Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7084 |
| ensemblid | ENSG00000166548.17 |
| hgncid | 11831 |
| symbol | TK2 |
| name | thymidine kinase 2 |
| refseq_nuc | NM_004614.5 |
| refseq_prot | NP_004605.4 |
| ensembl_nuc | ENST00000544898.6 |
| ensembl_prot | ENSP00000440898.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 66508003 |
| end | 66550122 |
| strand | - |
| ver | v1.2 |
| region | chr16:66508003-66550122 |
| region5000 | chr16:66503003-66555122 |
| regionname0 | TK2_chr16_66508003_66550122 |
| regionname5000 | TK2_chr16_66503003_66555122 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 265 | 297 | 83 | 54 | 122 | 6 | 30 | 89 | TK2_chr16_66503003_66555122 | TK2 | MLLWP others(260): Show |
chr16 | 66503003 | 66555122 |
| a0002 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | MLLWP others(260): Show |
chr16 | 66503003 | 66555122 |
| a0003 | 0/0 | 265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | MLLWP others(260): Show |
chr16 | 66503003 | 66555122 |
| a0004 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | MLLWP others(260): Show |
chr16 | 66503003 | 66555122 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 795 | 297 | 83 | 54 | 122 | 6 | 30 | TK2_chr16_66503003_66555122 | TK2 | ATGCT others(790): Show |
chr16 | 66503003 | 66555122 | ||
| a0002c0003 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | ATGCT others(790): Show |
chr16 | 66503003 | 66555122 | ||
| a0003c0004 | 0/0 | 795 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | ATGCT others(790): Show |
chr16 | 66503003 | 66555122 | ||
| a0004c0002 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | ATGCT others(790): Show |
chr16 | 66503003 | 66555122 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4824 | 100 | 25 | 23 | 36 | 3 | 11 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0002 | 0/0 | 4824 | 61 | 26 | 9 | 19 | 0 | 7 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0003 | 0/0 | 4823 | 45 | 2 | 12 | 27 | 2 | 2 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0004 | 0/0 | 4826 | 19 | 1 | 2 | 15 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0005 | 0/0 | 4826 | 11 | 0 | 0 | 7 | 0 | 4 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0006 | 0/0 | 4824 | 7 | 5 | 2 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0007 | 0/0 | 4824 | 7 | 0 | 5 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0008 | 0/0 | 4824 | 6 | 6 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0009 | 0/0 | 4826 | 5 | 5 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0010 | 0/0 | 4825 | 4 | 1 | 0 | 3 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4820): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0011 | 0/0 | 4823 | 2 | 1 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0012 | 0/0 | 4825 | 2 | 1 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4820): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0013 | 0/0 | 4826 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0014 | 0/0 | 4823 | 2 | 0 | 0 | 0 | 0 | 2 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0015 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0016 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0017 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0018 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0019 | 0/0 | 4823 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0020 | 0/0 | 4823 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0021 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0022 | 0/0 | 4824 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0023 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0024 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0025 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0026 | 0/0 | 4823 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0027 | 0/0 | 4823 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0028 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0029 | 0/0 | 4823 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0030 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0031 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0032 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0033 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0034 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0035 | 0/0 | 4825 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4820): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0036 | 0/0 | 4826 | 1 | 0 | 0 | 0 | 1 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0037 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4821): Show |
chr16 | 66503003 | 66555122 |
| a0001c0001t0038 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0002c0003t0003 | 0/0 | 4823 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4818): Show |
chr16 | 66503003 | 66555122 |
| a0003c0004t0002 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| a0004c0002t0002 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | AGTCG others(4819): Show |
chr16 | 66503003 | 66555122 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 14 | 1 | 6 | 5 | 1 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0004 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0010 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0001 | 0/0 | 16 | 0 | 7 | 7 | 1 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0007g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0007g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0008g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0010g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0010g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0011g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0013g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0013g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0014g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0015g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0016g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0017g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0018g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0020g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0021g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0022g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0023g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0024g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0025g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0026g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0027g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0028g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0029g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0030g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0031g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0032g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0033g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0034g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0035g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0036g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0037g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0001c0001t0038g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0003c0004t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| a0004c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0036 | g0201 | EUR | FIN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00438 | hp1 | a0001 | c0001 | t0026 | g0113 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0133 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00597 | hp2 | a0001 | c0001 | t0030 | g0146 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00673 | hp1 | a0002 | c0003 | t0003 | g0062 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | CHS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0198 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0184 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01256 | hp1 | a0001 | c0001 | t0035 | g0204 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0186 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0211 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0182 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0183 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | CDX | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0021 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0206 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0217 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0181 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0215 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0213 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02683 | hp1 | a0001 | c0001 | t0020 | g0042 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02717 | hp1 | a0003 | c0004 | t0002 | g0141 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0216 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02809 | hp2 | a0001 | c0001 | t0033 | g0189 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02886 | hp1 | a0001 | c0001 | t0027 | g0185 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02895 | hp2 | a0001 | c0001 | t0029 | g0180 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0179 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02922 | hp2 | a0001 | c0001 | t0028 | g0138 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0158 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0037 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0041 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03239 | hp1 | a0001 | c0001 | t0022 | g0110 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03491 | hp2 | a0001 | c0001 | t0014 | g0034 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0021 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03492 | hp2 | a0001 | c0001 | t0014 | g0034 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0014 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0040 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | STU | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | YRI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | YRI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18747 | hp1 | a0001 | c0001 | t0017 | g0060 | EAS | CHB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | YRI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18942 | hp2 | a0001 | c0001 | t0010 | g0026 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18965 | hp2 | a0001 | c0001 | t0019 | g0093 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18967 | hp1 | a0001 | c0001 | t0010 | g0026 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18975 | hp2 | a0001 | c0001 | t0025 | g0081 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18998 | hp1 | a0001 | c0001 | t0037 | g0197 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19000 | hp2 | a0001 | c0001 | t0013 | g0193 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19005 | hp1 | a0001 | c0001 | t0012 | g0116 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19010 | hp2 | a0001 | c0001 | t0018 | g0052 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19011 | hp1 | a0001 | c0001 | t0021 | g0107 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19030 | hp1 | a0001 | c0001 | t0024 | g0123 | AFR | LWK | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | LWK | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19062 | hp1 | a0004 | c0002 | t0002 | g0142 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19062 | hp2 | a0001 | c0001 | t0013 | g0202 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19070 | hp1 | a0001 | c0001 | t0015 | g0079 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19085 | hp2 | a0001 | c0001 | t0031 | g0149 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20129 | hp1 | a0001 | c0001 | t0032 | g0148 | AFR | ASW | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0130 | EUR | TSI | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | GIH | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | GIH | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0049 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03471 | hp1 | a0001 | c0001 | t0038 | g0220 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG06807 | hp1 | a0001 | c0001 | t0023 | g0075 | AFR | USA | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | USA | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20300 | hp1 | a0001 | c0001 | t0034 | g0218 | AFR | USA | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | TK2_chr16_66503003_66555122 | TK2 | chr16 | 66503003 | 66555122 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:66513736 | C | G | 1 | a0003 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.694G>C | p.Val232Leu | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/10 | 755/4824 | 694/798 | 232/265 | chr16 | 66513736 | |||
| chr16:66517807 | C | T | 1 | a0002 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.520G>A | p.Val174Met | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 7/10 | 581/4824 | 520/798 | 174/265 | chr16 | 66517807 | |||
| chr16:66531454 | C | T | 1 | a0004 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.301G>A | p.Asp101Asn | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/10 | 362/4824 | 301/798 | 101/265 | chr16 | 66531454 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:66508182 | G | A | 11 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0013 others(8): Show |
40 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*3786C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 3786 | chr16 | 66508182 | ||||||
| chr16:66508637 | G | A | 1 | a0001c0001t0013 | 2 | NA19000.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3331C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 3331 | chr16 | 66508637 | ||||||
| chr16:66508653 | C | T | 1 | a0001c0001t0027 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3315G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 3315 | chr16 | 66508653 | ||||||
| chr16:66509054 | G | A | 12 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(9): Show |
45 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2914C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2914 | chr16 | 66509054 | ||||||
| chr16:66509060 | T | C | 1 | a0001c0001t0019 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2908A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2908 | chr16 | 66509060 | ||||||
| chr16:66509117 | T | G | 1 | a0001c0001t0020 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2851A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2851 | chr16 | 66509117 | ||||||
| chr16:66509186 | G | A | 1 | a0001c0001t0022 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2782C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2782 | chr16 | 66509186 | ||||||
| chr16:66509331 | C | T | 1 | a0001c0001t0021 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2637G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2637 | chr16 | 66509331 | ||||||
| chr16:66509428 | C | A | 1 | a0001c0001t0011 | 2 | HG02258.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2540G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2540 | chr16 | 66509428 | ||||||
| chr16:66509481 | G | A | 1 | a0001c0001t0031 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2487C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2487 | chr16 | 66509481 | ||||||
| chr16:66509549 | G | A | 2 | a0001c0001t0006 a0001c0001t0029 |
8 | HG00738.hp2 HG01433.hp1 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2419C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2419 | chr16 | 66509549 | ||||||
| chr16:66509583 | G | A | 1 | a0001c0001t0023 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2385C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2385 | chr16 | 66509583 | ||||||
| chr16:66509670 | G | A | 1 | a0001c0001t0036 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2298C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2298 | chr16 | 66509670 | ||||||
| chr16:66509747 | A | G | 17 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(14): Show |
61 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2221T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 2221 | chr16 | 66509747 | ||||||
| chr16:66510057 | T | C | 1 | a0001c0001t0024 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1911A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1911 | chr16 | 66510057 | ||||||
| chr16:66510210 | C | CA | 3 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0035 |
7 | HG00544.hp2 HG01256.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1757dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1757 | chr16 | 66510210 | ||||||
| chr16:66510210 | C | CAA | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(5): Show |
41 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1756_*1757dupTT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1757 | chr16 | 66510210 | ||||||
| chr16:66510210 | CA | C | 9 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(6): Show |
55 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1757delT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1757 | chr16 | 66510210 | ||||||
| chr16:66510228 | A | G | 1 | a0001c0001t0027 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1740 | chr16 | 66510228 | ||||||
| chr16:66510287 | T | C | 1 | a0001c0001t0025 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1681A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1681 | chr16 | 66510287 | ||||||
| chr16:66510881 | G | A | 1 | a0001c0001t0032 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1087C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1087 | chr16 | 66510881 | ||||||
| chr16:66510881 | G | T | 1 | a0001c0001t0033 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 1087 | chr16 | 66510881 | ||||||
| chr16:66511048 | G | A | 1 | a0001c0001t0017 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*920C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 920 | chr16 | 66511048 | ||||||
| chr16:66511135 | A | C | 1 | a0001c0001t0018 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 833 | chr16 | 66511135 | ||||||
| chr16:66511203 | A | G | 17 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(14): Show |
61 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*765T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 765 | chr16 | 66511203 | ||||||
| chr16:66511208 | A | C | 1 | a0001c0001t0033 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 760 | chr16 | 66511208 | ||||||
| chr16:66511517 | C | T | 1 | a0001c0001t0028 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*451G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 451 | chr16 | 66511517 | ||||||
| chr16:66511582 | G | A | 1 | a0001c0001t0037 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*386C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 386 | chr16 | 66511582 | ||||||
| chr16:66511778 | C | T | 1 | a0001c0001t0015 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 190 | chr16 | 66511778 | ||||||
| chr16:66511823 | A | G | 1 | a0001c0001t0027 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 145 | chr16 | 66511823 | ||||||
| chr16:66511911 | T | C | 1 | a0001c0001t0026 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 10/10 | 57 | chr16 | 66511911 | ||||||
| chr16:66550070 | G | A | 1 | a0001c0001t0038 | 1 | HG03471.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/10 | chr16 | 66550070 | |||||||
| chr16:66550091 | G | C | 10 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 others(7): Show |
39 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-30C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/10 | 30 | chr16 | 66550091 | ||||||
| chr16:66550099 | T | C | 22 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(19): Show |
125 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(122): Show |
5_prime_UTR_variant | MODIFIER | c.-38A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/10 | 38 | chr16 | 66550099 | ||||||
| chr16:66550110 | G | A | 1 | a0001c0001t0014 | 2 | HG03491.hp2 HG03492.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/10 | chr16 | 66550110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:66512079 | C | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(46): Show |
65 | HG00544.hp2 HG00621.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.700-13G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66512079 | |||||||
| chr16:66512126 | C | T | 1 | a0001c0001t0011g0021 | 2 | HG02258.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.700-60G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66512126 | |||||||
| chr16:66512504 | G | A | 4 | a0001c0001t0004g0219 a0001c0001t0016g0041 a0001c0001t0034g0218 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-438C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66512504 | |||||||
| chr16:66512644 | A | G | 3 | a0001c0001t0002g0028 a0001c0001t0002g0167 a0001c0001t0002g0168 |
4 | HG03669.hp2 HG03927.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-578T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66512644 | |||||||
| chr16:66512884 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.700-818A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66512884 | |||||||
| chr16:66512887 | C | T | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
44 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.700-821G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66512887 | |||||||
| chr16:66513042 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.699+689C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66513042 | |||||||
| chr16:66513047 | G | C | 42 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(39): Show |
45 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.699+684C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66513047 | |||||||
| chr16:66513368 | A | C | 42 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(39): Show |
45 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.699+363T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66513368 | |||||||
| chr16:66513371 | T | C | 4 | a0001c0001t0002g0140 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+360A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66513371 | |||||||
| chr16:66513507 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.699+224A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66513507 | |||||||
| chr16:66513604 | C | A | 1 | a0001c0001t0013g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.699+127G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66513604 | |||||||
| chr16:66513652 | G | A | 2 | a0001c0001t0002g0154 a0001c0001t0002g0164 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.699+79C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 9/9 | chr16 | 66513652 | |||||||
| chr16:66513838 | C | T | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.619-27G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66513838 | |||||||
| chr16:66513864 | T | C | 56 | a0001c0001t0002g0031 a0001c0001t0004g0013 a0001c0001t0004g0191 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.619-53A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66513864 | |||||||
| chr16:66513874 | G | C | 56 | a0001c0001t0002g0031 a0001c0001t0004g0013 a0001c0001t0004g0191 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.619-63C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66513874 | |||||||
| chr16:66514127 | CCCCTCT | C | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-322_619-317del others(6): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514127 | |||||||
| chr16:66514197 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0085 a0001c0001t0001g0086 others(5): Show |
9 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-386G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514197 | |||||||
| chr16:66514218 | T | C | 2 | a0001c0001t0004g0203 a0001c0001t0005g0014 |
3 | HG00558.hp1 HG03831.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.619-407A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514218 | |||||||
| chr16:66514401 | G | A | 4 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-590C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514401 | |||||||
| chr16:66514406 | C | A | 1 | a0001c0001t0002g0145 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.619-595G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514406 | |||||||
| chr16:66514516 | A | G | 13 | a0001c0001t0002g0031 a0001c0001t0006g0179 a0001c0001t0006g0181 others(10): Show |
16 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.619-705T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514516 | |||||||
| chr16:66514523 | C | T | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-712G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514523 | |||||||
| chr16:66514687 | G | C | 2 | a0001c0001t0002g0137 a0001c0001t0028g0138 |
2 | HG00609.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.619-876C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514687 | |||||||
| chr16:66514937 | T | C | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.619-1126A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66514937 | |||||||
| chr16:66515033 | G | C | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
44 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.619-1222C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515033 | |||||||
| chr16:66515078 | A | G | 1 | a0001c0001t0003g0092 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.619-1267T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515078 | |||||||
| chr16:66515079 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.619-1268A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515079 | |||||||
| chr16:66515169 | TA | T | 44 | a0001c0001t0003g0097 a0001c0001t0004g0013 a0001c0001t0004g0191 others(41): Show |
47 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.619-1359delT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515169 | |||||||
| chr16:66515201 | G | A | 32 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(29): Show |
35 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.619-1390C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515201 | |||||||
| chr16:66515377 | T | C | 43 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(40): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.619-1566A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515377 | |||||||
| chr16:66515483 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0056 others(2): Show |
7 | HG00423.hp1 HG00597.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+1653G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515483 | |||||||
| chr16:66515594 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618+1542G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515594 | |||||||
| chr16:66515843 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.618+1293C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66515843 | |||||||
| chr16:66516083 | C | A | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.618+1053G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66516083 | |||||||
| chr16:66516085 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.618+1051T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66516085 | |||||||
| chr16:66516086 | T | C | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.618+1050A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66516086 | |||||||
| chr16:66516350 | T | C | 1 | a0001c0001t0005g0037 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.618+786A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66516350 | |||||||
| chr16:66516631 | T | C | 13 | a0001c0001t0002g0031 a0001c0001t0006g0179 a0001c0001t0006g0181 others(10): Show |
16 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.618+505A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66516631 | |||||||
| chr16:66516763 | G | C | 1 | a0001c0001t0017g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.618+373C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66516763 | |||||||
| chr16:66516801 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.618+335C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 8/9 | chr16 | 66516801 | |||||||
| chr16:66517235 | T | C | 1 | a0001c0001t0002g0030 | 2 | HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.539-20A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 7/9 | chr16 | 66517235 | |||||||
| chr16:66517275 | G | T | 2 | a0001c0001t0002g0024 a0001c0001t0012g0116 |
3 | NA18998.hp2 NA19005.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.539-60C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 7/9 | chr16 | 66517275 | |||||||
| chr16:66517371 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0051 others(5): Show |
10 | HG00423.hp1 HG00597.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.539-156A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 7/9 | chr16 | 66517371 | |||||||
| chr16:66517391 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0065 others(10): Show |
27 | HG01109.hp2 HG01168.hp2 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.539-176G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 7/9 | chr16 | 66517391 | |||||||
| chr16:66517704 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.538+85G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 7/9 | chr16 | 66517704 | |||||||
| chr16:66518007 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0035g0204 |
2 | HG01256.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.450-130C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66518007 | |||||||
| chr16:66518422 | C | T | 36 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(33): Show |
39 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.450-545G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66518422 | |||||||
| chr16:66518574 | T | C | 3 | a0001c0001t0006g0186 a0001c0001t0006g0187 a0001c0001t0006g0188 |
3 | HG01433.hp1 HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.450-697A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66518574 | |||||||
| chr16:66518579 | G | A | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.450-702C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66518579 | |||||||
| chr16:66518661 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.450-784A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66518661 | |||||||
| chr16:66518965 | T | A | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-1088A>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66518965 | |||||||
| chr16:66518985 | G | A | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
44 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.450-1108C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66518985 | |||||||
| chr16:66519119 | G | A | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.450-1242C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519119 | |||||||
| chr16:66519163 | G | A | 9 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0131 others(6): Show |
11 | HG01109.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.450-1286C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519163 | |||||||
| chr16:66519164 | T | C | 2 | a0001c0001t0002g0137 a0001c0001t0028g0138 |
2 | HG00609.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.450-1287A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519164 | |||||||
| chr16:66519282 | G | A | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
44 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.450-1405C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519282 | |||||||
| chr16:66519380 | T | G | 1 | a0001c0001t0004g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.450-1503A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519380 | |||||||
| chr16:66519555 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.450-1678C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519555 | |||||||
| chr16:66519739 | C | T | 1 | a0001c0001t0008g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.450-1862G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519739 | |||||||
| chr16:66519923 | G | T | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.450-2046C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66519923 | |||||||
| chr16:66520168 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.450-2291C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520168 | |||||||
| chr16:66520196 | T | C | 1 | a0001c0001t0001g0018 | 2 | NA18960.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.450-2319A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520196 | |||||||
| chr16:66520251 | C | T | 1 | a0001c0001t0003g0019 | 2 | NA19012.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.450-2374G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520251 | |||||||
| chr16:66520333 | G | A | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-2456C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520333 | |||||||
| chr16:66520402 | G | A | 11 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(8): Show |
12 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.450-2525C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520402 | |||||||
| chr16:66520448 | G | A | 1 | a0001c0001t0030g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.450-2571C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520448 | |||||||
| chr16:66520623 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0089 |
2 | HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.450-2746G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520623 | |||||||
| chr16:66520637 | G | A | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.450-2760C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520637 | |||||||
| chr16:66520684 | G | A | 51 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(48): Show |
67 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.450-2807C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520684 | |||||||
| chr16:66520929 | C | T | 1 | a0001c0001t0009g0214 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.450-3052G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66520929 | |||||||
| chr16:66521078 | T | C | 1 | a0001c0001t0002g0028 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.450-3201A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66521078 | |||||||
| chr16:66521081 | G | A | 10 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0131 others(7): Show |
12 | HG01109.hp1 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.450-3204C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66521081 | |||||||
| chr16:66521179 | C | A | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.450-3302G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66521179 | |||||||
| chr16:66521335 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.450-3458C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66521335 | |||||||
| chr16:66521607 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0003g0047 |
4 | HG02129.hp2 NA18612.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.450-3730C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66521607 | |||||||
| chr16:66521842 | T | C | 45 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(42): Show |
48 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.450-3965A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66521842 | |||||||
| chr16:66522075 | C | T | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.450-4198G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522075 | |||||||
| chr16:66522106 | C | A | 1 | a0001c0001t0002g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.450-4229G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522106 | |||||||
| chr16:66522118 | C | A | 1 | a0001c0001t0002g0030 | 2 | HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.450-4241G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522118 | |||||||
| chr16:66522133 | C | T | 1 | a0001c0001t0020g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.450-4256G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522133 | |||||||
| chr16:66522241 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.450-4364G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522241 | |||||||
| chr16:66522362 | A | C | 57 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(54): Show |
62 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.450-4485T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522362 | |||||||
| chr16:66522618 | G | A | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.450-4741C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522618 | |||||||
| chr16:66522722 | C | T | 1 | a0001c0001t0004g0219 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450-4845G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522722 | |||||||
| chr16:66522756 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.450-4879G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522756 | |||||||
| chr16:66522841 | G | C | 1 | a0001c0001t0003g0090 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.450-4964C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522841 | |||||||
| chr16:66522859 | C | T | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.450-4982G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522859 | |||||||
| chr16:66522860 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.450-4983C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66522860 | |||||||
| chr16:66523357 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0069 a0001c0001t0001g0077 others(2): Show |
5 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-5480G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66523357 | |||||||
| chr16:66523515 | A | G | 57 | a0001c0001t0002g0030 a0001c0001t0004g0013 a0001c0001t0004g0191 others(54): Show |
63 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.449+5479T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66523515 | |||||||
| chr16:66523538 | A | C | 36 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(33): Show |
39 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.449+5456T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66523538 | |||||||
| chr16:66523633 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.449+5361C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66523633 | |||||||
| chr16:66523891 | G | A | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
44 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.449+5103C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66523891 | |||||||
| chr16:66524135 | G | A | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449+4859C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66524135 | |||||||
| chr16:66524390 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.449+4604G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66524390 | |||||||
| chr16:66524527 | G | C | 2 | a0001c0001t0007g0190 a0001c0001t0007g0200 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.449+4467C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66524527 | |||||||
| chr16:66524988 | C | T | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.449+4006G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66524988 | |||||||
| chr16:66525083 | C | G | 1 | a0001c0001t0003g0091 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.449+3911G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525083 | |||||||
| chr16:66525100 | G | A | 3 | a0001c0001t0008g0033 a0001c0001t0008g0178 a0001c0001t0008g0182 |
4 | HG02055.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+3894C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525100 | |||||||
| chr16:66525145 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.449+3849G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525145 | |||||||
| chr16:66525331 | T | C | 3 | a0001c0001t0016g0041 a0001c0001t0034g0218 a0001c0001t0038g0220 |
3 | HG03041.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.449+3663A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525331 | |||||||
| chr16:66525414 | A | G | 1 | a0001c0001t0008g0032 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.449+3580T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525414 | |||||||
| chr16:66525503 | G | A | 9 | a0001c0001t0004g0219 a0001c0001t0009g0213 a0001c0001t0009g0214 others(6): Show |
9 | HG02258.hp2 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.449+3491C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525503 | |||||||
| chr16:66525543 | A | T | 107 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(104): Show |
127 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.449+3451T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525543 | |||||||
| chr16:66525636 | A | G | 1 | a0001c0001t0003g0090 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.449+3358T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525636 | |||||||
| chr16:66525643 | T | G | 1 | a0001c0001t0002g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.449+3351A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525643 | |||||||
| chr16:66525654 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.449+3340G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525654 | |||||||
| chr16:66525822 | T | C | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.449+3172A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525822 | |||||||
| chr16:66525912 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.449+3082C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66525912 | |||||||
| chr16:66526131 | G | A | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.449+2863C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526131 | |||||||
| chr16:66526147 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0165 |
5 | HG01256.hp2 HG01258.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.449+2847C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526147 | |||||||
| chr16:66526180 | G | C | 1 | a0001c0001t0021g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.449+2814C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526180 | |||||||
| chr16:66526469 | G | C | 57 | a0001c0001t0003g0038 a0001c0001t0004g0013 a0001c0001t0004g0191 others(54): Show |
62 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.449+2525C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526469 | |||||||
| chr16:66526541 | G | A | 8 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0131 others(5): Show |
10 | HG01109.hp1 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.449+2453C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526541 | |||||||
| chr16:66526634 | T | C | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.449+2360A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526634 | |||||||
| chr16:66526695 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.449+2299A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526695 | |||||||
| chr16:66526708 | T | C | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.449+2286A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526708 | |||||||
| chr16:66526808 | T | C | 1 | a0001c0001t0004g0208 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.449+2186A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526808 | |||||||
| chr16:66526870 | C | T | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.449+2124G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66526870 | |||||||
| chr16:66527126 | A | G | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.449+1868T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527126 | |||||||
| chr16:66527163 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0031g0149 |
2 | NA18950.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.449+1831G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527163 | |||||||
| chr16:66527208 | A | G | 1 | a0001c0001t0010g0133 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.449+1786T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527208 | |||||||
| chr16:66527241 | C | T | 2 | a0001c0001t0002g0137 a0001c0001t0028g0138 |
2 | HG00609.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.449+1753G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527241 | |||||||
| chr16:66527515 | G | T | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.449+1479C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527515 | |||||||
| chr16:66527546 | G | C | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.449+1448C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527546 | |||||||
| chr16:66527760 | T | C | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449+1234A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527760 | |||||||
| chr16:66527939 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.449+1055C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527939 | |||||||
| chr16:66527996 | T | TA | 39 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(36): Show |
42 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.449+997dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66527996 | |||||||
| chr16:66528013 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.449+981A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528013 | |||||||
| chr16:66528097 | C | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(173): Show |
229 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.449+897G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528097 | |||||||
| chr16:66528100 | G | A | 1 | a0001c0001t0024g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.449+894C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528100 | |||||||
| chr16:66528177 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.449+817A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528177 | |||||||
| chr16:66528186 | G | A | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449+808C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528186 | |||||||
| chr16:66528368 | G | C | 45 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(42): Show |
48 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.449+626C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528368 | |||||||
| chr16:66528371 | T | C | 4 | a0001c0001t0004g0219 a0001c0001t0016g0041 a0001c0001t0034g0218 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+623A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528371 | |||||||
| chr16:66528397 | T | C | 47 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(44): Show |
53 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.449+597A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528397 | |||||||
| chr16:66528430 | G | A | 1 | a0001c0001t0011g0021 | 2 | HG02258.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.449+564C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528430 | |||||||
| chr16:66528438 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0002g0139 |
2 | HG01069.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.449+556G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528438 | |||||||
| chr16:66528555 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.449+439G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528555 | |||||||
| chr16:66528617 | C | T | 2 | a0001c0001t0002g0137 a0001c0001t0028g0138 |
2 | HG00609.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.449+377G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528617 | |||||||
| chr16:66528619 | T | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.449+375A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528619 | |||||||
| chr16:66528652 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.449+342A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528652 | |||||||
| chr16:66528846 | G | A | 1 | a0001c0001t0003g0097 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.449+148C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528846 | |||||||
| chr16:66528864 | G | A | 10 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(7): Show |
11 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.449+130C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528864 | |||||||
| chr16:66528892 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.449+102G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528892 | |||||||
| chr16:66528900 | G | A | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.449+94C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528900 | |||||||
| chr16:66528980 | T | G | 2 | a0001c0001t0027g0185 a0001c0001t0033g0189 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.449+14A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 6/9 | chr16 | 66528980 | |||||||
| chr16:66529107 | A | G | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376-40T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529107 | |||||||
| chr16:66529186 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.376-119C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529186 | |||||||
| chr16:66529295 | C | G | 1 | a0001c0001t0002g0139 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.376-228G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529295 | |||||||
| chr16:66529327 | G | A | 11 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(8): Show |
13 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.376-260C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529327 | |||||||
| chr16:66529409 | C | T | 1 | a0001c0001t0009g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.376-342G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529409 | |||||||
| chr16:66529471 | C | T | 11 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(8): Show |
13 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.376-404G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529471 | |||||||
| chr16:66529514 | G | A | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376-447C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529514 | |||||||
| chr16:66529625 | C | T | 11 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(8): Show |
13 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.376-558G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529625 | |||||||
| chr16:66529924 | T | A | 1 | a0001c0001t0004g0199 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.376-857A>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529924 | |||||||
| chr16:66529994 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0157 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.376-927G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66529994 | |||||||
| chr16:66530110 | T | C | 1 | a0001c0001t0003g0098 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.376-1043A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530110 | |||||||
| chr16:66530225 | A | T | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.375+1155T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530225 | |||||||
| chr16:66530230 | C | A | 1 | a0001c0001t0003g0120 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.375+1150G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530230 | |||||||
| chr16:66530243 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.375+1137G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530243 | |||||||
| chr16:66530291 | C | T | 2 | a0001c0001t0002g0173 a0001c0001t0002g0175 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.375+1089G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530291 | |||||||
| chr16:66530357 | T | C | 3 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | HG02109.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.375+1023A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530357 | |||||||
| chr16:66530371 | G | A | 5 | a0001c0001t0004g0219 a0001c0001t0016g0041 a0001c0001t0034g0218 others(2): Show |
5 | HG02258.hp2 HG02717.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+1009C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530371 | |||||||
| chr16:66530397 | G | C | 1 | a0001c0001t0003g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.375+983C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530397 | |||||||
| chr16:66530643 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.375+737G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530643 | |||||||
| chr16:66530979 | T | C | 1 | a0001c0001t0003g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.375+401A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530979 | |||||||
| chr16:66530998 | C | T | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.375+382G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66530998 | |||||||
| chr16:66531107 | G | A | 1 | a0001c0001t0032g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.375+273C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66531107 | |||||||
| chr16:66531153 | A | T | 11 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(8): Show |
13 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.375+227T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66531153 | |||||||
| chr16:66531238 | G | A | 1 | a0001c0001t0032g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.375+142C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 5/9 | chr16 | 66531238 | |||||||
| chr16:66531500 | C | A | 2 | a0001c0001t0002g0137 a0001c0001t0028g0138 |
2 | HG00609.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.286-31G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66531500 | |||||||
| chr16:66531589 | A | G | 43 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 others(40): Show |
49 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.286-120T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66531589 | |||||||
| chr16:66531643 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.286-174T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66531643 | |||||||
| chr16:66531941 | A | C | 3 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | HG02109.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.286-472T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66531941 | |||||||
| chr16:66532099 | C | T | 1 | a0001c0001t0006g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.286-630G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532099 | |||||||
| chr16:66532129 | C | CA | 7 | a0001c0001t0001g0045 a0001c0001t0001g0105 a0001c0001t0002g0151 others(4): Show |
7 | HG02486.hp1 HG03688.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-661dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532129 | |||||||
| chr16:66532129 | CA | C | 17 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 others(14): Show |
18 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.286-661delT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532129 | |||||||
| chr16:66532129 | CAA | C | 38 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(35): Show |
45 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.286-662_286-661del others(2): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532129 | |||||||
| chr16:66532238 | T | C | 53 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(50): Show |
61 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.286-769A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532238 | |||||||
| chr16:66532336 | G | A | 51 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0020 others(48): Show |
77 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.286-867C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532336 | |||||||
| chr16:66532461 | T | G | 1 | a0001c0001t0004g0209 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.286-992A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532461 | |||||||
| chr16:66532485 | G | A | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.286-1016C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532485 | |||||||
| chr16:66532605 | GA | G | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.286-1137delT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532605 | |||||||
| chr16:66532621 | T | A | 2 | a0001c0001t0002g0030 a0001c0001t0003g0001 |
3 | HG02165.hp2 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.286-1152A>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532621 | |||||||
| chr16:66532664 | A | T | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.286-1195T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532664 | |||||||
| chr16:66532778 | T | C | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.286-1309A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532778 | |||||||
| chr16:66532868 | G | GA | 12 | a0001c0001t0006g0179 a0001c0001t0006g0181 a0001c0001t0006g0183 others(9): Show |
14 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.286-1400dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532868 | |||||||
| chr16:66532868 | GA | G | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
47 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.286-1400delT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532868 | |||||||
| chr16:66532947 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.286-1478C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66532947 | |||||||
| chr16:66533075 | C | CT | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.286-1607dupA | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533075 | |||||||
| chr16:66533172 | C | T | 3 | a0001c0001t0006g0179 a0001c0001t0006g0184 a0001c0001t0029g0180 |
3 | HG00738.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.286-1703G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533172 | |||||||
| chr16:66533261 | C | T | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.286-1792G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533261 | |||||||
| chr16:66533335 | C | CA | 48 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0100 others(45): Show |
54 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.286-1867dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533335 | |||||||
| chr16:66533335 | CA | C | 60 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0002g0006 others(57): Show |
75 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.286-1867delT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533335 | |||||||
| chr16:66533441 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.286-1972A>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533441 | |||||||
| chr16:66533547 | C | T | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.286-2078G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533547 | |||||||
| chr16:66533590 | G | A | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.286-2121C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533590 | |||||||
| chr16:66533738 | T | C | 39 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(36): Show |
45 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.286-2269A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533738 | |||||||
| chr16:66533747 | T | C | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(106): Show |
130 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.286-2278A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533747 | |||||||
| chr16:66533876 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.286-2407A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66533876 | |||||||
| chr16:66534007 | C | CA | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
224 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.286-2539dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534007 | |||||||
| chr16:66534007 | C | CAA | 52 | a0001c0001t0001g0105 a0001c0001t0002g0161 a0001c0001t0002g0163 others(49): Show |
60 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.286-2540_286-2539d others(4): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534007 | |||||||
| chr16:66534007 | C | CAAA | 6 | a0001c0001t0004g0195 a0001c0001t0004g0210 a0001c0001t0005g0043 others(3): Show |
6 | HG00621.hp1 HG00733.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2541_286-2539d others(5): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534007 | |||||||
| chr16:66534172 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.286-2703G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534172 | |||||||
| chr16:66534245 | T | C | 39 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(36): Show |
45 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.285+2719A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534245 | |||||||
| chr16:66534263 | T | C | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285+2701A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534263 | |||||||
| chr16:66534329 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.285+2635A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534329 | |||||||
| chr16:66534432 | C | G | 1 | a0001c0001t0002g0137 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.285+2532G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534432 | |||||||
| chr16:66534585 | T | C | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
47 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.285+2379A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534585 | |||||||
| chr16:66534626 | G | A | 39 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(36): Show |
45 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.285+2338C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534626 | |||||||
| chr16:66534702 | C | T | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285+2262G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534702 | |||||||
| chr16:66534853 | T | A | 1 | a0001c0001t0002g0147 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.285+2111A>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534853 | |||||||
| chr16:66534979 | G | A | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285+1985C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534979 | |||||||
| chr16:66534987 | C | A | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1977G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66534987 | |||||||
| chr16:66535129 | C | T | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285+1835G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66535129 | |||||||
| chr16:66535280 | T | C | 30 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(27): Show |
36 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.285+1684A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66535280 | |||||||
| chr16:66535297 | T | G | 1 | a0001c0001t0005g0014 | 2 | HG00558.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.285+1667A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66535297 | |||||||
| chr16:66535346 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.285+1618G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66535346 | |||||||
| chr16:66535493 | G | A | 1 | a0001c0001t0032g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.285+1471C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66535493 | |||||||
| chr16:66535990 | G | A | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0031g0149 |
3 | NA18950.hp2 NA19070.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.285+974C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66535990 | |||||||
| chr16:66536029 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+935G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536029 | |||||||
| chr16:66536065 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.285+899T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536065 | |||||||
| chr16:66536071 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.285+893C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536071 | |||||||
| chr16:66536119 | G | A | 39 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(36): Show |
45 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.285+845C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536119 | |||||||
| chr16:66536137 | G | C | 1 | a0001c0001t0027g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285+827C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536137 | |||||||
| chr16:66536202 | C | CAAA | 32 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0194 others(29): Show |
38 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.285+759_285+761dup others(3): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536202 | |||||||
| chr16:66536202 | CA | C | 11 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0131 others(8): Show |
13 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.285+761delT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536202 | |||||||
| chr16:66536272 | G | T | 1 | a0001c0001t0024g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+692C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536272 | |||||||
| chr16:66536667 | A | T | 1 | a0001c0001t0001g0065 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.285+297T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536667 | |||||||
| chr16:66536729 | G | C | 1 | a0001c0001t0021g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.285+235C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536729 | |||||||
| chr16:66536760 | T | G | 2 | a0001c0001t0001g0023 a0001c0001t0002g0153 |
3 | HG00609.hp1 NA18954.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.285+204A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 4/9 | chr16 | 66536760 | |||||||
| chr16:66537237 | A | C | 1 | a0003c0004t0002g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232-220T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66537237 | |||||||
| chr16:66537518 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0046 others(2): Show |
8 | HG01069.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.232-501G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66537518 | |||||||
| chr16:66537723 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.232-706C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66537723 | |||||||
| chr16:66538234 | T | C | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.232-1217A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66538234 | |||||||
| chr16:66538396 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.232-1379A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66538396 | |||||||
| chr16:66538402 | T | A | 1 | a0001c0001t0004g0219 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.232-1385A>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66538402 | |||||||
| chr16:66538923 | G | A | 1 | a0001c0001t0009g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.232-1906C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66538923 | |||||||
| chr16:66538924 | C | A | 1 | a0001c0001t0009g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.232-1907G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66538924 | |||||||
| chr16:66538925 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0046 others(1): Show |
7 | HG01167.hp1 HG01168.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.232-1908C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66538925 | |||||||
| chr16:66539287 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0115 a0001c0001t0022g0110 |
4 | HG00639.hp1 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-2270C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539287 | |||||||
| chr16:66539351 | C | A | 2 | a0001c0001t0001g0056 a0001c0001t0005g0040 |
2 | HG03834.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.232-2334G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539351 | |||||||
| chr16:66539592 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.231+2287G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539592 | |||||||
| chr16:66539602 | G | GA | 17 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0061 others(14): Show |
17 | HG00438.hp1 HG00673.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.231+2276dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539602 | |||||||
| chr16:66539602 | GAAAAAA | G | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+2271_231+2276d others(8): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539602 | |||||||
| chr16:66539621 | A | G | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+2258T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539621 | |||||||
| chr16:66539622 | A | G | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+2257T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539622 | |||||||
| chr16:66539626 | G | A | 43 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(40): Show |
49 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.231+2253C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539626 | |||||||
| chr16:66539626 | G | GAAGA | 11 | a0001c0001t0002g0031 a0001c0001t0006g0179 a0001c0001t0006g0181 others(8): Show |
14 | HG01433.hp1 HG02055.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.231+2249_231+2252d others(6): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539626 | |||||||
| chr16:66539770 | A | G | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+2109T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539770 | |||||||
| chr16:66539792 | C | A | 37 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(34): Show |
47 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.231+2087G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66539792 | |||||||
| chr16:66540173 | C | CT | 21 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0048 others(18): Show |
27 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.231+1705dupA | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66540173 | |||||||
| chr16:66540173 | C | CTTTTTTT | 32 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0196 others(29): Show |
38 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.231+1699_231+1705d others(9): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66540173 | |||||||
| chr16:66540173 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0007g0190 others(3): Show |
6 | HG02647.hp1 NA18995.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+1698_231+1705d others(10): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66540173 | |||||||
| chr16:66540173 | CT | C | 60 | a0001c0001t0001g0115 a0001c0001t0002g0006 a0001c0001t0002g0007 others(57): Show |
73 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.231+1705delA | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66540173 | |||||||
| chr16:66540911 | G | C | 41 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(38): Show |
47 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.231+968C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66540911 | |||||||
| chr16:66541192 | A | T | 1 | a0001c0001t0003g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.231+687T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66541192 | |||||||
| chr16:66541286 | C | T | 13 | a0001c0001t0002g0031 a0001c0001t0006g0179 a0001c0001t0006g0181 others(10): Show |
16 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.231+593G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66541286 | |||||||
| chr16:66541388 | A | ATG | 3 | a0001c0001t0001g0016 a0001c0001t0002g0173 a0001c0001t0012g0049 |
4 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+489_231+490dup others(2): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66541388 | |||||||
| chr16:66541407 | G | A | 3 | a0001c0001t0002g0137 a0001c0001t0002g0139 a0001c0001t0028g0138 |
3 | HG00609.hp2 HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.231+472C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66541407 | |||||||
| chr16:66541614 | G | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01109.hp1 HG02145.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+265C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66541614 | |||||||
| chr16:66541619 | G | A | 1 | a0001c0001t0002g0030 | 2 | HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.231+260C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66541619 | |||||||
| chr16:66541665 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0002g0153 |
3 | HG00609.hp1 NA18954.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.231+214G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 3/9 | chr16 | 66541665 | |||||||
| chr16:66541965 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.157-12G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66541965 | |||||||
| chr16:66542161 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-208G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542161 | |||||||
| chr16:66542194 | G | A | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157-241C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542194 | |||||||
| chr16:66542303 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.157-350C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542303 | |||||||
| chr16:66542413 | G | A | 39 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(36): Show |
45 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.157-460C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542413 | |||||||
| chr16:66542627 | G | C | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.157-674C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542627 | |||||||
| chr16:66542868 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.157-915G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542868 | |||||||
| chr16:66542908 | T | C | 1 | a0001c0001t0038g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157-955A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542908 | |||||||
| chr16:66542910 | T | C | 9 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0131 others(6): Show |
11 | HG01109.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-957A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66542910 | |||||||
| chr16:66543140 | C | T | 3 | a0001c0001t0002g0137 a0001c0001t0002g0139 a0001c0001t0028g0138 |
3 | HG00609.hp2 HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.157-1187G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543140 | |||||||
| chr16:66543154 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.157-1201C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543154 | |||||||
| chr16:66543226 | A | T | 54 | a0001c0001t0002g0031 a0001c0001t0004g0013 a0001c0001t0004g0191 others(51): Show |
63 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.157-1273T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543226 | |||||||
| chr16:66543227 | T | C | 1 | a0001c0001t0003g0117 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.157-1274A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543227 | |||||||
| chr16:66543399 | C | T | 1 | a0001c0001t0004g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.157-1446G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543399 | |||||||
| chr16:66543616 | A | G | 1 | a0001c0001t0002g0028 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.157-1663T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543616 | |||||||
| chr16:66543689 | C | T | 1 | a0001c0001t0008g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.157-1736G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543689 | |||||||
| chr16:66543798 | C | A | 13 | a0001c0001t0002g0031 a0001c0001t0006g0179 a0001c0001t0006g0181 others(10): Show |
16 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.157-1845G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543798 | |||||||
| chr16:66543812 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.157-1859G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66543812 | |||||||
| chr16:66544154 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157-2201C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544154 | |||||||
| chr16:66544214 | G | C | 39 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(36): Show |
45 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.157-2261C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544214 | |||||||
| chr16:66544415 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.157-2462T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544415 | |||||||
| chr16:66544631 | T | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0119 a0001c0001t0002g0153 |
4 | HG00609.hp1 NA18954.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-2678A>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544631 | |||||||
| chr16:66544817 | G | A | 1 | a0001c0001t0004g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.157-2864C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544817 | |||||||
| chr16:66544842 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.157-2889A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544842 | |||||||
| chr16:66544982 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.157-3029C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544982 | |||||||
| chr16:66544991 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.157-3038C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66544991 | |||||||
| chr16:66545094 | C | CA | 16 | a0001c0001t0001g0122 a0001c0001t0002g0031 a0001c0001t0004g0191 others(13): Show |
19 | HG00738.hp2 HG01109.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.157-3142dupT | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545094 | |||||||
| chr16:66545094 | C | CAA | 38 | a0001c0001t0004g0013 a0001c0001t0004g0192 a0001c0001t0004g0194 others(35): Show |
43 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.157-3143_157-3142d others(4): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545094 | |||||||
| chr16:66545180 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.157-3227A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545180 | |||||||
| chr16:66545311 | G | A | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.157-3358C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545311 | |||||||
| chr16:66545456 | C | G | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.157-3503G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545456 | |||||||
| chr16:66545621 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.156+3357G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545621 | |||||||
| chr16:66545676 | T | C | 1 | a0001c0001t0024g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.156+3302A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545676 | |||||||
| chr16:66545880 | C | T | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.156+3098G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545880 | |||||||
| chr16:66545903 | G | A | 54 | a0001c0001t0002g0031 a0001c0001t0004g0013 a0001c0001t0004g0191 others(51): Show |
63 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.156+3075C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66545903 | |||||||
| chr16:66546081 | T | C | 13 | a0001c0001t0002g0007 a0001c0001t0002g0155 a0001c0001t0002g0156 others(10): Show |
16 | HG01175.hp1 HG01884.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+2897A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546081 | |||||||
| chr16:66546100 | T | C | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.156+2878A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546100 | |||||||
| chr16:66546324 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.156+2654A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546324 | |||||||
| chr16:66546360 | T | C | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.156+2618A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546360 | |||||||
| chr16:66546425 | T | A | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.156+2553A>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546425 | |||||||
| chr16:66546705 | A | T | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.156+2273T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546705 | |||||||
| chr16:66546753 | AT | A | 42 | a0001c0001t0001g0125 a0001c0001t0002g0164 a0001c0001t0002g0165 others(39): Show |
48 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.156+2224delA | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546753 | |||||||
| chr16:66546812 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.156+2166A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546812 | |||||||
| chr16:66546878 | A | G | 1 | a0001c0001t0004g0219 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.156+2100T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546878 | |||||||
| chr16:66546895 | G | A | 1 | a0001c0001t0003g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.156+2083C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546895 | |||||||
| chr16:66546950 | G | T | 3 | a0001c0001t0016g0041 a0001c0001t0034g0218 a0001c0001t0038g0220 |
3 | HG03041.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.156+2028C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546950 | |||||||
| chr16:66546968 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.156+2010C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66546968 | |||||||
| chr16:66547046 | T | C | 64 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(61): Show |
76 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.156+1932A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547046 | |||||||
| chr16:66547047 | A | G | 40 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.156+1931T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547047 | |||||||
| chr16:66547237 | C | G | 38 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(35): Show |
43 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.156+1741G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547237 | |||||||
| chr16:66547254 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.156+1724C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547254 | |||||||
| chr16:66547555 | C | T | 1 | a0001c0001t0020g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.156+1423G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547555 | |||||||
| chr16:66547596 | GC | G | 5 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0135 others(2): Show |
5 | HG00544.hp2 HG02027.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+1381delG | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547596 | |||||||
| chr16:66547620 | C | T | 10 | a0001c0001t0004g0219 a0001c0001t0009g0213 a0001c0001t0009g0214 others(7): Show |
10 | HG02258.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+1358G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547620 | |||||||
| chr16:66547828 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.156+1150A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547828 | |||||||
| chr16:66547902 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.156+1076G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547902 | |||||||
| chr16:66547918 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.156+1060G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547918 | |||||||
| chr16:66547937 | A | G | 1 | a0001c0001t0003g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.156+1041T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66547937 | |||||||
| chr16:66548004 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.156+974G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548004 | |||||||
| chr16:66548041 | T | C | 3 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | HG02109.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.156+937A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548041 | |||||||
| chr16:66548058 | C | T | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+920G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548058 | |||||||
| chr16:66548142 | C | T | 27 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(24): Show |
32 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.156+836G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548142 | |||||||
| chr16:66548236 | C | T | 26 | a0001c0001t0004g0013 a0001c0001t0004g0191 a0001c0001t0004g0192 others(23): Show |
31 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.156+742G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548236 | |||||||
| chr16:66548600 | G | A | 13 | a0001c0001t0002g0031 a0001c0001t0006g0179 a0001c0001t0006g0181 others(10): Show |
16 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+378C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548600 | |||||||
| chr16:66548796 | T | C | 1 | a0001c0001t0002g0030 | 2 | HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.156+182A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548796 | |||||||
| chr16:66548963 | A | G | 13 | a0001c0001t0002g0031 a0001c0001t0006g0179 a0001c0001t0006g0181 others(10): Show |
16 | HG00738.hp2 HG01433.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+15T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 2/9 | chr16 | 66548963 | |||||||
| chr16:66549110 | TCCCTGGC others(30): Show |
T | 1 | a0001c0001t0001g0035 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.125-138_125-102del others(37): Show |
TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549110 | |||||||
| chr16:66549125 | C | T | 43 | a0001c0001t0001g0016 a0001c0001t0001g0085 a0001c0001t0001g0086 others(40): Show |
49 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.125-116G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549125 | |||||||
| chr16:66549237 | T | C | 1 | a0001c0001t0003g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.125-228A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549237 | |||||||
| chr16:66549296 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.125-287C>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549296 | |||||||
| chr16:66549347 | G | C | 3 | a0001c0001t0006g0186 a0001c0001t0006g0187 a0001c0001t0006g0188 |
3 | HG01433.hp1 HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-338C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549347 | |||||||
| chr16:66549541 | C | G | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.124+397G>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549541 | |||||||
| chr16:66549715 | G | C | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(100): Show |
124 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.124+223C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549715 | |||||||
| chr16:66549732 | G | C | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+206C>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549732 | |||||||
| chr16:66549736 | C | T | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+202G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549736 | |||||||
| chr16:66549737 | A | C | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+201T>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549737 | |||||||
| chr16:66549738 | A | T | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+200T>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549738 | |||||||
| chr16:66549740 | G | T | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+198C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549740 | |||||||
| chr16:66549742 | C | A | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+196G>T | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549742 | |||||||
| chr16:66549744 | A | G | 102 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(99): Show |
123 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.124+194T>C | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549744 | |||||||
| chr16:66549746 | C | T | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+192G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549746 | |||||||
| chr16:66549747 | G | T | 1 | a0001c0001t0007g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.124+191C>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549747 | |||||||
| chr16:66549802 | T | C | 48 | a0001c0001t0002g0031 a0001c0001t0004g0013 a0001c0001t0004g0191 others(45): Show |
56 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.124+136A>G | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549802 | |||||||
| chr16:66549836 | C | T | 1 | a0001c0001t0033g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.124+102G>A | TK2 | ENSG00000166548.17 | transcript | ENST00000544898.6 | protein_coding | 1/9 | chr16 | 66549836 |