Item | Value |
---|---|
geneid | 11137 |
ensemblid | ENSG00000136045.12 |
hgncid | 17015 |
symbol | PWP1 |
name | PWP1 homolog, endonuclein |
refseq_nuc | NM_007062.3 |
refseq_prot | NP_008993.1 |
ensembl_nuc | ENST00000412830.8 |
ensembl_prot | ENSP00000387365.3 |
mane_status | MANE Select |
chr | chr12 |
start | 107685799 |
end | 107713162 |
strand | + |
ver | v1.2 |
region | chr12:107685799-107713162 |
region5000 | chr12:107680799-107718162 |
regionname0 | PWP1_chr12_107685799_107713162 |
regionname5000 | PWP1_chr12_107680799_107718162 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 501 | 299 | 78 | 60 | 110 | 13 | 36 | 84 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0002 | 0/0 | 501 | 24 | 2 | 2 | 15 | 1 | 4 | 12 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0003 | 0/0 | 501 | 12 | 0 | 0 | 11 | 0 | 1 | 10 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0004 | 0/0 | 501 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0005 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0006 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0007 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0008 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
a0009 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | MNRSR others(496): Show |
chr12 | 107680799 | 107718162 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1503 | 277 | 57 | 59 | 110 | 13 | 36 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0001c0003 | 0/0 | 1503 | 18 | 17 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0001c0005 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0002c0002 | 0/0 | 1503 | 24 | 2 | 2 | 15 | 1 | 4 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0003c0004 | 0/0 | 1503 | 12 | 0 | 0 | 11 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0004c0006 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0005c0011 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0006c0008 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0007c0010 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0008c0009 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 | ||
a0009c0007 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | ATGAA others(1498): Show |
chr12 | 107680799 | 107718162 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2549 | 144 | 3 | 36 | 79 | 8 | 18 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0002 | 1/1 | 2549 | 111 | 39 | 22 | 27 | 4 | 17 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0003 | 0/0 | 2549 | 8 | 7 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0004 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0005 | 0/0 | 2549 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0006 | 0/0 | 2549 | 3 | 0 | 0 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0007 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0008 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0009 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0010 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0011 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0001t0012 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0003t0001 | 0/0 | 2549 | 18 | 17 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0001c0005t0004 | 0/0 | 2549 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0002c0002t0002 | 0/0 | 2549 | 24 | 2 | 2 | 15 | 1 | 4 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0003c0004t0002 | 0/0 | 2549 | 12 | 0 | 0 | 11 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0004c0006t0002 | 0/0 | 2549 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0005c0011t0007 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0006c0008t0002 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0007c0010t0002 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0008c0009t0001 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
a0009c0007t0002 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | AGCGG others(2544): Show |
chr12 | 107680799 | 107718162 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 0 | 9 | 8 | 1 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 3 | 1 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0002 | 0/0 | 17 | 0 | 6 | 7 | 0 | 4 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0003 | 1/0 | 12 | 9 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0010g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0012g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0005t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0005t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0005t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0004c0006t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0004c0006t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0005c0011t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0006c0008t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0007c0010t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0008c0009t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0009c0007t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0032 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00642 | hp1 | a0005 | c0011 | t0007 | g0042 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01261 | hp2 | a0006 | c0008 | t0002 | g0144 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0205 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02027 | hp1 | a0003 | c0004 | t0002 | g0048 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | CDX | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02293 | hp1 | a0001 | c0001 | t0010 | g0102 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02602 | hp2 | a0003 | c0004 | t0002 | g0009 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02647 | hp1 | a0001 | c0005 | t0004 | g0046 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0053 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0212 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02896 | hp1 | a0004 | c0006 | t0002 | g0220 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02897 | hp2 | a0004 | c0006 | t0002 | g0219 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0204 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03098 | hp1 | a0001 | c0005 | t0004 | g0045 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03453 | hp1 | a0007 | c0010 | t0002 | g0044 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03486 | hp1 | a0001 | c0005 | t0004 | g0017 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0207 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0193 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03942 | hp1 | a0008 | c0009 | t0001 | g0072 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CHB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18906 | hp2 | a0001 | c0005 | t0004 | g0017 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18954 | hp1 | a0003 | c0004 | t0002 | g0019 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18964 | hp1 | a0003 | c0004 | t0002 | g0047 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18983 | hp2 | a0003 | c0004 | t0002 | g0049 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18994 | hp2 | a0003 | c0004 | t0002 | g0009 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19004 | hp1 | a0003 | c0004 | t0002 | g0018 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19043 | hp2 | a0009 | c0007 | t0002 | g0089 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19055 | hp2 | a0003 | c0004 | t0002 | g0019 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19063 | hp2 | a0001 | c0001 | t0008 | g0100 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19065 | hp2 | a0003 | c0004 | t0002 | g0018 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19068 | hp2 | a0003 | c0004 | t0002 | g0009 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19081 | hp1 | a0003 | c0004 | t0002 | g0050 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ASW | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ASW | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | TSI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18955 | hp2 | a0003 | c0004 | t0002 | g0009 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0126 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0128 | REF | REF | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107688476 | G | A | 1 | a0003 | 12 | HG02027.hp1 HG02602.hp2 NA18954.hp1 others(9): Show |
missense_variant | MODERATE | c.101G>A | p.Arg34His | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 2/15 | 202/2549 | 101/1506 | 34/501 | chr12 | 107688476 | |||
chr12:107688682 | C | T | 1 | a0005 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.199C>T | p.Arg67Cys | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/15 | 300/2549 | 199/1506 | 67/501 | chr12 | 107688682 | |||
chr12:107688737 | G | A | 1 | a0009 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.254G>A | p.Arg85Lys | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/15 | 355/2549 | 254/1506 | 85/501 | chr12 | 107688737 | |||
chr12:107688797 | A | G | 1 | a0004 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.314A>G | p.Asp105Gly | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/15 | 415/2549 | 314/1506 | 105/501 | chr12 | 107688797 | |||
chr12:107696490 | A | C | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.519A>C | p.Glu173Asp | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/15 | 620/2549 | 519/1506 | 173/501 | chr12 | 107696490 | |||
chr12:107702992 | G | C | 1 | a0002 | 24 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(21): Show |
missense_variant | MODERATE | c.864G>C | p.Leu288Phe | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/15 | 965/2549 | 864/1506 | 288/501 | chr12 | 107702992 | |||
chr12:107708980 | A | G | 1 | a0008 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1132A>G | p.Ile378Val | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 12/15 | 1233/2549 | 1132/1506 | 378/501 | chr12 | 107708980 | |||
chr12:107712116 | G | A | 1 | a0006 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1402G>A | p.Glu468Lys | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 1503/2549 | 1402/1506 | 468/501 | chr12 | 107712116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107692857 | C | T | 1 | a0001c0005 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.363C>T | p.Tyr121Tyr | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 4/15 | 464/2549 | 363/1506 | 121/501 | chr12 | 107692857 | |||
chr12:107702941 | T | C | 1 | a0001c0003 | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
synonymous_variant | LOW | c.813T>C | p.Val271Val | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/15 | 914/2549 | 813/1506 | 271/501 | chr12 | 107702941 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107685811 | C | T | 1 | a0001c0001t0012 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-89C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/15 | 89 | chr12 | 107685811 | ||||||
chr12:107685856 | A | G | 1 | a0001c0001t0011 | 1 | HG02717.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/15 | chr12 | 107685856 | |||||||
chr12:107712227 | T | G | 1 | a0001c0001t0008 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 7 | chr12 | 107712227 | ||||||
chr12:107712281 | T | C | 4 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(1): Show |
11 | HG00642.hp1 HG01516.hp1 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*61T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 61 | chr12 | 107712281 | ||||||
chr12:107712378 | G | A | 1 | a0001c0001t0005 | 4 | HG02622.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*158G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 158 | chr12 | 107712378 | ||||||
chr12:107712480 | T | C | 2 | a0001c0001t0004 a0001c0005t0004 |
5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*260T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 260 | chr12 | 107712480 | ||||||
chr12:107712542 | G | A | 1 | a0001c0001t0010 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 322 | chr12 | 107712542 | ||||||
chr12:107712630 | G | C | 2 | a0001c0001t0007 a0005c0011t0007 |
2 | HG00642.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 410 | chr12 | 107712630 | ||||||
chr12:107712647 | C | T | 1 | a0001c0001t0006 | 3 | HG02155.hp1 NA18972.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*427C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 427 | chr12 | 107712647 | ||||||
chr12:107712771 | T | C | 2 | a0001c0001t0004 a0001c0005t0004 |
5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*551T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 551 | chr12 | 107712771 | ||||||
chr12:107713045 | G | A | 1 | a0001c0001t0009 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 825 | chr12 | 107713045 | ||||||
chr12:107713138 | T | C | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(6): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*918T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 918 | chr12 | 107713138 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107686044 | C | A | 1 | a0001c0005t0004g0017 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.72+73C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686044 | |||||||
chr12:107686089 | T | G | 1 | a0007c0010t0002g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+118T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686089 | |||||||
chr12:107686116 | G | T | 2 | a0001c0001t0005g0016 a0001c0001t0005g0223 |
4 | HG02622.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+145G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686116 | |||||||
chr12:107686193 | C | A | 1 | a0001c0005t0004g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.72+222C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686193 | |||||||
chr12:107686200 | C | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(92): Show |
133 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.72+229C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686200 | |||||||
chr12:107686205 | C | A | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+234C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686205 | |||||||
chr12:107686255 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.72+284G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686255 | |||||||
chr12:107686486 | T | A | 7 | a0003c0004t0002g0009 a0003c0004t0002g0018 a0003c0004t0002g0019 others(4): Show |
12 | HG02027.hp1 HG02602.hp2 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+515T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686486 | |||||||
chr12:107686502 | A | T | 22 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0033 others(19): Show |
42 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.72+531A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686502 | |||||||
chr12:107686662 | C | T | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72+691C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686662 | |||||||
chr12:107686735 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.72+764G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686735 | |||||||
chr12:107686760 | A | G | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.72+789A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686760 | |||||||
chr12:107686767 | G | C | 1 | a0001c0001t0006g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.72+796G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686767 | |||||||
chr12:107686773 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72+802T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686773 | |||||||
chr12:107686811 | AAAAAATT others(1058): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.72+851_73-562del | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686811 | ||||||
chr12:107686834 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.72+863T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686834 | |||||||
chr12:107686837 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.72+866A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686837 | |||||||
chr12:107686838 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.72+867T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686838 | |||||||
chr12:107686969 | CA | C | 47 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0012 others(44): Show |
75 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.72+1029delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | ||||||
chr12:107686969 | CAA | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0025 a0001c0001t0002g0026 others(4): Show |
9 | HG00558.hp1 HG01167.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+1028_72+1029del others(2): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | ||||||
chr12:107686969 | CAAA | C | 3 | a0001c0001t0005g0016 a0001c0001t0005g0223 a0001c0005t0004g0017 |
6 | HG02622.hp1 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+1027_72+1029del others(3): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | ||||||
chr12:107686969 | CAAAAA | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(4): Show |
9 | HG01109.hp2 HG01167.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+1025_72+1029del others(5): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | ||||||
chr12:107686969 | CAAAAAA | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(24): Show |
52 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.72+1024_72+1029del others(6): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | ||||||
chr12:107686969 | CAAAAAAA others(13): Show |
C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(110): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.72+1010_72+1029del others(20): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | ||||||
chr12:107687101 | C | T | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+1130C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687101 | |||||||
chr12:107687402 | C | T | 60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(57): Show |
88 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.73-1046C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687402 | |||||||
chr12:107687440 | C | T | 36 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(33): Show |
47 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.73-1008C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687440 | |||||||
chr12:107687629 | G | A | 7 | a0003c0004t0002g0009 a0003c0004t0002g0018 a0003c0004t0002g0019 others(4): Show |
11 | HG02027.hp1 NA18954.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-819G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687629 | |||||||
chr12:107687705 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.73-743G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687705 | |||||||
chr12:107687840 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(97): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.73-608C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687840 | |||||||
chr12:107687979 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.73-469C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687979 | |||||||
chr12:107687983 | A | G | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.73-465A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687983 | |||||||
chr12:107688005 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.73-443T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688005 | |||||||
chr12:107688030 | C | CA | 13 | a0001c0001t0001g0065 a0001c0001t0002g0012 a0001c0001t0002g0066 others(10): Show |
15 | HG00423.hp1 HG01358.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.73-388dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA | 5 | a0001c0001t0001g0040 a0001c0001t0001g0191 a0001c0001t0006g0148 others(2): Show |
6 | HG01243.hp2 HG01515.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-394_73-388dupAA others(5): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA others(1): Show |
21 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(18): Show |
33 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-395_73-388dupAA others(6): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA others(2): Show |
22 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0037 others(19): Show |
34 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-396_73-388dupAA others(7): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA others(3): Show |
14 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0055 others(11): Show |
17 | HG00438.hp1 HG01433.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.73-397_73-388dupAA others(8): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
5 | HG01123.hp1 HG01978.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-398_73-388dupAA others(9): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0151 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.73-403_73-388dupAA others(14): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-404_73-388dupAA others(15): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0149 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.73-405_73-388dupAA others(16): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | CA | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(59): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-388delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | CAA | C | 9 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(6): Show |
9 | HG01515.hp1 HG02976.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-389_73-388delAA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-397_73-388delAA others(8): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0216 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.73-400_73-388delAA others(11): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.73-401_73-388delAA others(12): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688030 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73-402_73-388delAA others(13): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | ||||||
chr12:107688129 | A | G | 1 | a0001c0005t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-319A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688129 | |||||||
chr12:107688263 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
4 | HG01081.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-185G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688263 | |||||||
chr12:107688289 | TC | T | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(58): Show |
89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.73-158delC | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688289 | |||||||
chr12:107688357 | C | T | 1 | a0007c0010t0002g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-91C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688357 | |||||||
chr12:107688395 | T | A | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73-53T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688395 | |||||||
chr12:107688838 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.319+36A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107688838 | |||||||
chr12:107689150 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.319+348C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689150 | |||||||
chr12:107689164 | C | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.319+362C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689164 | |||||||
chr12:107689178 | G | A | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+376G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689178 | |||||||
chr12:107689334 | G | A | 1 | a0001c0005t0004g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.319+532G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689334 | |||||||
chr12:107689558 | C | G | 1 | a0007c0010t0002g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+756C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689558 | |||||||
chr12:107689876 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.319+1074C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689876 | |||||||
chr12:107689882 | A | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(110): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.319+1080A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689882 | |||||||
chr12:107689904 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
4 | HG01081.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1102G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689904 | |||||||
chr12:107689915 | G | A | 2 | a0001c0003t0001g0056 a0001c0003t0001g0060 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.319+1113G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689915 | |||||||
chr12:107689952 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
5 | HG01109.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.319+1150C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689952 | |||||||
chr12:107690018 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.319+1216G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690018 | |||||||
chr12:107690123 | T | G | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+1321T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690123 | |||||||
chr12:107690341 | T | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(31): Show |
64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.319+1539T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690341 | |||||||
chr12:107690472 | T | G | 1 | a0001c0001t0005g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.319+1670T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690472 | |||||||
chr12:107690506 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
4 | HG01081.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1704C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690506 | |||||||
chr12:107690672 | G | A | 1 | a0001c0001t0005g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.319+1870G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690672 | |||||||
chr12:107690682 | C | G | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1880C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690682 | |||||||
chr12:107690859 | A | T | 6 | a0001c0001t0002g0092 a0001c0003t0001g0020 a0001c0003t0001g0054 others(3): Show |
7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-1955A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690859 | |||||||
chr12:107690913 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0099 a0001c0001t0001g0101 others(1): Show |
4 | NA18983.hp1 NA19063.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-1901G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690913 | |||||||
chr12:107690953 | C | T | 1 | a0001c0001t0009g0212 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.320-1861C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690953 | |||||||
chr12:107691086 | A | G | 1 | a0001c0001t0005g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.320-1728A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691086 | |||||||
chr12:107691546 | G | A | 1 | a0002c0002t0002g0200 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.320-1268G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691546 | |||||||
chr12:107691601 | A | G | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.320-1213A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691601 | |||||||
chr12:107691605 | G | A | 2 | a0001c0001t0005g0016 a0001c0001t0005g0223 |
4 | HG02622.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-1209G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691605 | |||||||
chr12:107691631 | G | A | 2 | a0001c0001t0002g0066 a0001c0001t0002g0075 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.320-1183G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691631 | |||||||
chr12:107691673 | CTTA | C | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.320-1136_320-1134d others(5): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 107691673 | ||||||
chr12:107691679 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0075 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.320-1135A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691679 | |||||||
chr12:107691746 | T | A | 20 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(17): Show |
22 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.320-1068T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691746 | |||||||
chr12:107691793 | G | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(116): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.320-1021G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691793 | |||||||
chr12:107691805 | C | T | 1 | a0001c0001t0002g0027 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.320-1009C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691805 | |||||||
chr12:107691824 | T | C | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.320-990T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691824 | |||||||
chr12:107692122 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0154 |
3 | NA18967.hp1 NA19064.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.320-692G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692122 | |||||||
chr12:107692213 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.320-601G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692213 | |||||||
chr12:107692217 | C | T | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.320-597C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692217 | |||||||
chr12:107692249 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.320-565C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692249 | |||||||
chr12:107692465 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.320-349T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692465 | |||||||
chr12:107692468 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.320-346T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692468 | |||||||
chr12:107692574 | G | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(94): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.320-240G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692574 | |||||||
chr12:107692732 | AGTCCAAG others(7): Show |
A | 2 | a0001c0001t0002g0135 a0001c0001t0002g0147 |
2 | NA18982.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.320-78_320-65delCA others(12): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 107692732 | ||||||
chr12:107692770 | A | G | 3 | a0001c0003t0001g0053 a0001c0003t0001g0058 a0001c0003t0001g0062 |
3 | HG02486.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.320-44A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692770 | |||||||
chr12:107692920 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.405+21T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 4/14 | chr12 | 107692920 | |||||||
chr12:107693119 | A | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(58): Show |
89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.502+23A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693119 | |||||||
chr12:107693185 | T | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0076 |
3 | HG01243.hp1 HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.502+89T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693185 | |||||||
chr12:107693337 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.502+241G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693337 | |||||||
chr12:107693462 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.502+366G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693462 | |||||||
chr12:107693479 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502+383C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693479 | |||||||
chr12:107693649 | C | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.502+553C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693649 | |||||||
chr12:107693900 | G | C | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.502+804G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693900 | |||||||
chr12:107693920 | C | T | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.502+824C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693920 | |||||||
chr12:107694019 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.502+923G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694019 | |||||||
chr12:107694109 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.502+1013G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694109 | |||||||
chr12:107694127 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.502+1031G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694127 | |||||||
chr12:107694195 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.502+1099T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694195 | |||||||
chr12:107694257 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0074 a0001c0001t0001g0125 |
4 | HG00597.hp2 HG02698.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1161A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694257 | |||||||
chr12:107694263 | G | A | 1 | a0007c0010t0002g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.502+1167G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694263 | |||||||
chr12:107694294 | G | T | 3 | a0003c0004t0002g0018 a0003c0004t0002g0019 a0003c0004t0002g0049 |
5 | NA18954.hp1 NA18983.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+1198G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694294 | |||||||
chr12:107694500 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.502+1404C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694500 | |||||||
chr12:107694610 | A | G | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1514A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694610 | |||||||
chr12:107694681 | A | G | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1585A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694681 | |||||||
chr12:107694905 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.503-1569A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694905 | |||||||
chr12:107694923 | G | C | 3 | a0001c0001t0006g0148 a0001c0001t0006g0167 a0001c0001t0006g0181 |
3 | HG02155.hp1 NA18972.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.503-1551G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694923 | |||||||
chr12:107694938 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.503-1536G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694938 | |||||||
chr12:107694988 | A | G | 1 | a0001c0003t0001g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.503-1486A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694988 | |||||||
chr12:107695099 | C | CA | 9 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0215 others(6): Show |
9 | HG02056.hp1 HG02622.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.503-1358dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107695099 | ||||||
chr12:107695099 | CA | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(74): Show |
120 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.503-1358delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107695099 | ||||||
chr12:107695182 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.503-1292C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695182 | |||||||
chr12:107695244 | C | T | 1 | a0006c0008t0002g0144 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.503-1230C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695244 | |||||||
chr12:107695265 | C | CA | 21 | a0001c0001t0002g0146 a0001c0003t0001g0020 a0001c0003t0001g0053 others(18): Show |
22 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.503-1197dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107695265 | ||||||
chr12:107695474 | T | C | 1 | a0001c0003t0001g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.503-1000T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695474 | |||||||
chr12:107695556 | G | A | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.503-918G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695556 | |||||||
chr12:107695593 | A | G | 4 | a0001c0001t0001g0029 a0001c0005t0004g0017 a0001c0005t0004g0045 others(1): Show |
6 | HG00280.hp1 HG00741.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-881A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695593 | |||||||
chr12:107695866 | T | C | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.503-608T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695866 | |||||||
chr12:107695966 | G | T | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.503-508G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695966 | |||||||
chr12:107695986 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.503-488G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695986 | |||||||
chr12:107696029 | C | CT | 51 | a0001c0001t0001g0074 a0001c0001t0001g0104 a0001c0001t0001g0105 others(48): Show |
65 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.503-424dupT | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107696029 | ||||||
chr12:107696029 | C | CTT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.503-425_503-424dup others(2): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107696029 | ||||||
chr12:107696029 | C | CTTT | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0103 others(11): Show |
16 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.503-426_503-424dup others(3): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107696029 | ||||||
chr12:107696221 | C | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(61): Show |
93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.503-253C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107696221 | |||||||
chr12:107696244 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.503-230G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107696244 | |||||||
chr12:107696667 | A | C | 1 | a0001c0001t0002g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.613+83A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696667 | |||||||
chr12:107696691 | T | C | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.613+107T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696691 | |||||||
chr12:107696741 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.613+157A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696741 | |||||||
chr12:107696900 | G | A | 2 | a0002c0002t0002g0200 a0002c0002t0002g0204 |
2 | HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.613+316G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696900 | |||||||
chr12:107696904 | C | T | 2 | a0002c0002t0002g0200 a0002c0002t0002g0204 |
2 | HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.613+320C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696904 | |||||||
chr12:107697019 | A | C | 1 | a0001c0001t0002g0034 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.613+435A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107697019 | |||||||
chr12:107697143 | A | G | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.614-324A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107697143 | |||||||
chr12:107697434 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.614-33G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107697434 | |||||||
chr12:107697848 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.744+251T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107697848 | |||||||
chr12:107697876 | C | G | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.744+279C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107697876 | |||||||
chr12:107697877 | G | A | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.744+280G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107697877 | |||||||
chr12:107698106 | A | C | 1 | a0001c0001t0002g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.744+509A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698106 | |||||||
chr12:107698269 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.744+672G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698269 | |||||||
chr12:107698418 | T | C | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.744+821T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698418 | |||||||
chr12:107698469 | T | C | 1 | a0001c0003t0001g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.744+872T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698469 | |||||||
chr12:107698514 | C | T | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.745-859C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698514 | |||||||
chr12:107698592 | C | T | 1 | a0002c0002t0002g0196 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.745-781C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698592 | |||||||
chr12:107698738 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.745-635G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698738 | |||||||
chr12:107698894 | T | C | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.745-479T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698894 | |||||||
chr12:107698914 | G | GTCTCTAA others(28): Show |
1 | a0001c0001t0008g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.745-435_745-434ins others(35): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 107698914 | ||||||
chr12:107698939 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.745-434A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698939 | |||||||
chr12:107698970 | A | C | 1 | a0001c0001t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.745-403A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698970 | |||||||
chr12:107698980 | T | C | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-393T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698980 | |||||||
chr12:107699028 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.745-345C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107699028 | |||||||
chr12:107699219 | A | G | 3 | a0002c0002t0002g0032 a0002c0002t0002g0098 a0002c0002t0002g0120 |
4 | HG00099.hp1 HG00735.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-154A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107699219 | |||||||
chr12:107699238 | A | G | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.745-135A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107699238 | |||||||
chr12:107699505 | C | G | 1 | a0001c0001t0005g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.806+71C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699505 | |||||||
chr12:107699603 | C | A | 8 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(5): Show |
9 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806+169C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699603 | |||||||
chr12:107699679 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0075 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.806+245A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699679 | |||||||
chr12:107699819 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.806+385C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699819 | |||||||
chr12:107700025 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.806+591G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700025 | |||||||
chr12:107700241 | G | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(96): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.806+807G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700241 | |||||||
chr12:107700288 | A | G | 1 | a0001c0001t0003g0209 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806+854A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700288 | |||||||
chr12:107700311 | G | A | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.806+877G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700311 | |||||||
chr12:107700450 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.806+1016A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700450 | |||||||
chr12:107700561 | C | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(55): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.806+1127C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700561 | |||||||
chr12:107700605 | G | A | 1 | a0008c0009t0001g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.806+1171G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700605 | |||||||
chr12:107700627 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.806+1193A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700627 | |||||||
chr12:107700882 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.806+1448G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700882 | |||||||
chr12:107700897 | T | TC | 37 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(34): Show |
67 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.806+1470dupC | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 107700897 | ||||||
chr12:107700930 | A | G | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.806+1496A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700930 | |||||||
chr12:107700964 | A | C | 1 | a0001c0001t0002g0052 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.806+1530A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700964 | |||||||
chr12:107701203 | T | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(31): Show |
64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.807-1732T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701203 | |||||||
chr12:107701240 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.807-1695A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701240 | |||||||
chr12:107701288 | T | G | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.807-1647T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701288 | |||||||
chr12:107701339 | A | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.807-1596A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701339 | |||||||
chr12:107701418 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.807-1517T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701418 | |||||||
chr12:107701429 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.807-1506G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701429 | |||||||
chr12:107701534 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
5 | HG01109.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-1401C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701534 | |||||||
chr12:107701563 | A | G | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.807-1372A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701563 | |||||||
chr12:107701766 | C | T | 1 | a0009c0007t0002g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.807-1169C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701766 | |||||||
chr12:107701803 | G | A | 1 | a0001c0003t0001g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.807-1132G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701803 | |||||||
chr12:107701936 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.807-999G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701936 | |||||||
chr12:107701977 | C | T | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.807-958C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701977 | |||||||
chr12:107702177 | T | C | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.807-758T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702177 | |||||||
chr12:107702243 | C | CT | 34 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(31): Show |
64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.807-683dupT | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 107702243 | ||||||
chr12:107702319 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.807-616T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702319 | |||||||
chr12:107702338 | T | C | 1 | a0001c0001t0007g0205 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.807-597T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702338 | |||||||
chr12:107702367 | G | A | 1 | a0001c0003t0001g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.807-568G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702367 | |||||||
chr12:107702403 | C | T | 1 | a0002c0002t0002g0194 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.807-532C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702403 | |||||||
chr12:107702614 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.807-321A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702614 | |||||||
chr12:107702755 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(34): Show |
68 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.807-180T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702755 | |||||||
chr12:107702780 | C | T | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.807-155C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702780 | |||||||
chr12:107703113 | T | C | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.903+82T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703113 | |||||||
chr12:107703348 | G | T | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.903+317G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703348 | |||||||
chr12:107703602 | C | T | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.904-83C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703602 | |||||||
chr12:107703658 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0099 a0001c0001t0001g0101 |
3 | NA18983.hp1 NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.904-27C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703658 | |||||||
chr12:107703678 | C | T | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.904-7C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703678 | |||||||
chr12:107704024 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.965+278G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704024 | |||||||
chr12:107704193 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.966-443G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704193 | |||||||
chr12:107704262 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(51): Show |
86 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.966-374T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704262 | |||||||
chr12:107704288 | G | C | 22 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0025 others(19): Show |
42 | HG00558.hp1 HG00597.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.966-348G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704288 | |||||||
chr12:107704339 | T | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0182 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.966-297T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704339 | |||||||
chr12:107704810 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(55): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1077+63G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704810 | |||||||
chr12:107704935 | T | C | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1077+188T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704935 | |||||||
chr12:107704961 | C | G | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077+214C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704961 | |||||||
chr12:107704974 | G | A | 3 | a0001c0001t0002g0068 a0001c0001t0002g0082 a0001c0001t0002g0113 |
3 | HG01167.hp1 HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1077+227G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704974 | |||||||
chr12:107705080 | G | T | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1077+333G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705080 | |||||||
chr12:107705149 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1077+402G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705149 | |||||||
chr12:107705179 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1077+432T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705179 | |||||||
chr12:107705264 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(25): Show |
58 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1077+517G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705264 | |||||||
chr12:107705355 | T | C | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077+608T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705355 | |||||||
chr12:107705361 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1077+614G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705361 | |||||||
chr12:107705388 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1077+641A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705388 | |||||||
chr12:107705505 | T | C | 23 | a0001c0001t0001g0073 a0001c0001t0001g0109 a0001c0001t0001g0112 others(20): Show |
30 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1077+758T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705505 | |||||||
chr12:107705518 | C | G | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1077+771C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705518 | |||||||
chr12:107705520 | T | TC | 42 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0112 others(39): Show |
50 | HG00597.hp1 HG00621.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1077+779dupC | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 107705520 | ||||||
chr12:107705524 | C | A | 1 | a0001c0001t0002g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1077+777C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705524 | |||||||
chr12:107705555 | T | A | 1 | a0001c0001t0002g0138 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1077+808T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705555 | |||||||
chr12:107705640 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1077+893A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705640 | |||||||
chr12:107705742 | A | C | 1 | a0001c0001t0004g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077+995A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705742 | |||||||
chr12:107705764 | A | C | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077+1017A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705764 | |||||||
chr12:107705772 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1077+1025A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705772 | |||||||
chr12:107705846 | CACATATG others(11): Show |
C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(58): Show |
89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1077+1100_1077+111 others(22): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705846 | |||||||
chr12:107705885 | A | C | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1077+1138A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705885 | |||||||
chr12:107705930 | G | A | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1077+1183G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705930 | |||||||
chr12:107706050 | C | G | 3 | a0001c0005t0004g0017 a0001c0005t0004g0045 a0001c0005t0004g0046 |
4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+1303C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706050 | |||||||
chr12:107706216 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1077+1469A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706216 | |||||||
chr12:107706308 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1077+1561G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706308 | |||||||
chr12:107706382 | G | A | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1077+1635G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706382 | |||||||
chr12:107706540 | A | T | 5 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0094 others(2): Show |
5 | HG01243.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077+1793A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706540 | |||||||
chr12:107706641 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1077+1894A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706641 | |||||||
chr12:107706709 | T | C | 4 | a0001c0001t0002g0069 a0001c0001t0002g0077 a0001c0001t0002g0084 others(1): Show |
4 | HG00323.hp1 HG01168.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+1962T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706709 | |||||||
chr12:107706844 | C | G | 3 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0001c0001t0002g0087 |
3 | HG02055.hp2 HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1078-2082C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706844 | |||||||
chr12:107706902 | T | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0075 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1078-2024T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706902 | |||||||
chr12:107706976 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1078-1950C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706976 | |||||||
chr12:107706985 | T | C | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1941T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706985 | |||||||
chr12:107706995 | T | A | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1931T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706995 | |||||||
chr12:107706996 | G | C | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1930G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706996 | |||||||
chr12:107706999 | T | C | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1927T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706999 | |||||||
chr12:107707000 | A | G | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1926A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707000 | |||||||
chr12:107707002 | T | G | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1924T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707002 | |||||||
chr12:107707008 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1078-1918A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707008 | |||||||
chr12:107707028 | A | T | 1 | a0001c0003t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1898A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707028 | |||||||
chr12:107707063 | T | C | 4 | a0001c0001t0002g0031 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
5 | HG01109.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-1863T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707063 | |||||||
chr12:107707094 | TCTC | T | 32 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0195 others(29): Show |
43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1078-1829_1078-182 others(7): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 107707094 | ||||||
chr12:107707118 | T | C | 2 | a0001c0001t0002g0085 a0001c0001t0002g0206 |
2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1078-1808T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707118 | |||||||
chr12:107707126 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1078-1800A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707126 | |||||||
chr12:107707162 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1764A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707162 | |||||||
chr12:107707163 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1763T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707163 | |||||||
chr12:107707194 | G | C | 1 | a0001c0001t0002g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1732G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707194 | |||||||
chr12:107707196 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1730T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707196 | |||||||
chr12:107707352 | T | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(33): Show |
67 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1078-1574T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707352 | |||||||
chr12:107707413 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1078-1513G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707413 | |||||||
chr12:107707418 | A | G | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1078-1508A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707418 | |||||||
chr12:107707794 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1078-1132C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707794 | |||||||
chr12:107707828 | C | G | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078-1098C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707828 | |||||||
chr12:107707861 | G | C | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1078-1065G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707861 | |||||||
chr12:107707883 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1078-1043G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707883 | |||||||
chr12:107708088 | A | G | 1 | a0007c0010t0002g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1078-838A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708088 | |||||||
chr12:107708089 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0216 |
2 | HG00408.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1078-837T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708089 | |||||||
chr12:107708127 | C | T | 1 | a0001c0003t0001g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1078-799C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708127 | |||||||
chr12:107708145 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1078-781T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708145 | |||||||
chr12:107708256 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1078-670C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708256 | |||||||
chr12:107708523 | T | C | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1078-403T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708523 | |||||||
chr12:107708525 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1078-401G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708525 | |||||||
chr12:107708538 | G | A | 1 | a0001c0003t0001g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1078-388G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708538 | |||||||
chr12:107708585 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1078-341T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708585 | |||||||
chr12:107708635 | C | T | 1 | a0002c0002t0002g0196 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1078-291C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708635 | |||||||
chr12:107708776 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1078-150C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708776 | |||||||
chr12:107708777 | G | A | 2 | a0004c0006t0002g0219 a0004c0006t0002g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1078-149G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708777 | |||||||
chr12:107709510 | C | CT | 35 | a0001c0001t0001g0073 a0001c0001t0001g0109 a0001c0001t0001g0112 others(32): Show |
46 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1290+295dupT | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 107709510 | ||||||
chr12:107709527 | T | A | 1 | a0001c0001t0005g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1290+295T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709527 | |||||||
chr12:107709527 | TA | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1290+299delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 107709527 | ||||||
chr12:107709528 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(83): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1290+296A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709528 | |||||||
chr12:107709535 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1290+303T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709535 | |||||||
chr12:107709577 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1290+345C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709577 | |||||||
chr12:107709655 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0183 |
2 | HG00642.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1290+423T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709655 | |||||||
chr12:107709806 | T | C | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1290+574T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709806 | |||||||
chr12:107709813 | GA | G | 4 | a0001c0001t0004g0088 a0001c0005t0004g0017 a0001c0005t0004g0045 others(1): Show |
5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1290+586delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 107709813 | ||||||
chr12:107709879 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1291-526C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709879 | |||||||
chr12:107709908 | T | G | 3 | a0004c0006t0002g0219 a0004c0006t0002g0220 a0007c0010t0002g0044 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1291-497T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709908 | |||||||
chr12:107710045 | A | T | 1 | a0001c0001t0002g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1291-360A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710045 | |||||||
chr12:107710060 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1291-345A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710060 | |||||||
chr12:107710143 | C | T | 1 | a0001c0001t0012g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-262C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710143 | |||||||
chr12:107710153 | T | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(31): Show |
64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1291-252T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710153 | |||||||
chr12:107710206 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1291-199C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710206 | |||||||
chr12:107710286 | A | C | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291-119A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710286 | |||||||
chr12:107710540 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0186 |
6 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+30C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710540 | |||||||
chr12:107710552 | T | TA | 15 | a0001c0001t0002g0027 a0001c0001t0002g0081 a0001c0001t0002g0117 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1396+63dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 107710552 | ||||||
chr12:107710552 | T | TAAA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0023 others(27): Show |
57 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1396+61_1396+63dup others(3): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 107710552 | ||||||
chr12:107710552 | TA | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
88 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1396+63delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 107710552 | ||||||
chr12:107710630 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(30): Show |
63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1396+120C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710630 | |||||||
chr12:107710640 | A | G | 1 | a0001c0001t0005g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1396+130A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710640 | |||||||
chr12:107710651 | T | C | 2 | a0002c0002t0002g0193 a0002c0002t0002g0207 |
2 | HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1396+141T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710651 | |||||||
chr12:107710757 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1396+247T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710757 | |||||||
chr12:107710992 | T | C | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0094 others(1): Show |
4 | HG01243.hp2 HG02486.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+482T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710992 | |||||||
chr12:107711200 | G | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(55): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1396+690G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711200 | |||||||
chr12:107711358 | G | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(88): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1397-753G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711358 | |||||||
chr12:107711396 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1397-715G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711396 | |||||||
chr12:107711456 | C | T | 17 | a0001c0003t0001g0020 a0001c0003t0001g0053 a0001c0003t0001g0054 others(14): Show |
18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1397-655C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711456 | |||||||
chr12:107711528 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1397-583G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711528 | |||||||
chr12:107711538 | C | T | 2 | a0001c0001t0002g0140 a0001c0001t0005g0016 |
4 | HG02083.hp2 HG02622.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-573C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711538 | |||||||
chr12:107711566 | C | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0035 others(28): Show |
41 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1397-545C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711566 | |||||||
chr12:107711609 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1397-502A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711609 | |||||||
chr12:107711747 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1397-364T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711747 | |||||||
chr12:107711778 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1397-333G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711778 | |||||||
chr12:107712057 | T | C | 4 | a0001c0001t0004g0088 a0001c0005t0004g0017 a0001c0005t0004g0045 others(1): Show |
5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1397-54T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107712057 |