Item | Value |
---|---|
geneid | 390928 |
ensemblid | ENSG00000183760.11 |
hgncid | 33781 |
symbol | ACP7 |
name | acid phosphatase 7, tartrate resistant (putative) |
refseq_nuc | NM_001004318.3 |
refseq_prot | NP_001004318.2 |
ensembl_nuc | ENST00000331256.10 |
ensembl_prot | ENSP00000327557.4 |
mane_status | MANE Select |
chr | chr19 |
start | 39084368 |
end | 39111493 |
strand | + |
ver | v1.2 |
region | chr19:39084368-39111493 |
region5000 | chr19:39079368-39116493 |
regionname0 | ACP7_chr19_39084368_39111493 |
regionname5000 | ACP7_chr19_39079368_39116493 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 438 | 395 | 82 | 80 | 175 | 16 | 40 | ACP7_chr19_39079368_39116493 | ACP7 | MHPLP others(433): Show |
chr19 | 39079368 | 39116493 |
a0002 | 0/0 | 438 | 3 | 0 | 3 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | MHPLP others(433): Show |
chr19 | 39079368 | 39116493 |
a0003 | 0/0 | 438 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | MHPLP others(433): Show |
chr19 | 39079368 | 39116493 |
a0004 | 0/0 | 438 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | MHPLP others(433): Show |
chr19 | 39079368 | 39116493 |
a0005 | 0/0 | 438 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | MHPLP others(433): Show |
chr19 | 39079368 | 39116493 |
a0006 | 0/0 | 438 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | MHPLP others(433): Show |
chr19 | 39079368 | 39116493 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1314 | 111 | 16 | 25 | 48 | 8 | 13 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0002 | 0/0 | 1314 | 103 | 2 | 23 | 57 | 5 | 16 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0003 | 1/0 | 1314 | 76 | 13 | 15 | 41 | 2 | 4 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0004 | 0/0 | 1314 | 52 | 5 | 13 | 28 | 1 | 5 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0005 | 0/0 | 1314 | 15 | 15 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0006 | 0/0 | 1314 | 15 | 14 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0007 | 0/0 | 1314 | 6 | 5 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0008 | 0/0 | 1314 | 5 | 5 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0009 | 0/0 | 1314 | 4 | 4 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0010 | 0/0 | 1314 | 4 | 3 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0012 | 0/0 | 1314 | 2 | 0 | 2 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0017 | 0/0 | 1314 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0001c0018 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0002c0011 | 0/0 | 1314 | 3 | 0 | 3 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0003c0014 | 0/0 | 1314 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0004c0013 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0005c0016 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 | ||
a0006c0015 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | ATGCA others(1309): Show |
chr19 | 39079368 | 39116493 |
acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2903 | 85 | 8 | 21 | 36 | 8 | 11 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0004 | 0/0 | 2903 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0006 | 0/0 | 2903 | 6 | 3 | 1 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0011 | 0/0 | 2906 | 7 | 0 | 0 | 7 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0013 | 0/0 | 2903 | 3 | 2 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0014 | 0/0 | 2906 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0015 | 0/0 | 2906 | 4 | 0 | 2 | 1 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0028 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0030 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0001t0033 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0002 | 0/0 | 2906 | 49 | 0 | 14 | 26 | 0 | 9 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0005 | 0/0 | 2903 | 34 | 2 | 8 | 21 | 1 | 2 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0007 | 0/0 | 2906 | 9 | 0 | 1 | 4 | 0 | 4 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0012 | 0/0 | 2903 | 3 | 0 | 0 | 0 | 3 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0021 | 0/0 | 2906 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0022 | 0/0 | 2903 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0023 | 0/0 | 2906 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0024 | 0/0 | 2906 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0027 | 0/0 | 2906 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0002t0031 | 0/0 | 2903 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0002 | 0/0 | 2906 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0003 | 0/0 | 2903 | 52 | 12 | 14 | 20 | 2 | 4 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0006 | 1/0 | 2903 | 14 | 0 | 0 | 13 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0014 | 0/0 | 2906 | 3 | 0 | 0 | 3 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0019 | 0/0 | 2903 | 3 | 0 | 0 | 3 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0020 | 0/0 | 2903 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0025 | 0/0 | 2878 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2873): Show |
chr19 | 39079368 | 39116493 |
a0001c0003t0032 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0004t0002 | 0/0 | 2906 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0004t0004 | 0/0 | 2903 | 40 | 1 | 10 | 24 | 1 | 4 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0004t0005 | 0/0 | 2903 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0004t0009 | 0/0 | 2903 | 4 | 4 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0004t0012 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0004t0017 | 0/0 | 2906 | 3 | 0 | 2 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0004t0020 | 0/0 | 2903 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0005t0001 | 0/0 | 2903 | 7 | 7 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0005t0006 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0005t0010 | 0/0 | 2903 | 5 | 5 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0006t0008 | 0/0 | 2903 | 9 | 8 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0006t0009 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0006t0010 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0007t0006 | 0/0 | 2903 | 6 | 5 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0008t0009 | 0/0 | 2903 | 2 | 2 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0008t0016 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0009t0005 | 0/0 | 2903 | 2 | 2 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0009t0026 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0009t0029 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0010t0004 | 0/0 | 2903 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0010t0018 | 0/0 | 2906 | 3 | 3 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0012t0006 | 0/0 | 2903 | 2 | 0 | 2 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0001c0017t0002 | 0/0 | 2906 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0001c0018t0002 | 0/0 | 2906 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2901): Show |
chr19 | 39079368 | 39116493 |
a0002c0011t0004 | 0/0 | 2903 | 3 | 0 | 3 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0003c0014t0001 | 0/0 | 2903 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0004c0013t0006 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0005c0016t0013 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
a0006c0015t0004 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | AGAGG others(2898): Show |
chr19 | 39079368 | 39116493 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0011g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0011g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0011g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0013g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0014g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0015g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0015g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0015g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0015g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0028g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0030g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0001t0033g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0005g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0007g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0012g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0012g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0012g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0021g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0021g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0022g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0023g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0024g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0027g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0002t0031g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0004 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0289 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0006g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0014g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0014g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0014g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0019g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0019g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0019g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0020g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0025g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0003t0032g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0009g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0012g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0017g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0017g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0017g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0004t0020g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0005t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0006t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0007t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0007t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0007t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0007t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0007t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0007t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0008t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0008t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0008t0016g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0008t0016g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0008t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0009t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0009t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0009t0026g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0009t0029g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0010t0004g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0010t0018g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0010t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0012t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0012t0006g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0017t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0001c0018t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0002c0011t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0002c0011t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0002c0011t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0003c0014t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0004c0013t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0005c0016t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
a0006c0015t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0005 | g0219 | EUR | GBR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0353 | EUR | GBR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00140 | hp1 | a0001 | c0003 | t0003 | g0275 | EUR | GBR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00140 | hp2 | a0001 | c0004 | t0004 | g0329 | EUR | GBR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00280 | hp2 | a0001 | c0002 | t0031 | g0312 | EUR | FIN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00408 | hp1 | a0001 | c0003 | t0019 | g0024 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00423 | hp1 | a0001 | c0004 | t0004 | g0048 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00558 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00558 | hp2 | a0001 | c0002 | t0005 | g0108 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00621 | hp1 | a0001 | c0004 | t0012 | g0271 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00621 | hp2 | a0001 | c0003 | t0003 | g0255 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00639 | hp2 | a0001 | c0003 | t0020 | g0253 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00642 | hp1 | a0001 | c0007 | t0006 | g0117 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0227 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00673 | hp1 | a0001 | c0002 | t0005 | g0080 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | CHS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0157 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00733 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00735 | hp1 | a0001 | c0002 | t0005 | g0368 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00738 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG00741 | hp2 | a0001 | c0004 | t0020 | g0268 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0155 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01069 | hp2 | a0001 | c0003 | t0003 | g0251 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01070 | hp2 | a0001 | c0004 | t0004 | g0059 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01071 | hp1 | a0001 | c0003 | t0003 | g0017 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01074 | hp1 | a0001 | c0004 | t0004 | g0082 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01081 | hp1 | a0001 | c0004 | t0017 | g0188 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01081 | hp2 | a0001 | c0002 | t0005 | g0325 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01099 | hp2 | a0001 | c0004 | t0004 | g0147 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01106 | hp1 | a0001 | c0001 | t0013 | g0243 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01106 | hp2 | a0001 | c0002 | t0005 | g0220 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01109 | hp2 | a0001 | c0006 | t0008 | g0035 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01167 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01168 | hp2 | a0001 | c0012 | t0006 | g0208 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01169 | hp2 | a0001 | c0012 | t0006 | g0207 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01175 | hp1 | a0001 | c0004 | t0004 | g0086 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01175 | hp2 | a0001 | c0002 | t0005 | g0237 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01192 | hp2 | a0001 | c0004 | t0004 | g0136 | AMR | PUR | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01255 | hp1 | a0001 | c0003 | t0003 | g0030 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01255 | hp2 | a0002 | c0011 | t0004 | g0075 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01256 | hp2 | a0001 | c0002 | t0005 | g0314 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01257 | hp1 | a0002 | c0011 | t0004 | g0083 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01257 | hp2 | a0001 | c0003 | t0003 | g0276 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01258 | hp1 | a0002 | c0011 | t0004 | g0084 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01261 | hp1 | a0001 | c0002 | t0005 | g0229 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01358 | hp2 | a0001 | c0002 | t0007 | g0242 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01361 | hp1 | a0001 | c0003 | t0003 | g0266 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01361 | hp2 | a0001 | c0003 | t0003 | g0215 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01496 | hp1 | a0001 | c0004 | t0004 | g0096 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01496 | hp2 | a0001 | c0004 | t0004 | g0072 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0357 | EUR | IBS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01515 | hp2 | a0001 | c0003 | t0003 | g0263 | EUR | IBS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01516 | hp1 | a0001 | c0002 | t0012 | g0331 | EUR | IBS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | IBS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0350 | EUR | IBS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01517 | hp2 | a0001 | c0002 | t0012 | g0330 | EUR | IBS | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01884 | hp1 | a0001 | c0006 | t0009 | g0005 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01884 | hp2 | a0001 | c0010 | t0018 | g0011 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01891 | hp1 | a0001 | c0006 | t0009 | g0031 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01891 | hp2 | a0001 | c0004 | t0004 | g0064 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01928 | hp1 | a0001 | c0003 | t0003 | g0001 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0137 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0121 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01975 | hp2 | a0001 | c0004 | t0017 | g0146 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01978 | hp1 | a0001 | c0003 | t0003 | g0282 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01978 | hp2 | a0001 | c0001 | t0015 | g0167 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01981 | hp1 | a0001 | c0004 | t0004 | g0051 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01981 | hp2 | a0003 | c0014 | t0001 | g0361 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0181 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02004 | hp2 | a0001 | c0004 | t0004 | g0071 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02040 | hp1 | a0001 | c0004 | t0004 | g0055 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02055 | hp1 | a0004 | c0013 | t0006 | g0116 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0203 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02056 | hp1 | a0001 | c0002 | t0005 | g0226 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02056 | hp2 | a0001 | c0002 | t0005 | g0094 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02074 | hp1 | a0001 | c0004 | t0005 | g0161 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02074 | hp2 | a0001 | c0002 | t0005 | g0088 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02080 | hp2 | a0001 | c0004 | t0004 | g0065 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02129 | hp1 | a0001 | c0002 | t0005 | g0069 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0054 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0261 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02132 | hp2 | a0001 | c0002 | t0007 | g0232 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02135 | hp1 | a0001 | c0004 | t0004 | g0077 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02135 | hp2 | a0001 | c0002 | t0023 | g0238 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02145 | hp1 | a0001 | c0001 | t0028 | g0217 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02145 | hp2 | a0001 | c0010 | t0018 | g0139 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02148 | hp1 | a0001 | c0003 | t0003 | g0284 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0175 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CDX | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CDX | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02165 | hp1 | a0001 | c0003 | t0003 | g0250 | EAS | CDX | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CDX | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02257 | hp1 | a0001 | c0005 | t0006 | g0135 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02257 | hp2 | a0001 | c0006 | t0008 | g0118 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02258 | hp2 | a0001 | c0004 | t0009 | g0102 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02273 | hp1 | a0001 | c0001 | t0015 | g0123 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02273 | hp2 | a0001 | c0003 | t0003 | g0017 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02280 | hp1 | a0001 | c0005 | t0010 | g0145 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02293 | hp1 | a0001 | c0003 | t0003 | g0278 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0127 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02300 | hp1 | a0001 | c0002 | t0005 | g0288 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02451 | hp1 | a0001 | c0007 | t0006 | g0115 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02451 | hp2 | a0001 | c0004 | t0009 | g0291 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02523 | hp2 | a0001 | c0003 | t0006 | g0049 | EAS | KHV | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02572 | hp2 | a0001 | c0003 | t0003 | g0272 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02602 | hp1 | a0001 | c0004 | t0004 | g0092 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02602 | hp2 | a0001 | c0004 | t0004 | g0095 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02615 | hp1 | a0001 | c0007 | t0006 | g0111 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0202 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02622 | hp1 | a0001 | c0006 | t0008 | g0037 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02622 | hp2 | a0001 | c0003 | t0003 | g0264 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0247 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02630 | hp2 | a0005 | c0016 | t0013 | g0248 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0362 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0367 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02698 | hp2 | a0001 | c0003 | t0003 | g0001 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02723 | hp1 | a0001 | c0005 | t0001 | g0198 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02723 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02738 | hp1 | a0001 | c0002 | t0007 | g0241 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02738 | hp2 | a0001 | c0003 | t0003 | g0224 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02809 | hp1 | a0001 | c0001 | t0033 | g0349 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02809 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02886 | hp1 | a0001 | c0004 | t0009 | g0019 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02886 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02896 | hp1 | a0001 | c0001 | t0013 | g0249 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02896 | hp2 | a0001 | c0003 | t0003 | g0265 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02897 | hp1 | a0001 | c0007 | t0006 | g0114 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02897 | hp2 | a0001 | c0003 | t0003 | g0273 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0204 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02922 | hp2 | a0001 | c0006 | t0008 | g0110 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02965 | hp1 | a0001 | c0005 | t0010 | g0141 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02965 | hp2 | a0001 | c0006 | t0008 | g0033 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02970 | hp1 | a0001 | c0002 | t0005 | g0228 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02970 | hp2 | a0001 | c0003 | t0003 | g0280 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02976 | hp1 | a0001 | c0002 | t0005 | g0218 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02976 | hp2 | a0001 | c0005 | t0001 | g0199 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0170 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03098 | hp1 | a0001 | c0008 | t0009 | g0142 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03098 | hp2 | a0001 | c0006 | t0008 | g0006 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03130 | hp1 | a0001 | c0004 | t0009 | g0019 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03139 | hp1 | a0001 | c0006 | t0008 | g0006 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03139 | hp2 | a0001 | c0009 | t0029 | g0210 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03225 | hp2 | a0001 | c0008 | t0009 | g0143 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03453 | hp2 | a0001 | c0005 | t0001 | g0212 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03486 | hp1 | a0001 | c0006 | t0008 | g0036 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03486 | hp2 | a0001 | c0006 | t0008 | g0032 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03490 | hp1 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03490 | hp2 | a0001 | c0002 | t0007 | g0233 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0150 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0171 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03492 | hp2 | a0001 | c0002 | t0007 | g0231 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03516 | hp1 | a0001 | c0003 | t0003 | g0286 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03516 | hp2 | a0001 | c0006 | t0010 | g0206 | AFR | ESN | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03540 | hp1 | a0001 | c0001 | t0030 | g0100 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03540 | hp2 | a0001 | c0003 | t0003 | g0281 | AFR | GWD | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03579 | hp1 | a0001 | c0005 | t0010 | g0201 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03579 | hp2 | a0001 | c0007 | t0006 | g0109 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0173 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03704 | hp2 | a0001 | c0002 | t0005 | g0326 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03710 | hp1 | a0001 | c0002 | t0027 | g0177 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0377 | SAS | PJL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0140 | SAS | BEB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03831 | hp2 | a0001 | c0017 | t0002 | g0176 | SAS | BEB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04115 | hp1 | a0001 | c0001 | t0015 | g0149 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04115 | hp2 | a0001 | c0010 | t0004 | g0344 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04184 | hp1 | a0001 | c0004 | t0004 | g0090 | SAS | BEB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0152 | SAS | BEB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04199 | hp1 | a0001 | c0004 | t0004 | g0079 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04199 | hp2 | a0001 | c0004 | t0017 | g0185 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04204 | hp1 | a0001 | c0001 | t0014 | g0138 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04228 | hp1 | a0001 | c0002 | t0005 | g0172 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG04228 | hp2 | a0001 | c0002 | t0007 | g0234 | SAS | STU | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18522 | hp1 | a0001 | c0006 | t0009 | g0005 | AFR | YRI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18522 | hp2 | a0001 | c0005 | t0006 | g0134 | AFR | YRI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18747 | hp1 | a0001 | c0002 | t0007 | g0225 | EAS | CHB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18747 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | CHB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | YRI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18906 | hp2 | a0001 | c0005 | t0006 | g0197 | AFR | YRI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18939 | hp1 | a0001 | c0004 | t0004 | g0008 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18940 | hp1 | a0001 | c0004 | t0002 | g0194 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18940 | hp2 | a0001 | c0003 | t0006 | g0334 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18941 | hp2 | a0001 | c0004 | t0004 | g0093 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18942 | hp2 | a0001 | c0003 | t0006 | g0290 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18943 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18943 | hp2 | a0001 | c0003 | t0014 | g0022 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18944 | hp1 | a0001 | c0004 | t0004 | g0073 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18944 | hp2 | a0001 | c0003 | t0003 | g0279 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18946 | hp1 | a0001 | c0004 | t0004 | g0081 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18949 | hp1 | a0001 | c0004 | t0004 | g0045 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18950 | hp1 | a0001 | c0004 | t0004 | g0078 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18950 | hp2 | a0001 | c0003 | t0019 | g0025 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18951 | hp2 | a0001 | c0002 | t0007 | g0235 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18952 | hp1 | a0001 | c0001 | t0011 | g0168 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18954 | hp2 | a0001 | c0002 | t0005 | g0106 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18957 | hp1 | a0001 | c0003 | t0014 | g0027 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18959 | hp2 | a0001 | c0003 | t0003 | g0252 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18960 | hp1 | a0001 | c0003 | t0006 | g0372 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18960 | hp2 | a0001 | c0002 | t0022 | g0184 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18961 | hp2 | a0001 | c0003 | t0006 | g0371 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18962 | hp1 | a0001 | c0004 | t0004 | g0008 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18963 | hp1 | a0001 | c0003 | t0003 | g0262 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18964 | hp2 | a0001 | c0003 | t0003 | g0213 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18965 | hp1 | a0001 | c0003 | t0006 | g0254 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18966 | hp1 | a0001 | c0003 | t0003 | g0257 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18966 | hp2 | a0001 | c0003 | t0006 | g0370 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18967 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18967 | hp2 | a0001 | c0002 | t0005 | g0125 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18968 | hp1 | a0001 | c0002 | t0005 | g0239 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18968 | hp2 | a0001 | c0004 | t0004 | g0097 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18970 | hp1 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18971 | hp1 | a0001 | c0003 | t0006 | g0373 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18971 | hp2 | a0001 | c0002 | t0005 | g0070 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18972 | hp1 | a0001 | c0002 | t0024 | g0230 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18972 | hp2 | a0001 | c0003 | t0006 | g0374 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18975 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18975 | hp2 | a0001 | c0004 | t0004 | g0056 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18979 | hp1 | a0001 | c0002 | t0005 | g0324 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18980 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18980 | hp2 | a0001 | c0004 | t0004 | g0060 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18981 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18981 | hp2 | a0001 | c0002 | t0021 | g0158 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18983 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18984 | hp2 | a0001 | c0002 | t0021 | g0180 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18986 | hp2 | a0006 | c0015 | t0004 | g0066 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18989 | hp1 | a0001 | c0002 | t0005 | g0063 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18990 | hp1 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18995 | hp1 | a0001 | c0018 | t0002 | g0186 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18998 | hp1 | a0001 | c0004 | t0005 | g0189 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA18999 | hp2 | a0001 | c0003 | t0003 | g0285 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19000 | hp1 | a0001 | c0001 | t0011 | g0164 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19000 | hp2 | a0001 | c0003 | t0006 | g0333 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19003 | hp2 | a0001 | c0004 | t0004 | g0068 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19004 | hp1 | a0001 | c0002 | t0007 | g0236 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19004 | hp2 | a0001 | c0004 | t0004 | g0044 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19005 | hp1 | a0001 | c0004 | t0004 | g0058 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19007 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19009 | hp1 | a0001 | c0004 | t0004 | g0050 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19010 | hp2 | a0001 | c0003 | t0006 | g0364 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19012 | hp1 | a0001 | c0001 | t0011 | g0166 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19012 | hp2 | a0001 | c0004 | t0004 | g0274 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19030 | hp1 | a0001 | c0008 | t0016 | g0113 | AFR | LWK | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19030 | hp2 | a0001 | c0005 | t0001 | g0200 | AFR | LWK | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19043 | hp1 | a0001 | c0005 | t0010 | g0193 | AFR | LWK | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19043 | hp2 | a0001 | c0009 | t0026 | g0196 | AFR | LWK | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19054 | hp2 | a0001 | c0003 | t0014 | g0026 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19056 | hp1 | a0001 | c0003 | t0003 | g0277 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0191 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19057 | hp1 | a0001 | c0003 | t0003 | g0256 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19057 | hp2 | a0001 | c0002 | t0005 | g0062 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19062 | hp1 | a0001 | c0001 | t0011 | g0165 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19064 | hp1 | a0001 | c0004 | t0004 | g0076 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19064 | hp2 | a0001 | c0003 | t0003 | g0258 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19065 | hp1 | a0001 | c0002 | t0005 | g0107 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19065 | hp2 | a0001 | c0004 | t0004 | g0053 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19067 | hp1 | a0001 | c0002 | t0005 | g0085 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19067 | hp2 | a0001 | c0003 | t0019 | g0021 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19070 | hp1 | a0001 | c0002 | t0005 | g0240 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19070 | hp2 | a0001 | c0001 | t0015 | g0190 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19072 | hp1 | a0001 | c0003 | t0003 | g0287 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19072 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19079 | hp1 | a0001 | c0003 | t0006 | g0259 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19081 | hp1 | a0001 | c0002 | t0005 | g0089 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19084 | hp1 | a0001 | c0004 | t0004 | g0061 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19086 | hp1 | a0001 | c0004 | t0004 | g0046 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19086 | hp2 | a0001 | c0002 | t0022 | g0179 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19087 | hp1 | a0001 | c0003 | t0003 | g0270 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19088 | hp1 | a0001 | c0004 | t0004 | g0067 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19088 | hp2 | a0001 | c0003 | t0006 | g0222 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19091 | hp1 | a0001 | c0003 | t0025 | g0260 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19240 | hp1 | a0001 | c0008 | t0016 | g0112 | AFR | YRI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA19240 | hp2 | a0001 | c0006 | t0010 | g0209 | AFR | YRI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20129 | hp1 | a0001 | c0003 | t0003 | g0004 | AFR | ASW | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20129 | hp2 | a0001 | c0007 | t0006 | g0038 | AFR | ASW | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20752 | hp1 | a0001 | c0002 | t0012 | g0246 | EUR | TSI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0322 | EUR | TSI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | TSI | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20905 | hp1 | a0001 | c0003 | t0003 | g0223 | SAS | GIH | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0029 | SAS | GIH | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01123 | hp1 | a0001 | c0004 | t0004 | g0074 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02486 | hp1 | a0001 | c0008 | t0016 | g0119 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0267 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG02559 | hp2 | a0001 | c0010 | t0018 | g0011 | AFR | ACB | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03471 | hp1 | a0001 | c0005 | t0001 | g0034 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG03471 | hp2 | a0001 | c0006 | t0010 | g0205 | AFR | MSL | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG06807 | hp1 | a0001 | c0009 | t0005 | g0133 | AFR | USA | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20300 | hp1 | a0001 | c0005 | t0010 | g0144 | AFR | USA | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA20300 | hp2 | a0001 | c0009 | t0005 | g0211 | AFR | USA | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA21309 | hp1 | a0001 | c0003 | t0032 | g0120 | AFR | LWK | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | LWK | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0308 | REF | REF | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
homoSapiens | grch38p0 | a0001 | c0003 | t0006 | g0289 | REF | REF | ACP7_chr19_39079368_39116493 | ACP7 | chr19 | 39079368 | 39116493 |
view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:39098602 | G | T | 1 | a0004 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.266G>T | p.Arg89Leu | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/13 | 477/2903 | 266/1317 | 89/438 | chr19 | 39098602 | |||
chr19:39099046 | G | A | 1 | a0003 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.409G>A | p.Ala137Thr | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/13 | 620/2903 | 409/1317 | 137/438 | chr19 | 39099046 | |||
chr19:39099075 | C | A | 1 | a0006 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.438C>A | p.Asn146Lys | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/13 | 649/2903 | 438/1317 | 146/438 | chr19 | 39099075 | |||
chr19:39099091 | C | T | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.454C>T | p.Arg152Trp | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/13 | 665/2903 | 454/1317 | 152/438 | chr19 | 39099091 | |||
chr19:39101189 | G | T | 1 | a0002 | 3 | HG01255.hp2 HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.955G>T | p.Asp319Tyr | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 9/13 | 1166/2903 | 955/1317 | 319/438 | chr19 | 39101189 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:39085347 | G | A | 7 | a0001c0005a0001c0006a0001c0007others(4): Show | 48 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(45): Show |
synonymous_variant | LOW | c.78G>A | p.Gly26Gly | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/13 | 289/2903 | 78/1317 | 26/438 | chr19 | 39085347 | |||
chr19:39098537 | G | A | 2 | a0001c0007a0004c0013 | 7 | HG00642.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
synonymous_variant | LOW | c.201G>A | p.Ser67Ser | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/13 | 412/2903 | 201/1317 | 67/438 | chr19 | 39098537 | |||
chr19:39098549 | C | T | 4 | a0001c0002a0001c0009a0001c0017others(1): Show | 109 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
synonymous_variant | LOW | c.213C>T | p.Pro71Pro | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/13 | 424/2903 | 213/1317 | 71/438 | chr19 | 39098549 | |||
chr19:39100283 | C | A | 1 | a0001c0017 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.562C>A | p.Arg188Arg | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 5/13 | 773/2903 | 562/1317 | 188/438 | chr19 | 39100283 | |||
chr19:39100315 | G | A | 12 | a0001c0001a0001c0002a0001c0005others(9): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
synonymous_variant | LOW | c.594G>A | p.Pro198Pro | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 5/13 | 805/2903 | 594/1317 | 198/438 | chr19 | 39100315 | |||
chr19:39101498 | C | T | 6 | a0001c0004a0001c0006a0001c0008others(3): Show | 80 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(77): Show |
synonymous_variant | LOW | c.1074C>T | p.Thr358Thr | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/13 | 1285/2903 | 1074/1317 | 358/438 | chr19 | 39101498 | |||
chr19:39101528 | A | G | 1 | a0001c0018 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.1104A>G | p.Thr368Thr | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/13 | 1315/2903 | 1104/1317 | 368/438 | chr19 | 39101528 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:39084397 | G | A | 12 | a0001c0001t0013a0001c0002t0007a0001c0002t0012others(9): Show | 77 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-182G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/13 | 873 | chr19 | 39084397 | ||||||
chr19:39085110 | T | C | 19 | a0001c0001t0011a0001c0001t0014a0001c0001t0015others(16): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-160T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/13 | 160 | chr19 | 39085110 | ||||||
chr19:39085130 | C | CCCT | 19 | a0001c0001t0011a0001c0001t0014a0001c0001t0015others(16): Show | 91 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-139_-137dupCCT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/13 | 136 | INFO_REALIGN_3_PRIME | chr19 | 39085130 | |||||
chr19:39085230 | C | T | 2 | a0001c0001t0028a0001c0010t0018 | 4 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/13 | 40 | chr19 | 39085230 | ||||||
chr19:39085244 | C | A | 1 | a0001c0001t0011 | 7 | NA18952.hp1 NA18983.hp1 NA19000.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-26C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/13 | 26 | chr19 | 39085244 | ||||||
chr19:39110241 | A | C | 4 | a0001c0004t0009a0001c0006t0009a0001c0008t0009others(1): Show | 12 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*123A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 123 | chr19 | 39110241 | ||||||
chr19:39110400 | G | A | 1 | a0001c0001t0030 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 282 | chr19 | 39110400 | ||||||
chr19:39110500 | T | C | 19 | a0001c0002t0002a0001c0002t0005a0001c0002t0007others(16): Show | 114 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*382T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 382 | chr19 | 39110500 | ||||||
chr19:39110530 | G | A | 17 | a0001c0002t0002a0001c0002t0005a0001c0002t0007others(14): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*412G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 412 | chr19 | 39110530 | ||||||
chr19:39110552 | C | T | 14 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(11): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 434 | chr19 | 39110552 | ||||||
chr19:39110633 | T | C | 2 | a0001c0006t0008a0001c0010t0018 | 12 | HG01109.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*515T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 515 | chr19 | 39110633 | ||||||
chr19:39110652 | G | A | 1 | a0001c0001t0033 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 534 | chr19 | 39110652 | ||||||
chr19:39110695 | G | A | 1 | a0001c0002t0021 | 2 | NA18981.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*577G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 577 | chr19 | 39110695 | ||||||
chr19:39110899 | C | T | 8 | a0001c0001t0004a0001c0003t0020a0001c0004t0004others(5): Show | 52 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*781C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 781 | chr19 | 39110899 | ||||||
chr19:39110949 | A | C | 1 | a0001c0002t0023 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 831 | chr19 | 39110949 | ||||||
chr19:39110966 | A | T | 1 | a0001c0002t0031 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848A>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 848 | chr19 | 39110966 | ||||||
chr19:39110997 | G | A | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(6): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*879G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 879 | chr19 | 39110997 | ||||||
chr19:39111175 | T | A | 4 | a0001c0004t0009a0001c0006t0009a0001c0008t0009others(1): Show | 12 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1057T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 1057 | chr19 | 39111175 | ||||||
chr19:39111268 | C | G | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(6): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1150C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 1150 | chr19 | 39111268 | ||||||
chr19:39111366 | AGGAGGTT others(18): Show |
A | 1 | a0001c0003t0025 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1250_*1274delGAGG others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 1250 | INFO_REALIGN_3_PRIME | chr19 | 39111366 | |||||
chr19:39111432 | C | A | 1 | a0001c0003t0032 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 13/13 | 1314 | chr19 | 39111432 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:39084509 | G | C | 11 | a0001c0002t0002g0028a0001c0002t0002g0029a0001c0003t0002g0023others(8): Show | 12 | HG00408.hp1 HG00597.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-179+109G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | chr19 | 39084509 | |||||||
chr19:39084509 | G | T | 1 | a0001c0001t0001g0377 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-179+109G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | chr19 | 39084509 | |||||||
chr19:39084510 | G | T | 1 | a0001c0001t0001g0376 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-179+110G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | chr19 | 39084510 | |||||||
chr19:39084536 | AG | A | 190 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(187): Show | 202 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.-179+139delG | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 39084536 | ||||||
chr19:39084598 | C | G | 1 | a0001c0001t0001g0375 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-179+198C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | chr19 | 39084598 | |||||||
chr19:39084795 | G | A | 106 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(103): Show | 110 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.-178-297G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | chr19 | 39084795 | |||||||
chr19:39084811 | C | G | 5 | a0001c0003t0006g0370a0001c0003t0006g0371a0001c0003t0006g0372others(2): Show | 5 | NA18960.hp1 NA18961.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178-281C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | chr19 | 39084811 | |||||||
chr19:39085017 | G | A | 9 | a0001c0005t0001g0034a0001c0006t0008g0006a0001c0006t0008g0032others(6): Show | 11 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-178-75G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 1/12 | chr19 | 39085017 | |||||||
chr19:39085423 | C | T | 1 | a0001c0001t0001g0369 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.121+33C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085423 | |||||||
chr19:39085433 | C | T | 1 | a0001c0002t0005g0368 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.121+43C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085433 | |||||||
chr19:39085613 | C | T | 9 | a0001c0003t0032g0120a0001c0005t0001g0198a0001c0005t0001g0199others(6): Show | 9 | HG02055.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+223C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085613 | |||||||
chr19:39085622 | G | A | 14 | a0001c0001t0015g0123a0001c0002t0002g0009a0001c0002t0002g0010others(11): Show | 16 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.121+232G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085622 | |||||||
chr19:39085646 | G | C | 2 | a0001c0003t0003g0213a0001c0003t0003g0214 | 2 | NA18964.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.121+256G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085646 | |||||||
chr19:39085665 | G | A | 2 | a0001c0003t0014g0026a0001c0003t0014g0027 | 2 | NA18957.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.121+275G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085665 | |||||||
chr19:39085737 | T | C | 1 | a0001c0007t0006g0038 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+347T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085737 | |||||||
chr19:39085747 | G | C | 1 | a0001c0003t0003g0215 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.121+357G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085747 | |||||||
chr19:39085810 | C | G | 23 | a0001c0005t0001g0034a0001c0006t0008g0006a0001c0006t0008g0032others(20): Show | 25 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.121+420C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085810 | |||||||
chr19:39085811 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.121+421G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085811 | |||||||
chr19:39085949 | T | G | 205 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(202): Show | 215 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.121+559T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085949 | |||||||
chr19:39085953 | C | T | 102 | a0001c0001t0001g0192a0001c0001t0001g0221a0001c0001t0011g0013others(99): Show | 109 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.121+563C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085953 | |||||||
chr19:39085966 | T | C | 2 | a0001c0001t0028g0217a0001c0009t0005g0133 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.121+576T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39085966 | |||||||
chr19:39086048 | G | A | 1 | a0001c0001t0013g0243 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.121+658G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086048 | |||||||
chr19:39086096 | G | GAAGGATC others(4): Show |
2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02486.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.121+707_121+717dup others(11): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39086096 | ||||||
chr19:39086104 | A | G | 113 | a0001c0001t0001g0192a0001c0001t0001g0221a0001c0001t0011g0013others(110): Show | 120 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.121+714A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086104 | |||||||
chr19:39086436 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.121+1046C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086436 | |||||||
chr19:39086629 | C | CA | 23 | a0001c0001t0006g0103a0001c0001t0006g0137a0001c0001t0014g0138others(20): Show | 27 | HG00140.hp1 HG00558.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.121+1251dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39086629 | ||||||
chr19:39086637 | A | G | 1 | a0001c0004t0002g0194 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.121+1247A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086637 | |||||||
chr19:39086641 | A | AG | 127 | a0001c0001t0001g0020a0001c0001t0001g0192a0001c0001t0001g0195others(124): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.121+1261dupG | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39086641 | ||||||
chr19:39086641 | AG | A | 68 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(65): Show | 71 | HG00280.hp1 HG00423.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.121+1261delG | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39086641 | ||||||
chr19:39086642 | G | A | 62 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0006g0098others(59): Show | 69 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.121+1252G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086642 | |||||||
chr19:39086643 | G | A | 54 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(51): Show | 56 | HG00280.hp1 HG00423.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.121+1253G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086643 | |||||||
chr19:39086644 | G | A | 2 | a0001c0002t0005g0218a0001c0009t0029g0210 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+1254G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086644 | |||||||
chr19:39086645 | G | C | 1 | a0001c0005t0001g0198 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.121+1255G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086645 | |||||||
chr19:39086659 | T | C | 193 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(190): Show | 202 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.121+1269T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086659 | |||||||
chr19:39086665 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.121+1275G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086665 | |||||||
chr19:39086724 | A | C | 189 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(186): Show | 198 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.121+1334A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086724 | |||||||
chr19:39086788 | G | C | 258 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(255): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.121+1398G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086788 | |||||||
chr19:39086833 | C | T | 3 | a0001c0005t0010g0141a0001c0005t0010g0144a0001c0005t0010g0145 | 3 | HG02280.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.121+1443C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086833 | |||||||
chr19:39086970 | A | C | 1 | a0001c0004t0002g0194 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.121+1580A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086970 | |||||||
chr19:39086972 | G | A | 13 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(10): Show | 14 | HG01884.hp2 HG01934.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.121+1582G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086972 | |||||||
chr19:39086981 | A | G | 3 | a0001c0002t0007g0242a0001c0002t0012g0330a0001c0002t0012g0331 | 3 | HG01358.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.121+1591A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39086981 | |||||||
chr19:39087084 | C | G | 2 | a0001c0002t0005g0218a0001c0009t0029g0210 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+1694C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087084 | |||||||
chr19:39087100 | G | A | 186 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(183): Show | 195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.121+1710G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087100 | |||||||
chr19:39087306 | C | A | 1 | a0001c0001t0015g0123 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.121+1916C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087306 | |||||||
chr19:39087465 | G | A | 1 | a0001c0009t0005g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.121+2075G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087465 | |||||||
chr19:39087632 | G | GT | 13 | a0001c0001t0001g0216a0001c0001t0001g0327a0001c0001t0001g0328others(10): Show | 13 | HG00140.hp2 HG00735.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.121+2261dupT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39087632 | ||||||
chr19:39087632 | GT | G | 226 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(223): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.121+2261delT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39087632 | ||||||
chr19:39087632 | GTT | G | 11 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(8): Show | 11 | HG01934.hp2 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.121+2260_121+2261d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39087632 | ||||||
chr19:39087637 | T | G | 12 | a0001c0001t0013g0247a0001c0001t0013g0249a0001c0003t0003g0272others(9): Show | 12 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.121+2247T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087637 | |||||||
chr19:39087638 | T | G | 173 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(170): Show | 182 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.121+2248T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087638 | |||||||
chr19:39087643 | T | G | 173 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(170): Show | 182 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.121+2253T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087643 | |||||||
chr19:39087648 | T | G | 172 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(169): Show | 181 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.121+2258T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087648 | |||||||
chr19:39087909 | C | T | 176 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0052others(173): Show | 185 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.121+2519C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39087909 | |||||||
chr19:39088030 | T | C | 1 | a0001c0003t0003g0287 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.121+2640T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088030 | |||||||
chr19:39088031 | C | T | 1 | a0001c0003t0003g0287 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.121+2641C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088031 | |||||||
chr19:39088215 | G | T | 2 | a0001c0003t0003g0269a0001c0003t0003g0270 | 2 | NA18970.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.121+2825G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088215 | |||||||
chr19:39088257 | A | G | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121+2867A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088257 | |||||||
chr19:39088303 | G | C | 1 | a0001c0005t0001g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.121+2913G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088303 | |||||||
chr19:39088419 | C | T | 82 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0057others(79): Show | 84 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.121+3029C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088419 | |||||||
chr19:39088491 | C | G | 1 | a0001c0005t0010g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.121+3101C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088491 | |||||||
chr19:39088559 | T | G | 23 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(20): Show | 23 | HG00642.hp1 HG01934.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+3169T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088559 | |||||||
chr19:39088667 | T | C | 2 | a0001c0002t0005g0226a0001c0002t0007g0225 | 2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.121+3277T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088667 | |||||||
chr19:39088724 | T | C | 1 | a0001c0002t0005g0325 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.121+3334T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088724 | |||||||
chr19:39088726 | G | GGTTT | 6 | a0001c0002t0022g0179a0001c0003t0003g0030a0001c0003t0003g0250others(3): Show | 6 | HG01255.hp1 HG02165.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+3369_121+3372d others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39088726 | ||||||
chr19:39088726 | GGTTT | G | 27 | a0001c0001t0001g0335a0001c0001t0015g0190a0001c0001t0028g0217others(24): Show | 29 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.121+3369_121+3372d others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39088726 | ||||||
chr19:39088726 | GGTTTGTT others(1): Show |
G | 123 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(120): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.121+3365_121+3372d others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39088726 | ||||||
chr19:39088726 | GGTTTGTT others(5): Show |
G | 84 | a0001c0001t0011g0013a0001c0001t0011g0164a0001c0001t0011g0165others(81): Show | 91 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.121+3361_121+3372d others(14): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39088726 | ||||||
chr19:39088781 | C | T | 2 | a0001c0012t0006g0207a0001c0012t0006g0208 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.121+3391C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088781 | |||||||
chr19:39088934 | A | G | 6 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+3544A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088934 | |||||||
chr19:39088934 | AT | A | 88 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0057others(85): Show | 89 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.121+3557delT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39088934 | ||||||
chr19:39088935 | T | G | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.121+3545T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39088935 | |||||||
chr19:39089118 | G | A | 7 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(4): Show | 8 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.121+3728G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089118 | |||||||
chr19:39089129 | G | T | 1 | a0001c0001t0013g0243 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.121+3739G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089129 | |||||||
chr19:39089225 | G | A | 2 | a0001c0005t0001g0199a0001c0005t0001g0200 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.121+3835G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089225 | |||||||
chr19:39089312 | C | T | 2 | a0001c0008t0009g0142a0001c0008t0009g0143 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.121+3922C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089312 | |||||||
chr19:39089327 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.121+3937C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089327 | |||||||
chr19:39089333 | G | A | 1 | a0001c0003t0002g0023 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.121+3943G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089333 | |||||||
chr19:39089358 | A | G | 316 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(313): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.121+3968A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089358 | |||||||
chr19:39089740 | G | A | 2 | a0001c0002t0021g0158a0001c0002t0021g0180 | 2 | NA18981.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.121+4350G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089740 | |||||||
chr19:39089872 | CTGTGACT others(6): Show |
C | 1 | a0001c0002t0023g0238 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.121+4486_121+4498d others(15): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39089872 | ||||||
chr19:39089917 | C | G | 2 | a0001c0012t0006g0207a0001c0012t0006g0208 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.121+4527C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39089917 | |||||||
chr19:39090079 | G | A | 2 | a0001c0005t0006g0134a0001c0005t0006g0135 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.121+4689G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090079 | |||||||
chr19:39090097 | A | G | 100 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0091others(97): Show | 105 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.121+4707A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090097 | |||||||
chr19:39090098 | T | G | 1 | a0001c0004t0004g0048 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.121+4708T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090098 | |||||||
chr19:39090449 | A | G | 1 | a0001c0002t0027g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.121+5059A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090449 | |||||||
chr19:39090465 | G | A | 2 | a0001c0003t0006g0049a0001c0004t0004g0050 | 2 | HG02523.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.121+5075G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090465 | |||||||
chr19:39090790 | C | CT | 127 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0057others(124): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.121+5417dupT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39090790 | ||||||
chr19:39090790 | C | CTT | 8 | a0001c0002t0002g0162a0001c0004t0004g0086a0001c0004t0009g0019others(5): Show | 9 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+5416_121+5417d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39090790 | ||||||
chr19:39090790 | CT | C | 6 | a0001c0001t0001g0292a0001c0001t0001g0336a0001c0002t0002g0124others(3): Show | 6 | HG01069.hp2 HG01943.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+5417delT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39090790 | ||||||
chr19:39090798 | T | G | 1 | a0001c0002t0007g0225 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.121+5408T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090798 | |||||||
chr19:39090827 | A | G | 2 | a0001c0012t0006g0207a0001c0012t0006g0208 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.121+5437A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090827 | |||||||
chr19:39090925 | T | C | 8 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(5): Show | 10 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+5535T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090925 | |||||||
chr19:39090927 | G | A | 1 | a0001c0002t0005g0227 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.121+5537G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39090927 | |||||||
chr19:39091086 | C | T | 122 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.121+5696C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091086 | |||||||
chr19:39091164 | C | CT | 12 | a0001c0002t0002g0140a0001c0002t0005g0085a0001c0006t0008g0006others(9): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.121+5789dupT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39091164 | ||||||
chr19:39091164 | CT | C | 11 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0337others(8): Show | 11 | HG01069.hp2 HG02004.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.121+5789delT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39091164 | ||||||
chr19:39091287 | C | T | 1 | a0001c0002t0023g0238 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.121+5897C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091287 | |||||||
chr19:39091310 | G | A | 1 | a0001c0001t0013g0247 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.121+5920G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091310 | |||||||
chr19:39091363 | A | G | 1 | a0001c0002t0005g0042 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.121+5973A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091363 | |||||||
chr19:39091478 | T | C | 89 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0091others(86): Show | 92 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+6088T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091478 | |||||||
chr19:39091561 | C | T | 1 | a0001c0001t0001g0363 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.121+6171C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091561 | |||||||
chr19:39091640 | C | T | 3 | a0001c0003t0032g0120a0001c0012t0006g0207a0001c0012t0006g0208 | 3 | HG01168.hp2 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.121+6250C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091640 | |||||||
chr19:39091697 | G | A | 2 | a0001c0002t0005g0054a0001c0004t0004g0055 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.121+6307G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091697 | |||||||
chr19:39091772 | G | A | 1 | a0001c0002t0012g0246 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.121+6382G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39091772 | |||||||
chr19:39091909 | CTAAAAAA others(1): Show |
C | 23 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(20): Show | 23 | HG00642.hp1 HG01934.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.122-6531_122-6524d others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39091909 | ||||||
chr19:39091918 | T | TA | 9 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(6): Show | 11 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.122-6533dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39091918 | ||||||
chr19:39092058 | G | A | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.122-6400G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092058 | |||||||
chr19:39092112 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.122-6346C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092112 | |||||||
chr19:39092370 | G | GTA | 30 | a0001c0002t0002g0131a0001c0002t0005g0108a0001c0002t0005g0226others(27): Show | 33 | HG00558.hp2 HG01175.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.122-6065_122-6064d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092370 | ||||||
chr19:39092370 | G | GTATA | 3 | a0001c0003t0003g0266a0001c0003t0003g0282a0001c0003t0032g0120 | 3 | HG01361.hp1 HG01978.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.122-6067_122-6064d others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092370 | ||||||
chr19:39092370 | G | GTATATAT others(1): Show |
3 | a0001c0002t0007g0242a0001c0002t0012g0330a0001c0002t0012g0331 | 3 | HG01358.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.122-6071_122-6064d others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092370 | ||||||
chr19:39092370 | GTA | G | 13 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0244others(10): Show | 13 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-6065_122-6064d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092370 | ||||||
chr19:39092370 | GTATA | G | 212 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(209): Show | 219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.122-6067_122-6064d others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092370 | ||||||
chr19:39092374 | A | G | 4 | a0001c0004t0002g0194a0001c0004t0005g0161a0001c0004t0005g0189others(1): Show | 4 | HG00621.hp1 HG02074.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-6084A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092374 | |||||||
chr19:39092376 | A | G | 93 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0091others(90): Show | 98 | HG00423.hp1 HG00673.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.122-6082A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092376 | |||||||
chr19:39092378 | A | G | 1 | a0001c0004t0004g0096 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.122-6080A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092378 | |||||||
chr19:39092417 | G | A | 2 | a0001c0001t0006g0098a0001c0001t0006g0099 | 2 | NA19072.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.122-6041G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092417 | |||||||
chr19:39092487 | G | A | 9 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(6): Show | 11 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.122-5971G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092487 | |||||||
chr19:39092519 | C | T | 1 | a0001c0003t0003g0262 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.122-5939C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092519 | |||||||
chr19:39092520 | G | A | 309 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(306): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.122-5938G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092520 | |||||||
chr19:39092709 | C | T | 1 | a0001c0001t0028g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122-5749C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092709 | |||||||
chr19:39092728 | C | A | 82 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0091others(79): Show | 84 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.122-5730C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092728 | |||||||
chr19:39092770 | TC | T | 6 | a0001c0003t0002g0023a0001c0003t0014g0022a0001c0003t0014g0026others(3): Show | 6 | HG00408.hp1 NA18943.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-5687delC | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092770 | |||||||
chr19:39092771 | C | CT | 94 | a0001c0001t0001g0057a0001c0001t0001g0091a0001c0001t0001g0104others(91): Show | 96 | HG00423.hp1 HG00673.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.122-5663dupT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092771 | ||||||
chr19:39092771 | C | CTT | 12 | a0001c0002t0005g0007a0001c0002t0005g0042a0001c0002t0005g0062others(9): Show | 14 | HG00621.hp1 HG01255.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.122-5664_122-5663d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092771 | ||||||
chr19:39092771 | C | T | 1 | a0001c0003t0019g0021 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.122-5687C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092771 | |||||||
chr19:39092771 | CT | C | 19 | a0001c0001t0001g0360a0001c0001t0028g0217a0001c0002t0002g0014others(16): Show | 20 | HG00741.hp1 HG01257.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-5663delT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092771 | ||||||
chr19:39092771 | CTT | C | 114 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(111): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.122-5664_122-5663d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39092771 | ||||||
chr19:39092787 | T | C | 130 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(127): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.122-5671T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092787 | |||||||
chr19:39092881 | G | C | 1 | a0001c0001t0001g0363 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.122-5577G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39092881 | |||||||
chr19:39093057 | C | T | 9 | a0001c0003t0032g0120a0001c0004t0009g0019a0001c0004t0009g0102others(6): Show | 10 | HG01168.hp2 HG01169.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-5401C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093057 | |||||||
chr19:39093070 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.122-5388G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093070 | |||||||
chr19:39093090 | T | TTTTC | 139 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(136): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.122-5360_122-5357d others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093090 | ||||||
chr19:39093099 | T | TTTCC | 83 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0091others(80): Show | 85 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(82): Show |
intron_variant | MODIFIER | c.122-5357_122-5356i others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093099 | ||||||
chr19:39093139 | C | G | 6 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-5319C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093139 | |||||||
chr19:39093140 | A | C | 6 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-5318A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093140 | |||||||
chr19:39093141 | C | CTGCT | 210 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(207): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.122-5316_122-5315i others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093141 | ||||||
chr19:39093141 | C | T | 6 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-5317C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093141 | |||||||
chr19:39093142 | T | TGCTTTCT others(11): Show |
14 | a0001c0005t0010g0193a0001c0006t0008g0006a0001c0006t0008g0032others(11): Show | 16 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-5316_122-5315i others(20): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093142 | |||||||
chr19:39093143 | C | T | 230 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(227): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.122-5315C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093143 | |||||||
chr19:39093172 | C | CTTTCTTT others(31): Show |
1 | a0001c0005t0010g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.122-5285_122-5284i others(40): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(39): Show |
1 | a0001c0005t0010g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.122-5285_122-5284i others(48): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(43): Show |
4 | a0001c0002t0005g0054a0001c0004t0004g0055a0001c0005t0010g0141others(1): Show | 4 | HG02040.hp1 HG02129.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(52): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(49): Show |
1 | a0001c0001t0001g0335 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.122-5285_122-5284i others(58): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(15): Show |
3 | a0001c0003t0032g0120a0001c0012t0006g0207a0001c0012t0006g0208 | 3 | HG01168.hp2 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-5285_122-5284i others(24): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(35): Show |
2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02486.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.122-5285_122-5284i others(44): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(19): Show |
1 | a0001c0001t0028g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122-5285_122-5284i others(28): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(23): Show |
1 | a0001c0001t0001g0376 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.122-5285_122-5284i others(32): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(27): Show |
12 | a0001c0001t0001g0087a0001c0001t0001g0322a0001c0001t0001g0363others(9): Show | 12 | HG01981.hp2 HG02698.hp1 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(36): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(31): Show |
25 | a0001c0001t0001g0216a0001c0001t0001g0315a0001c0001t0001g0316others(22): Show | 25 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(40): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(35): Show |
36 | a0001c0001t0001g0020a0001c0001t0001g0039a0001c0001t0001g0040others(33): Show | 37 | HG00280.hp2 HG00544.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(44): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(39): Show |
26 | a0001c0001t0001g0043a0001c0001t0001g0292a0001c0001t0001g0294others(23): Show | 26 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(48): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(43): Show |
55 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0192others(52): Show | 57 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(52): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(47): Show |
25 | a0001c0001t0001g0091a0001c0001t0001g0105a0001c0001t0001g0221others(22): Show | 26 | HG01192.hp1 HG01891.hp2 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(56): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(51): Show |
9 | a0001c0004t0002g0194a0001c0004t0004g0044a0001c0004t0004g0053others(6): Show | 9 | HG00621.hp1 HG01070.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(60): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(55): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0104a0001c0002t0002g0182others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(64): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(59): Show |
2 | a0001c0004t0004g0056a0001c0004t0004g0096 | 2 | HG01496.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.122-5285_122-5284i others(68): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(133): Show |
1 | a0001c0004t0009g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122-5285_122-5284i others(142): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(125): Show |
5 | a0001c0004t0009g0019a0001c0004t0009g0291a0001c0008t0016g0112others(2): Show | 6 | HG02451.hp2 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-5285_122-5284i others(134): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | CTTTCTTT others(47): Show |
1 | a0001c0004t0004g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.122-5285_122-5284i others(56): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39093172 | ||||||
chr19:39093172 | C | T | 14 | a0001c0005t0010g0193a0001c0006t0008g0006a0001c0006t0008g0032others(11): Show | 16 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-5286C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093172 | |||||||
chr19:39093179 | C | T | 3 | a0001c0003t0032g0120a0001c0012t0006g0207a0001c0012t0006g0208 | 3 | HG01168.hp2 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-5279C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093179 | |||||||
chr19:39093278 | T | C | 1 | a0001c0002t0005g0324 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.122-5180T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093278 | |||||||
chr19:39093340 | C | T | 3 | a0001c0002t0002g0157a0001c0002t0005g0220a0001c0002t0005g0229 | 3 | HG00733.hp1 HG01106.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.122-5118C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093340 | |||||||
chr19:39093402 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.122-5056C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093402 | |||||||
chr19:39093517 | G | A | 6 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-4941G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093517 | |||||||
chr19:39093543 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.122-4915C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093543 | |||||||
chr19:39093545 | C | T | 1 | a0001c0002t0002g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.122-4913C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093545 | |||||||
chr19:39093640 | T | G | 1 | a0001c0004t0004g0067 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.122-4818T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093640 | |||||||
chr19:39093759 | C | A | 14 | a0001c0003t0003g0280a0001c0003t0003g0281a0001c0005t0010g0193others(11): Show | 16 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-4699C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093759 | |||||||
chr19:39093814 | C | T | 1 | a0001c0004t0004g0078 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.122-4644C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39093814 | |||||||
chr19:39094093 | T | G | 124 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(121): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.122-4365T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094093 | |||||||
chr19:39094121 | G | A | 11 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(8): Show | 13 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-4337G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094121 | |||||||
chr19:39094219 | G | A | 3 | a0001c0001t0001g0221a0001c0002t0005g0239a0001c0002t0005g0240 | 3 | NA18942.hp1 NA18968.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.122-4239G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094219 | |||||||
chr19:39094236 | C | T | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-4222C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094236 | |||||||
chr19:39094238 | C | T | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-4220C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094238 | |||||||
chr19:39094251 | T | A | 1 | a0001c0005t0006g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-4207T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094251 | |||||||
chr19:39094279 | T | C | 12 | a0001c0005t0010g0193a0001c0006t0008g0006a0001c0006t0008g0032others(9): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-4179T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094279 | |||||||
chr19:39094359 | C | T | 1 | a0001c0003t0003g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.122-4099C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094359 | |||||||
chr19:39094360 | G | A | 5 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0006t0010g0205others(2): Show | 5 | HG03471.hp2 HG03516.hp2 NA19072.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-4098G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094360 | |||||||
chr19:39094374 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.122-4084G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094374 | |||||||
chr19:39094487 | A | T | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-3971A>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094487 | |||||||
chr19:39094502 | CA | C | 211 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(208): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.122-3941delA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39094502 | ||||||
chr19:39094502 | CAA | C | 86 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0091others(83): Show | 88 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.122-3942_122-3941d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39094502 | ||||||
chr19:39094537 | T | C | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-3921T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094537 | |||||||
chr19:39094546 | C | T | 59 | a0001c0001t0011g0013a0001c0001t0011g0164a0001c0001t0011g0165others(56): Show | 66 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.122-3912C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094546 | |||||||
chr19:39094560 | C | T | 1 | a0001c0003t0003g0262 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.122-3898C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094560 | |||||||
chr19:39094656 | C | G | 12 | a0001c0005t0010g0193a0001c0006t0008g0006a0001c0006t0008g0032others(9): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-3802C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094656 | |||||||
chr19:39094669 | A | T | 2 | a0001c0008t0009g0142a0001c0008t0009g0143 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.122-3789A>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094669 | |||||||
chr19:39094732 | C | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0091others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-3726C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094732 | |||||||
chr19:39094760 | G | T | 11 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(8): Show | 13 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-3698G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094760 | |||||||
chr19:39094985 | A | G | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-3473A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39094985 | |||||||
chr19:39095094 | T | C | 11 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(8): Show | 13 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-3364T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095094 | |||||||
chr19:39095105 | C | T | 2 | a0001c0005t0001g0202a0001c0005t0010g0201 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.122-3353C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095105 | |||||||
chr19:39095209 | C | T | 7 | a0001c0007t0006g0038a0001c0007t0006g0109a0001c0007t0006g0111others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-3249C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095209 | |||||||
chr19:39095227 | G | A | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-3231G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095227 | |||||||
chr19:39095239 | G | T | 1 | a0001c0002t0007g0236 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.122-3219G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095239 | |||||||
chr19:39095326 | C | T | 1 | a0001c0002t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.122-3132C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095326 | |||||||
chr19:39095330 | T | G | 1 | a0001c0001t0001g0039 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.122-3128T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095330 | |||||||
chr19:39095362 | A | G | 12 | a0001c0005t0010g0193a0001c0006t0008g0006a0001c0006t0008g0032others(9): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-3096A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095362 | |||||||
chr19:39095562 | T | G | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-2896T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095562 | |||||||
chr19:39095672 | G | A | 2 | a0001c0008t0009g0142a0001c0008t0009g0143 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.122-2786G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095672 | |||||||
chr19:39095835 | G | A | 1 | a0001c0005t0001g0202 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.122-2623G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39095835 | |||||||
chr19:39096012 | C | G | 15 | a0001c0001t0001g0221a0001c0001t0015g0190a0001c0002t0002g0159others(12): Show | 15 | NA18942.hp1 NA18952.hp2 NA18959.hp1 others(12): Show |
intron_variant | MODIFIER | c.122-2446C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096012 | |||||||
chr19:39096177 | G | A | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-2281G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096177 | |||||||
chr19:39096314 | A | G | 116 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(113): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.122-2144A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096314 | |||||||
chr19:39096338 | C | T | 1 | a0001c0004t0020g0268 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.122-2120C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096338 | |||||||
chr19:39096360 | C | T | 10 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(7): Show | 12 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-2098C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096360 | |||||||
chr19:39096464 | T | C | 1 | a0001c0002t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.122-1994T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096464 | |||||||
chr19:39096478 | A | G | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-1980A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096478 | |||||||
chr19:39096696 | A | G | 2 | a0001c0008t0009g0142a0001c0008t0009g0143 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.122-1762A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096696 | |||||||
chr19:39096863 | G | A | 18 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(15): Show | 18 | HG00642.hp1 HG01256.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.122-1595G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096863 | |||||||
chr19:39096877 | C | T | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122-1581C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096877 | |||||||
chr19:39096878 | G | A | 126 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(123): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.122-1580G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096878 | |||||||
chr19:39096895 | G | A | 2 | a0001c0008t0009g0142a0001c0008t0009g0143 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.122-1563G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096895 | |||||||
chr19:39096944 | G | A | 1 | a0001c0004t0004g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.122-1514G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096944 | |||||||
chr19:39096990 | T | C | 18 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(15): Show | 18 | HG00642.hp1 HG01934.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.122-1468T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39096990 | |||||||
chr19:39097007 | G | A | 1 | a0001c0003t0006g0049 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.122-1451G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097007 | |||||||
chr19:39097014 | A | C | 1 | a0001c0005t0006g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-1444A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097014 | |||||||
chr19:39097017 | G | A | 1 | a0001c0004t0004g0274 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.122-1441G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097017 | |||||||
chr19:39097017 | G | T | 78 | a0001c0001t0015g0190a0001c0002t0002g0148a0001c0002t0002g0159others(75): Show | 80 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.122-1441G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097017 | |||||||
chr19:39097021 | C | T | 3 | a0001c0005t0010g0141a0001c0005t0010g0144a0001c0005t0010g0145 | 3 | HG02280.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.122-1437C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097021 | |||||||
chr19:39097025 | C | T | 1 | a0001c0004t0004g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.122-1433C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097025 | |||||||
chr19:39097080 | A | G | 87 | a0001c0001t0015g0190a0001c0002t0002g0148a0001c0002t0002g0159others(84): Show | 90 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.122-1378A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097080 | |||||||
chr19:39097255 | C | T | 83 | a0001c0002t0002g0148a0001c0002t0002g0159a0001c0002t0002g0160others(80): Show | 86 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.122-1203C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097255 | |||||||
chr19:39097308 | T | C | 84 | a0001c0002t0002g0148a0001c0002t0002g0159a0001c0002t0002g0160others(81): Show | 87 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.122-1150T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097308 | |||||||
chr19:39097335 | C | G | 84 | a0001c0002t0002g0148a0001c0002t0002g0159a0001c0002t0002g0160others(81): Show | 87 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.122-1123C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097335 | |||||||
chr19:39097351 | C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0343 | 2 | NA19054.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.122-1107C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097351 | |||||||
chr19:39097352 | G | A | 84 | a0001c0002t0002g0148a0001c0002t0002g0159a0001c0002t0002g0160others(81): Show | 87 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.122-1106G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097352 | |||||||
chr19:39097359 | C | T | 83 | a0001c0002t0002g0148a0001c0002t0002g0159a0001c0002t0002g0160others(80): Show | 86 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.122-1099C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097359 | |||||||
chr19:39097399 | C | CA | 6 | a0001c0001t0001g0307a0001c0001t0001g0365a0001c0001t0015g0149others(3): Show | 6 | HG03471.hp1 HG03831.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-1044dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39097399 | ||||||
chr19:39097399 | C | CAAAAA | 74 | a0001c0002t0002g0148a0001c0002t0002g0159a0001c0002t0002g0160others(71): Show | 77 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.122-1048_122-1044d others(7): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39097399 | ||||||
chr19:39097399 | C | CAAAAAA | 10 | a0001c0002t0005g0042a0001c0002t0005g0239a0001c0004t0004g0050others(7): Show | 10 | HG00621.hp1 HG01175.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-1049_122-1044d others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39097399 | ||||||
chr19:39097479 | G | A | 86 | a0001c0001t0001g0309a0001c0002t0002g0148a0001c0002t0002g0159others(83): Show | 89 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.122-979G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097479 | |||||||
chr19:39097568 | GA | G | 8 | a0001c0001t0001g0321a0001c0001t0001g0351a0001c0001t0011g0191others(5): Show | 8 | HG01168.hp1 HG04228.hp1 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.122-875delA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39097568 | ||||||
chr19:39097568 | GAA | G | 57 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(54): Show | 59 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.122-876_122-875del others(2): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39097568 | ||||||
chr19:39097688 | T | C | 6 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-770T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097688 | |||||||
chr19:39097799 | G | C | 59 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.122-659G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097799 | |||||||
chr19:39097833 | C | G | 13 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(10): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.122-625C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097833 | |||||||
chr19:39097931 | A | C | 59 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.122-527A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39097931 | |||||||
chr19:39098106 | C | T | 59 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.122-352C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39098106 | |||||||
chr19:39098168 | T | C | 1 | a0001c0003t0006g0049 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.122-290T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39098168 | |||||||
chr19:39098177 | C | G | 59 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.122-281C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39098177 | |||||||
chr19:39098177 | C | T | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.122-281C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39098177 | |||||||
chr19:39098253 | C | CA | 15 | a0001c0001t0001g0245a0001c0001t0001g0299a0001c0001t0001g0360others(12): Show | 15 | HG00140.hp1 HG00741.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.122-179dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39098253 | ||||||
chr19:39098253 | CA | C | 144 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(141): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.122-179delA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39098253 | ||||||
chr19:39098253 | CAA | C | 26 | a0001c0001t0001g0296a0001c0001t0001g0313a0001c0001t0001g0358others(23): Show | 27 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.122-180_122-179del others(2): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39098253 | ||||||
chr19:39098253 | CAAA | C | 104 | a0001c0001t0001g0321a0001c0001t0006g0137a0001c0001t0014g0138others(101): Show | 111 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.122-181_122-179del others(3): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39098253 | ||||||
chr19:39098253 | CAAAAAAA others(3): Show |
C | 2 | a0001c0005t0001g0202a0001c0005t0010g0201 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.122-188_122-179del others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39098253 | ||||||
chr19:39098269 | AAAAAAAA others(4): Show |
A | 2 | a0001c0004t0004g0076a0001c0004t0004g0077 | 2 | HG02135.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.122-184_122-174del others(11): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 39098269 | ||||||
chr19:39098275 | A | G | 58 | a0001c0002t0005g0227a0001c0003t0006g0049a0001c0004t0002g0194others(55): Show | 60 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.122-183A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39098275 | |||||||
chr19:39098363 | T | C | 60 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(57): Show | 62 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.122-95T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | chr19 | 39098363 | |||||||
chr19:39098694 | G | A | 305 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(302): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.322+36G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/12 | chr19 | 39098694 | |||||||
chr19:39098782 | T | A | 6 | a0001c0003t0003g0017a0001c0003t0003g0215a0001c0003t0003g0251others(3): Show | 7 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.322+124T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/12 | chr19 | 39098782 | |||||||
chr19:39098878 | T | C | 52 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-82T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/12 | chr19 | 39098878 | |||||||
chr19:39098880 | CACCAGTC others(26): Show |
C | 52 | a0001c0003t0006g0049a0001c0004t0002g0194a0001c0004t0004g0008others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-79_323-47delAC others(31): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/12 | chr19 | 39098880 | |||||||
chr19:39098908 | G | A | 101 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(98): Show | 108 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.323-52G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/12 | chr19 | 39098908 | |||||||
chr19:39098909 | G | A | 18 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(15): Show | 18 | HG00642.hp1 HG01934.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.323-51G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/12 | chr19 | 39098909 | |||||||
chr19:39098911 | G | A | 1 | a0001c0002t0012g0246 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.323-49G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3/12 | chr19 | 39098911 | |||||||
chr19:39099152 | C | T | 12 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(9): Show | 15 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.505+10C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39099152 | |||||||
chr19:39099173 | C | CGGTGGGG others(15): Show |
1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.505+47_505+68dupCA others(20): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39099173 | ||||||
chr19:39099199 | GGGGGGCG others(8): Show |
G | 8 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(5): Show | 9 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.505+80_505+94delCG others(13): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39099199 | ||||||
chr19:39099223 | G | T | 1 | a0001c0004t0004g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.505+81G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39099223 | |||||||
chr19:39099229 | CG | C | 126 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(123): Show | 129 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.505+92delG | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39099229 | ||||||
chr19:39099652 | G | A | 249 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(246): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.505+510G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39099652 | |||||||
chr19:39099790 | C | G | 1 | a0001c0009t0005g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.506-437C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39099790 | |||||||
chr19:39099808 | C | A | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.506-419C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39099808 | |||||||
chr19:39099906 | C | T | 249 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(246): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.506-321C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39099906 | |||||||
chr19:39099992 | C | CA | 62 | a0001c0001t0001g0192a0001c0001t0006g0137a0001c0003t0003g0215others(59): Show | 64 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.506-212dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39099992 | ||||||
chr19:39099992 | C | CAA | 7 | a0001c0004t0004g0048a0001c0004t0004g0090a0001c0004t0004g0274others(4): Show | 7 | HG00423.hp1 HG02074.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-213_506-212dup others(2): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39099992 | ||||||
chr19:39099992 | CA | C | 222 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(219): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.506-212delA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39099992 | ||||||
chr19:39099992 | CAA | C | 11 | a0001c0001t0001g0311a0001c0001t0001g0320a0001c0001t0001g0366others(8): Show | 11 | HG01256.hp1 HG02280.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.506-213_506-212del others(2): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39099992 | ||||||
chr19:39100121 | G | A | 312 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.506-106G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39100121 | |||||||
chr19:39100173 | A | T | 6 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(3): Show | 7 | HG02257.hp2 HG02622.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-54A>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | chr19 | 39100173 | |||||||
chr19:39100213 | G | GC | 95 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(92): Show | 102 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
splice_region_variant&intron_variant | LOW | c.506-9dupC | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 39100213 | ||||||
chr19:39100359 | T | C | 1 | a0001c0009t0029g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.629+9T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 5/12 | chr19 | 39100359 | |||||||
chr19:39100890 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.807+37G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 7/12 | chr19 | 39100890 | |||||||
chr19:39101108 | G | A | 101 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(98): Show | 108 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.916-42G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 8/12 | chr19 | 39101108 | |||||||
chr19:39101118 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.916-32G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 8/12 | chr19 | 39101118 | |||||||
chr19:39101214 | G | T | 1 | a0001c0002t0007g0235 | 1 | NA18951.hp2 | splice_region_variant&intron_variant | LOW | c.973+7G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 9/12 | chr19 | 39101214 | |||||||
chr19:39101449 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1042-17G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 10/12 | chr19 | 39101449 | |||||||
chr19:39101459 | T | C | 2 | a0001c0004t0004g0076a0001c0004t0004g0077 | 2 | HG02135.hp1 NA19064.hp1 |
splice_region_variant&intron_variant | LOW | c.1042-7T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 10/12 | chr19 | 39101459 | |||||||
chr19:39101546 | G | A | 1 | a0001c0002t0005g0106 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1113+9G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101546 | |||||||
chr19:39101629 | A | G | 12 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(9): Show | 15 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+92A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101629 | |||||||
chr19:39101663 | C | T | 107 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(104): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1113+126C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101663 | |||||||
chr19:39101687 | T | C | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1113+150T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101687 | |||||||
chr19:39101692 | C | T | 102 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(99): Show | 109 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1113+155C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101692 | |||||||
chr19:39101805 | A | G | 1 | a0001c0004t0017g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+268A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101805 | |||||||
chr19:39101936 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1113+399T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101936 | |||||||
chr19:39101939 | A | C | 1 | a0001c0001t0015g0167 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1113+402A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101939 | |||||||
chr19:39101942 | C | CA | 126 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(123): Show | 132 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1113+421dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39101942 | ||||||
chr19:39101942 | C | CAA | 23 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0322others(20): Show | 23 | HG00642.hp1 HG01358.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1113+420_1113+421d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39101942 | ||||||
chr19:39101942 | CA | C | 62 | a0001c0002t0002g0159a0001c0003t0003g0261a0001c0004t0002g0194others(59): Show | 64 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1113+421delA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39101942 | ||||||
chr19:39101985 | TGGTGCTT others(38): Show |
T | 1 | a0001c0001t0011g0165 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1113+450_1113+494d others(47): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39101985 | ||||||
chr19:39101986 | G | T | 1 | a0001c0010t0018g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1113+449G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39101986 | |||||||
chr19:39102115 | TTC | T | 5 | a0001c0001t0001g0328a0001c0002t0005g0069a0001c0005t0001g0212others(2): Show | 5 | HG02129.hp1 HG03453.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+583_1113+584d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102115 | ||||||
chr19:39102118 | T | TCA | 50 | a0001c0001t0001g0293a0001c0001t0001g0304a0001c0001t0001g0321others(47): Show | 51 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1113+582_1113+583i others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102118 | T | TCACA | 84 | a0001c0001t0001g0335a0001c0001t0001g0376a0001c0001t0015g0190others(81): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1113+582_1113+583i others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102118 | T | TCACACA | 23 | a0001c0002t0002g0130a0001c0002t0002g0140a0001c0002t0002g0171others(20): Show | 24 | HG00423.hp1 HG00544.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1113+582_1113+583i others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102118 | T | TCACACAC others(1): Show |
14 | a0001c0001t0028g0217a0001c0002t0002g0124a0001c0002t0002g0157others(11): Show | 15 | HG00733.hp1 HG02027.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1113+582_1113+583i others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102118 | T | TCACACAC others(3): Show |
7 | a0001c0005t0010g0141a0001c0005t0010g0144a0001c0005t0010g0145others(4): Show | 8 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+582_1113+583i others(12): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102118 | T | TCACACAC others(5): Show |
1 | a0001c0004t0009g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1113+582_1113+583i others(14): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102118 | TCTCA | T | 3 | a0001c0001t0001g0306a0001c0012t0006g0207a0001c0012t0006g0208 | 3 | HG01168.hp2 HG01169.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1113+583_1113+586d others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102118 | TCTCACAC others(7): Show |
T | 2 | a0001c0002t0005g0324a0001c0005t0001g0034 | 2 | HG03471.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1113+583_1113+596d others(16): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102118 | ||||||
chr19:39102120 | T | A | 282 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(279): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1113+583T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102120 | |||||||
chr19:39102120 | T | TCA | 35 | a0001c0001t0006g0101a0001c0001t0006g0103a0001c0001t0006g0204others(32): Show | 43 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1113+620_1113+621d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102120 | ||||||
chr19:39102120 | T | TCACA | 13 | a0001c0001t0006g0137a0001c0003t0003g0264a0001c0003t0003g0287others(10): Show | 13 | HG01934.hp2 HG02622.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+618_1113+621d others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102120 | ||||||
chr19:39102120 | T | TCACACA | 9 | a0001c0003t0003g0270a0001c0003t0006g0372a0001c0003t0019g0021others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+616_1113+621d others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102120 | ||||||
chr19:39102120 | T | TCACACAC others(3): Show |
1 | a0001c0007t0006g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1113+612_1113+621d others(12): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102120 | ||||||
chr19:39102120 | TCA | T | 5 | a0001c0003t0003g0256a0001c0003t0003g0272a0001c0003t0003g0276others(2): Show | 5 | HG01257.hp2 HG02572.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+620_1113+621d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102120 | ||||||
chr19:39102122 | A | T | 1 | a0001c0003t0003g0278 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1113+585A>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102122 | |||||||
chr19:39102159 | A | C | 2 | a0001c0002t0002g0129a0001c0005t0001g0212 | 2 | HG02015.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1113+622A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102159 | |||||||
chr19:39102296 | G | C | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1113+759G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102296 | |||||||
chr19:39102381 | C | CT | 205 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(202): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1113+856dupT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102381 | ||||||
chr19:39102381 | C | CTT | 12 | a0001c0002t0002g0015a0001c0002t0002g0016a0001c0002t0002g0140others(9): Show | 14 | HG01069.hp1 HG01123.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.1113+855_1113+856d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102381 | ||||||
chr19:39102450 | C | T | 102 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(99): Show | 109 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1113+913C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102450 | |||||||
chr19:39102631 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1113+1094C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102631 | |||||||
chr19:39102657 | A | G | 218 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1113+1120A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102657 | |||||||
chr19:39102711 | A | G | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1174A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102711 | |||||||
chr19:39102714 | CT | C | 28 | a0001c0001t0001g0020a0001c0001t0001g0039a0001c0001t0001g0216others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1113+1181delT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102714 | ||||||
chr19:39102715 | T | TTAC | 11 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(8): Show | 11 | HG00280.hp2 HG00438.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+1179_1113+118 others(7): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTACTTTC | 18 | a0001c0002t0002g0010a0001c0002t0002g0124a0001c0002t0002g0131others(15): Show | 18 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1113+1179_1113+118 others(11): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTACTTTC others(4): Show |
13 | a0001c0002t0002g0009a0001c0002t0002g0014a0001c0002t0002g0028others(10): Show | 13 | HG00597.hp2 HG01175.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1113+1179_1113+118 others(15): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTACTTTC others(8): Show |
8 | a0001c0002t0002g0121a0001c0002t0002g0126a0001c0002t0002g0127others(5): Show | 8 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+1179_1113+118 others(19): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTACTTTC others(12): Show |
2 | a0001c0002t0005g0062a0001c0002t0005g0070 | 2 | NA18971.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1113+1179_1113+118 others(23): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTC | 27 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0043others(24): Show | 27 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1113+1180_1113+118 others(7): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTCTTTC | 30 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0057others(27): Show | 30 | HG00423.hp2 HG00438.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1113+1180_1113+118 others(11): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTCTTTC others(4): Show |
41 | a0001c0001t0001g0040a0001c0001t0001g0091a0001c0001t0001g0105others(38): Show | 41 | HG00673.hp2 HG01074.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1113+1180_1113+118 others(15): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTCTTTC others(8): Show |
25 | a0001c0001t0001g0245a0001c0001t0001g0305a0001c0001t0001g0313others(22): Show | 25 | HG00099.hp2 HG00597.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1113+1180_1113+118 others(19): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTCTTTC others(12): Show |
15 | a0001c0001t0001g0294a0001c0001t0001g0298a0001c0001t0001g0352others(12): Show | 15 | HG01106.hp1 HG01934.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1113+1180_1113+118 others(23): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTCTTTC others(16): Show |
4 | a0001c0001t0001g0320a0001c0001t0011g0013a0001c0002t0002g0012others(1): Show | 4 | HG02083.hp2 HG02735.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+1180_1113+118 others(27): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTCTTTC others(20): Show |
3 | a0001c0002t0021g0180a0001c0005t0010g0145a0001c0009t0005g0211 | 3 | HG02280.hp1 NA18984.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1113+1180_1113+118 others(31): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTTC | 11 | a0001c0003t0003g0001a0001c0003t0003g0002a0001c0003t0003g0017others(8): Show | 13 | HG00621.hp2 HG00738.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+1228_1113+123 others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTTCTTT others(1): Show |
21 | a0001c0001t0006g0137a0001c0003t0003g0001a0001c0003t0003g0003others(18): Show | 22 | HG00140.hp1 HG01515.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.1113+1224_1113+123 others(12): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTTCTTT others(5): Show |
20 | a0001c0001t0006g0098a0001c0001t0014g0138a0001c0003t0003g0001others(17): Show | 20 | HG00408.hp1 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+1220_1113+123 others(16): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTTCTTT others(9): Show |
15 | a0001c0001t0006g0103a0001c0001t0006g0204a0001c0003t0003g0003others(12): Show | 15 | HG00642.hp1 HG01255.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1113+1216_1113+123 others(20): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTTCTTT others(13): Show |
11 | a0001c0001t0006g0099a0001c0003t0003g0002a0001c0003t0003g0223others(8): Show | 11 | HG00733.hp2 HG01978.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+1212_1113+123 others(24): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102715 | T | TTTTCTTT others(17): Show |
1 | a0001c0003t0014g0027 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1113+1208_1113+123 others(28): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102715 | ||||||
chr19:39102718 | T | A | 8 | a0001c0002t0002g0140a0001c0002t0002g0154a0001c0002t0002g0169others(5): Show | 8 | HG00735.hp1 HG01256.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+1181T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102718 | |||||||
chr19:39102722 | T | A | 1 | a0001c0002t0027g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1113+1185T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102722 | |||||||
chr19:39102736 | T | G | 1 | a0001c0002t0002g0126 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1113+1199T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102736 | |||||||
chr19:39102753 | TTCTTTCT others(7): Show |
T | 2 | a0001c0010t0018g0011a0001c0010t0018g0139 | 3 | HG01884.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1113+1220_1113+123 others(18): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102753 | ||||||
chr19:39102764 | T | TTTCTTTC others(4): Show |
1 | a0001c0007t0006g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1113+1231_1113+123 others(15): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102764 | ||||||
chr19:39102764 | T | TTTCTTTC others(12): Show |
1 | a0001c0003t0003g0252 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1113+1231_1113+123 others(23): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102764 | ||||||
chr19:39102765 | T | C | 1 | a0001c0002t0027g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1113+1228T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102765 | |||||||
chr19:39102765 | T | TTCTTTCT others(7): Show |
1 | a0001c0008t0009g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1113+1231_1113+123 others(18): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102765 | ||||||
chr19:39102765 | T | TTCTTTCT others(15): Show |
1 | a0001c0003t0003g0286 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1113+1231_1113+123 others(26): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102765 | ||||||
chr19:39102765 | TTC | T | 7 | a0001c0004t0004g0059a0001c0004t0004g0079a0001c0004t0004g0092others(4): Show | 7 | HG01070.hp2 HG02257.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+1242_1113+124 others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102765 | ||||||
chr19:39102767 | C | CTT | 13 | a0001c0001t0001g0305a0001c0002t0005g0219a0001c0004t0004g0051others(10): Show | 13 | HG00099.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+1231_1113+123 others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102767 | ||||||
chr19:39102767 | C | CTTTCTT | 14 | a0001c0004t0004g0045a0001c0004t0004g0050a0001c0004t0004g0053others(11): Show | 14 | HG00140.hp2 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1113+1231_1113+123 others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102767 | ||||||
chr19:39102767 | C | CTTTCTTT others(3): Show |
21 | a0001c0001t0030g0100a0001c0004t0004g0008a0001c0004t0004g0048others(18): Show | 21 | HG00423.hp1 HG00741.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.1113+1231_1113+123 others(14): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102767 | ||||||
chr19:39102767 | C | CTTTCTTT others(7): Show |
12 | a0001c0004t0002g0194a0001c0004t0004g0044a0001c0004t0004g0073others(9): Show | 12 | HG00621.hp1 HG01123.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+1231_1113+123 others(18): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102767 | ||||||
chr19:39102767 | C | CTTTCTTT others(11): Show |
10 | a0001c0001t0006g0101a0001c0003t0006g0333a0001c0004t0004g0046others(7): Show | 10 | HG01891.hp2 HG02074.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1113+1231_1113+123 others(22): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102767 | ||||||
chr19:39102767 | C | CTTTCTTT others(15): Show |
1 | a0001c0004t0004g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1113+1231_1113+123 others(26): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102767 | ||||||
chr19:39102767 | C | CTTTCTTT others(21): Show |
1 | a0001c0004t0004g0008 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1113+1231_1113+123 others(32): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102767 | ||||||
chr19:39102769 | C | T | 110 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(107): Show | 113 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1113+1232C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102769 | |||||||
chr19:39102771 | C | T | 1 | a0001c0005t0001g0202 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1113+1234C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102771 | |||||||
chr19:39102773 | C | T | 2 | a0001c0001t0028g0217a0001c0009t0026g0196 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1113+1236C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102773 | |||||||
chr19:39102777 | C | T | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1113+1240C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102777 | |||||||
chr19:39102780 | T | TC | 7 | a0001c0003t0003g0285a0001c0003t0006g0333a0001c0003t0019g0025others(4): Show | 7 | HG00621.hp1 NA18940.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+1243_1113+124 others(5): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102780 | |||||||
chr19:39102781 | T | C | 214 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(211): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1113+1244T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102781 | |||||||
chr19:39102783 | C | T | 1 | a0001c0006t0008g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1113+1246C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102783 | |||||||
chr19:39102785 | C | CTCTT | 6 | a0001c0002t0002g0028a0001c0002t0005g0042a0001c0002t0005g0218others(3): Show | 6 | HG00597.hp2 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+1251_1113+125 others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102785 | ||||||
chr19:39102785 | C | CTT | 75 | a0001c0002t0002g0010a0001c0002t0002g0012a0001c0002t0002g0014others(72): Show | 81 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1113+1249_1113+125 others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102785 | ||||||
chr19:39102785 | C | T | 120 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(117): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1113+1248C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102785 | |||||||
chr19:39102791 | CTCTT | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0315a0001c0002t0027g0177 | 3 | HG03710.hp1 HG03834.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1113+1268_1113+127 others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102791 | ||||||
chr19:39102795 | T | C | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(210): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1113+1258T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102795 | |||||||
chr19:39102795 | T | TTCTCTCT others(3): Show |
1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1113+1261_1113+126 others(14): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39102795 | ||||||
chr19:39102889 | G | A | 1 | a0001c0002t0002g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1113+1352G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102889 | |||||||
chr19:39102903 | T | A | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1366T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102903 | |||||||
chr19:39102906 | C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0041 | 2 | NA19009.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1113+1369C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102906 | |||||||
chr19:39102913 | A | C | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1376A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39102913 | |||||||
chr19:39103058 | A | G | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1521A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103058 | |||||||
chr19:39103072 | G | A | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1535G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103072 | |||||||
chr19:39103129 | T | C | 109 | a0001c0001t0028g0217a0001c0002t0002g0009a0001c0002t0002g0010others(106): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+1592T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103129 | |||||||
chr19:39103192 | C | T | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1655C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103192 | |||||||
chr19:39103253 | ATTGT | A | 14 | a0001c0002t0005g0108a0001c0002t0005g0226a0001c0002t0007g0225others(11): Show | 14 | HG00558.hp2 HG01358.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1113+1719_1113+172 others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103253 | ||||||
chr19:39103269 | C | T | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1732C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103269 | |||||||
chr19:39103322 | G | C | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+1785G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103322 | |||||||
chr19:39103372 | C | T | 1 | a0001c0002t0005g0325 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1113+1835C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103372 | |||||||
chr19:39103441 | G | GT | 9 | a0001c0003t0003g0214a0001c0003t0003g0255a0001c0003t0003g0262others(6): Show | 9 | HG00621.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+1929dupT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | G | GTGTT | 11 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(8): Show | 14 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1113+1905_1113+190 others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | G | GTGTTT | 20 | a0001c0004t0004g0008a0001c0004t0004g0044a0001c0004t0004g0045others(17): Show | 21 | HG00423.hp1 HG01192.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+1905_1113+190 others(9): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | G | GTGTTTT | 21 | a0001c0004t0002g0194a0001c0004t0004g0050a0001c0004t0004g0051others(18): Show | 21 | HG00621.hp1 HG01081.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+1905_1113+190 others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | G | GTGTTTTT | 11 | a0001c0004t0004g0059a0001c0004t0004g0076a0001c0004t0004g0077others(8): Show | 11 | HG01070.hp2 HG01074.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+1905_1113+190 others(11): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | G | GTT | 11 | a0001c0001t0006g0103a0001c0001t0006g0137a0001c0001t0030g0100others(8): Show | 11 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+1928_1113+192 others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | G | GTTT | 8 | a0001c0001t0006g0099a0001c0001t0006g0101a0001c0001t0006g0204others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+1927_1113+192 others(7): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | GTT | G | 14 | a0001c0001t0011g0165a0001c0002t0002g0016a0001c0002t0002g0122others(11): Show | 15 | HG00673.hp1 HG01106.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+1928_1113+192 others(6): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | GTTT | G | 89 | a0001c0001t0001g0356a0001c0001t0001g0376a0001c0001t0011g0164others(86): Show | 95 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1113+1927_1113+192 others(7): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | GTTTT | G | 50 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0087others(47): Show | 52 | HG00544.hp2 HG00639.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1113+1926_1113+192 others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | GTTTTT | G | 57 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1113+1925_1113+192 others(9): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103441 | GTTTTTT | G | 6 | a0001c0001t0028g0217a0001c0005t0010g0141a0001c0005t0010g0144others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+1924_1113+192 others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39103441 | ||||||
chr19:39103449 | T | G | 3 | a0001c0004t0004g0051a0001c0004t0004g0071a0001c0004t0004g0092 | 3 | HG01981.hp1 HG02004.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1113+1912T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103449 | |||||||
chr19:39103556 | G | A | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+2019G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103556 | |||||||
chr19:39103579 | C | T | 3 | a0001c0002t0005g0218a0001c0005t0010g0193a0001c0009t0029g0210 | 3 | HG02976.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1113+2042C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103579 | |||||||
chr19:39103635 | T | A | 1 | a0001c0001t0001g0355 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1113+2098T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103635 | |||||||
chr19:39103689 | G | A | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+2152G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103689 | |||||||
chr19:39103767 | G | A | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1113+2230G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103767 | |||||||
chr19:39103882 | C | T | 5 | a0001c0001t0028g0217a0001c0005t0010g0141a0001c0005t0010g0144others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+2345C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103882 | |||||||
chr19:39103903 | T | C | 1 | a0001c0003t0003g0252 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1113+2366T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39103903 | |||||||
chr19:39104059 | A | G | 1 | a0001c0004t0009g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+2522A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104059 | |||||||
chr19:39104117 | T | A | 1 | a0001c0004t0004g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1113+2580T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104117 | |||||||
chr19:39104155 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1113+2618A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104155 | |||||||
chr19:39104392 | A | G | 1 | a0001c0002t0002g0028 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1114-2555A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104392 | |||||||
chr19:39104417 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1114-2530C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104417 | |||||||
chr19:39104528 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1114-2419G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104528 | |||||||
chr19:39104575 | G | T | 6 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-2372G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104575 | |||||||
chr19:39104606 | G | A | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1114-2341G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104606 | |||||||
chr19:39104613 | G | A | 1 | a0001c0003t0006g0370 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1114-2334G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104613 | |||||||
chr19:39104644 | G | A | 1 | a0001c0005t0010g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1114-2303G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104644 | |||||||
chr19:39104815 | G | A | 1 | a0001c0004t0004g0055 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1114-2132G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104815 | |||||||
chr19:39104816 | C | T | 74 | a0001c0004t0002g0194a0001c0004t0004g0008a0001c0004t0004g0044others(71): Show | 79 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1114-2131C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104816 | |||||||
chr19:39104826 | A | G | 1 | a0001c0004t0004g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1114-2121A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104826 | |||||||
chr19:39104839 | C | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0221a0001c0001t0001g0316 | 3 | NA18942.hp1 NA19007.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1114-2108C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39104839 | |||||||
chr19:39105007 | TTTTA | T | 114 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(111): Show | 117 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1114-1920_1114-191 others(8): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 39105007 | ||||||
chr19:39105176 | C | T | 3 | a0001c0003t0003g0255a0001c0003t0003g0258a0001c0003t0003g0279 | 3 | HG00621.hp2 NA18944.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1114-1771C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105176 | |||||||
chr19:39105261 | C | T | 8 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(5): Show | 9 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114-1686C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105261 | |||||||
chr19:39105305 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1114-1642G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105305 | |||||||
chr19:39105306 | T | C | 291 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(288): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1114-1641T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105306 | |||||||
chr19:39105336 | G | C | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1114-1611G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105336 | |||||||
chr19:39105481 | A | G | 311 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(308): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.1114-1466A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105481 | |||||||
chr19:39105589 | C | T | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1114-1358C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105589 | |||||||
chr19:39105709 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1114-1238G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105709 | |||||||
chr19:39105714 | G | A | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1114-1233G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105714 | |||||||
chr19:39105726 | G | A | 52 | a0001c0004t0002g0194a0001c0004t0004g0008a0001c0004t0004g0044others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1114-1221G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105726 | |||||||
chr19:39105763 | C | T | 3 | a0001c0004t0004g0065a0001c0004t0004g0073a0001c0004t0004g0093 | 3 | HG02080.hp2 NA18941.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1114-1184C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105763 | |||||||
chr19:39105880 | A | G | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1114-1067A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105880 | |||||||
chr19:39105893 | C | T | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1114-1054C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105893 | |||||||
chr19:39105932 | A | C | 49 | a0001c0004t0004g0008a0001c0004t0004g0044a0001c0004t0004g0045others(46): Show | 50 | HG00140.hp2 HG00423.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1114-1015A>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39105932 | |||||||
chr19:39106187 | G | A | 105 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(102): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1114-760G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39106187 | |||||||
chr19:39106435 | G | A | 15 | a0001c0006t0008g0006a0001c0006t0008g0032a0001c0006t0008g0033others(12): Show | 18 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1114-512G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39106435 | |||||||
chr19:39106599 | C | T | 9 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114-348C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39106599 | |||||||
chr19:39106736 | C | T | 1 | a0001c0001t0015g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1114-211C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39106736 | |||||||
chr19:39106872 | T | C | 1 | a0001c0017t0002g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1114-75T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39106872 | |||||||
chr19:39106899 | C | T | 9 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114-48C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | chr19 | 39106899 | |||||||
chr19:39107102 | C | A | 1 | a0001c0007t0006g0114 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1251+18C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107102 | |||||||
chr19:39107157 | G | A | 9 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(6): Show | 10 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1251+73G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107157 | |||||||
chr19:39107173 | G | A | 1 | a0001c0009t0026g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251+89G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107173 | |||||||
chr19:39107262 | C | T | 59 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1251+178C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107262 | |||||||
chr19:39107358 | G | A | 59 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1251+274G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107358 | |||||||
chr19:39107386 | T | C | 2 | a0001c0001t0001g0350a0001c0001t0001g0357 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1251+302T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107386 | |||||||
chr19:39107402 | G | A | 59 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1251+318G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107402 | |||||||
chr19:39107444 | C | T | 1 | a0001c0003t0003g0224 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1251+360C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107444 | |||||||
chr19:39107501 | G | A | 1 | a0001c0001t0004g0354 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1251+417G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107501 | |||||||
chr19:39107508 | C | T | 59 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1251+424C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107508 | |||||||
chr19:39107532 | C | T | 8 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(5): Show | 9 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251+448C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107532 | |||||||
chr19:39107539 | G | A | 5 | a0001c0001t0028g0217a0001c0005t0010g0141a0001c0005t0010g0144others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251+455G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107539 | |||||||
chr19:39107557 | C | G | 1 | a0001c0001t0001g0375 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1251+473C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107557 | |||||||
chr19:39107578 | C | CA | 29 | a0001c0001t0006g0137a0001c0002t0002g0140a0001c0002t0002g0152others(26): Show | 29 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1251+516dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39107578 | ||||||
chr19:39107578 | C | CAAAAAAA | 36 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(33): Show | 37 | HG00544.hp2 HG00741.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1251+510_1251+516d others(9): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39107578 | ||||||
chr19:39107578 | C | CAAAAAAA others(1): Show |
9 | a0001c0004t0004g0048a0001c0004t0004g0050a0001c0004t0004g0071others(6): Show | 9 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251+509_1251+516d others(10): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39107578 | ||||||
chr19:39107578 | CA | C | 120 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(117): Show | 126 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1251+516delA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39107578 | ||||||
chr19:39107578 | CAA | C | 6 | a0001c0001t0001g0302a0001c0001t0001g0313a0001c0001t0001g0321others(3): Show | 6 | HG01168.hp1 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+515_1251+516d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39107578 | ||||||
chr19:39107605 | G | T | 1 | a0001c0001t0011g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1251+521G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107605 | |||||||
chr19:39107622 | A | G | 50 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(47): Show | 51 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1251+538A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107622 | |||||||
chr19:39107628 | G | T | 4 | a0001c0005t0010g0141a0001c0005t0010g0144a0001c0005t0010g0145others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251+544G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107628 | |||||||
chr19:39107695 | G | T | 7 | a0001c0004t0004g0059a0001c0004t0004g0086a0001c0004t0004g0096others(4): Show | 7 | HG00140.hp2 HG01070.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251+611G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107695 | |||||||
chr19:39107851 | C | A | 1 | a0001c0003t0032g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1251+767C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107851 | |||||||
chr19:39107973 | T | C | 59 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(56): Show | 61 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1251+889T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39107973 | |||||||
chr19:39108064 | G | C | 1 | a0001c0002t0005g0314 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1251+980G>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108064 | |||||||
chr19:39108064 | G | T | 1 | a0001c0001t0001g0322 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1251+980G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108064 | |||||||
chr19:39108139 | A | AT | 122 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(119): Show | 127 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1251+1073dupT | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39108139 | ||||||
chr19:39108139 | ATTT | A | 60 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0004t0004g0008others(57): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1251+1071_1251+107 others(7): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39108139 | ||||||
chr19:39108196 | G | T | 1 | a0001c0001t0001g0319 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1251+1112G>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108196 | |||||||
chr19:39108285 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1251+1201G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108285 | |||||||
chr19:39108301 | G | A | 2 | a0001c0005t0006g0134a0001c0005t0006g0135 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1251+1217G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108301 | |||||||
chr19:39108360 | C | T | 1 | a0001c0001t0015g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1251+1276C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108360 | |||||||
chr19:39108385 | C | A | 1 | a0001c0001t0011g0165 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1251+1301C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108385 | |||||||
chr19:39108412 | A | G | 1 | a0001c0002t0031g0312 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1251+1328A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108412 | |||||||
chr19:39108495 | A | G | 3 | a0001c0006t0010g0205a0001c0006t0010g0206a0001c0006t0010g0209 | 3 | HG03471.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1251+1411A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108495 | |||||||
chr19:39108562 | C | T | 11 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(8): Show | 13 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1251+1478C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108562 | |||||||
chr19:39108640 | G | A | 1 | a0001c0003t0003g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1252-1413G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108640 | |||||||
chr19:39108648 | A | G | 1 | a0001c0004t0004g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1252-1405A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108648 | |||||||
chr19:39108667 | C | G | 62 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0003t0020g0253others(59): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1252-1386C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108667 | |||||||
chr19:39108854 | C | T | 62 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0003t0020g0253others(59): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1252-1199C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108854 | |||||||
chr19:39108859 | C | T | 105 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(102): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1252-1194C>T | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108859 | |||||||
chr19:39108866 | G | A | 62 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0003t0020g0253others(59): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1252-1187G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108866 | |||||||
chr19:39108914 | A | G | 62 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0003t0020g0253others(59): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1252-1139A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39108914 | |||||||
chr19:39109332 | A | G | 292 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(289): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1252-721A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109332 | |||||||
chr19:39109351 | A | G | 1 | a0001c0003t0006g0374 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1252-702A>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109351 | |||||||
chr19:39109396 | T | G | 52 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0003t0020g0253others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1252-657T>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109396 | |||||||
chr19:39109486 | C | G | 52 | a0001c0001t0004g0310a0001c0001t0004g0354a0001c0003t0020g0253others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1252-567C>G | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109486 | |||||||
chr19:39109586 | T | A | 17 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0101others(14): Show | 17 | HG00642.hp1 HG01934.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1252-467T>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109586 | |||||||
chr19:39109597 | T | C | 187 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(184): Show | 195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1252-456T>C | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109597 | |||||||
chr19:39109685 | T | TA | 113 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(110): Show | 118 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1252-344dupA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39109685 | ||||||
chr19:39109685 | T | TAA | 70 | a0001c0001t0001g0244a0001c0001t0001g0293a0001c0001t0001g0317others(67): Show | 73 | HG00140.hp2 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1252-345_1252-344d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39109685 | ||||||
chr19:39109685 | T | TAAA | 6 | a0001c0004t0004g0048a0001c0004t0004g0078a0001c0004t0004g0090others(3): Show | 6 | HG00423.hp1 HG00741.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1252-346_1252-344d others(5): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39109685 | ||||||
chr19:39109685 | TA | T | 88 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0012others(85): Show | 95 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1252-344delA | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39109685 | ||||||
chr19:39109685 | TAA | T | 7 | a0001c0002t0002g0183a0001c0002t0005g0239a0001c0002t0005g0314others(4): Show | 7 | HG01256.hp2 HG01516.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-345_1252-344d others(4): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 39109685 | ||||||
chr19:39109869 | G | A | 8 | a0001c0004t0009g0019a0001c0004t0009g0102a0001c0004t0009g0291others(5): Show | 10 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1252-184G>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109869 | |||||||
chr19:39109984 | C | A | 1 | a0001c0003t0003g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1252-69C>A | ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | chr19 | 39109984 |