Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9633 |
| ensemblid | ENSG00000132749.11 |
| hgncid | 7446 |
| symbol | TESMIN |
| name | testis expressed metallothionein like protein |
| refseq_nuc | NM_004923.3 |
| refseq_prot | NP_004914.2 |
| ensembl_nuc | ENST00000255087.10 |
| ensembl_prot | ENSP00000255087.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 68707440 |
| end | 68751520 |
| strand | - |
| ver | v1.2 |
| region | chr11:68707440-68751520 |
| region5000 | chr11:68702440-68756520 |
| regionname0 | TESMIN_chr11_68707440_68751520 |
| regionname5000 | TESMIN_chr11_68702440_68756520 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 508 | 281 | 79 | 57 | 116 | 3 | 24 | 88 | TESMIN_chr11_68702440_68756520 | TESMIN | MEEGP others(503): Show |
chr11 | 68702440 | 68756520 |
| a0002 | 0/0 | 508 | 12 | 2 | 4 | 2 | 3 | 1 | 2 | TESMIN_chr11_68702440_68756520 | TESMIN | MEEGP others(503): Show |
chr11 | 68702440 | 68756520 |
| a0003 | 0/0 | 508 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | MEEGP others(503): Show |
chr11 | 68702440 | 68756520 |
| a0004 | 0/0 | 508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | MEEGP others(503): Show |
chr11 | 68702440 | 68756520 |
| a0005 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | MEEGP others(503): Show |
chr11 | 68702440 | 68756520 |
| a0006 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | MEEGP others(503): Show |
chr11 | 68702440 | 68756520 |
| a0007 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | MEEGP others(503): Show |
chr11 | 68702440 | 68756520 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1524 | 277 | 75 | 57 | 116 | 3 | 24 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0001c0004 | 0/0 | 1524 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0001c0005 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0001c0009 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0002c0002 | 0/0 | 1524 | 12 | 2 | 4 | 2 | 3 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0003c0003 | 0/0 | 1524 | 3 | 0 | 0 | 3 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0004c0007 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0005c0010 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0006c0008 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 | ||
| a0007c0006 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ATGGA others(1519): Show |
chr11 | 68702440 | 68756520 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2535 | 264 | 68 | 55 | 113 | 3 | 23 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0002 | 0/0 | 2535 | 3 | 0 | 0 | 3 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0003 | 0/0 | 2535 | 3 | 2 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0004 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0005 | 0/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0006 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0007 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0008 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0001t0009 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0004t0001 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0005t0001 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0001c0009t0001 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0002c0002t0001 | 0/0 | 2535 | 12 | 2 | 4 | 2 | 3 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0003c0003t0001 | 0/0 | 2535 | 3 | 0 | 0 | 3 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0004c0007t0001 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0005c0010t0001 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0006c0008t0001 | 0/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| a0007c0006t0001 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | ACCCT others(2530): Show |
chr11 | 68702440 | 68756520 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 0 | 4 | 12 | 0 | 3 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 3 | 0 | 2 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0001g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0003g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0001c0009t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0003c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0004c0007t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0005c0010t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0006c0008t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| a0007c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0113 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01243 | hp1 | a0004 | c0007 | t0001 | g0135 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0018 | EUR | IBS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0064 | EUR | IBS | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0138 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02080 | hp2 | a0003 | c0003 | t0001 | g0035 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0035 | EAS | CDX | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0153 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02897 | hp1 | a0005 | c0010 | t0001 | g0208 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0148 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03453 | hp2 | a0001 | c0009 | t0001 | g0060 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03831 | hp2 | a0006 | c0008 | t0001 | g0142 | SAS | BEB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19056 | hp2 | a0007 | c0006 | t0001 | g0074 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0200 | AFR | ASW | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0018 | EUR | TSI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0201 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0206 | AFR | MSL | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0040 | REF | REF | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0209 | REF | REF | TESMIN_chr11_68702440_68756520 | TESMIN | chr11 | 68702440 | 68756520 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:68713389 | G | A | 1 | a0005 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.1039C>T | p.Pro347Ser | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/10 | 1179/2535 | 1039/1527 | 347/508 | chr11 | 68713389 | |||
| chr11:68715908 | A | G | 1 | a0006 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.949T>C | p.Cys317Arg | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/10 | 1089/2535 | 949/1527 | 317/508 | chr11 | 68715908 | |||
| chr11:68742367 | A | G | 1 | a0004 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.779T>C | p.Val260Ala | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/10 | 919/2535 | 779/1527 | 260/508 | chr11 | 68742367 | |||
| chr11:68745022 | C | G | 1 | a0007 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.720G>C | p.Gln240His | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/10 | 860/2535 | 720/1527 | 240/508 | chr11 | 68745022 | |||
| chr11:68745075 | A | G | 1 | a0002 | 12 | HG01169.hp1 HG01261.hp2 HG01516.hp1 others(9): Show |
missense_variant | MODERATE | c.667T>C | p.Cys223Arg | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/10 | 807/2535 | 667/1527 | 223/508 | chr11 | 68745075 | |||
| chr11:68750464 | G | C | 1 | a0003 | 3 | HG02080.hp2 HG02165.hp2 NA18939.hp2 |
missense_variant | MODERATE | c.197C>G | p.Ala66Gly | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/10 | 337/2535 | 197/1527 | 66/508 | chr11 | 68750464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:68713282 | G | A | 1 | a0001c0009 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1146C>T | p.Cys382Cys | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/10 | 1286/2535 | 1146/1527 | 382/508 | chr11 | 68713282 | |||
| chr11:68738759 | G | A | 1 | a0001c0004 | 2 | HG03471.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.858C>T | p.Asn286Asn | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/10 | 998/2535 | 858/1527 | 286/508 | chr11 | 68738759 | |||
| chr11:68750607 | C | T | 1 | a0001c0005 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.54G>A | p.Val18Val | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/10 | 194/2535 | 54/1527 | 18/508 | chr11 | 68750607 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:68707492 | C | G | 1 | a0001c0001t0003 | 3 | HG01346.hp2 HG02965.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*816G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 816 | chr11 | 68707492 | ||||||
| chr11:68707493 | G | A | 1 | a0001c0001t0006 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 815 | chr11 | 68707493 | ||||||
| chr11:68707512 | T | G | 1 | a0001c0001t0007 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 796 | chr11 | 68707512 | ||||||
| chr11:68707516 | C | T | 1 | a0001c0001t0006 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 792 | chr11 | 68707516 | ||||||
| chr11:68707533 | C | T | 1 | a0001c0001t0002 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*775G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 775 | chr11 | 68707533 | ||||||
| chr11:68707699 | G | A | 1 | a0001c0001t0008 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*609C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 609 | chr11 | 68707699 | ||||||
| chr11:68707705 | C | T | 1 | a0001c0001t0005 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 603 | chr11 | 68707705 | ||||||
| chr11:68707715 | C | T | 1 | a0001c0001t0002 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*593G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 593 | chr11 | 68707715 | ||||||
| chr11:68708200 | G | A | 1 | a0001c0001t0004 | 2 | HG02976.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*108C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 10/10 | 108 | chr11 | 68708200 | ||||||
| chr11:68750694 | G | A | 1 | a0001c0001t0009 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/10 | 34 | chr11 | 68750694 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:68708543 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
200 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.1335-43T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68708543 | |||||||
| chr11:68708750 | G | A | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1335-250C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68708750 | |||||||
| chr11:68708758 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.1335-259dupA | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68708758 | |||||||
| chr11:68708819 | C | G | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1335-319G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68708819 | |||||||
| chr11:68709050 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02922.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1335-550C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709050 | |||||||
| chr11:68709063 | T | TA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335-564dupT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709063 | |||||||
| chr11:68709089 | A | AAAAG | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1335-593_1335-590d others(6): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709089 | |||||||
| chr11:68709089 | A | AAAAGAAA others(1): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(24): Show |
38 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1335-597_1335-590d others(10): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709089 | |||||||
| chr11:68709169 | T | C | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1335-669A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709169 | |||||||
| chr11:68709175 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1335-675C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709175 | |||||||
| chr11:68709242 | C | T | 1 | a0001c0004t0001g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1335-742G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709242 | |||||||
| chr11:68709333 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02922.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1335-833G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709333 | |||||||
| chr11:68709334 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1335-834C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709334 | |||||||
| chr11:68709679 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1335-1179G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709679 | |||||||
| chr11:68709800 | C | A | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1334+1074G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68709800 | |||||||
| chr11:68710015 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0079 others(5): Show |
11 | HG00558.hp1 HG00621.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1334+859C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710015 | |||||||
| chr11:68710028 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0114 others(4): Show |
10 | HG01934.hp1 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1334+846G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710028 | |||||||
| chr11:68710099 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1334+775G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710099 | |||||||
| chr11:68710106 | T | G | 2 | a0001c0001t0001g0196 a0002c0002t0001g0194 |
2 | NA18950.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1334+768A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710106 | |||||||
| chr11:68710224 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1334+650A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710224 | |||||||
| chr11:68710332 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01109.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1334+542C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710332 | |||||||
| chr11:68710419 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1334+455G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710419 | |||||||
| chr11:68710450 | T | C | 1 | a0002c0002t0001g0061 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1334+424A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710450 | |||||||
| chr11:68710544 | A | G | 1 | a0001c0001t0006g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1334+330T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710544 | |||||||
| chr11:68710549 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1334+325G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710549 | |||||||
| chr11:68710739 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
202 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.1334+135T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 9/9 | chr11 | 68710739 | |||||||
| chr11:68711244 | T | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1159-195A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711244 | |||||||
| chr11:68711289 | G | T | 1 | a0001c0004t0001g0200 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1159-240C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711289 | |||||||
| chr11:68711305 | AGT | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1159-258_1159-257d others(4): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711305 | |||||||
| chr11:68711318 | T | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0046 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159-269A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711318 | |||||||
| chr11:68711337 | C | T | 1 | a0001c0001t0006g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1159-288G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711337 | |||||||
| chr11:68711390 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1159-341T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711390 | |||||||
| chr11:68711442 | A | AGT | 7 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0132 others(4): Show |
8 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1159-395_1159-394d others(4): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711442 | |||||||
| chr11:68711442 | AGTGT | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1159-397_1159-394d others(6): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711442 | |||||||
| chr11:68711483 | G | A | 1 | a0001c0005t0001g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1159-434C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711483 | |||||||
| chr11:68711529 | G | A | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1159-480C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711529 | |||||||
| chr11:68711793 | T | A | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1159-744A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711793 | |||||||
| chr11:68711985 | C | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1159-936G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68711985 | |||||||
| chr11:68712105 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1159-1056T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68712105 | |||||||
| chr11:68712246 | G | A | 1 | a0004c0007t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1158+1024C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68712246 | |||||||
| chr11:68712504 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1158+766C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68712504 | |||||||
| chr11:68712625 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1158+645G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68712625 | |||||||
| chr11:68712692 | C | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1158+578G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68712692 | |||||||
| chr11:68712925 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1158+345C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68712925 | |||||||
| chr11:68712927 | G | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158+343C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68712927 | |||||||
| chr11:68713082 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158+188C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68713082 | |||||||
| chr11:68713241 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158+29C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 8/9 | chr11 | 68713241 | |||||||
| chr11:68713563 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1021-156A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68713563 | |||||||
| chr11:68713592 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1021-185T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68713592 | |||||||
| chr11:68713782 | A | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(26): Show |
40 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1021-375T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68713782 | |||||||
| chr11:68713875 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1021-468C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68713875 | |||||||
| chr11:68713893 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0092 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1021-486G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68713893 | |||||||
| chr11:68713953 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1021-546T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68713953 | |||||||
| chr11:68714010 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1021-603C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714010 | |||||||
| chr11:68714022 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
133 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.1021-615T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714022 | |||||||
| chr11:68714050 | C | T | 1 | a0001c0001t0006g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1021-643G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714050 | |||||||
| chr11:68714061 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1021-654T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714061 | |||||||
| chr11:68714110 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1021-703C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714110 | |||||||
| chr11:68714165 | C | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
155 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1021-758G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714165 | |||||||
| chr11:68714359 | GTGTGCAC others(11): Show |
G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0179 |
3 | HG02886.hp2 HG03098.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1021-970_1021-953d others(20): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714359 | |||||||
| chr11:68714398 | C | T | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1021-991G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714398 | |||||||
| chr11:68714494 | A | G | 4 | a0002c0002t0001g0018 a0002c0002t0001g0063 a0002c0002t0001g0064 others(1): Show |
5 | HG01169.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-1087T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714494 | |||||||
| chr11:68714762 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1020+1075T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68714762 | |||||||
| chr11:68715021 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
132 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1020+816T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715021 | |||||||
| chr11:68715184 | CG | C | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1020+652delC | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715184 | |||||||
| chr11:68715372 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1020+465A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715372 | |||||||
| chr11:68715439 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(26): Show |
40 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1020+398G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715439 | |||||||
| chr11:68715485 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1020+352C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715485 | |||||||
| chr11:68715517 | A | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1020+320T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715517 | |||||||
| chr11:68715539 | TAAACTCC others(7): Show |
T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1020+284_1020+297d others(16): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715539 | |||||||
| chr11:68715551 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1020+286A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715551 | |||||||
| chr11:68715660 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1020+177T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 7/9 | chr11 | 68715660 | |||||||
| chr11:68716009 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918-70T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716009 | |||||||
| chr11:68716132 | G | A | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.918-193C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716132 | |||||||
| chr11:68716432 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.918-493C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716432 | |||||||
| chr11:68716546 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
203 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.918-607C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716546 | |||||||
| chr11:68716826 | C | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.918-887G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716826 | |||||||
| chr11:68716839 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918-900C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716839 | |||||||
| chr11:68716907 | A | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.918-968T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716907 | |||||||
| chr11:68716928 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.918-989C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716928 | |||||||
| chr11:68716960 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918-1021T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68716960 | |||||||
| chr11:68717006 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.918-1067G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717006 | |||||||
| chr11:68717082 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918-1143G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717082 | |||||||
| chr11:68717317 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01496.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.918-1378G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717317 | |||||||
| chr11:68717364 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.918-1425T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717364 | |||||||
| chr11:68717414 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.918-1475G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717414 | |||||||
| chr11:68717515 | C | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.918-1576G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717515 | |||||||
| chr11:68717585 | G | A | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.918-1646C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717585 | |||||||
| chr11:68717645 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.918-1706C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717645 | |||||||
| chr11:68717751 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
199 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.918-1812T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717751 | |||||||
| chr11:68717757 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
204 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.918-1818A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717757 | |||||||
| chr11:68717848 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.918-1909A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68717848 | |||||||
| chr11:68718083 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.918-2144C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718083 | |||||||
| chr11:68718083 | GGCCCAGT others(51): Show |
G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.918-2202_918-2145d others(60): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718083 | |||||||
| chr11:68718098 | C | T | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.918-2159G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718098 | |||||||
| chr11:68718127 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.918-2188G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718127 | |||||||
| chr11:68718147 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.918-2208C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718147 | |||||||
| chr11:68718158 | C | G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.918-2219G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718158 | |||||||
| chr11:68718167 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.918-2228C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718167 | |||||||
| chr11:68718167 | G | GCAGCCCC others(22): Show |
114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.918-2229_918-2228i others(31): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718167 | |||||||
| chr11:68718167 | G | GCAGGCCC others(22): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.918-2229_918-2228i others(31): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718167 | |||||||
| chr11:68718356 | C | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(29): Show |
43 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.918-2417G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718356 | |||||||
| chr11:68718562 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.918-2623C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718562 | |||||||
| chr11:68718686 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.918-2747A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718686 | |||||||
| chr11:68718688 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.918-2749G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718688 | |||||||
| chr11:68718796 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.918-2857A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718796 | |||||||
| chr11:68718942 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0168 a0001c0001t0001g0171 others(3): Show |
7 | HG02258.hp1 HG02486.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.918-3003G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718942 | |||||||
| chr11:68718946 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.918-3007G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68718946 | |||||||
| chr11:68719024 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.918-3085C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719024 | |||||||
| chr11:68719035 | G | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.918-3096C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719035 | |||||||
| chr11:68719140 | T | C | 1 | a0001c0009t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918-3201A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719140 | |||||||
| chr11:68719194 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.918-3255G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719194 | |||||||
| chr11:68719418 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918-3479G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719418 | |||||||
| chr11:68719480 | T | G | 1 | a0001c0005t0001g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.918-3541A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719480 | |||||||
| chr11:68719652 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.918-3713T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719652 | |||||||
| chr11:68719762 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.918-3823A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719762 | |||||||
| chr11:68719807 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0179 |
4 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.918-3868C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719807 | |||||||
| chr11:68719812 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0096 |
5 | HG00639.hp1 HG00738.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.918-3873T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68719812 | |||||||
| chr11:68720040 | T | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
203 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.918-4101A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720040 | |||||||
| chr11:68720045 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
194 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.918-4106T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720045 | |||||||
| chr11:68720177 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(27): Show |
41 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.918-4238C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720177 | |||||||
| chr11:68720186 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.918-4247C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720186 | |||||||
| chr11:68720351 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918-4412A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720351 | |||||||
| chr11:68720366 | T | C | 1 | a0001c0001t0009g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.918-4427A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720366 | |||||||
| chr11:68720575 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918-4636G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720575 | |||||||
| chr11:68720673 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0158 |
3 | HG01109.hp2 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.918-4734G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68720673 | |||||||
| chr11:68721006 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.918-5067A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721006 | |||||||
| chr11:68721060 | CTTTT | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.918-5125_918-5122d others(6): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721060 | |||||||
| chr11:68721255 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0193 |
2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.918-5316C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721255 | |||||||
| chr11:68721341 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.918-5402G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721341 | |||||||
| chr11:68721364 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0150 |
3 | HG02602.hp2 HG02683.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.918-5425T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721364 | |||||||
| chr11:68721369 | C | T | 1 | a0001c0001t0001g0022 | 2 | NA18957.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.918-5430G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721369 | |||||||
| chr11:68721407 | C | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
11 | HG01070.hp1 HG01175.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.918-5468G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721407 | |||||||
| chr11:68721430 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0002g0017 |
4 | HG00609.hp1 NA18961.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.918-5491C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721430 | |||||||
| chr11:68721461 | TG | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0179 |
4 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.918-5523delC | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721461 | |||||||
| chr11:68721698 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.918-5759A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721698 | |||||||
| chr11:68721705 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
200 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.918-5766G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721705 | |||||||
| chr11:68721718 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918-5779G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721718 | |||||||
| chr11:68721832 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.918-5893G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68721832 | |||||||
| chr11:68722006 | CCAGATAC others(9): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.918-6083_918-6068d others(18): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68722006 | |||||||
| chr11:68722186 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.918-6247A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68722186 | |||||||
| chr11:68722193 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.918-6254T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68722193 | |||||||
| chr11:68722349 | G | T | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.918-6410C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68722349 | |||||||
| chr11:68722909 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.918-6970A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68722909 | |||||||
| chr11:68723203 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.918-7264T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723203 | |||||||
| chr11:68723282 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(29): Show |
43 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.918-7343A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723282 | |||||||
| chr11:68723462 | T | TA | 33 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0031 others(30): Show |
44 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.918-7524dupT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723462 | |||||||
| chr11:68723462 | TA | T | 14 | a0001c0001t0001g0095 a0001c0001t0001g0111 a0001c0001t0001g0115 others(11): Show |
14 | HG01070.hp1 HG01167.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.918-7524delT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723462 | |||||||
| chr11:68723627 | G | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.918-7688C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723627 | |||||||
| chr11:68723678 | A | G | 1 | a0001c0001t0006g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.918-7739T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723678 | |||||||
| chr11:68723875 | A | G | 1 | a0001c0001t0001g0016 | 3 | HG02145.hp2 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.918-7936T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723875 | |||||||
| chr11:68723898 | C | A | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918-7959G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723898 | |||||||
| chr11:68723947 | C | T | 1 | a0001c0001t0006g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.918-8008G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68723947 | |||||||
| chr11:68724053 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.918-8114C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68724053 | |||||||
| chr11:68724234 | A | G | 1 | a0001c0005t0001g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.918-8295T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68724234 | |||||||
| chr11:68724301 | A | G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.918-8362T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68724301 | |||||||
| chr11:68724484 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0178 |
2 | HG02258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.918-8545C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68724484 | |||||||
| chr11:68724697 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.918-8758G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68724697 | |||||||
| chr11:68725234 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.918-9295A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68725234 | |||||||
| chr11:68725257 | G | A | 1 | a0001c0001t0005g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.918-9318C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68725257 | |||||||
| chr11:68725379 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.918-9440T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68725379 | |||||||
| chr11:68725623 | C | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0140 others(7): Show |
15 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.918-9684G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68725623 | |||||||
| chr11:68725638 | TTTG | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.918-9702_918-9700d others(5): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68725638 | |||||||
| chr11:68725641 | G | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02895.hp2 HG02897.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.918-9702C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68725641 | |||||||
| chr11:68725775 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
196 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.918-9836T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68725775 | |||||||
| chr11:68726128 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918-10189G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68726128 | |||||||
| chr11:68726244 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
203 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.918-10305A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68726244 | |||||||
| chr11:68726318 | TA | T | 9 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0061 others(6): Show |
11 | HG01169.hp1 HG01261.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.918-10380delT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68726318 | |||||||
| chr11:68726516 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.918-10577T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68726516 | |||||||
| chr11:68726546 | T | C | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.918-10607A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68726546 | |||||||
| chr11:68726856 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.918-10917A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68726856 | |||||||
| chr11:68726922 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918-10983T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68726922 | |||||||
| chr11:68727003 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.918-11064C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727003 | |||||||
| chr11:68727068 | C | CA | 9 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(6): Show |
10 | HG00609.hp2 HG02300.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.918-11130dupT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727068 | |||||||
| chr11:68727181 | C | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(22): Show |
36 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.918-11242G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727181 | |||||||
| chr11:68727287 | A | T | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918-11348T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727287 | |||||||
| chr11:68727493 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.917+11207G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727493 | |||||||
| chr11:68727606 | A | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.917+11094T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727606 | |||||||
| chr11:68727632 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.917+11068A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727632 | |||||||
| chr11:68727650 | G | A | 1 | a0001c0001t0001g0011 | 3 | HG00639.hp1 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.917+11050C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727650 | |||||||
| chr11:68727840 | C | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.917+10860G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727840 | |||||||
| chr11:68727905 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.917+10795C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727905 | |||||||
| chr11:68727994 | T | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
204 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.917+10706A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68727994 | |||||||
| chr11:68728008 | C | T | 1 | a0001c0001t0001g0014 | 3 | HG01891.hp2 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.917+10692G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68728008 | |||||||
| chr11:68728108 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.917+10592C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68728108 | |||||||
| chr11:68728172 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
196 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.917+10528T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68728172 | |||||||
| chr11:68728301 | G | A | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.917+10399C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68728301 | |||||||
| chr11:68728323 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.917+10377C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68728323 | |||||||
| chr11:68728361 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.917+10339G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68728361 | |||||||
| chr11:68728368 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.917+10332C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68728368 | |||||||
| chr11:68729199 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.917+9501C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729199 | |||||||
| chr11:68729325 | A | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0103 others(2): Show |
6 | NA18957.hp2 NA18979.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.917+9375T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729325 | |||||||
| chr11:68729350 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02922.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.917+9350G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729350 | |||||||
| chr11:68729369 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
204 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.917+9330delT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729369 | |||||||
| chr11:68729523 | C | CA | 9 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(6): Show |
9 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.917+9176dupT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729523 | |||||||
| chr11:68729523 | CA | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
35 | HG01070.hp2 HG01071.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.917+9176delT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729523 | |||||||
| chr11:68729757 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0165 |
5 | NA18940.hp2 NA18944.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.917+8943C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729757 | |||||||
| chr11:68729787 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0092 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.917+8913T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729787 | |||||||
| chr11:68729903 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
199 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.917+8797A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68729903 | |||||||
| chr11:68730194 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
153 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.917+8506C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730194 | |||||||
| chr11:68730264 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.917+8436C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730264 | |||||||
| chr11:68730477 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.917+8223A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730477 | |||||||
| chr11:68730625 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.917+8075A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730625 | |||||||
| chr11:68730687 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+8013G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730687 | |||||||
| chr11:68730691 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+8009T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730691 | |||||||
| chr11:68730693 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+8007C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730693 | |||||||
| chr11:68730695 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+8005A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730695 | |||||||
| chr11:68730696 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+8004C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730696 | |||||||
| chr11:68730699 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+8001C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730699 | |||||||
| chr11:68730704 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7996T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730704 | |||||||
| chr11:68730706 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7994T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730706 | |||||||
| chr11:68730707 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7993T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730707 | |||||||
| chr11:68730709 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7991A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730709 | |||||||
| chr11:68730717 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7983G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730717 | |||||||
| chr11:68730723 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7977T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730723 | |||||||
| chr11:68730724 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7976C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730724 | |||||||
| chr11:68730725 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7975C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730725 | |||||||
| chr11:68730728 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7972C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730728 | |||||||
| chr11:68730729 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7971T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730729 | |||||||
| chr11:68730730 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7970C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730730 | |||||||
| chr11:68730731 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7969C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730731 | |||||||
| chr11:68730734 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7966C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730734 | |||||||
| chr11:68730735 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7965G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730735 | |||||||
| chr11:68730737 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7963C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730737 | |||||||
| chr11:68730747 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.917+7953T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730747 | |||||||
| chr11:68730796 | CA | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0036 others(44): Show |
60 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.917+7903delT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730796 | |||||||
| chr11:68730883 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.917+7817T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730883 | |||||||
| chr11:68730941 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.917+7759G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730941 | |||||||
| chr11:68730994 | G | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0042 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.917+7706C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68730994 | |||||||
| chr11:68731066 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.917+7634G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731066 | |||||||
| chr11:68731166 | T | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(26): Show |
40 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.917+7534A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731166 | |||||||
| chr11:68731235 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.917+7465T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731235 | |||||||
| chr11:68731356 | G | C | 1 | a0001c0001t0001g0021 | 2 | NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.917+7344C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731356 | |||||||
| chr11:68731445 | T | TA | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
254 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.917+7254dupT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731445 | |||||||
| chr11:68731464 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.917+7236T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731464 | |||||||
| chr11:68731558 | T | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
196 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.917+7142A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731558 | |||||||
| chr11:68731585 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.917+7115C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731585 | |||||||
| chr11:68731592 | A | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.917+7108T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731592 | |||||||
| chr11:68731602 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.917+7098C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731602 | |||||||
| chr11:68731603 | G | T | 1 | a0002c0002t0001g0063 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.917+7097C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731603 | |||||||
| chr11:68731675 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.917+7025G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731675 | |||||||
| chr11:68731759 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.917+6941G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68731759 | |||||||
| chr11:68732073 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.917+6627C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732073 | |||||||
| chr11:68732088 | A | C | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.917+6612T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732088 | |||||||
| chr11:68732143 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0042 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.917+6557C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732143 | |||||||
| chr11:68732332 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.917+6368A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732332 | |||||||
| chr11:68732406 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
132 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.917+6294G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732406 | |||||||
| chr11:68732480 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.917+6220C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732480 | |||||||
| chr11:68732485 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.917+6215C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732485 | |||||||
| chr11:68732629 | C | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.917+6071G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732629 | |||||||
| chr11:68732662 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.917+6038C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732662 | |||||||
| chr11:68732673 | A | C | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.917+6027T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732673 | |||||||
| chr11:68732716 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.917+5984A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732716 | |||||||
| chr11:68732778 | T | C | 1 | a0001c0009t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.917+5922A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732778 | |||||||
| chr11:68732818 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.917+5882C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732818 | |||||||
| chr11:68732899 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.917+5801C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68732899 | |||||||
| chr11:68733121 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.917+5579T>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68733121 | |||||||
| chr11:68733149 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.917+5551C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68733149 | |||||||
| chr11:68733370 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0077 others(2): Show |
9 | HG02056.hp2 NA18951.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.917+5330A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68733370 | |||||||
| chr11:68733495 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.917+5205C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68733495 | |||||||
| chr11:68733565 | C | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.917+5135G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68733565 | |||||||
| chr11:68733864 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02922.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.917+4836T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68733864 | |||||||
| chr11:68734186 | T | A | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.917+4514A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68734186 | |||||||
| chr11:68734210 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.917+4490C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68734210 | |||||||
| chr11:68734434 | G | A | 2 | a0001c0001t0001g0141 a0006c0008t0001g0142 |
2 | HG01257.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.917+4266C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68734434 | |||||||
| chr11:68734519 | A | G | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0124 others(1): Show |
4 | HG00673.hp1 HG02071.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.917+4181T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68734519 | |||||||
| chr11:68734730 | T | A | 2 | a0001c0001t0001g0023 a0007c0006t0001g0074 |
3 | NA18952.hp2 NA18975.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.917+3970A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68734730 | |||||||
| chr11:68734877 | G | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0026 others(35): Show |
53 | HG01070.hp2 HG01071.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.917+3823C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68734877 | |||||||
| chr11:68734897 | C | A | 1 | a0001c0001t0001g0026 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.917+3803G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68734897 | |||||||
| chr11:68735055 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.917+3645G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68735055 | |||||||
| chr11:68735079 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0120 |
3 | HG02293.hp1 NA18957.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.917+3621C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68735079 | |||||||
| chr11:68735240 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.917+3460C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68735240 | |||||||
| chr11:68735305 | C | A | 1 | a0001c0005t0001g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.917+3395G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68735305 | |||||||
| chr11:68735442 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.917+3258G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68735442 | |||||||
| chr11:68735520 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.917+3180G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68735520 | |||||||
| chr11:68735735 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.917+2965C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68735735 | |||||||
| chr11:68736299 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.917+2401T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68736299 | |||||||
| chr11:68736902 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.917+1798A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68736902 | |||||||
| chr11:68736958 | G | A | 7 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0063 others(4): Show |
9 | HG01169.hp1 HG01261.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.917+1742C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68736958 | |||||||
| chr11:68737006 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.917+1694A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737006 | |||||||
| chr11:68737226 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0109 |
2 | NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.917+1474C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737226 | |||||||
| chr11:68737323 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.917+1377T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737323 | |||||||
| chr11:68737368 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.917+1332C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737368 | |||||||
| chr11:68737439 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.917+1261G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737439 | |||||||
| chr11:68737504 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(25): Show |
39 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.917+1196G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737504 | |||||||
| chr11:68737505 | G | A | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.917+1195C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737505 | |||||||
| chr11:68737596 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.917+1104T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737596 | |||||||
| chr11:68737626 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.917+1074T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737626 | |||||||
| chr11:68737684 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0118 |
3 | NA18965.hp2 NA18986.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.917+1016C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737684 | |||||||
| chr11:68737706 | T | C | 1 | a0001c0001t0007g0113 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.917+994A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737706 | |||||||
| chr11:68737794 | T | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
153 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.917+906A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737794 | |||||||
| chr11:68737839 | G | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0114 others(4): Show |
10 | HG01934.hp1 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.917+861C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737839 | |||||||
| chr11:68737907 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
203 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.917+793G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737907 | |||||||
| chr11:68737921 | AAAAC | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
153 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.917+775_917+778del others(4): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68737921 | |||||||
| chr11:68738279 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.917+421G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738279 | |||||||
| chr11:68738280 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0158 |
3 | HG01109.hp2 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.917+420C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738280 | |||||||
| chr11:68738284 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.917+416C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738284 | |||||||
| chr11:68738315 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.917+385G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738315 | |||||||
| chr11:68738324 | T | G | 4 | a0001c0001t0001g0184 a0001c0004t0001g0200 a0001c0004t0001g0201 others(1): Show |
4 | HG02717.hp2 HG03471.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.917+376A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738324 | |||||||
| chr11:68738355 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.917+345G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738355 | |||||||
| chr11:68738557 | T | C | 1 | a0002c0002t0001g0019 | 2 | HG01261.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.917+143A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738557 | |||||||
| chr11:68738694 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01109.hp2 HG01358.hp2 |
splice_region_variant&intron_variant | LOW | c.917+6G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 6/9 | chr11 | 68738694 | |||||||
| chr11:68738868 | A | G | 1 | a0001c0001t0001g0020 | 2 | NA19058.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.829-80T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68738868 | |||||||
| chr11:68739034 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.829-246A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739034 | |||||||
| chr11:68739056 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.829-268C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739056 | |||||||
| chr11:68739364 | G | A | 1 | a0001c0001t0009g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.829-576C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739364 | |||||||
| chr11:68739455 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.829-667A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739455 | |||||||
| chr11:68739688 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.829-900G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739688 | |||||||
| chr11:68739735 | G | A | 1 | a0001c0001t0006g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.829-947C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739735 | |||||||
| chr11:68739765 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.829-977C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739765 | |||||||
| chr11:68739791 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.829-1003G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739791 | |||||||
| chr11:68739891 | G | C | 1 | a0001c0001t0009g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.829-1103C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68739891 | |||||||
| chr11:68740009 | T | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0079 others(4): Show |
10 | HG00558.hp1 HG00621.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.829-1221A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740009 | |||||||
| chr11:68740097 | G | A | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.829-1309C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740097 | |||||||
| chr11:68740184 | C | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.829-1396G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740184 | |||||||
| chr11:68740403 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.829-1615C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740403 | |||||||
| chr11:68740451 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.829-1663A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740451 | |||||||
| chr11:68740508 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.829-1720A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740508 | |||||||
| chr11:68740570 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0042 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.828+1748C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740570 | |||||||
| chr11:68740580 | A | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.828+1738T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740580 | |||||||
| chr11:68740849 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.828+1469A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68740849 | |||||||
| chr11:68741003 | C | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
11 | HG01070.hp1 HG01175.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.828+1315G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741003 | |||||||
| chr11:68741244 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.828+1074G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741244 | |||||||
| chr11:68741317 | G | T | 3 | a0001c0001t0001g0027 a0003c0003t0001g0035 a0003c0003t0001g0181 |
5 | HG02027.hp1 HG02080.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.828+1001C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741317 | |||||||
| chr11:68741425 | T | TG | 12 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0009t0001g0060 others(9): Show |
14 | HG01169.hp1 HG01261.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.828+892dupC | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741425 | |||||||
| chr11:68741426 | G | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.828+892C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741426 | |||||||
| chr11:68741523 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.828+795T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741523 | |||||||
| chr11:68741777 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0046 others(3): Show |
6 | HG01243.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.828+541C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741777 | |||||||
| chr11:68741779 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0046 others(3): Show |
6 | HG01243.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.828+539C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741779 | |||||||
| chr11:68741895 | C | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.828+423G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741895 | |||||||
| chr11:68741996 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0169 others(5): Show |
11 | HG00609.hp1 HG01884.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.828+322G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68741996 | |||||||
| chr11:68742007 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.828+311C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68742007 | |||||||
| chr11:68742102 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.828+216G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68742102 | |||||||
| chr11:68742178 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.828+140G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 5/9 | chr11 | 68742178 | |||||||
| chr11:68742529 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.752-135C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68742529 | |||||||
| chr11:68742540 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.752-146A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68742540 | |||||||
| chr11:68742722 | C | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.752-328G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68742722 | |||||||
| chr11:68742819 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.752-425C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68742819 | |||||||
| chr11:68742925 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0004g0045 a0001c0001t0004g0047 |
3 | HG02976.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.752-531C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68742925 | |||||||
| chr11:68743016 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
204 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.752-622A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743016 | |||||||
| chr11:68743038 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.752-644A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743038 | |||||||
| chr11:68743111 | C | G | 1 | a0001c0001t0005g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.752-717G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743111 | |||||||
| chr11:68743112 | G | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02922.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.752-718C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743112 | |||||||
| chr11:68743234 | C | CT | 15 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0077 others(12): Show |
15 | HG02083.hp2 HG02486.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.752-841dupA | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743234 | |||||||
| chr11:68743234 | C | CTT | 19 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(16): Show |
30 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.752-842_752-841dup others(2): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743234 | |||||||
| chr11:68743234 | CT | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG00642.hp1 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.752-841delA | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743234 | |||||||
| chr11:68743234 | CTT | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0184 others(4): Show |
9 | HG00609.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-842_752-841del others(2): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743234 | |||||||
| chr11:68743669 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.752-1275G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743669 | |||||||
| chr11:68743686 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.752-1292T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743686 | |||||||
| chr11:68743824 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.751+1167A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743824 | |||||||
| chr11:68743901 | C | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.751+1090G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743901 | |||||||
| chr11:68743956 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.751+1035C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68743956 | |||||||
| chr11:68744092 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.751+899T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744092 | |||||||
| chr11:68744164 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.751+827C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744164 | |||||||
| chr11:68744223 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
277 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.751+768T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744223 | |||||||
| chr11:68744271 | C | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.751+720G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744271 | |||||||
| chr11:68744277 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.751+714A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744277 | |||||||
| chr11:68744306 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.751+685G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744306 | |||||||
| chr11:68744484 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.751+507C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744484 | |||||||
| chr11:68744677 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
153 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.751+314G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744677 | |||||||
| chr11:68744813 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.751+178T>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744813 | |||||||
| chr11:68744901 | G | T | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.751+90C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 4/9 | chr11 | 68744901 | |||||||
| chr11:68745164 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.631-53A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745164 | |||||||
| chr11:68745300 | C | CA | 20 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0046 others(17): Show |
21 | HG00423.hp2 HG00673.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.631-190dupT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745300 | |||||||
| chr11:68745317 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631-206T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745317 | |||||||
| chr11:68745614 | A | G | 1 | a0001c0009t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631-503T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745614 | |||||||
| chr11:68745773 | T | C | 5 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-662A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745773 | |||||||
| chr11:68745778 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
205 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.631-667T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745778 | |||||||
| chr11:68745979 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.631-868A>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745979 | |||||||
| chr11:68745998 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.631-887T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68745998 | |||||||
| chr11:68746170 | T | TAC | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
133 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.630+1036_630+1037d others(4): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746170 | |||||||
| chr11:68746170 | T | TACACACA others(17): Show |
1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.630+1014_630+1037d others(26): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746170 | |||||||
| chr11:68746170 | TAC | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(70): Show |
110 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(107): Show |
intron_variant | MODIFIER | c.630+1036_630+1037d others(4): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746170 | |||||||
| chr11:68746170 | TACAC | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
6 | HG00609.hp1 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+1034_630+1037d others(6): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746170 | |||||||
| chr11:68746321 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.630+887G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746321 | |||||||
| chr11:68746354 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.630+854C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746354 | |||||||
| chr11:68746438 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.630+770T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746438 | |||||||
| chr11:68746549 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0036 others(27): Show |
41 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.630+659C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746549 | |||||||
| chr11:68746797 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.630+411G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746797 | |||||||
| chr11:68746830 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.630+378C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746830 | |||||||
| chr11:68746878 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.630+330C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746878 | |||||||
| chr11:68746936 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.630+272A>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68746936 | |||||||
| chr11:68747028 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.630+180C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68747028 | |||||||
| chr11:68747056 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.630+152G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68747056 | |||||||
| chr11:68747059 | G | A | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.630+149C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68747059 | |||||||
| chr11:68747107 | C | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0141 others(2): Show |
9 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+101G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68747107 | |||||||
| chr11:68747107 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02922.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.630+101G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 3/9 | chr11 | 68747107 | |||||||
| chr11:68747530 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.472-164T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68747530 | |||||||
| chr11:68747771 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.472-405G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68747771 | |||||||
| chr11:68748067 | C | T | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.472-701G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68748067 | |||||||
| chr11:68748385 | CATATAAA others(10): Show |
C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-1036_472-1020d others(19): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68748385 | |||||||
| chr11:68748443 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.472-1077C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68748443 | |||||||
| chr11:68748713 | CAGAA | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02922.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.472-1351_472-1348d others(6): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68748713 | |||||||
| chr11:68748996 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.471+1194G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68748996 | |||||||
| chr11:68748997 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.471+1193C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68748997 | |||||||
| chr11:68749053 | T | C | 1 | a0004c0007t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.471+1137A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68749053 | |||||||
| chr11:68749358 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+832T>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68749358 | |||||||
| chr11:68749758 | G | GA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(33): Show |
49 | HG00642.hp1 HG00738.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.471+431dupT | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68749758 | |||||||
| chr11:68749848 | C | G | 1 | a0001c0001t0002g0017 | 3 | HG00609.hp1 NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.471+342G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68749848 | |||||||
| chr11:68749915 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.471+275C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68749915 | |||||||
| chr11:68749998 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.471+192C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68749998 | |||||||
| chr11:68750139 | T | C | 3 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0005t0001g0206 |
3 | HG03471.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.471+51A>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 2/9 | chr11 | 68750139 | |||||||
| chr11:68750768 | A | ACAGCCAA others(8): Show |
1 | a0001c0001t0001g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-39-84_-39-70dupCC others(13): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750768 | |||||||
| chr11:68750768 | ACAGCCAA others(8): Show |
A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.-39-84_-39-70delCC others(13): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750768 | |||||||
| chr11:68750788 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-39-89G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750788 | |||||||
| chr11:68750799 | C | T | 1 | a0001c0001t0001g0010 | 3 | HG00597.hp2 HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-39-100G>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750799 | |||||||
| chr11:68750811 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-39-112C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750811 | |||||||
| chr11:68750825 | GGC | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-39-128_-39-127del others(2): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750825 | |||||||
| chr11:68750904 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18959.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-39-205C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750904 | |||||||
| chr11:68750932 | T | TAGGTGAG others(8): Show |
2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-39-248_-39-234dup others(15): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750932 | |||||||
| chr11:68750932 | TAGGTGAG others(8): Show |
T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(14): Show |
intron_variant | MODIFIER | c.-39-248_-39-234del others(15): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750932 | |||||||
| chr11:68750943 | C | CGGCCAGG others(106): Show |
1 | a0001c0001t0006g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-39-357_-39-245dup others(113): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750943 | |||||||
| chr11:68750987 | G | A | 1 | a0001c0005t0001g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-39-288C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750987 | |||||||
| chr11:68750999 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-39-300C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68750999 | |||||||
| chr11:68751051 | GGAGGGGC others(21): Show |
G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0207 |
3 | HG00423.hp2 NA18939.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-40+341_-39-353del others(28): Show |
TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751051 | |||||||
| chr11:68751058 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-39-359G>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751058 | |||||||
| chr11:68751073 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0042 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-40+347C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751073 | |||||||
| chr11:68751116 | G | A | 1 | a0005c0010t0001g0208 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-40+304C>T | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751116 | |||||||
| chr11:68751158 | GC | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
297 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(294): Show |
intron_variant | MODIFIER | c.-40+261delG | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751158 | |||||||
| chr11:68751160 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-40+260G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751160 | |||||||
| chr11:68751162 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-40+258C>G | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751162 | |||||||
| chr11:68751164 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-40+256G>C | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751164 | |||||||
| chr11:68751258 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-40+162C>A | TESMIN | ENSG00000132749.11 | transcript | ENST00000255087.10 | protein_coding | 1/9 | chr11 | 68751258 |