Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4528 |
| ensemblid | ENSG00000085760.15 |
| hgncid | 7441 |
| symbol | MTIF2 |
| name | mitochondrial translational initiation factor 2 |
| refseq_nuc | NM_002453.3 |
| refseq_prot | NP_002444.2 |
| ensembl_nuc | ENST00000263629.9 |
| ensembl_prot | ENSP00000263629.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 55236595 |
| end | 55269231 |
| strand | - |
| ver | v1.2 |
| region | chr2:55236595-55269231 |
| region5000 | chr2:55231595-55274231 |
| regionname0 | MTIF2_chr2_55236595_55269231 |
| regionname5000 | MTIF2_chr2_55231595_55274231 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 727 | 213 | 36 | 58 | 88 | 8 | 23 | 69 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(722): Show |
chr2 | 55231595 | 55274231 |
| a0002 | 1/1 | 727 | 150 | 41 | 19 | 67 | 6 | 15 | 54 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(722): Show |
chr2 | 55231595 | 55274231 |
| a0003 | 0/0 | 727 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(722): Show |
chr2 | 55231595 | 55274231 |
| a0004 | 0/0 | 197 | 4 | 2 | 1 | 1 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(192): Show |
chr2 | 55231595 | 55274231 |
| a0005 | 0/0 | 727 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(722): Show |
chr2 | 55231595 | 55274231 |
| a0006 | 0/0 | 197 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(192): Show |
chr2 | 55231595 | 55274231 |
| a0007 | 0/0 | 727 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(722): Show |
chr2 | 55231595 | 55274231 |
| a0008 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | MNQKL others(722): Show |
chr2 | 55231595 | 55274231 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2181 | 171 | 34 | 36 | 79 | 7 | 15 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0001c0003 | 0/0 | 2181 | 39 | 1 | 21 | 8 | 1 | 8 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0001c0010 | 0/0 | 2181 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0001c0011 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0001c0012 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0002c0002 | 1/1 | 2181 | 132 | 41 | 14 | 57 | 4 | 14 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0002c0004 | 0/0 | 2181 | 18 | 0 | 5 | 10 | 2 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0003c0005 | 0/0 | 2181 | 9 | 0 | 0 | 9 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0004c0006 | 0/0 | 2182 | 4 | 2 | 1 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2177): Show |
chr2 | 55231595 | 55274231 | ||
| a0005c0007 | 0/0 | 2181 | 3 | 3 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0005c0014 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0006c0008 | 0/0 | 2182 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2177): Show |
chr2 | 55231595 | 55274231 | ||
| a0007c0009 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 | ||
| a0008c0013 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATGAA others(2176): Show |
chr2 | 55231595 | 55274231 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2536 | 171 | 34 | 36 | 79 | 7 | 15 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0001c0003t0001 | 0/0 | 2536 | 39 | 1 | 21 | 8 | 1 | 8 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0001c0010t0001 | 0/0 | 2536 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0001c0011t0001 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0001c0012t0001 | 0/0 | 2536 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0002c0002t0001 | 1/1 | 2536 | 131 | 40 | 14 | 57 | 4 | 14 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0002c0002t0003 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0002c0004t0001 | 0/0 | 2536 | 8 | 0 | 1 | 5 | 1 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0002c0004t0002 | 0/0 | 2536 | 10 | 0 | 4 | 5 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0003c0005t0001 | 0/0 | 2536 | 9 | 0 | 0 | 9 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0004c0006t0001 | 0/0 | 2537 | 4 | 2 | 1 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2532): Show |
chr2 | 55231595 | 55274231 |
| a0005c0007t0001 | 0/0 | 2536 | 3 | 3 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0005c0014t0001 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0006c0008t0001 | 0/0 | 2537 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2532): Show |
chr2 | 55231595 | 55274231 |
| a0007c0009t0002 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| a0008c0013t0001 | 0/0 | 2536 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | ATTCT others(2531): Show |
chr2 | 55231595 | 55274231 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 2 | 2 | 6 | 1 | 3 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0005 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0002 | 0/0 | 11 | 0 | 7 | 1 | 0 | 3 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0010t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0011t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0001c0012t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0002t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0002c0004t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0003c0005t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0003c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0003c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0004c0006t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0004c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0004c0006t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0004c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0005c0007t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0005c0007t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0005c0007t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0005c0014t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0006c0008t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0006c0008t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0007c0009t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| a0008c0013t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0013 | EUR | GBR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0084 | EUR | GBR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0241 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0230 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0237 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01070 | hp1 | a0002 | c0004 | t0002 | g0045 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0232 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01071 | hp2 | a0002 | c0004 | t0002 | g0045 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0263 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01261 | hp2 | a0002 | c0004 | t0002 | g0283 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01346 | hp2 | a0001 | c0010 | t0001 | g0193 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0124 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01433 | hp1 | a0002 | c0004 | t0002 | g0280 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0114 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0231 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01515 | hp1 | a0002 | c0004 | t0002 | g0285 | EUR | IBS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0259 | EUR | IBS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0038 | EUR | IBS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0013 | EUR | IBS | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0233 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01978 | hp1 | a0004 | c0006 | t0001 | g0202 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0257 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02015 | hp2 | a0002 | c0004 | t0002 | g0281 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02055 | hp2 | a0004 | c0006 | t0001 | g0147 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02071 | hp2 | a0002 | c0004 | t0001 | g0160 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0236 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | CDX | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02280 | hp1 | a0007 | c0009 | t0002 | g0284 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0238 | AMR | PEL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02630 | hp2 | a0005 | c0007 | t0001 | g0265 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02965 | hp1 | a0002 | c0002 | t0003 | g0278 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0276 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02976 | hp1 | a0005 | c0007 | t0001 | g0264 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0258 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0037 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | MSL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0227 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0087 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03654 | hp2 | a0002 | c0004 | t0001 | g0112 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0037 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | PJL | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | BEB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0235 | SAS | BEB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | BEB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0115 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0092 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | YRI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | YRI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18906 | hp2 | a0001 | c0011 | t0001 | g0054 | AFR | YRI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18949 | hp1 | a0003 | c0005 | t0001 | g0261 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18954 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18960 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18966 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18967 | hp1 | a0006 | c0008 | t0001 | g0071 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18969 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18970 | hp2 | a0002 | c0004 | t0002 | g0044 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18972 | hp1 | a0006 | c0008 | t0001 | g0153 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18973 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18975 | hp2 | a0002 | c0004 | t0002 | g0282 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18990 | hp1 | a0004 | c0006 | t0001 | g0207 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18990 | hp2 | a0002 | c0004 | t0001 | g0085 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18992 | hp2 | a0003 | c0005 | t0001 | g0132 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18994 | hp1 | a0008 | c0013 | t0001 | g0116 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19000 | hp2 | a0002 | c0004 | t0001 | g0125 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19002 | hp1 | a0002 | c0004 | t0002 | g0044 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | LWK | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19043 | hp1 | a0005 | c0007 | t0001 | g0063 | AFR | LWK | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19043 | hp2 | a0005 | c0014 | t0001 | g0066 | AFR | LWK | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19057 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19058 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19070 | hp1 | a0001 | c0012 | t0001 | g0162 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19074 | hp1 | a0002 | c0004 | t0001 | g0161 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19084 | hp1 | a0002 | c0004 | t0002 | g0279 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19086 | hp2 | a0002 | c0004 | t0001 | g0158 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | YRI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ASW | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20805 | hp1 | a0002 | c0004 | t0001 | g0159 | EUR | TSI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0096 | SAS | GIH | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | CLM | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02486 | hp1 | a0004 | c0006 | t0001 | g0164 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0275 | AFR | USA | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | USA | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | USA | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0110 | REF | REF | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0151 | REF | REF | MTIF2_chr2_55231595_55274231 | MTIF2 | chr2 | 55231595 | 55274231 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:55242979 | C | T | 3 | a0001 a0004 a0005 |
221 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(218): Show |
missense_variant | MODERATE | c.1666G>A | p.Val556Ile | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/16 | 1965/2536 | 1666/2184 | 556/727 | chr2 | 55242979 | |||
| chr2:55243000 | C | G | 1 | a0003 | 9 | NA18949.hp1 NA18954.hp2 NA18960.hp1 others(6): Show |
missense_variant | MODERATE | c.1645G>C | p.Val549Leu | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/16 | 1944/2536 | 1645/2184 | 549/727 | chr2 | 55243000 | |||
| chr2:55246385 | C | T | 1 | a0008 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.1058G>A | p.Gly353Asp | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/16 | 1357/2536 | 1058/2184 | 353/727 | chr2 | 55246385 | |||
| chr2:55254128 | T | TC | 2 | a0004 a0006 |
6 | HG01978.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
frameshift_variant | HIGH | c.576dupG | p.Lys193fs | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/16 | 875/2536 | 576/2184 | 192/727 | chr2 | 55254128 | |||
| chr2:55263683 | G | T | 3 | a0001 a0004 a0007 |
218 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(215): Show |
missense_variant | MODERATE | c.176C>A | p.Thr59Asn | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/16 | 475/2536 | 176/2184 | 59/727 | chr2 | 55263683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:55249455 | G | A | 1 | a0001c0010 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.921C>T | p.Tyr307Tyr | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/16 | 1220/2536 | 921/2184 | 307/727 | chr2 | 55249455 | |||
| chr2:55252648 | G | A | 1 | a0001c0011 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.670C>T | p.Leu224Leu | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/16 | 969/2536 | 670/2184 | 224/727 | chr2 | 55252648 | |||
| chr2:55254186 | T | A | 1 | a0001c0003 | 39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
synonymous_variant | LOW | c.519A>T | p.Pro173Pro | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/16 | 818/2536 | 519/2184 | 173/727 | chr2 | 55254186 | |||
| chr2:55263652 | T | C | 4 | a0001c0012 a0002c0004 a0003c0005 others(1): Show |
29 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(26): Show |
synonymous_variant | LOW | c.207A>G | p.Leu69Leu | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/16 | 506/2536 | 207/2184 | 69/727 | chr2 | 55263652 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:55268702 | G | A | 1 | a0002c0002t0003 | 1 | HG02965.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/16 | chr2 | 55268702 | |||||||
| chr2:55269225 | G | C | 2 | a0002c0004t0002 a0007c0009t0002 |
11 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-293C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 1/16 | chr2 | 55269225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:55236859 | TGATAA | T | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2012-44_2012-40del others(5): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 15/15 | chr2 | 55236859 | |||||||
| chr2:55236861 | A | G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0102 a0002c0002t0001g0103 |
4 | NA18961.hp1 NA19062.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2012-41T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 15/15 | chr2 | 55236861 | |||||||
| chr2:55237256 | A | G | 1 | a0002c0002t0001g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2011+32T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 15/15 | chr2 | 55237256 | |||||||
| chr2:55237544 | T | C | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1871-116A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237544 | |||||||
| chr2:55237564 | T | G | 19 | a0002c0004t0001g0085 a0002c0004t0001g0112 a0002c0004t0001g0124 others(16): Show |
27 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1871-136A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237564 | |||||||
| chr2:55237610 | A | C | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1871-182T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237610 | |||||||
| chr2:55237622 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1871-194A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237622 | |||||||
| chr2:55237649 | C | CT | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1871-222dupA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237649 | |||||||
| chr2:55237649 | C | CTT | 29 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0208 others(26): Show |
47 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1871-223_1871-222d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237649 | |||||||
| chr2:55237649 | CT | C | 9 | a0002c0002t0001g0018 a0002c0002t0001g0093 a0002c0002t0001g0121 others(6): Show |
10 | HG01358.hp1 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1871-222delA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237649 | |||||||
| chr2:55237649 | CTT | C | 73 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(70): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1871-223_1871-222d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237649 | |||||||
| chr2:55237743 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0128 others(6): Show |
10 | HG00140.hp2 HG00735.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1871-315C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237743 | |||||||
| chr2:55237776 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18944.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1871-348C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237776 | |||||||
| chr2:55237829 | TTAG | T | 6 | a0002c0002t0001g0023 a0002c0002t0001g0046 a0002c0002t0001g0047 others(3): Show |
7 | HG02109.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1871-404_1871-402d others(5): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237829 | |||||||
| chr2:55237921 | A | C | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1871-493T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237921 | |||||||
| chr2:55237950 | C | A | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1871-522G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237950 | |||||||
| chr2:55237978 | G | A | 20 | a0002c0004t0001g0085 a0002c0004t0001g0112 a0002c0004t0001g0124 others(17): Show |
28 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1871-550C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55237978 | |||||||
| chr2:55238059 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0194 |
3 | NA18970.hp1 NA18984.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1871-631T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238059 | |||||||
| chr2:55238067 | T | A | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1871-639A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238067 | |||||||
| chr2:55238099 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1871-671T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238099 | |||||||
| chr2:55238191 | C | CA | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(265): Show |
362 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(359): Show |
intron_variant | MODIFIER | c.1871-764dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238191 | |||||||
| chr2:55238285 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1871-857G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238285 | |||||||
| chr2:55238389 | G | GT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(119): Show |
166 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1871-962dupA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238389 | |||||||
| chr2:55238389 | G | GTT | 51 | a0001c0001t0001g0051 a0001c0001t0001g0190 a0001c0001t0001g0198 others(48): Show |
72 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1871-963_1871-962d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238389 | |||||||
| chr2:55238389 | G | GTTT | 12 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0081 others(9): Show |
13 | HG01167.hp2 HG01891.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1871-964_1871-962d others(5): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238389 | |||||||
| chr2:55238389 | GT | G | 24 | a0001c0003t0001g0232 a0002c0002t0001g0055 a0002c0002t0001g0148 others(21): Show |
32 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1871-962delA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238389 | |||||||
| chr2:55238454 | G | A | 20 | a0002c0004t0001g0085 a0002c0004t0001g0112 a0002c0004t0001g0124 others(17): Show |
28 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1871-1026C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238454 | |||||||
| chr2:55238497 | T | G | 83 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(80): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1871-1069A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238497 | |||||||
| chr2:55238502 | C | T | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1871-1074G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238502 | |||||||
| chr2:55238538 | T | A | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1871-1110A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238538 | |||||||
| chr2:55238620 | T | C | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1871-1192A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238620 | |||||||
| chr2:55238634 | G | A | 1 | a0007c0009t0002g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1871-1206C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238634 | |||||||
| chr2:55238791 | T | C | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1870+1220A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238791 | |||||||
| chr2:55238809 | C | T | 1 | a0001c0003t0001g0114 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1870+1202G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238809 | |||||||
| chr2:55238935 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0195 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1870+1076C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238935 | |||||||
| chr2:55238952 | T | C | 1 | a0002c0002t0001g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1870+1059A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55238952 | |||||||
| chr2:55239093 | G | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(58): Show |
83 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1870+918C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55239093 | |||||||
| chr2:55239280 | AG | A | 22 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(19): Show |
26 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1870+730delC | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55239280 | |||||||
| chr2:55239282 | C | A | 22 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(19): Show |
26 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1870+729G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55239282 | |||||||
| chr2:55239302 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1870+709G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55239302 | |||||||
| chr2:55239315 | T | C | 84 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(81): Show |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1870+696A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55239315 | |||||||
| chr2:55239827 | A | G | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1870+184T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 14/15 | chr2 | 55239827 | |||||||
| chr2:55240196 | C | A | 1 | a0002c0002t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1706-21G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55240196 | |||||||
| chr2:55240351 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1706-176G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55240351 | |||||||
| chr2:55240426 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1706-251G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55240426 | |||||||
| chr2:55240510 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1706-335G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55240510 | |||||||
| chr2:55240644 | C | T | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1706-469G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55240644 | |||||||
| chr2:55240685 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1706-510C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55240685 | |||||||
| chr2:55240999 | T | TAAA | 12 | a0002c0002t0001g0025 a0002c0002t0001g0062 a0002c0002t0001g0134 others(9): Show |
13 | HG00738.hp2 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1706-825_1706-824i others(5): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55240999 | |||||||
| chr2:55241001 | T | A | 12 | a0002c0002t0001g0025 a0002c0002t0001g0062 a0002c0002t0001g0134 others(9): Show |
13 | HG00738.hp2 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1706-826A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241001 | |||||||
| chr2:55241080 | A | G | 1 | a0001c0003t0001g0235 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1706-905T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241080 | |||||||
| chr2:55241140 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1706-965C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241140 | |||||||
| chr2:55241157 | C | T | 1 | a0001c0003t0001g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1706-982G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241157 | |||||||
| chr2:55241229 | C | G | 1 | a0002c0002t0001g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1706-1054G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241229 | |||||||
| chr2:55241374 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1706-1199G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241374 | |||||||
| chr2:55241417 | C | CA | 29 | a0001c0001t0001g0171 a0001c0001t0001g0192 a0001c0003t0001g0257 others(26): Show |
37 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1706-1243dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241417 | |||||||
| chr2:55241701 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
179 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1705+1239C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241701 | |||||||
| chr2:55241736 | G | A | 1 | a0002c0004t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1705+1204C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241736 | |||||||
| chr2:55241764 | A | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(17): Show |
28 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1705+1176T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55241764 | |||||||
| chr2:55242055 | G | A | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1705+885C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242055 | |||||||
| chr2:55242066 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1705+874A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242066 | |||||||
| chr2:55242113 | G | C | 1 | a0001c0001t0001g0172 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1705+827C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242113 | |||||||
| chr2:55242117 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1705+823C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242117 | |||||||
| chr2:55242142 | CA | C | 24 | a0001c0003t0001g0233 a0002c0002t0001g0012 a0002c0002t0001g0025 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1705+797delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242142 | |||||||
| chr2:55242157 | GA | G | 57 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(54): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1705+782delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242157 | |||||||
| chr2:55242177 | A | G | 28 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(25): Show |
42 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1705+763T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242177 | |||||||
| chr2:55242236 | A | G | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1705+704T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242236 | |||||||
| chr2:55242421 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1705+519T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242421 | |||||||
| chr2:55242575 | A | G | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1705+365T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242575 | |||||||
| chr2:55242664 | G | C | 1 | a0001c0012t0001g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1705+276C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242664 | |||||||
| chr2:55242683 | A | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(160): Show |
222 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1705+257T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242683 | |||||||
| chr2:55242684 | A | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(159): Show |
221 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1705+256T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242684 | |||||||
| chr2:55242685 | A | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0179 a0001c0001t0001g0196 others(3): Show |
6 | HG00609.hp1 HG02040.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1705+255T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242685 | |||||||
| chr2:55242699 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1705+241G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242699 | |||||||
| chr2:55242813 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0167 a0001c0001t0001g0222 others(2): Show |
6 | HG00099.hp2 HG01106.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1705+127T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 13/15 | chr2 | 55242813 | |||||||
| chr2:55243294 | C | A | 2 | a0002c0002t0001g0272 a0002c0002t0001g0273 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1564+122G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 12/15 | chr2 | 55243294 | |||||||
| chr2:55243389 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1564+27A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 12/15 | chr2 | 55243389 | |||||||
| chr2:55243709 | C | G | 1 | a0002c0002t0001g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1312-41G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 11/15 | chr2 | 55243709 | |||||||
| chr2:55243844 | T | C | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1312-176A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 11/15 | chr2 | 55243844 | |||||||
| chr2:55244246 | T | C | 57 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(54): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1107-13A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244246 | |||||||
| chr2:55244271 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(263): Show |
359 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.1107-38A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244271 | |||||||
| chr2:55244401 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1107-168C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244401 | |||||||
| chr2:55244410 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1107-177G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244410 | |||||||
| chr2:55244503 | T | C | 1 | a0001c0003t0001g0231 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1107-270A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244503 | |||||||
| chr2:55244652 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1107-419G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244652 | |||||||
| chr2:55244714 | A | C | 6 | a0001c0001t0001g0131 a0001c0001t0001g0179 a0001c0001t0001g0196 others(3): Show |
6 | HG00609.hp1 HG02040.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1107-481T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244714 | |||||||
| chr2:55244917 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1107-684G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55244917 | |||||||
| chr2:55245046 | C | CA | 57 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(54): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1107-814dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245046 | |||||||
| chr2:55245226 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.1107-993C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245226 | |||||||
| chr2:55245450 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1106+887C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245450 | |||||||
| chr2:55245538 | G | T | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1106+799C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245538 | |||||||
| chr2:55245542 | T | G | 1 | a0002c0002t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1106+795A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245542 | |||||||
| chr2:55245732 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1106+605C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245732 | |||||||
| chr2:55245751 | T | TA | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(152): Show |
214 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1106+585dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245751 | |||||||
| chr2:55245839 | C | A | 14 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0048 others(11): Show |
16 | HG00140.hp1 HG01167.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1106+498G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245839 | |||||||
| chr2:55245936 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1106+401G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55245936 | |||||||
| chr2:55246235 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
112 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+102T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55246235 | |||||||
| chr2:55246250 | CAT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1106+85_1106+86del others(2): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 10/15 | chr2 | 55246250 | |||||||
| chr2:55246535 | G | C | 6 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(3): Show |
6 | HG01123.hp1 HG01358.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-74C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55246535 | |||||||
| chr2:55246545 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.982-84T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55246545 | |||||||
| chr2:55246688 | C | G | 1 | a0002c0002t0001g0101 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.982-227G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55246688 | |||||||
| chr2:55246709 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.982-248G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55246709 | |||||||
| chr2:55246890 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0163 a0001c0001t0001g0183 others(3): Show |
10 | HG00639.hp2 HG00733.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.982-429T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55246890 | |||||||
| chr2:55246979 | T | G | 1 | a0002c0002t0001g0074 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.982-518A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55246979 | |||||||
| chr2:55246996 | T | C | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.982-535A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55246996 | |||||||
| chr2:55247284 | C | T | 40 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(37): Show |
60 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.982-823G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55247284 | |||||||
| chr2:55247468 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(204): Show |
278 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.982-1007T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55247468 | |||||||
| chr2:55247599 | A | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
219 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.982-1138T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55247599 | |||||||
| chr2:55247756 | T | A | 22 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(19): Show |
26 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.982-1295A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55247756 | |||||||
| chr2:55247827 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.982-1366C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55247827 | |||||||
| chr2:55247846 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0203 |
3 | NA18964.hp1 NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.982-1385G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55247846 | |||||||
| chr2:55248010 | C | G | 58 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(55): Show |
80 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.981+1385G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248010 | |||||||
| chr2:55248181 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.981+1214C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248181 | |||||||
| chr2:55248466 | A | T | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.981+929T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248466 | |||||||
| chr2:55248468 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.981+927T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248468 | |||||||
| chr2:55248778 | T | C | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.981+617A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248778 | |||||||
| chr2:55248851 | T | G | 1 | a0002c0002t0001g0157 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.981+544A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248851 | |||||||
| chr2:55248863 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.981+532A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248863 | |||||||
| chr2:55248937 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.981+458T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55248937 | |||||||
| chr2:55249010 | C | T | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.981+385G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55249010 | |||||||
| chr2:55249255 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.981+140G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55249255 | |||||||
| chr2:55249302 | T | C | 1 | a0002c0002t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.981+93A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55249302 | |||||||
| chr2:55249362 | C | G | 2 | a0002c0002t0001g0023 a0002c0002t0001g0055 |
3 | HG02109.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+33G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 9/15 | chr2 | 55249362 | |||||||
| chr2:55249706 | C | T | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.842-172G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55249706 | |||||||
| chr2:55249790 | CA | C | 42 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(39): Show |
62 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.842-257delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55249790 | |||||||
| chr2:55249801 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
179 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.842-267T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55249801 | |||||||
| chr2:55249820 | G | A | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.842-286C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55249820 | |||||||
| chr2:55249849 | T | G | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.842-315A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55249849 | |||||||
| chr2:55249950 | G | A | 22 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(19): Show |
26 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.842-416C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55249950 | |||||||
| chr2:55250234 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0180 |
3 | NA18939.hp2 NA19004.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.842-700A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250234 | |||||||
| chr2:55250417 | C | CA | 12 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0194 others(9): Show |
13 | HG00738.hp1 HG01123.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.842-884dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250417 | |||||||
| chr2:55250417 | CA | C | 7 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0213 others(4): Show |
7 | HG03669.hp1 HG03927.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.842-884delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250417 | |||||||
| chr2:55250426 | A | AAAC | 6 | a0001c0001t0001g0032 a0001c0001t0001g0175 a0001c0001t0001g0221 others(3): Show |
7 | HG02056.hp1 NA18944.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.842-893_842-892ins others(3): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250426 | |||||||
| chr2:55250434 | T | A | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.842-900A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250434 | |||||||
| chr2:55250479 | C | G | 3 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | NA18961.hp2 NA19062.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.842-945G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250479 | |||||||
| chr2:55250611 | C | T | 1 | a0002c0002t0001g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.842-1077G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250611 | |||||||
| chr2:55250712 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0203 |
3 | NA18964.hp1 NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.842-1178G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250712 | |||||||
| chr2:55250783 | T | C | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.842-1249A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250783 | |||||||
| chr2:55250848 | G | C | 1 | a0002c0002t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.842-1314C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250848 | |||||||
| chr2:55250897 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.842-1363C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55250897 | |||||||
| chr2:55251025 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.841+1452C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251025 | |||||||
| chr2:55251090 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
218 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.841+1387T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251090 | |||||||
| chr2:55251110 | CA | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(219): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.841+1366delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251110 | |||||||
| chr2:55251110 | CAA | C | 12 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0185 others(9): Show |
12 | HG01074.hp1 HG01168.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.841+1365_841+1366d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251110 | |||||||
| chr2:55251137 | A | G | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.841+1340T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251137 | |||||||
| chr2:55251266 | T | C | 1 | a0002c0002t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.841+1211A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251266 | |||||||
| chr2:55251295 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.841+1182C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251295 | |||||||
| chr2:55251456 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.841+1021C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251456 | |||||||
| chr2:55251561 | C | G | 1 | a0001c0003t0001g0240 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.841+916G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251561 | |||||||
| chr2:55251720 | T | C | 1 | a0002c0002t0001g0260 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.841+757A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251720 | |||||||
| chr2:55251848 | C | G | 20 | a0002c0004t0001g0085 a0002c0004t0001g0112 a0002c0004t0001g0124 others(17): Show |
28 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.841+629G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251848 | |||||||
| chr2:55251932 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.841+545C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55251932 | |||||||
| chr2:55252027 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
179 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.841+450A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55252027 | |||||||
| chr2:55252034 | G | C | 57 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(54): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.841+443C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55252034 | |||||||
| chr2:55252148 | T | C | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.841+329A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55252148 | |||||||
| chr2:55252255 | T | C | 1 | a0002c0002t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.841+222A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 8/15 | chr2 | 55252255 | |||||||
| chr2:55252886 | A | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(240): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.665-233T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55252886 | |||||||
| chr2:55252912 | A | C | 1 | a0002c0002t0001g0271 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.665-259T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55252912 | |||||||
| chr2:55253048 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.665-395A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253048 | |||||||
| chr2:55253076 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0205 |
4 | HG00642.hp2 HG01168.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-423G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253076 | |||||||
| chr2:55253137 | G | A | 13 | a0001c0001t0001g0041 a0001c0001t0001g0111 a0001c0001t0001g0145 others(10): Show |
14 | HG01074.hp1 HG01261.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.665-484C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253137 | |||||||
| chr2:55253211 | T | C | 1 | a0002c0002t0001g0148 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.665-558A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253211 | |||||||
| chr2:55253344 | A | G | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.665-691T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253344 | |||||||
| chr2:55253405 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.664+636C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253405 | |||||||
| chr2:55253489 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
4 | HG01346.hp1 HG02280.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+552C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253489 | |||||||
| chr2:55253522 | T | C | 2 | a0001c0001t0001g0146 a0004c0006t0001g0147 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.664+519A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253522 | |||||||
| chr2:55253591 | C | T | 22 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(19): Show |
26 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.664+450G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253591 | |||||||
| chr2:55253593 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.664+448C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253593 | |||||||
| chr2:55253709 | G | C | 21 | a0002c0004t0001g0085 a0002c0004t0001g0112 a0002c0004t0001g0124 others(18): Show |
29 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.664+332C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253709 | |||||||
| chr2:55253741 | GGAGGCA | G | 4 | a0001c0001t0001g0145 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | NA18952.hp1 NA18979.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+294_664+299del others(6): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253741 | |||||||
| chr2:55253759 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.664+282C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253759 | |||||||
| chr2:55253792 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.664+249C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253792 | |||||||
| chr2:55253793 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.664+248A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253793 | |||||||
| chr2:55253794 | GACAGAGT others(24): Show |
G | 1 | a0001c0001t0001g0058 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.664+216_664+246del others(31): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253794 | |||||||
| chr2:55253794 | GACAGAGT others(25): Show |
G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
146 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.664+215_664+246del others(32): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253794 | |||||||
| chr2:55253794 | GACAGAGT others(26): Show |
G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(47): Show |
70 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.664+214_664+246del others(33): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253794 | |||||||
| chr2:55253808 | C | CT | 22 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(19): Show |
26 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.664+232dupA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253808 | |||||||
| chr2:55253820 | GA | G | 81 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(78): Show |
107 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.664+220delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253820 | |||||||
| chr2:55253853 | C | T | 1 | a0002c0002t0001g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.664+188G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253853 | |||||||
| chr2:55253857 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.664+184G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55253857 | |||||||
| chr2:55254001 | G | C | 1 | a0001c0003t0001g0037 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.664+40C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55254001 | |||||||
| chr2:55254018 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.664+23A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 7/15 | chr2 | 55254018 | |||||||
| chr2:55254235 | A | G | 1 | a0002c0002t0001g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.504-34T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 6/15 | chr2 | 55254235 | |||||||
| chr2:55254350 | T | TATA | 269 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.504-150_504-149ins others(3): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 6/15 | chr2 | 55254350 | |||||||
| chr2:55254409 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.504-208C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 6/15 | chr2 | 55254409 | |||||||
| chr2:55254433 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.503+221A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 6/15 | chr2 | 55254433 | |||||||
| chr2:55255031 | C | T | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.332-206G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255031 | |||||||
| chr2:55255056 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0203 |
3 | NA18964.hp1 NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.332-231A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255056 | |||||||
| chr2:55255351 | T | C | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-526A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255351 | |||||||
| chr2:55255425 | AATATG | A | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.332-605_332-601del others(5): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255425 | |||||||
| chr2:55255440 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(180): Show |
246 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.332-615C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255440 | |||||||
| chr2:55255444 | AAT | A | 44 | a0001c0001t0001g0146 a0002c0002t0001g0003 a0002c0002t0001g0006 others(41): Show |
64 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.332-621_332-620del others(2): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255444 | |||||||
| chr2:55255498 | A | T | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.332-673T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255498 | |||||||
| chr2:55255548 | TA | T | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-724delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255548 | |||||||
| chr2:55255625 | G | A | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-800C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255625 | |||||||
| chr2:55255748 | G | A | 1 | a0002c0002t0001g0023 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.332-923C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255748 | |||||||
| chr2:55255775 | C | T | 40 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(37): Show |
60 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.332-950G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255775 | |||||||
| chr2:55255884 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(179): Show |
245 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.332-1059G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255884 | |||||||
| chr2:55255891 | T | G | 24 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.332-1066A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255891 | |||||||
| chr2:55255892 | T | G | 24 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.332-1067A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255892 | |||||||
| chr2:55255893 | T | G | 24 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.332-1068A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55255893 | |||||||
| chr2:55256058 | G | A | 1 | a0001c0003t0001g0064 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.332-1233C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256058 | |||||||
| chr2:55256301 | T | TACACACA others(3): Show |
1 | a0002c0002t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.332-1486_332-1477d others(12): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256301 | |||||||
| chr2:55256301 | TAC | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0111 a0001c0001t0001g0145 others(15): Show |
20 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.332-1478_332-1477d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256301 | |||||||
| chr2:55256301 | TACAC | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(199): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.332-1480_332-1477d others(6): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256301 | |||||||
| chr2:55256328 | A | ACACAATA others(1): Show |
21 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(18): Show |
25 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.332-1504_332-1503i others(10): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256328 | |||||||
| chr2:55256487 | C | A | 1 | a0001c0003t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.332-1662G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256487 | |||||||
| chr2:55256510 | A | C | 1 | a0002c0002t0001g0277 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.332-1685T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256510 | |||||||
| chr2:55256637 | G | A | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.332-1812C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256637 | |||||||
| chr2:55256687 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0205 |
4 | HG00642.hp2 HG01168.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-1862G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256687 | |||||||
| chr2:55256700 | C | CA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(153): Show |
205 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.332-1876dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256700 | |||||||
| chr2:55256700 | C | CAA | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.332-1877_332-1876d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256700 | |||||||
| chr2:55256766 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(179): Show |
245 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.332-1941T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256766 | |||||||
| chr2:55256873 | AT | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.332-2049delA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55256873 | |||||||
| chr2:55257037 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.332-2212G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257037 | |||||||
| chr2:55257202 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(179): Show |
245 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.332-2377C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257202 | |||||||
| chr2:55257264 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(269): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.332-2439T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257264 | |||||||
| chr2:55257363 | C | A | 2 | a0001c0003t0001g0038 a0001c0003t0001g0239 |
3 | HG01361.hp1 HG01516.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.332-2538G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257363 | |||||||
| chr2:55257541 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
9 | HG02257.hp2 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.332-2716A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257541 | |||||||
| chr2:55257612 | T | C | 1 | a0002c0002t0001g0026 | 2 | NA18951.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.332-2787A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257612 | |||||||
| chr2:55257817 | G | C | 1 | a0002c0002t0001g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.332-2992C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257817 | |||||||
| chr2:55257835 | G | A | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.332-3010C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257835 | |||||||
| chr2:55257915 | A | G | 1 | a0002c0002t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.332-3090T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55257915 | |||||||
| chr2:55258256 | G | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.332-3431C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258256 | |||||||
| chr2:55258314 | T | C | 1 | a0002c0002t0001g0096 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.332-3489A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258314 | |||||||
| chr2:55258332 | T | C | 1 | a0002c0002t0001g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332-3507A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258332 | |||||||
| chr2:55258574 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.331+3742C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258574 | |||||||
| chr2:55258673 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.331+3643C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258673 | |||||||
| chr2:55258689 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+3627C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258689 | |||||||
| chr2:55258795 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.331+3521C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258795 | |||||||
| chr2:55258811 | C | CA | 70 | a0001c0001t0001g0041 a0001c0001t0001g0111 a0001c0001t0001g0129 others(67): Show |
93 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.331+3504dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258811 | |||||||
| chr2:55258811 | C | CAA | 13 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(10): Show |
13 | HG02040.hp1 HG02083.hp1 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.331+3503_331+3504d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258811 | |||||||
| chr2:55258811 | CA | C | 8 | a0001c0001t0001g0176 a0001c0001t0001g0181 a0001c0001t0001g0182 others(5): Show |
8 | HG01069.hp2 HG01070.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.331+3504delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258811 | |||||||
| chr2:55258874 | G | C | 85 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(82): Show |
111 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.331+3442C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258874 | |||||||
| chr2:55258978 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
9 | HG02257.hp2 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+3338A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55258978 | |||||||
| chr2:55259028 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.331+3288G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259028 | |||||||
| chr2:55259192 | T | C | 1 | a0002c0002t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.331+3124A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259192 | |||||||
| chr2:55259352 | G | C | 6 | a0001c0001t0001g0145 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG02040.hp1 NA18952.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+2964C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259352 | |||||||
| chr2:55259436 | T | C | 6 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(3): Show |
6 | HG01123.hp1 HG01358.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+2880A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259436 | |||||||
| chr2:55259450 | T | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
218 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.331+2866A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259450 | |||||||
| chr2:55259504 | T | TA | 251 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(248): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.331+2811dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259504 | |||||||
| chr2:55259504 | T | TAA | 6 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(3): Show |
6 | HG01123.hp1 HG01358.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+2810_331+2811d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259504 | |||||||
| chr2:55259537 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.331+2779C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259537 | |||||||
| chr2:55259628 | A | G | 20 | a0002c0004t0001g0085 a0002c0004t0001g0112 a0002c0004t0001g0124 others(17): Show |
28 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.331+2688T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259628 | |||||||
| chr2:55259634 | G | C | 1 | a0001c0003t0001g0240 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.331+2682C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259634 | |||||||
| chr2:55259659 | G | C | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+2657C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259659 | |||||||
| chr2:55259671 | G | A | 3 | a0001c0003t0001g0039 a0001c0003t0001g0227 a0001c0003t0001g0240 |
4 | HG03491.hp1 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+2645C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259671 | |||||||
| chr2:55259673 | A | G | 1 | a0002c0002t0001g0272 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.331+2643T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259673 | |||||||
| chr2:55259851 | C | A | 13 | a0001c0001t0001g0041 a0001c0001t0001g0111 a0001c0001t0001g0145 others(10): Show |
14 | HG01074.hp1 HG01261.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.331+2465G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259851 | |||||||
| chr2:55259888 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.331+2428T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259888 | |||||||
| chr2:55259917 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.331+2399G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259917 | |||||||
| chr2:55259918 | T | C | 17 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(14): Show |
22 | HG00099.hp2 HG01106.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.331+2398A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55259918 | |||||||
| chr2:55260037 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.331+2279G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260037 | |||||||
| chr2:55260189 | C | T | 1 | a0001c0003t0001g0230 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.331+2127G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260189 | |||||||
| chr2:55260283 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.331+2033G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260283 | |||||||
| chr2:55260291 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18947.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.331+2025G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260291 | |||||||
| chr2:55260361 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
219 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.331+1955A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260361 | |||||||
| chr2:55260377 | T | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(242): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.331+1939A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260377 | |||||||
| chr2:55260399 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0208 a0001c0001t0001g0209 |
4 | HG00735.hp2 HG01928.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+1917A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260399 | |||||||
| chr2:55260400 | C | CA | 10 | a0001c0001t0001g0036 a0001c0001t0001g0167 a0001c0001t0001g0174 others(7): Show |
11 | HG01106.hp1 HG01109.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.331+1915dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260400 | |||||||
| chr2:55260400 | CA | C | 75 | a0001c0001t0001g0176 a0002c0002t0001g0003 a0002c0002t0001g0006 others(72): Show |
103 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.331+1915delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260400 | |||||||
| chr2:55260400 | CAA | C | 4 | a0002c0002t0001g0010 a0002c0002t0001g0088 a0002c0002t0001g0090 others(1): Show |
6 | HG00423.hp1 NA18957.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+1914_331+1915d others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260400 | |||||||
| chr2:55260442 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.331+1874A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260442 | |||||||
| chr2:55260504 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.331+1812A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260504 | |||||||
| chr2:55260517 | T | C | 1 | a0001c0003t0001g0228 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.331+1799A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260517 | |||||||
| chr2:55260702 | C | A | 57 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(54): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.331+1614G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260702 | |||||||
| chr2:55260793 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
112 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.331+1523G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260793 | |||||||
| chr2:55260993 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.331+1323A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55260993 | |||||||
| chr2:55261030 | A | G | 1 | a0002c0004t0002g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.331+1286T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261030 | |||||||
| chr2:55261049 | C | T | 2 | a0002c0002t0001g0088 a0002c0002t0001g0089 |
2 | NA18984.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.331+1267G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261049 | |||||||
| chr2:55261112 | G | A | 2 | a0001c0001t0001g0270 a0002c0002t0001g0276 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.331+1204C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261112 | |||||||
| chr2:55261161 | T | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
219 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.331+1155A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261161 | |||||||
| chr2:55261371 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
218 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.331+945G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261371 | |||||||
| chr2:55261532 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
219 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.331+784C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261532 | |||||||
| chr2:55261584 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
219 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.331+732C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261584 | |||||||
| chr2:55261940 | C | A | 1 | a0002c0002t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.331+376G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261940 | |||||||
| chr2:55261941 | C | A | 2 | a0001c0001t0001g0226 a0002c0002t0001g0143 |
2 | NA18522.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.331+375G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261941 | |||||||
| chr2:55261941 | C | CA | 24 | a0001c0001t0001g0256 a0001c0003t0001g0241 a0002c0002t0001g0012 others(21): Show |
28 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.331+374dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261941 | |||||||
| chr2:55261941 | CA | C | 59 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0001g0104 others(56): Show |
82 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.331+374delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261941 | |||||||
| chr2:55261942 | A | C | 1 | a0002c0002t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.331+374T>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55261942 | |||||||
| chr2:55262251 | T | C | 1 | a0002c0002t0001g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.331+65A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55262251 | |||||||
| chr2:55262267 | C | T | 1 | a0002c0004t0002g0280 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.331+49G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 5/15 | chr2 | 55262267 | |||||||
| chr2:55262493 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
219 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.220-66A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262493 | |||||||
| chr2:55262532 | T | C | 3 | a0005c0007t0001g0063 a0005c0007t0001g0264 a0005c0007t0001g0265 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.220-105A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262532 | |||||||
| chr2:55262540 | T | TC | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.220-114dupG | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262540 | |||||||
| chr2:55262541 | C | CT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(163): Show |
232 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.220-115dupA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262541 | |||||||
| chr2:55262541 | C | CTT | 11 | a0001c0001t0001g0049 a0001c0001t0001g0104 a0001c0001t0001g0169 others(8): Show |
11 | HG00621.hp2 HG02056.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-116_220-115dup others(2): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262541 | |||||||
| chr2:55262727 | T | G | 23 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(20): Show |
27 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.220-300A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262727 | |||||||
| chr2:55262728 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.220-301A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262728 | |||||||
| chr2:55262729 | T | G | 1 | a0001c0003t0001g0228 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.220-302A>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262729 | |||||||
| chr2:55262729 | TG | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
216 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.220-303delC | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262729 | |||||||
| chr2:55262730 | G | T | 2 | a0001c0001t0001g0111 a0001c0003t0001g0228 |
2 | HG02055.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.220-303C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262730 | |||||||
| chr2:55262742 | G | A | 1 | a0001c0003t0001g0040 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.220-315C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262742 | |||||||
| chr2:55262831 | C | T | 1 | a0005c0007t0001g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220-404G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262831 | |||||||
| chr2:55262922 | T | C | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.220-495A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262922 | |||||||
| chr2:55262994 | C | T | 1 | a0002c0002t0001g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.220-567G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55262994 | |||||||
| chr2:55263003 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01981.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.220-576T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55263003 | |||||||
| chr2:55263091 | G | A | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.219+549C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55263091 | |||||||
| chr2:55263189 | C | G | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.219+451G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55263189 | |||||||
| chr2:55263281 | A | G | 1 | a0001c0003t0001g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.219+359T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55263281 | |||||||
| chr2:55263362 | T | C | 1 | a0002c0004t0002g0279 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.219+278A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55263362 | |||||||
| chr2:55263463 | T | C | 24 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.219+177A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 4/15 | chr2 | 55263463 | |||||||
| chr2:55263871 | G | GA | 25 | a0001c0003t0001g0002 a0001c0003t0001g0037 a0001c0003t0001g0038 others(22): Show |
39 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.-7-7dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55263871 | |||||||
| chr2:55264194 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(153): Show |
215 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-7-329C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55264194 | |||||||
| chr2:55264355 | C | T | 1 | a0005c0007t0001g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-7-490G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55264355 | |||||||
| chr2:55264655 | T | C | 24 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7-790A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55264655 | |||||||
| chr2:55264711 | C | G | 1 | a0002c0002t0001g0267 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7-846G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55264711 | |||||||
| chr2:55264856 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-7-991G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55264856 | |||||||
| chr2:55264918 | A | G | 24 | a0002c0002t0001g0012 a0002c0002t0001g0025 a0002c0002t0001g0027 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7-1053T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55264918 | |||||||
| chr2:55264940 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(258): Show |
354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.-7-1075G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55264940 | |||||||
| chr2:55265018 | G | A | 56 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(53): Show |
77 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-7-1153C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265018 | |||||||
| chr2:55265030 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG01099.hp1 HG01106.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-1165C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265030 | |||||||
| chr2:55265221 | C | T | 2 | a0002c0002t0001g0272 a0002c0002t0001g0273 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-7-1356G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265221 | |||||||
| chr2:55265244 | GA | G | 28 | a0001c0001t0001g0059 a0001c0001t0001g0156 a0001c0001t0001g0163 others(25): Show |
36 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.-7-1380delT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265244 | |||||||
| chr2:55265299 | A | G | 21 | a0001c0012t0001g0162 a0002c0004t0001g0085 a0002c0004t0001g0112 others(18): Show |
29 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7-1434T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265299 | |||||||
| chr2:55265366 | CACAA | C | 53 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0010 others(50): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-7-1505_-7-1502del others(4): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265366 | |||||||
| chr2:55265525 | T | C | 3 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0250 |
3 | HG03225.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-1660A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265525 | |||||||
| chr2:55265554 | G | C | 1 | a0001c0001t0001g0041 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-1689C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265554 | |||||||
| chr2:55265664 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-7-1799T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265664 | |||||||
| chr2:55265752 | T | C | 1 | a0002c0002t0001g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8+1817A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265752 | |||||||
| chr2:55265774 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-8+1795A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265774 | |||||||
| chr2:55265819 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0059 others(4): Show |
10 | HG01109.hp1 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+1750C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265819 | |||||||
| chr2:55265821 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0252 |
3 | HG00597.hp1 HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-8+1748C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265821 | |||||||
| chr2:55265853 | T | A | 1 | a0001c0001t0001g0253 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-8+1716A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265853 | |||||||
| chr2:55265961 | C | A | 1 | a0002c0002t0001g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+1608G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55265961 | |||||||
| chr2:55266160 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8+1409C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266160 | |||||||
| chr2:55266174 | C | T | 1 | a0002c0002t0001g0023 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-8+1395G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266174 | |||||||
| chr2:55266306 | T | C | 2 | a0002c0002t0001g0106 a0002c0004t0002g0279 |
2 | NA18963.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-8+1263A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266306 | |||||||
| chr2:55266500 | G | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0049 others(16): Show |
26 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8+1069C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266500 | |||||||
| chr2:55266525 | C | CA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
210 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-8+1043dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266525 | |||||||
| chr2:55266525 | C | CAA | 7 | a0001c0001t0001g0043 a0001c0001t0001g0131 a0001c0001t0001g0255 others(4): Show |
8 | HG01109.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+1042_-8+1043dup others(2): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266525 | |||||||
| chr2:55266540 | T | A | 1 | a0002c0002t0001g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-8+1029A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266540 | |||||||
| chr2:55266763 | C | CT | 28 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(25): Show |
32 | HG00140.hp2 HG00423.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.-8+805dupA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266763 | |||||||
| chr2:55266763 | CT | C | 15 | a0001c0001t0001g0072 a0001c0001t0001g0262 a0001c0003t0001g0263 others(12): Show |
16 | HG00597.hp2 HG01257.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+805delA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266763 | |||||||
| chr2:55266763 | CTT | C | 60 | a0001c0001t0001g0017 a0001c0001t0001g0065 a0001c0001t0001g0067 others(57): Show |
82 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+804_-8+805delAA | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266763 | |||||||
| chr2:55266894 | C | G | 2 | a0001c0003t0001g0114 a0001c0003t0001g0115 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-8+675G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266894 | |||||||
| chr2:55266897 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0065 a0001c0001t0001g0067 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+672C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55266897 | |||||||
| chr2:55267061 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0049 others(26): Show |
37 | HG00140.hp1 HG01109.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.-8+508G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267061 | |||||||
| chr2:55267105 | A | G | 1 | a0001c0001t0001g0024 | 2 | NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-8+464T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267105 | |||||||
| chr2:55267108 | TTATGGTT others(15): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8+439_-8+460delCA others(20): Show |
MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267108 | |||||||
| chr2:55267196 | G | A | 1 | a0002c0004t0002g0285 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-8+373C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267196 | |||||||
| chr2:55267245 | C | A | 1 | a0002c0002t0001g0267 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8+324G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267245 | |||||||
| chr2:55267334 | T | C | 1 | a0002c0002t0003g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-8+235A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267334 | |||||||
| chr2:55267394 | G | C | 1 | a0002c0002t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-8+175C>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267394 | |||||||
| chr2:55267399 | T | A | 1 | a0002c0002t0001g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-8+170A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267399 | |||||||
| chr2:55267405 | C | T | 1 | a0002c0002t0001g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+164G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267405 | |||||||
| chr2:55267413 | C | A | 1 | a0001c0001t0001g0268 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8+156G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267413 | |||||||
| chr2:55267450 | C | T | 1 | a0002c0002t0001g0023 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-8+119G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267450 | |||||||
| chr2:55267520 | A | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(10): Show |
18 | HG00558.hp2 HG00597.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8+49T>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 3/15 | chr2 | 55267520 | |||||||
| chr2:55267707 | T | A | 1 | a0001c0001t0001g0269 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-74-72A>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55267707 | |||||||
| chr2:55267768 | C | G | 89 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(86): Show |
119 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-74-133G>C | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55267768 | |||||||
| chr2:55267839 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-74-204C>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55267839 | |||||||
| chr2:55267897 | C | T | 1 | a0002c0004t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-74-262G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55267897 | |||||||
| chr2:55268055 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-74-420G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268055 | |||||||
| chr2:55268058 | G | T | 1 | a0002c0004t0002g0044 | 2 | NA18970.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-74-423C>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268058 | |||||||
| chr2:55268115 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(85): Show |
117 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-75+463G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268115 | |||||||
| chr2:55268127 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-75+451G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268127 | |||||||
| chr2:55268252 | A | AG | 5 | a0001c0001t0001g0017 a0001c0001t0001g0065 a0001c0001t0001g0067 others(2): Show |
6 | HG02258.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-75+325dupC | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268252 | |||||||
| chr2:55268253 | G | GA | 15 | a0002c0002t0001g0271 a0002c0002t0001g0272 a0002c0002t0001g0273 others(12): Show |
17 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-75+324dupT | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268253 | |||||||
| chr2:55268361 | A | T | 2 | a0002c0002t0001g0046 a0002c0002t0001g0047 |
2 | HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-75+217T>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268361 | |||||||
| chr2:55268395 | T | C | 1 | a0002c0002t0001g0277 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-75+183A>G | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 2/15 | chr2 | 55268395 | |||||||
| chr2:55268934 | C | T | 1 | a0001c0003t0001g0064 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-236-195G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 1/15 | chr2 | 55268934 | |||||||
| chr2:55268942 | C | A | 9 | a0002c0004t0002g0044 a0002c0004t0002g0045 a0002c0004t0002g0279 others(6): Show |
11 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-236-203G>T | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 1/15 | chr2 | 55268942 | |||||||
| chr2:55268980 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0049 others(17): Show |
27 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-237+189G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 1/15 | chr2 | 55268980 | |||||||
| chr2:55269131 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-237+38G>A | MTIF2 | ENSG00000085760.15 | transcript | ENST00000263629.9 | protein_coding | 1/15 | chr2 | 55269131 |