Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4208 |
| ensemblid | ENSG00000081189.17 |
| hgncid | 6996 |
| symbol | MEF2C |
| name | myocyte enhancer factor 2C |
| refseq_nuc | NM_002397.5 |
| refseq_prot | NP_002388.2 |
| ensembl_nuc | ENST00000504921.7 |
| ensembl_prot | ENSP00000421925.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 88717117 |
| end | 88883184 |
| strand | - |
| ver | v1.2 |
| region | chr5:88717117-88883184 |
| region5000 | chr5:88712117-88888184 |
| regionname0 | MEF2C_chr5_88717117_88883184 |
| regionname5000 | MEF2C_chr5_88712117_88888184 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1419 | 302 | 78 | 56 | 122 | 14 | 30 | MEF2C_chr5_88712117_88888184 | MEF2C | ATGGG others(1414): Show |
chr5 | 88712117 | 88888184 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7281 | 78 | 11 | 17 | 37 | 4 | 9 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0002 | 0/0 | 7282 | 71 | 17 | 6 | 37 | 1 | 10 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0003 | 1/0 | 7281 | 54 | 6 | 15 | 26 | 2 | 4 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0004 | 0/1 | 7280 | 35 | 21 | 8 | 0 | 3 | 2 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7275): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0005 | 0/0 | 7280 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7275): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0006 | 0/0 | 7281 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0007 | 0/0 | 7281 | 5 | 5 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0008 | 0/0 | 7282 | 5 | 0 | 2 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0009 | 0/0 | 7280 | 4 | 0 | 1 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7275): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0010 | 0/0 | 7283 | 3 | 0 | 0 | 0 | 2 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7278): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0011 | 0/0 | 7282 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0012 | 0/0 | 7281 | 3 | 0 | 3 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0013 | 0/0 | 7281 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0014 | 0/0 | 7280 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7275): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0015 | 0/0 | 7281 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0016 | 0/0 | 7282 | 2 | 0 | 0 | 0 | 2 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0017 | 0/0 | 7281 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0018 | 0/0 | 7281 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0019 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0020 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7275): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0021 | 0/0 | 7282 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0022 | 0/0 | 7282 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0023 | 0/0 | 7282 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0024 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0025 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0026 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0027 | 0/0 | 7281 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0028 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0029 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0030 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7277): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0031 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0032 | 0/0 | 7281 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0033 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0034 | 0/0 | 7281 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0035 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0036 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7275): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0037 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| a0001c0001t0038 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | GCAGT others(7276): Show |
chr5 | 88712117 | 88888184 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0009g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0011g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0012g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0013g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0013g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0014g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0014g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0015g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0016g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0016g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0017g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0018g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0019g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0020g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0021g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0022g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0023g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0024g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0025g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0026g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0027g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0028g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0029g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0030g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0031g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0032g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0033g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0034g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0035g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0036g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0037g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| a0001c0001t0038g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0248 | EUR | GBR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0138 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0146 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00597 | hp2 | a0001 | c0001 | t0013 | g0150 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00639 | hp1 | a0001 | c0001 | t0034 | g0016 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00673 | hp2 | a0001 | c0001 | t0013 | g0149 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0062 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0156 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0073 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01433 | hp2 | a0001 | c0001 | t0012 | g0142 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0061 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01516 | hp1 | a0001 | c0001 | t0016 | g0078 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01517 | hp1 | a0001 | c0001 | t0010 | g0060 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01517 | hp2 | a0001 | c0001 | t0016 | g0083 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01891 | hp2 | a0001 | c0001 | t0019 | g0071 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0181 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01975 | hp1 | a0001 | c0001 | t0027 | g0264 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0035 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01978 | hp2 | a0001 | c0001 | t0018 | g0123 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0161 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02055 | hp1 | a0001 | c0001 | t0035 | g0091 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0072 | EAS | CDX | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0296 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02572 | hp2 | a0001 | c0001 | t0029 | g0023 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02602 | hp2 | a0001 | c0001 | t0031 | g0169 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02615 | hp1 | a0001 | c0001 | t0036 | g0017 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02622 | hp1 | a0001 | c0001 | t0025 | g0158 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0294 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02683 | hp1 | a0001 | c0001 | t0038 | g0298 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02735 | hp1 | a0001 | c0001 | t0028 | g0173 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02896 | hp2 | a0001 | c0001 | t0026 | g0037 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0291 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0286 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0085 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03225 | hp2 | a0001 | c0001 | t0024 | g0070 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0116 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0115 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03942 | hp1 | a0001 | c0001 | t0037 | g0233 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0252 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18522 | hp2 | a0001 | c0001 | t0015 | g0093 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18906 | hp2 | a0001 | c0001 | t0030 | g0113 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18941 | hp1 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18945 | hp2 | a0001 | c0001 | t0022 | g0194 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18966 | hp2 | a0001 | c0001 | t0009 | g0179 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18969 | hp2 | a0001 | c0001 | t0009 | g0180 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18979 | hp2 | a0001 | c0001 | t0021 | g0208 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18982 | hp2 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0050 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19009 | hp2 | a0001 | c0001 | t0023 | g0196 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19056 | hp1 | a0001 | c0001 | t0017 | g0253 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0111 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19086 | hp2 | a0001 | c0001 | t0011 | g0051 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19091 | hp1 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0297 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA20129 | hp1 | a0001 | c0001 | t0033 | g0064 | AFR | ASW | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ASW | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0118 | EUR | TSI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | TSI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | GIH | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA20905 | hp2 | a0001 | c0001 | t0010 | g0032 | SAS | GIH | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | USA | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA18955 | hp2 | a0001 | c0001 | t0032 | g0134 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0119 | REF | REF | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0141 | REF | REF | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:88823930 | G | T | 1 | a0001 | 1 | NA19056.hp1 | splice_region_variant | LOW | c.-142C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/11 | chr5 | 88823930 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:88717390 | T | C | 2 | a0001c0001t0006 a0001c0001t0009 |
9 | HG01928.hp1 NA18941.hp1 NA18945.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5214A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 5214 | chr5 | 88717390 | ||||||
| chr5:88717417 | T | G | 1 | a0001c0001t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5187A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 5187 | chr5 | 88717417 | ||||||
| chr5:88717769 | C | G | 1 | a0001c0001t0012 | 3 | HG01099.hp1 HG01255.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4835G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 4835 | chr5 | 88717769 | ||||||
| chr5:88717994 | A | G | 1 | a0001c0001t0026 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4610T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 4610 | chr5 | 88717994 | ||||||
| chr5:88718056 | G | A | 7 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0015 others(4): Show |
16 | HG00639.hp1 HG01243.hp1 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4548C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 4548 | chr5 | 88718056 | ||||||
| chr5:88718621 | C | T | 1 | a0001c0001t0022 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3983G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3983 | chr5 | 88718621 | ||||||
| chr5:88718706 | A | G | 1 | a0001c0001t0016 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3898T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3898 | chr5 | 88718706 | ||||||
| chr5:88719016 | T | C | 1 | a0001c0001t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3588A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3588 | chr5 | 88719016 | ||||||
| chr5:88719021 | T | G | 1 | a0001c0001t0033 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3583A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3583 | chr5 | 88719021 | ||||||
| chr5:88719140 | T | C | 1 | a0001c0001t0034 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3464A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3464 | chr5 | 88719140 | ||||||
| chr5:88719385 | T | C | 1 | a0001c0001t0011 | 3 | NA18982.hp2 NA18992.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3219A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3219 | chr5 | 88719385 | ||||||
| chr5:88719477 | C | T | 1 | a0001c0001t0014 | 2 | HG02922.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3127G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3127 | chr5 | 88719477 | ||||||
| chr5:88719490 | C | T | 1 | a0001c0001t0032 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3114G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3114 | chr5 | 88719490 | ||||||
| chr5:88719491 | G | A | 1 | a0001c0001t0023 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3113C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3113 | chr5 | 88719491 | ||||||
| chr5:88719726 | C | T | 1 | a0001c0001t0021 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2878G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2878 | chr5 | 88719726 | ||||||
| chr5:88719728 | A | C | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(17): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2876T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2876 | chr5 | 88719728 | ||||||
| chr5:88719966 | T | C | 1 | a0001c0001t0027 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2638A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2638 | chr5 | 88719966 | ||||||
| chr5:88720059 | A | G | 1 | a0001c0001t0031 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2545T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2545 | chr5 | 88720059 | ||||||
| chr5:88720191 | A | G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(26): Show |
205 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*2413T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2413 | chr5 | 88720191 | ||||||
| chr5:88720214 | G | A | 1 | a0001c0001t0013 | 3 | HG00597.hp2 HG00673.hp2 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2390C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2390 | chr5 | 88720214 | ||||||
| chr5:88720237 | T | A | 1 | a0001c0001t0035 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2367 | chr5 | 88720237 | ||||||
| chr5:88720336 | A | AT | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(21): Show |
194 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2267dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2267 | chr5 | 88720336 | ||||||
| chr5:88720336 | A | ATT | 4 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0029 others(1): Show |
7 | HG01515.hp1 HG01517.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2266_*2267dupAA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2267 | chr5 | 88720336 | ||||||
| chr5:88720546 | A | T | 1 | a0001c0001t0028 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2058T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2058 | chr5 | 88720546 | ||||||
| chr5:88720708 | T | C | 1 | a0001c0001t0037 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1896A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 1896 | chr5 | 88720708 | ||||||
| chr5:88720787 | AT | A | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(17): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1816delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 1816 | chr5 | 88720787 | ||||||
| chr5:88721798 | T | C | 1 | a0001c0001t0008 | 5 | HG01433.hp1 HG01975.hp2 HG02155.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*806A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 806 | chr5 | 88721798 | ||||||
| chr5:88722571 | GA | G | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0014 others(3): Show |
45 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*32delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 32 | chr5 | 88722571 | ||||||
| chr5:88722575 | A | G | 1 | a0001c0001t0018 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 29 | chr5 | 88722575 | ||||||
| chr5:88883019 | G | A | 1 | a0001c0001t0038 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-207C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/11 | 59231 | chr5 | 88883019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:88723063 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1101-138G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723063 | |||||||
| chr5:88723179 | G | A | 2 | a0001c0001t0029g0023 a0001c0001t0030g0113 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1101-254C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723179 | |||||||
| chr5:88723576 | C | T | 2 | a0001c0001t0014g0286 a0001c0001t0014g0291 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1101-651G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723576 | |||||||
| chr5:88723657 | G | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1101-732C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723657 | |||||||
| chr5:88723720 | G | A | 1 | a0001c0001t0012g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1101-795C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723720 | |||||||
| chr5:88723746 | T | C | 1 | a0001c0001t0023g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1101-821A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723746 | |||||||
| chr5:88723812 | T | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1101-887A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723812 | |||||||
| chr5:88723930 | G | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1101-1005C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723930 | |||||||
| chr5:88724059 | A | G | 1 | a0001c0001t0024g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1101-1134T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724059 | |||||||
| chr5:88724205 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1101-1280C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724205 | |||||||
| chr5:88724364 | C | T | 3 | a0001c0001t0004g0112 a0001c0001t0029g0023 a0001c0001t0030g0113 |
3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1101-1439G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724364 | |||||||
| chr5:88724502 | C | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1101-1577G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724502 | |||||||
| chr5:88724528 | T | C | 1 | a0001c0001t0003g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1101-1603A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724528 | |||||||
| chr5:88724574 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1101-1649A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724574 | |||||||
| chr5:88725017 | A | G | 9 | a0001c0001t0001g0069 a0001c0001t0002g0030 a0001c0001t0002g0041 others(6): Show |
9 | HG01515.hp1 HG01517.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1101-2092T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725017 | |||||||
| chr5:88725193 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0192 |
2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1101-2268A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725193 | |||||||
| chr5:88725494 | G | A | 1 | a0001c0001t0004g0118 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1101-2569C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725494 | |||||||
| chr5:88725512 | C | T | 1 | a0001c0001t0013g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1101-2587G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725512 | |||||||
| chr5:88725535 | T | C | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1101-2610A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725535 | |||||||
| chr5:88725574 | G | A | 22 | a0001c0001t0004g0004 a0001c0001t0004g0015 a0001c0001t0004g0088 others(19): Show |
23 | HG01192.hp2 HG01496.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1101-2649C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725574 | |||||||
| chr5:88725710 | T | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1100+2783A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725710 | |||||||
| chr5:88725905 | G | A | 5 | a0001c0001t0004g0015 a0001c0001t0004g0115 a0001c0001t0004g0116 others(2): Show |
5 | HG01192.hp2 HG01981.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100+2588C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725905 | |||||||
| chr5:88725982 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0276 |
2 | NA18959.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1100+2511A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725982 | |||||||
| chr5:88726001 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0168 |
2 | HG01070.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1100+2492A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726001 | |||||||
| chr5:88726515 | G | A | 3 | a0001c0001t0004g0112 a0001c0001t0029g0023 a0001c0001t0030g0113 |
3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1100+1978C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726515 | |||||||
| chr5:88726562 | G | A | 3 | a0001c0001t0002g0030 a0001c0001t0002g0041 a0001c0001t0002g0054 |
3 | HG03834.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1100+1931C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726562 | |||||||
| chr5:88726733 | CTGTCCCT others(4): Show |
C | 3 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0055 |
3 | NA18955.hp1 NA18966.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1100+1749_1100+175 others(15): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726733 | |||||||
| chr5:88727323 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1100+1170A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727323 | |||||||
| chr5:88727339 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1100+1154T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727339 | |||||||
| chr5:88727349 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1100+1144C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727349 | |||||||
| chr5:88727532 | A | T | 106 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(103): Show |
107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1100+961T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727532 | |||||||
| chr5:88727758 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1100+735C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727758 | |||||||
| chr5:88727805 | GA | G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1100+687delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727805 | |||||||
| chr5:88728382 | A | G | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG01243.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1100+111T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88728382 | |||||||
| chr5:88729055 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964+163C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 9/10 | chr5 | 88729055 | |||||||
| chr5:88729195 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0159 |
2 | NA19001.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.964+23A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 9/10 | chr5 | 88729195 | |||||||
| chr5:88729373 | A | C | 1 | a0001c0001t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.835-26T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88729373 | |||||||
| chr5:88729940 | A | G | 1 | a0001c0001t0037g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.834+271T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88729940 | |||||||
| chr5:88730005 | T | G | 1 | a0001c0001t0002g0074 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.834+206A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88730005 | |||||||
| chr5:88730028 | CA | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.834+182delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88730028 | |||||||
| chr5:88730196 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.834+15C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88730196 | |||||||
| chr5:88730328 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.811-94A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730328 | |||||||
| chr5:88730362 | A | G | 1 | a0001c0001t0033g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.811-128T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730362 | |||||||
| chr5:88730524 | A | G | 5 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(2): Show |
6 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.811-290T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730524 | |||||||
| chr5:88730645 | G | C | 1 | a0001c0001t0021g0208 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.811-411C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730645 | |||||||
| chr5:88730850 | A | G | 1 | a0001c0001t0004g0004 | 2 | HG01496.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.811-616T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730850 | |||||||
| chr5:88730995 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.810+734G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730995 | |||||||
| chr5:88731051 | A | C | 6 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0086 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.810+678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731051 | |||||||
| chr5:88731053 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.810+676G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731053 | |||||||
| chr5:88731085 | C | T | 131 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.810+644G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731085 | |||||||
| chr5:88731232 | G | A | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.810+497C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731232 | |||||||
| chr5:88731243 | A | C | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.810+486T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731243 | |||||||
| chr5:88731332 | G | A | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.810+397C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731332 | |||||||
| chr5:88731400 | T | C | 68 | a0001c0001t0001g0069 a0001c0001t0002g0002 a0001c0001t0002g0012 others(65): Show |
69 | HG00597.hp1 HG01433.hp1 HG01515.hp1 others(66): Show |
intron_variant | MODIFIER | c.810+329A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731400 | |||||||
| chr5:88731461 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+268C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731461 | |||||||
| chr5:88731525 | T | C | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.810+204A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731525 | |||||||
| chr5:88731530 | A | AT | 25 | a0001c0001t0001g0079 a0001c0001t0002g0024 a0001c0001t0002g0033 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.810+198dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731530 | |||||||
| chr5:88731530 | A | T | 19 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(16): Show |
20 | HG01496.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.810+199T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731530 | |||||||
| chr5:88731970 | A | G | 1 | a0001c0001t0010g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.638-69T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88731970 | |||||||
| chr5:88732476 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0002g0007 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.638-575T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732476 | |||||||
| chr5:88732477 | G | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.638-576C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732477 | |||||||
| chr5:88732637 | T | A | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-736A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732637 | |||||||
| chr5:88732667 | A | T | 1 | a0001c0001t0021g0208 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.638-766T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732667 | |||||||
| chr5:88732820 | G | C | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.638-919C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732820 | |||||||
| chr5:88732994 | G | T | 1 | a0001c0001t0001g0276 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.638-1093C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732994 | |||||||
| chr5:88733023 | C | T | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-1122G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733023 | |||||||
| chr5:88733167 | G | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 others(1): Show |
4 | NA18951.hp2 NA18969.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1266C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733167 | |||||||
| chr5:88733257 | T | C | 5 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 others(2): Show |
5 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-1356A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733257 | |||||||
| chr5:88733391 | T | C | 2 | a0001c0001t0002g0038 a0001c0001t0002g0176 |
2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.638-1490A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733391 | |||||||
| chr5:88733700 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.638-1799T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733700 | |||||||
| chr5:88733810 | C | T | 209 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(206): Show |
211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.638-1909G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733810 | |||||||
| chr5:88733890 | A | G | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-1989T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733890 | |||||||
| chr5:88733936 | C | T | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-2035G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733936 | |||||||
| chr5:88734013 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.638-2112G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734013 | |||||||
| chr5:88734037 | C | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.638-2136G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734037 | |||||||
| chr5:88734208 | A | G | 2 | a0001c0001t0005g0018 a0001c0001t0005g0019 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.638-2307T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734208 | |||||||
| chr5:88734475 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.638-2574C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734475 | |||||||
| chr5:88734479 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-2578G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734479 | |||||||
| chr5:88734561 | G | GT | 3 | a0001c0001t0004g0283 a0001c0001t0004g0284 a0001c0001t0015g0093 |
3 | HG02895.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.638-2661dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734561 | |||||||
| chr5:88734561 | G | T | 1 | a0001c0001t0004g0146 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.638-2660C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734561 | |||||||
| chr5:88734561 | GTTTGTTT others(10): Show |
G | 3 | a0001c0001t0002g0077 a0001c0001t0016g0078 a0001c0001t0016g0083 |
3 | HG01169.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.638-2677_638-2661d others(19): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734561 | |||||||
| chr5:88734565 | G | GT | 26 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0003g0048 others(23): Show |
27 | HG00642.hp1 HG01192.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.638-2665dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0002g0046 a0001c0001t0004g0084 a0001c0001t0030g0113 |
3 | HG00733.hp1 HG02735.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.638-2674_638-2665d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | G | GTTTTTTT others(4): Show |
4 | a0001c0001t0002g0053 a0001c0001t0002g0105 a0001c0001t0002g0136 others(1): Show |
4 | HG01496.hp2 NA18982.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-2675_638-2665d others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | G | GTTTTTTT others(5): Show |
3 | a0001c0001t0002g0047 a0001c0001t0011g0050 a0001c0001t0011g0051 |
3 | HG03490.hp1 NA18992.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.638-2676_638-2665d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0166 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.638-2677_638-2665d others(15): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | G | T | 9 | a0001c0001t0004g0102 a0001c0001t0004g0138 a0001c0001t0004g0146 others(6): Show |
9 | HG00280.hp1 HG00323.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-2664C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | GTTTTT | G | 16 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0082 others(13): Show |
16 | HG00673.hp2 HG01361.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-2669_638-2665d others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | GTTTTTT | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0026 others(82): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.638-2670_638-2665d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734565 | GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0003g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.638-2684_638-2665d others(22): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | |||||||
| chr5:88734567 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.638-2667_638-2666i others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734567 | |||||||
| chr5:88734568 | T | G | 1 | a0001c0001t0003g0236 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.638-2667A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734568 | |||||||
| chr5:88734574 | T | TTG | 11 | a0001c0001t0002g0066 a0001c0001t0002g0184 a0001c0001t0002g0185 others(8): Show |
11 | HG00597.hp1 HG02145.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.638-2674_638-2673i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734574 | |||||||
| chr5:88734575 | T | G | 1 | a0001c0001t0003g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.638-2674A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734575 | |||||||
| chr5:88734575 | T | TG | 53 | a0001c0001t0001g0069 a0001c0001t0002g0002 a0001c0001t0002g0012 others(50): Show |
54 | HG01433.hp1 HG02015.hp2 HG02027.hp1 others(51): Show |
intron_variant | MODIFIER | c.638-2675_638-2674i others(3): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734575 | |||||||
| chr5:88734576 | T | G | 4 | a0001c0001t0008g0035 a0001c0001t0010g0032 a0001c0001t0010g0060 others(1): Show |
4 | HG01515.hp1 HG01517.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-2675A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734576 | |||||||
| chr5:88734579 | T | G | 1 | a0001c0001t0003g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.638-2678A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734579 | |||||||
| chr5:88734580 | T | G | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0294 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-2679A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734580 | |||||||
| chr5:88734581 | T | G | 1 | a0001c0001t0003g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.638-2680A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734581 | |||||||
| chr5:88734582 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.638-2681A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734582 | |||||||
| chr5:88734585 | T | G | 4 | a0001c0001t0002g0030 a0001c0001t0002g0041 a0001c0001t0002g0054 others(1): Show |
4 | HG00673.hp1 HG03834.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-2684A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734585 | |||||||
| chr5:88734587 | T | G | 2 | a0001c0001t0005g0086 a0001c0001t0005g0087 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.638-2686A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734587 | |||||||
| chr5:88734588 | T | G | 1 | a0001c0001t0001g0043 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.638-2687A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734588 | |||||||
| chr5:88734853 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.638-2952G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734853 | |||||||
| chr5:88735119 | A | G | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.638-3218T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735119 | |||||||
| chr5:88735182 | G | A | 1 | a0001c0001t0002g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-3281C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735182 | |||||||
| chr5:88735294 | G | A | 1 | a0001c0001t0036g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.638-3393C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735294 | |||||||
| chr5:88735324 | T | C | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.638-3423A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735324 | |||||||
| chr5:88735498 | T | C | 1 | a0001c0001t0021g0208 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.638-3597A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735498 | |||||||
| chr5:88735734 | C | G | 1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.638-3833G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735734 | |||||||
| chr5:88735856 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-3955A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735856 | |||||||
| chr5:88735857 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-3956G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735857 | |||||||
| chr5:88735921 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.638-4020G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735921 | |||||||
| chr5:88735960 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.638-4059T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735960 | |||||||
| chr5:88735965 | A | C | 3 | a0001c0001t0004g0112 a0001c0001t0029g0023 a0001c0001t0030g0113 |
3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.638-4064T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735965 | |||||||
| chr5:88736003 | T | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-4102A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736003 | |||||||
| chr5:88736195 | TAAATATT others(323): Show |
T | 208 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(205): Show |
210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.638-4624_638-4295d others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736195 | |||||||
| chr5:88736356 | C | T | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-4455G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736356 | |||||||
| chr5:88736360 | G | T | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-4459C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736360 | |||||||
| chr5:88736363 | G | A | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-4462C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736363 | |||||||
| chr5:88736500 | C | CA | 14 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0049 others(11): Show |
14 | HG01361.hp1 HG01891.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.638-4600dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736500 | |||||||
| chr5:88736621 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.638-4720G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736621 | |||||||
| chr5:88736705 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-4804G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736705 | |||||||
| chr5:88736834 | G | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-4933C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736834 | |||||||
| chr5:88736903 | T | C | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.638-5002A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736903 | |||||||
| chr5:88737059 | A | T | 2 | a0001c0001t0011g0050 a0001c0001t0011g0051 |
2 | NA18992.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.638-5158T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737059 | |||||||
| chr5:88737284 | T | C | 68 | a0001c0001t0001g0069 a0001c0001t0002g0002 a0001c0001t0002g0012 others(65): Show |
69 | HG00597.hp1 HG01433.hp1 HG01515.hp1 others(66): Show |
intron_variant | MODIFIER | c.638-5383A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737284 | |||||||
| chr5:88737304 | G | A | 1 | a0001c0001t0010g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.638-5403C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737304 | |||||||
| chr5:88737512 | C | A | 3 | a0001c0001t0004g0112 a0001c0001t0029g0023 a0001c0001t0030g0113 |
3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.638-5611G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737512 | |||||||
| chr5:88737677 | A | G | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.638-5776T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737677 | |||||||
| chr5:88737773 | G | A | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-5872C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737773 | |||||||
| chr5:88737805 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-5904G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737805 | |||||||
| chr5:88738013 | G | C | 1 | a0001c0001t0015g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638-6112C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738013 | |||||||
| chr5:88738052 | G | C | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-6151C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738052 | |||||||
| chr5:88738333 | G | A | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.638-6432C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738333 | |||||||
| chr5:88738376 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.638-6475A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738376 | |||||||
| chr5:88738447 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.638-6546T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738447 | |||||||
| chr5:88738646 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.638-6745A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738646 | |||||||
| chr5:88738815 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.638-6914G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738815 | |||||||
| chr5:88739000 | G | C | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.638-7099C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739000 | |||||||
| chr5:88739050 | T | C | 208 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(205): Show |
210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.638-7149A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739050 | |||||||
| chr5:88739251 | A | C | 210 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(207): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.638-7350T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739251 | |||||||
| chr5:88739611 | T | A | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-7710A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739611 | |||||||
| chr5:88739715 | A | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0003g0014 others(3): Show |
6 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-7814T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739715 | |||||||
| chr5:88740024 | G | A | 2 | a0001c0001t0014g0286 a0001c0001t0014g0291 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.638-8123C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740024 | |||||||
| chr5:88740070 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-8169G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740070 | |||||||
| chr5:88740199 | C | T | 1 | a0001c0001t0037g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.638-8298G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740199 | |||||||
| chr5:88740233 | C | CGT | 86 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.638-8334_638-8333d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | C | CGTGT | 23 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0108 others(20): Show |
23 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.638-8336_638-8333d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | C | CGTGTGT | 46 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0002g0002 others(43): Show |
47 | HG00597.hp1 HG01081.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.638-8338_638-8333d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | C | CGTGTGTG others(1): Show |
14 | a0001c0001t0001g0094 a0001c0001t0001g0129 a0001c0001t0002g0012 others(11): Show |
14 | HG01884.hp1 HG02015.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.638-8340_638-8333d others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | C | CGTGTGTG others(3): Show |
8 | a0001c0001t0001g0130 a0001c0001t0001g0159 a0001c0001t0002g0057 others(5): Show |
8 | HG02145.hp2 HG02965.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-8342_638-8333d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.638-8344_638-8333d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | CGT | C | 85 | a0001c0001t0001g0261 a0001c0001t0002g0024 a0001c0001t0002g0049 others(82): Show |
87 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.638-8334_638-8333d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | CGTGT | C | 4 | a0001c0001t0001g0011 a0001c0001t0003g0235 a0001c0001t0004g0015 others(1): Show |
4 | HG01981.hp2 HG02135.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-8336_638-8333d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740233 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0276 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.638-8346_638-8333d others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | |||||||
| chr5:88740407 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.638-8506A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740407 | |||||||
| chr5:88740516 | G | A | 4 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0296 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+8554C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740516 | |||||||
| chr5:88740669 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+8401G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740669 | |||||||
| chr5:88740691 | A | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0114 others(4): Show |
7 | HG00639.hp2 HG01099.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+8379T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740691 | |||||||
| chr5:88740763 | T | C | 2 | a0001c0001t0009g0179 a0001c0001t0009g0180 |
2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.637+8307A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740763 | |||||||
| chr5:88740964 | A | G | 1 | a0001c0001t0025g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637+8106T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740964 | |||||||
| chr5:88741060 | C | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+8010G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741060 | |||||||
| chr5:88741107 | C | T | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.637+7963G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741107 | |||||||
| chr5:88741160 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.637+7910C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741160 | |||||||
| chr5:88741206 | G | A | 1 | a0001c0001t0008g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.637+7864C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741206 | |||||||
| chr5:88741339 | T | A | 2 | a0001c0001t0005g0086 a0001c0001t0005g0087 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.637+7731A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741339 | |||||||
| chr5:88741392 | T | A | 12 | a0001c0001t0003g0117 a0001c0001t0003g0172 a0001c0001t0003g0234 others(9): Show |
12 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+7678A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741392 | |||||||
| chr5:88741481 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.637+7589G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741481 | |||||||
| chr5:88741997 | T | G | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+7073A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741997 | |||||||
| chr5:88742160 | G | C | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+6910C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742160 | |||||||
| chr5:88742558 | T | A | 4 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0296 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+6512A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742558 | |||||||
| chr5:88742573 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+6497T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742573 | |||||||
| chr5:88742903 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.637+6167A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742903 | |||||||
| chr5:88742949 | A | C | 1 | a0001c0001t0026g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.637+6121T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742949 | |||||||
| chr5:88743028 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.637+6042G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743028 | |||||||
| chr5:88743141 | A | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+5929T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743141 | |||||||
| chr5:88743308 | C | G | 1 | a0001c0001t0002g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+5762G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743308 | |||||||
| chr5:88743421 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0136 |
2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.637+5649T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743421 | |||||||
| chr5:88743578 | C | G | 1 | a0001c0001t0002g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.637+5492G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743578 | |||||||
| chr5:88743689 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.637+5381C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743689 | |||||||
| chr5:88743843 | T | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+5227A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743843 | |||||||
| chr5:88743898 | C | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+5172G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743898 | |||||||
| chr5:88744197 | A | T | 1 | a0001c0001t0004g0107 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.637+4873T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744197 | |||||||
| chr5:88744204 | C | CA | 208 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(205): Show |
210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.637+4865dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744204 | |||||||
| chr5:88744329 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.637+4741C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744329 | |||||||
| chr5:88744369 | C | T | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.637+4701G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744369 | |||||||
| chr5:88744463 | G | C | 5 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0296 others(2): Show |
5 | HG00639.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+4607C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744463 | |||||||
| chr5:88744499 | C | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+4571G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744499 | |||||||
| chr5:88744654 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.637+4416G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744654 | |||||||
| chr5:88744659 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.637+4411T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744659 | |||||||
| chr5:88744664 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0144 |
2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.637+4406T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744664 | |||||||
| chr5:88744901 | T | A | 1 | a0001c0001t0036g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.637+4169A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744901 | |||||||
| chr5:88745042 | T | C | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+4028A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745042 | |||||||
| chr5:88745064 | T | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.637+4006A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745064 | |||||||
| chr5:88745165 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637+3905C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745165 | |||||||
| chr5:88745650 | G | GA | 207 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(204): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.637+3419dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745650 | |||||||
| chr5:88745705 | C | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+3365G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745705 | |||||||
| chr5:88745964 | G | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+3106C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745964 | |||||||
| chr5:88746037 | T | A | 24 | a0001c0001t0001g0079 a0001c0001t0002g0024 a0001c0001t0002g0033 others(21): Show |
24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+3033A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746037 | |||||||
| chr5:88746037 | T | C | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+3033A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746037 | |||||||
| chr5:88746115 | C | G | 210 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(207): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.637+2955G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746115 | |||||||
| chr5:88746202 | G | A | 24 | a0001c0001t0001g0079 a0001c0001t0002g0024 a0001c0001t0002g0033 others(21): Show |
24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+2868C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746202 | |||||||
| chr5:88746216 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+2854T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746216 | |||||||
| chr5:88746326 | T | C | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+2744A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746326 | |||||||
| chr5:88746441 | C | CT | 24 | a0001c0001t0001g0079 a0001c0001t0002g0024 a0001c0001t0002g0033 others(21): Show |
24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+2628dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746441 | |||||||
| chr5:88746455 | TTA | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+2613_637+2614d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746455 | |||||||
| chr5:88746479 | T | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.637+2591A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746479 | |||||||
| chr5:88746729 | G | A | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+2341C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746729 | |||||||
| chr5:88746952 | A | G | 4 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0296 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+2118T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746952 | |||||||
| chr5:88747210 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.637+1860T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747210 | |||||||
| chr5:88747321 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0003g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.637+1737_637+1748d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747321 | |||||||
| chr5:88747321 | TTTTTTTT others(321): Show |
T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.637+1421_637+1748d others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747321 | |||||||
| chr5:88747322 | TTTTTTTA others(320): Show |
T | 44 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0002g0024 others(41): Show |
44 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.637+1421_637+1747d others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747322 | |||||||
| chr5:88747333 | C | CT | 47 | a0001c0001t0001g0276 a0001c0001t0002g0049 a0001c0001t0002g0190 others(44): Show |
48 | HG00099.hp2 HG00642.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.637+1736dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747333 | C | CTT | 41 | a0001c0001t0001g0069 a0001c0001t0001g0261 a0001c0001t0002g0042 others(38): Show |
41 | HG01081.hp1 HG01243.hp2 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.637+1735_637+1736d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747333 | C | CTTT | 20 | a0001c0001t0002g0012 a0001c0001t0002g0025 a0001c0001t0002g0074 others(17): Show |
20 | HG01433.hp1 HG02027.hp1 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.637+1734_637+1736d others(5): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747333 | C | CTTTT | 9 | a0001c0001t0002g0027 a0001c0001t0002g0030 a0001c0001t0002g0041 others(6): Show |
9 | HG02145.hp2 HG02818.hp2 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+1733_637+1736d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747333 | C | CTTTTT | 8 | a0001c0001t0002g0002 a0001c0001t0002g0195 a0001c0001t0002g0209 others(5): Show |
8 | HG02129.hp2 NA18951.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+1732_637+1736d others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747333 | C | CTTTTTT | 9 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0188 others(6): Show |
9 | HG00597.hp1 HG03139.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+1731_637+1736d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747333 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0024g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+1727_637+1736d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747333 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.637+1725_637+1736d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | |||||||
| chr5:88747530 | T | C | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.637+1540A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747530 | |||||||
| chr5:88747539 | C | A | 1 | a0001c0001t0003g0236 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637+1531G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747539 | |||||||
| chr5:88747591 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.637+1479G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747591 | |||||||
| chr5:88747616 | T | C | 1 | a0001c0001t0017g0253 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.637+1454A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747616 | |||||||
| chr5:88747755 | C | T | 24 | a0001c0001t0001g0079 a0001c0001t0002g0024 a0001c0001t0002g0033 others(21): Show |
24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+1315G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747755 | |||||||
| chr5:88747839 | G | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.637+1231C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747839 | |||||||
| chr5:88748026 | T | C | 2 | a0001c0001t0014g0286 a0001c0001t0014g0291 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.637+1044A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748026 | |||||||
| chr5:88748073 | T | C | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+997A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748073 | |||||||
| chr5:88748349 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.637+721G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748349 | |||||||
| chr5:88748379 | T | G | 6 | a0001c0001t0001g0065 a0001c0001t0001g0137 a0001c0001t0001g0140 others(3): Show |
6 | HG01070.hp1 HG01255.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+691A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748379 | |||||||
| chr5:88748435 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.637+635C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748435 | |||||||
| chr5:88748641 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.637+429G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748641 | |||||||
| chr5:88748988 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.637+82A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748988 | |||||||
| chr5:88749212 | C | A | 15 | a0001c0001t0002g0024 a0001c0001t0002g0033 a0001c0001t0002g0038 others(12): Show |
15 | HG01069.hp1 HG01123.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.590-95G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749212 | |||||||
| chr5:88749428 | A | T | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.590-311T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749428 | |||||||
| chr5:88749758 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.590-641G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749758 | |||||||
| chr5:88749786 | T | G | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.590-669A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749786 | |||||||
| chr5:88749842 | A | C | 1 | a0001c0001t0004g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.590-725T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749842 | |||||||
| chr5:88749844 | C | G | 1 | a0001c0001t0004g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.590-727G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749844 | |||||||
| chr5:88749872 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.590-755A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749872 | |||||||
| chr5:88750016 | C | T | 3 | a0001c0001t0002g0185 a0001c0001t0008g0186 a0001c0001t0015g0093 |
3 | HG00597.hp1 NA18522.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.590-899G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750016 | |||||||
| chr5:88750119 | C | CGAGGCAA others(8): Show |
1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1003_590-1002i others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750119 | |||||||
| chr5:88750124 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1007T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750124 | |||||||
| chr5:88750125 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1008C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750125 | |||||||
| chr5:88750135 | G | C | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1018C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750135 | |||||||
| chr5:88750179 | T | G | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1062A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750179 | |||||||
| chr5:88750180 | G | T | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1063C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750180 | |||||||
| chr5:88750190 | A | T | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1073T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750190 | |||||||
| chr5:88750197 | T | A | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1080A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750197 | |||||||
| chr5:88750207 | A | AT | 25 | a0001c0001t0001g0079 a0001c0001t0002g0024 a0001c0001t0002g0030 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.590-1091dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750207 | |||||||
| chr5:88750207 | A | T | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1090T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750207 | |||||||
| chr5:88750208 | T | A | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1091A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750208 | |||||||
| chr5:88750209 | T | A | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1092A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750209 | |||||||
| chr5:88750234 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1117A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750234 | |||||||
| chr5:88750247 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-1130T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750247 | |||||||
| chr5:88750258 | T | G | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1141A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750258 | |||||||
| chr5:88750267 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1150A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750267 | |||||||
| chr5:88750290 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1173T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750290 | |||||||
| chr5:88750328 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00544.hp1 NA18747.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.590-1211G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750328 | |||||||
| chr5:88750337 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0003g0014 |
2 | HG02040.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.590-1220C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750337 | |||||||
| chr5:88750341 | C | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.590-1224G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750341 | |||||||
| chr5:88750374 | A | T | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.590-1257T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750374 | |||||||
| chr5:88750543 | A | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0167 a0001c0001t0001g0182 |
3 | NA18963.hp1 NA18971.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.589+1314T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750543 | |||||||
| chr5:88750773 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.589+1084G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750773 | |||||||
| chr5:88750824 | T | C | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.589+1033A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750824 | |||||||
| chr5:88751318 | A | G | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.589+539T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751318 | |||||||
| chr5:88751423 | A | C | 3 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0036g0017 |
3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.589+434T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751423 | |||||||
| chr5:88751426 | T | C | 1 | a0001c0001t0004g0015 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.589+431A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751426 | |||||||
| chr5:88751675 | G | A | 1 | a0001c0001t0004g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.589+182C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751675 | |||||||
| chr5:88752182 | T | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.403-139A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752182 | |||||||
| chr5:88752254 | T | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-211A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752254 | |||||||
| chr5:88752394 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.403-351C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752394 | |||||||
| chr5:88752640 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-597G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752640 | |||||||
| chr5:88752898 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.403-855G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752898 | |||||||
| chr5:88752941 | G | A | 1 | a0001c0001t0003g0277 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.403-898C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752941 | |||||||
| chr5:88752950 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-907T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752950 | |||||||
| chr5:88753190 | G | A | 4 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0296 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-1147C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753190 | |||||||
| chr5:88753524 | C | T | 208 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(205): Show |
210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.403-1481G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753524 | |||||||
| chr5:88753572 | G | C | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.403-1529C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753572 | |||||||
| chr5:88753721 | A | C | 1 | a0001c0001t0002g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.403-1678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753721 | |||||||
| chr5:88753781 | G | A | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403-1738C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753781 | |||||||
| chr5:88753784 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.403-1741C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753784 | |||||||
| chr5:88753912 | C | T | 1 | a0001c0001t0006g0154 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.403-1869G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753912 | |||||||
| chr5:88754207 | C | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403-2164G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754207 | |||||||
| chr5:88754251 | T | C | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.403-2208A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754251 | |||||||
| chr5:88754284 | C | T | 1 | a0001c0001t0004g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.403-2241G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754284 | |||||||
| chr5:88754366 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-2323A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754366 | |||||||
| chr5:88754570 | C | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | NA18949.hp2 NA19070.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.403-2527G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754570 | |||||||
| chr5:88754676 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.403-2633G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754676 | |||||||
| chr5:88754687 | A | G | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG02135.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.403-2644T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754687 | |||||||
| chr5:88755107 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.403-3064T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755107 | |||||||
| chr5:88755267 | GTATAGTT others(4): Show |
G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0202 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.403-3235_403-3225d others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755267 | |||||||
| chr5:88755322 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.403-3279A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755322 | |||||||
| chr5:88755502 | G | C | 1 | a0001c0001t0010g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.403-3459C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755502 | |||||||
| chr5:88755666 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0176 |
2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.403-3623G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755666 | |||||||
| chr5:88756028 | G | A | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.403-3985C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756028 | |||||||
| chr5:88756188 | G | T | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.403-4145C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756188 | |||||||
| chr5:88756406 | G | A | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403-4363C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756406 | |||||||
| chr5:88756639 | T | C | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.402+4546A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756639 | |||||||
| chr5:88756788 | AT | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(103): Show |
107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.402+4396delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756788 | |||||||
| chr5:88756870 | A | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.402+4315T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756870 | |||||||
| chr5:88756984 | G | A | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.402+4201C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756984 | |||||||
| chr5:88757013 | T | G | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.402+4172A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757013 | |||||||
| chr5:88757477 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.402+3708G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757477 | |||||||
| chr5:88757577 | C | T | 1 | a0001c0001t0003g0272 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.402+3608G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757577 | |||||||
| chr5:88757682 | G | A | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.402+3503C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757682 | |||||||
| chr5:88757951 | T | C | 2 | a0001c0001t0005g0086 a0001c0001t0005g0087 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.402+3234A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757951 | |||||||
| chr5:88758135 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.402+3050G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758135 | |||||||
| chr5:88758475 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+2710T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758475 | |||||||
| chr5:88758748 | G | A | 6 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0086 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+2437C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758748 | |||||||
| chr5:88758946 | C | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+2239G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758946 | |||||||
| chr5:88759092 | C | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.402+2093G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759092 | |||||||
| chr5:88759207 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.402+1978C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759207 | |||||||
| chr5:88759240 | T | C | 1 | a0001c0001t0002g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.402+1945A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759240 | |||||||
| chr5:88759318 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1867T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759318 | |||||||
| chr5:88759406 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1779G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759406 | |||||||
| chr5:88759478 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.402+1707C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759478 | |||||||
| chr5:88759496 | G | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1689C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759496 | |||||||
| chr5:88759652 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0136 |
2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.402+1533T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759652 | |||||||
| chr5:88759664 | T | C | 203 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.402+1521A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759664 | |||||||
| chr5:88759673 | T | TAGTC | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1511_402+1512i others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759673 | |||||||
| chr5:88759700 | T | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1485A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759700 | |||||||
| chr5:88759878 | G | A | 1 | a0001c0001t0011g0050 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.402+1307C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759878 | |||||||
| chr5:88759944 | A | G | 133 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(130): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.402+1241T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759944 | |||||||
| chr5:88760158 | C | A | 210 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(207): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.402+1027G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760158 | |||||||
| chr5:88760186 | A | G | 1 | a0001c0001t0003g0259 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.402+999T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760186 | |||||||
| chr5:88760630 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.402+555A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760630 | |||||||
| chr5:88760631 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.402+554A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760631 | |||||||
| chr5:88760731 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.402+454G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760731 | |||||||
| chr5:88761123 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.402+62A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88761123 | |||||||
| chr5:88761169 | T | C | 2 | a0001c0001t0014g0286 a0001c0001t0014g0291 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.402+16A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88761169 | |||||||
| chr5:88761357 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.259-29G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761357 | |||||||
| chr5:88761520 | C | T | 1 | a0001c0001t0011g0029 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.259-192G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761520 | |||||||
| chr5:88761614 | T | C | 1 | a0001c0001t0007g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.259-286A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761614 | |||||||
| chr5:88761973 | GAGA | G | 5 | a0001c0001t0003g0117 a0001c0001t0004g0015 a0001c0001t0004g0115 others(2): Show |
5 | HG01192.hp1 HG01981.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-648_259-646del others(3): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761973 | |||||||
| chr5:88761979 | G | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00544.hp1 NA18747.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.259-651C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761979 | |||||||
| chr5:88762098 | T | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.259-770A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762098 | |||||||
| chr5:88762142 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.259-814T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762142 | |||||||
| chr5:88762163 | T | G | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259-835A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762163 | |||||||
| chr5:88762346 | T | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-1018A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762346 | |||||||
| chr5:88762483 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.259-1155C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762483 | |||||||
| chr5:88762574 | A | C | 5 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(2): Show |
6 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1246T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762574 | |||||||
| chr5:88762583 | A | AT | 107 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.259-1256dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762583 | |||||||
| chr5:88762625 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.259-1297G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762625 | |||||||
| chr5:88762656 | G | C | 1 | a0001c0001t0002g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.259-1328C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762656 | |||||||
| chr5:88762749 | T | C | 1 | a0001c0001t0012g0156 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.259-1421A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762749 | |||||||
| chr5:88763104 | T | C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-1776A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763104 | |||||||
| chr5:88763143 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.259-1815A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763143 | |||||||
| chr5:88763642 | A | C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-2314T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763642 | |||||||
| chr5:88763716 | G | A | 1 | a0001c0001t0007g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.259-2388C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763716 | |||||||
| chr5:88763834 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.259-2506A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763834 | |||||||
| chr5:88764141 | T | C | 1 | a0001c0001t0004g0287 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259-2813A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764141 | |||||||
| chr5:88764356 | G | C | 1 | a0001c0001t0031g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-3028C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764356 | |||||||
| chr5:88764487 | T | C | 4 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0296 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-3159A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764487 | |||||||
| chr5:88764494 | G | T | 203 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.259-3166C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764494 | |||||||
| chr5:88764504 | G | A | 210 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(207): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.259-3176C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764504 | |||||||
| chr5:88764576 | GAGGC | G | 103 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.259-3252_259-3249d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764576 | |||||||
| chr5:88764676 | C | T | 3 | a0001c0001t0004g0112 a0001c0001t0029g0023 a0001c0001t0030g0113 |
3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-3348G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764676 | |||||||
| chr5:88764807 | C | CA | 13 | a0001c0001t0002g0049 a0001c0001t0002g0218 a0001c0001t0002g0220 others(10): Show |
13 | HG02257.hp1 HG02572.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.259-3480dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764807 | |||||||
| chr5:88764807 | CA | C | 15 | a0001c0001t0001g0065 a0001c0001t0001g0137 a0001c0001t0001g0140 others(12): Show |
15 | HG01070.hp1 HG01169.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-3480delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764807 | |||||||
| chr5:88764807 | CAA | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.259-3481_259-3480d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764807 | |||||||
| chr5:88764911 | T | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-3583A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764911 | |||||||
| chr5:88765199 | A | G | 1 | a0001c0001t0003g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.259-3871T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765199 | |||||||
| chr5:88765439 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0176 |
2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.259-4111T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765439 | |||||||
| chr5:88765716 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.259-4388C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765716 | |||||||
| chr5:88765782 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259-4454A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765782 | |||||||
| chr5:88765798 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259-4470C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765798 | |||||||
| chr5:88766256 | G | A | 2 | a0001c0001t0002g0188 a0001c0001t0002g0203 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.259-4928C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88766256 | |||||||
| chr5:88766482 | T | C | 5 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0055 others(2): Show |
5 | HG02132.hp1 NA18955.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-5154A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88766482 | |||||||
| chr5:88767174 | T | C | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.259-5846A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767174 | |||||||
| chr5:88767412 | G | GAA | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-6086_259-6085d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767412 | |||||||
| chr5:88767631 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.259-6303A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767631 | |||||||
| chr5:88767796 | A | G | 1 | a0001c0001t0004g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259-6468T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767796 | |||||||
| chr5:88767840 | C | A | 1 | a0001c0001t0005g0294 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.259-6512G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767840 | |||||||
| chr5:88767955 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.259-6627A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767955 | |||||||
| chr5:88768123 | G | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0002g0024 others(23): Show |
26 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.259-6795C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768123 | |||||||
| chr5:88768138 | T | C | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-6810A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768138 | |||||||
| chr5:88768195 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-6867G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768195 | |||||||
| chr5:88768278 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259-6950A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768278 | |||||||
| chr5:88768396 | T | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-7068A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768396 | |||||||
| chr5:88768460 | G | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-7132C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768460 | |||||||
| chr5:88768645 | T | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-7317A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768645 | |||||||
| chr5:88768784 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.259-7456C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768784 | |||||||
| chr5:88768813 | A | T | 4 | a0001c0001t0001g0069 a0001c0001t0010g0032 a0001c0001t0010g0060 others(1): Show |
4 | HG01515.hp1 HG01517.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-7485T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768813 | |||||||
| chr5:88768827 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.259-7499A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768827 | |||||||
| chr5:88768992 | G | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-7664C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768992 | |||||||
| chr5:88769313 | C | T | 12 | a0001c0001t0003g0172 a0001c0001t0003g0234 a0001c0001t0003g0235 others(9): Show |
12 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.259-7985G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769313 | |||||||
| chr5:88769424 | C | T | 1 | a0001c0001t0018g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.259-8096G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769424 | |||||||
| chr5:88769446 | G | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-8118C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769446 | |||||||
| chr5:88769703 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0003g0014 |
2 | HG02040.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.259-8375C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769703 | |||||||
| chr5:88769811 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-8483T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769811 | |||||||
| chr5:88769820 | G | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-8492C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769820 | |||||||
| chr5:88771068 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.259-9740T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771068 | |||||||
| chr5:88771344 | C | T | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-10016G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771344 | |||||||
| chr5:88771355 | C | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-10027G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771355 | |||||||
| chr5:88771628 | A | G | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-10300T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771628 | |||||||
| chr5:88771682 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.259-10354G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771682 | |||||||
| chr5:88771843 | C | T | 1 | a0001c0001t0003g0257 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.259-10515G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771843 | |||||||
| chr5:88773608 | A | G | 3 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0022 |
3 | HG02896.hp1 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259-12280T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773608 | |||||||
| chr5:88773651 | T | C | 4 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0019g0071 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-12323A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773651 | |||||||
| chr5:88773776 | G | T | 214 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(211): Show |
216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.259-12448C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773776 | |||||||
| chr5:88773801 | T | C | 5 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(2): Show |
6 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-12473A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773801 | |||||||
| chr5:88773986 | G | A | 2 | a0001c0001t0004g0283 a0001c0001t0004g0285 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.259-12658C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773986 | |||||||
| chr5:88774053 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.259-12725T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774053 | |||||||
| chr5:88774173 | T | TTAAC | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-12846_259-1284 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774173 | |||||||
| chr5:88774336 | C | CT | 104 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(101): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.259-13009dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774336 | |||||||
| chr5:88774448 | G | A | 1 | a0001c0001t0004g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.259-13120C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774448 | |||||||
| chr5:88774520 | C | T | 11 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(8): Show |
11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-13192G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774520 | |||||||
| chr5:88774526 | G | A | 11 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(8): Show |
11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-13198C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774526 | |||||||
| chr5:88774531 | C | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0202 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-13203G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774531 | |||||||
| chr5:88774574 | G | A | 1 | a0001c0001t0003g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.259-13246C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774574 | |||||||
| chr5:88774599 | T | C | 122 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(119): Show |
123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.259-13271A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774599 | |||||||
| chr5:88774694 | A | G | 1 | a0001c0001t0003g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.259-13366T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774694 | |||||||
| chr5:88774698 | G | T | 1 | a0001c0001t0011g0051 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.259-13370C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774698 | |||||||
| chr5:88774991 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.259-13663C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774991 | |||||||
| chr5:88775006 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02027.hp2 NA18959.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.259-13678C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775006 | |||||||
| chr5:88775259 | T | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0202 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-13931A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775259 | |||||||
| chr5:88775334 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259-14006T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775334 | |||||||
| chr5:88775733 | G | A | 1 | a0001c0001t0006g0154 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.259-14405C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775733 | |||||||
| chr5:88776116 | G | C | 111 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(108): Show |
112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.259-14788C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776116 | |||||||
| chr5:88776165 | T | C | 1 | a0001c0001t0025g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-14837A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776165 | |||||||
| chr5:88776198 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259-14870T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776198 | |||||||
| chr5:88776238 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-14910G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776238 | |||||||
| chr5:88776289 | G | A | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-14961C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776289 | |||||||
| chr5:88776533 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0101 a0001c0001t0001g0147 others(1): Show |
4 | HG02027.hp2 HG03239.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-15205C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776533 | |||||||
| chr5:88776546 | C | T | 1 | a0001c0001t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.259-15218G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776546 | |||||||
| chr5:88776849 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259-15521C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776849 | |||||||
| chr5:88777008 | T | A | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-15680A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777008 | |||||||
| chr5:88777024 | T | G | 11 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(8): Show |
11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-15696A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777024 | |||||||
| chr5:88777411 | T | A | 16 | a0001c0001t0001g0114 a0001c0001t0002g0024 a0001c0001t0002g0033 others(13): Show |
16 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-16083A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777411 | |||||||
| chr5:88777432 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259-16104C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777432 | |||||||
| chr5:88777802 | G | A | 127 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(124): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.259-16474C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777802 | |||||||
| chr5:88777886 | A | C | 12 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(9): Show |
12 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-16558T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777886 | |||||||
| chr5:88777899 | C | CT | 177 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0034 others(174): Show |
180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.259-16572dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777899 | |||||||
| chr5:88777899 | C | CTT | 11 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0147 others(8): Show |
11 | HG01081.hp1 HG01981.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-16573_259-1657 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777899 | |||||||
| chr5:88778155 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.259-16827C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778155 | |||||||
| chr5:88778363 | A | C | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.259-17035T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778363 | |||||||
| chr5:88778588 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.259-17260G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778588 | |||||||
| chr5:88778712 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(128): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.259-17384C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778712 | |||||||
| chr5:88778968 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0002g0007 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.259-17640G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778968 | |||||||
| chr5:88779006 | G | A | 7 | a0001c0001t0002g0030 a0001c0001t0002g0041 a0001c0001t0002g0054 others(4): Show |
7 | HG00280.hp1 HG00323.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-17678C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779006 | |||||||
| chr5:88779072 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0054 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.259-17744A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779072 | |||||||
| chr5:88779086 | G | T | 2 | a0001c0001t0003g0095 a0001c0001t0007g0020 |
2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.259-17758C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779086 | |||||||
| chr5:88779088 | AGTTT | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | NA18979.hp1 NA19057.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-17764_259-1776 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779088 | |||||||
| chr5:88779093 | A | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | NA18979.hp1 NA19057.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-17765T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779093 | |||||||
| chr5:88779137 | T | G | 2 | a0001c0001t0007g0021 a0001c0001t0007g0022 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-17809A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779137 | |||||||
| chr5:88779195 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.259-17867T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779195 | |||||||
| chr5:88779332 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-18004A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779332 | |||||||
| chr5:88779466 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.259-18138C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779466 | |||||||
| chr5:88779488 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259-18160T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779488 | |||||||
| chr5:88779496 | C | G | 1 | a0001c0001t0002g0058 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.259-18168G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779496 | |||||||
| chr5:88779601 | T | TTG | 156 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0034 others(153): Show |
158 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.259-18275_259-1827 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779601 | |||||||
| chr5:88779601 | T | TTGTG | 7 | a0001c0001t0001g0005 a0001c0001t0002g0057 a0001c0001t0002g0066 others(4): Show |
7 | HG01358.hp1 NA18955.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-18277_259-1827 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779601 | |||||||
| chr5:88779760 | G | GT | 112 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(109): Show |
113 | HG00544.hp1 HG00597.hp1 HG00741.hp1 others(110): Show |
intron_variant | MODIFIER | c.259-18433dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779760 | |||||||
| chr5:88779760 | G | GTT | 118 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(115): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.259-18434_259-1843 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779760 | |||||||
| chr5:88779760 | G | GTTT | 10 | a0001c0001t0001g0108 a0001c0001t0002g0041 a0001c0001t0002g0232 others(7): Show |
10 | HG00280.hp1 HG00323.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-18435_259-1843 others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779760 | |||||||
| chr5:88779864 | A | G | 2 | a0001c0001t0003g0266 a0001c0001t0003g0268 |
2 | NA18941.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.259-18536T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779864 | |||||||
| chr5:88779955 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259-18627C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779955 | |||||||
| chr5:88779993 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.259-18665T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779993 | |||||||
| chr5:88780533 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.259-19205A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780533 | |||||||
| chr5:88780617 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.259-19289G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780617 | |||||||
| chr5:88780634 | ATACT | A | 8 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(5): Show |
9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-19310_259-1930 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780634 | |||||||
| chr5:88780710 | T | C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-19382A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780710 | |||||||
| chr5:88780728 | A | G | 2 | a0001c0001t0007g0021 a0001c0001t0007g0022 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-19400T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780728 | |||||||
| chr5:88780792 | T | G | 3 | a0001c0001t0004g0112 a0001c0001t0030g0113 a0001c0001t0034g0016 |
3 | HG00639.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-19464A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780792 | |||||||
| chr5:88780866 | G | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG01261.hp1 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.259-19538C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780866 | |||||||
| chr5:88781182 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.259-19854A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781182 | |||||||
| chr5:88781306 | A | G | 1 | a0001c0001t0003g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-19978T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781306 | |||||||
| chr5:88781364 | T | C | 1 | a0001c0001t0003g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.259-20036A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781364 | |||||||
| chr5:88781374 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259-20046A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781374 | |||||||
| chr5:88781424 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.259-20096G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781424 | |||||||
| chr5:88781432 | C | T | 4 | a0001c0001t0002g0024 a0001c0001t0011g0029 a0001c0001t0011g0050 others(1): Show |
4 | HG02109.hp2 NA18982.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-20104G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781432 | |||||||
| chr5:88781520 | AC | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG01261.hp1 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.259-20193delG | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781520 | |||||||
| chr5:88781594 | T | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0202 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-20266A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781594 | |||||||
| chr5:88781631 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(128): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.259-20303C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781631 | |||||||
| chr5:88781711 | CCTGTAAT others(7): Show |
C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-20397_259-2038 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781711 | |||||||
| chr5:88781737 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.259-20409G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781737 | |||||||
| chr5:88781801 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259-20473G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781801 | |||||||
| chr5:88782464 | CA | C | 219 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(216): Show |
222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.259-21137delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782464 | |||||||
| chr5:88782472 | A | T | 3 | a0001c0001t0002g0077 a0001c0001t0016g0078 a0001c0001t0016g0083 |
3 | HG01169.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.259-21144T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782472 | |||||||
| chr5:88782508 | G | A | 138 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.259-21180C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782508 | |||||||
| chr5:88782941 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.259-21613A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782941 | |||||||
| chr5:88783067 | T | C | 4 | a0001c0001t0001g0079 a0001c0001t0004g0013 a0001c0001t0004g0075 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+21531A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783067 | |||||||
| chr5:88783123 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.258+21475G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783123 | |||||||
| chr5:88783193 | G | T | 219 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(216): Show |
222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.258+21405C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783193 | |||||||
| chr5:88783269 | T | G | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+21329A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783269 | |||||||
| chr5:88783322 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0004g0013 a0001c0001t0004g0075 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+21276G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783322 | |||||||
| chr5:88783366 | C | T | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+21232G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783366 | |||||||
| chr5:88783394 | C | T | 1 | a0001c0001t0023g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.258+21204G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783394 | |||||||
| chr5:88783553 | C | G | 1 | a0001c0001t0008g0186 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.258+21045G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783553 | |||||||
| chr5:88783554 | C | T | 10 | a0001c0001t0001g0065 a0001c0001t0001g0127 a0001c0001t0001g0137 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.258+21044G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783554 | |||||||
| chr5:88783682 | C | T | 127 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(124): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.258+20916G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783682 | |||||||
| chr5:88783888 | A | G | 3 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0055 |
3 | NA18955.hp1 NA18966.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.258+20710T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783888 | |||||||
| chr5:88784019 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.258+20579T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88784019 | |||||||
| chr5:88784235 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.258+20363T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88784235 | |||||||
| chr5:88784925 | T | C | 1 | a0001c0001t0032g0134 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.258+19673A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88784925 | |||||||
| chr5:88785279 | T | TAC | 19 | a0001c0001t0001g0011 a0001c0001t0002g0002 a0001c0001t0002g0007 others(16): Show |
19 | HG00673.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.258+19317_258+1931 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | T | TACAC | 8 | a0001c0001t0001g0063 a0001c0001t0002g0184 a0001c0001t0005g0018 others(5): Show |
8 | HG01099.hp1 HG01243.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+19315_258+1931 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | T | TACACAC | 6 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0002g0188 others(3): Show |
6 | HG01255.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+19313_258+1931 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0040 a0001c0001t0002g0176 a0001c0001t0003g0080 |
3 | HG01069.hp1 HG02040.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.258+19311_258+1931 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | T | TACACACA others(3): Show |
1 | a0001c0001t0002g0038 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.258+19309_258+1931 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | TAC | T | 50 | a0001c0001t0001g0056 a0001c0001t0001g0261 a0001c0001t0001g0276 others(47): Show |
51 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.258+19317_258+1931 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | TACAC | T | 28 | a0001c0001t0001g0114 a0001c0001t0002g0024 a0001c0001t0002g0033 others(25): Show |
29 | HG00639.hp2 HG01192.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.258+19315_258+1931 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | TACACAC | T | 7 | a0001c0001t0001g0094 a0001c0001t0001g0127 a0001c0001t0001g0135 others(4): Show |
7 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+19313_258+1931 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | TACACACA others(1): Show |
T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(82): Show |
86 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.258+19311_258+1931 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp1 HG00741.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+19309_258+1931 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785279 | TACACACA others(9): Show |
T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0036 |
2 | HG01978.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.258+19303_258+1931 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | |||||||
| chr5:88785617 | G | A | 1 | a0001c0001t0003g0267 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.258+18981C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785617 | |||||||
| chr5:88785679 | G | A | 16 | a0001c0001t0001g0114 a0001c0001t0002g0024 a0001c0001t0002g0033 others(13): Show |
16 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.258+18919C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785679 | |||||||
| chr5:88785762 | AAGTT | A | 127 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(124): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.258+18832_258+1883 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785762 | |||||||
| chr5:88785790 | G | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.258+18808C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785790 | |||||||
| chr5:88785845 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.258+18753T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785845 | |||||||
| chr5:88786084 | G | A | 2 | a0001c0001t0002g0025 a0001c0001t0003g0238 |
2 | HG01934.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.258+18514C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786084 | |||||||
| chr5:88786121 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.258+18477C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786121 | |||||||
| chr5:88786463 | G | GA | 20 | a0001c0001t0002g0077 a0001c0001t0003g0187 a0001c0001t0003g0255 others(17): Show |
20 | HG00741.hp1 HG01169.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.258+18134dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786463 | |||||||
| chr5:88786488 | TAAAC | T | 13 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0209 others(10): Show |
14 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+18106_258+1810 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786488 | |||||||
| chr5:88786673 | GCTACATA others(6): Show |
G | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+17912_258+1792 others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786673 | |||||||
| chr5:88786729 | T | G | 1 | a0001c0001t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+17869A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786729 | |||||||
| chr5:88786732 | A | G | 2 | a0001c0001t0003g0246 a0001c0001t0004g0247 |
2 | HG00642.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.258+17866T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786732 | |||||||
| chr5:88786862 | T | G | 1 | a0001c0001t0032g0134 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.258+17736A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786862 | |||||||
| chr5:88786887 | T | G | 1 | a0001c0001t0011g0051 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.258+17711A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786887 | |||||||
| chr5:88786922 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.258+17676T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786922 | |||||||
| chr5:88786925 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.258+17673A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786925 | |||||||
| chr5:88787077 | G | A | 4 | a0001c0001t0004g0281 a0001c0001t0004g0283 a0001c0001t0004g0284 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+17521C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787077 | |||||||
| chr5:88787116 | TTAA | T | 72 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0039 others(69): Show |
73 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.258+17479_258+1748 others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787116 | |||||||
| chr5:88787230 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0004g0102 |
2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.258+17368T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787230 | |||||||
| chr5:88787371 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.258+17227T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787371 | |||||||
| chr5:88787418 | TA | T | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+17179delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787418 | |||||||
| chr5:88787429 | G | C | 1 | a0001c0001t0031g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.258+17169C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787429 | |||||||
| chr5:88787458 | T | C | 5 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0246 others(2): Show |
5 | HG00642.hp1 HG01192.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+17140A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787458 | |||||||
| chr5:88787470 | A | T | 8 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(5): Show |
9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+17128T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787470 | |||||||
| chr5:88787485 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.258+17113G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787485 | |||||||
| chr5:88787636 | T | C | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+16962A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787636 | |||||||
| chr5:88787741 | A | C | 2 | a0001c0001t0003g0259 a0001c0001t0003g0288 |
2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.258+16857T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787741 | |||||||
| chr5:88787794 | A | T | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+16804T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787794 | |||||||
| chr5:88788158 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0057 others(4): Show |
7 | HG02027.hp1 NA18747.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+16440A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788158 | |||||||
| chr5:88788165 | AGTTT | A | 5 | a0001c0001t0002g0193 a0001c0001t0003g0095 a0001c0001t0007g0020 others(2): Show |
5 | HG02523.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+16429_258+1643 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788165 | |||||||
| chr5:88788174 | GTTTGTTT others(1): Show |
G | 70 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0039 others(67): Show |
71 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+16416_258+1642 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788174 | |||||||
| chr5:88788174 | GTTTGTTT others(9): Show |
G | 1 | a0001c0001t0002g0210 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.258+16408_258+1642 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788174 | |||||||
| chr5:88788178 | G | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+16420C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788178 | G | GTTTA | 15 | a0001c0001t0002g0041 a0001c0001t0002g0232 a0001c0001t0003g0230 others(12): Show |
16 | HG00280.hp1 HG00323.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.258+16416_258+1641 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788178 | G | GTTTATTT others(1): Show |
25 | a0001c0001t0001g0079 a0001c0001t0001g0114 a0001c0001t0002g0024 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.258+16412_258+1641 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788178 | G | GTTTATTT others(5): Show |
3 | a0001c0001t0002g0033 a0001c0001t0002g0052 a0001c0001t0004g0013 |
3 | HG01981.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.258+16408_258+1641 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788178 | G | GTTTATTT others(9): Show |
2 | a0001c0001t0002g0053 a0001c0001t0020g0008 |
2 | HG01496.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.258+16404_258+1641 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788178 | G | GTTTGTTT others(1): Show |
29 | a0001c0001t0001g0076 a0001c0001t0001g0094 a0001c0001t0001g0097 others(26): Show |
30 | HG00597.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.258+16419_258+1642 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788178 | G | GTTTGTTT others(5): Show |
1 | a0001c0001t0001g0081 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+16419_258+1642 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788178 | GTTTA | G | 21 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(18): Show |
21 | HG00741.hp1 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.258+16416_258+1641 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | |||||||
| chr5:88788182 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.258+16416T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788182 | |||||||
| chr5:88788199 | T | A | 27 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(24): Show |
28 | HG00597.hp2 HG00673.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.258+16399A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788199 | |||||||
| chr5:88788199 | T | TTTATTTA others(1): Show |
55 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0044 others(52): Show |
55 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.258+16398_258+1639 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788199 | |||||||
| chr5:88788286 | C | T | 13 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0209 others(10): Show |
14 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+16312G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788286 | |||||||
| chr5:88788305 | A | G | 1 | a0001c0001t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+16293T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788305 | |||||||
| chr5:88788713 | G | A | 1 | a0001c0001t0010g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.258+15885C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788713 | |||||||
| chr5:88789151 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.258+15447T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789151 | |||||||
| chr5:88789171 | CT | C | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+15426delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789171 | |||||||
| chr5:88789297 | G | T | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.258+15301C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789297 | |||||||
| chr5:88789409 | C | G | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.258+15189G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789409 | |||||||
| chr5:88789604 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0168 a0001c0001t0001g0170 |
3 | HG00280.hp2 HG01070.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.258+14994T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789604 | |||||||
| chr5:88789660 | A | T | 1 | a0001c0001t0004g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+14938T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789660 | |||||||
| chr5:88789922 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.258+14676T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789922 | |||||||
| chr5:88790008 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0289 |
2 | HG02132.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.258+14590G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790008 | |||||||
| chr5:88790028 | T | C | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+14570A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790028 | |||||||
| chr5:88790185 | CTTCCT | C | 3 | a0001c0001t0008g0035 a0001c0001t0008g0072 a0001c0001t0008g0073 |
3 | HG01433.hp1 HG01975.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.258+14408_258+1441 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790185 | |||||||
| chr5:88790250 | A | G | 1 | a0001c0001t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+14348T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790250 | |||||||
| chr5:88790283 | A | G | 3 | a0001c0001t0006g0001 a0001c0001t0006g0153 a0001c0001t0006g0154 |
4 | NA18945.hp1 NA18970.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+14315T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790283 | |||||||
| chr5:88790288 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.258+14310G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790288 | |||||||
| chr5:88790295 | T | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(125): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.258+14303A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790295 | |||||||
| chr5:88790307 | A | C | 132 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.258+14291T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790307 | |||||||
| chr5:88790454 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258+14144A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790454 | |||||||
| chr5:88790467 | A | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0054 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.258+14131T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790467 | |||||||
| chr5:88790729 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.258+13869A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790729 | |||||||
| chr5:88790863 | G | A | 1 | a0001c0001t0023g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.258+13735C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790863 | |||||||
| chr5:88790904 | C | G | 1 | a0001c0001t0003g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.258+13694G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790904 | |||||||
| chr5:88791579 | T | C | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+13019A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791579 | |||||||
| chr5:88791610 | A | G | 1 | a0001c0001t0029g0023 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258+12988T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791610 | |||||||
| chr5:88791856 | T | C | 8 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(5): Show |
9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+12742A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791856 | |||||||
| chr5:88791947 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.258+12651T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791947 | |||||||
| chr5:88792387 | G | A | 81 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(78): Show |
82 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.258+12211C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792387 | |||||||
| chr5:88792407 | T | C | 1 | a0001c0001t0003g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.258+12191A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792407 | |||||||
| chr5:88792421 | A | G | 1 | a0001c0001t0003g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+12177T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792421 | |||||||
| chr5:88792476 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.258+12122G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792476 | |||||||
| chr5:88792622 | G | C | 132 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.258+11976C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792622 | |||||||
| chr5:88792758 | G | A | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.258+11840C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792758 | |||||||
| chr5:88793015 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.258+11583A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793015 | |||||||
| chr5:88793244 | G | A | 1 | a0001c0001t0004g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.258+11354C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793244 | |||||||
| chr5:88793327 | TG | T | 73 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0039 others(70): Show |
74 | HG00544.hp1 HG00597.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.258+11270delC | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793327 | |||||||
| chr5:88793438 | T | C | 2 | a0001c0001t0004g0282 a0001c0001t0004g0287 |
2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.258+11160A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793438 | |||||||
| chr5:88793696 | C | A | 1 | a0001c0001t0021g0208 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.258+10902G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793696 | |||||||
| chr5:88793740 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.258+10858C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793740 | |||||||
| chr5:88794459 | G | A | 1 | a0001c0001t0010g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.258+10139C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88794459 | |||||||
| chr5:88794647 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.258+9951A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88794647 | |||||||
| chr5:88795143 | T | C | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0025g0158 |
3 | HG02622.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.258+9455A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795143 | |||||||
| chr5:88795271 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.258+9327G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795271 | |||||||
| chr5:88795615 | A | G | 8 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(5): Show |
9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+8983T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795615 | |||||||
| chr5:88795676 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.258+8922A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795676 | |||||||
| chr5:88796051 | T | G | 16 | a0001c0001t0001g0114 a0001c0001t0002g0024 a0001c0001t0002g0033 others(13): Show |
16 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.258+8547A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796051 | |||||||
| chr5:88796133 | A | T | 262 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(259): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.258+8465T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796133 | |||||||
| chr5:88796197 | T | C | 2 | a0001c0001t0005g0086 a0001c0001t0005g0087 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.258+8401A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796197 | |||||||
| chr5:88796376 | T | G | 1 | a0001c0001t0004g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.258+8222A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796376 | |||||||
| chr5:88796521 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.258+8077G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796521 | |||||||
| chr5:88796562 | T | C | 132 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.258+8036A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796562 | |||||||
| chr5:88796590 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+8008T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796590 | |||||||
| chr5:88796749 | T | C | 4 | a0001c0001t0002g0191 a0001c0001t0002g0197 a0001c0001t0002g0199 others(1): Show |
4 | NA18945.hp2 NA18982.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+7849A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796749 | |||||||
| chr5:88796764 | A | G | 1 | a0001c0001t0004g0004 | 2 | HG01496.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.258+7834T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796764 | |||||||
| chr5:88796908 | T | C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+7690A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796908 | |||||||
| chr5:88796910 | G | C | 132 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.258+7688C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796910 | |||||||
| chr5:88797017 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0136 |
2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.258+7581T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797017 | |||||||
| chr5:88797241 | T | C | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0294 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+7357A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797241 | |||||||
| chr5:88797322 | C | T | 9 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(6): Show |
10 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+7276G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797322 | |||||||
| chr5:88797336 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0144 |
2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.258+7262A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797336 | |||||||
| chr5:88797343 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.258+7255G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797343 | |||||||
| chr5:88797448 | C | T | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.258+7150G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797448 | |||||||
| chr5:88797449 | C | G | 1 | a0001c0001t0004g0116 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.258+7149G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797449 | |||||||
| chr5:88797453 | GC | G | 37 | a0001c0001t0001g0028 a0001c0001t0001g0076 a0001c0001t0001g0079 others(34): Show |
38 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.258+7144delG | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797453 | |||||||
| chr5:88797454 | C | CT | 21 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0065 others(18): Show |
21 | HG00597.hp2 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.258+7143_258+7144i others(3): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797454 | |||||||
| chr5:88797454 | C | CTT | 5 | a0001c0001t0001g0130 a0001c0001t0001g0228 a0001c0001t0002g0243 others(2): Show |
5 | HG02109.hp1 HG03209.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+7143_258+7144i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797454 | |||||||
| chr5:88797454 | CCTTTTTT others(9): Show |
C | 1 | a0001c0001t0009g0181 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.258+7128_258+7143d others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797454 | |||||||
| chr5:88797455 | C | CT | 67 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0039 others(64): Show |
68 | HG00544.hp1 HG00597.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.258+7142dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | |||||||
| chr5:88797455 | C | CTT | 14 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0069 others(11): Show |
14 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+7141_258+7142d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | |||||||
| chr5:88797455 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0044 others(91): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.258+7143G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | |||||||
| chr5:88797455 | CT | C | 33 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0002g0237 others(30): Show |
33 | HG00099.hp2 HG00673.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.258+7142delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | |||||||
| chr5:88797455 | CTT | C | 6 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0294 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+7141_258+7142d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | |||||||
| chr5:88797456 | T | G | 1 | a0001c0001t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.258+7142A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797456 | |||||||
| chr5:88797457 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.258+7141A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797457 | |||||||
| chr5:88797537 | T | C | 2 | a0001c0001t0010g0060 a0001c0001t0010g0061 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.258+7061A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797537 | |||||||
| chr5:88798176 | A | G | 1 | a0001c0001t0011g0029 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.258+6422T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798176 | |||||||
| chr5:88798418 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258+6180C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798418 | |||||||
| chr5:88798431 | G | A | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+6167C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798431 | |||||||
| chr5:88798452 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.258+6146G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798452 | |||||||
| chr5:88798564 | T | C | 2 | a0001c0001t0002g0185 a0001c0001t0008g0186 |
2 | HG00597.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.258+6034A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798564 | |||||||
| chr5:88798580 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.258+6018T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798580 | |||||||
| chr5:88798675 | T | C | 11 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(8): Show |
11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+5923A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798675 | |||||||
| chr5:88798790 | G | T | 1 | a0001c0001t0013g0161 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.258+5808C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798790 | |||||||
| chr5:88798795 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+5803A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798795 | |||||||
| chr5:88798806 | G | A | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+5792C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798806 | |||||||
| chr5:88798814 | G | A | 2 | a0001c0001t0007g0296 a0001c0001t0007g0297 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.258+5784C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798814 | |||||||
| chr5:88798859 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.258+5739A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798859 | |||||||
| chr5:88799373 | G | T | 1 | a0001c0001t0003g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+5225C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799373 | |||||||
| chr5:88799809 | T | C | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258+4789A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799809 | |||||||
| chr5:88799839 | G | T | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4759C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799839 | |||||||
| chr5:88799849 | TTC | T | 28 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0265 others(25): Show |
29 | HG01069.hp2 HG01070.hp2 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.258+4747_258+4748d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799849 | |||||||
| chr5:88799870 | T | A | 1 | a0001c0001t0003g0275 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.258+4728A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | T | TCA | 3 | a0001c0001t0003g0238 a0001c0001t0003g0255 a0001c0001t0004g0256 |
3 | HG00741.hp1 HG01934.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.258+4726_258+4727d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | T | TCATA | 6 | a0001c0001t0002g0030 a0001c0001t0002g0243 a0001c0001t0004g0112 others(3): Show |
6 | HG00280.hp1 HG02055.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+4727_258+4728i others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | T | TCATACA | 5 | a0001c0001t0002g0041 a0001c0001t0002g0054 a0001c0001t0003g0080 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+4727_258+4728i others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | T | TCATACAC others(3): Show |
1 | a0001c0001t0005g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.258+4727_258+4728i others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | T | TCATACAC others(5): Show |
1 | a0001c0001t0015g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258+4727_258+4728i others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | T | TCATACAC others(7): Show |
1 | a0001c0001t0036g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258+4727_258+4728i others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | TCA | T | 55 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0034 others(52): Show |
55 | HG00099.hp2 HG00544.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.258+4726_258+4727d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | TCACA | T | 12 | a0001c0001t0002g0025 a0001c0001t0002g0057 a0001c0001t0002g0058 others(9): Show |
12 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.258+4724_258+4727d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799870 | TCACACA | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0002g0049 others(8): Show |
11 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.258+4722_258+4727d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | |||||||
| chr5:88799871 | C | CAT | 3 | a0001c0001t0002g0007 a0001c0001t0004g0146 a0001c0001t0024g0070 |
3 | HG00323.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+4726_258+4727i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799871 | |||||||
| chr5:88799872 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.258+4726T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799872 | |||||||
| chr5:88799873 | C | T | 160 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(157): Show |
163 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.258+4725G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799873 | |||||||
| chr5:88799875 | C | T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0034 others(29): Show |
32 | HG00544.hp1 HG01069.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.258+4723G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799875 | |||||||
| chr5:88799877 | C | T | 8 | a0001c0001t0002g0025 a0001c0001t0002g0057 a0001c0001t0002g0058 others(5): Show |
8 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+4721G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799877 | |||||||
| chr5:88799879 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0002g0049 others(5): Show |
8 | HG02486.hp2 NA18953.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+4719G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799879 | |||||||
| chr5:88799901 | CACACACA others(9): Show |
C | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.258+4681_258+4696d others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799901 | |||||||
| chr5:88799903 | CACACACA others(7): Show |
C | 3 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0022 |
3 | HG02896.hp1 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.258+4681_258+4694d others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799903 | |||||||
| chr5:88799905 | CACACACA others(5): Show |
C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0120 a0001c0001t0001g0127 others(6): Show |
9 | HG00280.hp2 HG01070.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+4681_258+4692d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799905 | |||||||
| chr5:88799905 | CACACACA others(7): Show |
C | 6 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0089 others(3): Show |
7 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+4679_258+4692d others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799905 | |||||||
| chr5:88799907 | CACACACA others(3): Show |
C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0183 a0001c0001t0006g0153 others(3): Show |
6 | HG01884.hp1 HG02735.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+4681_258+4690d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799907 | |||||||
| chr5:88799909 | CACACAGA others(1): Show |
C | 49 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0067 others(46): Show |
49 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.258+4681_258+4688d others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799909 | |||||||
| chr5:88799909 | CACACAGA others(3): Show |
C | 3 | a0001c0001t0005g0086 a0001c0001t0006g0001 a0001c0001t0029g0023 |
4 | HG02572.hp2 HG02970.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4679_258+4688d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799909 | |||||||
| chr5:88799911 | CACAGAG | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0079 others(19): Show |
22 | HG00099.hp1 HG00673.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.258+4681_258+4686d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799911 | |||||||
| chr5:88799911 | CACAGAGA others(1): Show |
C | 4 | a0001c0001t0002g0052 a0001c0001t0004g0115 a0001c0001t0004g0116 others(1): Show |
4 | HG02451.hp1 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4679_258+4686d others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799911 | |||||||
| chr5:88799913 | C | G | 5 | a0001c0001t0002g0066 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+4685G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799913 | |||||||
| chr5:88799913 | CAG | C | 29 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0027 others(26): Show |
30 | HG00597.hp1 HG01123.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.258+4683_258+4684d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799913 | |||||||
| chr5:88799913 | CAGAG | C | 15 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0114 others(12): Show |
15 | HG00639.hp2 HG01169.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+4681_258+4684d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799913 | |||||||
| chr5:88799915 | G | C | 15 | a0001c0001t0002g0030 a0001c0001t0002g0041 a0001c0001t0002g0054 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.258+4683C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799915 | |||||||
| chr5:88799917 | G | C | 11 | a0001c0001t0002g0030 a0001c0001t0002g0041 a0001c0001t0002g0054 others(8): Show |
11 | HG00280.hp1 HG01123.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+4681C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799917 | |||||||
| chr5:88799919 | G | C | 13 | a0001c0001t0001g0114 a0001c0001t0002g0033 a0001c0001t0002g0046 others(10): Show |
13 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.258+4679C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799919 | |||||||
| chr5:88799968 | C | T | 132 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(129): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.258+4630G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799968 | |||||||
| chr5:88800043 | G | C | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4555C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800043 | |||||||
| chr5:88800509 | G | T | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.258+4089C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800509 | |||||||
| chr5:88800647 | G | C | 1 | a0001c0001t0002g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.258+3951C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800647 | |||||||
| chr5:88800858 | T | A | 1 | a0001c0001t0001g0159 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.258+3740A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800858 | |||||||
| chr5:88801494 | CT | C | 133 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(130): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.258+3103delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801494 | |||||||
| chr5:88801511 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0007g0296 a0001c0001t0007g0297 others(5): Show |
8 | HG00639.hp1 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+3087C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801511 | |||||||
| chr5:88801519 | G | A | 2 | a0001c0001t0002g0038 a0001c0001t0002g0176 |
2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.258+3079C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801519 | |||||||
| chr5:88801531 | C | T | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+3067G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801531 | |||||||
| chr5:88801585 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.258+3013G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801585 | |||||||
| chr5:88801606 | C | T | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+2992G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801606 | |||||||
| chr5:88801699 | G | A | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258+2899C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801699 | |||||||
| chr5:88801878 | T | C | 1 | a0001c0001t0003g0263 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.258+2720A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801878 | |||||||
| chr5:88802057 | C | A | 1 | a0001c0001t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+2541G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802057 | |||||||
| chr5:88802219 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.258+2379G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802219 | |||||||
| chr5:88802239 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+2359T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802239 | |||||||
| chr5:88802247 | A | T | 157 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0039 others(154): Show |
159 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.258+2351T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802247 | |||||||
| chr5:88802265 | C | T | 1 | a0001c0001t0004g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.258+2333G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802265 | |||||||
| chr5:88802303 | A | G | 164 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
166 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.258+2295T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802303 | |||||||
| chr5:88802308 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.258+2290A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802308 | |||||||
| chr5:88802444 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.258+2154A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802444 | |||||||
| chr5:88802556 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.258+2042G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802556 | |||||||
| chr5:88802622 | T | A | 2 | a0001c0001t0003g0238 a0001c0001t0003g0280 |
2 | HG01099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.258+1976A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802622 | |||||||
| chr5:88802728 | T | C | 168 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(165): Show |
170 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.258+1870A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802728 | |||||||
| chr5:88802749 | A | G | 3 | a0001c0001t0004g0103 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG01243.hp2 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.258+1849T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802749 | |||||||
| chr5:88803129 | T | A | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0025g0158 |
3 | HG02622.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.258+1469A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803129 | |||||||
| chr5:88803140 | T | C | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+1458A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803140 | |||||||
| chr5:88803179 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258+1419C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803179 | |||||||
| chr5:88803300 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1298G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803300 | |||||||
| chr5:88803621 | G | T | 2 | a0001c0001t0001g0056 a0001c0001t0003g0031 |
2 | NA19075.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.258+977C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803621 | |||||||
| chr5:88803854 | T | C | 70 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0237 others(67): Show |
71 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+744A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803854 | |||||||
| chr5:88803972 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0054 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.258+626G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803972 | |||||||
| chr5:88804134 | G | C | 75 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0039 others(72): Show |
76 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.258+464C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804134 | |||||||
| chr5:88804209 | G | A | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0053 others(1): Show |
4 | HG01123.hp2 HG01496.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+389C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804209 | |||||||
| chr5:88804210 | G | C | 1 | a0001c0001t0012g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.258+388C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804210 | |||||||
| chr5:88804443 | A | C | 32 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0265 others(29): Show |
33 | HG01069.hp2 HG01070.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.258+155T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804443 | |||||||
| chr5:88804832 | A | T | 1 | a0001c0001t0003g0292 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.55-31T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88804832 | |||||||
| chr5:88804846 | C | T | 2 | a0001c0001t0008g0035 a0001c0001t0008g0073 |
2 | HG01433.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.55-45G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88804846 | |||||||
| chr5:88805096 | T | A | 1 | a0001c0001t0002g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55-295A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805096 | |||||||
| chr5:88805278 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55-477T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805278 | |||||||
| chr5:88805325 | A | G | 164 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
166 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.55-524T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805325 | |||||||
| chr5:88805333 | C | T | 167 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(164): Show |
169 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.55-532G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805333 | |||||||
| chr5:88805434 | A | G | 13 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-633T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805434 | |||||||
| chr5:88805687 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.55-886A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805687 | |||||||
| chr5:88805739 | A | ATTTCACT others(1): Show |
8 | a0001c0001t0004g0112 a0001c0001t0007g0296 a0001c0001t0007g0297 others(5): Show |
8 | HG00639.hp1 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-946_55-939dupGA others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805739 | |||||||
| chr5:88805772 | T | A | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.55-971A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805772 | |||||||
| chr5:88805823 | C | CT | 54 | a0001c0001t0001g0068 a0001c0001t0001g0082 a0001c0001t0001g0099 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.55-1023dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | |||||||
| chr5:88805823 | C | CTT | 12 | a0001c0001t0001g0028 a0001c0001t0001g0065 a0001c0001t0001g0125 others(9): Show |
12 | HG00323.hp2 HG00733.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.55-1024_55-1023dup others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | |||||||
| chr5:88805823 | CT | C | 17 | a0001c0001t0001g0011 a0001c0001t0002g0049 a0001c0001t0002g0191 others(14): Show |
17 | HG00099.hp2 HG01069.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-1023delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | |||||||
| chr5:88805823 | CTT | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0034 others(65): Show |
69 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.55-1024_55-1023del others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | |||||||
| chr5:88805871 | A | G | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.55-1070T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805871 | |||||||
| chr5:88806030 | A | G | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1229T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806030 | |||||||
| chr5:88806143 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.55-1342A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806143 | |||||||
| chr5:88806265 | C | T | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1464G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806265 | |||||||
| chr5:88806416 | A | G | 11 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(8): Show |
11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.55-1615T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806416 | |||||||
| chr5:88806464 | T | G | 84 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(81): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.55-1663A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806464 | |||||||
| chr5:88806739 | A | AAAAATAT others(20): Show |
4 | a0001c0001t0002g0207 a0001c0001t0004g0006 a0001c0001t0019g0071 others(1): Show |
4 | HG01891.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-1965_55-1939dup others(27): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806739 | |||||||
| chr5:88806742 | A | G | 1 | a0001c0001t0003g0055 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.55-1941T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806742 | |||||||
| chr5:88807046 | T | C | 186 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
188 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.55-2245A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807046 | |||||||
| chr5:88807200 | T | C | 16 | a0001c0001t0003g0255 a0001c0001t0004g0103 a0001c0001t0004g0106 others(13): Show |
16 | HG00741.hp1 HG01243.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.55-2399A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807200 | |||||||
| chr5:88807368 | C | T | 3 | a0001c0001t0002g0207 a0001c0001t0007g0296 a0001c0001t0007g0297 |
3 | HG02572.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.55-2567G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807368 | |||||||
| chr5:88807396 | T | C | 19 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(16): Show |
19 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.55-2595A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807396 | |||||||
| chr5:88807471 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-2670G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807471 | |||||||
| chr5:88807504 | G | C | 3 | a0001c0001t0001g0039 a0001c0001t0012g0142 a0001c0001t0012g0156 |
3 | HG01255.hp2 HG01433.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.55-2703C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807504 | |||||||
| chr5:88807975 | T | A | 6 | a0001c0001t0004g0089 a0001c0001t0004g0090 a0001c0001t0004g0092 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-3174A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807975 | |||||||
| chr5:88808081 | T | C | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.55-3280A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808081 | |||||||
| chr5:88808442 | T | C | 1 | a0001c0001t0004g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.55-3641A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808442 | |||||||
| chr5:88808530 | C | T | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-3729G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808530 | |||||||
| chr5:88808543 | A | G | 19 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(16): Show |
19 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.55-3742T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808543 | |||||||
| chr5:88808605 | C | T | 19 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(16): Show |
19 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.55-3804G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808605 | |||||||
| chr5:88809289 | A | G | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.55-4488T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809289 | |||||||
| chr5:88809458 | A | G | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.55-4657T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809458 | |||||||
| chr5:88809644 | T | G | 2 | a0001c0001t0004g0138 a0001c0001t0004g0146 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.55-4843A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809644 | |||||||
| chr5:88809683 | C | A | 1 | a0001c0001t0002g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55-4882G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809683 | |||||||
| chr5:88809730 | C | T | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-4929G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809730 | |||||||
| chr5:88809797 | C | T | 186 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
189 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(186): Show |
intron_variant | MODIFIER | c.55-4996G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809797 | |||||||
| chr5:88810284 | T | C | 1 | a0001c0001t0007g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.55-5483A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810284 | |||||||
| chr5:88810441 | T | C | 186 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
189 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(186): Show |
intron_variant | MODIFIER | c.55-5640A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810441 | |||||||
| chr5:88810533 | CA | C | 184 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(181): Show |
187 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(184): Show |
intron_variant | MODIFIER | c.55-5733delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810533 | |||||||
| chr5:88810942 | T | G | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.55-6141A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810942 | |||||||
| chr5:88811036 | C | G | 7 | a0001c0001t0001g0114 a0001c0001t0002g0027 a0001c0001t0003g0117 others(4): Show |
7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-6235G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811036 | |||||||
| chr5:88811084 | A | G | 1 | a0001c0001t0032g0134 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.55-6283T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811084 | |||||||
| chr5:88811520 | C | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(81): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.55-6719G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811520 | |||||||
| chr5:88811752 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.55-6951T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811752 | |||||||
| chr5:88811791 | T | C | 13 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-6990A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811791 | |||||||
| chr5:88811985 | T | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0136 |
2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55-7184A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811985 | |||||||
| chr5:88812610 | TC | T | 71 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0197 others(68): Show |
73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.55-7810delG | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88812610 | |||||||
| chr5:88812636 | T | A | 171 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
174 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.55-7835A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88812636 | |||||||
| chr5:88812757 | G | A | 171 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
174 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.55-7956C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88812757 | |||||||
| chr5:88813065 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.55-8264C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813065 | |||||||
| chr5:88813471 | A | T | 2 | a0001c0001t0007g0021 a0001c0001t0007g0022 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.55-8670T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813471 | |||||||
| chr5:88813509 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.55-8708G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813509 | |||||||
| chr5:88813773 | C | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(15): Show |
18 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.55-8972G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813773 | |||||||
| chr5:88814267 | C | T | 167 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(164): Show |
170 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.55-9466G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814267 | |||||||
| chr5:88814276 | T | C | 3 | a0001c0001t0001g0101 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02027.hp2 NA18959.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.54+9459A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814276 | |||||||
| chr5:88814521 | A | G | 167 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(164): Show |
170 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.54+9214T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814521 | |||||||
| chr5:88814546 | C | T | 264 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(261): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.54+9189G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814546 | |||||||
| chr5:88814573 | C | A | 13 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+9162G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814573 | |||||||
| chr5:88815391 | C | T | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+8344G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815391 | |||||||
| chr5:88815392 | C | G | 264 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(261): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.54+8343G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815392 | |||||||
| chr5:88815527 | G | C | 10 | a0001c0001t0002g0188 a0001c0001t0002g0200 a0001c0001t0002g0201 others(7): Show |
10 | HG02145.hp2 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+8208C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815527 | |||||||
| chr5:88815587 | T | G | 1 | a0001c0001t0002g0190 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.54+8148A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815587 | |||||||
| chr5:88815932 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.54+7803C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815932 | |||||||
| chr5:88816126 | A | G | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.54+7609T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816126 | |||||||
| chr5:88816229 | C | T | 1 | a0001c0001t0010g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.54+7506G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816229 | |||||||
| chr5:88816303 | G | A | 1 | a0001c0001t0003g0272 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.54+7432C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816303 | |||||||
| chr5:88816406 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.54+7329C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816406 | |||||||
| chr5:88816411 | T | G | 1 | a0001c0001t0003g0055 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.54+7324A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816411 | |||||||
| chr5:88816465 | C | CT | 12 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0147 others(9): Show |
12 | HG00741.hp2 HG02027.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.54+7269dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816465 | |||||||
| chr5:88816465 | CT | C | 78 | a0001c0001t0001g0039 a0001c0001t0001g0069 a0001c0001t0001g0094 others(75): Show |
79 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.54+7269delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816465 | |||||||
| chr5:88816465 | CTT | C | 68 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0049 others(65): Show |
70 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.54+7268_54+7269del others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816465 | |||||||
| chr5:88816596 | C | T | 12 | a0001c0001t0004g0004 a0001c0001t0004g0088 a0001c0001t0004g0206 others(9): Show |
13 | HG01496.hp1 HG02055.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+7139G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816596 | |||||||
| chr5:88816708 | T | C | 1 | a0001c0001t0004g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+7027A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816708 | |||||||
| chr5:88816864 | C | T | 3 | a0001c0001t0004g0089 a0001c0001t0004g0090 a0001c0001t0004g0092 |
3 | HG01884.hp2 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.54+6871G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816864 | |||||||
| chr5:88816934 | C | A | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+6801G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816934 | |||||||
| chr5:88816944 | T | A | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+6791A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816944 | |||||||
| chr5:88817008 | C | T | 13 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+6727G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817008 | |||||||
| chr5:88817034 | C | CA | 4 | a0001c0001t0001g0039 a0001c0001t0012g0062 a0001c0001t0012g0142 others(1): Show |
4 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+6700dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817034 | |||||||
| chr5:88817218 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.54+6517C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817218 | |||||||
| chr5:88817411 | C | T | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+6324G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817411 | |||||||
| chr5:88817438 | T | C | 5 | a0001c0001t0004g0293 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+6297A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817438 | |||||||
| chr5:88817646 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.54+6089G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817646 | |||||||
| chr5:88817842 | C | G | 13 | a0001c0001t0002g0237 a0001c0001t0003g0234 a0001c0001t0003g0235 others(10): Show |
13 | HG00099.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+5893G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817842 | |||||||
| chr5:88817912 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.54+5823T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817912 | |||||||
| chr5:88818235 | A | C | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0294 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+5500T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818235 | |||||||
| chr5:88818447 | G | C | 1 | a0001c0001t0001g0043 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.54+5288C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818447 | |||||||
| chr5:88818659 | T | C | 167 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(164): Show |
170 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.54+5076A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818659 | |||||||
| chr5:88818727 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0067 others(6): Show |
9 | HG01358.hp1 NA18979.hp1 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+5008C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818727 | |||||||
| chr5:88818737 | G | T | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+4998C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818737 | |||||||
| chr5:88818885 | A | C | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.54+4850T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818885 | |||||||
| chr5:88818979 | C | T | 1 | a0001c0001t0004g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+4756G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818979 | |||||||
| chr5:88819056 | G | A | 13 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+4679C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819056 | |||||||
| chr5:88819361 | C | T | 13 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+4374G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819361 | |||||||
| chr5:88819425 | A | G | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+4310T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819425 | |||||||
| chr5:88819477 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.54+4258G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819477 | |||||||
| chr5:88819816 | C | T | 5 | a0001c0001t0002g0198 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+3919G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819816 | |||||||
| chr5:88820068 | T | A | 171 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
174 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.54+3667A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820068 | |||||||
| chr5:88820075 | TTA | T | 168 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(165): Show |
171 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(168): Show |
intron_variant | MODIFIER | c.54+3658_54+3659del others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820075 | |||||||
| chr5:88820499 | T | C | 1 | a0001c0001t0004g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.54+3236A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820499 | |||||||
| chr5:88820502 | C | T | 74 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0237 others(71): Show |
76 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.54+3233G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820502 | |||||||
| chr5:88820520 | T | C | 1 | a0001c0001t0033g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.54+3215A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820520 | |||||||
| chr5:88820533 | G | C | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.54+3202C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820533 | |||||||
| chr5:88820560 | A | T | 1 | a0001c0001t0004g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.54+3175T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820560 | |||||||
| chr5:88820588 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0012g0062 a0001c0001t0012g0142 others(1): Show |
4 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+3147A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820588 | |||||||
| chr5:88820711 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(15): Show |
18 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.54+3024G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820711 | |||||||
| chr5:88820787 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+2948C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820787 | |||||||
| chr5:88820853 | C | A | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+2882G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820853 | |||||||
| chr5:88821210 | A | T | 170 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
173 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(170): Show |
intron_variant | MODIFIER | c.54+2525T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821210 | |||||||
| chr5:88821259 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.54+2476A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821259 | |||||||
| chr5:88821260 | T | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0159 |
2 | NA19001.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.54+2475A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821260 | |||||||
| chr5:88821332 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.54+2403A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821332 | |||||||
| chr5:88821677 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+2058G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821677 | |||||||
| chr5:88821703 | T | A | 1 | a0001c0001t0004g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+2032A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821703 | |||||||
| chr5:88821704 | A | T | 8 | a0001c0001t0006g0001 a0001c0001t0006g0153 a0001c0001t0006g0154 others(5): Show |
9 | HG01928.hp1 NA18941.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+2031T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821704 | |||||||
| chr5:88821800 | G | C | 1 | a0001c0001t0003g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54+1935C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821800 | |||||||
| chr5:88822271 | C | T | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.54+1464G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822271 | |||||||
| chr5:88822577 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54+1158C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822577 | |||||||
| chr5:88822603 | T | G | 2 | a0001c0001t0002g0237 a0001c0001t0003g0249 |
2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.54+1132A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822603 | |||||||
| chr5:88822778 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.54+957C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822778 | |||||||
| chr5:88822837 | C | T | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.54+898G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822837 | |||||||
| chr5:88822964 | C | A | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.54+771G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822964 | |||||||
| chr5:88823041 | A | G | 167 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(164): Show |
170 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.54+694T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88823041 | |||||||
| chr5:88823562 | T | C | 2 | a0001c0001t0007g0296 a0001c0001t0007g0297 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54+173A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88823562 | |||||||
| chr5:88823968 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-142-38G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88823968 | |||||||
| chr5:88824262 | C | CCT | 166 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(163): Show |
169 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.-142-333_-142-332i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88824262 | |||||||
| chr5:88824509 | C | T | 2 | a0001c0001t0003g0236 a0001c0001t0037g0233 |
2 | HG01168.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-142-579G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88824509 | |||||||
| chr5:88824599 | T | C | 167 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(164): Show |
170 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.-142-669A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88824599 | |||||||
| chr5:88825089 | C | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-1159G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825089 | |||||||
| chr5:88825231 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-142-1301A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825231 | |||||||
| chr5:88825240 | T | G | 1 | a0001c0001t0003g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-142-1310A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825240 | |||||||
| chr5:88825265 | AT | A | 7 | a0001c0001t0001g0129 a0001c0001t0001g0151 a0001c0001t0001g0174 others(4): Show |
7 | HG01496.hp2 HG02129.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-1336delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825265 | |||||||
| chr5:88825371 | T | A | 167 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(164): Show |
170 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.-142-1441A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825371 | |||||||
| chr5:88825839 | G | A | 1 | a0001c0001t0003g0258 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-142-1909C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825839 | |||||||
| chr5:88826361 | C | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0184 a0001c0001t0002g0185 others(30): Show |
34 | HG00597.hp1 HG01433.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.-142-2431G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826361 | |||||||
| chr5:88826383 | A | T | 2 | a0001c0001t0003g0246 a0001c0001t0004g0247 |
2 | HG00642.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-142-2453T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826383 | |||||||
| chr5:88826416 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-142-2486G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826416 | |||||||
| chr5:88826908 | T | A | 1 | a0001c0001t0001g0028 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-142-2978A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826908 | |||||||
| chr5:88826908 | T | TA | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
115 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.-142-2979dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826908 | |||||||
| chr5:88827523 | T | A | 1 | a0001c0001t0004g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-142-3593A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827523 | |||||||
| chr5:88827608 | A | C | 1 | a0001c0001t0003g0254 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-142-3678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827608 | |||||||
| chr5:88827653 | T | C | 1 | a0001c0001t0025g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-142-3723A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827653 | |||||||
| chr5:88827733 | T | A | 71 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0237 others(68): Show |
73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.-142-3803A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827733 | |||||||
| chr5:88827912 | A | G | 3 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0055 |
3 | NA18955.hp1 NA18966.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-142-3982T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827912 | |||||||
| chr5:88827914 | T | TA | 121 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
123 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.-142-3985dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827914 | |||||||
| chr5:88828029 | T | A | 1 | a0001c0001t0002g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-142-4099A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828029 | |||||||
| chr5:88828306 | T | G | 171 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
174 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.-142-4376A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828306 | |||||||
| chr5:88828399 | T | A | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-142-4469A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828399 | |||||||
| chr5:88828441 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0004g0102 a0001c0001t0004g0106 |
3 | HG01891.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-142-4511T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828441 | |||||||
| chr5:88828511 | C | T | 3 | a0001c0001t0003g0254 a0001c0001t0003g0260 a0001c0001t0003g0290 |
3 | NA18999.hp2 NA19074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-142-4581G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828511 | |||||||
| chr5:88828850 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-142-4920G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828850 | |||||||
| chr5:88829112 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-142-5182G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829112 | |||||||
| chr5:88829206 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-142-5276A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829206 | |||||||
| chr5:88829413 | T | G | 11 | a0001c0001t0004g0112 a0001c0001t0004g0293 a0001c0001t0005g0018 others(8): Show |
11 | HG00639.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-142-5483A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829413 | |||||||
| chr5:88829518 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-142-5588G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829518 | |||||||
| chr5:88829676 | G | A | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-5746C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829676 | |||||||
| chr5:88829677 | C | G | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-5747G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829677 | |||||||
| chr5:88830036 | T | G | 156 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(153): Show |
159 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.-142-6106A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88830036 | |||||||
| chr5:88830522 | T | C | 3 | a0001c0001t0004g0103 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG01243.hp2 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-142-6592A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88830522 | |||||||
| chr5:88830624 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-142-6694A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88830624 | |||||||
| chr5:88831100 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-142-7170G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831100 | |||||||
| chr5:88831386 | T | C | 7 | a0001c0001t0001g0065 a0001c0001t0001g0127 a0001c0001t0001g0137 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-7456A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831386 | |||||||
| chr5:88831529 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-142-7599A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831529 | |||||||
| chr5:88831607 | T | C | 15 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(12): Show |
15 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-142-7677A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831607 | |||||||
| chr5:88831611 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-7681A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831611 | |||||||
| chr5:88832109 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0144 |
2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-142-8179G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832109 | |||||||
| chr5:88832219 | A | G | 4 | a0001c0001t0003g0095 a0001c0001t0007g0020 a0001c0001t0007g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-8289T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832219 | |||||||
| chr5:88832732 | T | C | 1 | a0001c0001t0030g0113 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-142-8802A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832732 | |||||||
| chr5:88832737 | C | T | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0025g0158 |
3 | HG02622.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-142-8807G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832737 | |||||||
| chr5:88832762 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0004g0102 |
2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-142-8832C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832762 | |||||||
| chr5:88832825 | A | T | 261 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(258): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-142-8895T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832825 | |||||||
| chr5:88832835 | G | T | 261 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(258): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-142-8905C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832835 | |||||||
| chr5:88832874 | T | A | 3 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0035g0091 |
3 | HG02055.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-142-8944A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832874 | |||||||
| chr5:88832875 | G | T | 3 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0035g0091 |
3 | HG02055.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-142-8945C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832875 | |||||||
| chr5:88833516 | C | T | 3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 |
3 | NA18969.hp1 NA19057.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-142-9586G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833516 | |||||||
| chr5:88833517 | G | A | 1 | a0001c0001t0008g0111 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-142-9587C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833517 | |||||||
| chr5:88833818 | A | G | 3 | a0001c0001t0008g0035 a0001c0001t0008g0072 a0001c0001t0008g0073 |
3 | HG01433.hp1 HG01975.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-142-9888T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833818 | |||||||
| chr5:88833894 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0175 |
2 | HG00733.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-142-9964C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833894 | |||||||
| chr5:88834075 | TG | T | 43 | a0001c0001t0002g0002 a0001c0001t0002g0184 a0001c0001t0002g0185 others(40): Show |
44 | HG00597.hp1 HG01433.hp1 HG01975.hp2 others(41): Show |
intron_variant | MODIFIER | c.-142-10146delC | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834075 | |||||||
| chr5:88834503 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-10573G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834503 | |||||||
| chr5:88834833 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-10903G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834833 | |||||||
| chr5:88834953 | ATAT | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0152 |
3 | NA18951.hp1 NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-142-11026_-142-11 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834953 | |||||||
| chr5:88835307 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-142-11377G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835307 | |||||||
| chr5:88835308 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-142-11378G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835308 | |||||||
| chr5:88835465 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-142-11535C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835465 | |||||||
| chr5:88835477 | C | A | 7 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-11547G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835477 | |||||||
| chr5:88835610 | G | A | 2 | a0001c0001t0014g0286 a0001c0001t0014g0291 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-142-11680C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835610 | |||||||
| chr5:88835675 | T | C | 2 | a0001c0001t0003g0242 a0001c0001t0003g0250 |
2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-142-11745A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835675 | |||||||
| chr5:88835679 | G | A | 1 | a0001c0001t0006g0155 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-142-11749C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835679 | |||||||
| chr5:88835813 | T | TA | 141 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
144 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.-142-11884dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835813 | |||||||
| chr5:88835813 | T | TAA | 14 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(11): Show |
14 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.-142-11885_-142-11 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835813 | |||||||
| chr5:88835848 | C | A | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-142-11918G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835848 | |||||||
| chr5:88836144 | T | C | 2 | a0001c0001t0010g0060 a0001c0001t0010g0061 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-142-12214A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88836144 | |||||||
| chr5:88836819 | G | T | 1 | a0001c0001t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-142-12889C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88836819 | |||||||
| chr5:88837002 | C | CA | 86 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0039 others(83): Show |
87 | HG00280.hp1 HG00544.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.-142-13073dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | |||||||
| chr5:88837002 | C | CAA | 71 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(68): Show |
72 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-142-13074_-142-13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | |||||||
| chr5:88837002 | C | CAAA | 14 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0164 others(11): Show |
14 | HG00323.hp2 HG01255.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-142-13075_-142-13 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | |||||||
| chr5:88837002 | CA | C | 10 | a0001c0001t0002g0057 a0001c0001t0002g0211 a0001c0001t0002g0237 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.-142-13073delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | |||||||
| chr5:88837002 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-142-13083_-142-13 others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | |||||||
| chr5:88837101 | A | G | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0034g0016 others(1): Show |
4 | HG00639.hp1 HG01243.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-13171T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837101 | |||||||
| chr5:88837452 | T | C | 7 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-13522A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837452 | |||||||
| chr5:88837590 | C | G | 1 | a0001c0001t0003g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-142-13660G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837590 | |||||||
| chr5:88837781 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-142-13851G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837781 | |||||||
| chr5:88837820 | T | C | 3 | a0001c0001t0003g0262 a0001c0001t0003g0273 a0001c0001t0003g0274 |
3 | NA18965.hp1 NA19063.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-142-13890A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837820 | |||||||
| chr5:88838068 | G | A | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-142-14138C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838068 | |||||||
| chr5:88838102 | A | G | 259 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.-142-14172T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838102 | |||||||
| chr5:88838296 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-142-14366C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838296 | |||||||
| chr5:88838377 | GT | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-142-14448delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838377 | |||||||
| chr5:88838493 | A | G | 165 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-14563T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838493 | |||||||
| chr5:88838695 | C | A | 1 | a0001c0001t0004g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-142-14765G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838695 | |||||||
| chr5:88839321 | A | ATC | 6 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG02027.hp2 HG03669.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.-142-15393_-142-15 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839321 | |||||||
| chr5:88839321 | ATC | A | 66 | a0001c0001t0001g0065 a0001c0001t0001g0097 a0001c0001t0001g0098 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-142-15393_-142-15 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839321 | |||||||
| chr5:88839347 | C | CTCTATCT others(1): Show |
17 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(14): Show |
17 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-142-15418_-142-15 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839347 | |||||||
| chr5:88839351 | C | A | 21 | a0001c0001t0001g0069 a0001c0001t0001g0076 a0001c0001t0001g0081 others(18): Show |
21 | HG00099.hp2 HG01243.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.-142-15421G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTATCTA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(12): Show |
15 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTATCTAT others(3): Show |
1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-15422_-142-15 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTA | 3 | a0001c0001t0002g0200 a0001c0001t0007g0296 a0001c0001t0007g0297 |
3 | HG02572.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-142-15425_-142-15 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTATCT others(1): Show |
61 | a0001c0001t0001g0114 a0001c0001t0001g0261 a0001c0001t0001g0276 others(58): Show |
62 | HG00639.hp2 HG00642.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.-142-15429_-142-15 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTATCT others(5): Show |
2 | a0001c0001t0002g0027 a0001c0001t0036g0017 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-142-15433_-142-15 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTCTA | 20 | a0001c0001t0002g0002 a0001c0001t0002g0184 a0001c0001t0002g0185 others(17): Show |
21 | HG00597.hp1 HG02132.hp2 HG02809.hp1 others(18): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTCTAT others(3): Show |
6 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0004g0282 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTCTCT others(1): Show |
13 | a0001c0001t0002g0188 a0001c0001t0002g0201 a0001c0001t0002g0202 others(10): Show |
13 | HG01243.hp2 HG01361.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTCTCT others(5): Show |
11 | a0001c0001t0003g0263 a0001c0001t0004g0004 a0001c0001t0004g0256 others(8): Show |
12 | HG01496.hp1 HG02615.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839351 | C | CTCTCTCT others(3): Show |
11 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0191 others(8): Show |
11 | HG02129.hp2 HG02148.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | |||||||
| chr5:88839355 | A | C | 1 | a0001c0001t0008g0035 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-142-15425T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839355 | |||||||
| chr5:88839645 | T | C | 164 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
167 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(164): Show |
intron_variant | MODIFIER | c.-142-15715A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839645 | |||||||
| chr5:88839661 | T | C | 2 | a0001c0001t0019g0071 a0001c0001t0024g0070 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-142-15731A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839661 | |||||||
| chr5:88839670 | G | A | 2 | a0001c0001t0028g0173 a0001c0001t0031g0169 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-142-15740C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839670 | |||||||
| chr5:88839791 | C | T | 2 | a0001c0001t0007g0021 a0001c0001t0007g0022 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-142-15861G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839791 | |||||||
| chr5:88839891 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-142-15961C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839891 | |||||||
| chr5:88839970 | C | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-16040G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839970 | |||||||
| chr5:88840599 | C | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0184 a0001c0001t0002g0185 others(41): Show |
45 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.-142-16669G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88840599 | |||||||
| chr5:88840862 | G | C | 1 | a0001c0001t0004g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-142-16932C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88840862 | |||||||
| chr5:88840893 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-142-16963A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88840893 | |||||||
| chr5:88841429 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-17499G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841429 | |||||||
| chr5:88841506 | CA | C | 142 | a0001c0001t0001g0069 a0001c0001t0001g0094 a0001c0001t0001g0114 others(139): Show |
145 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(142): Show |
intron_variant | MODIFIER | c.-142-17577delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841506 | |||||||
| chr5:88841506 | CAA | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
24 | HG00733.hp1 HG01081.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-142-17578_-142-17 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841506 | |||||||
| chr5:88841527 | GA | G | 72 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0027 others(69): Show |
74 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.-142-17598delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841527 | |||||||
| chr5:88841633 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-142-17703T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841633 | |||||||
| chr5:88841664 | T | A | 72 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0027 others(69): Show |
74 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.-142-17734A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841664 | |||||||
| chr5:88841830 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-17900G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841830 | |||||||
| chr5:88842208 | C | T | 1 | a0001c0001t0022g0194 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-142-18278G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842208 | |||||||
| chr5:88842225 | G | A | 165 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-18295C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842225 | |||||||
| chr5:88842345 | A | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0054 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-142-18415T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842345 | |||||||
| chr5:88842529 | G | A | 1 | a0001c0001t0019g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-142-18599C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842529 | |||||||
| chr5:88842541 | GA | G | 12 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(9): Show |
12 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-142-18612delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842541 | |||||||
| chr5:88842594 | C | CATTT | 165 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-18665_-142-18 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842594 | |||||||
| chr5:88842679 | T | C | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-142-18749A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842679 | |||||||
| chr5:88842730 | T | A | 33 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0265 others(30): Show |
34 | HG01069.hp2 HG01070.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.-142-18800A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842730 | |||||||
| chr5:88842773 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-142-18843G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842773 | |||||||
| chr5:88842901 | C | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-18971G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842901 | |||||||
| chr5:88842914 | C | T | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-18984G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842914 | |||||||
| chr5:88842989 | C | T | 1 | a0001c0001t0036g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-142-19059G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842989 | |||||||
| chr5:88843209 | C | CT | 119 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0034 others(116): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-142-19280dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843209 | |||||||
| chr5:88843251 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-19321G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843251 | |||||||
| chr5:88843271 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-142-19341A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843271 | |||||||
| chr5:88843353 | C | CA | 8 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0003g0250 others(5): Show |
8 | HG00639.hp2 HG01192.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-142-19424dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843353 | |||||||
| chr5:88843805 | C | CT | 6 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0079 others(3): Show |
6 | HG01433.hp1 HG02145.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-142-19876dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843805 | |||||||
| chr5:88843805 | CT | C | 93 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0114 others(90): Show |
95 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.-142-19876delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843805 | |||||||
| chr5:88843892 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-19962G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843892 | |||||||
| chr5:88843897 | C | T | 1 | a0001c0001t0004g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-142-19967G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843897 | |||||||
| chr5:88843961 | C | T | 1 | a0001c0001t0031g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-142-20031G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843961 | |||||||
| chr5:88843966 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-142-20036G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843966 | |||||||
| chr5:88844213 | G | A | 7 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-20283C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844213 | |||||||
| chr5:88844292 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-142-20362G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844292 | |||||||
| chr5:88844324 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-142-20394A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844324 | |||||||
| chr5:88844574 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-142-20644T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844574 | |||||||
| chr5:88844746 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-142-20816G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844746 | |||||||
| chr5:88845125 | G | A | 154 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(151): Show |
157 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.-142-21195C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845125 | |||||||
| chr5:88845145 | T | C | 148 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(145): Show |
151 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(148): Show |
intron_variant | MODIFIER | c.-142-21215A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845145 | |||||||
| chr5:88845181 | C | T | 7 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-21251G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845181 | |||||||
| chr5:88845213 | G | T | 164 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
167 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(164): Show |
intron_variant | MODIFIER | c.-142-21283C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845213 | |||||||
| chr5:88845441 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-142-21511A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845441 | |||||||
| chr5:88845473 | G | A | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-21543C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845473 | |||||||
| chr5:88845626 | A | G | 1 | a0001c0001t0003g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-142-21696T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845626 | |||||||
| chr5:88845655 | G | A | 3 | a0001c0001t0002g0077 a0001c0001t0016g0078 a0001c0001t0016g0083 |
3 | HG01169.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-142-21725C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845655 | |||||||
| chr5:88845723 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-21793C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845723 | |||||||
| chr5:88845770 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-142-21840C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845770 | |||||||
| chr5:88845772 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-142-21842C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845772 | |||||||
| chr5:88845945 | T | C | 1 | a0001c0001t0008g0111 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-142-22015A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845945 | |||||||
| chr5:88845984 | T | G | 2 | a0001c0001t0001g0040 a0001c0001t0003g0014 |
2 | HG02040.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-142-22054A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845984 | |||||||
| chr5:88846016 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-142-22086T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846016 | |||||||
| chr5:88846070 | CT | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0276 a0001c0001t0003g0275 others(5): Show |
8 | HG02132.hp1 NA18941.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-142-22141delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846070 | |||||||
| chr5:88846208 | C | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-22278G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846208 | |||||||
| chr5:88846230 | G | A | 5 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0015g0085 others(2): Show |
5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-22300C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846230 | |||||||
| chr5:88846358 | A | G | 1 | a0001c0001t0003g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-142-22428T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846358 | |||||||
| chr5:88846619 | G | C | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-22689C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846619 | |||||||
| chr5:88847392 | A | G | 1 | a0001c0001t0004g0107 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-142-23462T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847392 | |||||||
| chr5:88847709 | C | T | 165 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-23779G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847709 | |||||||
| chr5:88847809 | A | T | 15 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(12): Show |
15 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-142-23879T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847809 | |||||||
| chr5:88847932 | A | G | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(50): Show |
54 | HG00597.hp1 HG01243.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.-142-24002T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847932 | |||||||
| chr5:88847979 | C | T | 5 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0246 others(2): Show |
5 | HG00642.hp1 HG01192.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-24049G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847979 | |||||||
| chr5:88848209 | A | G | 165 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-24279T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848209 | |||||||
| chr5:88848274 | T | C | 76 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
77 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(74): Show |
intron_variant | MODIFIER | c.-142-24344A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848274 | |||||||
| chr5:88848417 | G | A | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
51 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(48): Show |
intron_variant | MODIFIER | c.-142-24487C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848417 | |||||||
| chr5:88848479 | G | C | 2 | a0001c0001t0002g0207 a0001c0001t0004g0006 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-142-24549C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848479 | |||||||
| chr5:88848703 | A | G | 164 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
167 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(164): Show |
intron_variant | MODIFIER | c.-142-24773T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848703 | |||||||
| chr5:88848852 | T | C | 72 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0027 others(69): Show |
74 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.-142-24922A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848852 | |||||||
| chr5:88848869 | T | C | 71 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0232 others(68): Show |
73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.-142-24939A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848869 | |||||||
| chr5:88848877 | G | T | 1 | a0001c0001t0002g0185 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-142-24947C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848877 | |||||||
| chr5:88849005 | G | A | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-142-25075C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849005 | |||||||
| chr5:88849008 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-142-25078C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849008 | |||||||
| chr5:88849083 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-142-25153T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849083 | |||||||
| chr5:88849145 | T | G | 19 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0209 others(16): Show |
20 | HG00597.hp1 HG04184.hp1 NA18944.hp1 others(17): Show |
intron_variant | MODIFIER | c.-142-25215A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849145 | |||||||
| chr5:88849150 | C | CA | 34 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0076 others(31): Show |
34 | HG00544.hp1 HG00597.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-142-25221dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | |||||||
| chr5:88849150 | C | CAA | 62 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0232 others(59): Show |
64 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.-142-25222_-142-25 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | |||||||
| chr5:88849150 | C | CAAA | 12 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0003g0230 others(9): Show |
12 | HG00639.hp2 HG01192.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-142-25223_-142-25 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | |||||||
| chr5:88849150 | CA | C | 21 | a0001c0001t0001g0056 a0001c0001t0001g0122 a0001c0001t0001g0133 others(18): Show |
21 | HG00639.hp1 HG01255.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-142-25221delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | |||||||
| chr5:88849172 | T | C | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-25242A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849172 | |||||||
| chr5:88849174 | C | A | 1 | a0001c0001t0035g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-142-25244G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849174 | |||||||
| chr5:88849267 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-142-25337G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849267 | |||||||
| chr5:88849306 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0002g0157 |
2 | NA18956.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-142-25376T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849306 | |||||||
| chr5:88849647 | T | C | 1 | a0001c0001t0013g0150 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-142-25717A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849647 | |||||||
| chr5:88849653 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-142-25723C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849653 | |||||||
| chr5:88849661 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-142-25731T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849661 | |||||||
| chr5:88850014 | C | T | 1 | a0001c0001t0033g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-142-26084G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850014 | |||||||
| chr5:88850084 | C | G | 15 | a0001c0001t0001g0069 a0001c0001t0002g0025 a0001c0001t0002g0049 others(12): Show |
15 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-142-26154G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850084 | |||||||
| chr5:88850105 | G | GA | 87 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0096 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-142-26176_-142-26 others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850105 | |||||||
| chr5:88850106 | C | G | 87 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0096 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-142-26176G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850106 | |||||||
| chr5:88850125 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-142-26195G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850125 | |||||||
| chr5:88850183 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-142-26253C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850183 | |||||||
| chr5:88850460 | G | A | 1 | a0001c0001t0008g0111 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-142-26530C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850460 | |||||||
| chr5:88850503 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-142-26573T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850503 | |||||||
| chr5:88850688 | A | G | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-26758T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850688 | |||||||
| chr5:88850721 | T | C | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-26791A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850721 | |||||||
| chr5:88850883 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-142-26953C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850883 | |||||||
| chr5:88850956 | T | G | 3 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0036g0017 |
3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-142-27026A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850956 | |||||||
| chr5:88851035 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-142-27105A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851035 | |||||||
| chr5:88851102 | G | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-27172C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851102 | |||||||
| chr5:88851188 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-142-27258C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851188 | |||||||
| chr5:88851233 | C | CA | 41 | a0001c0001t0001g0026 a0001c0001t0002g0024 a0001c0001t0002g0033 others(38): Show |
42 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-142-27304dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | |||||||
| chr5:88851233 | C | CAA | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0069 others(67): Show |
71 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-142-27305_-142-27 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | |||||||
| chr5:88851233 | C | CAAA | 13 | a0001c0001t0001g0011 a0001c0001t0002g0007 a0001c0001t0002g0012 others(10): Show |
13 | HG00597.hp1 HG01243.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-142-27306_-142-27 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | |||||||
| chr5:88851233 | CA | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0094 a0001c0001t0002g0046 others(3): Show |
6 | HG01884.hp1 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-27304delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | |||||||
| chr5:88851233 | CAA | C | 80 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0096 others(77): Show |
81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-142-27305_-142-27 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | |||||||
| chr5:88851268 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-142-27338A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851268 | |||||||
| chr5:88851281 | C | A | 2 | a0001c0001t0007g0021 a0001c0001t0007g0022 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-142-27351G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851281 | |||||||
| chr5:88851375 | T | C | 69 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0232 others(66): Show |
71 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.-142-27445A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851375 | |||||||
| chr5:88851443 | T | A | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-27513A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851443 | |||||||
| chr5:88851565 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-142-27635T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851565 | |||||||
| chr5:88851643 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-142-27713G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851643 | |||||||
| chr5:88851816 | A | C | 1 | a0001c0001t0008g0072 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-142-27886T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851816 | |||||||
| chr5:88851954 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28024C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851954 | |||||||
| chr5:88852072 | A | G | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-28142T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852072 | |||||||
| chr5:88852122 | C | T | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-28192G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852122 | |||||||
| chr5:88852224 | C | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28294G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852224 | |||||||
| chr5:88852233 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-28303A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852233 | |||||||
| chr5:88852620 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-142-28690G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852620 | |||||||
| chr5:88852698 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-142-28768G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852698 | |||||||
| chr5:88852700 | G | A | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-28770C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852700 | |||||||
| chr5:88852821 | A | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28891T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852821 | |||||||
| chr5:88852826 | A | C | 1 | a0001c0001t0025g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-142-28896T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852826 | |||||||
| chr5:88852872 | G | A | 3 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0036g0017 |
3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-142-28942C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852872 | |||||||
| chr5:88852879 | C | T | 9 | a0001c0001t0001g0069 a0001c0001t0005g0018 a0001c0001t0005g0019 others(6): Show |
9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-142-28949G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852879 | |||||||
| chr5:88852884 | C | T | 1 | a0001c0001t0012g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-142-28954G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852884 | |||||||
| chr5:88852893 | G | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28963C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852893 | |||||||
| chr5:88853002 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-142-29072A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853002 | |||||||
| chr5:88853041 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-29111A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853041 | |||||||
| chr5:88853106 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-142-29176G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853106 | |||||||
| chr5:88853182 | C | T | 2 | a0001c0001t0004g0089 a0001c0001t0004g0090 |
2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-142-29252G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853182 | |||||||
| chr5:88853474 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+29481T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853474 | |||||||
| chr5:88853509 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+29446C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853509 | |||||||
| chr5:88853592 | A | T | 1 | a0001c0001t0002g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-143+29363T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853592 | |||||||
| chr5:88853643 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0008g0072 a0001c0001t0008g0073 others(3): Show |
6 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+29312A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853643 | |||||||
| chr5:88853724 | G | T | 4 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0015g0085 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+29231C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853724 | |||||||
| chr5:88853831 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+29124G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853831 | |||||||
| chr5:88853836 | G | T | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-143+29119C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853836 | |||||||
| chr5:88853930 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+29025G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853930 | |||||||
| chr5:88853955 | T | C | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-143+29000A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853955 | |||||||
| chr5:88854129 | A | G | 37 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0265 others(34): Show |
38 | HG01069.hp2 HG01070.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.-143+28826T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854129 | |||||||
| chr5:88854358 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+28597C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854358 | |||||||
| chr5:88854472 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+28483C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854472 | |||||||
| chr5:88854567 | G | C | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+28388C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854567 | |||||||
| chr5:88854580 | T | C | 2 | a0001c0001t0005g0018 a0001c0001t0005g0019 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-143+28375A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854580 | |||||||
| chr5:88854606 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-143+28349A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854606 | |||||||
| chr5:88854650 | T | C | 1 | a0001c0001t0002g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-143+28305A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854650 | |||||||
| chr5:88854683 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-143+28272G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854683 | |||||||
| chr5:88854924 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-143+28031G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854924 | |||||||
| chr5:88854984 | T | G | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+27971A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854984 | |||||||
| chr5:88855175 | T | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+27780A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855175 | |||||||
| chr5:88855546 | C | G | 1 | a0001c0001t0003g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-143+27409G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855546 | |||||||
| chr5:88855610 | C | A | 7 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+27345G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855610 | |||||||
| chr5:88855817 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-143+27138A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855817 | |||||||
| chr5:88855853 | A | G | 1 | a0001c0001t0012g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-143+27102T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855853 | |||||||
| chr5:88855856 | G | A | 5 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0015g0085 others(2): Show |
5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+27099C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855856 | |||||||
| chr5:88855856 | G | T | 1 | a0001c0001t0003g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-143+27099C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855856 | |||||||
| chr5:88855971 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-143+26984G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855971 | |||||||
| chr5:88856067 | G | C | 3 | a0001c0001t0004g0088 a0001c0001t0005g0086 a0001c0001t0005g0087 |
3 | HG02451.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-143+26888C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856067 | |||||||
| chr5:88856300 | C | T | 247 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(244): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-143+26655G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856300 | |||||||
| chr5:88856385 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+26570A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856385 | |||||||
| chr5:88856521 | G | A | 1 | a0001c0001t0020g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-143+26434C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856521 | |||||||
| chr5:88856712 | C | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0184 a0001c0001t0002g0185 others(41): Show |
45 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.-143+26243G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856712 | |||||||
| chr5:88856757 | C | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+26198G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856757 | |||||||
| chr5:88857002 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0054 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-143+25953G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857002 | |||||||
| chr5:88857152 | T | C | 4 | a0001c0001t0004g0089 a0001c0001t0004g0090 a0001c0001t0004g0092 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+25803A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857152 | |||||||
| chr5:88857301 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-143+25654T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857301 | |||||||
| chr5:88857579 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-143+25376G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857579 | |||||||
| chr5:88857631 | C | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+25324G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857631 | |||||||
| chr5:88857635 | G | A | 5 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0015g0085 others(2): Show |
5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+25320C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857635 | |||||||
| chr5:88857872 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-143+25083G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857872 | |||||||
| chr5:88858024 | C | T | 1 | a0001c0001t0007g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143+24931G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858024 | |||||||
| chr5:88858057 | C | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+24898G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858057 | |||||||
| chr5:88858258 | T | A | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+24697A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858258 | |||||||
| chr5:88858434 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-143+24521A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858434 | |||||||
| chr5:88858542 | G | A | 3 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0036g0017 |
3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-143+24413C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858542 | |||||||
| chr5:88858798 | T | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+24157A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858798 | |||||||
| chr5:88858799 | A | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0184 a0001c0001t0002g0185 others(41): Show |
45 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.-143+24156T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858799 | |||||||
| chr5:88858920 | T | C | 3 | a0001c0001t0004g0088 a0001c0001t0005g0086 a0001c0001t0005g0087 |
3 | HG02451.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-143+24035A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858920 | |||||||
| chr5:88858953 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-143+24002A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858953 | |||||||
| chr5:88858981 | C | T | 1 | a0001c0001t0015g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-143+23974G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858981 | |||||||
| chr5:88859292 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+23663C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859292 | |||||||
| chr5:88859700 | T | C | 7 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+23255A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859700 | |||||||
| chr5:88859705 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-143+23250C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859705 | |||||||
| chr5:88859775 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-143+23180A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859775 | |||||||
| chr5:88860293 | G | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | NA18747.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-143+22662C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860293 | |||||||
| chr5:88860309 | A | C | 1 | a0001c0001t0033g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-143+22646T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860309 | |||||||
| chr5:88860323 | C | CT | 10 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+22631dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860323 | |||||||
| chr5:88860613 | C | T | 1 | a0001c0001t0037g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-143+22342G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860613 | |||||||
| chr5:88860637 | G | A | 11 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0043 others(8): Show |
11 | HG00544.hp1 HG02015.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-143+22318C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860637 | |||||||
| chr5:88860749 | T | C | 1 | a0001c0001t0028g0173 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-143+22206A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860749 | |||||||
| chr5:88860800 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+22155A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860800 | |||||||
| chr5:88860833 | T | C | 1 | a0001c0001t0003g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-143+22122A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860833 | |||||||
| chr5:88860897 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0002g0007 a0001c0001t0002g0012 |
3 | HG02486.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-143+22058A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860897 | |||||||
| chr5:88861006 | C | T | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143+21949G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861006 | |||||||
| chr5:88861153 | C | T | 282 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(279): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-143+21802G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861153 | |||||||
| chr5:88861164 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-143+21791G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861164 | |||||||
| chr5:88861467 | T | C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+21488A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861467 | |||||||
| chr5:88861484 | G | A | 2 | a0001c0001t0015g0085 a0001c0001t0015g0093 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143+21471C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861484 | |||||||
| chr5:88861735 | T | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0076 others(100): Show |
104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-143+21220A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861735 | |||||||
| chr5:88861846 | A | G | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-143+21109T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861846 | |||||||
| chr5:88861921 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-143+21034T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861921 | |||||||
| chr5:88862065 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0054 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-143+20890A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862065 | |||||||
| chr5:88862262 | T | C | 4 | a0001c0001t0006g0001 a0001c0001t0006g0153 a0001c0001t0006g0154 others(1): Show |
5 | NA18941.hp1 NA18945.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+20693A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862262 | |||||||
| chr5:88862329 | G | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(83): Show |
87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-143+20626C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862329 | |||||||
| chr5:88862650 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-143+20305A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862650 | |||||||
| chr5:88862669 | AT | A | 11 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0209 others(8): Show |
12 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.-143+20285delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862669 | |||||||
| chr5:88862847 | G | A | 2 | a0001c0001t0003g0259 a0001c0001t0003g0288 |
2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-143+20108C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862847 | |||||||
| chr5:88863274 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-143+19681A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863274 | |||||||
| chr5:88863356 | T | A | 245 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(242): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.-143+19599A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863356 | |||||||
| chr5:88863468 | C | T | 4 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0015g0085 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+19487G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863468 | |||||||
| chr5:88863474 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+19481C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863474 | |||||||
| chr5:88863509 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-143+19446T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863509 | |||||||
| chr5:88863706 | T | C | 1 | a0001c0001t0003g0055 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-143+19249A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863706 | |||||||
| chr5:88863824 | C | CT | 94 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(91): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-143+19130dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863824 | |||||||
| chr5:88863856 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-143+19099G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863856 | |||||||
| chr5:88863891 | G | A | 3 | a0001c0001t0002g0027 a0001c0001t0007g0021 a0001c0001t0007g0022 |
3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-143+19064C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863891 | |||||||
| chr5:88864023 | T | C | 2 | a0001c0001t0004g0075 a0001c0001t0004g0084 |
2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-143+18932A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864023 | |||||||
| chr5:88864149 | T | G | 91 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(88): Show |
92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-143+18806A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864149 | |||||||
| chr5:88864150 | TG | T | 91 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0094 others(88): Show |
92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-143+18804delC | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864150 | |||||||
| chr5:88864151 | G | T | 1 | a0001c0001t0007g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143+18804C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864151 | |||||||
| chr5:88864151 | GT | G | 153 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(150): Show |
156 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.-143+18803delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864151 | |||||||
| chr5:88864152 | T | G | 1 | a0001c0001t0007g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143+18803A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864152 | |||||||
| chr5:88864381 | A | C | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+18574T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864381 | |||||||
| chr5:88864537 | C | T | 101 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0076 others(98): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-143+18418G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864537 | |||||||
| chr5:88864643 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+18312C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864643 | |||||||
| chr5:88864725 | G | C | 5 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0015g0085 others(2): Show |
5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+18230C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864725 | |||||||
| chr5:88864767 | A | T | 3 | a0001c0001t0001g0145 a0001c0001t0002g0105 a0001c0001t0002g0136 |
3 | NA19065.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-143+18188T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864767 | |||||||
| chr5:88864767 | AT | A | 71 | a0001c0001t0001g0126 a0001c0001t0001g0276 a0001c0001t0002g0191 others(68): Show |
73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.-143+18187delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864767 | |||||||
| chr5:88864836 | G | A | 3 | a0001c0001t0005g0018 a0001c0001t0019g0071 a0001c0001t0024g0070 |
3 | HG01243.hp1 HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-143+18119C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864836 | |||||||
| chr5:88864846 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+18109G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864846 | |||||||
| chr5:88864895 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0002g0157 |
2 | NA18956.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-143+18060C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864895 | |||||||
| chr5:88864905 | T | C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+18050A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864905 | |||||||
| chr5:88864998 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-143+17957G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864998 | |||||||
| chr5:88865020 | C | T | 3 | a0001c0001t0004g0088 a0001c0001t0005g0086 a0001c0001t0005g0087 |
3 | HG02451.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-143+17935G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865020 | |||||||
| chr5:88865493 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-143+17462A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865493 | |||||||
| chr5:88865564 | G | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-143+17391C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865564 | |||||||
| chr5:88865600 | T | C | 101 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0076 others(98): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-143+17355A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865600 | |||||||
| chr5:88865834 | G | T | 7 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0296 others(4): Show |
7 | HG00639.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+17121C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865834 | |||||||
| chr5:88865853 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-143+17102A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865853 | |||||||
| chr5:88865893 | T | C | 4 | a0001c0001t0007g0296 a0001c0001t0007g0297 a0001c0001t0015g0085 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+17062A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865893 | |||||||
| chr5:88865899 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-143+17056A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865899 | |||||||
| chr5:88865947 | G | C | 1 | a0001c0001t0003g0031 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-143+17008C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865947 | |||||||
| chr5:88865967 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-143+16988G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865967 | |||||||
| chr5:88866032 | G | T | 9 | a0001c0001t0001g0069 a0001c0001t0005g0018 a0001c0001t0005g0019 others(6): Show |
9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+16923C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866032 | |||||||
| chr5:88866057 | G | A | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+16898C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866057 | |||||||
| chr5:88866165 | G | A | 9 | a0001c0001t0001g0069 a0001c0001t0005g0018 a0001c0001t0005g0019 others(6): Show |
9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+16790C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866165 | |||||||
| chr5:88866221 | T | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+16734A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866221 | |||||||
| chr5:88866277 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-143+16678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866277 | |||||||
| chr5:88866331 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-143+16624C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866331 | |||||||
| chr5:88866428 | C | G | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+16527G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866428 | |||||||
| chr5:88866485 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0003g0095 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+16470C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866485 | |||||||
| chr5:88866593 | G | A | 1 | a0001c0001t0003g0290 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-143+16362C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866593 | |||||||
| chr5:88866859 | T | C | 2 | a0001c0001t0003g0238 a0001c0001t0003g0280 |
2 | HG01099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-143+16096A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866859 | |||||||
| chr5:88866940 | G | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0185 a0001c0001t0002g0209 others(9): Show |
13 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.-143+16015C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866940 | |||||||
| chr5:88867032 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-143+15923G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867032 | |||||||
| chr5:88867117 | T | A | 8 | a0001c0001t0001g0056 a0001c0001t0002g0025 a0001c0001t0002g0057 others(5): Show |
8 | HG02027.hp1 NA18747.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.-143+15838A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867117 | |||||||
| chr5:88867520 | A | C | 1 | a0001c0001t0012g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-143+15435T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867520 | |||||||
| chr5:88867917 | C | T | 2 | a0001c0001t0003g0230 a0001c0001t0003g0231 |
2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-143+15038G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867917 | |||||||
| chr5:88867919 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-143+15036G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867919 | |||||||
| chr5:88867954 | G | A | 105 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0076 others(102): Show |
106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-143+15001C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867954 | |||||||
| chr5:88868251 | AT | A | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+14703delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868251 | |||||||
| chr5:88868260 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0003g0095 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+14695A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868260 | |||||||
| chr5:88868314 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-143+14641T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868314 | |||||||
| chr5:88868370 | C | A | 9 | a0001c0001t0001g0069 a0001c0001t0005g0018 a0001c0001t0005g0019 others(6): Show |
9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+14585G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868370 | |||||||
| chr5:88868412 | G | A | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-143+14543C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868412 | |||||||
| chr5:88868677 | T | A | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-143+14278A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868677 | |||||||
| chr5:88868782 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-143+14173C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868782 | |||||||
| chr5:88868906 | C | T | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-143+14049G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868906 | |||||||
| chr5:88869189 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-143+13766T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869189 | |||||||
| chr5:88869252 | C | CAT | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0165 |
3 | HG00642.hp2 HG01255.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-143+13701_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | |||||||
| chr5:88869252 | C | CATATATA others(3): Show |
1 | a0001c0001t0010g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-143+13693_-143+13 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | |||||||
| chr5:88869252 | C | CATATATA others(9): Show |
1 | a0001c0001t0003g0258 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-143+13687_-143+13 others(22): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | |||||||
| chr5:88869252 | CAT | C | 27 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(24): Show |
27 | HG00099.hp1 HG00733.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-143+13701_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | |||||||
| chr5:88869252 | CATATATA others(23): Show |
C | 1 | a0001c0001t0003g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-143+13673_-143+13 others(36): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | |||||||
| chr5:88869254 | T | TATATATA others(49): Show |
1 | a0001c0001t0002g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-143+13700_-143+13 others(62): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869254 | |||||||
| chr5:88869254 | T | TATATATA others(69): Show |
1 | a0001c0001t0022g0194 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-143+13700_-143+13 others(82): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869254 | |||||||
| chr5:88869254 | T | TATATATA others(33): Show |
1 | a0001c0001t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-143+13700_-143+13 others(46): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869254 | |||||||
| chr5:88869256 | T | TATATATA others(47): Show |
4 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0221 others(1): Show |
4 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+13698_-143+13 others(60): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869256 | |||||||
| chr5:88869258 | T | TATATATA others(69): Show |
2 | a0001c0001t0002g0191 a0001c0001t0002g0197 |
2 | NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-143+13696_-143+13 others(82): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869258 | |||||||
| chr5:88869260 | T | TATATATA others(29): Show |
1 | a0001c0001t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-143+13694_-143+13 others(42): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869260 | |||||||
| chr5:88869260 | TATATATA others(11): Show |
T | 7 | a0001c0001t0001g0114 a0001c0001t0003g0095 a0001c0001t0003g0117 others(4): Show |
7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(24): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869260 | |||||||
| chr5:88869262 | TATATATA others(9): Show |
T | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+13677_-143+13 others(22): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869262 | |||||||
| chr5:88869264 | T | C | 1 | a0001c0001t0003g0266 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-143+13691A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869264 | |||||||
| chr5:88869264 | TATATATA others(7): Show |
T | 4 | a0001c0001t0001g0094 a0001c0001t0002g0201 a0001c0001t0004g0206 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869264 | |||||||
| chr5:88869266 | TATATATA others(5): Show |
T | 25 | a0001c0001t0001g0040 a0001c0001t0002g0002 a0001c0001t0002g0184 others(22): Show |
26 | HG00597.hp1 HG01168.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869266 | |||||||
| chr5:88869267 | A | G | 1 | a0001c0001t0003g0268 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-143+13688T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869267 | |||||||
| chr5:88869268 | TATATATA others(3): Show |
T | 22 | a0001c0001t0001g0069 a0001c0001t0001g0120 a0001c0001t0002g0024 others(19): Show |
22 | HG01123.hp1 HG01496.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869268 | |||||||
| chr5:88869270 | TATATATA others(1): Show |
T | 18 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0043 others(15): Show |
18 | HG00544.hp1 HG01891.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869270 | |||||||
| chr5:88869272 | T | TATATATA others(53): Show |
1 | a0001c0001t0023g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-143+13682_-143+13 others(66): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869272 | |||||||
| chr5:88869272 | T | TATATATA others(35): Show |
1 | a0001c0001t0011g0029 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-143+13682_-143+13 others(48): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869272 | |||||||
| chr5:88869272 | TATATAC | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0039 others(16): Show |
19 | HG00642.hp1 HG01099.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869272 | |||||||
| chr5:88869274 | TATAC | T | 27 | a0001c0001t0001g0056 a0001c0001t0001g0096 a0001c0001t0001g0110 others(24): Show |
28 | HG01358.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869274 | |||||||
| chr5:88869274 | TATACATA others(15): Show |
T | 3 | a0001c0001t0002g0027 a0001c0001t0007g0021 a0001c0001t0007g0022 |
3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-143+13659_-143+13 others(28): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869274 | |||||||
| chr5:88869275 | A | ATATATAC others(77): Show |
1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-143+13679_-143+13 others(90): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869275 | |||||||
| chr5:88869276 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0004g0107 a0001c0001t0009g0181 |
3 | HG01358.hp1 HG01928.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-143+13679A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869276 | |||||||
| chr5:88869276 | TAC | T | 34 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0261 others(31): Show |
34 | HG00099.hp2 HG00673.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869276 | |||||||
| chr5:88869276 | TACATATA others(13): Show |
T | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-143+13659_-143+13 others(26): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869276 | |||||||
| chr5:88869277 | A | ATATATAC others(101): Show |
1 | a0001c0001t0001g0192 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-143+13677_-143+13 others(114): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869277 | |||||||
| chr5:88869278 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0026 others(35): Show |
38 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-143+13677G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869278 | |||||||
| chr5:88869280 | T | C | 16 | a0001c0001t0001g0096 a0001c0001t0001g0110 a0001c0001t0001g0133 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-143+13675A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | |||||||
| chr5:88869280 | T | TATATACA others(49): Show |
1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-143+13674_-143+13 others(62): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | |||||||
| chr5:88869280 | T | TATATACA others(63): Show |
1 | a0001c0001t0002g0199 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-143+13674_-143+13 others(76): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | |||||||
| chr5:88869280 | T | TATATATA others(29): Show |
3 | a0001c0001t0001g0165 a0001c0001t0002g0166 a0001c0001t0018g0123 |
3 | HG01123.hp2 HG01255.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-143+13639_-143+13 others(42): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | |||||||
| chr5:88869280 | T | TATATATA others(11): Show |
1 | a0001c0001t0001g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-143+13674_-143+13 others(24): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | |||||||
| chr5:88869280 | T | TATATATA others(15): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-143+13674_-143+13 others(28): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | |||||||
| chr5:88869281 | A | G | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+13674T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869281 | |||||||
| chr5:88869284 | T | C | 3 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0220 |
3 | HG02148.hp2 HG02273.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-143+13671A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869284 | |||||||
| chr5:88869286 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-143+13669A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869286 | |||||||
| chr5:88869294 | T | C | 3 | a0001c0001t0001g0101 a0001c0001t0004g0107 a0001c0001t0009g0181 |
3 | HG01928.hp1 HG02965.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-143+13661A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869294 | |||||||
| chr5:88869296 | C | T | 44 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0001g0114 others(41): Show |
44 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-143+13659G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869296 | |||||||
| chr5:88869296 | CACAT | C | 55 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(52): Show |
55 | HG00544.hp1 HG01123.hp1 HG01433.hp1 others(52): Show |
intron_variant | MODIFIER | c.-143+13655_-143+13 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869296 | |||||||
| chr5:88869296 | CACATAT | C | 89 | a0001c0001t0001g0094 a0001c0001t0001g0261 a0001c0001t0001g0276 others(86): Show |
92 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.-143+13653_-143+13 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869296 | |||||||
| chr5:88869298 | C | T | 30 | a0001c0001t0001g0101 a0001c0001t0001g0192 a0001c0001t0002g0007 others(27): Show |
30 | HG01243.hp1 HG01928.hp1 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.-143+13657G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869298 | |||||||
| chr5:88869300 | T | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0176 a0001c0001t0005g0018 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+13655A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | |||||||
| chr5:88869300 | T | TATATATA others(27): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0171 |
2 | HG01515.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-143+13654_-143+13 others(40): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | |||||||
| chr5:88869300 | T | TATATATA others(27): Show |
1 | a0001c0001t0004g0146 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-143+13654_-143+13 others(40): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | |||||||
| chr5:88869300 | T | TATATATA others(29): Show |
1 | a0001c0001t0001g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-143+13654_-143+13 others(42): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | |||||||
| chr5:88869302 | T | C | 12 | a0001c0001t0002g0191 a0001c0001t0002g0195 a0001c0001t0002g0197 others(9): Show |
12 | HG02129.hp2 HG03139.hp2 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.-143+13653A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869302 | |||||||
| chr5:88869302 | T | TATATACA others(57): Show |
1 | a0001c0001t0002g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-143+13652_-143+13 others(70): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869302 | |||||||
| chr5:88869303 | A | ACG | 4 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0221 others(1): Show |
4 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+13651_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | |||||||
| chr5:88869303 | A | ATATACAT others(47): Show |
1 | a0001c0001t0002g0190 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-143+13651_-143+13 others(60): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | |||||||
| chr5:88869303 | A | ATATACGT others(47): Show |
1 | a0001c0001t0002g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-143+13651_-143+13 others(60): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | |||||||
| chr5:88869303 | A | ATATATAC others(49): Show |
2 | a0001c0001t0002g0220 a0001c0001t0002g0226 |
2 | HG02132.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-143+13651_-143+13 others(62): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | |||||||
| chr5:88869303 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-143+13652T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | |||||||
| chr5:88869312 | TATAC | T | 4 | a0001c0001t0003g0255 a0001c0001t0003g0259 a0001c0001t0003g0288 others(1): Show |
4 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+13639_-143+13 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869312 | |||||||
| chr5:88869314 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-143+13641A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869314 | |||||||
| chr5:88869314 | TAC | T | 11 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0002g0027 others(8): Show |
11 | HG02451.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-143+13639_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869314 | |||||||
| chr5:88869316 | C | T | 187 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(184): Show |
190 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.-143+13639G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869316 | |||||||
| chr5:88869426 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-143+13529C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869426 | |||||||
| chr5:88869507 | G | C | 1 | a0001c0001t0033g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-143+13448C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869507 | |||||||
| chr5:88869607 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0168 a0001c0001t0004g0138 |
3 | HG00280.hp1 HG01070.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-143+13348T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869607 | |||||||
| chr5:88869714 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-143+13241G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869714 | |||||||
| chr5:88869862 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-143+13093C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869862 | |||||||
| chr5:88869866 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0007g0021 a0001c0001t0007g0022 |
3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-143+13089G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869866 | |||||||
| chr5:88869958 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-143+12997A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869958 | |||||||
| chr5:88870244 | G | A | 45 | a0001c0001t0001g0192 a0001c0001t0002g0002 a0001c0001t0002g0184 others(42): Show |
46 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.-143+12711C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88870244 | |||||||
| chr5:88870887 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-143+12068C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88870887 | |||||||
| chr5:88871458 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-143+11497G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871458 | |||||||
| chr5:88871463 | G | A | 2 | a0001c0001t0007g0296 a0001c0001t0007g0297 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-143+11492C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871463 | |||||||
| chr5:88871605 | T | C | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-143+11350A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871605 | |||||||
| chr5:88871824 | A | G | 56 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0034 others(53): Show |
56 | HG00544.hp1 HG01099.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.-143+11131T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871824 | |||||||
| chr5:88871923 | G | C | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.-143+11032C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871923 | |||||||
| chr5:88872196 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+10759G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872196 | |||||||
| chr5:88872578 | C | G | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.-143+10377G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872578 | |||||||
| chr5:88872580 | C | T | 294 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(291): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-143+10375G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872580 | |||||||
| chr5:88872681 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | NA18979.hp1 NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-143+10274A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872681 | |||||||
| chr5:88872817 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG01261.hp1 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-143+10138C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872817 | |||||||
| chr5:88872895 | A | G | 1 | a0001c0001t0006g0001 | 2 | NA18970.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-143+10060T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872895 | |||||||
| chr5:88872978 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-143+9977C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872978 | |||||||
| chr5:88873031 | C | T | 1 | a0001c0001t0003g0257 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-143+9924G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873031 | |||||||
| chr5:88873056 | T | TAC | 14 | a0001c0001t0002g0232 a0001c0001t0003g0255 a0001c0001t0004g0004 others(11): Show |
15 | HG00741.hp1 HG01496.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-143+9897_-143+989 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873056 | |||||||
| chr5:88873138 | C | A | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.-143+9817G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873138 | |||||||
| chr5:88873669 | C | T | 1 | a0001c0001t0038g0298 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-143+9286G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873669 | |||||||
| chr5:88873708 | A | AT | 18 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0124 others(15): Show |
18 | HG00741.hp2 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-143+9246dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | A | ATT | 11 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0133 others(8): Show |
11 | HG01934.hp1 HG02451.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.-143+9245_-143+924 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | AT | A | 23 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(20): Show |
23 | HG00280.hp2 HG00733.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-143+9246delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATT | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0108 others(7): Show |
10 | HG00733.hp1 HG01081.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-143+9245_-143+924 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTT | A | 10 | a0001c0001t0002g0232 a0001c0001t0003g0238 a0001c0001t0003g0242 others(7): Show |
10 | HG00741.hp1 HG01934.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-143+9241_-143+924 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTTT | A | 59 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0237 others(56): Show |
61 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-143+9240_-143+924 others(11): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTTT others(1): Show |
A | 15 | a0001c0001t0001g0094 a0001c0001t0001g0114 a0001c0001t0002g0188 others(12): Show |
15 | HG00639.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-143+9239_-143+924 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTTT others(2): Show |
A | 52 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
53 | HG00597.hp1 HG01192.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.-143+9238_-143+924 others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0002g0027 a0001c0001t0002g0215 a0001c0001t0007g0021 others(2): Show |
5 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+9237_-143+924 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-143+9236_-143+924 others(15): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0028 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-143+9234_-143+924 others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873708 | ATTTTTTT others(7): Show |
A | 51 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(48): Show |
51 | HG00544.hp1 HG01099.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.-143+9233_-143+924 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | |||||||
| chr5:88873750 | A | G | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.-143+9205T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873750 | |||||||
| chr5:88873835 | A | G | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.-143+9120T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873835 | |||||||
| chr5:88873916 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-143+9039T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873916 | |||||||
| chr5:88873935 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0003g0095 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+9020C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873935 | |||||||
| chr5:88874162 | G | A | 3 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0036g0017 |
3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-143+8793C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874162 | |||||||
| chr5:88874190 | C | T | 17 | a0001c0001t0002g0237 a0001c0001t0002g0243 a0001c0001t0002g0244 others(14): Show |
17 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-143+8765G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874190 | |||||||
| chr5:88874226 | C | T | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+8729G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874226 | |||||||
| chr5:88874249 | T | C | 203 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(200): Show |
206 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(203): Show |
intron_variant | MODIFIER | c.-143+8706A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874249 | |||||||
| chr5:88874437 | T | C | 1 | a0001c0001t0003g0292 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-143+8518A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874437 | |||||||
| chr5:88874514 | T | C | 194 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.-143+8441A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874514 | |||||||
| chr5:88874752 | T | C | 2 | a0001c0001t0007g0296 a0001c0001t0007g0297 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-143+8203A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874752 | |||||||
| chr5:88874759 | T | C | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+8196A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874759 | |||||||
| chr5:88875013 | G | A | 2 | a0001c0001t0003g0230 a0001c0001t0003g0231 |
2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-143+7942C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875013 | |||||||
| chr5:88875048 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-143+7907A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875048 | |||||||
| chr5:88875412 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-143+7543T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875412 | |||||||
| chr5:88875470 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-143+7485A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875470 | |||||||
| chr5:88875530 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-143+7425G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875530 | |||||||
| chr5:88875679 | A | T | 1 | a0001c0001t0003g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-143+7276T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875679 | |||||||
| chr5:88875817 | C | T | 1 | a0001c0001t0002g0007 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-143+7138G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875817 | |||||||
| chr5:88875908 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-143+7047A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875908 | |||||||
| chr5:88875947 | C | A | 2 | a0001c0001t0001g0094 a0001c0001t0003g0095 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+7008G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875947 | |||||||
| chr5:88876063 | G | GT | 6 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0001g0124 others(3): Show |
6 | HG01978.hp2 HG02135.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+6891dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876063 | |||||||
| chr5:88876063 | GT | G | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(122): Show |
126 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.-143+6891delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876063 | |||||||
| chr5:88876063 | GTT | G | 65 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0232 others(62): Show |
67 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-143+6890_-143+689 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876063 | |||||||
| chr5:88876193 | T | C | 1 | a0001c0001t0018g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-143+6762A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876193 | |||||||
| chr5:88876253 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-143+6702A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876253 | |||||||
| chr5:88877014 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-143+5941T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877014 | |||||||
| chr5:88877101 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-143+5854T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877101 | |||||||
| chr5:88877199 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0003g0095 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+5756C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877199 | |||||||
| chr5:88877362 | T | C | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+5593A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877362 | |||||||
| chr5:88877843 | A | T | 2 | a0001c0001t0003g0230 a0001c0001t0003g0231 |
2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-143+5112T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877843 | |||||||
| chr5:88878027 | C | T | 2 | a0001c0001t0002g0185 a0001c0001t0008g0186 |
2 | HG00597.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-143+4928G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88878027 | |||||||
| chr5:88878087 | A | G | 1 | a0001c0001t0004g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-143+4868T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88878087 | |||||||
| chr5:88878959 | A | G | 1 | a0001c0001t0007g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-143+3996T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88878959 | |||||||
| chr5:88879068 | T | C | 1 | a0001c0001t0004g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-143+3887A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879068 | |||||||
| chr5:88879102 | A | T | 1 | a0001c0001t0018g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-143+3853T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879102 | |||||||
| chr5:88879134 | C | T | 3 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0036g0017 |
3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-143+3821G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879134 | |||||||
| chr5:88879287 | T | C | 5 | a0001c0001t0001g0177 a0001c0001t0009g0178 a0001c0001t0009g0179 others(2): Show |
5 | HG01928.hp1 NA18953.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+3668A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879287 | |||||||
| chr5:88879382 | TTA | T | 192 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(189): Show |
195 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(192): Show |
intron_variant | MODIFIER | c.-143+3571_-143+357 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879382 | |||||||
| chr5:88879434 | C | G | 214 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
217 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.-143+3521G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879434 | |||||||
| chr5:88879505 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-143+3450C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879505 | |||||||
| chr5:88879634 | T | C | 5 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 others(2): Show |
5 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+3321A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879634 | |||||||
| chr5:88879669 | T | C | 1 | a0001c0001t0005g0294 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-143+3286A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879669 | |||||||
| chr5:88879742 | T | C | 2 | a0001c0001t0004g0112 a0001c0001t0030g0113 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+3213A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879742 | |||||||
| chr5:88879794 | G | T | 1 | a0001c0001t0034g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+3161C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879794 | |||||||
| chr5:88880405 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-143+2550C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880405 | |||||||
| chr5:88880482 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-143+2473A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880482 | |||||||
| chr5:88880522 | G | A | 1 | a0001c0001t0003g0295 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-143+2433C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880522 | |||||||
| chr5:88880580 | T | C | 6 | a0001c0001t0001g0114 a0001c0001t0003g0117 a0001c0001t0004g0015 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-143+2375A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880580 | |||||||
| chr5:88880618 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-143+2337C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880618 | |||||||
| chr5:88880662 | A | G | 1 | a0001c0001t0004g0015 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-143+2293T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880662 | |||||||
| chr5:88880857 | T | C | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-143+2098A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880857 | |||||||
| chr5:88880916 | A | G | 1 | a0001c0001t0003g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-143+2039T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880916 | |||||||
| chr5:88881044 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-143+1911C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881044 | |||||||
| chr5:88881160 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-143+1795T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881160 | |||||||
| chr5:88881726 | C | CT | 221 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(218): Show |
224 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(221): Show |
intron_variant | MODIFIER | c.-143+1228dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881726 | |||||||
| chr5:88881726 | C | CTT | 8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG01981.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-143+1227_-143+122 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881726 | |||||||
| chr5:88881782 | T | C | 45 | a0001c0001t0001g0192 a0001c0001t0002g0002 a0001c0001t0002g0184 others(42): Show |
46 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.-143+1173A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881782 | |||||||
| chr5:88882393 | C | G | 1 | a0001c0001t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-143+562G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882393 | |||||||
| chr5:88882653 | T | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG00741.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-143+302A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882653 | |||||||
| chr5:88882672 | G | T | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-143+283C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882672 | |||||||
| chr5:88882843 | T | G | 1 | a0001c0001t0001g0229 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-143+112A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882843 | |||||||
| chr5:88882866 | T | C | 69 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0002g0232 others(66): Show |
71 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.-143+89A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882866 | |||||||
| chr5:88882911 | T | C | 2 | a0001c0001t0007g0296 a0001c0001t0007g0297 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-143+44A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882911 |