Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83890 |
| ensemblid | ENSG00000145757.16 |
| hgncid | 22988 |
| symbol | SPATA9 |
| name | spermatogenesis associated 9 |
| refseq_nuc | NM_031952.4 |
| refseq_prot | NP_114158.2 |
| ensembl_nuc | ENST00000274432.13 |
| ensembl_prot | ENSP00000274432.8 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 95658315 |
| end | 95682991 |
| strand | - |
| ver | v1.2 |
| region | chr5:95658315-95682991 |
| region5000 | chr5:95653315-95687991 |
| regionname0 | SPATA9_chr5_95658315_95682991 |
| regionname5000 | SPATA9_chr5_95653315_95687991 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 254 | 362 | 83 | 65 | 149 | 18 | 45 | 110 | SPATA9_chr5_95653315_95687991 | SPATA9 | MPIKP others(249): Show |
chr5 | 95653315 | 95687991 |
| a0002 | 0/0 | 254 | 15 | 9 | 6 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | MPIKP others(249): Show |
chr5 | 95653315 | 95687991 |
| a0003 | 0/0 | 254 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | MPIKP others(249): Show |
chr5 | 95653315 | 95687991 |
| a0004 | 0/0 | 254 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | MPIKP others(249): Show |
chr5 | 95653315 | 95687991 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 762 | 313 | 81 | 55 | 124 | 14 | 37 | SPATA9_chr5_95653315_95687991 | SPATA9 | ATGCC others(757): Show |
chr5 | 95653315 | 95687991 | ||
| a0001c0002 | 0/0 | 762 | 46 | 2 | 10 | 22 | 4 | 8 | SPATA9_chr5_95653315_95687991 | SPATA9 | ATGCC others(757): Show |
chr5 | 95653315 | 95687991 | ||
| a0001c0004 | 0/0 | 762 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | ATGCC others(757): Show |
chr5 | 95653315 | 95687991 | ||
| a0002c0003 | 0/0 | 762 | 15 | 9 | 6 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | ATGCC others(757): Show |
chr5 | 95653315 | 95687991 | ||
| a0003c0005 | 0/0 | 762 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | ATGCC others(757): Show |
chr5 | 95653315 | 95687991 | ||
| a0004c0006 | 0/0 | 762 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | ATGCC others(757): Show |
chr5 | 95653315 | 95687991 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1210 | 222 | 51 | 48 | 83 | 12 | 27 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1205): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0002 | 0/1 | 1536 | 43 | 7 | 4 | 23 | 2 | 6 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0003 | 0/0 | 1537 | 9 | 0 | 0 | 9 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1532): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0004 | 0/0 | 1537 | 11 | 6 | 2 | 1 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1532): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0005 | 0/0 | 1210 | 8 | 8 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1205): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0006 | 0/0 | 1538 | 3 | 1 | 1 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1533): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0007 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0008 | 0/0 | 1535 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1530): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0009 | 0/0 | 1536 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0010 | 0/0 | 1210 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | AATGA others(1205): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0011 | 0/0 | 1210 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1205): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0012 | 0/0 | 1210 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1205): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0013 | 0/0 | 1538 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1533): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0014 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1532): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0015 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1532): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0017 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1532): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0018 | 0/0 | 1529 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1524): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0020 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1528): Show |
chr5 | 95653315 | 95687991 |
| a0001c0001t0021 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| a0001c0002t0002 | 0/0 | 1536 | 37 | 1 | 8 | 18 | 4 | 6 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| a0001c0002t0003 | 0/0 | 1537 | 5 | 0 | 2 | 1 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1532): Show |
chr5 | 95653315 | 95687991 |
| a0001c0002t0004 | 0/0 | 1537 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1532): Show |
chr5 | 95653315 | 95687991 |
| a0001c0002t0006 | 0/0 | 1538 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1533): Show |
chr5 | 95653315 | 95687991 |
| a0001c0002t0016 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| a0001c0002t0019 | 0/0 | 1535 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1530): Show |
chr5 | 95653315 | 95687991 |
| a0001c0004t0002 | 0/0 | 1536 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| a0002c0003t0001 | 0/0 | 1210 | 15 | 9 | 6 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1205): Show |
chr5 | 95653315 | 95687991 |
| a0003c0005t0001 | 0/0 | 1210 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1205): Show |
chr5 | 95653315 | 95687991 |
| a0004c0006t0007 | 0/0 | 1536 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | AGTGA others(1531): Show |
chr5 | 95653315 | 95687991 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 51 | 8 | 4 | 36 | 1 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0002 | 0/0 | 19 | 2 | 9 | 2 | 2 | 4 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0003 | 0/0 | 16 | 3 | 6 | 3 | 2 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0004 | 0/0 | 14 | 5 | 3 | 0 | 1 | 5 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0005 | 0/0 | 11 | 0 | 0 | 9 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0020 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0034 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0003g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0004g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0004g0019 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0004g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0005g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0005g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0006g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0008g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0018g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0020g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0001t0021g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0006 | 0/0 | 8 | 1 | 1 | 4 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0012 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0003g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0016g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0002t0019g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0001c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0002c0003t0001g0007 | 0/0 | 7 | 3 | 4 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0002c0003t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0002c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0002c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0003c0005t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| a0004c0006t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0027 | EUR | FIN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0012 | EUR | FIN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0062 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0050 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0039 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0134 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01496 | hp2 | a0004 | c0006 | t0007 | g0070 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0115 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0136 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02040 | hp1 | a0003 | c0005 | t0001 | g0036 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02129 | hp1 | a0001 | c0001 | t0021 | g0086 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02145 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CDX | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0133 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0076 | AMR | PEL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02523 | hp2 | a0001 | c0002 | t0019 | g0080 | EAS | KHV | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0141 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0031 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02698 | hp1 | a0001 | c0001 | t0013 | g0154 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0135 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0031 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0067 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03540 | hp2 | a0001 | c0001 | t0018 | g0147 | AFR | GWD | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03704 | hp2 | a0003 | c0005 | t0001 | g0036 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0079 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0039 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | BEB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG04228 | hp2 | a0001 | c0001 | t0010 | g0053 | SAS | STU | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | YRI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | YRI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18949 | hp1 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18953 | hp2 | a0001 | c0002 | t0016 | g0078 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18959 | hp1 | a0001 | c0001 | t0008 | g0085 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0162 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18984 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18987 | hp1 | a0001 | c0001 | t0020 | g0089 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0066 | AFR | LWK | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | LWK | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19058 | hp2 | a0001 | c0004 | t0002 | g0071 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19060 | hp2 | a0001 | c0004 | t0002 | g0073 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0149 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19086 | hp1 | a0001 | c0004 | t0002 | g0072 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | YRI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0012 | EUR | TSI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0057 | EUR | TSI | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | GIH | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0153 | SAS | GIH | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0031 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0096 | AFR | USA | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | USA | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | LWK | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0159 | REF | REF | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0129 | REF | REF | SPATA9_chr5_95653315_95687991 | SPATA9 | chr5 | 95653315 | 95687991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95658763 | T | C | 1 | a0002 | 15 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(12): Show |
missense_variant | MODERATE | c.625A>G | p.Lys209Glu | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 762/1210 | 625/765 | 209/254 | chr5 | 95658763 | |||
| chr5:95675417 | T | C | 1 | a0004 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.373A>G | p.Ile125Val | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/5 | 510/1210 | 373/765 | 125/254 | chr5 | 95675417 | |||
| chr5:95675485 | A | G | 1 | a0003 | 2 | HG02040.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.305T>C | p.Leu102Ser | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/5 | 442/1210 | 305/765 | 102/254 | chr5 | 95675485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95658635 | A | G | 2 | a0001c0002 a0001c0004 |
49 | HG00280.hp1 HG00323.hp1 HG01069.hp1 others(46): Show |
synonymous_variant | LOW | c.753T>C | p.Asn251Asn | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 890/1210 | 753/765 | 251/254 | chr5 | 95658635 | |||
| chr5:95675625 | C | T | 1 | a0001c0004 | 3 | NA19058.hp2 NA19060.hp2 NA19086.hp1 |
synonymous_variant | LOW | c.165G>A | p.Ala55Ala | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/5 | 302/1210 | 165/765 | 55/254 | chr5 | 95675625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95658423 | G | C | 4 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0017 others(1): Show |
5 | HG01496.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*200C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 200 | chr5 | 95658423 | ||||||
| chr5:95658447 | C | A | 1 | a0001c0001t0012 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 176 | chr5 | 95658447 | ||||||
| chr5:95658505 | T | TCTCTTTT others(312): Show |
1 | a0001c0001t0018 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(313): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(318): Show |
1 | a0001c0001t0008 | 3 | HG02056.hp1 NA18959.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(319): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(320): Show |
1 | a0001c0001t0015 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(321): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(318): Show |
1 | a0001c0002t0019 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(319): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(319): Show |
6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0021 others(3): Show |
86 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(320): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(319): Show |
1 | a0001c0001t0009 | 2 | NA18983.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(320): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(320): Show |
3 | a0001c0001t0004 a0001c0001t0014 a0001c0002t0004 |
13 | HG01081.hp1 HG01346.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(321): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(321): Show |
1 | a0001c0001t0013 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(322): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(319): Show |
1 | a0001c0002t0016 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(320): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(320): Show |
3 | a0001c0001t0003 a0001c0001t0017 a0001c0002t0003 |
15 | HG00621.hp1 HG00621.hp2 HG01099.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(321): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658505 | T | TCTCTTTT others(321): Show |
2 | a0001c0001t0006 a0001c0002t0006 |
4 | HG00597.hp2 HG01106.hp2 HG02257.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*117_*118insGGCCGG others(322): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 117 | chr5 | 95658505 | ||||||
| chr5:95658509 | T | TTTTTTTT others(316): Show |
1 | a0001c0001t0020 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113_*114insGAGGGC others(317): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 113 | chr5 | 95658509 | ||||||
| chr5:95658570 | G | A | 1 | a0001c0001t0021 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 53 | chr5 | 95658570 | ||||||
| chr5:95658577 | G | A | 1 | a0001c0001t0005 | 8 | HG01884.hp1 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*46C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 5/5 | 46 | chr5 | 95658577 | ||||||
| chr5:95682878 | A | T | 1 | a0001c0001t0011 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-24T>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 1/5 | 24 | chr5 | 95682878 | ||||||
| chr5:95682990 | C | T | 1 | a0001c0001t0010 | 1 | HG04228.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-136G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 1/5 | chr5 | 95682990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95659236 | A | C | 1 | a0002c0003t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.475-323T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659236 | |||||||
| chr5:95659295 | T | G | 11 | a0001c0001t0005g0033 a0001c0001t0005g0045 a0001c0001t0005g0048 others(8): Show |
23 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.475-382A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659295 | |||||||
| chr5:95659416 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0140 |
2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.475-503T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659416 | |||||||
| chr5:95659484 | A | G | 7 | a0002c0003t0001g0007 a0002c0003t0001g0031 a0002c0003t0001g0133 others(4): Show |
15 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.475-571T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659484 | |||||||
| chr5:95659565 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.475-652G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659565 | |||||||
| chr5:95659673 | C | T | 1 | a0001c0001t0012g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.475-760G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659673 | |||||||
| chr5:95659785 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0090 others(3): Show |
12 | HG01243.hp2 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.475-872C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659785 | |||||||
| chr5:95659801 | C | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0099 others(2): Show |
8 | HG01255.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-888G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659801 | |||||||
| chr5:95659911 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.475-998T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95659911 | |||||||
| chr5:95660061 | G | A | 1 | a0001c0002t0002g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.475-1148C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660061 | |||||||
| chr5:95660238 | A | G | 101 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0032 others(98): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.475-1325T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660238 | |||||||
| chr5:95660453 | A | G | 1 | a0001c0001t0001g0025 | 3 | HG03669.hp2 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.475-1540T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660453 | |||||||
| chr5:95660482 | G | A | 83 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0060 others(80): Show |
145 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.475-1569C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660482 | |||||||
| chr5:95660579 | C | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-1666G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660579 | |||||||
| chr5:95660587 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.475-1674C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660587 | |||||||
| chr5:95660716 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.475-1803G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660716 | |||||||
| chr5:95660760 | T | C | 1 | a0003c0005t0001g0036 | 2 | HG02040.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.475-1847A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660760 | |||||||
| chr5:95660946 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0099 |
4 | HG01255.hp1 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-2033A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660946 | |||||||
| chr5:95660964 | GTCT | G | 69 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0020 others(66): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.475-2054_475-2052d others(5): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660964 | |||||||
| chr5:95660967 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0138 a0001c0001t0011g0054 |
5 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-2054A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95660967 | |||||||
| chr5:95661053 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.475-2140A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661053 | |||||||
| chr5:95661261 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0095 others(4): Show |
10 | HG01255.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-2348G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661261 | |||||||
| chr5:95661330 | T | C | 4 | a0001c0001t0005g0033 a0001c0001t0005g0045 a0001c0001t0005g0048 others(1): Show |
8 | HG01884.hp1 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-2417A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661330 | |||||||
| chr5:95661414 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475-2501T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661414 | |||||||
| chr5:95661464 | G | T | 1 | a0001c0001t0012g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.474+2489C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661464 | |||||||
| chr5:95661621 | T | C | 1 | a0001c0004t0002g0072 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.474+2332A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661621 | |||||||
| chr5:95661690 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.474+2263A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661690 | |||||||
| chr5:95661922 | CA | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0138 |
4 | HG02976.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+2030delT | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661922 | |||||||
| chr5:95661958 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.474+1995T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95661958 | |||||||
| chr5:95662181 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474+1772G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662181 | |||||||
| chr5:95662185 | T | C | 70 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0020 others(67): Show |
129 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.474+1768A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662185 | |||||||
| chr5:95662469 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0099 |
4 | HG01255.hp1 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+1484G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662469 | |||||||
| chr5:95662489 | G | A | 1 | a0001c0001t0012g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.474+1464C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662489 | |||||||
| chr5:95662599 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.474+1354T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662599 | |||||||
| chr5:95662634 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.474+1319A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662634 | |||||||
| chr5:95662716 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.474+1237G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662716 | |||||||
| chr5:95662765 | A | T | 1 | a0001c0001t0002g0047 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.474+1188T>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662765 | |||||||
| chr5:95662775 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.474+1178C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662775 | |||||||
| chr5:95662822 | AGATGCAA others(16): Show |
A | 1 | a0001c0001t0001g0023 | 3 | HG00741.hp2 HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.474+1108_474+1130d others(25): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662822 | |||||||
| chr5:95662909 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0138 a0001c0001t0011g0054 |
5 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+1044C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662909 | |||||||
| chr5:95662929 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.474+1024T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662929 | |||||||
| chr5:95662974 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.474+979C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662974 | |||||||
| chr5:95662996 | C | T | 5 | a0001c0002t0002g0058 a0001c0002t0002g0077 a0001c0004t0002g0071 others(2): Show |
5 | HG02071.hp1 NA19058.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+957G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95662996 | |||||||
| chr5:95663267 | C | T | 1 | a0001c0001t0012g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.474+686G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95663267 | |||||||
| chr5:95663268 | A | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0028 others(102): Show |
199 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.474+685T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95663268 | |||||||
| chr5:95663656 | C | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0120 |
3 | NA18984.hp2 NA18985.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.474+297G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 4/4 | chr5 | 95663656 | |||||||
| chr5:95664282 | G | A | 7 | a0002c0003t0001g0007 a0002c0003t0001g0031 a0002c0003t0001g0133 others(4): Show |
15 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-234C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95664282 | |||||||
| chr5:95664284 | T | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0155 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.379-236A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95664284 | |||||||
| chr5:95664621 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0140 |
2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.379-573A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95664621 | |||||||
| chr5:95664920 | CA | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0069 |
5 | HG00408.hp2 HG01943.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-873delT | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95664920 | |||||||
| chr5:95665058 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0090 a0001c0001t0001g0091 |
7 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-1010T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665058 | |||||||
| chr5:95665100 | T | C | 2 | a0001c0001t0002g0151 a0001c0001t0002g0155 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.379-1052A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665100 | |||||||
| chr5:95665136 | A | G | 9 | a0001c0001t0005g0045 a0001c0001t0005g0132 a0002c0003t0001g0007 others(6): Show |
18 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.379-1088T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665136 | |||||||
| chr5:95665258 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0140 |
2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.379-1210A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665258 | |||||||
| chr5:95665321 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0140 |
2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.379-1273A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665321 | |||||||
| chr5:95665556 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.379-1508A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665556 | |||||||
| chr5:95665617 | C | CA | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1570_379-1569i others(3): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665617 | |||||||
| chr5:95665619 | G | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1571C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665619 | |||||||
| chr5:95665620 | T | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1572A>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665620 | |||||||
| chr5:95665621 | G | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1573C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665621 | |||||||
| chr5:95665622 | G | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1574C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665622 | |||||||
| chr5:95665623 | T | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1575A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665623 | |||||||
| chr5:95665624 | T | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1576A>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665624 | |||||||
| chr5:95665625 | G | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1577C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665625 | |||||||
| chr5:95665626 | G | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1578C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665626 | |||||||
| chr5:95665881 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.379-1833T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665881 | |||||||
| chr5:95665900 | CAG | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0095 others(4): Show |
10 | HG01255.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-1854_379-1853d others(4): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95665900 | |||||||
| chr5:95666025 | G | A | 3 | a0001c0001t0002g0034 a0001c0001t0015g0096 a0001c0001t0018g0147 |
5 | HG02818.hp1 HG02965.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1977C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666025 | |||||||
| chr5:95666106 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0102 a0001c0001t0001g0103 |
6 | NA18612.hp1 NA18974.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-2058A>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666106 | |||||||
| chr5:95666363 | A | G | 1 | a0001c0001t0004g0018 | 4 | HG02258.hp1 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-2315T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666363 | |||||||
| chr5:95666417 | T | G | 70 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0020 others(67): Show |
129 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.379-2369A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666417 | |||||||
| chr5:95666445 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.379-2397T>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666445 | |||||||
| chr5:95666597 | C | T | 1 | a0001c0001t0005g0048 | 2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.379-2549G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666597 | |||||||
| chr5:95666623 | A | G | 1 | a0001c0001t0012g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.379-2575T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666623 | |||||||
| chr5:95666698 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.379-2650G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666698 | |||||||
| chr5:95666735 | GCAT | G | 92 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0060 others(89): Show |
163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-2690_379-2688d others(5): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666735 | |||||||
| chr5:95666738 | T | G | 2 | a0001c0001t0002g0158 a0001c0001t0003g0157 |
2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.379-2690A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95666738 | |||||||
| chr5:95667069 | A | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0140 |
2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.379-3021T>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95667069 | |||||||
| chr5:95667233 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.379-3185G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95667233 | |||||||
| chr5:95667402 | G | A | 2 | a0001c0002t0002g0027 a0001c0002t0003g0039 |
5 | HG00280.hp1 HG01070.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-3354C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95667402 | |||||||
| chr5:95667413 | G | T | 2 | a0001c0001t0005g0045 a0001c0001t0005g0132 |
3 | HG01884.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.379-3365C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95667413 | |||||||
| chr5:95667497 | A | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0145 others(1): Show |
4 | HG00741.hp1 HG01106.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-3449T>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95667497 | |||||||
| chr5:95667580 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.379-3532A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95667580 | |||||||
| chr5:95667625 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0140 |
2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.379-3577A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95667625 | |||||||
| chr5:95668263 | T | G | 1 | a0001c0001t0012g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.379-4215A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95668263 | |||||||
| chr5:95668309 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01106.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.379-4261A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95668309 | |||||||
| chr5:95668402 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.379-4354G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95668402 | |||||||
| chr5:95668499 | G | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
10 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.379-4451C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95668499 | |||||||
| chr5:95668779 | G | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(43): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.379-4731C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95668779 | |||||||
| chr5:95669135 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0099 others(2): Show |
8 | HG01255.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-5087A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669135 | |||||||
| chr5:95669272 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.379-5224T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669272 | |||||||
| chr5:95669284 | T | C | 1 | a0001c0001t0004g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.379-5236A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669284 | |||||||
| chr5:95669311 | C | T | 1 | a0001c0001t0001g0032 | 3 | HG02572.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.379-5263G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669311 | |||||||
| chr5:95669490 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.379-5442G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669490 | |||||||
| chr5:95669574 | T | C | 1 | a0001c0001t0001g0026 | 3 | NA18985.hp1 NA19002.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.379-5526A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669574 | |||||||
| chr5:95669657 | T | G | 1 | a0001c0001t0001g0032 | 3 | HG02572.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.379-5609A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669657 | |||||||
| chr5:95669723 | C | T | 2 | a0001c0002t0002g0015 a0001c0002t0002g0074 |
5 | NA18943.hp2 NA18951.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-5675G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669723 | |||||||
| chr5:95669955 | T | G | 1 | a0002c0003t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.378+5457A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669955 | |||||||
| chr5:95669996 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0163 |
2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.378+5416A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95669996 | |||||||
| chr5:95670128 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.378+5284C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95670128 | |||||||
| chr5:95670241 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.378+5171T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95670241 | |||||||
| chr5:95670335 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0022 others(26): Show |
60 | HG00140.hp2 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.378+5077A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95670335 | |||||||
| chr5:95670373 | A | C | 1 | a0001c0001t0012g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.378+5039T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95670373 | |||||||
| chr5:95670453 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.378+4959T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95670453 | |||||||
| chr5:95670819 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.378+4593A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95670819 | |||||||
| chr5:95671099 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0123 a0001c0001t0001g0124 |
7 | HG00408.hp1 HG00423.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+4313C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671099 | |||||||
| chr5:95671300 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0018g0147 |
4 | HG02818.hp1 HG02965.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+4112G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671300 | |||||||
| chr5:95671463 | T | G | 18 | a0001c0001t0001g0156 a0001c0001t0002g0005 a0001c0001t0002g0009 others(15): Show |
39 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.378+3949A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671463 | |||||||
| chr5:95671566 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
231 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.378+3846G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671566 | |||||||
| chr5:95671661 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
233 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.378+3751T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671661 | |||||||
| chr5:95671755 | A | G | 1 | a0001c0001t0005g0132 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.378+3657T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671755 | |||||||
| chr5:95671787 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG00408.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.378+3625A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671787 | |||||||
| chr5:95671922 | T | TA | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
231 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.378+3489dupT | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95671922 | |||||||
| chr5:95672179 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.378+3233T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672179 | |||||||
| chr5:95672373 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.378+3039T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672373 | |||||||
| chr5:95672425 | G | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(58): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.378+2987C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672425 | |||||||
| chr5:95672455 | G | GT | 11 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0041 others(8): Show |
18 | HG00741.hp1 HG01243.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+2956dupA | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672455 | |||||||
| chr5:95672455 | G | GTT | 5 | a0001c0001t0005g0045 a0001c0001t0005g0132 a0002c0003t0001g0007 others(2): Show |
12 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.378+2955_378+2956d others(4): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672455 | |||||||
| chr5:95672455 | GT | G | 8 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0111 others(5): Show |
8 | HG00673.hp1 HG00738.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+2956delA | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672455 | |||||||
| chr5:95672459 | T | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(93): Show |
196 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.378+2953A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672459 | |||||||
| chr5:95672460 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.378+2952A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672460 | |||||||
| chr5:95672476 | TAAAC | T | 3 | a0001c0002t0002g0010 a0001c0002t0002g0087 a0001c0002t0006g0075 |
7 | HG02135.hp1 NA18947.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+2932_378+2935d others(6): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672476 | |||||||
| chr5:95672480 | C | T | 1 | a0001c0002t0002g0006 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.378+2932G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672480 | |||||||
| chr5:95672481 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.378+2931T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672481 | |||||||
| chr5:95672728 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0015g0096 |
2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.378+2684A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95672728 | |||||||
| chr5:95673016 | G | A | 1 | a0001c0004t0002g0073 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.378+2396C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673016 | |||||||
| chr5:95673032 | G | A | 11 | a0001c0001t0001g0032 a0001c0001t0001g0145 a0001c0001t0001g0163 others(8): Show |
22 | HG00741.hp1 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.378+2380C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673032 | |||||||
| chr5:95673254 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01106.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.378+2158G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673254 | |||||||
| chr5:95673255 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(120): Show |
251 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.378+2157T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673255 | |||||||
| chr5:95673376 | T | TTG | 7 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0007g0065 others(4): Show |
7 | HG01496.hp2 HG02055.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+2034_378+2035d others(4): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673376 | |||||||
| chr5:95673376 | TTG | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(74): Show |
153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.378+2034_378+2035d others(4): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673376 | |||||||
| chr5:95673419 | A | G | 1 | a0001c0002t0002g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.378+1993T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673419 | |||||||
| chr5:95673694 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.378+1718C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673694 | |||||||
| chr5:95673752 | C | CT | 13 | a0001c0001t0001g0032 a0001c0001t0001g0114 a0001c0001t0001g0145 others(10): Show |
24 | HG00741.hp1 HG01243.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.378+1659dupA | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673752 | |||||||
| chr5:95673911 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.378+1501A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95673911 | |||||||
| chr5:95674101 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.378+1311G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674101 | |||||||
| chr5:95674187 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0123 others(1): Show |
10 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+1225C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674187 | |||||||
| chr5:95674246 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.378+1166T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674246 | |||||||
| chr5:95674324 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
346 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.378+1088A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674324 | |||||||
| chr5:95674560 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.378+852C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674560 | |||||||
| chr5:95674576 | A | G | 1 | a0001c0002t0003g0062 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.378+836T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674576 | |||||||
| chr5:95674604 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.378+808G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674604 | |||||||
| chr5:95674663 | T | C | 1 | a0002c0003t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.378+749A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674663 | |||||||
| chr5:95674771 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.378+641C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674771 | |||||||
| chr5:95674889 | C | T | 12 | a0001c0001t0002g0005 a0001c0001t0002g0055 a0001c0001t0002g0104 others(9): Show |
27 | HG00438.hp1 HG00597.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.378+523G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674889 | |||||||
| chr5:95674985 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378+427A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674985 | |||||||
| chr5:95674998 | A | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0048 |
5 | HG02280.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+414T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95674998 | |||||||
| chr5:95675079 | A | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(58): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.378+333T>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95675079 | |||||||
| chr5:95675112 | C | A | 31 | a0001c0001t0001g0156 a0001c0001t0002g0005 a0001c0001t0002g0009 others(28): Show |
65 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.378+300G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95675112 | |||||||
| chr5:95675122 | T | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0099 others(2): Show |
8 | HG01255.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+290A>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95675122 | |||||||
| chr5:95675169 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
10 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.378+243A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95675169 | |||||||
| chr5:95675376 | A | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0099 others(2): Show |
8 | HG01255.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+36T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95675376 | |||||||
| chr5:95675384 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.378+28C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 3/4 | chr5 | 95675384 | |||||||
| chr5:95675668 | G | A | 2 | a0001c0001t0005g0045 a0001c0001t0005g0132 |
3 | HG01884.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151-29C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675668 | |||||||
| chr5:95675722 | A | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(58): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.151-83T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675722 | |||||||
| chr5:95675819 | C | CT | 11 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0041 others(8): Show |
15 | HG00642.hp1 HG01255.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-181dupA | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675819 | |||||||
| chr5:95675819 | C | CTTT | 9 | a0001c0001t0001g0032 a0001c0001t0001g0145 a0001c0001t0001g0163 others(6): Show |
20 | HG00741.hp1 HG01243.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.151-183_151-181dup others(3): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675819 | |||||||
| chr5:95675819 | CT | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(84): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.151-181delA | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675819 | |||||||
| chr5:95675819 | CTT | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0128 others(7): Show |
29 | HG00423.hp1 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.151-182_151-181del others(2): Show |
SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675819 | |||||||
| chr5:95675841 | T | A | 1 | a0001c0001t0001g0052 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.151-202A>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675841 | |||||||
| chr5:95675885 | G | A | 1 | a0001c0001t0002g0034 | 3 | HG02818.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.151-246C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675885 | |||||||
| chr5:95675945 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0090 a0001c0001t0001g0091 |
7 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-306G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675945 | |||||||
| chr5:95675965 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.151-326C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95675965 | |||||||
| chr5:95676088 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0163 |
2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.151-449G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95676088 | |||||||
| chr5:95676199 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG00642.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.151-560A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95676199 | |||||||
| chr5:95676233 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151-594C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95676233 | |||||||
| chr5:95676271 | A | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(58): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.151-632T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95676271 | |||||||
| chr5:95676504 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.151-865G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95676504 | |||||||
| chr5:95677116 | C | T | 1 | a0001c0001t0018g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.151-1477G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95677116 | |||||||
| chr5:95677123 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(53): Show |
114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.151-1484A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95677123 | |||||||
| chr5:95677227 | T | A | 10 | a0001c0001t0001g0032 a0001c0001t0005g0045 a0001c0001t0005g0132 others(7): Show |
21 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.151-1588A>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95677227 | |||||||
| chr5:95677314 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-1675G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95677314 | |||||||
| chr5:95677380 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.151-1741T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95677380 | |||||||
| chr5:95677872 | A | T | 1 | a0001c0001t0001g0017 | 4 | HG01069.hp2 HG01071.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-2233T>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95677872 | |||||||
| chr5:95677937 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.151-2298T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95677937 | |||||||
| chr5:95678112 | C | T | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0156 others(31): Show |
71 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.151-2473G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678112 | |||||||
| chr5:95678115 | A | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(113): Show |
230 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.151-2476T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678115 | |||||||
| chr5:95678117 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0102 a0001c0001t0001g0103 |
6 | NA18612.hp1 NA18974.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-2478G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678117 | |||||||
| chr5:95678341 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(107): Show |
221 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.151-2702A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678341 | |||||||
| chr5:95678367 | A | G | 1 | a0002c0003t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.151-2728T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678367 | |||||||
| chr5:95678512 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.151-2873G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678512 | |||||||
| chr5:95678603 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(58): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.151-2964C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678603 | |||||||
| chr5:95678635 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0099 others(2): Show |
8 | HG01255.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.151-2996T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678635 | |||||||
| chr5:95678703 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.151-3064A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678703 | |||||||
| chr5:95678737 | T | A | 1 | a0001c0002t0002g0012 | 5 | HG00323.hp1 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-3098A>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95678737 | |||||||
| chr5:95679214 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0006g0161 |
5 | HG00597.hp2 NA18961.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+3314C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679214 | |||||||
| chr5:95679287 | G | A | 1 | a0001c0001t0009g0162 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.150+3241C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679287 | |||||||
| chr5:95679313 | C | T | 1 | a0002c0003t0001g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.150+3215G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679313 | |||||||
| chr5:95679393 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0099 others(2): Show |
8 | HG01255.hp1 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+3135T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679393 | |||||||
| chr5:95679590 | T | C | 1 | a0001c0001t0004g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+2938A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679590 | |||||||
| chr5:95679607 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.150+2921G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679607 | |||||||
| chr5:95679858 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.150+2670G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679858 | |||||||
| chr5:95679908 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.150+2620C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679908 | |||||||
| chr5:95679924 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.150+2604T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679924 | |||||||
| chr5:95679928 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.150+2600G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679928 | |||||||
| chr5:95679971 | C | T | 1 | a0001c0001t0002g0047 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.150+2557G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679971 | |||||||
| chr5:95679993 | G | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(60): Show |
126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.150+2535C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95679993 | |||||||
| chr5:95680035 | C | T | 2 | a0001c0001t0005g0045 a0001c0001t0005g0132 |
3 | HG01884.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.150+2493G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680035 | |||||||
| chr5:95680092 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0163 |
2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.150+2436C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680092 | |||||||
| chr5:95680117 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0005g0045 a0001c0001t0005g0132 others(6): Show |
20 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.150+2411G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680117 | |||||||
| chr5:95680125 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0015g0096 |
2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.150+2403G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680125 | |||||||
| chr5:95680441 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 |
7 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+2087G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680441 | |||||||
| chr5:95680640 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0163 |
2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.150+1888G>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680640 | |||||||
| chr5:95680689 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.150+1839A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680689 | |||||||
| chr5:95680731 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+1797T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680731 | |||||||
| chr5:95680977 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.150+1551T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95680977 | |||||||
| chr5:95681041 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.150+1487C>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681041 | |||||||
| chr5:95681092 | C | G | 1 | a0001c0001t0008g0046 | 2 | HG02056.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.150+1436G>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681092 | |||||||
| chr5:95681118 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.150+1410A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681118 | |||||||
| chr5:95681138 | T | C | 1 | a0002c0003t0001g0136 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.150+1390A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681138 | |||||||
| chr5:95681437 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.150+1091T>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681437 | |||||||
| chr5:95681602 | G | A | 34 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0156 others(31): Show |
71 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.150+926C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681602 | |||||||
| chr5:95681689 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.150+839C>T | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681689 | |||||||
| chr5:95681780 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.150+748G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681780 | |||||||
| chr5:95681827 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(59): Show |
125 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.150+701G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681827 | |||||||
| chr5:95681853 | A | G | 2 | a0001c0002t0002g0057 a0001c0002t0004g0056 |
2 | HG02109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.150+675T>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681853 | |||||||
| chr5:95681901 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0005g0045 a0001c0001t0005g0132 others(6): Show |
20 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.150+627G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95681901 | |||||||
| chr5:95682023 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(107): Show |
221 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.150+505A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95682023 | |||||||
| chr5:95682148 | T | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0165 |
17 | HG00738.hp2 HG01175.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.150+380A>C | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95682148 | |||||||
| chr5:95682292 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.150+236A>G | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 2/4 | chr5 | 95682292 | |||||||
| chr5:95682678 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(54): Show |
115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.62-62C>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 1/4 | chr5 | 95682678 | |||||||
| chr5:95682702 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.62-86G>A | SPATA9 | ENSG00000145757.16 | transcript | ENST00000274432.13 | protein_coding | 1/4 | chr5 | 95682702 |