Item | Value |
---|---|
geneid | 353324 |
ensemblid | ENSG00000186451.2 |
hgncid | 23221 |
symbol | SPATA12 |
name | spermatogenesis associated 12 |
refseq_nuc | NM_181727.2 |
refseq_prot | NP_859078.1 |
ensembl_nuc | ENST00000334325.2 |
ensembl_prot | ENSP00000335392.1 |
mane_status | MANE Select |
chr | chr3 |
start | 57060664 |
end | 57075432 |
strand | + |
ver | v1.2 |
region | chr3:57060664-57075432 |
region5000 | chr3:57055664-57080432 |
regionname0 | SPATA12_chr3_57060664_57075432 |
regionname5000 | SPATA12_chr3_57055664_57080432 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 190 | 433 | 97 | 73 | 199 | 15 | 47 | 155 | SPATA12_chr3_57055664_57080432 | SPATA12 | MSSSA others(185): Show |
chr3 | 57055664 | 57080432 |
a0002 | 0/0 | 190 | 6 | 0 | 3 | 1 | 1 | 1 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | MSSSA others(185): Show |
chr3 | 57055664 | 57080432 |
a0003 | 0/0 | 190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | MSSSA others(185): Show |
chr3 | 57055664 | 57080432 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 570 | 432 | 97 | 73 | 198 | 15 | 47 | SPATA12_chr3_57055664_57080432 | SPATA12 | ATGTC others(565): Show |
chr3 | 57055664 | 57080432 | ||
a0001c0004 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ATGTC others(565): Show |
chr3 | 57055664 | 57080432 | ||
a0002c0002 | 0/0 | 570 | 6 | 0 | 3 | 1 | 1 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | ATGTC others(565): Show |
chr3 | 57055664 | 57080432 | ||
a0003c0003 | 0/0 | 570 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ATGTC others(565): Show |
chr3 | 57055664 | 57080432 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2190 | 182 | 59 | 42 | 36 | 14 | 29 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0002 | 0/0 | 2190 | 102 | 2 | 1 | 96 | 0 | 3 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0003 | 0/0 | 2190 | 100 | 5 | 25 | 59 | 0 | 11 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0004 | 0/0 | 2190 | 19 | 18 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0006 | 0/0 | 2190 | 5 | 4 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | AAAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0007 | 0/0 | 2190 | 5 | 0 | 0 | 1 | 0 | 4 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0008 | 0/0 | 2190 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0009 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0010 | 0/0 | 2190 | 2 | 0 | 1 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0011 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0012 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0014 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0015 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0016 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0017 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0018 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0019 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0020 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0001t0021 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0001c0004t0003 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0002c0002t0005 | 0/0 | 2190 | 6 | 0 | 3 | 1 | 1 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
a0003c0003t0013 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | ACAGT others(2185): Show |
chr3 | 57055664 | 57080432 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0003 | 0/0 | 14 | 1 | 7 | 0 | 2 | 4 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0004 | 0/0 | 19 | 1 | 4 | 8 | 3 | 3 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0007 | 0/0 | 6 | 2 | 3 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0018 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0025 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0030 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0033 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0060 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0002 | 0/0 | 21 | 0 | 0 | 21 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0006 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0001 | 0/0 | 16 | 1 | 5 | 7 | 0 | 3 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0005 | 0/0 | 14 | 0 | 2 | 12 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0010 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0007g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0008g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0009g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0010g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0010g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0012g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0015g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0016g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0018g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0019g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0020g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0001t0021g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0001c0004t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0002c0002t0005g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0002c0002t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0002c0002t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0002c0002t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
a0003c0003t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00099 | hp2 | a0002 | c0002 | t0005 | g0166 | EUR | GBR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00408 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00639 | hp1 | a0001 | c0001 | t0017 | g0001 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00639 | hp2 | a0002 | c0002 | t0005 | g0052 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00735 | hp1 | a0001 | c0001 | t0016 | g0003 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01099 | hp1 | a0002 | c0002 | t0005 | g0052 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0161 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01346 | hp1 | a0002 | c0002 | t0005 | g0165 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01496 | hp2 | a0001 | c0001 | t0010 | g0100 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02132 | hp2 | a0001 | c0001 | t0021 | g0006 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CDX | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CDX | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02523 | hp2 | a0001 | c0001 | t0015 | g0008 | EAS | KHV | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02970 | hp2 | a0001 | c0001 | t0014 | g0007 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03017 | hp1 | a0002 | c0002 | t0005 | g0213 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03130 | hp1 | a0003 | c0003 | t0013 | g0159 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03209 | hp2 | a0001 | c0001 | t0018 | g0186 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | ESN | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | GWD | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03654 | hp1 | a0001 | c0001 | t0007 | g0007 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0007 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0018 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0058 | SAS | STU | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | YRI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0043 | EAS | CHB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18947 | hp1 | a0002 | c0002 | t0005 | g0058 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19011 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | LWK | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | LWK | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19054 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19064 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19074 | hp1 | a0001 | c0004 | t0003 | g0123 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | YRI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20752 | hp2 | a0001 | c0001 | t0010 | g0212 | EUR | TSI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | TSI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02486 | hp2 | a0001 | c0001 | t0020 | g0181 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | ACB | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | MSL | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | USA | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
HG06807 | hp2 | a0001 | c0001 | t0019 | g0197 | AFR | USA | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | USA | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | LWK | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0124 | REF | REF | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | SPATA12_chr3_57055664_57080432 | SPATA12 | chr3 | 57055664 | 57080432 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57074073 | C | T | 1 | a0002 | 6 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(3): Show |
missense_variant | MODERATE | c.379C>T | p.Pro127Ser | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 831/2190 | 379/573 | 127/190 | chr3 | 57074073 | |||
chr3:57074254 | A | G | 1 | a0003 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.560A>G | p.His187Arg | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 1012/2190 | 560/573 | 187/190 | chr3 | 57074254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57073886 | C | T | 1 | a0001c0004 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.192C>T | p.Ala64Ala | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 644/2190 | 192/573 | 64/190 | chr3 | 57073886 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57060665 | C | A | 1 | a0001c0001t0006 | 5 | HG01099.hp2 HG01884.hp1 HG03139.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-451C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/2 | 13030 | chr3 | 57060665 | ||||||
chr3:57073436 | C | T | 1 | a0001c0001t0021 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-259C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 259 | chr3 | 57073436 | ||||||
chr3:57073485 | A | C | 4 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0019 others(1): Show |
24 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-210A>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | chr3 | 57073485 | |||||||
chr3:57073544 | G | A | 1 | a0001c0001t0012 | 1 | NA19054.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 151 | chr3 | 57073544 | ||||||
chr3:57073551 | T | C | 1 | a0003c0003t0013 | 1 | HG03130.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-144T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | chr3 | 57073551 | |||||||
chr3:57074372 | G | A | 1 | a0001c0001t0007 | 5 | HG03654.hp1 HG03688.hp1 HG03834.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*105G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 105 | chr3 | 57074372 | ||||||
chr3:57074380 | C | T | 1 | a0001c0001t0018 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 113 | chr3 | 57074380 | ||||||
chr3:57074473 | G | A | 1 | a0002c0002t0005 | 6 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*206G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 206 | chr3 | 57074473 | ||||||
chr3:57074484 | T | G | 1 | a0001c0001t0014 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217T>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 217 | chr3 | 57074484 | ||||||
chr3:57074523 | C | A | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0015 others(2): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 256 | chr3 | 57074523 | ||||||
chr3:57074715 | C | T | 1 | a0001c0001t0020 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*448C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 448 | chr3 | 57074715 | ||||||
chr3:57074762 | G | A | 1 | a0001c0001t0010 | 2 | HG01496.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*495G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 495 | chr3 | 57074762 | ||||||
chr3:57074817 | T | C | 4 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0016 others(1): Show |
7 | HG00735.hp1 HG02451.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*550T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 550 | chr3 | 57074817 | ||||||
chr3:57074844 | A | G | 1 | a0001c0001t0015 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*577A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 577 | chr3 | 57074844 | ||||||
chr3:57075039 | G | T | 1 | a0001c0001t0017 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*772G>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 772 | chr3 | 57075039 | ||||||
chr3:57075067 | T | C | 5 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0017 others(2): Show |
105 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*800T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 800 | chr3 | 57075067 | ||||||
chr3:57075398 | C | A | 1 | a0001c0001t0008 | 3 | HG00408.hp1 NA18612.hp2 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1131C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 1131 | chr3 | 57075398 | ||||||
chr3:57075411 | T | A | 2 | a0001c0001t0009 a0001c0001t0011 |
5 | HG02451.hp2 HG02723.hp1 HG03516.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1144T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 2/2 | 1144 | chr3 | 57075411 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:57060817 | C | A | 1 | a0001c0001t0002g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-330+31C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57060817 | |||||||
chr3:57060823 | A | AAC | 4 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG01891.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+51_-330+52dup others(2): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57060823 | ||||||
chr3:57060871 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-330+85C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57060871 | |||||||
chr3:57060905 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-330+119A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57060905 | |||||||
chr3:57060993 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0224 others(1): Show |
4 | HG02559.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-330+207C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57060993 | |||||||
chr3:57061171 | C | T | 1 | a0001c0001t0004g0223 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-330+385C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57061171 | |||||||
chr3:57061218 | T | C | 1 | a0001c0001t0002g0034 | 2 | NA19055.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-330+432T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57061218 | |||||||
chr3:57061307 | T | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
398 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.-330+521T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57061307 | |||||||
chr3:57061707 | T | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.-330+921T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57061707 | |||||||
chr3:57062129 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-330+1343T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57062129 | |||||||
chr3:57062170 | T | TCAAA | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.-330+1386_-330+138 others(8): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57062170 | ||||||
chr3:57062484 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.-330+1698A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57062484 | |||||||
chr3:57062698 | A | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0191 |
6 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+1912A>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57062698 | |||||||
chr3:57062702 | G | GCA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0055 others(3): Show |
12 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-330+1933_-330+193 others(6): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57062702 | ||||||
chr3:57062887 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0191 |
6 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+2101G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57062887 | |||||||
chr3:57063024 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0191 |
6 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+2238T>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57063024 | |||||||
chr3:57063096 | G | C | 1 | a0001c0001t0002g0071 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-330+2310G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57063096 | |||||||
chr3:57063143 | G | A | 1 | a0003c0003t0013g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-330+2357G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57063143 | |||||||
chr3:57063284 | GCAGC | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(95): Show |
164 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.-330+2505_-330+250 others(8): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57063284 | ||||||
chr3:57063300 | A | C | 1 | a0001c0001t0004g0206 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-330+2514A>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57063300 | |||||||
chr3:57063706 | C | T | 6 | a0001c0001t0001g0056 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
7 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+2920C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57063706 | |||||||
chr3:57063959 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0045 others(14): Show |
22 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-330+3173C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57063959 | |||||||
chr3:57064037 | G | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.-330+3251G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57064037 | |||||||
chr3:57064064 | C | G | 1 | a0001c0001t0003g0203 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-330+3278C>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57064064 | |||||||
chr3:57064284 | C | T | 1 | a0001c0001t0018g0186 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-330+3498C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57064284 | |||||||
chr3:57064323 | C | CT | 18 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
23 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-330+3546dupT | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57064323 | ||||||
chr3:57064467 | T | G | 2 | a0001c0001t0001g0121 a0001c0001t0004g0223 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-330+3681T>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57064467 | |||||||
chr3:57064679 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(78): Show |
146 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-330+3893C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57064679 | |||||||
chr3:57064831 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-330+4045C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57064831 | |||||||
chr3:57064928 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(26): Show |
55 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-330+4142T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57064928 | |||||||
chr3:57065176 | C | A | 1 | a0001c0001t0003g0198 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-330+4390C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065176 | |||||||
chr3:57065176 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(78): Show |
146 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-330+4390C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065176 | |||||||
chr3:57065222 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-330+4436G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065222 | |||||||
chr3:57065223 | A | G | 1 | a0001c0001t0002g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-330+4437A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065223 | |||||||
chr3:57065306 | A | G | 1 | a0001c0001t0002g0054 | 2 | HG00423.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-330+4520A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065306 | |||||||
chr3:57065329 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-330+4543T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065329 | |||||||
chr3:57065330 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0143 a0001c0001t0002g0013 |
5 | NA18950.hp1 NA18951.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.-330+4544G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065330 | |||||||
chr3:57065333 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-330+4547C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065333 | |||||||
chr3:57065444 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0004g0225 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-330+4658G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065444 | |||||||
chr3:57065653 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0003g0072 |
5 | HG01192.hp1 HG01928.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-330+4867G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065653 | |||||||
chr3:57065747 | G | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(77): Show |
140 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-330+4961G>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065747 | |||||||
chr3:57065759 | C | T | 4 | a0001c0001t0004g0115 a0001c0001t0004g0204 a0001c0001t0004g0205 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+4973C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065759 | |||||||
chr3:57065778 | T | C | 40 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(37): Show |
76 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-330+4992T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065778 | |||||||
chr3:57065791 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0006g0015 a0001c0001t0006g0161 |
7 | HG01099.hp2 HG01884.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-330+5005G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065791 | |||||||
chr3:57065825 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-330+5039C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065825 | |||||||
chr3:57065840 | T | G | 17 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0044 others(14): Show |
24 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.-330+5054T>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57065840 | |||||||
chr3:57066040 | C | CA | 6 | a0001c0001t0001g0056 a0001c0001t0001g0164 a0001c0001t0001g0210 others(3): Show |
7 | HG02922.hp1 HG03453.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+5266dupA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57066040 | ||||||
chr3:57066040 | CA | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0160 others(1): Show |
7 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+5266delA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57066040 | ||||||
chr3:57066043 | A | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0191 |
6 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-330+5257A>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066043 | |||||||
chr3:57066044 | A | AC | 7 | a0001c0001t0004g0028 a0001c0001t0004g0057 a0001c0001t0004g0180 others(4): Show |
12 | HG02451.hp2 HG02486.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-330+5258_-330+525 others(5): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066044 | |||||||
chr3:57066049 | AAAAC | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(75): Show |
138 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-330+5264_-330+526 others(8): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066049 | |||||||
chr3:57066085 | G | C | 1 | a0001c0001t0002g0038 | 2 | NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-330+5299G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066085 | |||||||
chr3:57066260 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-330+5474T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066260 | |||||||
chr3:57066411 | G | A | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG02165.hp1 NA18959.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-330+5625G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066411 | |||||||
chr3:57066510 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-330+5724G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066510 | |||||||
chr3:57066616 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-330+5830G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066616 | |||||||
chr3:57066945 | T | C | 1 | a0001c0001t0004g0187 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-330+6159T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066945 | |||||||
chr3:57066967 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-330+6181T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57066967 | |||||||
chr3:57067221 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0226 |
3 | HG02109.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-329-6145G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067221 | |||||||
chr3:57067315 | C | A | 1 | a0001c0001t0003g0076 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-329-6051C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067315 | |||||||
chr3:57067348 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-329-6018G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067348 | |||||||
chr3:57067377 | C | G | 1 | a0003c0003t0013g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-329-5989C>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067377 | |||||||
chr3:57067412 | G | A | 1 | a0003c0003t0013g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-329-5954G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067412 | |||||||
chr3:57067454 | A | AAAT | 28 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0056 others(25): Show |
34 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(31): Show |
intron_variant | MODIFIER | c.-329-5877_-329-587 others(7): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067454 | ||||||
chr3:57067454 | A | AAATAAT | 21 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0055 others(18): Show |
36 | HG01081.hp1 HG01891.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.-329-5880_-329-587 others(10): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067454 | ||||||
chr3:57067454 | A | AAATAATA others(2): Show |
64 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0035 others(61): Show |
114 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-329-5883_-329-587 others(13): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067454 | ||||||
chr3:57067454 | A | AAATAATA others(5): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0021 others(43): Show |
87 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-329-5886_-329-587 others(16): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067454 | ||||||
chr3:57067454 | A | AAATAATA others(8): Show |
8 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0078 others(5): Show |
11 | HG01346.hp1 HG02280.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.-329-5889_-329-587 others(19): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067454 | ||||||
chr3:57067454 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-329-5912A>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067454 | |||||||
chr3:57067454 | AAAT | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0164 others(11): Show |
33 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-329-5877_-329-587 others(7): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067454 | ||||||
chr3:57067454 | AAATAAT | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0221 a0001c0001t0001g0224 others(5): Show |
9 | HG01255.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-329-5880_-329-587 others(10): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067454 | ||||||
chr3:57067492 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-329-5874T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067492 | |||||||
chr3:57067494 | T | G | 1 | a0001c0001t0003g0198 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-329-5872T>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067494 | |||||||
chr3:57067587 | C | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | NA18940.hp2 NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-329-5779C>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067587 | |||||||
chr3:57067624 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-329-5742C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067624 | |||||||
chr3:57067696 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0064 |
3 | HG03453.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-329-5670G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067696 | |||||||
chr3:57067747 | C | T | 1 | a0001c0001t0001g0055 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-329-5619C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067747 | |||||||
chr3:57067815 | T | TA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(87): Show |
157 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-329-5539dupA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067815 | ||||||
chr3:57067815 | T | TAA | 7 | a0001c0001t0001g0056 a0001c0001t0001g0095 a0001c0001t0001g0118 others(4): Show |
8 | HG00609.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-329-5540_-329-553 others(6): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067815 | ||||||
chr3:57067828 | C | A | 2 | a0001c0001t0003g0079 a0001c0001t0003g0200 |
2 | NA18941.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-329-5538C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067828 | |||||||
chr3:57067859 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-329-5507G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067859 | |||||||
chr3:57067868 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.-329-5498T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067868 | |||||||
chr3:57067898 | G | A | 1 | a0001c0001t0003g0067 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-329-5468G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067898 | |||||||
chr3:57067907 | G | A | 15 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
20 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-329-5459G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067907 | |||||||
chr3:57067968 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-329-5398C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067968 | |||||||
chr3:57067984 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-329-5382C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57067984 | |||||||
chr3:57067989 | C | CA | 16 | a0001c0001t0001g0121 a0001c0001t0001g0224 a0001c0001t0002g0073 others(13): Show |
22 | HG01255.hp1 HG01891.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.-329-5369dupA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57067989 | ||||||
chr3:57068015 | C | T | 3 | a0002c0002t0005g0052 a0002c0002t0005g0165 a0002c0002t0005g0166 |
4 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-5351C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068015 | |||||||
chr3:57068154 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0003g0027 |
3 | HG02071.hp2 HG02155.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-329-5212C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068154 | |||||||
chr3:57068156 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0142 |
3 | HG02040.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-329-5210C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068156 | |||||||
chr3:57068162 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0191 |
6 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-329-5204C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068162 | |||||||
chr3:57068168 | T | C | 1 | a0001c0001t0003g0096 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-329-5198T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068168 | |||||||
chr3:57068168 | T | TAC | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(95): Show |
193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-329-5177_-329-517 others(6): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57068168 | ||||||
chr3:57068168 | T | TACAC | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(94): Show |
168 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.-329-5179_-329-517 others(8): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57068168 | ||||||
chr3:57068168 | T | TACACAC | 12 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0066 others(9): Show |
15 | HG02258.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-5181_-329-517 others(10): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57068168 | ||||||
chr3:57068168 | TAC | T | 3 | a0002c0002t0005g0052 a0002c0002t0005g0165 a0002c0002t0005g0166 |
4 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-5177_-329-517 others(6): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57068168 | ||||||
chr3:57068174 | C | CACACAG | 2 | a0001c0001t0001g0017 a0001c0001t0001g0191 |
5 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-5187_-329-518 others(10): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57068174 | ||||||
chr3:57068269 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-329-5097C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068269 | |||||||
chr3:57068330 | C | T | 3 | a0002c0002t0005g0052 a0002c0002t0005g0165 a0002c0002t0005g0166 |
4 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-5036C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068330 | |||||||
chr3:57068487 | T | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0222 |
6 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-329-4879T>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068487 | |||||||
chr3:57068587 | T | C | 7 | a0001c0001t0004g0028 a0001c0001t0004g0057 a0001c0001t0004g0180 others(4): Show |
12 | HG02451.hp2 HG02486.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-329-4779T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068587 | |||||||
chr3:57068652 | C | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0196 a0001c0001t0001g0217 others(6): Show |
10 | NA18947.hp2 NA18962.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.-329-4714C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068652 | |||||||
chr3:57068655 | C | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0191 |
5 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-4711C>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068655 | |||||||
chr3:57068819 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(78): Show |
144 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-329-4547A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068819 | |||||||
chr3:57068822 | C | T | 42 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(39): Show |
80 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-329-4544C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068822 | |||||||
chr3:57068916 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-329-4450C>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068916 | |||||||
chr3:57068919 | A | AT | 55 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0048 others(52): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-329-4429dupT | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57068919 | ||||||
chr3:57068919 | AT | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0188 others(7): Show |
12 | HG01069.hp2 HG02135.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-329-4429delT | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57068919 | ||||||
chr3:57068921 | T | C | 7 | a0001c0001t0004g0028 a0001c0001t0004g0057 a0001c0001t0004g0180 others(4): Show |
12 | HG02451.hp2 HG02486.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-329-4445T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068921 | |||||||
chr3:57068933 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0188 others(2): Show |
7 | HG02572.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-4433T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068933 | |||||||
chr3:57068953 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0167 others(7): Show |
17 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.-329-4413G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57068953 | |||||||
chr3:57069057 | G | T | 3 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 |
3 | HG02559.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-329-4309G>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069057 | |||||||
chr3:57069096 | T | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(35): Show |
76 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-329-4270T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069096 | |||||||
chr3:57069112 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-329-4254G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069112 | |||||||
chr3:57069135 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.-329-4231C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069135 | |||||||
chr3:57069212 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-329-4154C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069212 | |||||||
chr3:57069318 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-329-4048T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069318 | |||||||
chr3:57069320 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-329-4046T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069320 | |||||||
chr3:57069321 | T | C | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-329-4045T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069321 | |||||||
chr3:57069324 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-329-4042A>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069324 | |||||||
chr3:57069325 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-329-4041A>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069325 | |||||||
chr3:57069376 | A | AAC | 23 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0110 others(20): Show |
37 | HG00642.hp2 HG01069.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.-329-3956_-329-395 others(6): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069376 | A | AACAC | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(33): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.-329-3958_-329-395 others(8): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069376 | A | AACACAC | 20 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0030 others(17): Show |
30 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-329-3960_-329-395 others(10): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069376 | A | AACACACA others(1): Show |
5 | a0001c0001t0001g0121 a0001c0001t0001g0130 a0001c0001t0001g0169 others(2): Show |
6 | HG00323.hp1 HG01891.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-329-3962_-329-395 others(12): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069376 | A | AACACACA others(3): Show |
3 | a0001c0001t0004g0057 a0001c0001t0004g0162 a0001c0001t0004g0187 |
4 | HG01255.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-3964_-329-395 others(14): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069376 | A | AACACACA others(7): Show |
5 | a0001c0001t0004g0028 a0001c0001t0004g0180 a0001c0001t0004g0223 others(2): Show |
9 | HG02451.hp2 HG02723.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.-329-3968_-329-395 others(18): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069376 | AAC | A | 44 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0033 others(41): Show |
59 | HG00408.hp1 HG01070.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-329-3956_-329-395 others(6): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069376 | AACAC | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0044 others(8): Show |
18 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-329-3958_-329-395 others(8): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069376 | ||||||
chr3:57069386 | C | CACACAT | 3 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 |
3 | HG02559.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-329-3975_-329-397 others(10): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069386 | ||||||
chr3:57069412 | T | C | 2 | a0001c0001t0003g0001 a0001c0001t0003g0005 |
2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-329-3954T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069412 | |||||||
chr3:57069414 | G | C | 2 | a0001c0001t0001g0224 a0001c0001t0004g0225 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-329-3952G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069414 | |||||||
chr3:57069415 | T | A | 2 | a0001c0001t0001g0224 a0001c0001t0004g0225 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-329-3951T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069415 | |||||||
chr3:57069543 | A | G | 1 | a0003c0003t0013g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-329-3823A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069543 | |||||||
chr3:57069603 | C | T | 42 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(39): Show |
80 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-329-3763C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069603 | |||||||
chr3:57069648 | CT | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.-329-3708delT | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57069648 | ||||||
chr3:57069684 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(77): Show |
143 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.-329-3682C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069684 | |||||||
chr3:57069697 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0042 |
5 | HG01257.hp2 HG01258.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-3669T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069697 | |||||||
chr3:57069737 | G | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.-329-3629G>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069737 | |||||||
chr3:57069841 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(95): Show |
169 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-329-3525C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069841 | |||||||
chr3:57069857 | C | T | 1 | a0001c0001t0004g0028 | 3 | HG02723.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-329-3509C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069857 | |||||||
chr3:57069858 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-329-3508G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57069858 | |||||||
chr3:57070273 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-329-3093T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070273 | |||||||
chr3:57070324 | T | TTAGACTA others(17): Show |
12 | a0001c0001t0001g0224 a0001c0001t0004g0053 a0001c0001t0004g0115 others(9): Show |
13 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-329-3042_-329-304 others(28): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070324 | |||||||
chr3:57070400 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(95): Show |
169 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-329-2966C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070400 | |||||||
chr3:57070470 | G | C | 1 | a0001c0001t0002g0153 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-329-2896G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070470 | |||||||
chr3:57070512 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0003g0134 |
2 | NA18970.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-329-2854T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070512 | |||||||
chr3:57070550 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0191 |
6 | HG02145.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-329-2816A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070550 | |||||||
chr3:57070568 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-329-2798T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070568 | |||||||
chr3:57070578 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(150): Show |
263 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.-329-2788G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070578 | |||||||
chr3:57070644 | G | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
7 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-2722G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070644 | |||||||
chr3:57070694 | A | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.-329-2672A>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070694 | |||||||
chr3:57070742 | T | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(35): Show |
76 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-329-2624T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070742 | |||||||
chr3:57070745 | G | A | 1 | a0001c0001t0010g0100 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-329-2621G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070745 | |||||||
chr3:57070825 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(95): Show |
169 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-329-2541A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070825 | |||||||
chr3:57070971 | C | CA | 33 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0066 others(30): Show |
42 | HG01255.hp1 HG01515.hp2 HG01517.hp1 others(39): Show |
intron_variant | MODIFIER | c.-329-2379dupA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57070971 | ||||||
chr3:57070971 | CA | C | 5 | a0001c0001t0003g0127 a0001c0001t0003g0198 a0002c0002t0005g0052 others(2): Show |
6 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-329-2379delA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57070971 | ||||||
chr3:57070984 | AAAAGAAA others(1): Show |
A | 37 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(34): Show |
73 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-329-2370_-329-236 others(12): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57070984 | ||||||
chr3:57070988 | G | A | 12 | a0001c0001t0001g0224 a0001c0001t0004g0053 a0001c0001t0004g0115 others(9): Show |
13 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-329-2378G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57070988 | |||||||
chr3:57071023 | G | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(35): Show |
76 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-329-2343G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071023 | |||||||
chr3:57071038 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(95): Show |
169 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-329-2328C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071038 | |||||||
chr3:57071093 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(95): Show |
169 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-329-2273C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071093 | |||||||
chr3:57071174 | T | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0056 others(9): Show |
16 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-329-2192T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071174 | |||||||
chr3:57071232 | A | T | 19 | a0001c0001t0001g0224 a0001c0001t0004g0028 a0001c0001t0004g0053 others(16): Show |
25 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-329-2134A>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071232 | |||||||
chr3:57071388 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0051 others(11): Show |
35 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-329-1978G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071388 | |||||||
chr3:57071498 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-329-1868A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071498 | |||||||
chr3:57071659 | C | CA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0017 others(20): Show |
51 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-329-1690dupA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57071659 | ||||||
chr3:57071659 | CA | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(88): Show |
156 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-329-1690delA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57071659 | ||||||
chr3:57071715 | C | A | 1 | a0003c0003t0013g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-329-1651C>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071715 | |||||||
chr3:57071785 | A | G | 38 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(35): Show |
76 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-329-1581A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071785 | |||||||
chr3:57071856 | T | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0135 a0001c0001t0001g0136 |
5 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-329-1510T>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57071856 | |||||||
chr3:57071923 | TAA | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0114 |
4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-329-1441_-329-144 others(6): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57071923 | ||||||
chr3:57072117 | TAAC | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0149 others(35): Show |
76 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-329-1246_-329-124 others(7): Show |
SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57072117 | ||||||
chr3:57072206 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0154 |
2 | HG00597.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-329-1160T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072206 | |||||||
chr3:57072207 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0004g0225 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-329-1159T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072207 | |||||||
chr3:57072239 | A | T | 1 | a0001c0001t0003g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-329-1127A>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072239 | |||||||
chr3:57072318 | T | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0056 others(8): Show |
15 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-1048T>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072318 | |||||||
chr3:57072336 | G | C | 1 | a0001c0001t0002g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-329-1030G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072336 | |||||||
chr3:57072360 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-329-1006G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072360 | |||||||
chr3:57072443 | T | TA | 60 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-329-910dupA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57072443 | ||||||
chr3:57072483 | G | A | 15 | a0001c0001t0001g0224 a0001c0001t0004g0028 a0001c0001t0004g0053 others(12): Show |
21 | HG01255.hp1 HG01891.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-329-883G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072483 | |||||||
chr3:57072483 | G | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(55): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-329-883G>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072483 | |||||||
chr3:57072627 | A | G | 1 | a0001c0001t0007g0216 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-329-739A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072627 | |||||||
chr3:57072669 | G | C | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-329-697G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072669 | |||||||
chr3:57072726 | C | CA | 52 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0056 others(49): Show |
91 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-329-623dupA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57072726 | ||||||
chr3:57072726 | CA | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(56): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-329-623delA | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr3 | 57072726 | ||||||
chr3:57072743 | A | G | 1 | a0001c0001t0001g0051 | 2 | NA19082.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-329-623A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072743 | |||||||
chr3:57072832 | G | A | 3 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 |
3 | HG02559.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-329-534G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072832 | |||||||
chr3:57072839 | G | T | 1 | a0001c0001t0003g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-329-527G>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072839 | |||||||
chr3:57072881 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(92): Show |
161 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-329-485C>T | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57072881 | |||||||
chr3:57073021 | G | C | 7 | a0001c0001t0004g0028 a0001c0001t0004g0057 a0001c0001t0004g0180 others(4): Show |
12 | HG02451.hp2 HG02486.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-329-345G>C | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57073021 | |||||||
chr3:57073120 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-329-246A>G | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57073120 | |||||||
chr3:57073317 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-329-49G>A | SPATA12 | ENSG00000186451.2 | transcript | ENST00000334325.2 | protein_coding | 1/1 | chr3 | 57073317 |