Item | Value |
---|---|
geneid | 54872 |
ensemblid | ENSG00000174227.16 |
hgncid | 25985 |
symbol | PIGG |
name | phosphatidylinositol glycan anchor biosynthesis class G |
refseq_nuc | NM_001127178.3 |
refseq_prot | NP_001120650.1 |
ensembl_nuc | ENST00000453061.7 |
ensembl_prot | ENSP00000415203.2 |
mane_status | MANE Select |
chr | chr4 |
start | 499210 |
end | 540200 |
strand | + |
ver | v1.2 |
region | chr4:499210-540200 |
region5000 | chr4:494210-545200 |
regionname0 | PIGG_chr4_499210_540200 |
regionname5000 | PIGG_chr4_494210_545200 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 983 | 214 | 44 | 59 | 69 | 8 | 32 | 47 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0002 | 0/0 | 983 | 67 | 4 | 6 | 49 | 2 | 6 | 40 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0003 | 0/0 | 983 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0004 | 0/0 | 983 | 12 | 1 | 0 | 7 | 0 | 4 | 7 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0005 | 0/0 | 983 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0006 | 0/0 | 983 | 7 | 1 | 0 | 5 | 0 | 1 | 5 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0007 | 0/0 | 983 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0008 | 0/0 | 983 | 5 | 1 | 1 | 3 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0009 | 0/0 | 983 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0010 | 0/0 | 983 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0011 | 0/0 | 983 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0012 | 0/0 | 983 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0013 | 0/0 | 983 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0014 | 0/0 | 983 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0015 | 0/0 | 983 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0016 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(726): Show |
chr4 | 494210 | 545200 |
a0017 | 0/0 | 983 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0018 | 0/0 | 983 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0019 | 0/0 | 983 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0020 | 0/0 | 983 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0021 | 0/0 | 983 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
a0022 | 0/0 | 983 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | MRLGS others(978): Show |
chr4 | 494210 | 545200 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2949 | 211 | 44 | 59 | 66 | 8 | 32 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0001c0023 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0001c0024 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0001c0029 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0002c0002 | 0/0 | 2949 | 61 | 4 | 3 | 48 | 2 | 4 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0002c0007 | 0/0 | 2949 | 5 | 0 | 3 | 0 | 0 | 2 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0002c0028 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0003c0003 | 0/0 | 2949 | 13 | 12 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0004c0004 | 0/0 | 2949 | 12 | 1 | 0 | 7 | 0 | 4 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0005c0008 | 0/0 | 2949 | 5 | 5 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0005c0009 | 0/0 | 2949 | 5 | 5 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0005c0021 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0006c0005 | 0/0 | 2949 | 7 | 1 | 0 | 5 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0007c0006 | 0/0 | 2949 | 6 | 5 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0008c0012 | 0/0 | 2949 | 4 | 1 | 1 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0008c0027 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0009c0010 | 0/0 | 2949 | 4 | 3 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0010c0011 | 0/0 | 2949 | 4 | 4 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0011c0013 | 0/0 | 2949 | 3 | 1 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0012c0016 | 0/0 | 2949 | 2 | 1 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0012c0018 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0013c0014 | 0/0 | 2949 | 3 | 0 | 0 | 3 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0014c0015 | 0/0 | 2949 | 2 | 2 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0015c0030 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0016c0020 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0017c0017 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0018c0026 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0019c0031 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0020c0022 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0021c0025 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 | ||
a0022c0019 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ATGCG others(2944): Show |
chr4 | 494210 | 545200 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3909 | 189 | 28 | 58 | 66 | 8 | 27 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0001c0001t0003 | 0/0 | 3909 | 20 | 14 | 1 | 0 | 0 | 5 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0001c0001t0006 | 0/0 | 3909 | 2 | 2 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0001c0023t0001 | 0/0 | 3909 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0001c0024t0001 | 0/0 | 3909 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0001c0029t0001 | 0/0 | 3909 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0002c0002t0002 | 0/0 | 3908 | 61 | 4 | 3 | 48 | 2 | 4 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0002c0007t0002 | 0/0 | 3908 | 5 | 0 | 3 | 0 | 0 | 2 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0002c0028t0002 | 0/0 | 3908 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0003c0003t0002 | 0/0 | 3908 | 12 | 11 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0003c0003t0008 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0004c0004t0002 | 0/0 | 3908 | 11 | 1 | 0 | 7 | 0 | 3 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0004c0004t0009 | 0/0 | 3908 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0005c0008t0004 | 0/0 | 3907 | 5 | 5 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3902): Show |
chr4 | 494210 | 545200 |
a0005c0009t0002 | 0/0 | 3908 | 4 | 4 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0005c0009t0007 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0005c0021t0004 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3902): Show |
chr4 | 494210 | 545200 |
a0006c0005t0002 | 0/0 | 3908 | 7 | 1 | 0 | 5 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0007c0006t0001 | 0/0 | 3909 | 6 | 5 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0008c0012t0001 | 0/0 | 3909 | 4 | 1 | 1 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0008c0027t0001 | 0/0 | 3909 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0009c0010t0002 | 0/0 | 3908 | 4 | 3 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0010c0011t0005 | 0/0 | 3909 | 4 | 4 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0011c0013t0001 | 0/0 | 3909 | 3 | 1 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0012c0016t0001 | 0/0 | 3909 | 2 | 1 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0012c0018t0001 | 0/0 | 3909 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0013c0014t0001 | 0/0 | 3909 | 3 | 0 | 0 | 3 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0014c0015t0003 | 0/0 | 3909 | 2 | 2 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0015c0030t0003 | 0/0 | 3909 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0016c0020t0002 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0017c0017t0003 | 0/0 | 3909 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0018c0026t0002 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3903): Show |
chr4 | 494210 | 545200 |
a0019c0031t0001 | 0/0 | 3909 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0020c0022t0001 | 0/0 | 3909 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0021c0025t0001 | 0/0 | 3909 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
a0022c0019t0001 | 0/0 | 3909 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | ACTGT others(3904): Show |
chr4 | 494210 | 545200 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0023t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0024t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0001c0029t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0007t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0007t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0007t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0007t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0007t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0002c0028t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0003c0003t0008g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0004c0004t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0008t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0008t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0008t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0008t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0008t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0009t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0009t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0009t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0009t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0005c0021t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0006c0005t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0006c0005t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0006c0005t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0006c0005t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0006c0005t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0006c0005t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0007c0006t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0007c0006t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0007c0006t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0007c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0007c0006t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0007c0006t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0008c0012t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0008c0012t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0008c0012t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0008c0012t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0008c0027t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0009c0010t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0009c0010t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0009c0010t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0009c0010t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0010c0011t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0010c0011t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0010c0011t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0010c0011t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0011c0013t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0011c0013t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0011c0013t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0012c0016t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0012c0016t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0012c0018t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0013c0014t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0013c0014t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0014c0015t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0014c0015t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0015c0030t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0016c0020t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0017c0017t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0018c0026t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0019c0031t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0020c0022t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0021c0025t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
a0022c0019t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0313 | EUR | GBR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00597 | hp1 | a0008 | c0012 | t0001 | g0199 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00642 | hp1 | a0002 | c0007 | t0002 | g0104 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00642 | hp2 | a0011 | c0013 | t0001 | g0100 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01243 | hp1 | a0009 | c0010 | t0002 | g0294 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01243 | hp2 | a0007 | c0006 | t0001 | g0140 | AMR | PUR | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01261 | hp2 | a0002 | c0007 | t0002 | g0127 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01358 | hp2 | a0002 | c0007 | t0002 | g0150 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0266 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01884 | hp1 | a0009 | c0010 | t0002 | g0291 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01975 | hp1 | a0003 | c0003 | t0002 | g0265 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01981 | hp1 | a0008 | c0012 | t0001 | g0312 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0269 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02015 | hp1 | a0001 | c0023 | t0001 | g0156 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02040 | hp2 | a0008 | c0027 | t0001 | g0020 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02055 | hp1 | a0014 | c0015 | t0003 | g0214 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02055 | hp2 | a0005 | c0008 | t0004 | g0295 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02071 | hp2 | a0008 | c0012 | t0001 | g0180 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02145 | hp2 | a0015 | c0030 | t0003 | g0303 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CDX | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | CDX | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02258 | hp1 | a0005 | c0021 | t0004 | g0226 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02622 | hp2 | a0004 | c0004 | t0002 | g0095 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02630 | hp1 | a0009 | c0010 | t0002 | g0290 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02630 | hp2 | a0016 | c0020 | t0002 | g0090 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02647 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02683 | hp2 | a0002 | c0007 | t0002 | g0109 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0314 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02717 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02717 | hp2 | a0007 | c0006 | t0001 | g0279 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0321 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02723 | hp2 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02738 | hp1 | a0006 | c0005 | t0002 | g0052 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02809 | hp2 | a0003 | c0003 | t0002 | g0211 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02818 | hp1 | a0017 | c0017 | t0003 | g0292 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02818 | hp2 | a0005 | c0009 | t0002 | g0010 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02886 | hp2 | a0011 | c0013 | t0001 | g0251 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02895 | hp1 | a0005 | c0009 | t0002 | g0129 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02896 | hp2 | a0007 | c0006 | t0001 | g0288 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02922 | hp1 | a0003 | c0003 | t0002 | g0021 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02922 | hp2 | a0005 | c0009 | t0002 | g0319 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02965 | hp1 | a0005 | c0008 | t0004 | g0297 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02970 | hp1 | a0003 | c0003 | t0002 | g0028 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03017 | hp1 | a0004 | c0004 | t0002 | g0179 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03041 | hp2 | a0007 | c0006 | t0001 | g0154 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03130 | hp1 | a0012 | c0016 | t0001 | g0302 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03130 | hp2 | a0007 | c0006 | t0001 | g0287 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03139 | hp1 | a0014 | c0015 | t0003 | g0213 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03195 | hp1 | a0018 | c0026 | t0002 | g0036 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03195 | hp2 | a0006 | c0005 | t0002 | g0285 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0224 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03209 | hp2 | a0005 | c0008 | t0004 | g0038 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03225 | hp1 | a0007 | c0006 | t0001 | g0131 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03453 | hp1 | a0010 | c0011 | t0005 | g0293 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03486 | hp2 | a0003 | c0003 | t0002 | g0264 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03490 | hp2 | a0002 | c0007 | t0002 | g0108 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03516 | hp1 | a0005 | c0008 | t0004 | g0275 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03579 | hp1 | a0008 | c0012 | t0001 | g0277 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03579 | hp2 | a0003 | c0003 | t0002 | g0304 | AFR | MSL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03654 | hp2 | a0019 | c0031 | t0001 | g0067 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03669 | hp1 | a0004 | c0004 | t0002 | g0227 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0209 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0271 | SAS | PJL | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03831 | hp1 | a0011 | c0013 | t0001 | g0092 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03831 | hp2 | a0004 | c0004 | t0009 | g0069 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03942 | hp1 | a0004 | c0004 | t0002 | g0208 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04184 | hp2 | a0020 | c0022 | t0001 | g0055 | SAS | BEB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0307 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0306 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18522 | hp1 | a0003 | c0003 | t0002 | g0028 | AFR | YRI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18522 | hp2 | a0003 | c0003 | t0008 | g0124 | AFR | YRI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18906 | hp2 | a0010 | c0011 | t0005 | g0234 | AFR | YRI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18939 | hp2 | a0013 | c0014 | t0001 | g0015 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18948 | hp1 | a0004 | c0004 | t0002 | g0013 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18953 | hp1 | a0001 | c0029 | t0001 | g0268 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18953 | hp2 | a0012 | c0018 | t0001 | g0195 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18956 | hp1 | a0004 | c0004 | t0002 | g0094 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18969 | hp1 | a0001 | c0024 | t0001 | g0299 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18973 | hp2 | a0013 | c0014 | t0001 | g0015 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18987 | hp1 | a0004 | c0004 | t0002 | g0114 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18993 | hp2 | a0004 | c0004 | t0002 | g0115 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19009 | hp1 | a0013 | c0014 | t0001 | g0117 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19009 | hp2 | a0006 | c0005 | t0002 | g0230 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19012 | hp2 | a0021 | c0025 | t0001 | g0031 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | LWK | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19030 | hp2 | a0010 | c0011 | t0005 | g0225 | AFR | LWK | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19054 | hp2 | a0004 | c0004 | t0002 | g0111 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19062 | hp2 | a0006 | c0005 | t0002 | g0231 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19063 | hp2 | a0022 | c0019 | t0001 | g0163 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19068 | hp1 | a0012 | c0016 | t0001 | g0126 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19072 | hp2 | a0002 | c0028 | t0002 | g0270 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19074 | hp1 | a0006 | c0005 | t0002 | g0023 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19078 | hp1 | a0006 | c0005 | t0002 | g0164 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19084 | hp2 | a0004 | c0004 | t0002 | g0113 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19087 | hp2 | a0004 | c0004 | t0002 | g0013 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19091 | hp1 | a0006 | c0005 | t0002 | g0023 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19240 | hp1 | a0003 | c0003 | t0002 | g0021 | AFR | YRI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA19240 | hp2 | a0010 | c0011 | t0005 | g0212 | AFR | YRI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20129 | hp1 | a0005 | c0009 | t0007 | g0280 | AFR | ASW | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ASW | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0267 | EUR | TSI | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0320 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG02559 | hp2 | a0005 | c0008 | t0004 | g0249 | AFR | ACB | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | USA | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20300 | hp1 | a0009 | c0010 | t0002 | g0284 | AFR | USA | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA20300 | hp2 | a0003 | c0003 | t0002 | g0250 | AFR | USA | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA21309 | hp1 | a0005 | c0009 | t0002 | g0010 | AFR | LWK | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | LWK | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0106 | REF | REF | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0308 | REF | REF | PIGG_chr4_494210_545200 | PIGG | chr4 | 494210 | 545200 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:499412 | G | T | 1 | a0019 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.77G>T | p.Gly26Val | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/13 | 203/3909 | 77/2952 | 26/983 | chr4 | 499412 | |||
chr4:500399 | C | A | 1 | a0014 | 2 | HG02055.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.158C>A | p.Ala53Asp | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/13 | 284/3909 | 158/2952 | 53/983 | chr4 | 500399 | |||
chr4:500405 | C | A | 2 | a0009 a0017 |
5 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.164C>A | p.Ser55Tyr | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/13 | 290/3909 | 164/2952 | 55/983 | chr4 | 500405 | |||
chr4:500425 | C | T | 1 | a0015 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.184C>T | p.Pro62Ser | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/13 | 310/3909 | 184/2952 | 62/983 | chr4 | 500425 | |||
chr4:521139 | G | A | 1 | a0022 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.1198G>A | p.Val400Ile | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 7/13 | 1324/3909 | 1198/2952 | 400/983 | chr4 | 521139 | |||
chr4:521699 | C | T | 1 | a0008 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1372C>T | p.Arg458Cys | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/13 | 1498/3909 | 1372/2952 | 458/983 | chr4 | 521699 | |||
chr4:521700 | G | A | 9 | a0002 a0003 a0005 others(6): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
missense_variant | MODERATE | c.1373G>A | p.Arg458His | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/13 | 1499/3909 | 1373/2952 | 458/983 | chr4 | 521700 | |||
chr4:521847 | C | T | 1 | a0018 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1520C>T | p.Ala507Val | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/13 | 1646/3909 | 1520/2952 | 507/983 | chr4 | 521847 | |||
chr4:521873 | T | A | 1 | a0020 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1546T>A | p.Ser516Thr | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/13 | 1672/3909 | 1546/2952 | 516/983 | chr4 | 521873 | |||
chr4:523672 | T | C | 10 | a0002 a0003 a0004 others(7): Show |
119 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
missense_variant | MODERATE | c.1828T>C | p.Cys610Arg | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/13 | 1954/3909 | 1828/2952 | 610/983 | chr4 | 523672 | |||
chr4:523774 | G | A | 1 | a0018 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1930G>A | p.Glu644Lys | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/13 | 2056/3909 | 1930/2952 | 644/983 | chr4 | 523774 | |||
chr4:523811 | C | T | 1 | a0007 | 6 | HG01243.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
missense_variant | MODERATE | c.1967C>T | p.Ala656Val | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/13 | 2093/3909 | 1967/2952 | 656/983 | chr4 | 523811 | |||
chr4:523849 | C | T | 1 | a0021 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.2005C>T | p.Arg669Cys | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/13 | 2131/3909 | 2005/2952 | 669/983 | chr4 | 523849 | |||
chr4:527064 | G | A | 8 | a0002 a0003 a0004 others(5): Show |
104 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(101): Show |
missense_variant | MODERATE | c.2095G>A | p.Val699Ile | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/13 | 2221/3909 | 2095/2952 | 699/983 | chr4 | 527064 | |||
chr4:527160 | G | A | 3 | a0003 a0009 a0017 |
18 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(15): Show |
missense_variant | MODERATE | c.2191G>A | p.Val731Ile | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/13 | 2317/3909 | 2191/2952 | 731/983 | chr4 | 527160 | |||
chr4:527165 | C | G | 1 | a0016 | 1 | HG02630.hp2 | stop_gained | HIGH | c.2196C>G | p.Tyr732* | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/13 | 2322/3909 | 2196/2952 | 732/983 | chr4 | 527165 | |||
chr4:533888 | T | C | 8 | a0002 a0003 a0004 others(5): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
missense_variant | MODERATE | c.2642T>C | p.Ile881Thr | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/13 | 2768/3909 | 2642/2952 | 881/983 | chr4 | 533888 | |||
chr4:539212 | T | C | 8 | a0002 a0003 a0004 others(5): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
missense_variant | MODERATE | c.2795T>C | p.Phe932Ser | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 2921/3909 | 2795/2952 | 932/983 | chr4 | 539212 | |||
chr4:539308 | T | C | 1 | a0013 | 3 | NA18939.hp2 NA18973.hp2 NA19009.hp1 |
missense_variant | MODERATE | c.2891T>C | p.Ile964Thr | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 3017/3909 | 2891/2952 | 964/983 | chr4 | 539308 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:508936 | G | T | 2 | a0001c0029 a0002c0028 |
2 | NA18953.hp1 NA19072.hp2 |
synonymous_variant | LOW | c.867G>T | p.Leu289Leu | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/13 | 993/3909 | 867/2952 | 289/983 | chr4 | 508936 | |||
chr4:516061 | T | C | 2 | a0002c0007 a0005c0008 |
10 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(7): Show |
synonymous_variant | LOW | c.990T>C | p.Ser330Ser | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/13 | 1116/3909 | 990/2952 | 330/983 | chr4 | 516061 | |||
chr4:516172 | G | A | 1 | a0012c0018 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.1101G>A | p.Pro367Pro | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/13 | 1227/3909 | 1101/2952 | 367/983 | chr4 | 516172 | |||
chr4:521887 | T | C | 1 | a0001c0023 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.1560T>C | p.Cys520Cys | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/13 | 1686/3909 | 1560/2952 | 520/983 | chr4 | 521887 | |||
chr4:521908 | C | T | 1 | a0005c0021 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1581C>T | p.Thr527Thr | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/13 | 1707/3909 | 1581/2952 | 527/983 | chr4 | 521908 | |||
chr4:523587 | T | C | 15 | a0002c0002 a0002c0007 a0002c0028 others(12): Show |
119 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
synonymous_variant | LOW | c.1743T>C | p.Leu581Leu | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/13 | 1869/3909 | 1743/2952 | 581/983 | chr4 | 523587 | |||
chr4:523833 | C | T | 15 | a0002c0002 a0002c0007 a0002c0028 others(12): Show |
119 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
synonymous_variant | LOW | c.1989C>T | p.Ala663Ala | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/13 | 2115/3909 | 1989/2952 | 663/983 | chr4 | 523833 | |||
chr4:539186 | C | T | 1 | a0001c0024 | 1 | NA18969.hp1 | synonymous_variant | LOW | c.2769C>T | p.Tyr923Tyr | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 2895/3909 | 2769/2952 | 923/983 | chr4 | 539186 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:539610 | G | A | 20 | a0001c0001t0003 a0002c0002t0002 a0002c0007t0002 others(17): Show |
144 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*241G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 241 | chr4 | 539610 | ||||||
chr4:539633 | A | G | 1 | a0004c0004t0009 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*264A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 264 | chr4 | 539633 | ||||||
chr4:539655 | G | A | 1 | a0005c0009t0007 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 286 | chr4 | 539655 | ||||||
chr4:539857 | G | A | 15 | a0002c0002t0002 a0002c0007t0002 a0002c0028t0002 others(12): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*488G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 488 | chr4 | 539857 | ||||||
chr4:539858 | A | T | 16 | a0002c0002t0002 a0002c0007t0002 a0002c0028t0002 others(13): Show |
120 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*489A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 489 | chr4 | 539858 | ||||||
chr4:539904 | CA | C | 2 | a0005c0008t0004 a0005c0021t0004 |
6 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*536delA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 536 | chr4 | 539904 | ||||||
chr4:539909 | A | G | 1 | a0001c0001t0006 | 2 | HG02145.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*540A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 540 | chr4 | 539909 | ||||||
chr4:540090 | C | T | 1 | a0003c0003t0008 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 721 | chr4 | 540090 | ||||||
chr4:540171 | GA | G | 15 | a0002c0002t0002 a0002c0007t0002 a0002c0028t0002 others(12): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*808delA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 13/13 | 808 | INFO_REALIGN_3_PRIME | chr4 | 540171 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:499531 | A | T | 1 | a0002c0002t0002g0322 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.154+42A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 499531 | |||||||
chr4:499587 | C | T | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.154+98C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 499587 | |||||||
chr4:499655 | T | G | 1 | a0021c0025t0001g0031 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.154+166T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 499655 | |||||||
chr4:499719 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.154+230C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 499719 | |||||||
chr4:499779 | C | G | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.154+290C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 499779 | |||||||
chr4:499878 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.154+389G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 499878 | |||||||
chr4:500037 | A | T | 1 | a0001c0001t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.155-359A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 500037 | |||||||
chr4:500050 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.155-346A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 500050 | |||||||
chr4:500257 | A | G | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.155-139A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 500257 | |||||||
chr4:500297 | G | T | 1 | a0001c0001t0001g0316 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.155-99G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 500297 | |||||||
chr4:500299 | A | G | 1 | a0003c0003t0002g0007 | 3 | HG02647.hp1 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.155-97A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 1/12 | chr4 | 500299 | |||||||
chr4:500645 | T | C | 2 | a0001c0001t0003g0033 a0001c0001t0003g0034 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.360+44T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 500645 | |||||||
chr4:500676 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.360+75C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 500676 | |||||||
chr4:500869 | A | G | 4 | a0002c0002t0002g0029 a0002c0002t0002g0313 a0002c0002t0002g0314 others(1): Show |
5 | HG00099.hp2 HG01346.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+268A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 500869 | |||||||
chr4:500907 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.360+306C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 500907 | |||||||
chr4:501043 | G | A | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.360+442G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501043 | |||||||
chr4:501209 | G | A | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.360+608G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501209 | |||||||
chr4:501446 | G | A | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.360+845G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501446 | |||||||
chr4:501495 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.360+894G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501495 | |||||||
chr4:501532 | T | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.360+931T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501532 | |||||||
chr4:501561 | G | C | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.360+960G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501561 | |||||||
chr4:501692 | A | G | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.360+1091A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501692 | |||||||
chr4:501848 | A | T | 1 | a0001c0001t0001g0305 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.360+1247A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501848 | |||||||
chr4:501858 | G | A | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG00733.hp2 HG01884.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+1257G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501858 | |||||||
chr4:501890 | A | G | 1 | a0021c0025t0001g0031 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.360+1289A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501890 | |||||||
chr4:501902 | GCT | G | 8 | a0001c0001t0003g0027 a0001c0001t0003g0300 a0001c0001t0003g0301 others(5): Show |
10 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+1304_360+1305d others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 501902 | ||||||
chr4:501930 | G | C | 1 | a0001c0001t0003g0300 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.360+1329G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501930 | |||||||
chr4:501959 | G | T | 77 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0255 others(74): Show |
80 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.360+1358G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 501959 | |||||||
chr4:502046 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.360+1445T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502046 | |||||||
chr4:502060 | G | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.360+1459G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502060 | |||||||
chr4:502129 | C | G | 1 | a0004c0004t0002g0227 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.360+1528C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502129 | |||||||
chr4:502188 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.360+1587G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502188 | |||||||
chr4:502408 | G | T | 2 | a0005c0021t0004g0226 a0010c0011t0005g0225 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.360+1807G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502408 | |||||||
chr4:502728 | A | G | 1 | a0002c0002t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.360+2127A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502728 | |||||||
chr4:502805 | G | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(39): Show |
48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.360+2204G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502805 | |||||||
chr4:502934 | G | A | 6 | a0002c0002t0002g0228 a0002c0002t0002g0229 a0002c0002t0002g0232 others(3): Show |
6 | NA18939.hp1 NA18964.hp1 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+2333G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502934 | |||||||
chr4:502969 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.360+2368G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502969 | |||||||
chr4:502980 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0051 |
4 | HG01109.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+2379G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 502980 | |||||||
chr4:503187 | T | C | 1 | a0005c0008t0004g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.361-2531T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503187 | |||||||
chr4:503349 | G | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.361-2369G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503349 | |||||||
chr4:503381 | C | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.361-2337C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503381 | |||||||
chr4:503409 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.361-2309C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503409 | |||||||
chr4:503412 | T | G | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.361-2306T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503412 | |||||||
chr4:503451 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.361-2267C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503451 | |||||||
chr4:503523 | C | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(13): Show |
27 | HG00621.hp1 HG00733.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.361-2195C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503523 | |||||||
chr4:503544 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.361-2174T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503544 | |||||||
chr4:503670 | GTACAGC | G | 3 | a0001c0001t0003g0300 a0003c0003t0002g0028 a0003c0003t0002g0304 |
4 | HG02970.hp1 HG03579.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-2043_361-2038d others(8): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503670 | ||||||
chr4:503803 | A | G | 1 | a0015c0030t0003g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.361-1915A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503803 | |||||||
chr4:503845 | T | TAC | 46 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
50 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.361-1833_361-1832d others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | T | TACAC | 22 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(19): Show |
23 | HG00738.hp1 HG02559.hp2 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.361-1835_361-1832d others(6): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | T | TACACAC | 12 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0044 others(9): Show |
12 | HG02040.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.361-1837_361-1832d others(8): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG01069.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.361-1839_361-1832d others(10): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | T | TACACACA others(3): Show |
2 | a0002c0002t0002g0228 a0010c0011t0005g0234 |
2 | NA18906.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.361-1841_361-1832d others(12): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | TAC | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(76): Show |
95 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.361-1833_361-1832d others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | TACAC | T | 13 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
14 | HG00597.hp1 HG00738.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-1835_361-1832d others(6): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | TACACAC | T | 9 | a0001c0001t0001g0206 a0003c0003t0002g0007 a0006c0005t0002g0052 others(6): Show |
11 | HG00544.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.361-1837_361-1832d others(8): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | TACACACA others(1): Show |
T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0207 a0001c0001t0003g0296 others(4): Show |
7 | HG01255.hp2 HG02055.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-1839_361-1832d others(10): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | TACACACA others(3): Show |
T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(43): Show |
53 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.361-1841_361-1832d others(12): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503845 | TACACACA others(5): Show |
T | 10 | a0001c0001t0001g0210 a0002c0002t0002g0029 a0002c0002t0002g0313 others(7): Show |
12 | HG00099.hp2 HG01346.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.361-1843_361-1832d others(14): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 503845 | ||||||
chr4:503963 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361-1755A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 503963 | |||||||
chr4:504061 | G | A | 8 | a0001c0001t0003g0027 a0001c0001t0003g0300 a0001c0001t0003g0301 others(5): Show |
10 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-1657G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504061 | |||||||
chr4:504078 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0005c0009t0002g0010 others(1): Show |
5 | HG02630.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-1640C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504078 | |||||||
chr4:504222 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361-1496T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504222 | |||||||
chr4:504367 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.361-1351G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504367 | |||||||
chr4:504444 | T | C | 5 | a0004c0004t0002g0013 a0004c0004t0002g0094 a0004c0004t0002g0113 others(2): Show |
6 | NA18948.hp1 NA18956.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.361-1274T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504444 | |||||||
chr4:504480 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.361-1238A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504480 | |||||||
chr4:504550 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0005c0009t0002g0010 others(1): Show |
5 | HG02630.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-1168C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504550 | |||||||
chr4:504670 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(47): Show |
58 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.361-1048C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 504670 | |||||||
chr4:505014 | C | A | 1 | a0002c0002t0002g0229 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.361-704C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505014 | |||||||
chr4:505148 | A | G | 1 | a0002c0002t0002g0281 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.361-570A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505148 | |||||||
chr4:505183 | G | A | 3 | a0001c0001t0003g0300 a0003c0003t0002g0028 a0003c0003t0002g0304 |
4 | HG02970.hp1 HG03579.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-535G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505183 | |||||||
chr4:505203 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0003g0047 |
3 | HG00733.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.361-515C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505203 | |||||||
chr4:505233 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361-485G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505233 | |||||||
chr4:505317 | T | C | 5 | a0001c0001t0001g0116 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | NA18942.hp2 NA18950.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-401T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505317 | |||||||
chr4:505347 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.361-371T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505347 | |||||||
chr4:505459 | C | CA | 37 | a0001c0001t0001g0054 a0001c0001t0001g0099 a0001c0001t0001g0118 others(34): Show |
37 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.361-232dupA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505459 | ||||||
chr4:505459 | CA | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.361-232delA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505459 | ||||||
chr4:505459 | CAA | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0112 others(3): Show |
7 | HG02735.hp1 HG02970.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-233_361-232del others(2): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505459 | ||||||
chr4:505459 | CAAAAAAA others(4): Show |
C | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.361-242_361-232del others(11): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505459 | ||||||
chr4:505459 | CAAAAAAA others(5): Show |
C | 2 | a0014c0015t0003g0214 a0016c0020t0002g0090 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.361-243_361-232del others(12): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505459 | ||||||
chr4:505486 | A | T | 8 | a0001c0001t0003g0027 a0001c0001t0003g0300 a0001c0001t0003g0301 others(5): Show |
10 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-232A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505486 | |||||||
chr4:505632 | C | CA | 10 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0172 others(7): Show |
11 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.361-69dupA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505632 | ||||||
chr4:505632 | C | CAA | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(34): Show |
43 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.361-70_361-69dupAA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505632 | ||||||
chr4:505632 | C | CAAA | 6 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0001g0088 others(3): Show |
7 | HG02486.hp1 HG02738.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-71_361-69dupAA others(1): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 505632 | ||||||
chr4:505650 | T | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(39): Show |
48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.361-68T>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 2/12 | chr4 | 505650 | |||||||
chr4:505956 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.570+29A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 505956 | |||||||
chr4:506016 | A | C | 2 | a0001c0001t0001g0098 a0004c0004t0002g0111 |
2 | NA19054.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.570+89A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506016 | |||||||
chr4:506244 | G | T | 13 | a0002c0002t0002g0029 a0002c0002t0002g0209 a0002c0002t0002g0313 others(10): Show |
15 | HG00099.hp2 HG01346.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+317G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506244 | |||||||
chr4:506455 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0005c0009t0002g0010 |
4 | HG02818.hp2 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+528T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506455 | |||||||
chr4:506615 | G | A | 4 | a0002c0002t0002g0122 a0002c0002t0002g0123 a0002c0002t0002g0155 others(1): Show |
4 | NA18941.hp1 NA18955.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+688G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506615 | |||||||
chr4:506711 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(55): Show |
64 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.571-694T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506711 | |||||||
chr4:506729 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.571-676C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506729 | |||||||
chr4:506786 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.571-619T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506786 | |||||||
chr4:506818 | C | T | 1 | a0012c0018t0001g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.571-587C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506818 | |||||||
chr4:506820 | T | G | 10 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0023t0001g0156 others(7): Show |
11 | HG00423.hp1 HG00642.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-585T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506820 | |||||||
chr4:506833 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.571-572A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506833 | |||||||
chr4:506840 | T | C | 1 | a0005c0009t0002g0010 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.571-565T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506840 | |||||||
chr4:506842 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.571-563A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506842 | |||||||
chr4:506898 | G | T | 1 | a0021c0025t0001g0031 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.571-507G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506898 | |||||||
chr4:506930 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | HG02040.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.571-475A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 506930 | |||||||
chr4:507067 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.571-338A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 507067 | |||||||
chr4:507104 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.571-301A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 507104 | |||||||
chr4:507241 | A | G | 5 | a0005c0021t0004g0226 a0010c0011t0005g0225 a0010c0011t0005g0293 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-164A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 507241 | |||||||
chr4:507345 | G | A | 2 | a0003c0003t0002g0021 a0003c0003t0002g0211 |
3 | HG02809.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.571-60G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 3/12 | chr4 | 507345 | |||||||
chr4:507609 | G | A | 3 | a0003c0003t0008g0124 a0009c0010t0002g0284 a0009c0010t0002g0294 |
3 | HG01243.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.759+16G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507609 | |||||||
chr4:507647 | C | G | 1 | a0002c0002t0002g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.759+54C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507647 | |||||||
chr4:507684 | C | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
61 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.759+91C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507684 | |||||||
chr4:507850 | T | C | 2 | a0005c0009t0002g0319 a0010c0011t0005g0212 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.759+257T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507850 | |||||||
chr4:507871 | C | T | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.759+278C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507871 | |||||||
chr4:507919 | G | GTTCTGTG others(27): Show |
1 | a0002c0002t0002g0083 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.759+362_759+395dup others(34): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 507919 | ||||||
chr4:507971 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0012 |
5 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+378T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507971 | |||||||
chr4:507973 | C | A | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.759+380C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507973 | |||||||
chr4:507994 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.759+401G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 507994 | |||||||
chr4:508083 | C | T | 4 | a0001c0001t0001g0207 a0002c0002t0002g0209 a0004c0004t0002g0227 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+490C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 508083 | |||||||
chr4:508252 | G | T | 2 | a0014c0015t0003g0213 a0014c0015t0003g0214 |
2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.760-577G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 508252 | |||||||
chr4:508303 | C | T | 2 | a0001c0001t0003g0300 a0003c0003t0002g0250 |
2 | HG04199.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.760-526C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 508303 | |||||||
chr4:508320 | C | G | 5 | a0001c0001t0001g0207 a0002c0002t0002g0209 a0004c0004t0002g0208 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-509C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 4/12 | chr4 | 508320 | |||||||
chr4:509122 | T | C | 105 | a0001c0001t0001g0101 a0001c0001t0001g0207 a0001c0001t0001g0235 others(102): Show |
114 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.901+152T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509122 | |||||||
chr4:509130 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901+160G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509130 | |||||||
chr4:509266 | T | C | 1 | a0002c0002t0002g0258 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.901+296T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509266 | |||||||
chr4:509281 | G | A | 1 | a0004c0004t0002g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.901+311G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509281 | |||||||
chr4:509289 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.901+319C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509289 | |||||||
chr4:509348 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.901+378A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509348 | |||||||
chr4:509457 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.901+487C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509457 | |||||||
chr4:509467 | T | C | 103 | a0001c0001t0001g0101 a0001c0001t0001g0235 a0001c0001t0001g0240 others(100): Show |
112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.901+497T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509467 | |||||||
chr4:509588 | C | A | 5 | a0001c0001t0001g0207 a0002c0002t0002g0209 a0004c0004t0002g0208 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.901+618C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509588 | |||||||
chr4:509605 | G | A | 1 | a0012c0016t0001g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.901+635G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509605 | |||||||
chr4:509610 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.901+640C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509610 | |||||||
chr4:509615 | G | A | 10 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0264 others(7): Show |
13 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.901+645G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509615 | |||||||
chr4:509659 | G | A | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.901+689G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 509659 | |||||||
chr4:510006 | C | T | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.901+1036C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510006 | |||||||
chr4:510042 | G | T | 5 | a0001c0001t0001g0207 a0002c0002t0002g0209 a0004c0004t0002g0208 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.901+1072G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510042 | |||||||
chr4:510045 | C | T | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.901+1075C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510045 | |||||||
chr4:510058 | G | A | 5 | a0001c0001t0001g0207 a0002c0002t0002g0209 a0004c0004t0002g0208 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.901+1088G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510058 | |||||||
chr4:510223 | G | T | 85 | a0001c0001t0001g0101 a0001c0001t0001g0207 a0001c0001t0001g0235 others(82): Show |
91 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.901+1253G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510223 | |||||||
chr4:510708 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.901+1738G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510708 | |||||||
chr4:510875 | G | A | 99 | a0001c0001t0001g0101 a0001c0001t0001g0207 a0001c0001t0001g0235 others(96): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.901+1905G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510875 | |||||||
chr4:510960 | A | T | 1 | a0011c0013t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.901+1990A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 510960 | |||||||
chr4:511084 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0183 |
2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.901+2114G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511084 | |||||||
chr4:511122 | C | T | 1 | a0004c0004t0002g0227 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.901+2152C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511122 | |||||||
chr4:511123 | G | A | 4 | a0001c0001t0003g0027 a0001c0001t0003g0045 a0001c0001t0003g0301 others(1): Show |
5 | HG02145.hp2 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.901+2153G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511123 | |||||||
chr4:511166 | G | A | 60 | a0001c0001t0001g0101 a0001c0001t0001g0235 a0001c0001t0001g0240 others(57): Show |
62 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.901+2196G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511166 | |||||||
chr4:511295 | T | TA | 7 | a0001c0001t0001g0257 a0001c0001t0003g0034 a0002c0002t0002g0175 others(4): Show |
7 | HG00140.hp2 HG02129.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.901+2325_901+2326i others(3): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511295 | |||||||
chr4:511295 | T | TAA | 62 | a0001c0001t0001g0101 a0001c0001t0001g0235 a0001c0001t0001g0240 others(59): Show |
67 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.901+2325_901+2326i others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511295 | |||||||
chr4:511295 | T | TAAA | 14 | a0001c0001t0001g0207 a0001c0001t0003g0243 a0002c0002t0002g0026 others(11): Show |
15 | HG01884.hp1 HG02615.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.901+2325_901+2326i others(5): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511295 | |||||||
chr4:511296 | T | A | 84 | a0001c0001t0001g0101 a0001c0001t0001g0207 a0001c0001t0001g0235 others(81): Show |
90 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.901+2326T>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511296 | |||||||
chr4:511296 | T | TA | 21 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0003g0027 others(18): Show |
24 | HG00099.hp2 HG01243.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.901+2347dupA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 511296 | ||||||
chr4:511296 | TA | T | 10 | a0001c0001t0001g0082 a0001c0001t0001g0161 a0001c0001t0001g0170 others(7): Show |
11 | HG01081.hp2 HG02698.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.901+2347delA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 511296 | ||||||
chr4:511479 | A | C | 5 | a0001c0001t0003g0300 a0003c0003t0002g0250 a0005c0021t0004g0226 others(2): Show |
5 | HG02258.hp1 HG03453.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.901+2509A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511479 | |||||||
chr4:511529 | G | A | 1 | a0002c0002t0002g0258 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.901+2559G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511529 | |||||||
chr4:511602 | C | T | 79 | a0001c0001t0001g0101 a0001c0001t0001g0235 a0001c0001t0001g0240 others(76): Show |
85 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.901+2632C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511602 | |||||||
chr4:511876 | T | C | 13 | a0003c0003t0002g0007 a0003c0003t0002g0021 a0003c0003t0002g0028 others(10): Show |
17 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.901+2906T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511876 | |||||||
chr4:511918 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.901+2948C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511918 | |||||||
chr4:511944 | T | C | 1 | a0008c0012t0001g0277 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901+2974T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511944 | |||||||
chr4:511975 | C | T | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.901+3005C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 511975 | |||||||
chr4:512001 | T | C | 1 | a0001c0001t0003g0274 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.901+3031T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512001 | |||||||
chr4:512216 | C | CT | 10 | a0001c0001t0001g0081 a0001c0001t0001g0105 a0002c0002t0002g0169 others(7): Show |
10 | HG01175.hp2 HG02055.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.901+3267dupT | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 512216 | ||||||
chr4:512216 | CT | C | 101 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0053 others(98): Show |
110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.901+3267delT | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 512216 | ||||||
chr4:512229 | T | C | 1 | a0002c0028t0002g0270 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.901+3259T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512229 | |||||||
chr4:512265 | G | A | 2 | a0005c0009t0002g0319 a0010c0011t0005g0212 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.901+3295G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512265 | |||||||
chr4:512288 | C | T | 2 | a0005c0009t0002g0319 a0010c0011t0005g0212 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.901+3318C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512288 | |||||||
chr4:512318 | C | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0153 others(5): Show |
14 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.901+3348C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512318 | |||||||
chr4:512323 | T | G | 3 | a0005c0021t0004g0226 a0010c0011t0005g0225 a0010c0011t0005g0293 |
3 | HG02258.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.901+3353T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512323 | |||||||
chr4:512365 | A | G | 24 | a0001c0001t0001g0137 a0002c0002t0002g0209 a0002c0002t0002g0224 others(21): Show |
29 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.901+3395A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512365 | |||||||
chr4:512366 | C | T | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.901+3396C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512366 | |||||||
chr4:512367 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0210 a0001c0001t0003g0062 |
4 | HG00735.hp2 HG02602.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+3397C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512367 | |||||||
chr4:512369 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0205 |
3 | HG00735.hp2 HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.901+3399A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512369 | |||||||
chr4:512406 | A | G | 1 | a0002c0002t0002g0281 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.901+3436A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512406 | |||||||
chr4:512466 | C | T | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+3496C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512466 | |||||||
chr4:512479 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(128): Show |
148 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.902-3494A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512479 | |||||||
chr4:512487 | A | C | 2 | a0002c0002t0002g0026 a0002c0002t0002g0244 |
3 | NA18965.hp1 NA18983.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.902-3486A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512487 | |||||||
chr4:512541 | T | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.902-3432T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512541 | |||||||
chr4:512545 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.902-3428A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512545 | |||||||
chr4:512561 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.902-3412A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512561 | |||||||
chr4:512563 | T | C | 3 | a0002c0002t0002g0029 a0002c0002t0002g0224 a0008c0012t0001g0312 |
4 | HG01346.hp1 HG01981.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-3410T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512563 | |||||||
chr4:512582 | C | T | 19 | a0001c0001t0001g0207 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
22 | HG01884.hp1 HG01975.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.902-3391C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512582 | |||||||
chr4:512583 | A | G | 20 | a0001c0001t0001g0207 a0001c0001t0003g0033 a0001c0001t0003g0034 others(17): Show |
23 | HG01884.hp1 HG01975.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.902-3390A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512583 | |||||||
chr4:512587 | C | T | 1 | a0008c0012t0001g0277 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.902-3386C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512587 | |||||||
chr4:512591 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.902-3382T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512591 | |||||||
chr4:512591 | T | G | 1 | a0004c0004t0002g0094 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.902-3382T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512591 | |||||||
chr4:512612 | C | T | 1 | a0001c0001t0003g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.902-3361C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512612 | |||||||
chr4:512625 | A | G | 1 | a0002c0002t0002g0017 | 2 | HG00621.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.902-3348A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512625 | |||||||
chr4:512632 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0013c0014t0001g0015 others(1): Show |
5 | HG02056.hp1 NA18939.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.902-3341C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512632 | |||||||
chr4:512643 | C | T | 1 | a0001c0001t0003g0301 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.902-3330C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512643 | |||||||
chr4:512657 | G | A | 2 | a0003c0003t0002g0021 a0009c0010t0002g0294 |
3 | HG01243.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.902-3316G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512657 | |||||||
chr4:512674 | A | G | 1 | a0002c0002t0002g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.902-3299A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512674 | |||||||
chr4:512675 | T | C | 1 | a0002c0002t0002g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.902-3298T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512675 | |||||||
chr4:512682 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
262 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.902-3291G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512682 | |||||||
chr4:512685 | G | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0076 others(1): Show |
4 | NA18988.hp1 NA18989.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-3288G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512685 | |||||||
chr4:512687 | C | T | 2 | a0001c0001t0001g0119 a0020c0022t0001g0055 |
2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.902-3286C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512687 | |||||||
chr4:512688 | G | A | 5 | a0001c0001t0001g0283 a0001c0001t0003g0047 a0001c0001t0003g0238 others(2): Show |
5 | HG01255.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.902-3285G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512688 | |||||||
chr4:512695 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.902-3278A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512695 | |||||||
chr4:512703 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.902-3270T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512703 | |||||||
chr4:512708 | A | G | 12 | a0001c0001t0001g0044 a0002c0002t0002g0232 a0002c0002t0002g0246 others(9): Show |
13 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.902-3265A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512708 | |||||||
chr4:512725 | G | C | 2 | a0008c0012t0001g0277 a0010c0011t0005g0234 |
2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.902-3248G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512725 | |||||||
chr4:512740 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.902-3233G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512740 | |||||||
chr4:512747 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.902-3226A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512747 | |||||||
chr4:512769 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0088 others(42): Show |
51 | HG00423.hp2 HG00597.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.902-3204C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512769 | |||||||
chr4:512795 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.902-3178C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 512795 | |||||||
chr4:513058 | G | A | 2 | a0001c0001t0001g0056 a0002c0002t0002g0314 |
2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.902-2915G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513058 | |||||||
chr4:513212 | C | T | 92 | a0001c0001t0001g0101 a0001c0001t0003g0027 a0001c0001t0003g0045 others(89): Show |
98 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.902-2761C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513212 | |||||||
chr4:513369 | G | A | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.902-2604G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513369 | |||||||
chr4:513376 | G | A | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.902-2597G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513376 | |||||||
chr4:513415 | A | AC | 3 | a0001c0001t0001g0084 a0002c0002t0002g0123 a0006c0005t0002g0231 |
3 | NA18941.hp1 NA18965.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.902-2556dupC | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 513415 | ||||||
chr4:513750 | C | G | 1 | a0004c0004t0002g0111 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.902-2223C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513750 | |||||||
chr4:513757 | G | A | 1 | a0016c0020t0002g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.902-2216G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513757 | |||||||
chr4:513780 | C | A | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.902-2193C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513780 | |||||||
chr4:513826 | G | T | 1 | a0004c0004t0002g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.902-2147G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 513826 | |||||||
chr4:514123 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.902-1850A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514123 | |||||||
chr4:514177 | A | G | 7 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0003c0003t0002g0007 others(4): Show |
10 | HG01975.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.902-1796A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514177 | |||||||
chr4:514220 | G | A | 3 | a0008c0012t0001g0277 a0010c0011t0005g0212 a0010c0011t0005g0234 |
3 | HG03579.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.902-1753G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514220 | |||||||
chr4:514673 | C | T | 1 | a0005c0008t0004g0297 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.902-1300C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514673 | |||||||
chr4:514725 | C | G | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.902-1248C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514725 | |||||||
chr4:514813 | A | C | 1 | a0006c0005t0002g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.902-1160A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514813 | |||||||
chr4:514816 | C | T | 1 | a0006c0005t0002g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.902-1157C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514816 | |||||||
chr4:514819 | A | G | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.902-1154A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514819 | |||||||
chr4:514978 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.902-995G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 514978 | |||||||
chr4:515062 | G | C | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.902-911G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 515062 | |||||||
chr4:515151 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0130 |
2 | HG00558.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.902-822G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 515151 | |||||||
chr4:515173 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.902-800G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 515173 | |||||||
chr4:515222 | G | A | 2 | a0001c0001t0001g0207 a0011c0013t0001g0251 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.902-751G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 515222 | |||||||
chr4:515389 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0063 |
2 | HG01175.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.902-584G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 515389 | |||||||
chr4:515658 | C | T | 3 | a0005c0009t0007g0280 a0012c0016t0001g0302 a0016c0020t0002g0090 |
3 | HG02630.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.902-315C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 5/12 | chr4 | 515658 | |||||||
chr4:516194 | A | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0064 others(4): Show |
8 | HG00408.hp1 HG00423.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114+9A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516194 | |||||||
chr4:516287 | AT | A | 6 | a0007c0006t0001g0131 a0007c0006t0001g0140 a0007c0006t0001g0154 others(3): Show |
6 | HG01243.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+108delT | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 516287 | ||||||
chr4:516382 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1114+197T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516382 | |||||||
chr4:516411 | C | G | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1114+226C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516411 | |||||||
chr4:516505 | C | G | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1114+320C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516505 | |||||||
chr4:516771 | G | A | 1 | a0002c0007t0002g0108 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1114+586G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516771 | |||||||
chr4:516840 | G | A | 14 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0004c0004t0002g0013 others(11): Show |
16 | HG00642.hp2 HG01243.hp1 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.1114+655G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516840 | |||||||
chr4:516854 | C | CA | 41 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0057 others(38): Show |
46 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.1114+693dupA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 516854 | ||||||
chr4:516854 | C | CAA | 56 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0083 others(53): Show |
58 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1114+692_1114+693d others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 516854 | ||||||
chr4:516854 | C | CAAA | 8 | a0002c0002t0002g0075 a0002c0002t0002g0237 a0002c0002t0002g0241 others(5): Show |
8 | HG02135.hp1 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114+691_1114+693d others(5): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 516854 | ||||||
chr4:516854 | CA | C | 7 | a0001c0001t0001g0097 a0001c0001t0001g0138 a0001c0001t0001g0196 others(4): Show |
7 | HG01256.hp1 HG02273.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+693delA | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 516854 | ||||||
chr4:516895 | G | A | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1114+710G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516895 | |||||||
chr4:516944 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1114+759G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 516944 | |||||||
chr4:517039 | G | A | 6 | a0007c0006t0001g0131 a0007c0006t0001g0140 a0007c0006t0001g0154 others(3): Show |
6 | HG01243.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+854G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517039 | |||||||
chr4:517086 | A | G | 98 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(95): Show |
106 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1114+901A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517086 | |||||||
chr4:517158 | A | G | 1 | a0002c0002t0002g0266 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1114+973A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517158 | |||||||
chr4:517196 | G | A | 24 | a0002c0002t0002g0320 a0002c0002t0002g0321 a0003c0003t0002g0021 others(21): Show |
27 | HG00642.hp2 HG01243.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1114+1011G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517196 | |||||||
chr4:517224 | G | A | 2 | a0002c0002t0002g0125 a0002c0002t0002g0174 |
2 | NA19010.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1114+1039G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517224 | |||||||
chr4:517358 | A | C | 1 | a0005c0021t0004g0226 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1114+1173A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517358 | |||||||
chr4:517367 | G | A | 12 | a0004c0004t0002g0013 a0004c0004t0002g0094 a0004c0004t0002g0111 others(9): Show |
13 | HG00642.hp2 HG02258.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.1114+1182G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517367 | |||||||
chr4:517402 | C | T | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+1217C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517402 | |||||||
chr4:517550 | T | G | 112 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(109): Show |
121 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.1114+1365T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517550 | |||||||
chr4:517566 | G | A | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1114+1381G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517566 | |||||||
chr4:517572 | G | T | 3 | a0002c0002t0002g0193 a0002c0002t0002g0229 a0002c0002t0002g0232 |
3 | NA18939.hp1 NA19005.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1114+1387G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517572 | |||||||
chr4:517849 | C | T | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1114+1664C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 517849 | |||||||
chr4:518224 | G | T | 3 | a0002c0007t0002g0104 a0002c0007t0002g0109 a0002c0007t0002g0150 |
3 | HG00642.hp1 HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1114+2039G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518224 | |||||||
chr4:518331 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1114+2146C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518331 | |||||||
chr4:518375 | C | T | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1114+2190C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518375 | |||||||
chr4:518377 | A | AG | 4 | a0002c0002t0002g0029 a0002c0002t0002g0313 a0002c0002t0002g0314 others(1): Show |
5 | HG00099.hp2 HG01346.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114+2194dupG | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 518377 | ||||||
chr4:518474 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1114+2289G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518474 | |||||||
chr4:518525 | G | A | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1114+2340G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518525 | |||||||
chr4:518588 | A | G | 47 | a0001c0001t0003g0027 a0001c0001t0003g0045 a0001c0001t0003g0301 others(44): Show |
53 | HG00642.hp1 HG00642.hp2 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.1114+2403A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518588 | |||||||
chr4:518749 | AAC | A | 86 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(83): Show |
91 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1115-2303_1115-230 others(6): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 518749 | ||||||
chr4:518772 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0091 a0001c0001t0001g0093 |
3 | HG00597.hp2 HG02040.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1115-2284C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518772 | |||||||
chr4:518777 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1115-2279C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518777 | |||||||
chr4:518782 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0317 |
2 | HG00544.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1115-2274G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518782 | |||||||
chr4:518809 | C | A | 96 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(93): Show |
104 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1115-2247C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518809 | |||||||
chr4:518854 | C | T | 98 | a0001c0001t0001g0317 a0002c0002t0002g0017 a0002c0002t0002g0026 others(95): Show |
106 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1115-2202C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518854 | |||||||
chr4:518883 | A | G | 1 | a0002c0002t0002g0314 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1115-2173A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518883 | |||||||
chr4:518962 | A | G | 113 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(110): Show |
122 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1115-2094A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 518962 | |||||||
chr4:519039 | T | C | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-2017T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519039 | |||||||
chr4:519042 | C | T | 1 | a0021c0025t0001g0031 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1115-2014C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519042 | |||||||
chr4:519143 | T | C | 61 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(58): Show |
64 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1115-1913T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519143 | |||||||
chr4:519206 | G | A | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1115-1850G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519206 | |||||||
chr4:519216 | G | A | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1115-1840G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519216 | |||||||
chr4:519225 | T | C | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-1831T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519225 | |||||||
chr4:519330 | C | T | 1 | a0002c0002t0002g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1115-1726C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519330 | |||||||
chr4:519331 | G | A | 1 | a0002c0002t0002g0125 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1115-1725G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519331 | |||||||
chr4:519334 | G | A | 1 | a0005c0021t0004g0226 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1115-1722G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519334 | |||||||
chr4:519351 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1115-1705A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519351 | |||||||
chr4:519389 | T | C | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-1667T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519389 | |||||||
chr4:519412 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1115-1644G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519412 | |||||||
chr4:519448 | A | G | 101 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(98): Show |
109 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1115-1608A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519448 | |||||||
chr4:519458 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0110 |
4 | HG01069.hp2 HG01071.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-1598A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519458 | |||||||
chr4:519511 | A | G | 1 | a0002c0002t0002g0177 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1115-1545A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519511 | |||||||
chr4:519571 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1115-1485G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519571 | |||||||
chr4:519572 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1115-1484G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519572 | |||||||
chr4:519625 | C | T | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-1431C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519625 | |||||||
chr4:519671 | CACCTGGT others(105): Show |
C | 101 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(98): Show |
109 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1115-1197_1115-108 others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 519671 | ||||||
chr4:519767 | T | C | 7 | a0001c0001t0001g0137 a0007c0006t0001g0131 a0007c0006t0001g0140 others(4): Show |
7 | HG01243.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115-1289T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519767 | |||||||
chr4:519806 | G | C | 61 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(58): Show |
64 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1115-1250G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519806 | |||||||
chr4:519924 | C | CTGCAGGC others(49): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0003g0248 |
3 | HG01884.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1115-1113_1115-105 others(60): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 519924 | ||||||
chr4:519932 | G | A | 13 | a0002c0002t0002g0204 a0002c0002t0002g0237 a0002c0002t0002g0241 others(10): Show |
13 | HG00423.hp2 HG02056.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1115-1124G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519932 | |||||||
chr4:519977 | T | C | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-1079T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 519977 | |||||||
chr4:520032 | G | A | 1 | a0001c0001t0003g0307 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1115-1024G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520032 | |||||||
chr4:520247 | G | T | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1115-809G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520247 | |||||||
chr4:520252 | A | G | 101 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(98): Show |
109 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1115-804A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520252 | |||||||
chr4:520300 | G | A | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-756G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520300 | |||||||
chr4:520344 | A | G | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-712A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520344 | |||||||
chr4:520391 | T | G | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-665T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520391 | |||||||
chr4:520412 | G | T | 5 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0185 others(2): Show |
5 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115-644G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520412 | |||||||
chr4:520480 | G | GCTCCT | 113 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(110): Show |
122 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1115-573_1115-572i others(7): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 520480 | ||||||
chr4:520526 | C | T | 1 | a0002c0002t0002g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1115-530C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520526 | |||||||
chr4:520542 | T | C | 1 | a0005c0009t0002g0010 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1115-514T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520542 | |||||||
chr4:520587 | G | A | 1 | a0006c0005t0002g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1115-469G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520587 | |||||||
chr4:520811 | G | A | 12 | a0004c0004t0002g0013 a0004c0004t0002g0094 a0004c0004t0002g0111 others(9): Show |
13 | HG00642.hp2 HG03017.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.1115-245G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520811 | |||||||
chr4:520813 | A | G | 100 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(97): Show |
108 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1115-243A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520813 | |||||||
chr4:520836 | C | T | 26 | a0002c0002t0002g0224 a0002c0002t0002g0320 a0002c0002t0002g0321 others(23): Show |
28 | HG00642.hp1 HG01243.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1115-220C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520836 | |||||||
chr4:520840 | A | G | 113 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(110): Show |
122 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1115-216A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520840 | |||||||
chr4:520882 | A | G | 5 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0264 others(2): Show |
8 | HG01975.hp1 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115-174A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520882 | |||||||
chr4:520905 | C | G | 5 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0264 others(2): Show |
8 | HG01975.hp1 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115-151C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 520905 | |||||||
chr4:521028 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1115-28G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 6/12 | chr4 | 521028 | |||||||
chr4:521407 | G | A | 12 | a0004c0004t0002g0013 a0004c0004t0002g0094 a0004c0004t0002g0111 others(9): Show |
13 | HG00642.hp2 HG03017.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.1332+134G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 7/12 | chr4 | 521407 | |||||||
chr4:521454 | A | G | 61 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(58): Show |
64 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1332+181A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 7/12 | chr4 | 521454 | |||||||
chr4:521974 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1614+33A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 521974 | |||||||
chr4:522055 | C | A | 94 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(91): Show |
102 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1614+114C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522055 | |||||||
chr4:522188 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1614+247G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522188 | |||||||
chr4:522252 | C | A | 3 | a0002c0002t0002g0029 a0002c0002t0002g0313 a0002c0002t0002g0314 |
4 | HG00099.hp2 HG01346.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+311C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522252 | |||||||
chr4:522373 | T | TCATCCTG others(14): Show |
1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1614+442_1614+462d others(23): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 522373 | ||||||
chr4:522403 | C | T | 3 | a0001c0001t0003g0062 a0001c0001t0003g0274 a0001c0001t0003g0307 |
3 | HG02602.hp1 HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1614+462C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522403 | |||||||
chr4:522470 | A | G | 2 | a0005c0009t0002g0129 a0005c0009t0007g0280 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1614+529A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522470 | |||||||
chr4:522490 | G | C | 1 | a0006c0005t0002g0285 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1614+549G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522490 | |||||||
chr4:522512 | G | A | 3 | a0002c0002t0002g0029 a0002c0002t0002g0313 a0008c0012t0001g0312 |
4 | HG00099.hp2 HG01346.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614+571G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522512 | |||||||
chr4:522523 | A | G | 1 | a0001c0001t0001g0004 | 3 | HG01167.hp1 HG01169.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1614+582A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522523 | |||||||
chr4:522593 | C | T | 6 | a0001c0001t0001g0149 a0002c0007t0002g0104 a0002c0007t0002g0108 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+652C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522593 | |||||||
chr4:522609 | G | A | 80 | a0001c0001t0001g0149 a0002c0002t0002g0017 a0002c0002t0002g0026 others(77): Show |
86 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1614+668G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522609 | |||||||
chr4:522700 | C | G | 2 | a0005c0009t0002g0129 a0005c0009t0007g0280 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1614+759C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522700 | |||||||
chr4:522788 | T | C | 1 | a0006c0005t0002g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-671T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522788 | |||||||
chr4:522796 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1615-663C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522796 | |||||||
chr4:522797 | G | A | 106 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0002c0002t0002g0017 others(103): Show |
115 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.1615-662G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522797 | |||||||
chr4:522960 | T | G | 1 | a0001c0001t0003g0037 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1615-499T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522960 | |||||||
chr4:522977 | G | A | 73 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(70): Show |
79 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1615-482G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 522977 | |||||||
chr4:523004 | G | C | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1615-455G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523004 | |||||||
chr4:523107 | T | C | 110 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(107): Show |
119 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.1615-352T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523107 | |||||||
chr4:523174 | C | G | 110 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(107): Show |
119 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.1615-285C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523174 | |||||||
chr4:523215 | G | T | 1 | a0005c0009t0002g0010 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1615-244G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523215 | |||||||
chr4:523221 | T | C | 1 | a0001c0001t0003g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1615-238T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523221 | |||||||
chr4:523353 | T | C | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1615-106T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523353 | |||||||
chr4:523409 | G | A | 110 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(107): Show |
119 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.1615-50G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523409 | |||||||
chr4:523427 | G | A | 2 | a0001c0023t0001g0156 a0012c0016t0001g0126 |
2 | HG02015.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1615-32G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 8/12 | chr4 | 523427 | |||||||
chr4:523922 | G | T | 5 | a0001c0001t0003g0037 a0001c0001t0003g0236 a0001c0001t0003g0238 others(2): Show |
5 | HG01255.hp2 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069+9G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 523922 | |||||||
chr4:523929 | C | T | 2 | a0005c0009t0002g0129 a0005c0009t0007g0280 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2069+16C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 523929 | |||||||
chr4:523952 | ACGGCCGA others(8): Show |
A | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2069+41_2069+55del others(15): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 523952 | ||||||
chr4:523992 | T | C | 1 | a0002c0002t0002g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2069+79T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 523992 | |||||||
chr4:524049 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2069+136A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524049 | |||||||
chr4:524262 | T | C | 12 | a0004c0004t0002g0013 a0004c0004t0002g0094 a0004c0004t0002g0111 others(9): Show |
13 | HG00642.hp2 HG03017.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.2069+349T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524262 | |||||||
chr4:524272 | G | C | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069+359G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524272 | |||||||
chr4:524278 | C | T | 4 | a0001c0001t0003g0062 a0001c0001t0003g0306 a0001c0001t0003g0307 others(1): Show |
4 | HG02602.hp1 HG04184.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069+365C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524278 | |||||||
chr4:524315 | G | A | 2 | a0005c0009t0002g0129 a0005c0009t0007g0280 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2069+402G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524315 | |||||||
chr4:524433 | G | C | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2069+520G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524433 | |||||||
chr4:524449 | G | A | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2069+536G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524449 | |||||||
chr4:524458 | G | A | 1 | a0009c0010t0002g0284 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2069+545G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524458 | |||||||
chr4:524486 | G | A | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2069+573G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524486 | |||||||
chr4:524518 | A | G | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2069+605A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524518 | |||||||
chr4:524534 | T | C | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2069+621T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524534 | |||||||
chr4:524549 | C | A | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2069+636C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524549 | |||||||
chr4:524557 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2069+644C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524557 | |||||||
chr4:524599 | A | C | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2069+686A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524599 | |||||||
chr4:524635 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0085 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069+722C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524635 | |||||||
chr4:524696 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2069+783C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524696 | |||||||
chr4:524765 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2069+852C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524765 | |||||||
chr4:524806 | C | T | 24 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(21): Show |
26 | HG00642.hp1 HG00642.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2069+893C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524806 | |||||||
chr4:524942 | G | C | 1 | a0016c0020t0002g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2069+1029G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524942 | |||||||
chr4:524995 | A | G | 1 | a0002c0002t0002g0281 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2069+1082A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 524995 | |||||||
chr4:525115 | T | C | 75 | a0001c0001t0003g0062 a0002c0002t0002g0017 a0002c0002t0002g0026 others(72): Show |
78 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.2069+1202T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525115 | |||||||
chr4:525123 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2069+1210G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525123 | |||||||
chr4:525246 | A | G | 2 | a0002c0002t0002g0188 a0002c0002t0002g0191 |
2 | HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.2069+1333A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525246 | |||||||
chr4:525269 | C | T | 1 | a0001c0001t0001g0005 | 3 | NA18987.hp2 NA19080.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2069+1356C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525269 | |||||||
chr4:525291 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0063 |
2 | HG01175.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2069+1378G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525291 | |||||||
chr4:525315 | C | T | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069+1402C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525315 | |||||||
chr4:525364 | C | G | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2069+1451C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525364 | |||||||
chr4:525535 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2070-1504T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525535 | |||||||
chr4:525584 | G | A | 1 | a0003c0003t0002g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2070-1455G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525584 | |||||||
chr4:525617 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2070-1422T>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525617 | |||||||
chr4:525778 | G | A | 7 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0005c0009t0002g0010 others(4): Show |
9 | HG01243.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2070-1261G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525778 | |||||||
chr4:525847 | C | T | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070-1192C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525847 | |||||||
chr4:525852 | G | C | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070-1187G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525852 | |||||||
chr4:525895 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2070-1144G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525895 | |||||||
chr4:525925 | G | A | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2070-1114G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525925 | |||||||
chr4:525975 | T | C | 1 | a0012c0016t0001g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2070-1064T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 525975 | |||||||
chr4:526008 | AGAATTGG others(38): Show |
A | 4 | a0002c0002t0002g0175 a0002c0002t0002g0272 a0002c0002t0002g0273 others(1): Show |
4 | HG02129.hp2 NA18944.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.2070-1029_2070-985 others(48): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 526008 | ||||||
chr4:526025 | C | T | 1 | a0003c0003t0002g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2070-1014C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526025 | |||||||
chr4:526038 | A | G | 1 | a0008c0012t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2070-1001A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526038 | |||||||
chr4:526062 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0240 a0001c0001t0001g0255 others(2): Show |
5 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2070-977C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526062 | |||||||
chr4:526078 | C | G | 6 | a0005c0008t0004g0038 a0005c0008t0004g0249 a0005c0008t0004g0275 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070-961C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526078 | |||||||
chr4:526188 | A | G | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2070-851A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526188 | |||||||
chr4:526216 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2070-823G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526216 | |||||||
chr4:526239 | T | C | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2070-800T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526239 | |||||||
chr4:526259 | C | T | 1 | a0008c0012t0001g0277 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2070-780C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526259 | |||||||
chr4:526435 | T | C | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2070-604T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526435 | |||||||
chr4:526502 | T | A | 2 | a0001c0001t0003g0033 a0001c0001t0003g0034 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2070-537T>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526502 | |||||||
chr4:526516 | TC | T | 10 | a0005c0008t0004g0038 a0005c0008t0004g0249 a0005c0008t0004g0275 others(7): Show |
11 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2070-522delC | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526516 | |||||||
chr4:526698 | G | A | 6 | a0007c0006t0001g0131 a0007c0006t0001g0140 a0007c0006t0001g0154 others(3): Show |
6 | HG01243.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070-341G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526698 | |||||||
chr4:526717 | C | CT | 6 | a0002c0007t0002g0104 a0002c0007t0002g0109 a0002c0007t0002g0127 others(3): Show |
6 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070-306dupT | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 526717 | ||||||
chr4:526717 | CT | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0128 others(8): Show |
11 | HG00099.hp2 HG01167.hp2 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.2070-306delT | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 526717 | ||||||
chr4:526717 | CTT | C | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2070-307_2070-306d others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 526717 | ||||||
chr4:526795 | G | A | 1 | a0009c0010t0002g0290 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2070-244G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526795 | |||||||
chr4:526800 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA18982.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2070-239G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 9/12 | chr4 | 526800 | |||||||
chr4:527270 | A | G | 1 | a0001c0001t0003g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2261+40A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527270 | |||||||
chr4:527279 | A | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2261+49A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527279 | |||||||
chr4:527289 | GAC | G | 14 | a0003c0003t0002g0007 a0003c0003t0002g0021 a0003c0003t0002g0028 others(11): Show |
18 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.2261+62_2261+63del others(2): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 527289 | ||||||
chr4:527293 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0171 |
2 | HG00733.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2261+63C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527293 | |||||||
chr4:527294 | G | T | 14 | a0003c0003t0002g0007 a0003c0003t0002g0021 a0003c0003t0002g0028 others(11): Show |
18 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.2261+64G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527294 | |||||||
chr4:527313 | C | T | 14 | a0003c0003t0002g0007 a0003c0003t0002g0021 a0003c0003t0002g0028 others(11): Show |
18 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.2261+83C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527313 | |||||||
chr4:527524 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0107 |
2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2261+294T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527524 | |||||||
chr4:527578 | C | T | 4 | a0001c0001t0003g0062 a0001c0001t0003g0274 a0001c0001t0003g0306 others(1): Show |
4 | HG02602.hp1 HG03239.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2261+348C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527578 | |||||||
chr4:527691 | T | C | 72 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(69): Show |
78 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.2261+461T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527691 | |||||||
chr4:527712 | G | A | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
114 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.2261+482G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527712 | |||||||
chr4:527945 | G | A | 12 | a0004c0004t0002g0013 a0004c0004t0002g0094 a0004c0004t0002g0111 others(9): Show |
13 | HG00642.hp2 HG03017.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.2261+715G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 527945 | |||||||
chr4:528066 | C | G | 1 | a0016c0020t0002g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2261+836C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528066 | |||||||
chr4:528088 | G | T | 2 | a0010c0011t0005g0212 a0010c0011t0005g0234 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2261+858G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528088 | |||||||
chr4:528157 | C | G | 1 | a0002c0002t0002g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2261+927C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528157 | |||||||
chr4:528229 | T | G | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2261+999T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528229 | |||||||
chr4:528270 | T | C | 2 | a0005c0009t0002g0129 a0005c0009t0007g0280 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2261+1040T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528270 | |||||||
chr4:528357 | A | G | 1 | a0001c0001t0003g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2261+1127A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528357 | |||||||
chr4:528506 | G | A | 1 | a0004c0004t0002g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2261+1276G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528506 | |||||||
chr4:528545 | G | A | 1 | a0001c0001t0003g0274 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2261+1315G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528545 | |||||||
chr4:528601 | T | G | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2261+1371T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528601 | |||||||
chr4:528767 | T | A | 1 | a0006c0005t0002g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2261+1537T>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528767 | |||||||
chr4:528907 | C | T | 2 | a0005c0009t0002g0129 a0005c0009t0007g0280 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2262-1529C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528907 | |||||||
chr4:528954 | T | C | 3 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0009c0010t0002g0294 |
4 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2262-1482T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528954 | |||||||
chr4:528973 | C | G | 5 | a0002c0002t0002g0075 a0002c0002t0002g0122 a0002c0002t0002g0123 others(2): Show |
5 | NA18941.hp1 NA18950.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2262-1463C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 528973 | |||||||
chr4:529003 | T | C | 57 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0075 others(54): Show |
59 | HG00423.hp2 HG00621.hp2 HG01433.hp1 others(56): Show |
intron_variant | MODIFIER | c.2262-1433T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 529003 | |||||||
chr4:529120 | C | T | 1 | a0002c0002t0002g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2262-1316C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 529120 | |||||||
chr4:529320 | A | G | 2 | a0005c0009t0002g0129 a0005c0009t0007g0280 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2262-1116A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 529320 | |||||||
chr4:529347 | T | TAC | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2262-1088_2262-108 others(6): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 529347 | ||||||
chr4:529533 | TACG | T | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2262-901_2262-899d others(5): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 529533 | ||||||
chr4:529729 | C | G | 1 | a0009c0010t0002g0284 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2262-707C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 529729 | |||||||
chr4:530078 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2262-358T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530078 | |||||||
chr4:530085 | G | T | 1 | a0002c0002t0002g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2262-351G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530085 | |||||||
chr4:530138 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2262-298C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530138 | |||||||
chr4:530189 | C | G | 1 | a0005c0009t0007g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2262-247C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530189 | |||||||
chr4:530190 | G | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2262-246G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530190 | |||||||
chr4:530226 | G | A | 66 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0070 others(63): Show |
71 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2262-210G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530226 | |||||||
chr4:530240 | A | G | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2262-196A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530240 | |||||||
chr4:530330 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2262-106G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530330 | |||||||
chr4:530348 | G | T | 1 | a0011c0013t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2262-88G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530348 | |||||||
chr4:530349 | G | C | 1 | a0011c0013t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2262-87G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530349 | |||||||
chr4:530380 | T | G | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2262-56T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 10/12 | chr4 | 530380 | |||||||
chr4:530918 | C | T | 7 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0005c0008t0004g0038 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2571+173C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 530918 | |||||||
chr4:530920 | C | G | 115 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0003g0027 others(112): Show |
126 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.2571+175C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 530920 | |||||||
chr4:530949 | T | G | 105 | a0001c0001t0001g0040 a0001c0001t0003g0027 a0001c0001t0003g0045 others(102): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2571+204T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 530949 | |||||||
chr4:530999 | C | A | 1 | a0007c0006t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2571+254C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 530999 | |||||||
chr4:531093 | G | A | 108 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0002c0002t0002g0017 others(105): Show |
118 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.2571+348G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531093 | |||||||
chr4:531115 | A | G | 109 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0003g0047 others(106): Show |
119 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.2571+370A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531115 | |||||||
chr4:531154 | G | A | 1 | a0002c0002t0002g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2571+409G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531154 | |||||||
chr4:531240 | G | GCAGACGG others(55): Show |
84 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(81): Show |
90 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.2571+525_2571+526i others(64): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 531240 | ||||||
chr4:531240 | G | GCAGACGG others(54): Show |
1 | a0004c0004t0002g0113 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2571+525_2571+526i others(63): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 531240 | ||||||
chr4:531240 | G | GCAGACGG others(55): Show |
22 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0003c0003t0002g0007 others(19): Show |
26 | HG01884.hp1 HG01975.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2571+500_2571+561d others(64): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 531240 | ||||||
chr4:531245 | C | CGGGGCCT others(55): Show |
1 | a0004c0004t0002g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2571+525_2571+526i others(64): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 531245 | ||||||
chr4:531245 | C | CGGGGCCT others(55): Show |
2 | a0010c0011t0005g0212 a0010c0011t0005g0234 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2571+558_2571+619d others(64): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 531245 | ||||||
chr4:531245 | C | CGGGGCCT others(55): Show |
2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2571+524_2571+525i others(64): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 531245 | ||||||
chr4:531355 | G | GCTGGTTC others(6): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0181 others(5): Show |
11 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+610_2571+611i others(15): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531355 | |||||||
chr4:531358 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0181 others(5): Show |
11 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+613A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531358 | |||||||
chr4:531361 | A | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0181 others(5): Show |
11 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+616A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531361 | |||||||
chr4:531362 | G | GACT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0181 others(5): Show |
11 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+617_2571+618i others(5): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531362 | |||||||
chr4:531363 | G | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0181 others(5): Show |
11 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+618G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531363 | |||||||
chr4:531431 | G | A | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2571+686G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531431 | |||||||
chr4:531696 | A | G | 2 | a0010c0011t0005g0212 a0010c0011t0005g0234 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2571+951A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531696 | |||||||
chr4:531753 | C | T | 2 | a0010c0011t0005g0212 a0010c0011t0005g0234 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2571+1008C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531753 | |||||||
chr4:531783 | C | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2571+1038C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531783 | |||||||
chr4:531822 | G | A | 44 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(41): Show |
50 | HG00642.hp1 HG01243.hp1 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.2571+1077G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531822 | |||||||
chr4:531956 | C | T | 2 | a0002c0002t0002g0026 a0002c0002t0002g0244 |
3 | NA18965.hp1 NA18983.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2571+1211C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531956 | |||||||
chr4:531957 | G | A | 5 | a0003c0003t0002g0250 a0003c0003t0008g0124 a0009c0010t0002g0284 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.2571+1212G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 531957 | |||||||
chr4:532053 | G | A | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2571+1308G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532053 | |||||||
chr4:532089 | C | G | 59 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0075 others(56): Show |
62 | HG00423.hp2 HG00621.hp2 HG01433.hp1 others(59): Show |
intron_variant | MODIFIER | c.2571+1344C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532089 | |||||||
chr4:532356 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1462T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532356 | |||||||
chr4:532380 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1438A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532380 | |||||||
chr4:532428 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1390A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532428 | |||||||
chr4:532490 | A | T | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1328A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532490 | |||||||
chr4:532517 | G | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1301G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532517 | |||||||
chr4:532618 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1200A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532618 | |||||||
chr4:532619 | A | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1199A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532619 | |||||||
chr4:532654 | C | T | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-1164C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532654 | |||||||
chr4:532717 | T | C | 11 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(8): Show |
15 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.2572-1101T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532717 | |||||||
chr4:532929 | A | AGGAGTGG others(14): Show |
106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-880_2572-860d others(23): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 532929 | ||||||
chr4:532929 | A | AGGAGTGG others(119): Show |
1 | a0004c0004t0002g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2572-860_2572-859i others(128): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 532929 | ||||||
chr4:532964 | G | A | 2 | a0001c0001t0003g0033 a0001c0001t0003g0034 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2572-854G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 532964 | |||||||
chr4:533056 | C | G | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2572-762C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533056 | |||||||
chr4:533059 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-759A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533059 | |||||||
chr4:533072 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2572-746C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533072 | |||||||
chr4:533084 | C | T | 8 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(5): Show |
8 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.2572-734C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533084 | |||||||
chr4:533322 | T | G | 1 | a0005c0009t0002g0010 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2572-496T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533322 | |||||||
chr4:533336 | C | T | 1 | a0007c0006t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2572-482C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533336 | |||||||
chr4:533361 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2572-457C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533361 | |||||||
chr4:533387 | G | C | 110 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(107): Show |
120 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.2572-431G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533387 | |||||||
chr4:533428 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0185 |
2 | HG01081.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2572-390G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533428 | |||||||
chr4:533446 | C | T | 8 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(5): Show |
8 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.2572-372C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533446 | |||||||
chr4:533537 | G | A | 6 | a0005c0008t0004g0038 a0005c0008t0004g0249 a0005c0008t0004g0275 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2572-281G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533537 | |||||||
chr4:533544 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-274T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533544 | |||||||
chr4:533570 | G | A | 2 | a0005c0009t0002g0129 a0018c0026t0002g0036 |
2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2572-248G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533570 | |||||||
chr4:533613 | G | T | 2 | a0010c0011t0005g0212 a0010c0011t0005g0234 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2572-205G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533613 | |||||||
chr4:533630 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-188T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533630 | |||||||
chr4:533661 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0151 others(1): Show |
6 | HG01074.hp2 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2572-157C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533661 | |||||||
chr4:533696 | G | A | 1 | a0001c0001t0001g0005 | 3 | NA18987.hp2 NA19080.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2572-122G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533696 | |||||||
chr4:533700 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2572-118C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533700 | |||||||
chr4:533745 | G | A | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2572-73G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533745 | |||||||
chr4:533794 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0064 others(4): Show |
8 | HG00408.hp1 HG00423.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.2572-24G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 11/12 | chr4 | 533794 | |||||||
chr4:534098 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2735+117A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534098 | |||||||
chr4:534191 | G | A | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2735+210G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534191 | |||||||
chr4:534414 | C | CAGGACCC others(6): Show |
10 | a0003c0003t0008g0124 a0005c0008t0004g0038 a0005c0008t0004g0249 others(7): Show |
11 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2735+437_2735+449d others(15): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 534414 | ||||||
chr4:534495 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2735+514A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534495 | |||||||
chr4:534500 | A | C | 106 | a0001c0001t0001g0189 a0002c0002t0002g0017 a0002c0002t0002g0026 others(103): Show |
116 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2735+519A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534500 | |||||||
chr4:534500 | A | T | 1 | a0009c0010t0002g0284 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2735+519A>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534500 | |||||||
chr4:534507 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2735+526T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534507 | |||||||
chr4:534511 | G | C | 107 | a0001c0001t0001g0189 a0002c0002t0002g0017 a0002c0002t0002g0026 others(104): Show |
117 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2735+530G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534511 | |||||||
chr4:534608 | C | T | 5 | a0002c0007t0002g0104 a0002c0007t0002g0108 a0002c0007t0002g0109 others(2): Show |
5 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.2735+627C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534608 | |||||||
chr4:534614 | T | C | 98 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(95): Show |
108 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.2735+633T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534614 | |||||||
chr4:534617 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2735+636C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534617 | |||||||
chr4:534692 | C | T | 98 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(95): Show |
108 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.2735+711C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534692 | |||||||
chr4:534708 | C | T | 98 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(95): Show |
108 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.2735+727C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534708 | |||||||
chr4:534776 | G | A | 1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2735+795G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534776 | |||||||
chr4:534902 | T | C | 127 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0049 others(124): Show |
138 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.2735+921T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534902 | |||||||
chr4:534978 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0153 others(4): Show |
13 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2735+997G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 534978 | |||||||
chr4:535048 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2735+1067C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535048 | |||||||
chr4:535152 | G | T | 8 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(5): Show |
8 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.2735+1171G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535152 | |||||||
chr4:535203 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2735+1222G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535203 | |||||||
chr4:535297 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2735+1316C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535297 | |||||||
chr4:535297 | CT | C | 110 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(107): Show |
120 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.2735+1319delT | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 535297 | ||||||
chr4:535400 | A | G | 104 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(101): Show |
114 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.2735+1419A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535400 | |||||||
chr4:535406 | G | GCGTGTAC others(89): Show |
10 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(7): Show |
13 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2735+1430_2735+143 others(100): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 535406 | ||||||
chr4:535406 | G | GTGTGTGC others(41): Show |
1 | a0006c0005t0002g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2735+1425_2735+142 others(52): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535406 | |||||||
chr4:535408 | G | A | 1 | a0001c0024t0001g0299 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2735+1427G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535408 | |||||||
chr4:535421 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2735+1440G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535421 | |||||||
chr4:535424 | C | A | 13 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0003c0003t0002g0007 others(10): Show |
16 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.2735+1443C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535424 | |||||||
chr4:535424 | C | CGCCGCGG others(41): Show |
84 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(81): Show |
90 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.2735+1443_2735+144 others(52): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535424 | |||||||
chr4:535424 | C | CGCCGCGG others(233): Show |
7 | a0005c0008t0004g0038 a0005c0008t0004g0249 a0005c0008t0004g0275 others(4): Show |
8 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2735+1443_2735+144 others(244): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535424 | |||||||
chr4:535424 | C | CGCCGCGG others(89): Show |
1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2735+1443_2735+144 others(100): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535424 | |||||||
chr4:535424 | C | CGCCGCGG others(89): Show |
1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2735+1443_2735+144 others(100): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535424 | |||||||
chr4:535424 | C | CGCCGGGG others(41): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | NA18942.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2735+1443_2735+144 others(52): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535424 | |||||||
chr4:535441 | C | G | 106 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0002c0002t0002g0017 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2735+1460C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535441 | |||||||
chr4:535585 | T | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0289 |
2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2735+1604T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535585 | |||||||
chr4:535592 | T | C | 3 | a0002c0002t0002g0168 a0002c0002t0002g0239 a0002c0002t0002g0247 |
3 | NA18988.hp2 NA19006.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2735+1611T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535592 | |||||||
chr4:535642 | A | G | 105 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(102): Show |
115 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.2735+1661A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535642 | |||||||
chr4:535645 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2735+1664G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535645 | |||||||
chr4:535747 | C | A | 4 | a0010c0011t0005g0212 a0010c0011t0005g0225 a0010c0011t0005g0234 others(1): Show |
4 | HG03453.hp1 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2735+1766C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535747 | |||||||
chr4:535758 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2735+1777T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535758 | |||||||
chr4:535766 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0148 |
2 | HG00438.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2735+1785C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535766 | |||||||
chr4:535767 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2735+1786G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535767 | |||||||
chr4:535812 | T | C | 1 | a0002c0002t0002g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2735+1831T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535812 | |||||||
chr4:535821 | C | T | 10 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(7): Show |
13 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2735+1840C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535821 | |||||||
chr4:535926 | C | T | 15 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0004c0004t0002g0013 others(12): Show |
17 | HG01243.hp1 HG02738.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.2735+1945C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535926 | |||||||
chr4:535934 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2735+1953C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 535934 | |||||||
chr4:536079 | T | C | 105 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(102): Show |
115 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.2735+2098T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536079 | |||||||
chr4:536083 | G | C | 61 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(58): Show |
65 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.2735+2102G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536083 | |||||||
chr4:536112 | G | A | 96 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(93): Show |
103 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.2735+2131G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536112 | |||||||
chr4:536142 | G | T | 99 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(96): Show |
106 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.2735+2161G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536142 | |||||||
chr4:536246 | T | A | 1 | a0002c0002t0002g0267 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2735+2265T>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536246 | |||||||
chr4:536367 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2735+2386C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536367 | |||||||
chr4:536426 | G | A | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2735+2445G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536426 | |||||||
chr4:536427 | C | A | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2735+2446C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536427 | |||||||
chr4:536467 | C | T | 2 | a0003c0003t0008g0124 a0005c0009t0002g0010 |
3 | HG02818.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2735+2486C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536467 | |||||||
chr4:536561 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2735+2580A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536561 | |||||||
chr4:536647 | G | A | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2736-2506G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536647 | |||||||
chr4:536662 | C | G | 103 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(100): Show |
113 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.2736-2491C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536662 | |||||||
chr4:536753 | G | A | 1 | a0001c0001t0003g0301 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2736-2400G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536753 | |||||||
chr4:536787 | G | A | 1 | a0001c0001t0003g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2736-2366G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536787 | |||||||
chr4:536793 | G | C | 1 | a0005c0009t0002g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2736-2360G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536793 | |||||||
chr4:536887 | G | A | 15 | a0003c0003t0002g0021 a0003c0003t0002g0211 a0004c0004t0002g0013 others(12): Show |
17 | HG01243.hp1 HG02738.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.2736-2266G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536887 | |||||||
chr4:536900 | G | C | 1 | a0005c0008t0004g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2736-2253G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 536900 | |||||||
chr4:537057 | A | G | 8 | a0003c0003t0008g0124 a0005c0008t0004g0038 a0005c0008t0004g0249 others(5): Show |
9 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2736-2096A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537057 | |||||||
chr4:537062 | C | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-2091C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537062 | |||||||
chr4:537084 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-2069A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537084 | |||||||
chr4:537262 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2736-1891C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537262 | |||||||
chr4:537352 | G | A | 96 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(93): Show |
105 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.2736-1801G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537352 | |||||||
chr4:537425 | TC | T | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-1724delC | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 537425 | ||||||
chr4:537431 | T | C | 110 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(107): Show |
120 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.2736-1722T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537431 | |||||||
chr4:537476 | T | G | 110 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(107): Show |
120 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.2736-1677T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537476 | |||||||
chr4:537510 | G | A | 2 | a0010c0011t0005g0212 a0010c0011t0005g0234 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2736-1643G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537510 | |||||||
chr4:537539 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-1614T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537539 | |||||||
chr4:537824 | T | G | 1 | a0002c0002t0002g0193 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2736-1329T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537824 | |||||||
chr4:537903 | G | T | 6 | a0005c0008t0004g0038 a0005c0008t0004g0249 a0005c0008t0004g0275 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2736-1250G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537903 | |||||||
chr4:537930 | A | G | 1 | a0001c0001t0003g0301 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2736-1223A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537930 | |||||||
chr4:537931 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-1222T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537931 | |||||||
chr4:537970 | C | T | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2736-1183C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537970 | |||||||
chr4:537988 | T | C | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2736-1165T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537988 | |||||||
chr4:537992 | G | A | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2736-1161G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537992 | |||||||
chr4:537997 | G | C | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2736-1156G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 537997 | |||||||
chr4:538005 | T | C | 1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2736-1148T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538005 | |||||||
chr4:538009 | T | G | 4 | a0002c0002t0002g0125 a0002c0002t0002g0174 a0002c0002t0002g0245 others(1): Show |
4 | NA18968.hp2 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2736-1144T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538009 | |||||||
chr4:538021 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-1132T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538021 | |||||||
chr4:538026 | A | AGCCCTTT others(60): Show |
7 | a0005c0008t0004g0038 a0005c0008t0004g0249 a0005c0008t0004g0275 others(4): Show |
7 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2736-1090_2736-108 others(71): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538026 | ||||||
chr4:538026 | A | AGCCCTTT others(60): Show |
1 | a0003c0003t0008g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2736-1090_2736-108 others(71): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538026 | ||||||
chr4:538026 | A | G | 67 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(64): Show |
72 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.2736-1127A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538026 | |||||||
chr4:538057 | A | ACCCAGAC others(62): Show |
1 | a0005c0009t0007g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2736-1095_2736-109 others(73): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538057 | ||||||
chr4:538057 | A | ACCCAGAC others(125): Show |
19 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(16): Show |
20 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.2736-1095_2736-109 others(136): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538057 | ||||||
chr4:538060 | C | G | 20 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(17): Show |
21 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.2736-1093C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538060 | |||||||
chr4:538061 | C | A | 20 | a0002c0002t0002g0224 a0002c0007t0002g0104 a0002c0007t0002g0108 others(17): Show |
21 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.2736-1092C>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538061 | |||||||
chr4:538061 | C | CCACACAC others(123): Show |
1 | a0005c0009t0002g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2736-1079_2736-107 others(134): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538061 | ||||||
chr4:538061 | C | CCACACAC others(60): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2736-1084_2736-108 others(71): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538061 | ||||||
chr4:538061 | C | CCAGA | 10 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(7): Show |
14 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2736-1090_2736-108 others(8): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538061 | ||||||
chr4:538061 | C | CCAGACAC others(64): Show |
1 | a0018c0026t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2736-1090_2736-108 others(75): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538061 | ||||||
chr4:538071 | G | TTGCCGAC others(56): Show |
1 | a0005c0009t0002g0010 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2736-1083_2736-108 others(67): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538071 | |||||||
chr4:538075 | T | C | 40 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0002c0002t0002g0224 others(37): Show |
45 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.2736-1078T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538075 | |||||||
chr4:538075 | T | TGACAGGA others(60): Show |
71 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0064 others(68): Show |
77 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.2736-1069_2736-100 others(71): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538075 | ||||||
chr4:538075 | T | TGACAGGA others(127): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0216 |
2 | NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2736-1003_2736-100 others(138): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538075 | ||||||
chr4:538075 | T | TGACAGGA others(60): Show |
1 | a0006c0005t0002g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2736-1044_2736-104 others(71): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538075 | ||||||
chr4:538084 | C | T | 2 | a0001c0001t0001g0084 a0012c0018t0001g0195 |
2 | NA18953.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.2736-1069C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538084 | |||||||
chr4:538099 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2736-1054A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538099 | |||||||
chr4:538116 | C | G | 1 | a0003c0003t0002g0265 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2736-1037C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538116 | |||||||
chr4:538127 | G | C | 4 | a0001c0001t0001g0145 a0005c0009t0002g0010 a0005c0009t0002g0129 others(1): Show |
5 | HG02818.hp2 HG02895.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2736-1026G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538127 | |||||||
chr4:538137 | C | T | 9 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(6): Show |
12 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2736-1016C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538137 | |||||||
chr4:538142 | C | T | 10 | a0003c0003t0008g0124 a0005c0008t0004g0038 a0005c0008t0004g0249 others(7): Show |
11 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2736-1011C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538142 | |||||||
chr4:538143 | G | T | 10 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(7): Show |
13 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2736-1010G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538143 | |||||||
chr4:538157 | T | G | 62 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(59): Show |
66 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2736-996T>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538157 | |||||||
chr4:538170 | T | C | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-983T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538170 | |||||||
chr4:538173 | G | A | 2 | a0003c0003t0008g0124 a0005c0009t0002g0010 |
3 | HG02818.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2736-980G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538173 | |||||||
chr4:538225 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2736-928G>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538225 | |||||||
chr4:538268 | A | AC | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-885_2736-884i others(3): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538268 | |||||||
chr4:538314 | TC | T | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-838delC | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538314 | |||||||
chr4:538316 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-837A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538316 | |||||||
chr4:538330 | C | T | 2 | a0010c0011t0005g0225 a0010c0011t0005g0293 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2736-823C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538330 | |||||||
chr4:538411 | A | G | 88 | a0001c0001t0001g0185 a0002c0002t0002g0017 a0002c0002t0002g0026 others(85): Show |
98 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.2736-742A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538411 | |||||||
chr4:538576 | G | A | 9 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0250 others(6): Show |
12 | HG01884.hp1 HG01975.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2736-577G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538576 | |||||||
chr4:538589 | G | A | 2 | a0005c0009t0002g0129 a0018c0026t0002g0036 |
2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2736-564G>A | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538589 | |||||||
chr4:538660 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2736-493C>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538660 | |||||||
chr4:538674 | ACT | A | 2 | a0003c0003t0008g0124 a0005c0009t0002g0010 |
3 | HG02818.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2736-477_2736-476d others(4): Show |
PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 538674 | ||||||
chr4:538819 | G | T | 11 | a0003c0003t0008g0124 a0005c0008t0004g0038 a0005c0008t0004g0249 others(8): Show |
12 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2736-334G>T | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538819 | |||||||
chr4:538828 | A | C | 1 | a0002c0002t0002g0125 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2736-325A>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538828 | |||||||
chr4:538968 | C | G | 1 | a0019c0031t0001g0067 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2736-185C>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 538968 | |||||||
chr4:539023 | A | G | 106 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0029 others(103): Show |
116 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.2736-130A>G | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 539023 | |||||||
chr4:539128 | T | C | 4 | a0002c0002t0002g0083 a0002c0002t0002g0125 a0002c0002t0002g0174 others(1): Show |
4 | NA18977.hp2 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2736-25T>C | PIGG | ENSG00000174227.16 | transcript | ENST00000453061.7 | protein_coding | 12/12 | chr4 | 539128 |