Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6947 |
| ensemblid | ENSG00000134827.8 |
| hgncid | 11652 |
| symbol | TCN1 |
| name | transcobalamin 1 |
| refseq_nuc | NM_001062.4 |
| refseq_prot | NP_001053.2 |
| ensembl_nuc | ENST00000257264.4 |
| ensembl_prot | ENSP00000257264.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 59852808 |
| end | 59866487 |
| strand | - |
| ver | v1.2 |
| region | chr11:59852808-59866487 |
| region5000 | chr11:59847808-59871487 |
| regionname0 | TCN1_chr11_59852808_59866487 |
| regionname5000 | TCN1_chr11_59847808_59871487 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 433 | 308 | 88 | 58 | 116 | 13 | 31 | 84 | TCN1_chr11_59847808_59871487 | TCN1 | MRQSH others(428): Show |
chr11 | 59847808 | 59871487 |
| a0002 | 0/0 | 433 | 18 | 7 | 8 | 0 | 2 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | MRQSH others(428): Show |
chr11 | 59847808 | 59871487 |
| a0003 | 0/0 | 433 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | MRQSH others(428): Show |
chr11 | 59847808 | 59871487 |
| a0004 | 0/0 | 433 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | MRQSH others(428): Show |
chr11 | 59847808 | 59871487 |
| a0005 | 0/0 | 433 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | MRQSH others(428): Show |
chr11 | 59847808 | 59871487 |
| a0006 | 0/0 | 433 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | MRQSH others(428): Show |
chr11 | 59847808 | 59871487 |
| a0007 | 0/0 | 433 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | MRQSH others(428): Show |
chr11 | 59847808 | 59871487 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1299 | 200 | 42 | 45 | 82 | 11 | 18 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 | ||
| a0001c0002 | 0/0 | 1299 | 108 | 46 | 13 | 34 | 2 | 13 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 | ||
| a0002c0003 | 0/0 | 1299 | 18 | 7 | 8 | 0 | 2 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 | ||
| a0003c0004 | 0/0 | 1299 | 4 | 0 | 2 | 0 | 2 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 | ||
| a0004c0005 | 0/0 | 1299 | 2 | 0 | 0 | 2 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 | ||
| a0005c0006 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 | ||
| a0006c0007 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 | ||
| a0007c0008 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | ATGAG others(1294): Show |
chr11 | 59847808 | 59871487 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1486 | 199 | 42 | 45 | 81 | 11 | 18 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0001c0001t0002 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0001c0002t0001 | 0/0 | 1486 | 108 | 46 | 13 | 34 | 2 | 13 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0002c0003t0001 | 0/0 | 1486 | 18 | 7 | 8 | 0 | 2 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0003c0004t0001 | 0/0 | 1486 | 4 | 0 | 2 | 0 | 2 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0004c0005t0001 | 0/0 | 1486 | 2 | 0 | 0 | 2 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0005c0006t0001 | 0/0 | 1486 | 2 | 2 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0006c0007t0001 | 0/0 | 1486 | 1 | 0 | 0 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| a0007c0008t0001 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | GGTAC others(1481): Show |
chr11 | 59847808 | 59871487 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 78 | 11 | 20 | 40 | 1 | 6 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0003 | 1/1 | 35 | 4 | 9 | 17 | 1 | 2 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0007 | 0/0 | 7 | 1 | 1 | 0 | 4 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 3 | 1 | 2 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0002 | 0/0 | 45 | 4 | 5 | 26 | 2 | 8 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0006 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0002c0003t0001g0004 | 0/0 | 15 | 7 | 7 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0003c0004t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0003c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0004c0005t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0005c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0005c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0006c0007t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| a0007c0008t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00140 | hp1 | a0003 | c0004 | t0001 | g0018 | EUR | GBR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0018 | EUR | FIN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00423 | hp2 | a0004 | c0005 | t0001 | g0022 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00639 | hp2 | a0003 | c0004 | t0001 | g0018 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01070 | hp1 | a0003 | c0004 | t0001 | g0057 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01515 | hp2 | a0006 | c0007 | t0001 | g0040 | EUR | IBS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0034 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02145 | hp2 | a0007 | c0008 | t0001 | g0058 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02165 | hp1 | a0004 | c0005 | t0001 | g0022 | EAS | CDX | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03453 | hp2 | a0005 | c0006 | t0001 | g0095 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03540 | hp1 | a0005 | c0006 | t0001 | g0094 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0042 | SAS | BEB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | STU | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | YRI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | YRI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | YRI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | YRI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | LWK | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | LWK | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | LWK | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | YRI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | YRI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0004 | EUR | TSI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0082 | EUR | TSI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | MSL | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | USA | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | USA | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | LWK | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0003 | REF | REF | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | TCN1_chr11_59847808_59871487 | TCN1 | chr11 | 59847808 | 59871487 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59855881 | C | T | 1 | a0006 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.925G>A | p.Val309Ile | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 6/9 | 942/1486 | 925/1302 | 309/433 | chr11 | 59855881 | |||
| chr11:59855905 | C | A | 1 | a0002 | 18 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
missense_variant | MODERATE | c.901G>T | p.Asp301Tyr | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 6/9 | 918/1486 | 901/1302 | 301/433 | chr11 | 59855905 | |||
| chr11:59859171 | C | A | 1 | a0005 | 2 | HG03453.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.653G>T | p.Ser218Ile | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/9 | 670/1486 | 653/1302 | 218/433 | chr11 | 59859171 | |||
| chr11:59862613 | T | G | 1 | a0007 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.369A>C | p.Glu123Asp | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/9 | 386/1486 | 369/1302 | 123/433 | chr11 | 59862613 | |||
| chr11:59864006 | C | T | 1 | a0004 | 2 | HG00423.hp2 HG02165.hp1 |
missense_variant | MODERATE | c.160G>A | p.Ala54Thr | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/9 | 177/1486 | 160/1302 | 54/433 | chr11 | 59864006 | |||
| chr11:59864062 | C | T | 1 | a0003 | 4 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(1): Show |
missense_variant | MODERATE | c.104G>A | p.Arg35His | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/9 | 121/1486 | 104/1302 | 35/433 | chr11 | 59864062 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59855960 | G | A | 3 | a0001c0002 a0004c0005 a0005c0006 |
112 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(109): Show |
synonymous_variant | LOW | c.846C>T | p.Ser282Ser | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 6/9 | 863/1486 | 846/1302 | 282/433 | chr11 | 59855960 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59852882 | G | A | 1 | a0001c0001t0002 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 9/9 | 93 | chr11 | 59852882 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59853052 | A | C | 1 | a0001c0002t0001g0067 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1241-16T>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 8/8 | chr11 | 59853052 | |||||||
| chr11:59853180 | T | C | 4 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0062 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+23A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 8/8 | chr11 | 59853180 | |||||||
| chr11:59853537 | G | T | 14 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0041 others(11): Show |
16 | HG01109.hp1 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1122-216C>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59853537 | |||||||
| chr11:59853611 | G | C | 17 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(14): Show |
26 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.1122-290C>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59853611 | |||||||
| chr11:59853911 | G | A | 2 | a0001c0002t0001g0052 a0007c0008t0001g0058 |
2 | HG01261.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1122-590C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59853911 | |||||||
| chr11:59853923 | ATGATAAA others(516): Show |
A | 7 | a0001c0001t0001g0030 a0001c0002t0001g0017 a0001c0002t0001g0032 others(4): Show |
10 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1121+206_1122-603d others(2): Show |
TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59853923 | |||||||
| chr11:59854050 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121+602A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59854050 | |||||||
| chr11:59854227 | AAAAT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0059 others(4): Show |
9 | HG01109.hp2 HG01261.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121+421_1121+424d others(6): Show |
TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59854227 | |||||||
| chr11:59854436 | T | C | 1 | a0001c0001t0001g0001 | 8 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+216A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59854436 | |||||||
| chr11:59854447 | A | G | 7 | a0001c0001t0001g0030 a0001c0002t0001g0017 a0001c0002t0001g0032 others(4): Show |
10 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1121+205T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59854447 | |||||||
| chr11:59854463 | C | G | 1 | a0001c0002t0001g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1121+189G>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 7/8 | chr11 | 59854463 | |||||||
| chr11:59855116 | A | AT | 6 | a0001c0002t0001g0025 a0001c0002t0001g0047 a0001c0002t0001g0048 others(3): Show |
7 | HG01168.hp1 HG01169.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.938-282dupA | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 6/8 | chr11 | 59855116 | |||||||
| chr11:59855484 | A | C | 1 | a0001c0002t0001g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.937+385T>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 6/8 | chr11 | 59855484 | |||||||
| chr11:59855675 | C | G | 1 | a0001c0002t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.937+194G>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 6/8 | chr11 | 59855675 | |||||||
| chr11:59855714 | A | T | 4 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0005c0006t0001g0094 others(1): Show |
4 | HG03453.hp2 HG03540.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+155T>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 6/8 | chr11 | 59855714 | |||||||
| chr11:59856078 | T | TG | 7 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0087 others(4): Show |
13 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-21dupC | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856078 | |||||||
| chr11:59856167 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.748-109T>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856167 | |||||||
| chr11:59856250 | T | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0089 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.748-192A>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856250 | |||||||
| chr11:59856402 | G | C | 1 | a0002c0003t0001g0042 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.748-344C>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856402 | |||||||
| chr11:59856489 | A | G | 1 | a0004c0005t0001g0022 | 2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.748-431T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856489 | |||||||
| chr11:59856724 | G | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.748-666C>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856724 | |||||||
| chr11:59856778 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.748-720C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856778 | |||||||
| chr11:59856801 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.748-743G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856801 | |||||||
| chr11:59856803 | A | T | 1 | a0001c0002t0001g0024 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.748-745T>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856803 | |||||||
| chr11:59856848 | T | C | 1 | a0001c0001t0001g0005 | 5 | NA18940.hp2 NA18965.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-790A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856848 | |||||||
| chr11:59856969 | G | A | 1 | a0001c0002t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.748-911C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59856969 | |||||||
| chr11:59857063 | A | T | 25 | a0001c0001t0001g0008 a0001c0002t0001g0002 a0001c0002t0001g0006 others(22): Show |
96 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.748-1005T>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59857063 | |||||||
| chr11:59857550 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.748-1492G>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59857550 | |||||||
| chr11:59857582 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.747+1495G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59857582 | |||||||
| chr11:59857758 | C | T | 1 | a0001c0002t0001g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.747+1319G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59857758 | |||||||
| chr11:59857943 | G | C | 2 | a0005c0006t0001g0094 a0005c0006t0001g0095 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.747+1134C>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59857943 | |||||||
| chr11:59858177 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.747+900G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858177 | |||||||
| chr11:59858181 | T | C | 2 | a0005c0006t0001g0094 a0005c0006t0001g0095 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.747+896A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858181 | |||||||
| chr11:59858336 | G | GTTGT | 40 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0002t0001g0002 others(37): Show |
121 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.747+740_747+741ins others(4): Show |
TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858336 | |||||||
| chr11:59858336 | G | T | 2 | a0005c0006t0001g0094 a0005c0006t0001g0095 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.747+741C>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858336 | |||||||
| chr11:59858602 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747+475G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858602 | |||||||
| chr11:59858695 | G | A | 2 | a0005c0006t0001g0094 a0005c0006t0001g0095 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.747+382C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858695 | |||||||
| chr11:59858772 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.747+305G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858772 | |||||||
| chr11:59858814 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.747+263C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858814 | |||||||
| chr11:59858826 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.747+251G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858826 | |||||||
| chr11:59858918 | G | A | 2 | a0005c0006t0001g0094 a0005c0006t0001g0095 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.747+159C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858918 | |||||||
| chr11:59858935 | G | A | 3 | a0001c0002t0001g0017 a0001c0002t0001g0045 a0001c0002t0001g0046 |
5 | HG01884.hp1 HG02809.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+142C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59858935 | |||||||
| chr11:59859004 | TA | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0035 others(6): Show |
19 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(16): Show |
intron_variant | MODIFIER | c.747+72delT | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59859004 | |||||||
| chr11:59859013 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.747+64T>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59859013 | |||||||
| chr11:59859058 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.747+19C>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 5/8 | chr11 | 59859058 | |||||||
| chr11:59859331 | G | A | 3 | a0001c0002t0001g0017 a0001c0002t0001g0045 a0001c0002t0001g0046 |
5 | HG01884.hp1 HG02809.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-64C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859331 | |||||||
| chr11:59859385 | T | G | 1 | a0001c0002t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.557-118A>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859385 | |||||||
| chr11:59859423 | C | T | 3 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 |
3 | HG02258.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.557-156G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859423 | |||||||
| chr11:59859519 | A | T | 1 | a0001c0001t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.557-252T>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859519 | |||||||
| chr11:59859530 | C | A | 1 | a0001c0002t0001g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.557-263G>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859530 | |||||||
| chr11:59859730 | T | C | 1 | a0001c0001t0001g0016 | 3 | HG03704.hp2 HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.557-463A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859730 | |||||||
| chr11:59859739 | T | A | 19 | a0001c0001t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(16): Show |
29 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.557-472A>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859739 | |||||||
| chr11:59859917 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.557-650C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859917 | |||||||
| chr11:59859957 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.557-690T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59859957 | |||||||
| chr11:59860064 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.557-797C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860064 | |||||||
| chr11:59860078 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.557-811G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860078 | |||||||
| chr11:59860117 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.557-850A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860117 | |||||||
| chr11:59860217 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0064 a0001c0001t0001g0072 |
6 | HG01099.hp1 HG01943.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.557-950G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860217 | |||||||
| chr11:59860348 | T | C | 1 | a0001c0002t0001g0011 | 5 | HG01243.hp1 HG02258.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-1081A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860348 | |||||||
| chr11:59860620 | A | C | 7 | a0001c0002t0001g0021 a0001c0002t0001g0032 a0001c0002t0001g0033 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.556+907T>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860620 | |||||||
| chr11:59860634 | T | G | 3 | a0001c0002t0001g0017 a0001c0002t0001g0045 a0001c0002t0001g0046 |
5 | HG01884.hp1 HG02809.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+893A>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860634 | |||||||
| chr11:59860784 | G | A | 1 | a0001c0002t0001g0026 | 2 | HG01975.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.556+743C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860784 | |||||||
| chr11:59860922 | A | C | 1 | a0001c0002t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.556+605T>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59860922 | |||||||
| chr11:59861058 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.556+469A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59861058 | |||||||
| chr11:59861208 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.556+319T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59861208 | |||||||
| chr11:59861215 | G | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0035 others(1): Show |
8 | HG01071.hp2 HG01192.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.556+312C>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59861215 | |||||||
| chr11:59861242 | C | T | 7 | a0001c0002t0001g0021 a0001c0002t0001g0032 a0001c0002t0001g0033 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.556+285G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59861242 | |||||||
| chr11:59861338 | C | A | 2 | a0001c0002t0001g0071 a0001c0002t0001g0088 |
2 | HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.556+189G>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59861338 | |||||||
| chr11:59861444 | A | G | 3 | a0001c0002t0001g0021 a0001c0002t0001g0054 a0001c0002t0001g0055 |
4 | HG01109.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.556+83T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 4/8 | chr11 | 59861444 | |||||||
| chr11:59861691 | G | A | 1 | a0001c0002t0001g0015 | 4 | HG02451.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-9C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/8 | chr11 | 59861691 | |||||||
| chr11:59861832 | C | T | 23 | a0001c0001t0001g0008 a0001c0002t0001g0002 a0001c0002t0001g0006 others(20): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.401-150G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/8 | chr11 | 59861832 | |||||||
| chr11:59861995 | C | T | 1 | a0001c0002t0001g0065 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.401-313G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/8 | chr11 | 59861995 | |||||||
| chr11:59862290 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.400+292C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/8 | chr11 | 59862290 | |||||||
| chr11:59862319 | ATG | A | 3 | a0001c0002t0001g0021 a0001c0002t0001g0054 a0001c0002t0001g0055 |
4 | HG01109.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+261_400+262del others(2): Show |
TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/8 | chr11 | 59862319 | |||||||
| chr11:59862507 | G | A | 1 | a0001c0002t0001g0015 | 4 | HG02451.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+75C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/8 | chr11 | 59862507 | |||||||
| chr11:59862519 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.400+63A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 3/8 | chr11 | 59862519 | |||||||
| chr11:59862741 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.260-19T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59862741 | |||||||
| chr11:59862866 | A | G | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.260-144T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59862866 | |||||||
| chr11:59862872 | A | G | 3 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 |
3 | HG02258.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.260-150T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59862872 | |||||||
| chr11:59863121 | C | A | 1 | a0001c0002t0001g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-399G>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863121 | |||||||
| chr11:59863263 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0060 |
3 | NA18747.hp2 NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.260-541T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863263 | |||||||
| chr11:59863299 | G | GA | 19 | a0001c0001t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(16): Show |
29 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.260-578dupT | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863299 | |||||||
| chr11:59863325 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.259+582G>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863325 | |||||||
| chr11:59863335 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259+572C>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863335 | |||||||
| chr11:59863359 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.259+548C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863359 | |||||||
| chr11:59863363 | G | T | 1 | a0001c0001t0001g0019 | 3 | HG00280.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.259+544C>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863363 | |||||||
| chr11:59863444 | A | G | 1 | a0007c0008t0001g0058 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.259+463T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863444 | |||||||
| chr11:59863478 | C | T | 5 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+429G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863478 | |||||||
| chr11:59863505 | C | T | 1 | a0002c0003t0001g0034 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.259+402G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863505 | |||||||
| chr11:59863540 | C | A | 1 | a0001c0002t0001g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.259+367G>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863540 | |||||||
| chr11:59863882 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.259+25A>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 2/8 | chr11 | 59863882 | |||||||
| chr11:59864243 | C | T | 2 | a0005c0006t0001g0094 a0005c0006t0001g0095 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.80-157G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59864243 | |||||||
| chr11:59864250 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.80-164G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59864250 | |||||||
| chr11:59864272 | T | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0090 |
6 | HG01884.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-186A>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59864272 | |||||||
| chr11:59864430 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.80-344C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59864430 | |||||||
| chr11:59864737 | A | G | 19 | a0001c0001t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(16): Show |
29 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.80-651T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59864737 | |||||||
| chr11:59864874 | G | T | 1 | a0002c0003t0001g0034 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.80-788C>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59864874 | |||||||
| chr11:59864966 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.80-880A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59864966 | |||||||
| chr11:59865406 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.79+986G>A | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59865406 | |||||||
| chr11:59865411 | T | A | 1 | a0001c0001t0001g0031 | 2 | HG00673.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.79+981A>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59865411 | |||||||
| chr11:59865636 | GA | G | 3 | a0001c0002t0001g0017 a0001c0002t0001g0045 a0001c0002t0001g0046 |
5 | HG01884.hp1 HG02809.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+755delT | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59865636 | |||||||
| chr11:59865771 | G | A | 1 | a0001c0002t0001g0015 | 4 | HG02451.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+621C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59865771 | |||||||
| chr11:59865786 | A | G | 1 | a0001c0001t0001g0009 | 5 | HG00642.hp2 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+606T>C | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59865786 | |||||||
| chr11:59865872 | G | C | 1 | a0001c0001t0001g0005 | 11 | HG00558.hp2 HG02074.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+520C>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59865872 | |||||||
| chr11:59866020 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(76): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.79+372C>T | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59866020 | |||||||
| chr11:59866030 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79+362A>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59866030 | |||||||
| chr11:59866114 | A | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.79+278T>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59866114 | |||||||
| chr11:59866152 | G | C | 2 | a0005c0006t0001g0094 a0005c0006t0001g0095 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+240C>G | TCN1 | ENSG00000134827.8 | transcript | ENST00000257264.4 | protein_coding | 1/8 | chr11 | 59866152 |