 | 252/521 | chr1 | 156477111 | |||
| chr1:156480927 | G | A | 2 | a0001c0002 a0003c0006 |
97 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(94): Show |
synonymous_variant | LOW | c.303C>T | p.Pro101Pro | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 4/12 | 731/5912 | 303/1566 | 101/521 | chr1 | 156480927 | |||
| chr1:156480948 | G | A | 1 | a0001c0001 | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
synonymous_variant | LOW | c.282C>T | p.Asn94Asn | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 4/12 | 710/5912 | 282/1566 | 94/521 | chr1 | 156480948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156463921 | G | A | 1 | a0001c0003t0031 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3724C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 3724 | chr1 | 156463921 | ||||||
| chr1:156464137 | G | A | 2 | a0001c0003t0014 a0001c0003t0042 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3508C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 3508 | chr1 | 156464137 | ||||||
| chr1:156464417 | G | T | 1 | a0001c0001t0028 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3228C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 3228 | chr1 | 156464417 | ||||||
| chr1:156464448 | T | TG | 5 | a0001c0001t0011 a0001c0002t0012 a0001c0003t0007 others(2): Show |
16 | HG00741.hp1 HG01175.hp1 HG01433.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3196dupC | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 3196 | chr1 | 156464448 | ||||||
| chr1:156464453 | G | C | 1 | a0001c0001t0029 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3192C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 3192 | chr1 | 156464453 | ||||||
| chr1:156464649 | G | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2996C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2996 | chr1 | 156464649 | ||||||
| chr1:156464833 | G | A | 1 | a0001c0002t0035 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2812C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2812 | chr1 | 156464833 | ||||||
| chr1:156464911 | G | T | 13 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0021 others(10): Show |
120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2734C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2734 | chr1 | 156464911 | ||||||
| chr1:156465019 | G | T | 1 | a0001c0003t0038 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2626C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2626 | chr1 | 156465019 | ||||||
| chr1:156465121 | G | A | 1 | a0001c0002t0032 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2524C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2524 | chr1 | 156465121 | ||||||
| chr1:156465153 | C | G | 1 | a0001c0003t0010 | 4 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2492G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2492 | chr1 | 156465153 | ||||||
| chr1:156465168 | G | A | 1 | a0001c0001t0033 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2477C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2477 | chr1 | 156465168 | ||||||
| chr1:156465350 | G | A | 1 | a0001c0003t0010 | 4 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2295C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2295 | chr1 | 156465350 | ||||||
| chr1:156465359 | C | T | 1 | a0001c0001t0022 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2286G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 2286 | chr1 | 156465359 | ||||||
| chr1:156465666 | C | T | 1 | a0001c0003t0010 | 4 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1979G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1979 | chr1 | 156465666 | ||||||
| chr1:156465681 | T | C | 1 | a0001c0002t0004 | 12 | HG00673.hp1 HG01070.hp1 HG02080.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1964A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1964 | chr1 | 156465681 | ||||||
| chr1:156465681 | T | TAC | 9 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0018 others(6): Show |
39 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1962_*1963dupGT | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1963 | chr1 | 156465681 | ||||||
| chr1:156465762 | C | T | 1 | a0001c0002t0027 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1883G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1883 | chr1 | 156465762 | ||||||
| chr1:156465929 | G | T | 1 | a0001c0003t0026 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1716C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1716 | chr1 | 156465929 | ||||||
| chr1:156466004 | A | C | 1 | a0001c0002t0016 | 2 | NA18963.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1641T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1641 | chr1 | 156466004 | ||||||
| chr1:156466109 | C | T | 1 | a0001c0001t0025 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1536 | chr1 | 156466109 | ||||||
| chr1:156466110 | G | A | 3 | a0001c0002t0034 a0001c0002t0035 a0001c0002t0036 |
3 | HG02965.hp1 HG03139.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1535 | chr1 | 156466110 | ||||||
| chr1:156466126 | C | A | 1 | a0001c0002t0036 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1519G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1519 | chr1 | 156466126 | ||||||
| chr1:156466127 | T | C | 3 | a0001c0003t0013 a0001c0003t0014 a0001c0003t0042 |
7 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1518A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1518 | chr1 | 156466127 | ||||||
| chr1:156466182 | G | A | 1 | a0001c0002t0039 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1463C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1463 | chr1 | 156466182 | ||||||
| chr1:156466211 | C | T | 1 | a0001c0003t0014 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1434G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1434 | chr1 | 156466211 | ||||||
| chr1:156466300 | C | A | 1 | a0001c0002t0019 | 2 | HG01975.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1345G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1345 | chr1 | 156466300 | ||||||
| chr1:156466300 | C | CA | 10 | a0001c0001t0037 a0001c0002t0018 a0001c0003t0006 others(7): Show |
32 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1344dupT | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1344 | chr1 | 156466300 | ||||||
| chr1:156466309 | A | C | 2 | a0001c0002t0009 a0001c0002t0016 |
6 | HG00733.hp1 HG03942.hp1 NA18963.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1336T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1336 | chr1 | 156466309 | ||||||
| chr1:156466439 | G | A | 1 | a0001c0003t0038 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1206 | chr1 | 156466439 | ||||||
| chr1:156466614 | C | T | 1 | a0001c0001t0024 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1031G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1031 | chr1 | 156466614 | ||||||
| chr1:156466631 | C | T | 1 | a0001c0003t0008 | 5 | HG02257.hp2 HG03486.hp2 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1014G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 1014 | chr1 | 156466631 | ||||||
| chr1:156466884 | T | C | 2 | a0001c0003t0014 a0001c0003t0042 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*761A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 761 | chr1 | 156466884 | ||||||
| chr1:156466929 | CCT | C | 2 | a0001c0002t0005 a0001c0002t0039 |
10 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*714_*715delAG | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 714 | chr1 | 156466929 | ||||||
| chr1:156467301 | A | T | 1 | a0001c0002t0015 | 2 | HG02280.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*344T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 344 | chr1 | 156467301 | ||||||
| chr1:156467530 | C | T | 1 | a0001c0002t0023 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 115 | chr1 | 156467530 | ||||||
| chr1:156467591 | G | A | 1 | a0001c0003t0040 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 12/12 | 54 | chr1 | 156467591 | ||||||
| chr1:156483304 | G | T | 1 | a0001c0001t0022 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/12 | 12 | chr1 | 156483304 | ||||||
| chr1:156483335 | T | C | 1 | a0001c0001t0041 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/12 | 43 | chr1 | 156483335 | ||||||
| chr1:156500693 | G | T | 1 | a0001c0001t0021 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-346C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/12 | 17401 | chr1 | 156500693 | ||||||
| chr1:156500699 | G | C | 2 | a0001c0003t0014 a0001c0003t0042 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-352C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/12 | 17407 | chr1 | 156500699 | ||||||
| chr1:156500705 | G | C | 1 | a0001c0002t0020 | 1 | HG01516.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-358C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/12 | chr1 | 156500705 | |||||||
| chr1:156500706 | A | T | 1 | a0001c0002t0020 | 1 | HG01516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-359T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/12 | 17414 | chr1 | 156500706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156467874 | C | T | 1 | a0001c0003t0003g0037 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1554+119G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 11/11 | chr1 | 156467874 | |||||||
| chr1:156467962 | C | A | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1554+31G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 11/11 | chr1 | 156467962 | |||||||
| chr1:156468406 | G | A | 12 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(9): Show |
16 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1248-107C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 10/11 | chr1 | 156468406 | |||||||
| chr1:156468637 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG01261.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1247+143A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 10/11 | chr1 | 156468637 | |||||||
| chr1:156468709 | C | T | 2 | a0001c0002t0002g0210 a0001c0002t0002g0211 |
2 | HG02135.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1247+71G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 10/11 | chr1 | 156468709 | |||||||
| chr1:156468725 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
10 | HG02055.hp2 HG02258.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1247+55A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 10/11 | chr1 | 156468725 | |||||||
| chr1:156469054 | T | C | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1007-34A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469054 | |||||||
| chr1:156469061 | G | A | 1 | a0002c0004t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1007-41C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469061 | |||||||
| chr1:156469179 | G | C | 1 | a0001c0003t0038g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1007-159C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469179 | |||||||
| chr1:156469208 | T | C | 103 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0003 others(100): Show |
126 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(123): Show |
intron_variant | MODIFIER | c.1007-188A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469208 | |||||||
| chr1:156469416 | C | A | 18 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(15): Show |
23 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1007-396G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469416 | |||||||
| chr1:156469475 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1007-455G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469475 | |||||||
| chr1:156469509 | C | T | 3 | a0001c0002t0004g0158 a0001c0002t0004g0192 a0001c0002t0004g0200 |
3 | HG02080.hp2 NA18961.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1007-489G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469509 | |||||||
| chr1:156469589 | T | TA | 21 | a0001c0002t0003g0169 a0001c0002t0004g0201 a0001c0002t0005g0007 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1007-570dupT | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469589 | |||||||
| chr1:156469589 | T | TAA | 77 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0003 others(74): Show |
96 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.1007-571_1007-570d others(4): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469589 | |||||||
| chr1:156469603 | A | AAC | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(78): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1007-584_1007-583i others(4): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469603 | |||||||
| chr1:156469603 | A | AC | 2 | a0001c0001t0001g0022 a0001c0001t0001g0100 |
3 | HG01070.hp2 NA19057.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1007-584_1007-583i others(3): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469603 | |||||||
| chr1:156469607 | C | G | 1 | a0001c0003t0002g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1007-587G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469607 | |||||||
| chr1:156469625 | A | G | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1007-605T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469625 | |||||||
| chr1:156469712 | A | T | 1 | a0001c0002t0016g0147 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1007-692T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469712 | |||||||
| chr1:156469747 | G | A | 1 | a0001c0003t0006g0008 | 3 | HG02572.hp2 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1007-727C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469747 | |||||||
| chr1:156469768 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(205): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1007-748A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469768 | |||||||
| chr1:156469778 | C | A | 4 | a0001c0003t0008g0019 a0001c0003t0008g0067 a0001c0003t0008g0069 others(1): Show |
5 | HG02257.hp2 HG03486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007-758G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469778 | |||||||
| chr1:156469882 | A | G | 1 | a0001c0002t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1007-862T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156469882 | |||||||
| chr1:156470004 | G | C | 1 | a0001c0003t0013g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1007-984C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156470004 | |||||||
| chr1:156470287 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1007-1267G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156470287 | |||||||
| chr1:156470350 | T | C | 2 | a0001c0002t0003g0153 a0001c0002t0003g0169 |
2 | NA19003.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1007-1330A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156470350 | |||||||
| chr1:156470445 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1007-1425C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156470445 | |||||||
| chr1:156470452 | A | T | 18 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(15): Show |
23 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1007-1432T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156470452 | |||||||
| chr1:156470982 | C | T | 1 | a0001c0002t0002g0167 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1007-1962G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156470982 | |||||||
| chr1:156471255 | C | T | 3 | a0001c0003t0002g0002 a0001c0003t0002g0043 a0001c0003t0002g0044 |
8 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-2235G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156471255 | |||||||
| chr1:156471319 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1007-2299G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156471319 | |||||||
| chr1:156471419 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1007-2399C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156471419 | |||||||
| chr1:156471666 | G | A | 1 | a0001c0002t0002g0170 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1007-2646C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156471666 | |||||||
| chr1:156471946 | G | A | 6 | a0001c0002t0009g0142 a0001c0002t0009g0146 a0001c0002t0009g0150 others(3): Show |
6 | HG00733.hp1 HG03942.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-2926C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156471946 | |||||||
| chr1:156471980 | G | A | 1 | a0001c0005t0002g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1007-2960C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156471980 | |||||||
| chr1:156472190 | C | T | 1 | a0001c0002t0002g0157 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1006+2918G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472190 | |||||||
| chr1:156472198 | C | T | 4 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+2910G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472198 | |||||||
| chr1:156472321 | T | G | 4 | a0001c0003t0008g0019 a0001c0003t0008g0067 a0001c0003t0008g0069 others(1): Show |
5 | HG02257.hp2 HG03486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006+2787A>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472321 | |||||||
| chr1:156472479 | G | A | 2 | a0001c0002t0004g0198 a0001c0002t0004g0201 |
2 | NA18977.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1006+2629C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472479 | |||||||
| chr1:156472715 | A | AT | 8 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0001g0116 others(5): Show |
8 | HG01169.hp2 HG01346.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+2392dupA | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472715 | |||||||
| chr1:156472770 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1006+2338G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472770 | |||||||
| chr1:156472834 | C | G | 1 | a0001c0001t0001g0021 | 2 | HG01261.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1006+2274G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472834 | |||||||
| chr1:156472953 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1006+2155C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156472953 | |||||||
| chr1:156473075 | T | C | 1 | a0001c0002t0005g0050 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1006+2033A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473075 | |||||||
| chr1:156473164 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1006+1944G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473164 | |||||||
| chr1:156473180 | G | C | 1 | a0001c0001t0011g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1006+1928C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473180 | |||||||
| chr1:156473406 | G | A | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006+1702C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473406 | |||||||
| chr1:156473440 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0021g0030 |
2 | HG01106.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1006+1668T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473440 | |||||||
| chr1:156473560 | G | A | 5 | a0001c0002t0005g0007 a0001c0002t0005g0047 a0001c0002t0005g0048 others(2): Show |
7 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+1548C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473560 | |||||||
| chr1:156473566 | G | A | 1 | a0001c0003t0002g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1006+1542C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473566 | |||||||
| chr1:156473587 | C | T | 1 | a0001c0002t0004g0198 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1006+1521G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473587 | |||||||
| chr1:156473598 | A | G | 1 | a0001c0002t0009g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1006+1510T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473598 | |||||||
| chr1:156473635 | C | G | 2 | a0001c0003t0006g0075 a0001c0003t0006g0087 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1006+1473G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473635 | |||||||
| chr1:156473652 | C | T | 3 | a0001c0003t0007g0078 a0001c0003t0007g0082 a0001c0003t0007g0083 |
3 | HG02723.hp2 HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1006+1456G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473652 | |||||||
| chr1:156473711 | C | T | 1 | a0001c0002t0002g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1006+1397G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473711 | |||||||
| chr1:156473861 | A | C | 11 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(8): Show |
15 | HG01175.hp2 HG01884.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1006+1247T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473861 | |||||||
| chr1:156473880 | G | A | 3 | a0001c0003t0013g0068 a0001c0003t0013g0072 a0001c0003t0013g0081 |
3 | HG02109.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1006+1228C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156473880 | |||||||
| chr1:156474080 | C | CT | 5 | a0001c0002t0005g0007 a0001c0002t0005g0047 a0001c0002t0005g0048 others(2): Show |
7 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+1027dupA | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474080 | |||||||
| chr1:156474451 | A | G | 1 | a0001c0003t0031g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1006+657T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474451 | |||||||
| chr1:156474455 | CAA | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0109 others(1): Show |
4 | NA18973.hp1 NA19007.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+651_1006+652d others(4): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474455 | |||||||
| chr1:156474477 | C | T | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006+631G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474477 | |||||||
| chr1:156474521 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1006+587C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474521 | |||||||
| chr1:156474538 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1006+570C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474538 | |||||||
| chr1:156474571 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1006+537C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474571 | |||||||
| chr1:156474700 | C | A | 5 | a0001c0003t0007g0009 a0001c0003t0007g0078 a0001c0003t0007g0082 others(2): Show |
7 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006+408G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474700 | |||||||
| chr1:156474843 | A | G | 2 | a0001c0003t0017g0039 a0001c0003t0017g0040 |
2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1006+265T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 9/11 | chr1 | 156474843 | |||||||
| chr1:156475257 | G | A | 4 | a0001c0003t0008g0019 a0001c0003t0008g0067 a0001c0003t0008g0069 others(1): Show |
5 | HG02257.hp2 HG03486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-20C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475257 | |||||||
| chr1:156475421 | A | AG | 3 | a0001c0003t0006g0008 a0001c0003t0006g0074 a0001c0003t0040g0077 |
5 | HG02572.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-185dupC | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475421 | |||||||
| chr1:156475447 | T | C | 1 | a0001c0001t0033g0135 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.877-210A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475447 | |||||||
| chr1:156475460 | C | T | 2 | a0001c0002t0016g0147 a0001c0002t0016g0148 |
2 | NA18963.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.877-223G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475460 | |||||||
| chr1:156475654 | C | T | 1 | a0001c0002t0003g0166 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.877-417G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475654 | |||||||
| chr1:156475660 | G | A | 1 | a0001c0002t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.877-423C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475660 | |||||||
| chr1:156475711 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.877-474G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475711 | |||||||
| chr1:156475732 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0011g0204 |
3 | NA18949.hp1 NA18986.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.877-495G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475732 | |||||||
| chr1:156475890 | A | G | 1 | a0001c0001t0029g0108 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.876+604T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475890 | |||||||
| chr1:156475966 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0059 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.876+528C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156475966 | |||||||
| chr1:156476147 | C | T | 1 | a0001c0002t0012g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.876+347G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156476147 | |||||||
| chr1:156476228 | A | G | 1 | a0001c0003t0006g0076 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.876+266T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156476228 | |||||||
| chr1:156476308 | C | G | 1 | a0001c0001t0021g0030 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.876+186G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156476308 | |||||||
| chr1:156476438 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.876+56G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156476438 | |||||||
| chr1:156476450 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.876+44G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 8/11 | chr1 | 156476450 | |||||||
| chr1:156476604 | C | T | 1 | a0001c0002t0005g0016 | 2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.856-90G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 7/11 | chr1 | 156476604 | |||||||
| chr1:156476632 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.856-118G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 7/11 | chr1 | 156476632 | |||||||
| chr1:156476658 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.856-144G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 7/11 | chr1 | 156476658 | |||||||
| chr1:156476798 | C | CT | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.855+213dupA | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 7/11 | chr1 | 156476798 | |||||||
| chr1:156476969 | T | C | 1 | a0002c0004t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.855+43A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 7/11 | chr1 | 156476969 | |||||||
| chr1:156476973 | A | G | 1 | a0001c0002t0002g0155 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.855+39T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 7/11 | chr1 | 156476973 | |||||||
| chr1:156477334 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.665-132T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156477334 | |||||||
| chr1:156477411 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0011g0204 |
3 | NA18949.hp1 NA18986.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.665-209C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156477411 | |||||||
| chr1:156477414 | C | T | 1 | a0001c0003t0013g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.665-212G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156477414 | |||||||
| chr1:156477484 | G | T | 1 | a0001c0003t0031g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665-282C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156477484 | |||||||
| chr1:156477488 | G | A | 3 | a0001c0003t0014g0028 a0001c0003t0014g0213 a0001c0003t0042g0212 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-286C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156477488 | |||||||
| chr1:156477550 | G | A | 2 | a0001c0003t0026g0063 a0001c0003t0038g0064 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.665-348C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156477550 | |||||||
| chr1:156477566 | A | C | 19 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(16): Show |
24 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.665-364T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156477566 | |||||||
| chr1:156478083 | G | A | 3 | a0001c0003t0014g0028 a0001c0003t0014g0213 a0001c0003t0042g0212 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-881C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478083 | |||||||
| chr1:156478417 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(81): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.664+873A>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478417 | |||||||
| chr1:156478426 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0011g0057 |
2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.664+864G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478426 | |||||||
| chr1:156478464 | G | A | 7 | a0001c0002t0005g0007 a0001c0002t0005g0016 a0001c0002t0005g0046 others(4): Show |
10 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.664+826C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478464 | |||||||
| chr1:156478469 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(203): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.664+821A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478469 | |||||||
| chr1:156478553 | G | A | 1 | a0001c0001t0028g0055 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.664+737C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478553 | |||||||
| chr1:156478560 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.664+730G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478560 | |||||||
| chr1:156478573 | C | T | 1 | a0002c0004t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.664+717G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478573 | |||||||
| chr1:156478634 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(81): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.664+656C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478634 | |||||||
| chr1:156478755 | C | CCCGACCT others(11): Show |
13 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(10): Show |
17 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.664+517_664+534dup others(18): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478755 | |||||||
| chr1:156478778 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(203): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.664+512A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478778 | |||||||
| chr1:156478804 | A | T | 1 | a0001c0002t0009g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.664+486T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 6/11 | chr1 | 156478804 | |||||||
| chr1:156479388 | G | A | 3 | a0001c0002t0034g0173 a0001c0002t0035g0160 a0001c0002t0036g0174 |
3 | HG02965.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.608-42C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 5/11 | chr1 | 156479388 | |||||||
| chr1:156479398 | T | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0129 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.608-52A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 5/11 | chr1 | 156479398 | |||||||
| chr1:156479435 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.608-89C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 5/11 | chr1 | 156479435 | |||||||
| chr1:156479802 | C | T | 1 | a0001c0003t0002g0043 | 1 | HG00738.hp2 | splice_region_variant&intron_variant | LOW | c.397-6G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 4/11 | chr1 | 156479802 | |||||||
| chr1:156479821 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.397-25C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 4/11 | chr1 | 156479821 | |||||||
| chr1:156480183 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0100 a0001c0001t0001g0126 others(1): Show |
5 | HG01261.hp2 HG02004.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.397-387G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 4/11 | chr1 | 156480183 | |||||||
| chr1:156480225 | C | A | 2 | a0001c0003t0026g0063 a0001c0003t0038g0064 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.397-429G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 4/11 | chr1 | 156480225 | |||||||
| chr1:156480711 | G | T | 3 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0165 |
3 | NA18995.hp2 NA19007.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.396+123C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 4/11 | chr1 | 156480711 | |||||||
| chr1:156481081 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(103): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.259-110A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156481081 | |||||||
| chr1:156481177 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.259-206C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156481177 | |||||||
| chr1:156481344 | T | C | 2 | a0001c0002t0015g0143 a0001c0002t0015g0149 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.259-373A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156481344 | |||||||
| chr1:156481472 | C | T | 69 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0003 others(66): Show |
83 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.259-501G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156481472 | |||||||
| chr1:156481557 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(81): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.259-586A>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156481557 | |||||||
| chr1:156481750 | C | T | 1 | a0001c0003t0002g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.258+687G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156481750 | |||||||
| chr1:156481998 | G | A | 1 | a0001c0002t0002g0034 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.258+439C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156481998 | |||||||
| chr1:156482156 | A | G | 1 | a0001c0001t0033g0135 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.258+281T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156482156 | |||||||
| chr1:156482167 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG00140.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.258+270G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156482167 | |||||||
| chr1:156482301 | G | A | 69 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0003 others(66): Show |
83 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.258+136C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156482301 | |||||||
| chr1:156482302 | C | G | 3 | a0001c0003t0013g0068 a0001c0003t0013g0072 a0001c0003t0013g0081 |
3 | HG02109.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.258+135G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 3/11 | chr1 | 156482302 | |||||||
| chr1:156482745 | C | T | 1 | a0001c0002t0005g0016 | 2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.55-105G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/11 | chr1 | 156482745 | |||||||
| chr1:156482850 | A | G | 19 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(16): Show |
24 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.55-210T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/11 | chr1 | 156482850 | |||||||
| chr1:156482942 | T | A | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.54+297A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/11 | chr1 | 156482942 | |||||||
| chr1:156482991 | A | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(203): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.54+248T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/11 | chr1 | 156482991 | |||||||
| chr1:156483078 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.54+161C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/11 | chr1 | 156483078 | |||||||
| chr1:156483112 | T | A | 1 | a0001c0003t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+127A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/11 | chr1 | 156483112 | |||||||
| chr1:156483170 | T | C | 2 | a0001c0003t0026g0063 a0001c0003t0038g0064 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.54+69A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 2/11 | chr1 | 156483170 | |||||||
| chr1:156483455 | T | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-138-25A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156483455 | |||||||
| chr1:156483565 | T | C | 3 | a0001c0003t0014g0028 a0001c0003t0014g0213 a0001c0003t0042g0212 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138-135A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156483565 | |||||||
| chr1:156483617 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-138-187T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156483617 | |||||||
| chr1:156483649 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-138-219G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156483649 | |||||||
| chr1:156483864 | C | A | 4 | a0001c0003t0008g0019 a0001c0003t0008g0067 a0001c0003t0008g0069 others(1): Show |
5 | HG02257.hp2 HG03486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-434G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156483864 | |||||||
| chr1:156483932 | A | G | 2 | a0001c0002t0002g0154 a0001c0002t0002g0155 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-138-502T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156483932 | |||||||
| chr1:156484201 | T | C | 2 | a0001c0003t0017g0039 a0001c0003t0017g0040 |
2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-138-771A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156484201 | |||||||
| chr1:156484591 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(179): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-138-1161T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156484591 | |||||||
| chr1:156484592 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(179): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-138-1162T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156484592 | |||||||
| chr1:156484602 | T | A | 3 | a0001c0003t0014g0028 a0001c0003t0014g0213 a0001c0003t0042g0212 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138-1172A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156484602 | |||||||
| chr1:156484603 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-138-1173T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156484603 | |||||||
| chr1:156484682 | C | T | 12 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(9): Show |
16 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-138-1252G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156484682 | |||||||
| chr1:156484772 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(179): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-138-1342T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156484772 | |||||||
| chr1:156485020 | A | G | 1 | a0001c0001t0028g0055 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-138-1590T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485020 | |||||||
| chr1:156485205 | C | T | 4 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138-1775G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485205 | |||||||
| chr1:156485364 | A | G | 2 | a0001c0002t0003g0163 a0001c0002t0018g0175 |
2 | NA18950.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-138-1934T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485364 | |||||||
| chr1:156485381 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-138-1951C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485381 | |||||||
| chr1:156485505 | C | T | 2 | a0001c0003t0008g0019 a0001c0003t0008g0070 |
3 | HG02257.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-138-2075G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485505 | |||||||
| chr1:156485522 | CT | C | 35 | a0001c0001t0001g0065 a0001c0002t0004g0159 a0001c0002t0005g0007 others(32): Show |
43 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-138-2093delA | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485522 | |||||||
| chr1:156485522 | CTT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(93): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-138-2094_-138-209 others(6): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485522 | |||||||
| chr1:156485522 | CTTT | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0116 others(3): Show |
6 | HG00140.hp1 HG02451.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-138-2095_-138-209 others(7): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485522 | |||||||
| chr1:156485526 | T | C | 1 | a0001c0003t0008g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-138-2096A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485526 | |||||||
| chr1:156485550 | T | G | 16 | a0001c0002t0002g0006 a0001c0002t0002g0162 a0001c0002t0002g0180 others(13): Show |
19 | HG01123.hp1 HG01346.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-138-2120A>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485550 | |||||||
| chr1:156485600 | A | G | 1 | a0001c0001t0028g0055 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-138-2170T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485600 | |||||||
| chr1:156485674 | C | T | 2 | a0001c0003t0008g0019 a0001c0003t0008g0070 |
3 | HG02257.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-138-2244G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485674 | |||||||
| chr1:156485701 | CT | C | 4 | a0001c0002t0002g0023 a0001c0002t0002g0187 a0001c0002t0012g0188 others(1): Show |
5 | HG00741.hp1 HG01074.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-2272delA | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485701 | |||||||
| chr1:156485787 | G | A | 12 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(9): Show |
16 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-138-2357C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485787 | |||||||
| chr1:156485818 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0056 |
2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-138-2388A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156485818 | |||||||
| chr1:156486006 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-138-2576G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486006 | |||||||
| chr1:156486106 | G | A | 81 | a0001c0001t0001g0141 a0001c0002t0001g0164 a0001c0002t0001g0176 others(78): Show |
98 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.-138-2676C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486106 | |||||||
| chr1:156486292 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-138-2862G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486292 | |||||||
| chr1:156486316 | ACTGTG | A | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-138-2891_-138-288 others(9): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486316 | |||||||
| chr1:156486505 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(208): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-138-3075G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486505 | |||||||
| chr1:156486509 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-138-3079G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486509 | |||||||
| chr1:156486568 | A | T | 1 | a0001c0001t0030g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-138-3138T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486568 | |||||||
| chr1:156486692 | T | C | 1 | a0001c0002t0002g0033 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-138-3262A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486692 | |||||||
| chr1:156486737 | T | G | 69 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0003 others(66): Show |
83 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.-138-3307A>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156486737 | |||||||
| chr1:156487211 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-138-3781C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487211 | |||||||
| chr1:156487353 | T | A | 1 | a0001c0001t0030g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-138-3923A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487353 | |||||||
| chr1:156487511 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-138-4081G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487511 | |||||||
| chr1:156487673 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-138-4243G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487673 | |||||||
| chr1:156487741 | A | G | 19 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(16): Show |
24 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.-138-4311T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487741 | |||||||
| chr1:156487793 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-138-4363G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487793 | |||||||
| chr1:156487852 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-138-4422T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487852 | |||||||
| chr1:156487854 | G | A | 1 | a0001c0003t0003g0037 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-138-4424C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156487854 | |||||||
| chr1:156488035 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-138-4605T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488035 | |||||||
| chr1:156488244 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-138-4814A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488244 | |||||||
| chr1:156488269 | C | A | 12 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(9): Show |
16 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-138-4839G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488269 | |||||||
| chr1:156488583 | T | C | 1 | a0001c0002t0002g0012 | 3 | HG01069.hp1 HG01071.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-138-5153A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488583 | |||||||
| chr1:156488669 | C | T | 7 | a0001c0002t0005g0007 a0001c0002t0005g0016 a0001c0002t0005g0046 others(4): Show |
10 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-5239G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488669 | |||||||
| chr1:156488677 | A | G | 1 | a0001c0002t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-138-5247T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488677 | |||||||
| chr1:156488815 | C | T | 1 | a0001c0002t0002g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-138-5385G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488815 | |||||||
| chr1:156488885 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-138-5455G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488885 | |||||||
| chr1:156488892 | C | G | 2 | a0001c0003t0013g0068 a0001c0003t0013g0072 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-138-5462G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488892 | |||||||
| chr1:156488956 | A | C | 1 | a0001c0002t0012g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-138-5526T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156488956 | |||||||
| chr1:156489006 | T | C | 2 | a0001c0002t0019g0171 a0001c0002t0019g0184 |
2 | HG01975.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-138-5576A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489006 | |||||||
| chr1:156489048 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-138-5618G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489048 | |||||||
| chr1:156489089 | A | T | 1 | a0001c0002t0002g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-138-5659T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489089 | |||||||
| chr1:156489125 | A | G | 13 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(10): Show |
17 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-138-5695T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489125 | |||||||
| chr1:156489242 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-138-5812G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489242 | |||||||
| chr1:156489374 | A | C | 1 | a0001c0002t0002g0210 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-138-5944T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489374 | |||||||
| chr1:156489743 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-138-6313G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489743 | |||||||
| chr1:156489805 | C | T | 7 | a0001c0002t0005g0007 a0001c0002t0005g0016 a0001c0002t0005g0046 others(4): Show |
10 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-6375G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489805 | |||||||
| chr1:156489881 | T | C | 7 | a0001c0002t0005g0007 a0001c0002t0005g0016 a0001c0002t0005g0046 others(4): Show |
10 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-6451A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489881 | |||||||
| chr1:156489907 | A | T | 73 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0003 others(70): Show |
87 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.-138-6477T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156489907 | |||||||
| chr1:156490015 | G | C | 1 | a0001c0002t0002g0172 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-138-6585C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490015 | |||||||
| chr1:156490472 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-138-7042C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490472 | |||||||
| chr1:156490516 | T | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(203): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-138-7086A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490516 | |||||||
| chr1:156490583 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-138-7153C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490583 | |||||||
| chr1:156490711 | C | G | 7 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(4): Show |
11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-138-7281G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490711 | |||||||
| chr1:156490719 | C | T | 71 | a0001c0002t0001g0164 a0001c0002t0001g0176 a0001c0002t0002g0003 others(68): Show |
85 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.-138-7289G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490719 | |||||||
| chr1:156490721 | G | A | 1 | a0001c0002t0004g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-138-7291C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490721 | |||||||
| chr1:156490942 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-138-7512C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490942 | |||||||
| chr1:156490993 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0126 a0001c0001t0030g0101 |
3 | NA18961.hp1 NA19057.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-138-7563G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156490993 | |||||||
| chr1:156491120 | G | C | 19 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(16): Show |
24 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.-138-7690C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156491120 | |||||||
| chr1:156491327 | G | A | 1 | a0001c0002t0009g0150 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-138-7897C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156491327 | |||||||
| chr1:156491597 | G | A | 12 | a0001c0003t0006g0008 a0001c0003t0006g0041 a0001c0003t0006g0074 others(9): Show |
16 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-138-8167C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156491597 | |||||||
| chr1:156491741 | A | G | 2 | a0001c0003t0026g0063 a0001c0003t0038g0064 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-138-8311T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156491741 | |||||||
| chr1:156491758 | C | T | 4 | a0001c0002t0002g0023 a0001c0002t0002g0187 a0001c0002t0012g0188 others(1): Show |
5 | HG00741.hp1 HG01074.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-8328G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156491758 | |||||||
| chr1:156491915 | A | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-138-8485T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156491915 | |||||||
| chr1:156492000 | A | C | 2 | a0001c0003t0026g0063 a0001c0003t0038g0064 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-139+8486T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492000 | |||||||
| chr1:156492189 | G | T | 6 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(3): Show |
10 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-139+8297C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492189 | |||||||
| chr1:156492287 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-139+8199A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492287 | |||||||
| chr1:156492715 | C | T | 4 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-139+7771G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492715 | |||||||
| chr1:156492716 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-139+7770C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492716 | |||||||
| chr1:156492743 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-139+7743G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492743 | |||||||
| chr1:156492854 | C | T | 1 | a0001c0001t0011g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-139+7632G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492854 | |||||||
| chr1:156492888 | G | A | 1 | a0002c0004t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-139+7598C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156492888 | |||||||
| chr1:156493056 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(203): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-139+7430A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156493056 | |||||||
| chr1:156493419 | A | C | 1 | a0001c0002t0009g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-139+7067T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156493419 | |||||||
| chr1:156493457 | C | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0065 |
3 | HG02886.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-139+7029G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156493457 | |||||||
| chr1:156493638 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-139+6848A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156493638 | |||||||
| chr1:156493676 | G | A | 2 | a0001c0003t0026g0063 a0001c0003t0038g0064 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-139+6810C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156493676 | |||||||
| chr1:156494059 | A | C | 5 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0125 others(2): Show |
5 | HG00140.hp1 HG01109.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139+6427T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494059 | |||||||
| chr1:156494275 | C | T | 2 | a0001c0002t0002g0154 a0001c0002t0002g0155 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-139+6211G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494275 | |||||||
| chr1:156494397 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-139+6089G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494397 | |||||||
| chr1:156494486 | G | T | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139+6000C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494486 | |||||||
| chr1:156494596 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-139+5890G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494596 | |||||||
| chr1:156494631 | G | C | 10 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-139+5855C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494631 | |||||||
| chr1:156494637 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(81): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-139+5849G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494637 | |||||||
| chr1:156494692 | C | G | 1 | a0001c0001t0028g0055 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-139+5794G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494692 | |||||||
| chr1:156494753 | C | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0042 others(4): Show |
10 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.-139+5733G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494753 | |||||||
| chr1:156494878 | G | A | 10 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-139+5608C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494878 | |||||||
| chr1:156494953 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-139+5533A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156494953 | |||||||
| chr1:156495038 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-139+5448G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495038 | |||||||
| chr1:156495237 | C | G | 70 | a0001c0001t0001g0144 a0001c0002t0001g0164 a0001c0002t0001g0176 others(67): Show |
84 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.-139+5249G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495237 | |||||||
| chr1:156495653 | G | A | 1 | a0001c0003t0008g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-139+4833C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495653 | |||||||
| chr1:156495762 | C | CAAAAAAA others(1): Show |
6 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(3): Show |
11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-139+4716_-139+472 others(12): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495762 | |||||||
| chr1:156495762 | C | CAAAAAAA others(3): Show |
7 | a0001c0001t0001g0053 a0001c0001t0001g0088 a0001c0001t0001g0132 others(4): Show |
7 | HG01516.hp1 HG02155.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-139+4714_-139+472 others(14): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495762 | |||||||
| chr1:156495762 | C | CAAAAAAA others(4): Show |
126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(123): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-139+4713_-139+472 others(15): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495762 | |||||||
| chr1:156495762 | C | CAAAAAAA others(5): Show |
36 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0065 others(33): Show |
42 | HG00323.hp1 HG00733.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-139+4712_-139+472 others(16): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495762 | |||||||
| chr1:156495762 | C | CAAAAAAA others(6): Show |
9 | a0001c0001t0001g0051 a0001c0001t0001g0130 a0001c0002t0002g0183 others(6): Show |
11 | HG01192.hp2 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-139+4711_-139+472 others(17): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495762 | |||||||
| chr1:156495762 | C | CAAAAAAA others(7): Show |
10 | a0001c0003t0002g0205 a0001c0003t0002g0206 a0001c0003t0002g0207 others(7): Show |
12 | HG00735.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-139+4710_-139+472 others(18): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495762 | |||||||
| chr1:156495762 | C | CAAAAAAA others(8): Show |
4 | a0001c0003t0002g0208 a0001c0003t0002g0209 a0001c0003t0006g0041 others(1): Show |
4 | HG01175.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139+4709_-139+472 others(19): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156495762 | |||||||
| chr1:156496330 | C | T | 10 | a0001c0003t0002g0080 a0001c0003t0002g0084 a0001c0003t0002g0085 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-139+4156G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156496330 | |||||||
| chr1:156496374 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0066 |
4 | HG02615.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139+4112C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156496374 | |||||||
| chr1:156496544 | G | T | 1 | a0001c0002t0003g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-139+3942C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156496544 | |||||||
| chr1:156496545 | T | G | 1 | a0001c0002t0003g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-139+3941A>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156496545 | |||||||
| chr1:156496546 | G | T | 1 | a0001c0002t0003g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-139+3940C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156496546 | |||||||
| chr1:156496831 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-139+3655A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156496831 | |||||||
| chr1:156496907 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-139+3579C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156496907 | |||||||
| chr1:156497062 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-139+3424G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497062 | |||||||
| chr1:156497066 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-139+3420G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497066 | |||||||
| chr1:156497124 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-139+3362T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497124 | |||||||
| chr1:156497158 | C | A | 5 | a0001c0003t0002g0052 a0001c0003t0008g0019 a0001c0003t0008g0067 others(2): Show |
6 | HG02257.hp2 HG03139.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-139+3328G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497158 | |||||||
| chr1:156497212 | T | G | 2 | a0001c0003t0003g0014 a0001c0003t0003g0038 |
3 | HG02145.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-139+3274A>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497212 | |||||||
| chr1:156497358 | G | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG02109.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139+3128C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497358 | |||||||
| chr1:156497517 | T | C | 2 | a0001c0002t0002g0185 a0001c0002t0002g0186 |
2 | HG00738.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-139+2969A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497517 | |||||||
| chr1:156497751 | G | C | 1 | a0001c0001t0011g0204 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-139+2735C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156497751 | |||||||
| chr1:156498101 | T | TA | 26 | a0001c0002t0002g0034 a0001c0002t0002g0187 a0001c0002t0002g0190 others(23): Show |
34 | HG00673.hp1 HG00741.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-139+2384dupT | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498101 | |||||||
| chr1:156498101 | T | TAA | 14 | a0001c0002t0004g0198 a0001c0002t0004g0199 a0001c0003t0006g0008 others(11): Show |
16 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-139+2383_-139+238 others(6): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498101 | |||||||
| chr1:156498101 | T | TAAA | 14 | a0001c0002t0004g0200 a0001c0002t0004g0201 a0001c0002t0005g0047 others(11): Show |
16 | HG01168.hp2 HG02080.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-139+2382_-139+238 others(7): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498101 | |||||||
| chr1:156498101 | T | TAAAA | 9 | a0001c0002t0005g0007 a0001c0002t0005g0048 a0001c0002t0005g0050 others(6): Show |
11 | HG00099.hp1 HG00323.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-139+2381_-139+238 others(8): Show |
MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498101 | |||||||
| chr1:156498101 | TA | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(67): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-139+2384delT | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498101 | |||||||
| chr1:156498119 | A | C | 2 | a0001c0002t0002g0154 a0001c0002t0002g0155 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-139+2367T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498119 | |||||||
| chr1:156498162 | A | G | 1 | a0001c0003t0002g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-139+2324T>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498162 | |||||||
| chr1:156498217 | C | T | 1 | a0001c0002t0003g0153 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-139+2269G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498217 | |||||||
| chr1:156498383 | G | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG02109.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139+2103C>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498383 | |||||||
| chr1:156498451 | T | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-139+2035A>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498451 | |||||||
| chr1:156498587 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-139+1899G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498587 | |||||||
| chr1:156498610 | C | G | 1 | a0001c0002t0009g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-139+1876G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498610 | |||||||
| chr1:156498631 | A | C | 1 | a0001c0002t0009g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-139+1855T>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498631 | |||||||
| chr1:156498716 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-139+1770C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498716 | |||||||
| chr1:156498750 | C | T | 7 | a0001c0002t0005g0007 a0001c0002t0005g0016 a0001c0002t0005g0046 others(4): Show |
10 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-139+1736G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498750 | |||||||
| chr1:156498900 | A | T | 12 | a0001c0001t0001g0144 a0001c0002t0002g0145 a0001c0002t0009g0142 others(9): Show |
12 | HG00733.hp1 HG01433.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-139+1586T>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156498900 | |||||||
| chr1:156499455 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(205): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-139+1031A>G | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156499455 | |||||||
| chr1:156499572 | G | A | 73 | a0001c0001t0001g0144 a0001c0002t0001g0164 a0001c0002t0001g0176 others(70): Show |
87 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.-139+914C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156499572 | |||||||
| chr1:156499949 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-139+537G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156499949 | |||||||
| chr1:156500048 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
5 | HG02300.hp2 NA18949.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139+438C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156500048 | |||||||
| chr1:156500116 | G | A | 5 | a0001c0003t0002g0205 a0001c0003t0002g0206 a0001c0003t0002g0207 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139+370C>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156500116 | |||||||
| chr1:156500205 | C | G | 1 | a0001c0003t0006g0041 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-139+281G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156500205 | |||||||
| chr1:156500291 | C | T | 9 | a0001c0003t0003g0005 a0001c0003t0003g0014 a0001c0003t0003g0037 others(6): Show |
14 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139+195G>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156500291 | |||||||
| chr1:156500322 | C | A | 2 | a0001c0002t0002g0210 a0001c0002t0002g0211 |
2 | HG02135.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-139+164G>T | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156500322 | |||||||
| chr1:156500364 | C | G | 3 | a0001c0002t0002g0032 a0001c0002t0002g0033 a0001c0002t0002g0034 |
3 | NA18948.hp2 NA18978.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-139+122G>C | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156500364 | |||||||
| chr1:156500392 | G | T | 1 | a0001c0001t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-139+94C>A | MEF2D | ENSG00000116604.19 | transcript | ENST00000348159.9 | protein_coding | 1/11 | chr1 | 156500392 |