Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23483 |
| ensemblid | ENSG00000088451.11 |
| hgncid | 20324 |
| symbol | TGDS |
| name | TDP-glucose 4,6-dehydratase |
| refseq_nuc | NM_014305.4 |
| refseq_prot | NP_055120.1 |
| ensembl_nuc | ENST00000261296.7 |
| ensembl_prot | ENSP00000261296.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 94574054 |
| end | 94596152 |
| strand | - |
| ver | v1.2 |
| region | chr13:94574054-94596152 |
| region5000 | chr13:94569054-94601152 |
| regionname0 | TGDS_chr13_94574054_94596152 |
| regionname5000 | TGDS_chr13_94569054_94601152 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 350 | 373 | 91 | 70 | 154 | 12 | 44 | 116 | TGDS_chr13_94569054_94601152 | TGDS | MSAAC others(345): Show |
chr13 | 94569054 | 94601152 |
| a0002 | 0/0 | 350 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | MSAAC others(345): Show |
chr13 | 94569054 | 94601152 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 367 | 85 | 70 | 154 | 12 | 44 | TGDS_chr13_94569054_94601152 | TGDS | ATGTC others(1045): Show |
chr13 | 94569054 | 94601152 | ||
| a0001c0002 | 0/0 | 1050 | 6 | 6 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ATGTC others(1045): Show |
chr13 | 94569054 | 94601152 | ||
| a0002c0003 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ATGTC others(1045): Show |
chr13 | 94569054 | 94601152 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1797 | 351 | 74 | 66 | 153 | 12 | 44 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0002 | 0/0 | 1797 | 5 | 4 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0003 | 0/0 | 1797 | 3 | 2 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0004 | 0/0 | 1797 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0005 | 0/0 | 1797 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0006 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0007 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0008 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0001t0009 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0001c0002t0001 | 0/0 | 1797 | 6 | 6 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| a0002c0003t0001 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | ACTGC others(1792): Show |
chr13 | 94569054 | 94601152 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 37 | 3 | 5 | 19 | 2 | 6 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0002 | 0/0 | 25 | 1 | 12 | 9 | 1 | 2 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0003 | 0/0 | 23 | 0 | 3 | 16 | 0 | 4 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 2 | 1 | 2 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0012 | 0/0 | 5 | 1 | 0 | 0 | 2 | 2 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0002g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0001t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0002t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| a0002c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0114 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01934 | hp2 | a0001 | c0001 | t0009 | g0137 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0167 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | LWK | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ASW | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | USA | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | USA | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0050 | AFR | USA | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TGDS_chr13_94569054_94601152 | TGDS | chr13 | 94569054 | 94601152 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94596094 | C | T | 1 | a0002 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.43G>A | p.Gly15Ser | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/12 | 59/1797 | 43/1053 | 15/350 | chr13 | 94596094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94590869 | G | A | 1 | a0001c0002 | 6 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
synonymous_variant | LOW | c.297C>T | p.Ala99Ala | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/12 | 313/1797 | 297/1053 | 99/350 | chr13 | 94590869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94574063 | A | T | 1 | a0001c0001t0005 | 2 | HG03041.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*719T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 719 | chr13 | 94574063 | ||||||
| chr13:94574072 | T | A | 1 | a0001c0001t0008 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 710 | chr13 | 94574072 | ||||||
| chr13:94574082 | C | T | 1 | a0001c0001t0007 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*700G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 700 | chr13 | 94574082 | ||||||
| chr13:94574460 | T | A | 2 | a0001c0001t0003 a0001c0001t0004 |
5 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*322A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 322 | chr13 | 94574460 | ||||||
| chr13:94574541 | C | G | 1 | a0001c0001t0002 | 5 | HG01981.hp1 HG02559.hp1 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*241G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 241 | chr13 | 94574541 | ||||||
| chr13:94574612 | T | C | 1 | a0001c0001t0009 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*170A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 170 | chr13 | 94574612 | ||||||
| chr13:94574662 | A | G | 1 | a0001c0001t0004 | 2 | HG02970.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*120T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 120 | chr13 | 94574662 | ||||||
| chr13:94574707 | C | T | 1 | a0001c0001t0006 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 12/12 | 75 | chr13 | 94574707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:94574884 | AAAG | A | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
73 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.983-35_983-33delCT others(1): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94574884 | |||||||
| chr13:94574885 | AAG | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
14 | HG02055.hp1 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.983-35_983-34delCT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94574885 | |||||||
| chr13:94574978 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0060 others(1): Show |
9 | HG00735.hp2 HG01943.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.983-126G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94574978 | |||||||
| chr13:94575086 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.983-234G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575086 | |||||||
| chr13:94575159 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0098 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.983-307C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575159 | |||||||
| chr13:94575272 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0066 others(6): Show |
15 | HG00423.hp2 HG02027.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.983-420C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575272 | |||||||
| chr13:94575285 | C | CT | 47 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(44): Show |
76 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.983-434dupA | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575285 | |||||||
| chr13:94575285 | C | CTT | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0151 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.983-435_983-434dup others(2): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575285 | |||||||
| chr13:94575285 | CT | C | 12 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0065 others(9): Show |
13 | HG01069.hp2 HG01256.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.983-434delA | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575285 | |||||||
| chr13:94575307 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.983-455T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575307 | |||||||
| chr13:94575322 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0060 others(1): Show |
9 | HG00735.hp2 HG01943.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.983-470G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575322 | |||||||
| chr13:94575680 | AT | A | 3 | a0001c0002t0001g0018 a0001c0002t0001g0149 a0001c0002t0001g0193 |
6 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.982+633delA | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575680 | |||||||
| chr13:94575691 | CT | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0098 |
3 | HG02809.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.982+622delA | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575691 | |||||||
| chr13:94575715 | T | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0150 a0001c0001t0001g0157 others(3): Show |
10 | HG01192.hp2 HG01243.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+599A>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94575715 | |||||||
| chr13:94576020 | T | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0163 others(6): Show |
14 | HG01891.hp1 HG02083.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.982+294A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94576020 | |||||||
| chr13:94576070 | T | A | 1 | a0001c0001t0001g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.982+244A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94576070 | |||||||
| chr13:94576124 | G | A | 4 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 others(1): Show |
5 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.982+190C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94576124 | |||||||
| chr13:94576206 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.982+108C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94576206 | |||||||
| chr13:94576249 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.982+65C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 11/11 | chr13 | 94576249 | |||||||
| chr13:94576575 | T | A | 1 | a0002c0003t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.885-164A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94576575 | |||||||
| chr13:94576576 | A | T | 3 | a0001c0002t0001g0018 a0001c0002t0001g0149 a0001c0002t0001g0193 |
6 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-165T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94576576 | |||||||
| chr13:94576641 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.885-230C>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94576641 | |||||||
| chr13:94576764 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.885-353A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94576764 | |||||||
| chr13:94576840 | T | C | 3 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG01109.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.885-429A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94576840 | |||||||
| chr13:94576922 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.884+449C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94576922 | |||||||
| chr13:94576994 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.884+377C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94576994 | |||||||
| chr13:94577033 | C | T | 1 | a0001c0001t0004g0044 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.884+338G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94577033 | |||||||
| chr13:94577034 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.884+337T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94577034 | |||||||
| chr13:94577051 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.884+320C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94577051 | |||||||
| chr13:94577101 | C | CA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0105 others(4): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.884+269dupT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94577101 | |||||||
| chr13:94577270 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0134 |
2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.884+101T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 10/11 | chr13 | 94577270 | |||||||
| chr13:94577443 | A | G | 4 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 others(1): Show |
5 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.826-14T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 9/11 | chr13 | 94577443 | |||||||
| chr13:94577481 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(17): Show |
34 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.826-52T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 9/11 | chr13 | 94577481 | |||||||
| chr13:94577676 | T | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0146 others(8): Show |
19 | HG00140.hp1 HG00323.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.826-247A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 9/11 | chr13 | 94577676 | |||||||
| chr13:94577748 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
12 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.825+257G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 9/11 | chr13 | 94577748 | |||||||
| chr13:94577852 | CTTAAT | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0047 others(9): Show |
20 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.825+148_825+152del others(5): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 9/11 | chr13 | 94577852 | |||||||
| chr13:94577895 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.825+110A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 9/11 | chr13 | 94577895 | |||||||
| chr13:94578200 | A | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0164 a0001c0001t0001g0175 |
4 | HG02922.hp1 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.660-30T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 8/11 | chr13 | 94578200 | |||||||
| chr13:94578230 | T | C | 1 | a0001c0001t0001g0030 | 2 | NA18960.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.660-60A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 8/11 | chr13 | 94578230 | |||||||
| chr13:94578370 | A | AAGTGGCA others(8): Show |
129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.660-201_660-200ins others(15): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 8/11 | chr13 | 94578370 | |||||||
| chr13:94578623 | G | A | 53 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
88 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.659+107C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 8/11 | chr13 | 94578623 | |||||||
| chr13:94578637 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.659+93A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 8/11 | chr13 | 94578637 | |||||||
| chr13:94578981 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0022 others(42): Show |
83 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.616-208A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94578981 | |||||||
| chr13:94579031 | T | C | 1 | a0001c0001t0004g0044 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.616-258A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579031 | |||||||
| chr13:94579078 | A | G | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0163 others(3): Show |
8 | HG01891.hp1 HG02083.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.616-305T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579078 | |||||||
| chr13:94579091 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0076 others(1): Show |
8 | NA18952.hp2 NA18965.hp1 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.616-318T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579091 | |||||||
| chr13:94579335 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.615+559A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579335 | |||||||
| chr13:94579348 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.615+546T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579348 | |||||||
| chr13:94579501 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.615+393G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579501 | |||||||
| chr13:94579570 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.615+324G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579570 | |||||||
| chr13:94579571 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
149 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.615+323C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579571 | |||||||
| chr13:94579650 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0006g0147 |
2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.615+244A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579650 | |||||||
| chr13:94579727 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.615+167A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579727 | |||||||
| chr13:94579800 | T | A | 4 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 others(1): Show |
5 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+94A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 7/11 | chr13 | 94579800 | |||||||
| chr13:94580172 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.556-219G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580172 | |||||||
| chr13:94580228 | T | G | 4 | a0001c0001t0001g0080 a0001c0001t0003g0101 a0001c0001t0003g0191 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-275A>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580228 | |||||||
| chr13:94580238 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.556-285G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580238 | |||||||
| chr13:94580239 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.556-286C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580239 | |||||||
| chr13:94580394 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.556-441A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580394 | |||||||
| chr13:94580718 | T | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0109 |
2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.555+373A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580718 | |||||||
| chr13:94580740 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0163 others(6): Show |
14 | HG01891.hp1 HG02083.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.555+351G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580740 | |||||||
| chr13:94580756 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
14 | HG02055.hp1 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.555+335T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580756 | |||||||
| chr13:94580877 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.555+214C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 6/11 | chr13 | 94580877 | |||||||
| chr13:94581256 | G | A | 1 | a0002c0003t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.457-67C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581256 | |||||||
| chr13:94581295 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.457-106T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581295 | |||||||
| chr13:94581353 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.457-164C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581353 | |||||||
| chr13:94581526 | T | G | 2 | a0001c0001t0001g0179 a0002c0003t0001g0050 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.457-337A>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581526 | |||||||
| chr13:94581621 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.457-432C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581621 | |||||||
| chr13:94581704 | A | C | 1 | a0001c0001t0001g0028 | 2 | NA18939.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.457-515T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581704 | |||||||
| chr13:94581718 | C | A | 2 | a0001c0001t0001g0179 a0002c0003t0001g0050 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.457-529G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581718 | |||||||
| chr13:94581933 | C | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0146 others(9): Show |
20 | HG00140.hp1 HG00323.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.457-744G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581933 | |||||||
| chr13:94581969 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.457-780C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581969 | |||||||
| chr13:94581997 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.457-808G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94581997 | |||||||
| chr13:94582025 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.457-836G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582025 | |||||||
| chr13:94582034 | T | A | 1 | a0001c0001t0001g0036 | 2 | NA19003.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.457-845A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582034 | |||||||
| chr13:94582099 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0098 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.457-910C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582099 | |||||||
| chr13:94582199 | C | CA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
156 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.456+894dupT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582199 | |||||||
| chr13:94582303 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.456+791A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582303 | |||||||
| chr13:94582319 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.456+775T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582319 | |||||||
| chr13:94582406 | T | C | 1 | a0001c0002t0001g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.456+688A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582406 | |||||||
| chr13:94582414 | T | C | 3 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG01109.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.456+680A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582414 | |||||||
| chr13:94582458 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.456+636G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582458 | |||||||
| chr13:94582525 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0081 |
2 | HG00558.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.456+569A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582525 | |||||||
| chr13:94582880 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.456+214T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582880 | |||||||
| chr13:94582910 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.456+184A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582910 | |||||||
| chr13:94582921 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.456+173A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582921 | |||||||
| chr13:94582951 | T | C | 1 | a0002c0003t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.456+143A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 5/11 | chr13 | 94582951 | |||||||
| chr13:94583303 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
13 | HG02055.hp1 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-67T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583303 | |||||||
| chr13:94583372 | A | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0047 others(9): Show |
20 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.314-136T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583372 | |||||||
| chr13:94583469 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.314-233T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583469 | |||||||
| chr13:94583543 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.314-307A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583543 | |||||||
| chr13:94583553 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.314-317G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583553 | |||||||
| chr13:94583636 | C | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.314-400G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583636 | |||||||
| chr13:94583733 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.314-497T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583733 | |||||||
| chr13:94583905 | A | T | 3 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG01109.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.314-669T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583905 | |||||||
| chr13:94583976 | C | T | 3 | a0001c0002t0001g0018 a0001c0002t0001g0149 a0001c0002t0001g0193 |
6 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-740G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94583976 | |||||||
| chr13:94584092 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0111 |
3 | HG00323.hp1 HG01081.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.314-856T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584092 | |||||||
| chr13:94584117 | C | T | 1 | a0001c0001t0001g0020 | 3 | NA18969.hp2 NA18970.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.314-881G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584117 | |||||||
| chr13:94584138 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.314-902T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584138 | |||||||
| chr13:94584301 | AG | A | 3 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG01109.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.314-1066delC | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584301 | |||||||
| chr13:94584363 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.314-1127G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584363 | |||||||
| chr13:94584397 | T | G | 1 | a0001c0001t0001g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.314-1161A>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584397 | |||||||
| chr13:94584490 | G | C | 4 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 others(1): Show |
5 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-1254C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584490 | |||||||
| chr13:94584494 | G | A | 1 | a0001c0001t0001g0037 | 2 | NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.314-1258C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584494 | |||||||
| chr13:94584571 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
151 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.314-1335T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584571 | |||||||
| chr13:94584594 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(17): Show |
34 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.314-1358T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584594 | |||||||
| chr13:94584631 | C | A | 1 | a0001c0001t0003g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.314-1395G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584631 | |||||||
| chr13:94584677 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.314-1441T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584677 | |||||||
| chr13:94584709 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.314-1473A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94584709 | |||||||
| chr13:94585140 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0161 a0001c0001t0001g0183 |
4 | HG01069.hp1 HG01071.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-1904G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585140 | |||||||
| chr13:94585206 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.314-1970G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585206 | |||||||
| chr13:94585272 | G | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.314-2036C>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585272 | |||||||
| chr13:94585539 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.314-2303G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585539 | |||||||
| chr13:94585643 | C | A | 2 | a0001c0001t0001g0179 a0002c0003t0001g0050 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.314-2407G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585643 | |||||||
| chr13:94585769 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0174 |
2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.314-2533A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585769 | |||||||
| chr13:94585770 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.314-2534C>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585770 | |||||||
| chr13:94585776 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.314-2540C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585776 | |||||||
| chr13:94585786 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.314-2550G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585786 | |||||||
| chr13:94585799 | C | CA | 6 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0092 others(3): Show |
6 | HG02132.hp1 HG02280.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-2564dupT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585799 | |||||||
| chr13:94585799 | CA | C | 12 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0109 others(9): Show |
13 | HG00738.hp1 HG01192.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-2564delT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585799 | |||||||
| chr13:94585799 | CAA | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
233 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.314-2565_314-2564d others(4): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585799 | |||||||
| chr13:94585842 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.314-2606T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585842 | |||||||
| chr13:94585900 | T | C | 53 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
88 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.314-2664A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94585900 | |||||||
| chr13:94586211 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.314-2975C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586211 | |||||||
| chr13:94586212 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.314-2976T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586212 | |||||||
| chr13:94586216 | G | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.314-2980C>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586216 | |||||||
| chr13:94586542 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0100 |
2 | HG01243.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.314-3306T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586542 | |||||||
| chr13:94586568 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0039 others(4): Show |
16 | HG00544.hp1 NA18747.hp2 NA18952.hp1 others(13): Show |
intron_variant | MODIFIER | c.314-3332G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586568 | |||||||
| chr13:94586630 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.314-3394C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586630 | |||||||
| chr13:94586634 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.314-3398C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586634 | |||||||
| chr13:94586747 | AATT | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
135 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.314-3514_314-3512d others(5): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586747 | |||||||
| chr13:94586748 | ATTATTT | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0146 others(9): Show |
20 | HG00323.hp2 HG01109.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.314-3518_314-3513d others(8): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586748 | |||||||
| chr13:94586748 | ATTATTTT | A | 40 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(37): Show |
68 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.314-3519_314-3513d others(9): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586748 | |||||||
| chr13:94586749 | TTA | T | 13 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(10): Show |
13 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-3515_314-3514d others(4): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586749 | |||||||
| chr13:94586751 | A | AT | 13 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0059 others(10): Show |
18 | HG00544.hp2 HG01081.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.314-3516dupA | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586751 | |||||||
| chr13:94586751 | A | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0002c0003t0001g0050 |
3 | HG01975.hp2 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.314-3515T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586751 | |||||||
| chr13:94586751 | A | T | 2 | a0001c0001t0001g0100 a0001c0001t0003g0101 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.314-3515T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586751 | |||||||
| chr13:94586752 | T | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.314-3516A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586752 | |||||||
| chr13:94586753 | T | C | 13 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(10): Show |
13 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-3517A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586753 | |||||||
| chr13:94586754 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(51): Show |
132 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.314-3518A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586754 | |||||||
| chr13:94586755 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.314-3519A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586755 | |||||||
| chr13:94586756 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.314-3520A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586756 | |||||||
| chr13:94586757 | T | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0146 others(9): Show |
20 | HG00323.hp2 HG01109.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.314-3521A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586757 | |||||||
| chr13:94586758 | T | C | 40 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(37): Show |
68 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.314-3522A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586758 | |||||||
| chr13:94586759 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.314-3523A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586759 | |||||||
| chr13:94586814 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
242 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.314-3578T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586814 | |||||||
| chr13:94586841 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0103 a0001c0001t0001g0106 others(1): Show |
5 | HG00609.hp1 HG00673.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-3605G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586841 | |||||||
| chr13:94586904 | A | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
149 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.314-3668T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94586904 | |||||||
| chr13:94587037 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.314-3801A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587037 | |||||||
| chr13:94587173 | G | GA | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+3679dupT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587173 | |||||||
| chr13:94587178 | C | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.313+3675G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587178 | |||||||
| chr13:94587182 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+3671T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587182 | |||||||
| chr13:94587206 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+3647G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587206 | |||||||
| chr13:94587232 | T | C | 3 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG01109.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.313+3621A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587232 | |||||||
| chr13:94587267 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.313+3586T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587267 | |||||||
| chr13:94587288 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+3565T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587288 | |||||||
| chr13:94587289 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+3564A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587289 | |||||||
| chr13:94587290 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+3563T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587290 | |||||||
| chr13:94587377 | T | A | 3 | a0001c0002t0001g0018 a0001c0002t0001g0149 a0001c0002t0001g0193 |
6 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+3476A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587377 | |||||||
| chr13:94587515 | C | CAAAAGTT others(11): Show |
3 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG01109.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.313+3337_313+3338i others(20): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587515 | |||||||
| chr13:94587626 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313+3227T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587626 | |||||||
| chr13:94587788 | G | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0095 |
2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.313+3065C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587788 | |||||||
| chr13:94587800 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.313+3053C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587800 | |||||||
| chr13:94587832 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
247 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.313+3021A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587832 | |||||||
| chr13:94587854 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+2999C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587854 | |||||||
| chr13:94587856 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.313+2997C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587856 | |||||||
| chr13:94587998 | C | CA | 8 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0083 others(5): Show |
8 | HG01361.hp2 HG02280.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+2854dupT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587998 | |||||||
| chr13:94587998 | CA | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0051 others(11): Show |
18 | HG01109.hp2 HG01243.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.313+2854delT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587998 | |||||||
| chr13:94587998 | CAA | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.313+2853_313+2854d others(4): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94587998 | |||||||
| chr13:94588037 | C | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+2816G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588037 | |||||||
| chr13:94588143 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.313+2710G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588143 | |||||||
| chr13:94588176 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.313+2677G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588176 | |||||||
| chr13:94588186 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+2667T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588186 | |||||||
| chr13:94588187 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+2666G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588187 | |||||||
| chr13:94588307 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+2546A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588307 | |||||||
| chr13:94588338 | G | C | 3 | a0001c0001t0003g0101 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG01109.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.313+2515C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588338 | |||||||
| chr13:94588357 | A | T | 3 | a0001c0002t0001g0018 a0001c0002t0001g0149 a0001c0002t0001g0193 |
6 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+2496T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588357 | |||||||
| chr13:94588384 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.313+2469A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588384 | |||||||
| chr13:94588411 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.313+2442C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588411 | |||||||
| chr13:94588421 | C | CA | 20 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
26 | HG00544.hp2 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.313+2431dupT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588421 | |||||||
| chr13:94588421 | CAAA | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0022 others(22): Show |
37 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.313+2429_313+2431d others(5): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588421 | |||||||
| chr13:94588421 | CAAAA | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(58): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.313+2428_313+2431d others(6): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588421 | |||||||
| chr13:94588421 | CAAAAA | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(19): Show |
43 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.313+2427_313+2431d others(7): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588421 | |||||||
| chr13:94588421 | CAAAAAA | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
11 | HG01891.hp1 HG02083.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+2426_313+2431d others(8): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588421 | |||||||
| chr13:94588421 | CAAAAAAA | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0056 a0001c0001t0001g0166 others(3): Show |
9 | HG02055.hp1 HG02647.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.313+2425_313+2431d others(9): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588421 | |||||||
| chr13:94588500 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+2353A>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588500 | |||||||
| chr13:94588501 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+2352C>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588501 | |||||||
| chr13:94588686 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.313+2167A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588686 | |||||||
| chr13:94588912 | T | C | 1 | a0001c0001t0004g0044 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.313+1941A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588912 | |||||||
| chr13:94588970 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0131 a0001c0001t0001g0132 |
5 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+1883A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94588970 | |||||||
| chr13:94589053 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+1800C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589053 | |||||||
| chr13:94589166 | T | C | 1 | a0002c0003t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.313+1687A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589166 | |||||||
| chr13:94589173 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.313+1680A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589173 | |||||||
| chr13:94589293 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313+1560G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589293 | |||||||
| chr13:94589304 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0100 |
2 | HG01243.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.313+1549T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589304 | |||||||
| chr13:94589314 | G | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+1539C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589314 | |||||||
| chr13:94589319 | C | CT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.313+1533dupA | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589319 | |||||||
| chr13:94589319 | C | CTTT | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0163 others(3): Show |
8 | HG01891.hp1 HG02083.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+1531_313+1533d others(5): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589319 | |||||||
| chr13:94589380 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.313+1473G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589380 | |||||||
| chr13:94589403 | C | G | 1 | a0001c0001t0004g0044 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.313+1450G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589403 | |||||||
| chr13:94589468 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.313+1385G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589468 | |||||||
| chr13:94589539 | T | C | 1 | a0001c0001t0009g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.313+1314A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589539 | |||||||
| chr13:94589582 | G | C | 1 | a0001c0001t0001g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313+1271C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589582 | |||||||
| chr13:94589627 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0146 others(8): Show |
19 | HG00140.hp1 HG00323.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.313+1226C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589627 | |||||||
| chr13:94589782 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.313+1071A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94589782 | |||||||
| chr13:94590028 | AACT | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.313+822_313+824del others(3): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590028 | |||||||
| chr13:94590041 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.313+812A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590041 | |||||||
| chr13:94590053 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.313+800A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590053 | |||||||
| chr13:94590079 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0100 a0001c0001t0001g0179 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.313+774G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590079 | |||||||
| chr13:94590098 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+755C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590098 | |||||||
| chr13:94590104 | A | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(17): Show |
34 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.313+749T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590104 | |||||||
| chr13:94590132 | C | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+721G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590132 | |||||||
| chr13:94590176 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0139 |
3 | NA18979.hp2 NA18981.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.313+677A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590176 | |||||||
| chr13:94590262 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0100 |
2 | HG01243.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.313+591C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590262 | |||||||
| chr13:94590273 | T | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
149 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.313+580A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590273 | |||||||
| chr13:94590306 | CA | C | 3 | a0001c0002t0001g0018 a0001c0002t0001g0149 a0001c0002t0001g0193 |
6 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+546delT | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590306 | |||||||
| chr13:94590317 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.313+536C>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590317 | |||||||
| chr13:94590573 | A | T | 1 | a0001c0001t0003g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.313+280T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590573 | |||||||
| chr13:94590722 | T | C | 1 | a0001c0002t0001g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.313+131A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 4/11 | chr13 | 94590722 | |||||||
| chr13:94591016 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.223-73C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591016 | |||||||
| chr13:94591299 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.223-356A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591299 | |||||||
| chr13:94591331 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.223-388T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591331 | |||||||
| chr13:94591403 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.223-460C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591403 | |||||||
| chr13:94591465 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.223-522G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591465 | |||||||
| chr13:94591525 | A | T | 1 | a0001c0002t0001g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.223-582T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591525 | |||||||
| chr13:94591530 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.223-587A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591530 | |||||||
| chr13:94591702 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.222+539T>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591702 | |||||||
| chr13:94591753 | A | C | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
90 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.222+488T>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591753 | |||||||
| chr13:94591833 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.222+408A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94591833 | |||||||
| chr13:94592146 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.222+95A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94592146 | |||||||
| chr13:94592210 | G | A | 1 | a0001c0001t0001g0013 | 5 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+31C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 3/11 | chr13 | 94592210 | |||||||
| chr13:94592475 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.154-166G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 2/11 | chr13 | 94592475 | |||||||
| chr13:94592514 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0056 a0001c0001t0001g0180 others(2): Show |
8 | HG02055.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-205C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 2/11 | chr13 | 94592514 | |||||||
| chr13:94592623 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.154-314A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 2/11 | chr13 | 94592623 | |||||||
| chr13:94592834 | C | G | 1 | a0001c0001t0006g0147 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.154-525G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 2/11 | chr13 | 94592834 | |||||||
| chr13:94593174 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.153+667A>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 2/11 | chr13 | 94593174 | |||||||
| chr13:94593331 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.153+510A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 2/11 | chr13 | 94593331 | |||||||
| chr13:94593945 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.87-38A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94593945 | |||||||
| chr13:94593951 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.87-44G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94593951 | |||||||
| chr13:94594077 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.87-170G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594077 | |||||||
| chr13:94594186 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
253 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.87-279G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594186 | |||||||
| chr13:94594205 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.87-298T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594205 | |||||||
| chr13:94594297 | G | C | 5 | a0001c0001t0001g0100 a0001c0001t0003g0101 a0001c0001t0003g0191 others(2): Show |
5 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.87-390C>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594297 | |||||||
| chr13:94594399 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.87-492G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594399 | |||||||
| chr13:94594629 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.87-722G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594629 | |||||||
| chr13:94594632 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.87-725G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594632 | |||||||
| chr13:94594697 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.87-790G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594697 | |||||||
| chr13:94594710 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA19078.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.87-803A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594710 | |||||||
| chr13:94594763 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.87-856C>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594763 | |||||||
| chr13:94594883 | TTA | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
144 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.87-978_87-977delTA | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594883 | |||||||
| chr13:94594969 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.87-1062A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94594969 | |||||||
| chr13:94595045 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.86+1006A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595045 | |||||||
| chr13:94595075 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0185 a0001c0001t0001g0186 |
8 | HG00741.hp2 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.86+976A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595075 | |||||||
| chr13:94595372 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.86+679A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595372 | |||||||
| chr13:94595481 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18968.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.86+570A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595481 | |||||||
| chr13:94595518 | G | GAAACGGG others(37): Show |
1 | a0001c0001t0001g0057 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.86+489_86+532dupAA others(42): Show |
TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595518 | |||||||
| chr13:94595529 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.86+522G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595529 | |||||||
| chr13:94595675 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.86+376G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595675 | |||||||
| chr13:94595748 | C | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG02109.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.86+303G>T | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595748 | |||||||
| chr13:94595831 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.86+220G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595831 | |||||||
| chr13:94595935 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86+116T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595935 | |||||||
| chr13:94595975 | C | G | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.86+76G>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94595975 | |||||||
| chr13:94596003 | T | C | 3 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0002t0001g0193 |
3 | HG01109.hp2 HG02258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.86+48A>G | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94596003 | |||||||
| chr13:94596018 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.86+33T>C | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94596018 | |||||||
| chr13:94596035 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.86+16G>A | TGDS | ENSG00000088451.11 | transcript | ENST00000261296.7 | protein_coding | 1/11 | chr13 | 94596035 |