Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23788 |
| ensemblid | ENSG00000109919.10 |
| hgncid | 17587 |
| symbol | MTCH2 |
| name | mitochondrial carrier 2 |
| refseq_nuc | NM_014342.4 |
| refseq_prot | NP_055157.1 |
| ensembl_nuc | ENST00000302503.8 |
| ensembl_prot | ENSP00000303222.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 47617317 |
| end | 47642559 |
| strand | - |
| ver | v1.2 |
| region | chr11:47617317-47642559 |
| region5000 | chr11:47612317-47647559 |
| regionname0 | MTCH2_chr11_47617317_47642559 |
| regionname5000 | MTCH2_chr11_47612317_47647559 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 303 | 279 | 84 | 43 | 114 | 10 | 26 | 89 | MTCH2_chr11_47612317_47647559 | MTCH2 | MADAA others(298): Show |
chr11 | 47612317 | 47647559 |
| a0002 | 0/0 | 303 | 88 | 5 | 21 | 46 | 2 | 14 | 41 | MTCH2_chr11_47612317_47647559 | MTCH2 | MADAA others(298): Show |
chr11 | 47612317 | 47647559 |
| a0003 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | MADAA others(298): Show |
chr11 | 47612317 | 47647559 |
| a0004 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | MADAA others(298): Show |
chr11 | 47612317 | 47647559 |
| a0005 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | MADAA others(298): Show |
chr11 | 47612317 | 47647559 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 909 | 279 | 84 | 43 | 114 | 10 | 26 | MTCH2_chr11_47612317_47647559 | MTCH2 | ATGGC others(904): Show |
chr11 | 47612317 | 47647559 | ||
| a0002c0002 | 0/0 | 909 | 88 | 5 | 21 | 46 | 2 | 14 | MTCH2_chr11_47612317_47647559 | MTCH2 | ATGGC others(904): Show |
chr11 | 47612317 | 47647559 | ||
| a0003c0003 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | ATGGC others(904): Show |
chr11 | 47612317 | 47647559 | ||
| a0004c0004 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | ATGGC others(904): Show |
chr11 | 47612317 | 47647559 | ||
| a0005c0005 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | ATGGC others(904): Show |
chr11 | 47612317 | 47647559 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2522 | 235 | 50 | 38 | 113 | 9 | 24 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0002 | 0/0 | 2522 | 16 | 16 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0003 | 0/0 | 2522 | 6 | 0 | 3 | 0 | 1 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0004 | 0/0 | 2522 | 5 | 5 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0005 | 1/0 | 2522 | 5 | 4 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0006 | 0/0 | 2522 | 4 | 4 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0007 | 0/0 | 2518 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2513): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0008 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0010 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0011 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0012 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0001c0001t0013 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0002c0002t0001 | 0/0 | 2522 | 87 | 5 | 21 | 45 | 2 | 14 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0002c0002t0009 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0003c0003t0001 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0004c0004t0001 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| a0005c0005t0001 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | AGTGA others(2517): Show |
chr11 | 47612317 | 47647559 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 1 | 11 | 1 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0005g0017 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0011g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0001c0001t0013g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0002 | 0/0 | 10 | 0 | 4 | 5 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0002c0002t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0004c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| a0005c0005t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0047 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0036 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0268 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0089 | EUR | IBS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0096 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0050 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0216 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02735 | hp2 | a0004 | c0004 | t0001 | g0235 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0120 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0123 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0126 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03017 | hp2 | a0005 | c0005 | t0001 | g0264 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0087 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0277 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0102 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0082 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0070 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0076 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | CHB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0097 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18961 | hp1 | a0002 | c0002 | t0009 | g0099 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18993 | hp1 | a0001 | c0001 | t0010 | g0157 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ASW | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0193 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | GIH | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0103 | SAS | GIH | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0129 | REF | REF | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0017 | REF | REF | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47618877 | G | C | 1 | a0002 | 88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
missense_variant | MODERATE | c.868C>G | p.Pro290Ala | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 962/2522 | 868/912 | 290/303 | chr11 | 47618877 | |||
| chr11:47622717 | C | T | 1 | a0004 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.809G>A | p.Cys270Tyr | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/13 | 903/2522 | 809/912 | 270/303 | chr11 | 47622717 | |||
| chr11:47630596 | T | C | 1 | a0005 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.498A>G | p.Ile166Met | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/13 | 592/2522 | 498/912 | 166/303 | chr11 | 47630596 | |||
| chr11:47638776 | G | T | 1 | a0003 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.202C>A | p.Arg68Ser | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/13 | 296/2522 | 202/912 | 68/303 | chr11 | 47638776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47617458 | C | A | 2 | a0001c0001t0002 a0001c0001t0006 |
20 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1375G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1375 | chr11 | 47617458 | ||||||
| chr11:47617479 | A | G | 1 | a0002c0002t0009 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1354 | chr11 | 47617479 | ||||||
| chr11:47617511 | G | A | 1 | a0001c0001t0003 | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1322C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1322 | chr11 | 47617511 | ||||||
| chr11:47617601 | A | C | 1 | a0001c0001t0002 | 16 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1232T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1232 | chr11 | 47617601 | ||||||
| chr11:47617861 | T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 972 | chr11 | 47617861 | ||||||
| chr11:47617973 | T | G | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(13): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*860A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 860 | chr11 | 47617973 | ||||||
| chr11:47618006 | G | C | 1 | a0001c0001t0011 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*827C>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 827 | chr11 | 47618006 | ||||||
| chr11:47618042 | C | G | 2 | a0001c0001t0004 a0001c0001t0007 |
8 | HG02647.hp2 HG02809.hp2 HG02897.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*791G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 791 | chr11 | 47618042 | ||||||
| chr11:47618073 | CCTTT | C | 1 | a0001c0001t0007 | 3 | HG02809.hp2 HG02897.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*756_*759delAAAG | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 756 | chr11 | 47618073 | ||||||
| chr11:47618178 | T | A | 1 | a0001c0001t0012 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*655A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 655 | chr11 | 47618178 | ||||||
| chr11:47618581 | T | C | 1 | a0001c0001t0013 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 252 | chr11 | 47618581 | ||||||
| chr11:47618649 | G | A | 1 | a0001c0001t0003 | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*184C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 184 | chr11 | 47618649 | ||||||
| chr11:47642484 | A | C | 1 | a0001c0001t0008 | 1 | HG01168.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/13 | 19 | chr11 | 47642484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47619109 | T | C | 2 | a0002c0002t0001g0066 a0002c0002t0001g0067 |
2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.826-190A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619109 | |||||||
| chr11:47619210 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0111 a0001c0001t0001g0113 others(1): Show |
8 | HG00323.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.826-291A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619210 | |||||||
| chr11:47619316 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.826-397T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619316 | |||||||
| chr11:47619339 | C | T | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(83): Show |
108 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.826-420G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619339 | |||||||
| chr11:47619470 | G | A | 1 | a0002c0002t0001g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.826-551C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619470 | |||||||
| chr11:47619623 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.826-704A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619623 | |||||||
| chr11:47619681 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.826-762G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619681 | |||||||
| chr11:47619915 | A | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0275 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.826-996T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619915 | |||||||
| chr11:47620002 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.826-1083C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620002 | |||||||
| chr11:47620021 | G | A | 1 | a0002c0002t0001g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.826-1102C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620021 | |||||||
| chr11:47620031 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.826-1112G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620031 | |||||||
| chr11:47620071 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.826-1152G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620071 | |||||||
| chr11:47620195 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0115 |
2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.826-1276C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620195 | |||||||
| chr11:47620326 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826-1407C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620326 | |||||||
| chr11:47620335 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0174 others(4): Show |
8 | HG00408.hp1 NA18947.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.826-1416C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620335 | |||||||
| chr11:47620346 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.826-1427C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620346 | |||||||
| chr11:47620666 | A | G | 8 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0213 others(5): Show |
10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.826-1747T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620666 | |||||||
| chr11:47620677 | A | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.826-1758T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620677 | |||||||
| chr11:47620845 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(16): Show |
24 | HG00544.hp1 HG02083.hp2 HG02148.hp2 others(21): Show |
intron_variant | MODIFIER | c.825+1856G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620845 | |||||||
| chr11:47621021 | A | G | 1 | a0002c0002t0001g0093 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.825+1680T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47621021 | |||||||
| chr11:47621436 | CT | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.825+1264delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47621436 | |||||||
| chr11:47621581 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0275 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.825+1120G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47621581 | |||||||
| chr11:47622059 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0212 |
3 | HG02258.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.825+642A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47622059 | |||||||
| chr11:47622297 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.825+404T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47622297 | |||||||
| chr11:47622339 | T | A | 77 | a0001c0001t0001g0004 a0001c0001t0001g0204 a0001c0001t0001g0205 others(74): Show |
99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.825+362A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47622339 | |||||||
| chr11:47622853 | A | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG03704.hp1 HG03834.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.750-77T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47622853 | |||||||
| chr11:47623258 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.750-482C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623258 | |||||||
| chr11:47623369 | CT | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0134 others(97): Show |
123 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.750-594delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623369 | |||||||
| chr11:47623375 | T | A | 15 | a0001c0001t0002g0016 a0001c0001t0002g0030 a0001c0001t0002g0031 others(12): Show |
19 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.750-599A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623375 | |||||||
| chr11:47623375 | T | TA | 8 | a0001c0001t0001g0032 a0001c0001t0001g0175 a0001c0001t0001g0225 others(5): Show |
9 | HG01106.hp1 HG01346.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.750-600_750-599ins others(1): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623375 | |||||||
| chr11:47623375 | TTA | T | 9 | a0001c0001t0001g0133 a0001c0001t0003g0192 a0002c0002t0001g0043 others(6): Show |
9 | HG00323.hp1 HG01071.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.750-601_750-600del others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623375 | |||||||
| chr11:47623376 | T | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.750-600A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623376 | |||||||
| chr11:47623377 | A | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.750-601T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623377 | |||||||
| chr11:47623868 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.750-1092T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623868 | |||||||
| chr11:47623935 | C | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0147 |
4 | NA18945.hp1 NA18949.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.750-1159G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623935 | |||||||
| chr11:47624213 | C | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0003c0003t0001g0104 |
3 | HG01243.hp1 HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.750-1437G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624213 | |||||||
| chr11:47624231 | C | CA | 37 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0155 others(34): Show |
39 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.749+1442dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624231 | |||||||
| chr11:47624231 | CA | C | 7 | a0001c0001t0013g0268 a0002c0002t0001g0020 a0002c0002t0001g0039 others(4): Show |
8 | HG01168.hp2 NA18939.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.749+1442delT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624231 | |||||||
| chr11:47624262 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.749+1412G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624262 | |||||||
| chr11:47624286 | T | A | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.749+1388A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624286 | |||||||
| chr11:47624299 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.749+1375T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624299 | |||||||
| chr11:47624823 | C | CA | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.749+850dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624823 | |||||||
| chr11:47625028 | C | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.749+646G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625028 | |||||||
| chr11:47625036 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.749+638G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625036 | |||||||
| chr11:47625088 | AAAAAAC | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(85): Show |
111 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.749+580_749+585del others(6): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625088 | |||||||
| chr11:47625191 | C | T | 1 | a0001c0001t0002g0031 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.749+483G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625191 | |||||||
| chr11:47625218 | C | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0174 others(6): Show |
10 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.749+456G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625218 | |||||||
| chr11:47625225 | A | G | 1 | a0002c0002t0001g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.749+449T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625225 | |||||||
| chr11:47625422 | CA | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0105 others(97): Show |
124 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.749+251delT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625422 | |||||||
| chr11:47625434 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0204 a0001c0001t0001g0205 others(5): Show |
13 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.749+240T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625434 | |||||||
| chr11:47625435 | AAT | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0111 a0001c0001t0001g0130 others(13): Show |
17 | HG00544.hp2 HG01496.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.749+237_749+238del others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625435 | |||||||
| chr11:47625436 | AT | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(151): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.749+237delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625436 | |||||||
| chr11:47625437 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0165 |
2 | NA18939.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.749+237A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625437 | |||||||
| chr11:47625548 | C | G | 1 | a0001c0001t0001g0033 | 2 | NA18971.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.749+126G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625548 | |||||||
| chr11:47625568 | C | G | 1 | a0002c0002t0001g0098 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.749+106G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625568 | |||||||
| chr11:47625884 | TAC | T | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-145_682-144del others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47625884 | |||||||
| chr11:47625992 | C | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0174 others(6): Show |
10 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.682-251G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47625992 | |||||||
| chr11:47626018 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.682-277A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626018 | |||||||
| chr11:47626113 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.682-372G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626113 | |||||||
| chr11:47626237 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.682-496C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626237 | |||||||
| chr11:47626266 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.682-525C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626266 | |||||||
| chr11:47626356 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0165 |
2 | NA18939.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.682-615A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626356 | |||||||
| chr11:47626490 | G | A | 71 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(68): Show |
88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.681+590C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626490 | |||||||
| chr11:47626550 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.681+530T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626550 | |||||||
| chr11:47627010 | C | G | 26 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
30 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.681+70G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47627010 | |||||||
| chr11:47627357 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.634-230C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627357 | |||||||
| chr11:47627628 | A | AT | 15 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0184 others(12): Show |
19 | HG01243.hp1 HG01884.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.634-502dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627628 | |||||||
| chr11:47627628 | AT | A | 6 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(3): Show |
6 | HG02896.hp2 HG03098.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.634-502delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627628 | |||||||
| chr11:47627980 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.634-853A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627980 | |||||||
| chr11:47628066 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.633+887C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628066 | |||||||
| chr11:47628164 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.633+789G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628164 | |||||||
| chr11:47628298 | G | A | 2 | a0002c0002t0001g0061 a0002c0002t0001g0077 |
2 | NA18940.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.633+655C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628298 | |||||||
| chr11:47628586 | AT | A | 77 | a0001c0001t0001g0004 a0001c0001t0001g0204 a0001c0001t0001g0205 others(74): Show |
99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.633+366delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628586 | |||||||
| chr11:47628607 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.633+346A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628607 | |||||||
| chr11:47628636 | G | A | 1 | a0001c0001t0005g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.633+317C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628636 | |||||||
| chr11:47628766 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.633+187G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628766 | |||||||
| chr11:47629076 | C | G | 1 | a0001c0001t0006g0126 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.540-30G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629076 | |||||||
| chr11:47629132 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.540-86A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629132 | |||||||
| chr11:47629194 | A | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0275 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.540-148T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629194 | |||||||
| chr11:47629339 | G | A | 1 | a0002c0002t0001g0061 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.540-293C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629339 | |||||||
| chr11:47629441 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(86): Show |
112 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.540-395G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629441 | |||||||
| chr11:47629557 | G | A | 1 | a0002c0002t0001g0093 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.540-511C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629557 | |||||||
| chr11:47629587 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.540-541T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629587 | |||||||
| chr11:47629612 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.540-566G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629612 | |||||||
| chr11:47629751 | T | TA | 18 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0107 others(15): Show |
25 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.540-706dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629751 | |||||||
| chr11:47629765 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.540-719G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629765 | |||||||
| chr11:47629780 | C | T | 5 | a0001c0001t0001g0229 a0001c0001t0001g0250 a0001c0001t0001g0254 others(2): Show |
5 | HG00438.hp1 NA18960.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-734G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629780 | |||||||
| chr11:47629852 | G | T | 3 | a0002c0002t0001g0042 a0002c0002t0001g0063 a0002c0002t0001g0074 |
3 | HG00597.hp1 NA18962.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.539+703C>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629852 | |||||||
| chr11:47630025 | TATTA | T | 5 | a0001c0001t0003g0029 a0001c0001t0003g0192 a0001c0001t0003g0193 others(2): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+526_539+529del others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630025 | |||||||
| chr11:47630052 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.539+503C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630052 | |||||||
| chr11:47630287 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0196 |
4 | HG02723.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+268C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630287 | |||||||
| chr11:47630320 | G | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0162 others(2): Show |
8 | HG00733.hp1 HG01081.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.539+235C>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630320 | |||||||
| chr11:47630924 | A | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0249 a0001c0001t0001g0253 |
3 | HG00639.hp2 HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.479+112T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 7/12 | chr11 | 47630924 | |||||||
| chr11:47630951 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+85C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 7/12 | chr11 | 47630951 | |||||||
| chr11:47631378 | C | T | 4 | a0002c0002t0001g0009 a0002c0002t0001g0040 a0002c0002t0001g0041 others(1): Show |
7 | NA18944.hp1 NA18945.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+276G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 6/12 | chr11 | 47631378 | |||||||
| chr11:47631792 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.370-81C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47631792 | |||||||
| chr11:47631811 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.370-100A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47631811 | |||||||
| chr11:47632000 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.370-289T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632000 | |||||||
| chr11:47632159 | C | T | 5 | a0001c0001t0003g0029 a0001c0001t0003g0192 a0001c0001t0003g0193 others(2): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-448G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632159 | |||||||
| chr11:47632357 | A | AT | 7 | a0001c0001t0001g0142 a0001c0001t0001g0227 a0001c0001t0001g0241 others(4): Show |
7 | HG03688.hp2 HG03831.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-647dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632357 | |||||||
| chr11:47632513 | C | T | 4 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0065 others(1): Show |
4 | HG01943.hp2 HG01975.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-802G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632513 | |||||||
| chr11:47632548 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.370-837C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632548 | |||||||
| chr11:47632621 | C | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.370-910G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632621 | |||||||
| chr11:47632705 | T | C | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-994A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632705 | |||||||
| chr11:47632839 | C | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.370-1128G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632839 | |||||||
| chr11:47632890 | T | C | 1 | a0002c0002t0001g0047 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.370-1179A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632890 | |||||||
| chr11:47632947 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.370-1236C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632947 | |||||||
| chr11:47633114 | C | CT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.370-1404dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633114 | |||||||
| chr11:47633114 | C | CTT | 8 | a0001c0001t0001g0179 a0001c0001t0001g0240 a0001c0001t0006g0125 others(5): Show |
8 | HG01433.hp1 HG02615.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-1405_370-1404d others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633114 | |||||||
| chr11:47633210 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.369+1462G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633210 | |||||||
| chr11:47633254 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.369+1418G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633254 | |||||||
| chr11:47633361 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0185 |
2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.369+1311G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633361 | |||||||
| chr11:47633505 | A | AAT | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0213 others(3): Show |
8 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1165_369+1166d others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATAT | 6 | a0001c0001t0002g0221 a0002c0002t0001g0053 a0002c0002t0001g0071 others(3): Show |
6 | HG02965.hp1 NA18990.hp1 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1163_369+1166d others(6): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(1): Show |
4 | a0002c0002t0001g0043 a0002c0002t0001g0070 a0002c0002t0001g0082 others(1): Show |
4 | HG02735.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+1159_369+1166d others(10): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(3): Show |
13 | a0001c0001t0001g0007 a0001c0001t0001g0131 a0001c0001t0001g0143 others(10): Show |
17 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+1157_369+1166d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(5): Show |
17 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0130 others(14): Show |
23 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.369+1155_369+1166d others(14): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(7): Show |
24 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0136 others(21): Show |
27 | HG00408.hp1 HG00544.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.369+1153_369+1166d others(16): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(9): Show |
14 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0026 others(11): Show |
21 | HG02071.hp1 HG02145.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.369+1151_369+1166d others(18): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(11): Show |
6 | a0001c0001t0001g0154 a0001c0001t0001g0185 a0001c0001t0012g0216 others(3): Show |
8 | HG01346.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1149_369+1166d others(20): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(13): Show |
4 | a0001c0001t0001g0141 a0001c0001t0001g0179 a0001c0001t0001g0222 others(1): Show |
4 | HG04228.hp2 NA18986.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1147_369+1166d others(22): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(15): Show |
5 | a0001c0001t0001g0153 a0001c0001t0001g0168 a0002c0002t0001g0019 others(2): Show |
6 | HG01261.hp1 HG02273.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1145_369+1166d others(24): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(17): Show |
3 | a0001c0001t0001g0167 a0002c0002t0001g0090 a0002c0002t0001g0102 |
3 | HG00741.hp1 HG01243.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.369+1166_369+1167i others(26): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(19): Show |
5 | a0001c0001t0001g0152 a0002c0002t0001g0060 a0002c0002t0001g0061 others(2): Show |
5 | HG01074.hp2 HG02155.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1166_369+1167i others(28): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(21): Show |
1 | a0002c0002t0001g0059 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.369+1166_369+1167i others(30): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(23): Show |
4 | a0002c0002t0001g0047 a0002c0002t0001g0057 a0002c0002t0001g0058 others(1): Show |
4 | HG00323.hp1 HG01891.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1166_369+1167i others(32): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(25): Show |
2 | a0001c0001t0001g0199 a0001c0001t0001g0206 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.369+1166_369+1167i others(34): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(27): Show |
1 | a0002c0002t0001g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.369+1166_369+1167i others(36): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(29): Show |
1 | a0002c0002t0001g0018 | 2 | HG01175.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.369+1166_369+1167i others(38): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633505 | A | AATATATA others(31): Show |
1 | a0002c0002t0001g0039 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.369+1166_369+1167i others(40): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | |||||||
| chr11:47633516 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.369+1140_369+1155d others(18): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633516 | |||||||
| chr11:47633520 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.369+1141_369+1151d others(13): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633520 | |||||||
| chr11:47633522 | ATATATTT others(3): Show |
A | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG01168.hp2 HG01358.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+1140_369+1149d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633522 | |||||||
| chr11:47633524 | ATATTTTT others(3): Show |
A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(51): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.369+1138_369+1147d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633524 | |||||||
| chr11:47633524 | ATATTTTT others(4): Show |
A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0035 |
2 | NA18947.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.369+1137_369+1147d others(13): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633524 | |||||||
| chr11:47633526 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(23): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0004 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369+1145_369+1146i others(33): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.369+1145_369+1146i others(43): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(29): Show |
1 | a0002c0002t0001g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.369+1145_369+1146i others(38): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0004 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(39): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(27): Show |
1 | a0002c0002t0001g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(36): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(24): Show |
1 | a0002c0002t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(33): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.369+1145_369+1146i others(28): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(26): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | ATTTTTTT others(2): Show |
A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(4): Show |
8 | HG02004.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1137_369+1145d others(11): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633526 | ATTTTTTT others(3): Show |
A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0037 others(6): Show |
10 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.369+1136_369+1145d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | |||||||
| chr11:47633527 | T | TATA | 7 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0198 others(4): Show |
7 | HG02132.hp2 HG02280.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(5): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(2): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0140 a0001c0001t0001g0163 others(2): Show |
6 | HG01099.hp1 HG01109.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(11): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(4): Show |
8 | a0001c0001t0001g0278 a0001c0001t0002g0197 a0001c0001t0003g0194 others(5): Show |
8 | HG02257.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(13): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(6): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0001g0166 others(3): Show |
7 | HG02148.hp2 HG02300.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(15): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(8): Show |
5 | a0001c0001t0001g0148 a0001c0001t0001g0207 a0001c0001t0001g0212 others(2): Show |
6 | HG02258.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(17): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(10): Show |
4 | a0002c0002t0001g0002 a0002c0002t0001g0042 a0002c0002t0001g0074 others(1): Show |
4 | HG00597.hp1 HG01358.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(19): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(12): Show |
6 | a0001c0001t0001g0025 a0001c0001t0001g0144 a0001c0001t0001g0170 others(3): Show |
6 | HG02630.hp1 HG03041.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(21): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(14): Show |
5 | a0001c0001t0001g0025 a0002c0002t0001g0002 a0002c0002t0001g0045 others(2): Show |
5 | HG00438.hp2 HG02809.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(23): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(16): Show |
1 | a0001c0001t0003g0029 | 2 | HG01257.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(25): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(18): Show |
3 | a0002c0002t0001g0002 a0002c0002t0001g0052 a0002c0002t0001g0100 |
3 | HG00735.hp2 HG01192.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(27): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(20): Show |
1 | a0002c0002t0001g0002 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.369+1144_369+1145i others(29): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(22): Show |
3 | a0002c0002t0001g0048 a0002c0002t0001g0075 a0002c0002t0001g0089 |
3 | HG01515.hp1 HG03654.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(31): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(24): Show |
4 | a0001c0001t0003g0192 a0002c0002t0001g0002 a0002c0002t0001g0041 others(1): Show |
6 | HG01071.hp1 HG01074.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(33): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(26): Show |
5 | a0001c0001t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0020 others(2): Show |
5 | HG03239.hp2 HG03540.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(35): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(28): Show |
2 | a0002c0002t0001g0040 a0002c0002t0001g0073 |
2 | NA18981.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(37): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(30): Show |
1 | a0002c0002t0001g0009 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.369+1144_369+1145i others(39): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATATATA others(32): Show |
1 | a0002c0002t0001g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.369+1144_369+1145i others(41): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633527 | T | TATTATAT others(11): Show |
1 | a0001c0001t0001g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.369+1144_369+1145i others(20): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | |||||||
| chr11:47633528 | T | A | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(105): Show |
132 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.369+1144A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633528 | |||||||
| chr11:47633529 | T | A | 58 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(55): Show |
70 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.369+1143A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633529 | |||||||
| chr11:47633530 | T | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(94): Show |
117 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.369+1142A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633530 | |||||||
| chr11:47633531 | T | A | 41 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0144 others(38): Show |
47 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.369+1141A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633531 | |||||||
| chr11:47633532 | T | A | 65 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(62): Show |
74 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.369+1140A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633532 | |||||||
| chr11:47633533 | T | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0144 a0001c0001t0001g0166 others(18): Show |
22 | HG00438.hp2 HG01109.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.369+1139A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633533 | |||||||
| chr11:47633534 | T | A | 21 | a0001c0001t0001g0146 a0001c0001t0001g0174 a0001c0001t0001g0184 others(18): Show |
23 | HG00408.hp1 HG01074.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.369+1138A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633534 | |||||||
| chr11:47633535 | T | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
6 | HG02132.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1137A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633535 | |||||||
| chr11:47633536 | T | A | 4 | a0001c0001t0001g0232 a0002c0002t0001g0084 a0002c0002t0001g0101 others(1): Show |
4 | NA18942.hp2 NA18956.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1136A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633536 | |||||||
| chr11:47633537 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.369+1135A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633537 | |||||||
| chr11:47633538 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.369+1134A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633538 | |||||||
| chr11:47633779 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.369+893G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633779 | |||||||
| chr11:47633828 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.369+844G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633828 | |||||||
| chr11:47633833 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.369+839T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633833 | |||||||
| chr11:47634103 | T | C | 1 | a0002c0002t0001g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.369+569A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634103 | |||||||
| chr11:47634200 | C | T | 71 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(68): Show |
88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.369+472G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634200 | |||||||
| chr11:47634322 | T | G | 2 | a0002c0002t0001g0043 a0002c0002t0001g0097 |
2 | HG02735.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.369+350A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634322 | |||||||
| chr11:47634390 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.369+282G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634390 | |||||||
| chr11:47634443 | C | T | 1 | a0002c0002t0001g0100 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.369+229G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634443 | |||||||
| chr11:47634769 | A | AT | 38 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
49 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.307-36dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | |||||||
| chr11:47634769 | A | ATT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0033 others(49): Show |
74 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.307-37_307-36dupAA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | |||||||
| chr11:47634769 | A | ATTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0239 others(5): Show |
16 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.307-38_307-36dupAA others(1): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | |||||||
| chr11:47634769 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.307-45_307-36delAA others(8): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | |||||||
| chr11:47634808 | T | G | 1 | a0001c0001t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.307-74A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634808 | |||||||
| chr11:47634842 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.307-108C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634842 | |||||||
| chr11:47634962 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.307-228C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634962 | |||||||
| chr11:47634993 | G | C | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-259C>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634993 | |||||||
| chr11:47635067 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.307-333C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635067 | |||||||
| chr11:47635098 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.307-364C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635098 | |||||||
| chr11:47635111 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.307-377C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635111 | |||||||
| chr11:47635374 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.306+171G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635374 | |||||||
| chr11:47635421 | T | C | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.306+124A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635421 | |||||||
| chr11:47635684 | T | C | 1 | a0002c0002t0001g0049 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.280-113A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635684 | |||||||
| chr11:47635739 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280-168T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635739 | |||||||
| chr11:47635795 | T | C | 1 | a0001c0001t0005g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.280-224A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635795 | |||||||
| chr11:47635838 | A | G | 1 | a0002c0002t0001g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.280-267T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635838 | |||||||
| chr11:47635845 | G | A | 16 | a0001c0001t0002g0016 a0001c0001t0002g0030 a0001c0001t0002g0031 others(13): Show |
20 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.280-274C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635845 | |||||||
| chr11:47635984 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280-413C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635984 | |||||||
| chr11:47636128 | A | G | 1 | a0001c0001t0004g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.280-557T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636128 | |||||||
| chr11:47636519 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.280-948C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636519 | |||||||
| chr11:47636593 | G | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0196 a0001c0001t0002g0197 |
5 | HG02723.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-1022C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636593 | |||||||
| chr11:47636622 | C | A | 26 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
30 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.280-1051G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636622 | |||||||
| chr11:47636623 | G | A | 12 | a0001c0001t0002g0016 a0001c0001t0002g0030 a0001c0001t0002g0031 others(9): Show |
16 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-1052C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636623 | |||||||
| chr11:47636741 | A | C | 1 | a0001c0001t0006g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-1170T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636741 | |||||||
| chr11:47636762 | C | T | 71 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(68): Show |
88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.280-1191G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636762 | |||||||
| chr11:47636790 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280-1219C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636790 | |||||||
| chr11:47636931 | C | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0174 others(6): Show |
10 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.280-1360G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636931 | |||||||
| chr11:47636951 | C | G | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1380G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636951 | |||||||
| chr11:47636961 | G | GT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.280-1391dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636961 | |||||||
| chr11:47636961 | G | GTT | 12 | a0001c0001t0001g0108 a0001c0001t0001g0132 a0001c0001t0001g0149 others(9): Show |
12 | HG00741.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.280-1392_280-1391d others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636961 | |||||||
| chr11:47637019 | GCAATCTC others(25): Show |
G | 1 | a0002c0002t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.280-1480_280-1449d others(34): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637019 | |||||||
| chr11:47637452 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0206 a0001c0001t0001g0217 |
8 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+1247C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637452 | |||||||
| chr11:47637499 | G | GT | 6 | a0001c0001t0001g0148 a0001c0001t0001g0203 a0001c0001t0001g0247 others(3): Show |
6 | HG03041.hp2 HG03831.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1199dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637499 | |||||||
| chr11:47637578 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02257.hp1 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279+1121C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637578 | |||||||
| chr11:47637579 | T | G | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02257.hp1 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279+1120A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637579 | |||||||
| chr11:47637583 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0032 others(39): Show |
67 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+1116C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637583 | |||||||
| chr11:47637890 | T | G | 1 | a0002c0002t0001g0088 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.279+809A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637890 | |||||||
| chr11:47638129 | T | C | 1 | a0002c0002t0001g0100 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.279+570A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638129 | |||||||
| chr11:47638333 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.279+366C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638333 | |||||||
| chr11:47638360 | G | GAACACGG others(4543): Show |
1 | a0001c0001t0001g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0179 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0012g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02257.hp1 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0226 |
3 | HG01071.hp2 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4539): Show |
1 | a0001c0001t0001g0224 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0005c0005t0001g0264 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0181 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0182 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4543): Show |
5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG00408.hp1 HG02486.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0001c0001t0001g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0202 |
2 | HG03041.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4543): Show |
1 | a0001c0001t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0208 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(55): Show |
77 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4538): Show |
1 | a0001c0001t0001g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4545): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0137 others(3): Show |
7 | HG02280.hp1 HG03130.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
6 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0006g0125 others(3): Show |
6 | HG02071.hp2 HG02523.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0113 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4539): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0267 a0001c0001t0013g0268 |
3 | HG01168.hp2 HG02145.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0035 | 2 | NA19005.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0269 |
2 | HG01175.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0225 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0001c0001t0001g0227 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4539): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00639.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18949.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4549): Show |
1 | a0001c0001t0005g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4556): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4547): Show |
1 | a0001c0001t0005g0118 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4554): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18942.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0234 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0013 | 3 | HG02965.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0004c0004t0001g0235 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
3 | a0001c0001t0002g0016 a0001c0001t0002g0196 a0001c0001t0002g0197 |
5 | HG02723.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0001c0001t0002g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
5 | a0001c0001t0003g0029 a0001c0001t0003g0192 a0001c0001t0003g0193 others(2): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0001c0001t0011g0277 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0204 a0001c0001t0001g0217 others(1): Show |
9 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0146 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
8 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0213 others(5): Show |
10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4538): Show |
2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4545): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0147 |
4 | NA18945.hp1 NA18949.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0002c0002t0001g0096 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
2 | a0002c0002t0001g0092 a0002c0002t0001g0101 |
2 | NA18956.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
2 | a0002c0002t0001g0094 a0002c0002t0001g0095 |
2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
1 | a0002c0002t0001g0098 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
52 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(49): Show |
69 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 |
3 | HG00323.hp1 NA18994.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0049 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4539): Show |
1 | a0002c0002t0001g0090 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0050 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4542): Show |
1 | a0002c0002t0001g0051 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4543): Show |
1 | a0002c0002t0001g0093 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4541): Show |
1 | a0001c0001t0001g0276 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638360 | G | GAACACGG others(4540): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0003c0003t0001g0104 |
3 | HG01243.hp1 HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | |||||||
| chr11:47638367 | G | GTGAAACC others(4519): Show |
1 | a0002c0002t0001g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.279+331_279+332ins others(4526): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638367 | |||||||
| chr11:47638376 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.279+323A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638376 | |||||||
| chr11:47638386 | A | AAAAATAC others(4532): Show |
1 | a0001c0001t0001g0136 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.279+312_279+313ins others(4539): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638386 | |||||||
| chr11:47638449 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.279+250C>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638449 | |||||||
| chr11:47638488 | G | A | 1 | a0002c0002t0009g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.279+211C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638488 | |||||||
| chr11:47638491 | A | G | 1 | a0002c0002t0001g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.279+208T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638491 | |||||||
| chr11:47638503 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.279+196C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638503 | |||||||
| chr11:47638545 | C | CA | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.279+153dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638545 | |||||||
| chr11:47638545 | C | CAA | 22 | a0001c0001t0001g0115 a0001c0001t0001g0209 a0001c0001t0001g0210 others(19): Show |
24 | HG00544.hp1 HG01192.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+152_279+153dup others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638545 | |||||||
| chr11:47639331 | G | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG02630.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.88-280C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639331 | |||||||
| chr11:47639500 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.88-449T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639500 | |||||||
| chr11:47639556 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.88-505C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639556 | |||||||
| chr11:47639762 | C | T | 1 | a0002c0002t0001g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.88-711G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639762 | |||||||
| chr11:47639803 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.88-752T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639803 | |||||||
| chr11:47639867 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.88-816T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639867 | |||||||
| chr11:47639936 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.88-885C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639936 | |||||||
| chr11:47639946 | C | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(11): Show |
24 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-895G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639946 | |||||||
| chr11:47639989 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.88-938C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639989 | |||||||
| chr11:47640064 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88-1013G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640064 | |||||||
| chr11:47640203 | C | A | 1 | a0001c0001t0006g0128 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.88-1152G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640203 | |||||||
| chr11:47640203 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.88-1152G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640203 | |||||||
| chr11:47640446 | C | T | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-1395G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640446 | |||||||
| chr11:47640556 | C | T | 7 | a0001c0001t0004g0022 a0001c0001t0004g0121 a0001c0001t0004g0122 others(4): Show |
8 | HG02647.hp2 HG02809.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.88-1505G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640556 | |||||||
| chr11:47640580 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.88-1529A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640580 | |||||||
| chr11:47640681 | G | A | 1 | a0002c0002t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.88-1630C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640681 | |||||||
| chr11:47640785 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.87+1594A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640785 | |||||||
| chr11:47640806 | T | TAAGAATA others(284): Show |
1 | a0001c0001t0001g0271 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.87+1572_87+1573ins others(291): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640806 | |||||||
| chr11:47640806 | T | TAAGAATA others(285): Show |
1 | a0001c0001t0001g0272 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.87+1572_87+1573ins others(292): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640806 | |||||||
| chr11:47640806 | T | TAAGAATA others(286): Show |
1 | a0001c0001t0001g0273 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.87+1572_87+1573ins others(293): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640806 | |||||||
| chr11:47640956 | G | A | 1 | a0002c0002t0001g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.87+1423C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640956 | |||||||
| chr11:47641037 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(14): Show |
27 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.87+1342G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641037 | |||||||
| chr11:47641226 | C | T | 5 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+1153G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641226 | |||||||
| chr11:47641380 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(58): Show |
91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.87+999A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641380 | |||||||
| chr11:47641497 | A | G | 71 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(68): Show |
88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.87+882T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641497 | |||||||
| chr11:47641558 | T | C | 1 | a0001c0001t0004g0274 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.87+821A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641558 | |||||||
| chr11:47641596 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.87+783A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641596 | |||||||
| chr11:47641793 | T | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.87+586A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641793 | |||||||
| chr11:47641794 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.87+585G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641794 | |||||||
| chr11:47642090 | C | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.87+289G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47642090 | |||||||
| chr11:47642340 | G | A | 5 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+39C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47642340 |