Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7014 |
| ensemblid | ENSG00000132604.11 |
| hgncid | 11729 |
| symbol | TERF2 |
| name | telomeric repeat binding factor 2 |
| refseq_nuc | NM_005652.5 |
| refseq_prot | NP_005643.2 |
| ensembl_nuc | ENST00000254942.8 |
| ensembl_prot | ENSP00000254942.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 69355567 |
| end | 69386007 |
| strand | - |
| ver | v1.2 |
| region | chr16:69355567-69386007 |
| region5000 | chr16:69350567-69391007 |
| regionname0 | TERF2_chr16_69355567_69386007 |
| regionname5000 | TERF2_chr16_69350567_69391007 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 542 | 332 | 85 | 66 | 127 | 14 | 38 | 100 | TERF2_chr16_69350567_69391007 | TERF2 | MAAGA others(537): Show |
chr16 | 69350567 | 69391007 |
| a0002 | 0/0 | 542 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | MAAGA others(537): Show |
chr16 | 69350567 | 69391007 |
| a0003 | 0/0 | 542 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | MAAGA others(537): Show |
chr16 | 69350567 | 69391007 |
| a0004 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | MAGGG others(495): Show |
chr16 | 69350567 | 69391007 |
| a0005 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | MAAGA others(537): Show |
chr16 | 69350567 | 69391007 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1626 | 323 | 79 | 66 | 127 | 14 | 35 | TERF2_chr16_69350567_69391007 | TERF2 | ATGGC others(1621): Show |
chr16 | 69350567 | 69391007 | ||
| a0001c0002 | 0/0 | 1626 | 6 | 6 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | ATGGC others(1621): Show |
chr16 | 69350567 | 69391007 | ||
| a0001c0005 | 0/0 | 1626 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | ATGGC others(1621): Show |
chr16 | 69350567 | 69391007 | ||
| a0001c0007 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | ATGGC others(1621): Show |
chr16 | 69350567 | 69391007 | ||
| a0002c0003 | 0/0 | 1626 | 4 | 4 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | ATGGC others(1621): Show |
chr16 | 69350567 | 69391007 | ||
| a0003c0004 | 0/0 | 1626 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | ATGGC others(1621): Show |
chr16 | 69350567 | 69391007 | ||
| a0004c0008 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | GTGGC others(1621): Show |
chr16 | 69350567 | 69391007 | ||
| a0005c0006 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | ATGGC others(1621): Show |
chr16 | 69350567 | 69391007 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2996 | 249 | 55 | 53 | 101 | 11 | 28 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0002 | 0/1 | 2996 | 23 | 4 | 5 | 7 | 3 | 3 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0003 | 0/0 | 2996 | 10 | 10 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0004 | 0/0 | 2996 | 11 | 0 | 0 | 11 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0005 | 0/0 | 2997 | 7 | 1 | 3 | 3 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0007 | 0/0 | 2997 | 4 | 3 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0008 | 0/0 | 2996 | 4 | 0 | 0 | 4 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0009 | 0/0 | 2996 | 4 | 0 | 2 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0010 | 0/0 | 2997 | 2 | 2 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0011 | 0/0 | 2996 | 2 | 0 | 1 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0012 | 0/0 | 2996 | 2 | 2 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0013 | 0/0 | 2997 | 2 | 0 | 1 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0016 | 0/0 | 2996 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0017 | 0/0 | 2997 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0001t0018 | 0/0 | 2997 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0002t0006 | 0/0 | 2997 | 4 | 4 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0002t0014 | 0/0 | 2997 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0002t0015 | 0/0 | 2997 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2992): Show |
chr16 | 69350567 | 69391007 |
| a0001c0005t0002 | 0/0 | 2996 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0001c0007t0001 | 0/0 | 2996 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0002c0003t0003 | 0/0 | 2996 | 4 | 4 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0003c0004t0001 | 0/0 | 2996 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0004c0008t0004 | 0/0 | 2996 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| a0005c0006t0001 | 0/0 | 2996 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | AGAAG others(2991): Show |
chr16 | 69350567 | 69391007 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 4 | 2 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0002 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0028 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0007g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0010g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0011g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0013g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0013g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0016g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0017g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0001t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0002t0006g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0002t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0002t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0002t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0001c0007t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0002c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0002c0003t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0002c0003t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0002c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0003c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0003c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0004c0008t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| a0005c0006t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0250 | EUR | GBR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | FIN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0221 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0140 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0193 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0202 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0036 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01496 | hp1 | a0001 | c0001 | t0013 | g0218 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0235 | EUR | IBS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | IBS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01891 | hp2 | a0001 | c0002 | t0014 | g0054 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02015 | hp2 | a0004 | c0008 | t0004 | g0274 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02055 | hp2 | a0001 | c0001 | t0017 | g0178 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0119 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02257 | hp1 | a0001 | c0002 | t0006 | g0050 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02280 | hp2 | a0001 | c0002 | t0006 | g0052 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0062 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02451 | hp2 | a0002 | c0003 | t0003 | g0173 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | KHV | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02602 | hp2 | a0001 | c0001 | t0011 | g0220 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02622 | hp1 | a0001 | c0001 | t0018 | g0242 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02630 | hp2 | a0002 | c0003 | t0003 | g0174 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02738 | hp2 | a0003 | c0004 | t0001 | g0201 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02818 | hp1 | a0002 | c0003 | t0003 | g0177 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0243 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0093 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0273 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0272 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03453 | hp1 | a0001 | c0002 | t0006 | g0016 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03491 | hp2 | a0001 | c0005 | t0002 | g0224 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03492 | hp2 | a0001 | c0005 | t0002 | g0225 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0016 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03942 | hp2 | a0001 | c0007 | t0001 | g0196 | SAS | BEB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG04204 | hp1 | a0003 | c0004 | t0001 | g0200 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | YRI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0120 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18962 | hp1 | a0001 | c0001 | t0016 | g0122 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0123 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0099 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0181 | AFR | LWK | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19072 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0219 | SAS | GIH | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0092 | SAS | GIH | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0094 | AMR | CLM | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG03471 | hp2 | a0002 | c0003 | t0003 | g0179 | AFR | MSL | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG06807 | hp1 | a0001 | c0002 | t0015 | g0051 | AFR | USA | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | USA | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | USA | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA20300 | hp2 | a0005 | c0006 | t0001 | g0048 | AFR | USA | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0236 | REF | REF | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0028 | REF | REF | TERF2_chr16_69350567_69391007 | TERF2 | chr16 | 69350567 | 69391007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69366892 | G | C | 1 | a0002 | 4 | HG02451.hp2 HG02630.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.1255C>G | p.Leu419Val | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/10 | 1291/2996 | 1255/1629 | 419/542 | chr16 | 69366892 | |||
| chr16:69366898 | C | T | 1 | a0003 | 2 | HG02738.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.1249G>A | p.Ala417Thr | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/10 | 1285/2996 | 1249/1629 | 417/542 | chr16 | 69366898 | |||
| chr16:69367182 | G | T | 1 | a0005 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.965C>A | p.Pro322Gln | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/10 | 1001/2996 | 965/1629 | 322/542 | chr16 | 69367182 | |||
| chr16:69385971 | T | C | 1 | a0004 | 1 | HG02015.hp2 | start_lost | HIGH | c.1A>G | p.Met1? | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 1/10 | 37/2996 | 1/1629 | 1/542 | chr16 | 69385971 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69368402 | C | T | 1 | a0001c0002 | 6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
synonymous_variant | LOW | c.921G>A | p.Val307Val | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/10 | 957/2996 | 921/1629 | 307/542 | chr16 | 69368402 | |||
| chr16:69368453 | G | A | 1 | a0001c0005 | 2 | HG03491.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.870C>T | p.Ser290Ser | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/10 | 906/2996 | 870/1629 | 290/542 | chr16 | 69368453 | |||
| chr16:69370558 | T | G | 1 | a0001c0007 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.765A>C | p.Ser255Ser | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/10 | 801/2996 | 765/1629 | 255/542 | chr16 | 69370558 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69355763 | C | T | 1 | a0001c0002t0015 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1135G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 1135 | chr16 | 69355763 | ||||||
| chr16:69355835 | A | C | 1 | a0001c0001t0007 | 4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1063T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 1063 | chr16 | 69355835 | ||||||
| chr16:69355838 | C | CA | 5 | a0001c0001t0007 a0001c0001t0010 a0001c0002t0006 others(2): Show |
12 | HG01433.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1059_*1060insT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 1059 | chr16 | 69355838 | ||||||
| chr16:69355881 | T | C | 2 | a0001c0001t0004 a0004c0008t0004 |
12 | HG02015.hp2 HG02040.hp1 HG02083.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 1017 | chr16 | 69355881 | ||||||
| chr16:69356042 | A | G | 3 | a0001c0002t0006 a0001c0002t0014 a0001c0002t0015 |
6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*856T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 856 | chr16 | 69356042 | ||||||
| chr16:69356070 | A | G | 1 | a0001c0001t0011 | 2 | HG00735.hp1 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*828T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 828 | chr16 | 69356070 | ||||||
| chr16:69356296 | G | T | 1 | a0001c0002t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*602C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 602 | chr16 | 69356296 | ||||||
| chr16:69356363 | G | A | 1 | a0001c0001t0016 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 535 | chr16 | 69356363 | ||||||
| chr16:69356520 | G | A | 1 | a0001c0001t0018 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 378 | chr16 | 69356520 | ||||||
| chr16:69356669 | G | A | 2 | a0001c0001t0008 a0001c0001t0016 |
5 | HG02129.hp2 NA18946.hp2 NA18962.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*229C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 229 | chr16 | 69356669 | ||||||
| chr16:69356678 | T | C | 1 | a0001c0001t0009 | 4 | HG01123.hp2 HG02300.hp1 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 220 | chr16 | 69356678 | ||||||
| chr16:69356739 | G | A | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0013 others(1): Show |
28 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*159C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 159 | chr16 | 69356739 | ||||||
| chr16:69356756 | C | T | 3 | a0001c0001t0003 a0001c0001t0017 a0002c0003t0003 |
15 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*142G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 142 | chr16 | 69356756 | ||||||
| chr16:69356783 | G | C | 1 | a0001c0001t0012 | 2 | HG02976.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 115 | chr16 | 69356783 | ||||||
| chr16:69356799 | C | CA | 4 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(1): Show |
11 | HG01070.hp2 HG01109.hp1 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*98dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 10/10 | 98 | chr16 | 69356799 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69357110 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
6 | HG00738.hp1 HG02145.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1471-54T>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 9/9 | chr16 | 69357110 | |||||||
| chr16:69357756 | C | A | 12 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0168 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1427-195G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69357756 | |||||||
| chr16:69357811 | C | G | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1427-250G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69357811 | |||||||
| chr16:69357846 | C | CT | 13 | a0001c0001t0001g0078 a0001c0001t0001g0100 a0001c0001t0001g0114 others(10): Show |
13 | HG00621.hp2 HG00741.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1427-286dupA | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69357846 | |||||||
| chr16:69357846 | CT | C | 90 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(87): Show |
99 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1427-286delA | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69357846 | |||||||
| chr16:69357854 | T | C | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1427-293A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69357854 | |||||||
| chr16:69357877 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1427-316G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69357877 | |||||||
| chr16:69357884 | C | G | 6 | a0001c0001t0002g0031 a0001c0001t0002g0213 a0001c0001t0002g0216 others(3): Show |
7 | HG00621.hp1 NA18968.hp2 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.1427-323G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69357884 | |||||||
| chr16:69358300 | A | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
9 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1427-739T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69358300 | |||||||
| chr16:69358303 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
6 | HG00738.hp1 HG02145.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1427-742C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69358303 | |||||||
| chr16:69358599 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1427-1038C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69358599 | |||||||
| chr16:69358723 | C | CA | 11 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(8): Show |
11 | HG00544.hp1 HG01346.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1427-1163dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69358723 | |||||||
| chr16:69358786 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1427-1225A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69358786 | |||||||
| chr16:69358909 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0114 |
3 | HG02129.hp1 NA18951.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1427-1348G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69358909 | |||||||
| chr16:69358935 | G | A | 1 | a0001c0001t0018g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1427-1374C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69358935 | |||||||
| chr16:69359140 | G | A | 4 | a0001c0002t0006g0016 a0001c0002t0006g0050 a0001c0002t0006g0052 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427-1579C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359140 | |||||||
| chr16:69359303 | G | A | 1 | a0001c0001t0004g0066 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1427-1742C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359303 | |||||||
| chr16:69359320 | G | C | 3 | a0001c0001t0004g0063 a0001c0001t0004g0067 a0001c0001t0004g0073 |
3 | NA18973.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1427-1759C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359320 | |||||||
| chr16:69359387 | G | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1427-1826C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359387 | |||||||
| chr16:69359527 | CA | C | 82 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(79): Show |
91 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1426+1876delT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359527 | |||||||
| chr16:69359528 | A | G | 1 | a0001c0001t0004g0064 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1426+1876T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359528 | |||||||
| chr16:69359618 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0089 |
2 | HG00642.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1426+1786A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359618 | |||||||
| chr16:69359627 | A | AT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(85): Show |
106 | HG00280.hp2 HG00609.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.1426+1776dupA | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359627 | |||||||
| chr16:69359627 | A | ATT | 12 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0070 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1426+1775_1426+177 others(6): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359627 | |||||||
| chr16:69359627 | A | ATTT | 5 | a0001c0001t0001g0153 a0001c0001t0007g0007 a0001c0002t0006g0016 others(2): Show |
8 | HG00544.hp2 HG02257.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1426+1774_1426+177 others(7): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359627 | |||||||
| chr16:69359627 | AT | A | 38 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(35): Show |
41 | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1426+1776delA | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359627 | |||||||
| chr16:69359627 | ATT | A | 40 | a0001c0001t0001g0014 a0001c0001t0001g0211 a0001c0001t0001g0212 others(37): Show |
43 | HG00280.hp1 HG00738.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.1426+1775_1426+177 others(6): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359627 | |||||||
| chr16:69359627 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0005g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1426+1767_1426+177 others(14): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359627 | |||||||
| chr16:69359627 | ATTTTTTT others(4): Show |
A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0182 others(6): Show |
12 | HG00738.hp1 HG02615.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1426+1766_1426+177 others(15): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359627 | |||||||
| chr16:69359861 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1426+1543G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359861 | |||||||
| chr16:69359862 | G | A | 5 | a0001c0002t0006g0016 a0001c0002t0006g0050 a0001c0002t0006g0052 others(2): Show |
6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1426+1542C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69359862 | |||||||
| chr16:69360006 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1426+1398C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360006 | |||||||
| chr16:69360009 | T | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
9 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1426+1395A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360009 | |||||||
| chr16:69360055 | G | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
9 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1426+1349C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360055 | |||||||
| chr16:69360157 | C | T | 2 | a0003c0004t0001g0200 a0003c0004t0001g0201 |
2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1426+1247G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360157 | |||||||
| chr16:69360221 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1426+1183G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360221 | |||||||
| chr16:69360232 | A | G | 1 | a0001c0001t0012g0243 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1426+1172T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360232 | |||||||
| chr16:69360241 | C | T | 2 | a0001c0001t0011g0220 a0001c0001t0011g0221 |
2 | HG00735.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1426+1163G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360241 | |||||||
| chr16:69360279 | G | A | 9 | a0001c0001t0007g0007 a0001c0001t0007g0036 a0001c0001t0010g0272 others(6): Show |
12 | HG01433.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1426+1125C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360279 | |||||||
| chr16:69360378 | G | C | 9 | a0001c0001t0007g0007 a0001c0001t0007g0036 a0001c0001t0010g0272 others(6): Show |
12 | HG01433.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1426+1026C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360378 | |||||||
| chr16:69360534 | G | T | 9 | a0001c0001t0007g0007 a0001c0001t0007g0036 a0001c0001t0010g0272 others(6): Show |
12 | HG01433.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1426+870C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360534 | |||||||
| chr16:69360568 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0049 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1426+836G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360568 | |||||||
| chr16:69360705 | C | CA | 82 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(79): Show |
92 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1426+698dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360705 | |||||||
| chr16:69360705 | C | CAA | 14 | a0001c0001t0001g0228 a0001c0001t0001g0231 a0001c0001t0001g0241 others(11): Show |
14 | HG00099.hp2 HG00738.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426+697_1426+698d others(4): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360705 | |||||||
| chr16:69360705 | C | CAAA | 12 | a0001c0001t0002g0208 a0001c0001t0003g0166 a0001c0001t0003g0167 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1426+696_1426+698d others(5): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360705 | |||||||
| chr16:69360834 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1426+570G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360834 | |||||||
| chr16:69360869 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1426+535T>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69360869 | |||||||
| chr16:69361141 | G | A | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1426+263C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69361141 | |||||||
| chr16:69361238 | G | GA | 28 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0035 others(25): Show |
30 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1426+165dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69361238 | |||||||
| chr16:69361308 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1426+96G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69361308 | |||||||
| chr16:69361309 | G | A | 11 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(8): Show |
11 | HG00544.hp1 HG01346.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1426+95C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 8/9 | chr16 | 69361309 | |||||||
| chr16:69361531 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(49): Show |
82 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1341-42T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361531 | |||||||
| chr16:69361532 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1341-43G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361532 | |||||||
| chr16:69361565 | C | G | 1 | a0001c0007t0001g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1341-76G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361565 | |||||||
| chr16:69361831 | C | G | 5 | a0001c0002t0006g0016 a0001c0002t0006g0050 a0001c0002t0006g0052 others(2): Show |
6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1341-342G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361831 | |||||||
| chr16:69361886 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1341-397C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361886 | |||||||
| chr16:69361890 | C | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341-401G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361890 | |||||||
| chr16:69361917 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0147 |
2 | NA18945.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1341-428C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361917 | |||||||
| chr16:69361931 | T | TTCCACTA others(306): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
11 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(315): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(307): Show |
1 | a0001c0001t0018g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1341-443_1341-442i others(316): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(309): Show |
2 | a0001c0001t0001g0261 a0001c0001t0012g0243 |
2 | HG02976.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1341-443_1341-442i others(318): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(310): Show |
9 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(6): Show |
9 | HG00544.hp1 HG01346.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(319): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(311): Show |
1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1341-443_1341-442i others(320): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(314): Show |
1 | a0001c0001t0003g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1341-443_1341-442i others(323): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(314): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1341-443_1341-442i others(323): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(315): Show |
1 | a0001c0001t0003g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1341-443_1341-442i others(324): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(315): Show |
10 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0169 others(7): Show |
10 | HG02280.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(324): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(316): Show |
4 | a0001c0001t0003g0171 a0001c0001t0003g0180 a0001c0001t0012g0181 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(325): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(318): Show |
5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
5 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(327): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(319): Show |
22 | a0001c0001t0001g0231 a0001c0001t0001g0238 a0001c0001t0001g0239 others(19): Show |
23 | HG00735.hp1 HG00738.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(328): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(320): Show |
8 | a0001c0001t0001g0237 a0001c0001t0002g0208 a0001c0001t0002g0217 others(5): Show |
8 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(329): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(321): Show |
1 | a0001c0001t0001g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1341-443_1341-442i others(330): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(324): Show |
1 | a0001c0001t0001g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1341-443_1341-442i others(333): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(324): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0258 others(1): Show |
5 | HG01346.hp1 HG01496.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1341-443_1341-442i others(333): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(325): Show |
1 | a0001c0001t0001g0254 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1341-443_1341-442i others(334): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(326): Show |
2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1341-443_1341-442i others(335): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69361931 | T | TTCCACTA others(327): Show |
1 | a0001c0001t0001g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1341-443_1341-442i others(336): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69361931 | |||||||
| chr16:69362115 | G | C | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1341-626C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362115 | |||||||
| chr16:69362171 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1341-682G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362171 | |||||||
| chr16:69362333 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1341-844T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362333 | |||||||
| chr16:69362527 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1341-1038A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362527 | |||||||
| chr16:69362543 | A | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0102 a0001c0001t0001g0103 others(6): Show |
9 | HG01891.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1341-1054T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362543 | |||||||
| chr16:69362555 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1341-1066G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362555 | |||||||
| chr16:69362617 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1341-1128A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362617 | |||||||
| chr16:69362682 | C | T | 102 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(99): Show |
114 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1341-1193G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362682 | |||||||
| chr16:69362715 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
12 | HG02602.hp1 HG02622.hp1 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.1341-1226A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362715 | |||||||
| chr16:69362719 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1341-1230A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362719 | |||||||
| chr16:69362856 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1341-1367G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69362856 | |||||||
| chr16:69363004 | T | C | 1 | a0001c0001t0012g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1341-1515A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363004 | |||||||
| chr16:69363035 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1341-1546C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363035 | |||||||
| chr16:69363437 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1341-1948G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363437 | |||||||
| chr16:69363490 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(64): Show |
98 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1341-2001A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363490 | |||||||
| chr16:69363609 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1341-2120C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363609 | |||||||
| chr16:69363654 | T | C | 11 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(8): Show |
11 | HG00544.hp1 HG01346.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1341-2165A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363654 | |||||||
| chr16:69363707 | G | T | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1341-2218C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363707 | |||||||
| chr16:69363968 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1341-2479G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363968 | |||||||
| chr16:69363969 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0012g0243 |
2 | HG02976.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1341-2480C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363969 | |||||||
| chr16:69363981 | C | G | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341-2492G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69363981 | |||||||
| chr16:69364017 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1341-2528T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69364017 | |||||||
| chr16:69364271 | T | C | 4 | a0001c0002t0006g0016 a0001c0002t0006g0050 a0001c0002t0006g0052 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1340+2536A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69364271 | |||||||
| chr16:69364340 | C | A | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1340+2467G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69364340 | |||||||
| chr16:69364450 | G | T | 56 | a0001c0001t0001g0034 a0001c0001t0001g0228 a0001c0001t0001g0229 others(53): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1340+2357C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69364450 | |||||||
| chr16:69364722 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1340+2085G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69364722 | |||||||
| chr16:69364747 | C | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
9 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1340+2060G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69364747 | |||||||
| chr16:69364792 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1340+2015T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69364792 | |||||||
| chr16:69365001 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0152 |
2 | NA18971.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1340+1806G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69365001 | |||||||
| chr16:69365339 | C | T | 1 | a0001c0001t0002g0031 | 2 | NA18968.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1340+1468G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69365339 | |||||||
| chr16:69365417 | C | G | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1340+1390G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69365417 | |||||||
| chr16:69365418 | C | T | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1340+1389G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69365418 | |||||||
| chr16:69365683 | G | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
9 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1340+1124C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69365683 | |||||||
| chr16:69366057 | G | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
11 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.1340+750C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69366057 | |||||||
| chr16:69366239 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1340+568A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69366239 | |||||||
| chr16:69366304 | T | G | 82 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(79): Show |
88 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1340+503A>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69366304 | |||||||
| chr16:69366352 | A | C | 1 | a0001c0002t0014g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1340+455T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69366352 | |||||||
| chr16:69366496 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1340+311T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69366496 | |||||||
| chr16:69366564 | C | T | 1 | a0001c0001t0005g0099 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1340+243G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 7/9 | chr16 | 69366564 | |||||||
| chr16:69367252 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.948-53G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367252 | |||||||
| chr16:69367279 | T | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0132 |
2 | HG01074.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.948-80A>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367279 | |||||||
| chr16:69367361 | C | G | 1 | a0001c0001t0003g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.948-162G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367361 | |||||||
| chr16:69367533 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0182 others(6): Show |
12 | HG00738.hp1 HG02145.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-334C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367533 | |||||||
| chr16:69367562 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.948-363G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367562 | |||||||
| chr16:69367745 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.948-546A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367745 | |||||||
| chr16:69367776 | T | A | 1 | a0001c0002t0014g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.948-577A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367776 | |||||||
| chr16:69367988 | G | A | 5 | a0001c0002t0006g0016 a0001c0002t0006g0050 a0001c0002t0006g0052 others(2): Show |
6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+388C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69367988 | |||||||
| chr16:69368003 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.947+373A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69368003 | |||||||
| chr16:69368034 | G | A | 82 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(79): Show |
88 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.947+342C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69368034 | |||||||
| chr16:69368332 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.947+44G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69368332 | |||||||
| chr16:69368349 | C | T | 20 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.947+27G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 6/9 | chr16 | 69368349 | |||||||
| chr16:69368608 | C | T | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.841-126G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69368608 | |||||||
| chr16:69368621 | A | T | 1 | a0001c0001t0018g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.841-139T>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69368621 | |||||||
| chr16:69368864 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0102 a0001c0001t0001g0103 others(6): Show |
9 | HG01891.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.841-382G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69368864 | |||||||
| chr16:69368912 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.841-430C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69368912 | |||||||
| chr16:69368928 | A | G | 93 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(90): Show |
102 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.841-446T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69368928 | |||||||
| chr16:69368958 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.841-476C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69368958 | |||||||
| chr16:69369108 | CA | C | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-627delT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369108 | |||||||
| chr16:69369110 | G | T | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-628C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369110 | |||||||
| chr16:69369111 | G | T | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-629C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369111 | |||||||
| chr16:69369116 | T | TAACTCCA others(111): Show |
1 | a0001c0001t0002g0213 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.841-635_841-634ins others(118): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369116 | |||||||
| chr16:69369116 | T | TAACTCCA others(110): Show |
90 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(87): Show |
99 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.841-635_841-634ins others(117): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369116 | |||||||
| chr16:69369116 | T | TAACTCCA others(110): Show |
1 | a0001c0001t0003g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.841-635_841-634ins others(117): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369116 | |||||||
| chr16:69369119 | G | C | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-637C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369119 | |||||||
| chr16:69369122 | T | TCCACA | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-641_841-640ins others(5): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369122 | |||||||
| chr16:69369123 | T | C | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-641A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369123 | |||||||
| chr16:69369125 | T | C | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-643A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369125 | |||||||
| chr16:69369127 | T | C | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-645A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369127 | |||||||
| chr16:69369131 | T | C | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-649A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369131 | |||||||
| chr16:69369132 | A | AGCAGC | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.841-651_841-650ins others(5): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369132 | |||||||
| chr16:69369180 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.841-698T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369180 | |||||||
| chr16:69369310 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.841-828C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369310 | |||||||
| chr16:69369435 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.841-953T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369435 | |||||||
| chr16:69369500 | T | C | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+983A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369500 | |||||||
| chr16:69369647 | C | G | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.840+836G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369647 | |||||||
| chr16:69369680 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.840+803C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369680 | |||||||
| chr16:69369994 | T | A | 1 | a0001c0001t0004g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.840+489A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69369994 | |||||||
| chr16:69370014 | T | A | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.840+469A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69370014 | |||||||
| chr16:69370080 | G | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.840+403C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69370080 | |||||||
| chr16:69370338 | G | A | 56 | a0001c0001t0001g0034 a0001c0001t0001g0228 a0001c0001t0001g0229 others(53): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.840+145C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 5/9 | chr16 | 69370338 | |||||||
| chr16:69370635 | C | T | 1 | a0001c0002t0006g0050 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.694-6G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370635 | |||||||
| chr16:69370930 | G | T | 1 | a0001c0001t0008g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.694-301C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370930 | |||||||
| chr16:69370951 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.694-322C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370951 | |||||||
| chr16:69370994 | T | TAC | 38 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0029 others(35): Show |
42 | HG00544.hp1 HG00741.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.694-367_694-366dup others(2): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370994 | |||||||
| chr16:69370994 | T | TACAC | 13 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(10): Show |
13 | HG01109.hp2 HG01192.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.694-369_694-366dup others(4): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370994 | |||||||
| chr16:69370994 | T | TACACAC | 50 | a0001c0001t0001g0034 a0001c0001t0001g0211 a0001c0001t0001g0212 others(47): Show |
53 | HG00280.hp1 HG00621.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.694-371_694-366dup others(6): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370994 | |||||||
| chr16:69370994 | T | TACACACA others(1): Show |
11 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
15 | HG00099.hp2 HG00738.hp2 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.694-373_694-366dup others(8): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370994 | |||||||
| chr16:69370994 | T | TACACACA others(3): Show |
1 | a0001c0001t0012g0243 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.694-375_694-366dup others(10): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69370994 | |||||||
| chr16:69371500 | C | CA | 7 | a0001c0001t0001g0072 a0001c0001t0001g0104 a0001c0001t0001g0260 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+768dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69371500 | |||||||
| chr16:69371500 | CA | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0229 others(8): Show |
13 | HG01168.hp2 HG01346.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.693+768delT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69371500 | |||||||
| chr16:69371627 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.693+642G>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69371627 | |||||||
| chr16:69371835 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.693+434A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69371835 | |||||||
| chr16:69372078 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.693+191A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 4/9 | chr16 | 69372078 | |||||||
| chr16:69372501 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0146 |
4 | HG02015.hp1 HG02083.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-146C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69372501 | |||||||
| chr16:69372707 | A | G | 1 | a0001c0002t0014g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.607-352T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69372707 | |||||||
| chr16:69372884 | C | A | 1 | a0001c0001t0002g0223 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.607-529G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69372884 | |||||||
| chr16:69373083 | A | G | 92 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(89): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.607-728T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373083 | |||||||
| chr16:69373266 | A | G | 1 | a0001c0001t0002g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.607-911T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373266 | |||||||
| chr16:69373335 | A | C | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.607-980T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373335 | |||||||
| chr16:69373458 | T | C | 1 | a0001c0001t0003g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.607-1103A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373458 | |||||||
| chr16:69373578 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.607-1223A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373578 | |||||||
| chr16:69373588 | T | G | 1 | a0001c0001t0017g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.607-1233A>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373588 | |||||||
| chr16:69373766 | G | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0067 a0001c0001t0004g0073 |
3 | NA18973.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.607-1411C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373766 | |||||||
| chr16:69373773 | C | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0067 a0001c0001t0004g0073 |
3 | NA18973.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.607-1418G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373773 | |||||||
| chr16:69373819 | C | T | 1 | a0001c0001t0004g0064 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.607-1464G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373819 | |||||||
| chr16:69373896 | CAG | C | 37 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.607-1543_607-1542d others(4): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69373896 | |||||||
| chr16:69374012 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.607-1657G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374012 | |||||||
| chr16:69374063 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.607-1708T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374063 | |||||||
| chr16:69374243 | C | T | 5 | a0001c0002t0006g0016 a0001c0002t0006g0050 a0001c0002t0006g0052 others(2): Show |
6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-1888G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374243 | |||||||
| chr16:69374413 | T | C | 1 | a0001c0001t0012g0243 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.607-2058A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374413 | |||||||
| chr16:69374484 | T | G | 1 | a0001c0001t0018g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.607-2129A>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374484 | |||||||
| chr16:69374574 | G | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0067 a0001c0001t0004g0073 |
3 | NA18973.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.607-2219C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374574 | |||||||
| chr16:69374625 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.607-2270A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374625 | |||||||
| chr16:69374627 | T | TAAAAAAA others(12): Show |
1 | a0002c0003t0003g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.607-2291_607-2273d others(21): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(2): Show |
T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(6): Show |
11 | HG01074.hp1 HG01258.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.607-2281_607-2273d others(11): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(3): Show |
T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0197 |
3 | HG03942.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.607-2282_607-2273d others(12): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(4): Show |
T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0154 others(4): Show |
10 | HG01261.hp1 HG01361.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-2283_607-2273d others(13): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(5): Show |
T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0095 others(8): Show |
19 | HG00642.hp2 HG01123.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.607-2284_607-2273d others(14): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(6): Show |
T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0118 a0001c0001t0001g0139 others(7): Show |
12 | HG01070.hp2 HG01081.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.607-2285_607-2273d others(15): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(7): Show |
T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0138 a0001c0001t0001g0153 others(1): Show |
4 | HG00544.hp2 HG01255.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-2286_607-2273d others(16): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(8): Show |
T | 6 | a0001c0001t0001g0109 a0001c0001t0001g0137 a0001c0001t0001g0187 others(3): Show |
6 | HG00738.hp1 HG01099.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-2287_607-2273d others(17): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(9): Show |
T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
19 | HG00642.hp1 HG01109.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.607-2288_607-2273d others(18): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(10): Show |
T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0035 others(27): Show |
42 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.607-2289_607-2273d others(19): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(11): Show |
T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(35): Show |
53 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.607-2290_607-2273d others(20): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(12): Show |
T | 29 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0055 others(26): Show |
29 | HG00738.hp2 HG01074.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.607-2291_607-2273d others(21): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(13): Show |
T | 10 | a0001c0001t0001g0037 a0001c0001t0001g0101 a0001c0001t0002g0217 others(7): Show |
10 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.607-2292_607-2273d others(22): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(14): Show |
T | 10 | a0001c0001t0001g0130 a0001c0001t0001g0231 a0001c0001t0001g0232 others(7): Show |
11 | HG01496.hp1 HG02451.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.607-2293_607-2273d others(23): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(15): Show |
T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0199 others(1): Show |
5 | HG00408.hp1 HG01884.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-2294_607-2273d others(24): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(16): Show |
T | 6 | a0001c0001t0001g0262 a0001c0001t0001g0265 a0001c0001t0001g0267 others(3): Show |
6 | HG01361.hp1 HG02622.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-2295_607-2273d others(25): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(17): Show |
T | 8 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0001g0264 others(5): Show |
8 | HG00544.hp1 HG01346.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.607-2296_607-2273d others(26): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(18): Show |
T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0129 others(3): Show |
8 | HG02723.hp1 HG02976.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.607-2297_607-2273d others(27): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(19): Show |
T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0032 others(4): Show |
11 | HG02300.hp1 HG02602.hp1 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.607-2298_607-2273d others(28): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(22): Show |
T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0005g0202 others(2): Show |
5 | HG01123.hp1 HG01175.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-2301_607-2273d others(31): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(24): Show |
T | 1 | a0001c0001t0003g0180 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.607-2303_607-2273d others(33): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(25): Show |
T | 1 | a0001c0001t0001g0061 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.607-2304_607-2273d others(34): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(26): Show |
T | 3 | a0001c0001t0001g0126 a0001c0001t0002g0215 a0001c0002t0014g0054 |
3 | HG01891.hp2 HG03139.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.607-2305_607-2273d others(35): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(27): Show |
T | 8 | a0001c0001t0001g0124 a0001c0001t0003g0169 a0001c0001t0004g0125 others(5): Show |
9 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.607-2306_607-2273d others(36): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(28): Show |
T | 8 | a0001c0001t0002g0249 a0001c0001t0003g0166 a0001c0001t0003g0167 others(5): Show |
8 | HG01192.hp2 HG02129.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.607-2307_607-2273d others(37): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(29): Show |
T | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-2308_607-2273d others(38): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(30): Show |
T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0229 a0001c0001t0001g0230 others(7): Show |
11 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.607-2309_607-2273d others(39): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(31): Show |
T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0059 others(1): Show |
6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-2310_607-2273d others(40): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374627 | TAAAAAAA others(32): Show |
T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0237 others(1): Show |
4 | HG03195.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-2311_607-2273d others(41): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374627 | |||||||
| chr16:69374694 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.607-2339C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374694 | |||||||
| chr16:69374704 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.607-2349C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374704 | |||||||
| chr16:69374835 | C | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0182 others(7): Show |
13 | HG00738.hp1 HG02145.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.607-2480G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374835 | |||||||
| chr16:69374944 | AAC | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0005g0098 others(1): Show |
4 | HG00621.hp2 NA18985.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-2591_607-2590d others(4): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69374944 | |||||||
| chr16:69375224 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.607-2869A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69375224 | |||||||
| chr16:69375270 | G | C | 16 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0168 others(13): Show |
16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.607-2915C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69375270 | |||||||
| chr16:69375506 | A | G | 101 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(98): Show |
113 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.607-3151T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69375506 | |||||||
| chr16:69375599 | A | G | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG01346.hp2 HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.607-3244T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69375599 | |||||||
| chr16:69375920 | T | C | 13 | a0001c0001t0002g0214 a0001c0001t0002g0222 a0001c0001t0002g0223 others(10): Show |
13 | HG00280.hp1 HG00735.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.607-3565A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69375920 | |||||||
| chr16:69376122 | G | A | 1 | a0001c0002t0014g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.607-3767C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376122 | |||||||
| chr16:69376400 | A | C | 1 | a0001c0001t0018g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.607-4045T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376400 | |||||||
| chr16:69376542 | T | C | 1 | a0001c0001t0002g0031 | 2 | NA18968.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.607-4187A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376542 | |||||||
| chr16:69376674 | G | C | 1 | a0001c0001t0001g0269 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.607-4319C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376674 | |||||||
| chr16:69376691 | C | CA | 44 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0053 others(41): Show |
46 | HG00408.hp1 HG00544.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.607-4337dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376691 | |||||||
| chr16:69376691 | CA | C | 11 | a0001c0001t0001g0118 a0001c0001t0001g0211 a0001c0001t0001g0212 others(8): Show |
13 | HG01167.hp1 HG01168.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.607-4337delT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376691 | |||||||
| chr16:69376863 | G | GA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
137 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.607-4509dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376863 | |||||||
| chr16:69376863 | G | GAA | 66 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(63): Show |
71 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.607-4510_607-4509d others(4): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376863 | |||||||
| chr16:69376863 | G | GAAA | 33 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(30): Show |
37 | HG00544.hp1 HG01346.hp1 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.607-4511_607-4509d others(5): Show |
TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376863 | |||||||
| chr16:69376939 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.607-4584C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376939 | |||||||
| chr16:69376992 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.607-4637C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69376992 | |||||||
| chr16:69377003 | C | A | 1 | a0001c0002t0014g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.607-4648G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377003 | |||||||
| chr16:69377101 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.607-4746C>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377101 | |||||||
| chr16:69377148 | A | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.607-4793T>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377148 | |||||||
| chr16:69377186 | G | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG03098.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.607-4831C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377186 | |||||||
| chr16:69377202 | C | CA | 21 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
26 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.607-4848dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377202 | |||||||
| chr16:69377217 | G | C | 1 | a0001c0001t0001g0258 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.607-4862C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377217 | |||||||
| chr16:69377323 | C | A | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.607-4968G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377323 | |||||||
| chr16:69377564 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.607-5209T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377564 | |||||||
| chr16:69377568 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18973.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.607-5213G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377568 | |||||||
| chr16:69377586 | A | T | 1 | a0001c0001t0010g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.607-5231T>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377586 | |||||||
| chr16:69377842 | AT | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
8 | HG02135.hp2 HG02155.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.607-5488delA | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69377842 | |||||||
| chr16:69378422 | C | T | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-6067G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69378422 | |||||||
| chr16:69378571 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.606+6009G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69378571 | |||||||
| chr16:69378745 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.606+5835A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69378745 | |||||||
| chr16:69378789 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.606+5791C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69378789 | |||||||
| chr16:69378950 | T | TG | 31 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0032 others(28): Show |
37 | HG00280.hp1 HG00738.hp1 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.606+5629dupC | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69378950 | |||||||
| chr16:69378961 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
15 | HG02602.hp1 HG02976.hp1 HG03540.hp2 others(12): Show |
intron_variant | MODIFIER | c.606+5619T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69378961 | |||||||
| chr16:69379015 | T | C | 18 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0168 others(15): Show |
18 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.606+5565A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379015 | |||||||
| chr16:69379227 | C | T | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+5353G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379227 | |||||||
| chr16:69379407 | T | C | 5 | a0001c0002t0006g0016 a0001c0002t0006g0050 a0001c0002t0006g0052 others(2): Show |
6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+5173A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379407 | |||||||
| chr16:69379446 | G | A | 1 | a0001c0002t0014g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.606+5134C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379446 | |||||||
| chr16:69379586 | A | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0182 others(7): Show |
13 | HG00738.hp1 HG02145.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.606+4994T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379586 | |||||||
| chr16:69379719 | T | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
5 | HG01346.hp1 HG01358.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+4861A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379719 | |||||||
| chr16:69379725 | A | C | 7 | a0001c0001t0007g0007 a0001c0001t0007g0036 a0001c0002t0006g0016 others(4): Show |
10 | HG01433.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.606+4855T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379725 | |||||||
| chr16:69379852 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.606+4728G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69379852 | |||||||
| chr16:69380016 | C | T | 48 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.606+4564G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69380016 | |||||||
| chr16:69380655 | T | TA | 29 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(26): Show |
36 | HG00408.hp1 HG00738.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.606+3924dupT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69380655 | |||||||
| chr16:69380655 | TA | T | 6 | a0001c0001t0001g0053 a0001c0001t0002g0213 a0001c0002t0006g0016 others(3): Show |
7 | HG02257.hp1 HG02280.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.606+3924delT | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69380655 | |||||||
| chr16:69380802 | AT | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(6): Show |
10 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+3777delA | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69380802 | |||||||
| chr16:69380935 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.606+3645C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69380935 | |||||||
| chr16:69381477 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.606+3103A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69381477 | |||||||
| chr16:69381706 | C | T | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.606+2874G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69381706 | |||||||
| chr16:69381715 | A | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0005c0006t0001g0048 |
3 | HG02145.hp2 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.606+2865T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69381715 | |||||||
| chr16:69381938 | A | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
12 | NA18945.hp1 NA18948.hp1 NA18957.hp2 others(9): Show |
intron_variant | MODIFIER | c.606+2642T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69381938 | |||||||
| chr16:69382025 | C | A | 11 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(8): Show |
11 | HG00544.hp1 HG01346.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.606+2555G>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69382025 | |||||||
| chr16:69382198 | G | C | 2 | a0003c0004t0001g0200 a0003c0004t0001g0201 |
2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.606+2382C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69382198 | |||||||
| chr16:69382471 | G | C | 1 | a0001c0001t0005g0202 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.606+2109C>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69382471 | |||||||
| chr16:69382542 | T | C | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.606+2038A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69382542 | |||||||
| chr16:69382756 | T | C | 7 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(4): Show |
7 | HG00099.hp2 HG00738.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.606+1824A>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69382756 | |||||||
| chr16:69383090 | A | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.606+1490T>G | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69383090 | |||||||
| chr16:69383124 | C | T | 3 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 |
3 | HG02572.hp1 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.606+1456G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69383124 | |||||||
| chr16:69383144 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
9 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1436G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69383144 | |||||||
| chr16:69383235 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.606+1345G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69383235 | |||||||
| chr16:69383399 | T | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG01070.hp1 HG01071.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.606+1181A>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69383399 | |||||||
| chr16:69383692 | C | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(6): Show |
10 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+888G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69383692 | |||||||
| chr16:69384339 | A | G | 2 | a0001c0001t0007g0007 a0001c0001t0007g0036 |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+241T>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 3/9 | chr16 | 69384339 | |||||||
| chr16:69385089 | T | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18979.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.475+302A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 2/9 | chr16 | 69385089 | |||||||
| chr16:69385128 | T | A | 68 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(65): Show |
74 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.475+263A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 2/9 | chr16 | 69385128 | |||||||
| chr16:69385180 | T | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0253 a0001c0001t0001g0254 others(6): Show |
10 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+211A>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 2/9 | chr16 | 69385180 | |||||||
| chr16:69385491 | G | A | 11 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(8): Show |
11 | HG00544.hp1 HG01346.hp2 HG01361.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.380-5C>T | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 1/9 | chr16 | 69385491 | |||||||
| chr16:69385510 | T | G | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.380-24A>C | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 1/9 | chr16 | 69385510 | |||||||
| chr16:69385564 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.379+29G>A | TERF2 | ENSG00000132604.11 | transcript | ENST00000254942.8 | protein_coding | 1/9 | chr16 | 69385564 |