Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 124045 |
| ensemblid | ENSG00000167523.15 |
| hgncid | 26463 |
| symbol | SPATA33 |
| name | spermatogenesis associated 33 |
| refseq_nuc | NM_001271907.2 |
| refseq_prot | NP_001258836.1 |
| ensembl_nuc | ENST00000579310.6 |
| ensembl_prot | ENSP00000462996.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89657836 |
| end | 89670458 |
| strand | + |
| ver | v1.2 |
| region | chr16:89657836-89670458 |
| region5000 | chr16:89652836-89675458 |
| regionname0 | SPATA33_chr16_89657836_89670458 |
| regionname5000 | SPATA33_chr16_89652836_89675458 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 140 | 409 | 94 | 69 | 180 | 17 | 47 | 136 | SPATA33_chr16_89652836_89675458 | SPATA33 | MGLSK others(135): Show |
chr16 | 89652836 | 89675458 |
| a0002 | 0/0 | 140 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | MGLSK others(135): Show |
chr16 | 89652836 | 89675458 |
| a0003 | 0/0 | 140 | 3 | 0 | 2 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | MGLSK others(135): Show |
chr16 | 89652836 | 89675458 |
| a0004 | 0/0 | 140 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | MGLSK others(135): Show |
chr16 | 89652836 | 89675458 |
| a0005 | 0/0 | 140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | MGLSK others(135): Show |
chr16 | 89652836 | 89675458 |
| a0006 | 0/0 | 140 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | MGLSK others(135): Show |
chr16 | 89652836 | 89675458 |
| a0007 | 0/0 | 140 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | MGLSK others(135): Show |
chr16 | 89652836 | 89675458 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 420 | 409 | 94 | 69 | 180 | 17 | 47 | SPATA33_chr16_89652836_89675458 | SPATA33 | ATGGG others(415): Show |
chr16 | 89652836 | 89675458 | ||
| a0002c0002 | 0/0 | 420 | 6 | 5 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | ATGGG others(415): Show |
chr16 | 89652836 | 89675458 | ||
| a0003c0003 | 0/0 | 420 | 3 | 0 | 2 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | ATGGG others(415): Show |
chr16 | 89652836 | 89675458 | ||
| a0004c0005 | 0/0 | 420 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | ATGGG others(415): Show |
chr16 | 89652836 | 89675458 | ||
| a0005c0004 | 0/0 | 420 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | ATGGG others(415): Show |
chr16 | 89652836 | 89675458 | ||
| a0006c0007 | 0/0 | 420 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | ATGGG others(415): Show |
chr16 | 89652836 | 89675458 | ||
| a0007c0006 | 0/0 | 420 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | ATGGG others(415): Show |
chr16 | 89652836 | 89675458 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1460 | 97 | 28 | 15 | 43 | 3 | 8 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0002 | 0/0 | 1460 | 79 | 29 | 10 | 27 | 1 | 12 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0003 | 0/0 | 1460 | 61 | 9 | 27 | 6 | 10 | 9 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0004 | 0/0 | 1460 | 61 | 0 | 0 | 58 | 0 | 3 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0005 | 0/1 | 1460 | 40 | 0 | 7 | 27 | 1 | 4 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0006 | 0/0 | 1460 | 32 | 12 | 7 | 1 | 2 | 10 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0007 | 0/0 | 1460 | 10 | 0 | 0 | 10 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0008 | 1/0 | 1460 | 8 | 5 | 2 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0009 | 0/0 | 1460 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0010 | 0/0 | 1460 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0011 | 0/0 | 1460 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0012 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0013 | 0/0 | 1460 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0014 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0015 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0017 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0018 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0019 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0020 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0021 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0022 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0023 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0025 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0001c0001t0027 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0002c0002t0003 | 0/0 | 1460 | 6 | 5 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0003c0003t0005 | 0/0 | 1460 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0003c0003t0026 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0004c0005t0012 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0005c0004t0016 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0006c0007t0024 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| a0007c0006t0003 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | GTGAG others(1455): Show |
chr16 | 89652836 | 89675458 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 56 | 2 | 12 | 36 | 0 | 6 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0004 | 0/0 | 31 | 4 | 5 | 15 | 1 | 6 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0006 | 0/0 | 21 | 1 | 3 | 5 | 6 | 6 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0023 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0002 | 0/0 | 46 | 0 | 0 | 43 | 0 | 3 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0003 | 0/1 | 31 | 0 | 7 | 19 | 1 | 3 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0005 | 0/0 | 19 | 6 | 2 | 1 | 2 | 8 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0013 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0007g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0008g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0008g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0011g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0014g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0015g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0017g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0018g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0021g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0025g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0001c0001t0027g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0002c0002t0003g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0002c0002t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0003c0003t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0003c0003t0026g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0004c0005t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0005c0004t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0006c0007t0024g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| a0007c0006t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0005 | EUR | GBR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | GBR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | GBR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0124 | EUR | GBR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | FIN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | FIN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0005 | EUR | FIN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00408 | hp2 | a0003 | c0003 | t0026 | g0063 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0094 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0015 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0126 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0074 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01243 | hp2 | a0003 | c0003 | t0005 | g0003 | AMR | PUR | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0127 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02015 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02027 | hp2 | a0001 | c0001 | t0012 | g0003 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02040 | hp1 | a0001 | c0001 | t0007 | g0097 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02080 | hp2 | a0001 | c0001 | t0015 | g0021 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02083 | hp2 | a0004 | c0005 | t0012 | g0003 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02148 | hp2 | a0003 | c0003 | t0005 | g0003 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CDX | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CDX | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CDX | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0049 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02622 | hp2 | a0005 | c0004 | t0016 | g0048 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0037 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0066 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0070 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0075 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0037 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0042 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0042 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0120 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02970 | hp2 | a0001 | c0001 | t0018 | g0119 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0121 | AFR | ESN | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | GWD | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03669 | hp1 | a0001 | c0001 | t0014 | g0058 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04204 | hp1 | a0006 | c0007 | t0024 | g0027 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0062 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18612 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | CHB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18747 | hp1 | a0001 | c0001 | t0019 | g0093 | EAS | CHB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18962 | hp2 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18970 | hp2 | a0001 | c0001 | t0021 | g0092 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18985 | hp2 | a0001 | c0001 | t0025 | g0102 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18998 | hp1 | a0001 | c0001 | t0023 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19079 | hp1 | a0001 | c0001 | t0022 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ASW | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20752 | hp1 | a0007 | c0006 | t0003 | g0117 | EUR | TSI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | TSI | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | GIH | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0005 | SAS | GIH | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0090 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG02559 | hp2 | a0001 | c0001 | t0017 | g0079 | AFR | ACB | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | USA | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | USA | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | USA | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0003 | REF | REF | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0107 | REF | REF | SPATA33_chr16_89652836_89675458 | SPATA33 | chr16 | 89652836 | 89675458 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89658259 | A | C | 1 | a0006 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.49A>C | p.Lys17Gln | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/3 | 125/1460 | 49/423 | 17/140 | chr16 | 89658259 | |||
| chr16:89658281 | T | C | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.71T>C | p.Val24Ala | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/3 | 147/1460 | 71/423 | 24/140 | chr16 | 89658281 | |||
| chr16:89658347 | C | T | 1 | a0007 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.137C>T | p.Ser46Leu | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/3 | 213/1460 | 137/423 | 46/140 | chr16 | 89658347 | |||
| chr16:89658394 | C | T | 1 | a0003 | 3 | HG00408.hp2 HG01243.hp2 HG02148.hp2 |
missense_variant | MODERATE | c.184C>T | p.His62Tyr | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/3 | 260/1460 | 184/423 | 62/140 | chr16 | 89658394 | |||
| chr16:89669338 | G | T | 1 | a0004 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.264G>T | p.Gln88His | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 340/1460 | 264/423 | 88/140 | chr16 | 89669338 | |||
| chr16:89669463 | C | T | 1 | a0002 | 6 | HG00639.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
missense_variant | MODERATE | c.389C>T | p.Thr130Ile | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 465/1460 | 389/423 | 130/140 | chr16 | 89669463 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89657860 | C | T | 8 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0012 others(5): Show |
48 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(45): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-52C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/3 | chr16 | 89657860 | |||||||
| chr16:89657874 | G | T | 1 | a0006c0007t0024 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/3 | 38 | chr16 | 89657874 | ||||||
| chr16:89657882 | C | T | 1 | a0001c0001t0023 | 1 | NA18998.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/3 | 30 | chr16 | 89657882 | ||||||
| chr16:89657905 | C | G | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0019 others(4): Show |
76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
5_prime_UTR_variant | MODIFIER | c.-7C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/3 | 7 | chr16 | 89657905 | ||||||
| chr16:89669515 | G | C | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(3): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*18G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 18 | chr16 | 89669515 | ||||||
| chr16:89669533 | G | A | 1 | a0001c0001t0007 | 10 | HG00597.hp2 HG02015.hp2 HG02040.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*36G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 36 | chr16 | 89669533 | ||||||
| chr16:89669597 | C | T | 1 | a0001c0001t0014 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 100 | chr16 | 89669597 | ||||||
| chr16:89669749 | C | T | 1 | a0001c0001t0027 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 252 | chr16 | 89669749 | ||||||
| chr16:89669755 | G | A | 1 | a0001c0001t0015 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*258G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 258 | chr16 | 89669755 | ||||||
| chr16:89669893 | A | G | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
3_prime_UTR_variant | MODIFIER | c.*396A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 396 | chr16 | 89669893 | ||||||
| chr16:89669944 | G | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*447G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 447 | chr16 | 89669944 | ||||||
| chr16:89669959 | C | T | 2 | a0001c0001t0010 a0001c0001t0017 |
3 | HG02559.hp2 HG02965.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*462C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 462 | chr16 | 89669959 | ||||||
| chr16:89670084 | C | G | 1 | a0001c0001t0021 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*587C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 587 | chr16 | 89670084 | ||||||
| chr16:89670109 | G | A | 1 | a0001c0001t0018 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*612G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 612 | chr16 | 89670109 | ||||||
| chr16:89670112 | C | G | 2 | a0001c0001t0009 a0001c0001t0010 |
6 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*615C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 615 | chr16 | 89670112 | ||||||
| chr16:89670134 | G | A | 3 | a0001c0001t0012 a0001c0001t0019 a0004c0005t0012 |
3 | HG02027.hp2 HG02083.hp2 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*637G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 637 | chr16 | 89670134 | ||||||
| chr16:89670283 | G | A | 1 | a0001c0001t0013 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*786G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 786 | chr16 | 89670283 | ||||||
| chr16:89670310 | C | T | 1 | a0001c0001t0020 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*813C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 813 | chr16 | 89670310 | ||||||
| chr16:89670312 | T | C | 1 | a0001c0001t0020 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 815 | chr16 | 89670312 | ||||||
| chr16:89670314 | T | A | 1 | a0005c0004t0016 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817T>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 817 | chr16 | 89670314 | ||||||
| chr16:89670330 | G | A | 1 | a0001c0001t0013 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*833G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 833 | chr16 | 89670330 | ||||||
| chr16:89670343 | A | G | 1 | a0001c0001t0025 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*846A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 3/3 | 846 | chr16 | 89670343 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89658029 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.37+81G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/2 | chr16 | 89658029 | |||||||
| chr16:89658138 | G | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | HG00673.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.38-110G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/2 | chr16 | 89658138 | |||||||
| chr16:89658164 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0008g0017 a0001c0001t0008g0125 others(2): Show |
9 | HG01069.hp1 HG01256.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-84C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/2 | chr16 | 89658164 | |||||||
| chr16:89658182 | G | A | 1 | a0001c0001t0003g0018 | 3 | HG00738.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.38-66G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 1/2 | chr16 | 89658182 | |||||||
| chr16:89658470 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.211+49C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658470 | |||||||
| chr16:89658486 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+65G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658486 | |||||||
| chr16:89658487 | A | T | 1 | a0001c0001t0002g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+66A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658487 | |||||||
| chr16:89658594 | C | T | 1 | a0001c0001t0006g0013 | 5 | HG00741.hp2 HG01169.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+173C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658594 | |||||||
| chr16:89658669 | G | T | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG01074.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.211+248G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658669 | |||||||
| chr16:89658742 | C | G | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+321C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658742 | |||||||
| chr16:89658842 | G | A | 1 | a0001c0001t0004g0046 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.211+421G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658842 | |||||||
| chr16:89658933 | A | G | 1 | a0001c0001t0018g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.211+512A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658933 | |||||||
| chr16:89658995 | T | A | 1 | a0001c0001t0002g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.211+574T>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89658995 | |||||||
| chr16:89659156 | T | C | 1 | a0005c0004t0016g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.211+735T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659156 | |||||||
| chr16:89659227 | C | T | 1 | a0001c0001t0004g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.211+806C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659227 | |||||||
| chr16:89659312 | G | A | 1 | a0005c0004t0016g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.211+891G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659312 | |||||||
| chr16:89659398 | G | A | 1 | a0001c0001t0003g0009 | 5 | HG01074.hp1 HG01123.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+977G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659398 | |||||||
| chr16:89659487 | A | G | 4 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0124 others(1): Show |
8 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+1066A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659487 | |||||||
| chr16:89659512 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.211+1091A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659512 | |||||||
| chr16:89659527 | A | G | 1 | a0001c0001t0011g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.211+1106A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659527 | |||||||
| chr16:89659563 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0115 |
3 | HG02809.hp1 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.211+1142A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659563 | |||||||
| chr16:89659627 | T | C | 115 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(112): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.211+1206T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659627 | |||||||
| chr16:89659631 | G | A | 1 | a0001c0001t0006g0025 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.211+1210G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659631 | |||||||
| chr16:89659687 | GA | G | 5 | a0001c0001t0003g0014 a0001c0001t0004g0103 a0001c0001t0025g0102 others(2): Show |
12 | HG00639.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+1279delA | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89659687 | ||||||
| chr16:89659698 | A | T | 1 | a0001c0001t0003g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.211+1277A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659698 | |||||||
| chr16:89659839 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211+1418G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659839 | |||||||
| chr16:89659922 | C | T | 1 | a0001c0001t0004g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.211+1501C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659922 | |||||||
| chr16:89659928 | C | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0020 others(17): Show |
77 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.211+1507C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89659928 | |||||||
| chr16:89660003 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.211+1582C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660003 | |||||||
| chr16:89660003 | C | T | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+1582C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660003 | |||||||
| chr16:89660067 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.211+1646A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660067 | |||||||
| chr16:89660076 | G | A | 58 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(55): Show |
170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.211+1655G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660076 | |||||||
| chr16:89660142 | G | A | 1 | a0001c0001t0027g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.211+1721G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660142 | |||||||
| chr16:89660144 | G | A | 1 | a0001c0001t0009g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.211+1723G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660144 | |||||||
| chr16:89660185 | G | C | 1 | a0001c0001t0027g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.211+1764G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660185 | |||||||
| chr16:89660317 | G | A | 1 | a0001c0001t0005g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.211+1896G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660317 | |||||||
| chr16:89660320 | A | G | 1 | a0001c0001t0009g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.211+1899A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660320 | |||||||
| chr16:89660335 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.211+1914G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660335 | |||||||
| chr16:89660411 | G | A | 2 | a0001c0001t0003g0023 a0007c0006t0003g0117 |
4 | HG03704.hp1 HG06807.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+1990G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660411 | |||||||
| chr16:89660463 | A | G | 3 | a0001c0001t0003g0014 a0002c0002t0003g0015 a0002c0002t0003g0037 |
10 | HG00639.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+2042A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660463 | |||||||
| chr16:89660590 | C | T | 1 | a0001c0001t0004g0099 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.211+2169C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660590 | |||||||
| chr16:89660591 | G | A | 2 | a0001c0001t0003g0076 a0005c0004t0016g0048 |
2 | HG02622.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.211+2170G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660591 | |||||||
| chr16:89660739 | C | G | 3 | a0001c0001t0003g0014 a0002c0002t0003g0015 a0002c0002t0003g0037 |
10 | HG00639.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+2318C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660739 | |||||||
| chr16:89660781 | G | A | 4 | a0001c0001t0006g0051 a0001c0001t0006g0053 a0001c0001t0006g0054 others(1): Show |
4 | HG02451.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2360G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660781 | |||||||
| chr16:89660853 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.211+2432G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660853 | |||||||
| chr16:89660878 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0089 |
5 | HG01516.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+2457C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660878 | |||||||
| chr16:89660984 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0114 |
4 | NA18949.hp1 NA18979.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2563C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89660984 | |||||||
| chr16:89661018 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.211+2597T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661018 | |||||||
| chr16:89661031 | G | A | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+2610G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661031 | |||||||
| chr16:89661088 | C | A | 1 | a0001c0001t0003g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.211+2667C>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661088 | |||||||
| chr16:89661187 | C | T | 106 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(103): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.211+2766C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661187 | |||||||
| chr16:89661198 | G | A | 1 | a0001c0001t0006g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.211+2777G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661198 | |||||||
| chr16:89661275 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0012 others(18): Show |
58 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.211+2854G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661275 | |||||||
| chr16:89661398 | T | C | 1 | a0001c0001t0005g0057 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.211+2977T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661398 | |||||||
| chr16:89661432 | A | G | 1 | a0001c0001t0013g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.211+3011A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661432 | |||||||
| chr16:89661438 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0001t0001g0112 others(1): Show |
7 | HG02615.hp1 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+3017C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661438 | |||||||
| chr16:89661455 | G | A | 1 | a0001c0001t0004g0020 | 3 | NA18948.hp1 NA18959.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.211+3034G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661455 | |||||||
| chr16:89661493 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(132): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.211+3072C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661493 | |||||||
| chr16:89661526 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.211+3105C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661526 | |||||||
| chr16:89661575 | G | T | 1 | a0001c0001t0002g0073 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.211+3154G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661575 | |||||||
| chr16:89661777 | G | A | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+3356G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661777 | |||||||
| chr16:89661783 | G | C | 1 | a0001c0001t0021g0092 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.211+3362G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661783 | |||||||
| chr16:89661884 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0032 |
7 | HG01243.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+3463C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661884 | |||||||
| chr16:89661910 | T | C | 1 | a0001c0001t0017g0079 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.211+3489T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661910 | |||||||
| chr16:89661925 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0059 others(1): Show |
14 | HG02280.hp1 HG02717.hp2 HG03195.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+3504G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661925 | |||||||
| chr16:89661945 | T | C | 1 | a0001c0001t0005g0060 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.211+3524T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661945 | |||||||
| chr16:89661981 | A | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0059 a0001c0001t0014g0058 |
7 | HG03239.hp2 HG03669.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+3560A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89661981 | |||||||
| chr16:89662067 | G | A | 14 | a0001c0001t0005g0003 a0001c0001t0005g0026 a0001c0001t0005g0050 others(11): Show |
45 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.211+3646G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662067 | |||||||
| chr16:89662069 | A | T | 1 | a0001c0001t0008g0127 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.211+3648A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662069 | |||||||
| chr16:89662072 | A | T | 1 | a0005c0004t0016g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.211+3651A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662072 | |||||||
| chr16:89662212 | G | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(109): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.211+3791G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662212 | |||||||
| chr16:89662245 | G | A | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+3824G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662245 | |||||||
| chr16:89662252 | C | T | 2 | a0001c0001t0003g0035 a0001c0001t0003g0083 |
3 | HG01123.hp1 HG01168.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.211+3831C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662252 | |||||||
| chr16:89662271 | G | C | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+3850G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662271 | |||||||
| chr16:89662293 | C | CA | 67 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(64): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.211+3884dupA | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89662293 | ||||||
| chr16:89662380 | G | C | 1 | a0001c0001t0018g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.211+3959G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662380 | |||||||
| chr16:89662473 | A | G | 1 | a0001c0001t0018g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.211+4052A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662473 | |||||||
| chr16:89662483 | C | G | 1 | a0001c0001t0003g0082 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.211+4062C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662483 | |||||||
| chr16:89662617 | A | G | 66 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(63): Show |
177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.211+4196A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662617 | |||||||
| chr16:89662618 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.211+4197G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662618 | |||||||
| chr16:89662663 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.211+4242C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662663 | |||||||
| chr16:89662670 | A | C | 1 | a0001c0001t0002g0129 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.211+4249A>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662670 | |||||||
| chr16:89662698 | A | G | 1 | a0001c0001t0002g0041 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.211+4277A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662698 | |||||||
| chr16:89662717 | G | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(60): Show |
174 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.211+4296G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662717 | |||||||
| chr16:89662751 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+4330G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662751 | |||||||
| chr16:89662761 | A | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(61): Show |
175 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.211+4340A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662761 | |||||||
| chr16:89662840 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
4 | HG01516.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+4419C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662840 | |||||||
| chr16:89662849 | A | G | 1 | a0001c0001t0017g0079 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.211+4428A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662849 | |||||||
| chr16:89662880 | G | A | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+4459G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662880 | |||||||
| chr16:89662887 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0106 others(3): Show |
10 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+4466G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662887 | |||||||
| chr16:89662919 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(46): Show |
129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.211+4498G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662919 | |||||||
| chr16:89662928 | A | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(77): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.211+4507A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662928 | |||||||
| chr16:89662989 | T | C | 1 | a0001c0001t0005g0096 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.211+4568T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89662989 | |||||||
| chr16:89663059 | C | G | 1 | a0001c0001t0003g0083 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.211+4638C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663059 | |||||||
| chr16:89663083 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.211+4662C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663083 | |||||||
| chr16:89663166 | T | G | 26 | a0001c0001t0001g0088 a0001c0001t0003g0006 a0001c0001t0003g0009 others(23): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.211+4745T>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663166 | |||||||
| chr16:89663167 | A | C | 1 | a0001c0001t0008g0127 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.211+4746A>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663167 | |||||||
| chr16:89663241 | C | CT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
71 | HG00438.hp1 HG00558.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.211+4836dupT | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89663241 | ||||||
| chr16:89663241 | CT | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(22): Show |
52 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.211+4836delT | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89663241 | ||||||
| chr16:89663330 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(76): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.211+4909G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663330 | |||||||
| chr16:89663336 | C | T | 1 | a0001c0001t0005g0026 | 2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.211+4915C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663336 | |||||||
| chr16:89663399 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.211+4978G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663399 | |||||||
| chr16:89663436 | C | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(61): Show |
176 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.211+5015C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663436 | |||||||
| chr16:89663676 | G | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(46): Show |
129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.211+5255G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663676 | |||||||
| chr16:89663698 | G | A | 19 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0020 others(16): Show |
76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.211+5277G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663698 | |||||||
| chr16:89663744 | T | A | 1 | a0001c0001t0006g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.211+5323T>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663744 | |||||||
| chr16:89663798 | G | A | 1 | a0001c0001t0006g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211+5377G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663798 | |||||||
| chr16:89663906 | C | T | 25 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0012 others(22): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.212-5380C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89663906 | |||||||
| chr16:89664045 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(132): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.212-5241T>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664045 | |||||||
| chr16:89664051 | T | C | 6 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0067 others(3): Show |
8 | HG01192.hp2 HG01891.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-5235T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664051 | |||||||
| chr16:89664053 | G | T | 3 | a0001c0001t0003g0014 a0002c0002t0003g0015 a0002c0002t0003g0037 |
10 | HG00639.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-5233G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664053 | |||||||
| chr16:89664071 | A | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(46): Show |
130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.212-5215A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664071 | |||||||
| chr16:89664120 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.212-5166G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664120 | |||||||
| chr16:89664161 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.212-5125G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664161 | |||||||
| chr16:89664246 | A | G | 6 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0067 others(3): Show |
8 | HG01192.hp2 HG01891.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-5040A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664246 | |||||||
| chr16:89664294 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.212-4992C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664294 | |||||||
| chr16:89664353 | C | CTT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(131): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.212-4933_212-4932i others(4): Show |
SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664353 | |||||||
| chr16:89664416 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0015g0021 |
3 | HG02080.hp2 HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.212-4870G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664416 | |||||||
| chr16:89664419 | T | C | 26 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0012 others(23): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.212-4867T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664419 | |||||||
| chr16:89664509 | TGGGCCCG others(45): Show |
T | 1 | a0001c0001t0008g0126 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.212-4625_212-4574d others(54): Show |
SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89664509 | ||||||
| chr16:89664560 | T | C | 1 | a0001c0001t0002g0011 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.212-4726T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664560 | |||||||
| chr16:89664659 | C | A | 5 | a0001c0001t0004g0007 a0001c0001t0007g0007 a0001c0001t0007g0094 others(2): Show |
14 | HG00438.hp2 HG00597.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.212-4627C>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664659 | |||||||
| chr16:89664665 | A | AGGGCCCG others(45): Show |
1 | a0001c0001t0003g0014 | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-4574_212-4573i others(54): Show |
SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89664665 | ||||||
| chr16:89664665 | A | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(110): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.212-4621A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664665 | |||||||
| chr16:89664725 | G | A | 1 | a0001c0001t0005g0061 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.212-4561G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664725 | |||||||
| chr16:89664747 | T | C | 5 | a0001c0001t0003g0014 a0001c0001t0003g0077 a0001c0001t0018g0119 others(2): Show |
12 | HG00639.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-4539T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664747 | |||||||
| chr16:89664777 | A | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(112): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.212-4509A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664777 | |||||||
| chr16:89664830 | G | A | 1 | a0001c0001t0009g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.212-4456G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664830 | |||||||
| chr16:89664902 | A | T | 1 | a0001c0001t0007g0097 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.212-4384A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89664902 | |||||||
| chr16:89665022 | C | G | 1 | a0001c0001t0002g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-4264C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665022 | |||||||
| chr16:89665150 | A | G | 1 | a0001c0001t0011g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.212-4136A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665150 | |||||||
| chr16:89665254 | C | A | 1 | a0001c0001t0001g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.212-4032C>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665254 | |||||||
| chr16:89665284 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.212-4002C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665284 | |||||||
| chr16:89665285 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.212-4001G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665285 | |||||||
| chr16:89665308 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.212-3978T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665308 | |||||||
| chr16:89665309 | C | CT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0106 others(2): Show |
9 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-3966dupT | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89665309 | ||||||
| chr16:89665327 | G | C | 1 | a0001c0001t0005g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.212-3959G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665327 | |||||||
| chr16:89665330 | T | C | 1 | a0001c0001t0008g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.212-3956T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665330 | |||||||
| chr16:89665351 | G | T | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.212-3935G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665351 | |||||||
| chr16:89665391 | G | A | 1 | a0001c0001t0002g0028 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.212-3895G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665391 | |||||||
| chr16:89665429 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0055 |
3 | HG02055.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-3857C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665429 | |||||||
| chr16:89665480 | A | AT | 23 | a0001c0001t0001g0088 a0001c0001t0002g0072 a0001c0001t0003g0006 others(20): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.212-3792dupT | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr16 | 89665480 | ||||||
| chr16:89665494 | T | A | 1 | a0001c0001t0018g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212-3792T>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665494 | |||||||
| chr16:89665497 | G | C | 14 | a0001c0001t0005g0003 a0001c0001t0005g0026 a0001c0001t0005g0050 others(11): Show |
45 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.212-3789G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665497 | |||||||
| chr16:89665560 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.212-3726C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665560 | |||||||
| chr16:89665616 | A | T | 21 | a0001c0001t0001g0088 a0001c0001t0003g0006 a0001c0001t0003g0009 others(18): Show |
58 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.212-3670A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665616 | |||||||
| chr16:89665635 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-3651C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665635 | |||||||
| chr16:89665642 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(110): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.212-3644T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665642 | |||||||
| chr16:89665718 | G | C | 1 | a0001c0001t0005g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.212-3568G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665718 | |||||||
| chr16:89665812 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.212-3474G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665812 | |||||||
| chr16:89665830 | C | T | 28 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0012 others(25): Show |
72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.212-3456C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665830 | |||||||
| chr16:89665831 | G | C | 2 | a0002c0002t0003g0015 a0002c0002t0003g0037 |
6 | HG00639.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-3455G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665831 | |||||||
| chr16:89665872 | G | C | 1 | a0001c0001t0002g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.212-3414G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665872 | |||||||
| chr16:89665888 | T | G | 1 | a0005c0004t0016g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-3398T>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89665888 | |||||||
| chr16:89666035 | T | C | 1 | a0001c0001t0002g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.212-3251T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666035 | |||||||
| chr16:89666182 | A | T | 1 | a0001c0001t0004g0020 | 3 | NA18948.hp1 NA18959.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.212-3104A>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666182 | |||||||
| chr16:89666260 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0021 others(17): Show |
85 | HG00438.hp1 HG00558.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.212-3026G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666260 | |||||||
| chr16:89666306 | C | G | 1 | a0001c0001t0014g0058 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.212-2980C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666306 | |||||||
| chr16:89666415 | C | T | 1 | a0001c0001t0017g0079 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.212-2871C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666415 | |||||||
| chr16:89666593 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2693G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666593 | |||||||
| chr16:89666612 | G | T | 1 | a0002c0002t0003g0037 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.212-2674G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666612 | |||||||
| chr16:89666728 | A | C | 1 | a0001c0001t0004g0036 | 2 | NA18951.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.212-2558A>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666728 | |||||||
| chr16:89666798 | G | A | 14 | a0001c0001t0005g0003 a0001c0001t0005g0026 a0001c0001t0005g0050 others(11): Show |
45 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.212-2488G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666798 | |||||||
| chr16:89666879 | T | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0077 a0002c0002t0003g0015 others(1): Show |
11 | HG00639.hp1 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.212-2407T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666879 | |||||||
| chr16:89666951 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.212-2335T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666951 | |||||||
| chr16:89666963 | G | C | 1 | a0001c0001t0003g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.212-2323G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89666963 | |||||||
| chr16:89667016 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(74): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.212-2270C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667016 | |||||||
| chr16:89667068 | T | C | 1 | a0001c0001t0009g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.212-2218T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667068 | |||||||
| chr16:89667200 | G | A | 1 | a0001c0001t0005g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.212-2086G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667200 | |||||||
| chr16:89667205 | C | T | 19 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0020 others(16): Show |
76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.212-2081C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667205 | |||||||
| chr16:89667206 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(132): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.212-2080A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667206 | |||||||
| chr16:89667249 | A | G | 19 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0020 others(16): Show |
76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.212-2037A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667249 | |||||||
| chr16:89667372 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0068 |
4 | HG01192.hp2 HG01891.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-1914G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667372 | |||||||
| chr16:89667381 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.212-1905C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667381 | |||||||
| chr16:89667483 | C | A | 1 | a0001c0001t0006g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.212-1803C>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667483 | |||||||
| chr16:89667518 | C | T | 7 | a0001c0001t0003g0012 a0001c0001t0003g0014 a0001c0001t0003g0018 others(4): Show |
20 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-1768C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667518 | |||||||
| chr16:89667519 | C | T | 1 | a0001c0001t0002g0008 | 7 | HG02280.hp1 HG02717.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-1767C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667519 | |||||||
| chr16:89667567 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.212-1719G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667567 | |||||||
| chr16:89667680 | A | G | 79 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(76): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.212-1606A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667680 | |||||||
| chr16:89667685 | G | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(107): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.212-1601G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667685 | |||||||
| chr16:89667744 | C | T | 2 | a0001c0001t0009g0075 a0001c0001t0017g0079 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.212-1542C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667744 | |||||||
| chr16:89667777 | C | T | 1 | a0001c0001t0010g0121 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.212-1509C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667777 | |||||||
| chr16:89667788 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0091 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212-1498G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667788 | |||||||
| chr16:89667869 | G | C | 1 | a0001c0001t0002g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.212-1417G>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667869 | |||||||
| chr16:89667941 | T | C | 26 | a0001c0001t0001g0088 a0001c0001t0003g0006 a0001c0001t0003g0009 others(23): Show |
63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.212-1345T>C | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667941 | |||||||
| chr16:89667989 | C | G | 1 | a0005c0004t0016g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-1297C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89667989 | |||||||
| chr16:89668009 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.212-1277G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668009 | |||||||
| chr16:89668010 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0077 a0002c0002t0003g0015 others(1): Show |
11 | HG00639.hp1 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.212-1276C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668010 | |||||||
| chr16:89668040 | A | G | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.212-1246A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668040 | |||||||
| chr16:89668047 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.212-1239C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668047 | |||||||
| chr16:89668049 | C | A | 1 | a0007c0006t0003g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.212-1237C>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668049 | |||||||
| chr16:89668050 | G | A | 4 | a0001c0001t0009g0052 a0001c0001t0009g0071 a0001c0001t0009g0075 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-1236G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668050 | |||||||
| chr16:89668070 | G | T | 1 | a0005c0004t0016g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-1216G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668070 | |||||||
| chr16:89668146 | T | A | 1 | a0001c0001t0004g0098 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.212-1140T>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668146 | |||||||
| chr16:89668166 | C | T | 1 | a0001c0001t0017g0079 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.212-1120C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668166 | |||||||
| chr16:89668380 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(43): Show |
127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.212-906C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668380 | |||||||
| chr16:89668423 | A | G | 46 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(43): Show |
127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.212-863A>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668423 | |||||||
| chr16:89668477 | G | GT | 113 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(110): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.212-809_212-808ins others(1): Show |
SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668477 | |||||||
| chr16:89668509 | C | T | 4 | a0001c0001t0003g0034 a0001c0001t0003g0076 a0001c0001t0003g0122 others(1): Show |
5 | HG01074.hp2 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-777C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668509 | |||||||
| chr16:89668521 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.212-765C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668521 | |||||||
| chr16:89668584 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.212-702G>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668584 | |||||||
| chr16:89668613 | C | G | 2 | a0001c0001t0010g0120 a0001c0001t0010g0121 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.212-673C>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668613 | |||||||
| chr16:89668663 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG01099.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.212-623C>T | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668663 | |||||||
| chr16:89668664 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(12): Show |
45 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.212-622G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668664 | |||||||
| chr16:89668687 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.212-599G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668687 | |||||||
| chr16:89668693 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0086 |
3 | HG02572.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-593G>A | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668693 | |||||||
| chr16:89668996 | T | G | 1 | a0005c0004t0016g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-290T>G | SPATA33 | ENSG00000167523.15 | transcript | ENST00000579310.6 | protein_coding | 2/2 | chr16 | 89668996 |