geneid | 57540 |
---|---|
ensemblid | ENSG00000204624.8 |
hgncid | 29251 |
symbol | DISP3 |
name | dispatched RND transporter family member 3 |
refseq_nuc | NM_020780.2 |
refseq_prot | NP_065831.1 |
ensembl_nuc | ENST00000294484.7 |
ensembl_prot | ENSP00000294484.6 |
mane_status | MANE Select |
chr | chr1 |
start | 11479155 |
end | 11537551 |
strand | + |
ver | v1.2 |
region | chr1:11479155-11537551 |
region5000 | chr1:11474155-11542551 |
regionname0 | DISP3_chr1_11479155_11537551 |
regionname5000 | DISP3_chr1_11474155_11542551 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1392 | 100 | 29 | 7 | 55 | 0 | 7 | 43 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002 | 0/0 | 1392 | 75 | 5 | 4 | 54 | 1 | 11 | 39 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003 | 0/0 | 1392 | 68 | 2 | 16 | 38 | 6 | 6 | 29 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004 | 0/0 | 1392 | 58 | 35 | 7 | 8 | 1 | 7 | 8 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0005 | 0/0 | 1392 | 12 | 0 | 3 | 6 | 0 | 3 | 4 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0006 | 0/0 | 1392 | 9 | 0 | 7 | 0 | 0 | 2 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0007 | 0/0 | 1392 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0008 | 0/0 | 1392 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009 | 0/0 | 1392 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0010 | 0/0 | 1392 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0011 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0012 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0013 | 0/0 | 1392 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0014 | 0/0 | 1392 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0015 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0016 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0017 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0018 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0019 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0020 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0021 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0022 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0023 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0024 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4179 | 69 | 5 | 6 | 50 | 0 | 6 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0002 | 0/0 | 4179 | 61 | 3 | 3 | 47 | 1 | 7 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0003 | 0/0 | 4179 | 58 | 2 | 12 | 33 | 6 | 5 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0004 | 0/0 | 4179 | 38 | 17 | 6 | 8 | 1 | 6 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0005 | 0/0 | 4179 | 15 | 10 | 0 | 4 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0006 | 0/0 | 4179 | 12 | 0 | 3 | 6 | 0 | 3 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0007 | 0/0 | 4179 | 11 | 11 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0008 | 0/0 | 4179 | 9 | 0 | 4 | 4 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0009 | 0/0 | 4179 | 9 | 0 | 7 | 0 | 0 | 2 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0010 | 0/0 | 4179 | 8 | 8 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0011 | 0/0 | 4179 | 7 | 0 | 0 | 4 | 0 | 3 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0012 | 0/0 | 4179 | 4 | 0 | 4 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0013 | 0/0 | 4179 | 4 | 3 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0014 | 0/0 | 4179 | 4 | 0 | 0 | 4 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0015 | 0/0 | 4179 | 3 | 3 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0016 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0017 | 0/0 | 4179 | 2 | 0 | 1 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0018 | 0/0 | 4179 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0019 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0020 | 0/0 | 4179 | 2 | 0 | 0 | 0 | 2 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0021 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0022 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0023 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0024 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0025 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0026 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0027 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0028 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0029 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0030 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0031 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0032 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0033 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0034 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0035 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0036 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0037 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0038 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0039 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0040 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0041 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0042 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0043 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0044 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0045 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0046 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0047 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0048 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0049 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0050 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0051 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0052 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0053 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
c0054 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1087 | 100 | 5 | 32 | 42 | 6 | 13 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0002 | 0/0 | 1087 | 79 | 5 | 9 | 56 | 1 | 8 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0003 | 0/0 | 1088 | 66 | 3 | 5 | 49 | 2 | 7 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0004 | 0/0 | 1087 | 46 | 31 | 5 | 6 | 1 | 3 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0005 | 0/0 | 1087 | 13 | 13 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0006 | 0/0 | 1087 | 12 | 1 | 0 | 6 | 0 | 5 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0007 | 0/0 | 1085 | 7 | 7 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0008 | 0/0 | 1087 | 6 | 5 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0009 | 0/0 | 1087 | 4 | 3 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0010 | 0/0 | 1087 | 3 | 3 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0011 | 0/0 | 1087 | 3 | 0 | 0 | 2 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0012 | 0/0 | 1087 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0013 | 0/0 | 1087 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0014 | 0/0 | 1087 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0015 | 0/0 | 1087 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0016 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0017 | 0/0 | 1087 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0018 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0019 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0020 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0021 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0022 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0023 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0024 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0025 | 0/0 | 1088 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
t0026 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0002 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4179 | 69 | 5 | 6 | 50 | 0 | 6 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0005 | 0/0 | 4179 | 15 | 10 | 0 | 4 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0007 | 0/0 | 4179 | 11 | 11 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0021 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0043 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0044 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0050 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0002 | 0/0 | 4179 | 61 | 3 | 3 | 47 | 1 | 7 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0011 | 0/0 | 4179 | 7 | 0 | 0 | 4 | 0 | 3 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0018 | 0/0 | 4179 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0039 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0040 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0041 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0048 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0051 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0003 | 0/0 | 4179 | 58 | 2 | 12 | 33 | 6 | 5 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0008 | 0/0 | 4179 | 9 | 0 | 4 | 4 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0032 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0004 | 0/0 | 4179 | 38 | 17 | 6 | 8 | 1 | 6 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0010 | 0/0 | 4179 | 8 | 8 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0015 | 0/0 | 4179 | 3 | 3 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0016 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0017 | 0/0 | 4179 | 2 | 0 | 1 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0024 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0025 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0026 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0027 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0028 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0005c0006 | 0/0 | 4179 | 12 | 0 | 3 | 6 | 0 | 3 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0006c0009 | 0/0 | 4179 | 9 | 0 | 7 | 0 | 0 | 2 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0007c0013 | 0/0 | 4179 | 4 | 3 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0007c0037 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0008c0014 | 0/0 | 4179 | 4 | 0 | 0 | 4 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0008c0054 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009c0019 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009c0042 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009c0049 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0010c0012 | 0/0 | 4179 | 4 | 0 | 4 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0011c0022 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0012c0045 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0012c0046 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0013c0020 | 0/0 | 4179 | 2 | 0 | 0 | 0 | 2 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0014c0034 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0014c0035 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0015c0053 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0016c0030 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0017c0038 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0018c0047 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0019c0052 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0020c0036 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0021c0033 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0022c0031 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0023c0029 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0024c0023 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5265 | 6 | 0 | 2 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0001t0002 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0001t0003 | 0/0 | 5266 | 59 | 3 | 4 | 46 | 0 | 6 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0001t0007 | 0/0 | 5263 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0001t0011 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0005t0004 | 0/0 | 5265 | 11 | 6 | 0 | 4 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0005t0005 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0005t0006 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0005t0015 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0007t0005 | 0/0 | 5265 | 11 | 11 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0021t0008 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0043t0002 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0044t0005 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0001c0050t0001 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0002t0001 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0002t0002 | 0/0 | 5265 | 58 | 3 | 3 | 44 | 1 | 7 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0002t0022 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0002t0026 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0011t0001 | 0/0 | 5265 | 4 | 0 | 0 | 2 | 0 | 2 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0011t0003 | 0/0 | 5266 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0011t0011 | 0/0 | 5265 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0018t0002 | 0/0 | 5265 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0039t0002 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0040t0002 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0041t0004 | 0/0 | 5265 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0048t0002 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0002c0051t0004 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0003t0001 | 0/0 | 5265 | 56 | 2 | 12 | 31 | 6 | 5 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0003t0003 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0003t0024 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0008t0002 | 0/0 | 5265 | 6 | 0 | 4 | 1 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0008t0013 | 0/0 | 5265 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0008t0023 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0003c0032t0001 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0004t0004 | 0/0 | 5265 | 25 | 16 | 5 | 2 | 1 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0004t0006 | 0/0 | 5265 | 11 | 0 | 0 | 6 | 0 | 5 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0004t0008 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0004t0016 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0010t0004 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0010t0007 | 0/0 | 5263 | 4 | 4 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0010t0014 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0015t0004 | 0/0 | 5265 | 3 | 3 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0016t0012 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0016t0020 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0017t0001 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0017t0025 | 0/0 | 5266 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0024t0019 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0025t0008 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0026t0004 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0027t0001 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0004c0028t0012 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0005c0006t0001 | 0/0 | 5265 | 11 | 0 | 3 | 5 | 0 | 3 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0005c0006t0018 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0006c0009t0001 | 0/0 | 5265 | 9 | 0 | 7 | 0 | 0 | 2 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0007c0013t0009 | 0/0 | 5265 | 4 | 3 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0007c0037t0004 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0008c0014t0002 | 0/0 | 5265 | 4 | 0 | 0 | 4 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0008c0054t0011 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009c0019t0008 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009c0019t0010 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009c0042t0001 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0009c0049t0001 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0010c0012t0001 | 0/0 | 5265 | 3 | 0 | 3 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0010c0012t0003 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0011c0022t0010 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0012c0045t0004 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0012c0046t0021 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0013c0020t0003 | 0/0 | 5266 | 2 | 0 | 0 | 0 | 2 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0014c0034t0002 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0014c0035t0001 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0015c0053t0007 | 0/0 | 5263 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0016c0030t0002 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0017c0038t0017 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0018c0047t0002 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0019c0052t0002 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0020c0036t0008 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0021c0033t0001 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0022c0031t0001 | 0/0 | 5265 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0023c0029t0001 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
a0024c0023t0003 | 0/0 | 5266 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | copy fasta | chr1 | 11474155 | 11542551 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0001g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0007g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0015g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0005t0015g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0007t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0021t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0021t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0043t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0044t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0001c0050t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0022g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0002t0026g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0011t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0011t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0011t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0011t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0011t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0011t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0011t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0018t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0018t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0039t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0040t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0041t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0048t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0002c0051t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0003t0024g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0013g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0013g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0008t0023g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0003c0032t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0008g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0004t0016g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0014g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0010t0014g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0015t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0015t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0015t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0016t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0016t0020g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0017t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0017t0025g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0024t0019g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0025t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0026t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0027t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0004c0028t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0005c0006t0018g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0006c0009t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0007c0013t0009g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0007c0013t0009g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0007c0013t0009g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0007c0013t0009g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0007c0037t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0008c0014t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0008c0014t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0008c0014t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0008c0014t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0008c0054t0011g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0009c0019t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0009c0019t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0009c0042t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0009c0049t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0010c0012t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0010c0012t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0010c0012t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0010c0012t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0011c0022t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0011c0022t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0012c0045t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0012c0046t0021g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0013c0020t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0013c0020t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0014c0034t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0014c0035t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0015c0053t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0016c0030t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0017c0038t0017g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0018c0047t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0019c0052t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0020c0036t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0021c0033t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0022c0031t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0023c0029t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
a0024c0023t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0004 | t0004 | g0205 | EUR | GBR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0203 | EUR | GBR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0100 | EUR | FIN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0271 | EUR | FIN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00408 | hp2 | a0016 | c0030 | t0002 | g0167 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00438 | hp1 | a0002 | c0002 | t0026 | g0030 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00438 | hp2 | a0008 | c0014 | t0002 | g0187 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00558 | hp1 | a0003 | c0003 | t0001 | g0268 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00609 | hp1 | a0008 | c0014 | t0002 | g0154 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0262 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00639 | hp1 | a0003 | c0008 | t0002 | g0242 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00639 | hp2 | a0002 | c0040 | t0002 | g0309 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0229 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00673 | hp1 | a0005 | c0006 | t0001 | g0282 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | CHS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0231 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00735 | hp2 | a0004 | c0017 | t0001 | g0328 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0334 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00738 | hp2 | a0003 | c0008 | t0002 | g0222 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00741 | hp1 | a0018 | c0047 | t0002 | g0202 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG00741 | hp2 | a0005 | c0006 | t0001 | g0143 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01069 | hp1 | a0004 | c0004 | t0004 | g0012 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01069 | hp2 | a0003 | c0003 | t0001 | g0275 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01070 | hp1 | a0004 | c0004 | t0004 | g0012 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01070 | hp2 | a0003 | c0003 | t0001 | g0216 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01081 | hp1 | a0004 | c0004 | t0004 | g0322 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01081 | hp2 | a0005 | c0006 | t0001 | g0190 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01099 | hp1 | a0006 | c0009 | t0001 | g0270 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0223 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01106 | hp2 | a0003 | c0003 | t0001 | g0228 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0175 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0257 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0218 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01167 | hp2 | a0004 | c0004 | t0008 | g0308 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01168 | hp1 | a0010 | c0012 | t0003 | g0232 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01175 | hp1 | a0006 | c0009 | t0001 | g0010 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01175 | hp2 | a0003 | c0003 | t0001 | g0255 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01243 | hp1 | a0001 | c0050 | t0001 | g0314 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01243 | hp2 | a0007 | c0013 | t0009 | g0332 | AMR | PUR | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01255 | hp1 | a0003 | c0008 | t0002 | g0241 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01255 | hp2 | a0010 | c0012 | t0001 | g0220 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01256 | hp2 | a0006 | c0009 | t0001 | g0265 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01257 | hp1 | a0023 | c0029 | t0001 | g0140 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01257 | hp2 | a0004 | c0004 | t0004 | g0320 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01258 | hp2 | a0006 | c0009 | t0001 | g0010 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01433 | hp2 | a0005 | c0006 | t0001 | g0151 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01496 | hp1 | a0006 | c0009 | t0001 | g0250 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01496 | hp2 | a0014 | c0035 | t0001 | g0230 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01515 | hp1 | a0013 | c0020 | t0003 | g0002 | EUR | IBS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0243 | EUR | IBS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01516 | hp1 | a0013 | c0020 | t0003 | g0079 | EUR | IBS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0245 | EUR | IBS | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01891 | hp1 | a0004 | c0028 | t0012 | g0047 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01891 | hp2 | a0009 | c0042 | t0001 | g0015 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01934 | hp1 | a0010 | c0012 | t0001 | g0221 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01934 | hp2 | a0021 | c0033 | t0001 | g0283 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01952 | hp1 | a0004 | c0004 | t0004 | g0323 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01952 | hp2 | a0006 | c0009 | t0001 | g0263 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02004 | hp2 | a0003 | c0008 | t0002 | g0240 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0285 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02040 | hp1 | a0003 | c0003 | t0001 | g0278 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02055 | hp1 | a0004 | c0016 | t0012 | g0054 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02055 | hp2 | a0001 | c0007 | t0005 | g0005 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0267 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0098 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02071 | hp2 | a0002 | c0011 | t0001 | g0138 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02080 | hp2 | a0003 | c0003 | t0001 | g0280 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02083 | hp1 | a0001 | c0043 | t0002 | g0102 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02083 | hp2 | a0008 | c0014 | t0002 | g0173 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02129 | hp1 | a0002 | c0011 | t0003 | g0131 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02129 | hp2 | a0002 | c0018 | t0002 | g0160 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02145 | hp1 | a0011 | c0022 | t0010 | g0024 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02145 | hp2 | a0004 | c0004 | t0004 | g0217 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | CDX | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02165 | hp2 | a0001 | c0001 | t0011 | g0233 | EAS | CDX | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02258 | hp1 | a0004 | c0004 | t0004 | g0145 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02258 | hp2 | a0007 | c0013 | t0009 | g0333 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02273 | hp1 | a0006 | c0009 | t0001 | g0264 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02273 | hp2 | a0017 | c0038 | t0017 | g0153 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02280 | hp1 | a0004 | c0004 | t0004 | g0214 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02280 | hp2 | a0007 | c0013 | t0009 | g0331 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0148 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02293 | hp2 | a0003 | c0003 | t0001 | g0224 | AMR | PEL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02523 | hp1 | a0003 | c0003 | t0003 | g0251 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02523 | hp2 | a0005 | c0006 | t0001 | g0106 | EAS | KHV | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02572 | hp1 | a0001 | c0005 | t0015 | g0343 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02572 | hp2 | a0009 | c0049 | t0001 | g0013 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02602 | hp1 | a0004 | c0004 | t0006 | g0025 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0234 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02615 | hp1 | a0004 | c0004 | t0004 | g0341 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02615 | hp2 | a0004 | c0010 | t0004 | g0290 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02622 | hp1 | a0004 | c0004 | t0004 | g0293 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02630 | hp1 | a0001 | c0005 | t0004 | g0296 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02647 | hp1 | a0001 | c0005 | t0006 | g0038 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02647 | hp2 | a0001 | c0007 | t0005 | g0113 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02698 | hp1 | a0024 | c0023 | t0003 | g0061 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02698 | hp2 | a0005 | c0006 | t0001 | g0051 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02717 | hp1 | a0004 | c0010 | t0014 | g0291 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02717 | hp2 | a0004 | c0004 | t0004 | g0319 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02809 | hp1 | a0004 | c0004 | t0004 | g0313 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02818 | hp1 | a0004 | c0010 | t0007 | g0338 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02818 | hp2 | a0004 | c0004 | t0004 | g0340 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02886 | hp1 | a0004 | c0010 | t0007 | g0335 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02886 | hp2 | a0004 | c0016 | t0020 | g0017 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02895 | hp1 | a0001 | c0007 | t0005 | g0115 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02895 | hp2 | a0004 | c0010 | t0007 | g0336 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02897 | hp1 | a0004 | c0010 | t0014 | g0292 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02897 | hp2 | a0001 | c0007 | t0005 | g0114 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0276 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02922 | hp2 | a0001 | c0007 | t0005 | g0006 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02965 | hp1 | a0012 | c0046 | t0021 | g0016 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02965 | hp2 | a0001 | c0005 | t0005 | g0118 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02970 | hp1 | a0001 | c0007 | t0005 | g0006 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02970 | hp2 | a0020 | c0036 | t0008 | g0315 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02976 | hp1 | a0004 | c0004 | t0004 | g0213 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02976 | hp2 | a0004 | c0004 | t0004 | g0302 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03017 | hp1 | a0004 | c0004 | t0006 | g0022 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03017 | hp2 | a0005 | c0006 | t0001 | g0152 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03041 | hp1 | a0004 | c0010 | t0004 | g0312 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03041 | hp2 | a0004 | c0015 | t0004 | g0321 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03098 | hp1 | a0004 | c0004 | t0004 | g0304 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0146 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03130 | hp1 | a0014 | c0034 | t0002 | g0019 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03130 | hp2 | a0004 | c0015 | t0004 | g0318 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03139 | hp1 | a0004 | c0004 | t0004 | g0306 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03139 | hp2 | a0001 | c0005 | t0004 | g0295 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03195 | hp1 | a0004 | c0004 | t0004 | g0303 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03195 | hp2 | a0011 | c0022 | t0010 | g0023 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03209 | hp1 | a0001 | c0005 | t0004 | g0297 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03209 | hp2 | a0001 | c0005 | t0004 | g0298 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0274 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03225 | hp2 | a0004 | c0004 | t0004 | g0305 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03239 | hp1 | a0002 | c0011 | t0001 | g0144 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0235 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03453 | hp1 | a0015 | c0053 | t0007 | g0300 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03453 | hp2 | a0001 | c0005 | t0004 | g0294 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03486 | hp1 | a0002 | c0051 | t0004 | g0172 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03486 | hp2 | a0007 | c0037 | t0004 | g0330 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03490 | hp1 | a0003 | c0003 | t0001 | g0238 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03491 | hp1 | a0003 | c0003 | t0001 | g0227 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03491 | hp2 | a0004 | c0004 | t0006 | g0026 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03492 | hp2 | a0004 | c0004 | t0006 | g0027 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03516 | hp1 | a0001 | c0005 | t0015 | g0342 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03516 | hp2 | a0001 | c0007 | t0005 | g0005 | AFR | ESN | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03540 | hp1 | a0004 | c0025 | t0008 | g0053 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03540 | hp2 | a0004 | c0004 | t0004 | g0301 | AFR | GWD | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03579 | hp1 | a0001 | c0021 | t0008 | g0194 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03579 | hp2 | a0001 | c0044 | t0005 | g0117 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03669 | hp1 | a0004 | c0004 | t0006 | g0029 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03669 | hp2 | a0006 | c0009 | t0001 | g0273 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0339 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0327 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0226 | SAS | PJL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03831 | hp1 | a0004 | c0017 | t0025 | g0028 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03831 | hp2 | a0003 | c0003 | t0001 | g0247 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03834 | hp1 | a0004 | c0004 | t0004 | g0324 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03834 | hp2 | a0022 | c0031 | t0001 | g0246 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03927 | hp1 | a0002 | c0041 | t0004 | g0142 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03942 | hp1 | a0006 | c0009 | t0001 | g0288 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0178 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04115 | hp1 | a0001 | c0005 | t0004 | g0059 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04115 | hp2 | a0002 | c0011 | t0001 | g0201 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0326 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0186 | SAS | BEB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04199 | hp2 | a0003 | c0008 | t0002 | g0239 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04228 | hp1 | a0002 | c0011 | t0011 | g0137 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | STU | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18522 | hp1 | a0004 | c0010 | t0007 | g0337 | AFR | YRI | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18522 | hp2 | a0001 | c0007 | t0005 | g0120 | AFR | YRI | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | CHB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | CHB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0237 | EAS | CHB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | CHB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18906 | hp1 | a0007 | c0013 | t0009 | g0316 | AFR | YRI | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18906 | hp2 | a0004 | c0027 | t0001 | g0310 | AFR | YRI | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18940 | hp1 | a0004 | c0004 | t0004 | g0139 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18940 | hp2 | a0005 | c0006 | t0001 | g0071 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0200 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18942 | hp2 | a0004 | c0004 | t0004 | g0329 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0266 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18948 | hp1 | a0004 | c0004 | t0006 | g0034 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18948 | hp2 | a0003 | c0008 | t0023 | g0281 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18954 | hp1 | a0019 | c0052 | t0002 | g0135 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18954 | hp2 | a0005 | c0006 | t0001 | g0133 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18959 | hp2 | a0004 | c0004 | t0006 | g0036 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18960 | hp1 | a0002 | c0002 | t0022 | g0168 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18962 | hp1 | a0001 | c0005 | t0004 | g0209 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18962 | hp2 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0197 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18971 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18971 | hp2 | a0008 | c0014 | t0002 | g0188 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18973 | hp1 | a0003 | c0003 | t0001 | g0249 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18974 | hp1 | a0003 | c0008 | t0013 | g0244 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18977 | hp1 | a0005 | c0006 | t0018 | g0176 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18979 | hp1 | a0002 | c0018 | t0002 | g0166 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0259 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18985 | hp1 | a0004 | c0004 | t0006 | g0035 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0258 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18994 | hp1 | a0003 | c0032 | t0001 | g0279 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18994 | hp2 | a0002 | c0048 | t0002 | g0136 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18999 | hp1 | a0008 | c0054 | t0011 | g0189 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19002 | hp1 | a0005 | c0006 | t0001 | g0180 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19003 | hp1 | a0001 | c0005 | t0004 | g0208 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19010 | hp1 | a0001 | c0005 | t0004 | g0155 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0198 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19030 | hp1 | a0004 | c0015 | t0004 | g0317 | AFR | LWK | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19030 | hp2 | a0001 | c0007 | t0005 | g0119 | AFR | LWK | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19043 | hp1 | a0001 | c0021 | t0008 | g0212 | AFR | LWK | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19043 | hp2 | a0001 | c0007 | t0005 | g0116 | AFR | LWK | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19054 | hp1 | a0004 | c0004 | t0006 | g0033 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19055 | hp1 | a0002 | c0011 | t0001 | g0164 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19057 | hp2 | a0003 | c0003 | t0001 | g0248 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0253 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19063 | hp2 | a0003 | c0003 | t0001 | g0284 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19074 | hp2 | a0004 | c0004 | t0006 | g0037 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19079 | hp1 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19080 | hp1 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19080 | hp2 | a0004 | c0004 | t0006 | g0032 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19081 | hp2 | a0002 | c0011 | t0003 | g0159 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19085 | hp1 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19086 | hp1 | a0003 | c0008 | t0002 | g0277 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19088 | hp1 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19090 | hp1 | a0003 | c0003 | t0001 | g0252 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19090 | hp2 | a0003 | c0003 | t0024 | g0031 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0219 | AFR | ASW | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20129 | hp2 | a0001 | c0005 | t0004 | g0020 | AFR | ASW | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20752 | hp1 | a0003 | c0003 | t0001 | g0008 | EUR | TSI | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0256 | EUR | TSI | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0008 | SAS | GIH | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20905 | hp2 | a0005 | c0006 | t0001 | g0206 | SAS | GIH | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01123 | hp1 | a0010 | c0012 | t0001 | g0225 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02109 | hp1 | a0004 | c0004 | t0004 | g0215 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02109 | hp2 | a0001 | c0007 | t0005 | g0046 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02486 | hp1 | a0002 | c0039 | t0002 | g0141 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02559 | hp1 | a0012 | c0045 | t0004 | g0018 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG02559 | hp2 | a0009 | c0019 | t0008 | g0014 | AFR | ACB | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03471 | hp1 | a0004 | c0024 | t0019 | g0325 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
HG03471 | hp2 | a0009 | c0019 | t0010 | g0112 | AFR | MSL | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18955 | hp1 | a0003 | c0008 | t0013 | g0272 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA18955 | hp2 | a0001 | c0005 | t0004 | g0097 | EAS | JPT | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | USA | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | USA | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA21309 | hp1 | a0004 | c0004 | t0016 | g0307 | AFR | LWK | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
NA21309 | hp2 | a0004 | c0026 | t0004 | g0311 | AFR | LWK | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0150 | REF | REF | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0299 | REF | REF | DISP3_chr1_11474155_11542551 | DISP3 | chr1 | 11474155 | 11542551 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11501008
|
G | C | 1 | a0024 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.16G>C | p.Asp6His | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 237/5265 | 16/4179 | 6/1392 | chr1 | 11501008 | ||
chr1:11501107
|
G | A | 1 | a0004 | 58 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(55): Show |
missense_variant | MODERATE | c.115G>A | p.Gly39Arg | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 336/5265 | 115/4179 | 39/1392 | chr1 | 11501107 | ||
chr1:11501143
|
C | G | 1 | a0008 | 5 | HG00438.hp2 HG00609.hp1 HG02083.hp2 others(2): Show |
missense_variant | MODERATE | c.151C>G | p.Leu51Val | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 372/5265 | 151/4179 | 51/1392 | chr1 | 11501143 | ||
chr1:11501200
|
A | G | 1 | a0015 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.208A>G | p.Asn70Asp | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 429/5265 | 208/4179 | 70/1392 | chr1 | 11501200 | ||
chr1:11501311
|
G | C | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.319G>C | p.Ala107Pro | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 540/5265 | 319/4179 | 107/1392 | chr1 | 11501311 | ||
chr1:11501312
|
C | G | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.320C>G | p.Ala107Gly | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 541/5265 | 320/4179 | 107/1392 | chr1 | 11501312 | ||
chr1:11501332
|
G | A | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.340G>A | p.Glu114Lys | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 561/5265 | 340/4179 | 114/1392 | chr1 | 11501332 | ||
chr1:11501333
|
A | G | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.341A>G | p.Glu114Gly | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 562/5265 | 341/4179 | 114/1392 | chr1 | 11501333 | ||
chr1:11501334
|
G | C | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.342G>C | p.Glu114Asp | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 563/5265 | 342/4179 | 114/1392 | chr1 | 11501334 | ||
chr1:11501336
|
C | G | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.344C>G | p.Ala115Gly | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 565/5265 | 344/4179 | 115/1392 | chr1 | 11501336 | ||
chr1:11501432
|
C | T | 1 | a0011 | 2 | HG02145.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.440C>T | p.Thr147Met | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 661/5265 | 440/4179 | 147/1392 | chr1 | 11501432 | ||
chr1:11501489
|
G | A | 1 | a0016 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.497G>A | p.Arg166Gln | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 718/5265 | 497/4179 | 166/1392 | chr1 | 11501489 | ||
chr1:11501521
|
G | C | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.529G>C | p.Ala177Pro | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 750/5265 | 529/4179 | 177/1392 | chr1 | 11501521 | ||
chr1:11501536
|
G | A | 8 | a0003a0006a0007others(5): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(88): Show |
missense_variant | MODERATE | c.544G>A | p.Gly182Ser | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 765/5265 | 544/4179 | 182/1392 | chr1 | 11501536 | ||
chr1:11501543
|
G | T | 1 | a0019 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.551G>T | p.Gly184Val | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 772/5265 | 551/4179 | 184/1392 | chr1 | 11501543 | ||
chr1:11501691
|
G | C | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.699G>C | p.Gln233His | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 920/5265 | 699/4179 | 233/1392 | chr1 | 11501691 | ||
chr1:11501692
|
C | G | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.700C>G | p.Pro234Ala | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 921/5265 | 700/4179 | 234/1392 | chr1 | 11501692 | ||
chr1:11502076
|
G | C | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1084G>C | p.Ala362Pro | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 1305/5265 | 1084/4179 | 362/1392 | chr1 | 11502076 | ||
chr1:11502077
|
C | G | 1 | a0023 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1085C>G | p.Ala362Gly | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 1306/5265 | 1085/4179 | 362/1392 | chr1 | 11502077 | ||
chr1:11519413
|
G | A | 6 | a0003a0005a0006others(3): Show | 92 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(89): Show |
missense_variant | MODERATE | c.1948G>A | p.Ala650Thr | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/21 | 2169/5265 | 1948/4179 | 650/1392 | chr1 | 11519413 | ||
chr1:11519414
|
C | T | 1 | a0018 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1949C>T | p.Ala650Val | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/21 | 2170/5265 | 1949/4179 | 650/1392 | chr1 | 11519414 | ||
chr1:11519447
|
G | C | 6 | a0002a0008a0014others(3): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
missense_variant | MODERATE | c.1982G>C | p.Gly661Ala | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/21 | 2203/5265 | 1982/4179 | 661/1392 | chr1 | 11519447 | ||
chr1:11524047
|
C | A | 2 | a0009a0020 | 5 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(2): Show |
missense_variant | MODERATE | c.2468C>A | p.Thr823Asn | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/21 | 2689/5265 | 2468/4179 | 823/1392 | chr1 | 11524047 | ||
chr1:11524052
|
C | G | 2 | a0007a0012 | 7 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.2473C>G | p.Gln825Glu | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/21 | 2694/5265 | 2473/4179 | 825/1392 | chr1 | 11524052 | ||
chr1:11525251
|
C | T | 2 | a0006a0017 | 10 | HG01099.hp1 HG01175.hp1 HG01256.hp2 others(7): Show |
missense_variant | MODERATE | c.2552C>T | p.Ala851Val | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/21 | 2773/5265 | 2552/4179 | 851/1392 | chr1 | 11525251 | ||
chr1:11529838
|
C | T | 1 | a0021 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.2981C>T | p.Thr994Met | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/21 | 3202/5265 | 2981/4179 | 994/1392 | chr1 | 11529838 | ||
chr1:11531681
|
G | A | 1 | a0022 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.3346G>A | p.Val1116Met | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/21 | 3567/5265 | 3346/4179 | 1116/1392 | chr1 | 11531681 | ||
chr1:11535585
|
G | A | 1 | a0013 | 2 | HG01515.hp1 HG01516.hp1 |
missense_variant | MODERATE | c.3757G>A | p.Val1253Ile | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/21 | 3978/5265 | 3757/4179 | 1253/1392 | chr1 | 11535585 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11501520
|
C | G | 1 | a0023c0029 | 1 | HG01257.hp1 | synonymous_variant | LOW | c.528C>G | p.Pro176Pro | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 749/5265 | 528/4179 | 176/1392 | chr1 | 11501520 | ||
chr1:11501706
|
C | T | 1 | a0004c0028 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.714C>T | p.Pro238Pro | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 935/5265 | 714/4179 | 238/1392 | chr1 | 11501706 | ||
chr1:11501880
|
C | T | 10 | a0004c0004a0004c0010a0004c0015others(7): Show | 58 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(55): Show |
synonymous_variant | LOW | c.888C>T | p.Val296Val | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 1109/5265 | 888/4179 | 296/1392 | chr1 | 11501880 | ||
chr1:11501958
|
C | G | 1 | a0002c0051 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.966C>G | p.Leu322Leu | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 1187/5265 | 966/4179 | 322/1392 | chr1 | 11501958 | ||
chr1:11502057
|
C | T | 1 | a0001c0050 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1065C>T | p.Asp355Asp | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/21 | 1286/5265 | 1065/4179 | 355/1392 | chr1 | 11502057 | ||
chr1:11502682
|
C | T | 1 | a0009c0049 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1101C>T | p.Ser367Ser | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/21 | 1322/5265 | 1101/4179 | 367/1392 | chr1 | 11502682 | ||
chr1:11502856
|
C | T | 5 | a0004c0004a0004c0015a0004c0017others(2): Show | 45 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(42): Show |
synonymous_variant | LOW | c.1275C>T | p.Phe425Phe | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/21 | 1496/5265 | 1275/4179 | 425/1392 | chr1 | 11502856 | ||
chr1:11516149
|
C | T | 3 | a0002c0048a0007c0013a0007c0037 | 6 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
synonymous_variant | LOW | c.1737C>T | p.Asn579Asn | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/21 | 1958/5265 | 1737/4179 | 579/1392 | chr1 | 11516149 | ||
chr1:11519762
|
C | T | 10 | a0001c0007a0001c0021a0001c0044others(7): Show | 25 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(22): Show |
synonymous_variant | LOW | c.2082C>T | p.Pro694Pro | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/21 | 2303/5265 | 2082/4179 | 694/1392 | chr1 | 11519762 | ||
chr1:11529815
|
C | T | 1 | a0004c0015 | 3 | HG03041.hp2 HG03130.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.2958C>T | p.Phe986Phe | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/21 | 3179/5265 | 2958/4179 | 986/1392 | chr1 | 11529815 | ||
chr1:11529854
|
G | A | 13 | a0001c0043a0002c0002a0002c0018others(10): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
synonymous_variant | LOW | c.2997G>A | p.Pro999Pro | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/21 | 3218/5265 | 2997/4179 | 999/1392 | chr1 | 11529854 | ||
chr1:11530960
|
G | T | 1 | a0003c0032 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.3156G>T | p.Leu1052Leu | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 16/21 | 3377/5265 | 3156/4179 | 1052/1392 | chr1 | 11530960 | ||
chr1:11530981
|
C | T | 1 | a0001c0044 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.3177C>T | p.Ile1059Ile | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 16/21 | 3398/5265 | 3177/4179 | 1059/1392 | chr1 | 11530981 | ||
chr1:11531617
|
G | A | 2 | a0001c0050a0009c0049 | 2 | HG01243.hp1 HG02572.hp2 |
synonymous_variant | LOW | c.3282G>A | p.Leu1094Leu | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/21 | 3503/5265 | 3282/4179 | 1094/1392 | chr1 | 11531617 | ||
chr1:11534404
|
C | T | 1 | a0002c0040 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.3399C>T | p.Ser1133Ser | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/21 | 3620/5265 | 3399/4179 | 1133/1392 | chr1 | 11534404 | ||
chr1:11535030
|
C | T | 1 | a0002c0039 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.3555C>T | p.Cys1185Cys | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/21 | 3776/5265 | 3555/4179 | 1185/1392 | chr1 | 11535030 | ||
chr1:11535515
|
C | T | 5 | a0004c0025a0007c0013a0009c0019others(2): Show | 9 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
synonymous_variant | LOW | c.3687C>T | p.Ser1229Ser | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/21 | 3908/5265 | 3687/4179 | 1229/1392 | chr1 | 11535515 | ||
chr1:11535584
|
C | T | 1 | a0002c0018 | 2 | HG02129.hp2 NA18979.hp1 |
synonymous_variant | LOW | c.3756C>T | p.Cys1252Cys | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/21 | 3977/5265 | 3756/4179 | 1252/1392 | chr1 | 11535584 | ||
chr1:11536398
|
C | T | 12 | a0001c0005a0001c0007a0001c0044others(9): Show | 82 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(79): Show |
synonymous_variant | LOW | c.3891C>T | p.Ala1297Ala | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 4112/5265 | 3891/4179 | 1297/1392 | chr1 | 11536398 | ||
chr1:11536521
|
C | T | 1 | a0004c0026 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.4014C>T | p.Thr1338Thr | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 4235/5265 | 4014/4179 | 1338/1392 | chr1 | 11536521 | ||
chr1:11536572
|
C | T | 1 | a0004c0024 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.4065C>T | p.Ser1355Ser | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 4286/5265 | 4065/4179 | 1355/1392 | chr1 | 11536572 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11479166
|
T | C | 5 | a0001c0005t0005a0001c0007t0005a0001c0044t0005others(2): Show | 16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-210T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/21 | 21827 | chr1 | 11479166 | |||||
chr1:11479169
|
G | T | 1 | a0001c0005t0015 | 2 | HG02572.hp1 HG03516.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-207G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/21 | chr1 | 11479169 | ||||||
chr1:11479171
|
A | T | 5 | a0001c0005t0006a0002c0002t0026a0003c0003t0024others(2): Show | 15 | HG00438.hp1 HG02602.hp1 HG02647.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-205A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/21 | 21822 | chr1 | 11479171 | |||||
chr1:11479198
|
G | T | 1 | a0001c0005t0015 | 2 | HG02572.hp1 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-178G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/21 | 21795 | chr1 | 11479198 | |||||
chr1:11479241
|
G | A | 1 | a0004c0004t0016 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-135G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/21 | 21752 | chr1 | 11479241 | |||||
chr1:11479252
|
C | T | 1 | a0003c0008t0023 | 1 | NA18948.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/21 | 21741 | chr1 | 11479252 | |||||
chr1:11536705
|
C | T | 49 | a0001c0001t0002a0001c0001t0007a0001c0005t0004others(46): Show | 184 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*19C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 19 | chr1 | 11536705 | |||||
chr1:11536724
|
A | G | 1 | a0004c0010t0014 | 2 | HG02717.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*38A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 38 | chr1 | 11536724 | |||||
chr1:11536807
|
A | G | 20 | a0001c0001t0007a0001c0005t0004a0001c0005t0005others(17): Show | 83 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*121A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 121 | chr1 | 11536807 | |||||
chr1:11536845
|
T | C | 1 | a0017c0038t0017 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 159 | chr1 | 11536845 | |||||
chr1:11536855
|
T | C | 20 | a0001c0001t0007a0001c0005t0004a0001c0005t0005others(17): Show | 83 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 169 | chr1 | 11536855 | |||||
chr1:11536971
|
G | C | 3 | a0004c0016t0012a0004c0016t0020a0004c0028t0012 | 3 | HG01891.hp1 HG02055.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*285G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 285 | chr1 | 11536971 | |||||
chr1:11536989
|
T | C | 1 | a0012c0046t0021 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 303 | chr1 | 11536989 | |||||
chr1:11537063
|
T | C | 2 | a0002c0002t0026a0003c0008t0013 | 3 | HG00438.hp1 NA18955.hp1 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 377 | chr1 | 11537063 | |||||
chr1:11537077
|
CTG | C | 3 | a0001c0001t0007a0004c0010t0007a0015c0053t0007 | 7 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*392_*393delTG | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 392 | chr1 | 11537077 | |||||
chr1:11537106
|
G | A | 2 | a0004c0016t0012a0004c0028t0012 | 2 | HG01891.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*420G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 420 | chr1 | 11537106 | |||||
chr1:11537108
|
C | T | 3 | a0001c0001t0011a0002c0011t0011a0008c0054t0011 | 3 | HG02165.hp2 HG04228.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*422C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 422 | chr1 | 11537108 | |||||
chr1:11537145
|
G | T | 7 | a0001c0001t0007a0001c0001t0011a0002c0011t0011others(4): Show | 11 | HG02165.hp2 HG02622.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*459G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 459 | chr1 | 11537145 | |||||
chr1:11537152
|
C | T | 1 | a0002c0002t0022 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 466 | chr1 | 11537152 | |||||
chr1:11537199
|
G | A | 17 | a0001c0001t0002a0001c0043t0002a0002c0002t0002others(14): Show | 84 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 513 | chr1 | 11537199 | |||||
chr1:11537224
|
C | G | 4 | a0001c0001t0011a0002c0011t0011a0004c0024t0019others(1): Show | 4 | HG02165.hp2 HG03471.hp1 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*538C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 538 | chr1 | 11537224 | |||||
chr1:11537249
|
C | T | 1 | a0007c0013t0009 | 4 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*563C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 563 | chr1 | 11537249 | |||||
chr1:11537250
|
G | A | 1 | a0005c0006t0018 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 564 | chr1 | 11537250 | |||||
chr1:11537380
|
C | T | 3 | a0001c0001t0011a0002c0011t0011a0008c0054t0011 | 3 | HG02165.hp2 HG04228.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*694C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 694 | chr1 | 11537380 | |||||
chr1:11537387
|
T | TG | 7 | a0001c0001t0003a0002c0011t0003a0003c0003t0003others(4): Show | 67 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*706dupG | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 21/21 | 707 | INFO_REALIGN_3_PRIME | chr1 | 11537387 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11479565
|
C | T | 2 | a0001c0005t0015g0342a0001c0005t0015g0343 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-4+193C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11479565 | ||||||
chr1:11479581
|
C | T | 2 | a0001c0005t0015g0342a0001c0005t0015g0343 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-4+209C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11479581 | ||||||
chr1:11479731
|
C | T | 42 | a0001c0050t0001g0314a0002c0002t0002g0326a0002c0002t0002g0327others(39): Show | 43 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-4+359C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11479731 | ||||||
chr1:11479835
|
T | C | 335 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(332): Show | 348 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.-4+463T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11479835 | ||||||
chr1:11479853
|
G | A | 3 | a0009c0019t0008g0014a0009c0042t0001g0015a0009c0049t0001g0013 | 3 | HG01891.hp2 HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-4+481G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11479853 | ||||||
chr1:11480091
|
CG | C | 6 | a0004c0004t0004g0301a0004c0004t0004g0302a0004c0004t0004g0303others(3): Show | 6 | HG02976.hp2 HG03098.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+722delG | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480091 | |||||
chr1:11480209
|
C | T | 3 | a0004c0010t0004g0290a0004c0010t0014g0291a0004c0010t0014g0292 | 3 | HG02615.hp2 HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-4+837C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480209 | ||||||
chr1:11480260
|
G | A | 5 | a0001c0005t0004g0020a0004c0016t0020g0017a0012c0045t0004g0018others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+888G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480260 | ||||||
chr1:11480348
|
C | T | 1 | a0002c0002t0002g0289 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-4+976C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480348 | ||||||
chr1:11480464
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-4+1092G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480464 | ||||||
chr1:11480473
|
C | T | 1 | a0006c0009t0001g0288 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-4+1101C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480473 | ||||||
chr1:11480592
|
C | T | 54 | a0002c0002t0002g0274a0003c0003t0001g0009a0003c0003t0001g0237others(51): Show | 56 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.-4+1220C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480592 | ||||||
chr1:11480602
|
T | C | 253 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(250): Show | 263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-4+1230T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480602 | ||||||
chr1:11480674
|
C | T | 2 | a0001c0005t0004g0020a0001c0021t0008g0212 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-4+1302C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480674 | ||||||
chr1:11480675
|
G | A | 4 | a0004c0016t0020g0017a0012c0045t0004g0018a0012c0046t0021g0016others(1): Show | 4 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+1303G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480675 | ||||||
chr1:11480676
|
T | C | 5 | a0001c0005t0004g0020a0004c0016t0020g0017a0012c0045t0004g0018others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+1304T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480676 | ||||||
chr1:11480677
|
G | A | 5 | a0001c0005t0004g0020a0004c0016t0020g0017a0012c0045t0004g0018others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+1305G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480677 | ||||||
chr1:11480677
|
G | GCA | 50 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(47): Show | 53 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-4+1341_-4+1342dup others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
G | GCACA | 14 | a0003c0003t0001g0008a0003c0003t0001g0218a0003c0003t0001g0219others(11): Show | 15 | HG00639.hp1 HG01167.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+1339_-4+1342dup others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
G | GCACACA | 4 | a0003c0003t0001g0216a0003c0003t0001g0237a0003c0003t0001g0238others(1): Show | 4 | HG01070.hp2 HG02145.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+1337_-4+1342dup others(6): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
G | GCACACAC others(1): Show |
4 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+1335_-4+1342dup others(8): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
GCA | G | 16 | a0002c0040t0002g0309a0003c0003t0001g0280a0003c0003t0001g0284others(13): Show | 16 | HG00639.hp2 HG00673.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4+1341_-4+1342del others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
GCACA | G | 52 | a0001c0001t0011g0233a0001c0005t0006g0038a0001c0050t0001g0314others(49): Show | 53 | HG00438.hp1 HG00735.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-4+1339_-4+1342del others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
GCACACA | G | 24 | a0001c0001t0003g0021a0001c0001t0003g0039a0001c0001t0003g0040others(21): Show | 24 | HG00642.hp1 HG01168.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-4+1337_-4+1342del others(6): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
GCACACAC others(1): Show |
G | 167 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(164): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-4+1335_-4+1342del others(8): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480677
|
GCACACAC others(3): Show |
G | 1 | a0002c0002t0002g0211 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-4+1333_-4+1342del others(10): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480677 | |||||
chr1:11480761
|
C | G | 3 | a0001c0005t0004g0208a0001c0005t0004g0209a0002c0002t0002g0210 | 3 | NA18962.hp1 NA19003.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-4+1389C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480761 | ||||||
chr1:11480897
|
C | T | 6 | a0001c0005t0004g0020a0001c0021t0008g0212a0004c0016t0020g0017others(3): Show | 6 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+1525C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11480897 | ||||||
chr1:11480928
|
AAT | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.-4+1558_-4+1559del others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11480928 | |||||
chr1:11481038
|
T | TTC | 3 | a0003c0003t0001g0231a0003c0003t0001g0278a0012c0046t0021g0016 | 3 | HG00735.hp1 HG02040.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-4+1691_-4+1692dup others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481038 | |||||
chr1:11481038
|
T | TTCTC | 7 | a0001c0005t0004g0020a0004c0010t0004g0290a0004c0010t0014g0291others(4): Show | 7 | HG02559.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+1689_-4+1692dup others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481038 | |||||
chr1:11481038
|
T | TTCTCTC | 3 | a0001c0001t0003g0236a0001c0001t0011g0233a0002c0002t0002g0234 | 3 | HG02165.hp2 HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-4+1687_-4+1692dup others(6): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481038 | |||||
chr1:11481038
|
T | TTCTCTCT others(1): Show |
5 | a0002c0002t0002g0235a0004c0004t0004g0213a0004c0004t0004g0214others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+1685_-4+1692dup others(8): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481038 | |||||
chr1:11481061
|
T | TCA | 35 | a0001c0005t0005g0118a0001c0007t0005g0005a0001c0007t0005g0006others(32): Show | 37 | HG00423.hp1 HG00621.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4+1690_-4+1691ins others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481061 | |||||
chr1:11481061
|
T | TCACA | 68 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(65): Show | 74 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-4+1690_-4+1691ins others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481061 | |||||
chr1:11481063
|
T | A | 104 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(101): Show | 112 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-4+1691T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11481063 | ||||||
chr1:11481063
|
T | TCA | 124 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-4+1698_-4+1699dup others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481063 | |||||
chr1:11481063
|
T | TCTCA | 4 | a0001c0005t0015g0342a0001c0005t0015g0343a0009c0019t0008g0014others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+1692_-4+1693ins others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481063 | |||||
chr1:11481063
|
T | TCTCACAC others(1): Show |
15 | a0001c0005t0006g0038a0002c0002t0026g0030a0003c0003t0024g0031others(12): Show | 15 | HG00438.hp1 HG02602.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+1692_-4+1693ins others(8): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481063 | |||||
chr1:11481072
|
T | TAC | 7 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+1713_-4+1714dup others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11481072 | |||||
chr1:11481263
|
A | G | 3 | a0004c0016t0012g0054a0004c0025t0008g0053a0004c0028t0012g0047 | 3 | HG01891.hp1 HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-4+1891A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11481263 | ||||||
chr1:11481624
|
T | A | 7 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+2252T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11481624 | ||||||
chr1:11481988
|
T | C | 6 | a0001c0005t0004g0020a0001c0021t0008g0212a0004c0016t0020g0017others(3): Show | 6 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+2616T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11481988 | ||||||
chr1:11482254
|
G | C | 1 | a0002c0048t0002g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-4+2882G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11482254 | ||||||
chr1:11482569
|
G | A | 4 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+3197G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11482569 | ||||||
chr1:11482842
|
C | T | 143 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-4+3470C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11482842 | ||||||
chr1:11482900
|
A | C | 82 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(79): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-4+3528A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11482900 | ||||||
chr1:11483088
|
G | A | 2 | a0001c0005t0015g0342a0001c0005t0015g0343 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-4+3716G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483088 | ||||||
chr1:11483107
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-4+3735C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483107 | ||||||
chr1:11483147
|
G | A | 1 | a0002c0011t0011g0137 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-4+3775G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483147 | ||||||
chr1:11483288
|
C | T | 1 | a0004c0016t0012g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-4+3916C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483288 | ||||||
chr1:11483300
|
G | A | 1 | a0002c0011t0001g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-4+3928G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483300 | ||||||
chr1:11483612
|
G | A | 2 | a0001c0005t0015g0342a0001c0005t0015g0343 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-4+4240G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483612 | ||||||
chr1:11483634
|
G | T | 1 | a0002c0002t0002g0207 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-4+4262G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483634 | ||||||
chr1:11483967
|
G | C | 21 | a0001c0005t0005g0118a0001c0007t0005g0005a0001c0007t0005g0006others(18): Show | 23 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4+4595G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11483967 | ||||||
chr1:11484131
|
A | G | 5 | a0003c0003t0001g0238a0003c0003t0001g0245a0003c0003t0001g0247others(2): Show | 5 | HG01069.hp2 HG01516.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+4759A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11484131 | ||||||
chr1:11484432
|
C | T | 1 | a0005c0006t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-4+5060C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11484432 | ||||||
chr1:11484512
|
C | T | 5 | a0001c0005t0004g0020a0004c0016t0020g0017a0012c0045t0004g0018others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+5140C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11484512 | ||||||
chr1:11484551
|
T | A | 1 | a0001c0021t0008g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-4+5179T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11484551 | ||||||
chr1:11484597
|
G | A | 1 | a0002c0011t0001g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-4+5225G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11484597 | ||||||
chr1:11484871
|
A | G | 1 | a0004c0004t0004g0341 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4+5499A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11484871 | ||||||
chr1:11484923
|
A | G | 7 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+5551A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11484923 | ||||||
chr1:11485221
|
G | A | 53 | a0003c0003t0001g0009a0003c0003t0001g0237a0003c0003t0001g0238others(50): Show | 55 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-4+5849G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485221 | ||||||
chr1:11485514
|
C | T | 1 | a0004c0004t0004g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-4+6142C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485514 | ||||||
chr1:11485557
|
G | A | 1 | a0004c0015t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+6185G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485557 | ||||||
chr1:11485640
|
G | A | 1 | a0004c0004t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-4+6268G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485640 | ||||||
chr1:11485668
|
T | C | 12 | a0001c0005t0004g0020a0004c0004t0004g0213a0004c0004t0004g0214others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4+6296T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485668 | ||||||
chr1:11485788
|
G | A | 1 | a0003c0003t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-4+6416G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485788 | ||||||
chr1:11485789
|
G | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(212): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-4+6417G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485789 | ||||||
chr1:11485805
|
C | T | 246 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(243): Show | 256 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.-4+6433C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485805 | ||||||
chr1:11485823
|
A | C | 7 | a0004c0004t0004g0301a0004c0004t0004g0302a0004c0004t0004g0303others(4): Show | 7 | HG02818.hp2 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+6451A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485823 | ||||||
chr1:11485837
|
G | C | 1 | a0001c0001t0003g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-4+6465G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485837 | ||||||
chr1:11485889
|
G | A | 2 | a0001c0001t0001g0007a0023c0029t0001g0140 | 3 | HG01123.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-4+6517G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11485889 | ||||||
chr1:11486139
|
C | T | 1 | a0001c0005t0006g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4+6767C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486139 | ||||||
chr1:11486223
|
G | A | 1 | a0004c0004t0008g0308 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-4+6851G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486223 | ||||||
chr1:11486233
|
G | A | 1 | a0004c0015t0004g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-4+6861G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486233 | ||||||
chr1:11486281
|
T | G | 2 | a0001c0005t0015g0342a0001c0005t0015g0343 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-4+6909T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486281 | ||||||
chr1:11486412
|
G | A | 2 | a0001c0005t0015g0342a0001c0005t0015g0343 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-4+7040G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486412 | ||||||
chr1:11486433
|
T | C | 1 | a0003c0003t0001g0249 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-4+7061T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486433 | ||||||
chr1:11486535
|
T | G | 30 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(27): Show | 32 | HG00438.hp1 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-4+7163T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486535 | ||||||
chr1:11486603
|
C | T | 1 | a0006c0009t0001g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-4+7231C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486603 | ||||||
chr1:11486683
|
A | AGATTTTT others(319): Show |
1 | a0002c0002t0002g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-4+7327_-4+7328ins others(326): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11486683 | |||||
chr1:11486685
|
A | AT | 18 | a0001c0005t0006g0038a0002c0002t0002g0234a0002c0002t0026g0030others(15): Show | 18 | HG00438.hp1 HG02602.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4+7327dupT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11486685 | |||||
chr1:11486712
|
C | T | 1 | a0004c0004t0004g0313 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-4+7340C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11486712 | ||||||
chr1:11487007
|
C | T | 257 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(254): Show | 267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-4+7635C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487007 | ||||||
chr1:11487221
|
A | G | 257 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(254): Show | 267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-4+7849A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487221 | ||||||
chr1:11487255
|
C | T | 1 | a0004c0010t0004g0312 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-4+7883C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487255 | ||||||
chr1:11487350
|
G | A | 30 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(27): Show | 32 | HG00438.hp1 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-4+7978G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487350 | ||||||
chr1:11487393
|
G | T | 7 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+8021G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487393 | ||||||
chr1:11487407
|
G | A | 65 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(62): Show | 71 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-4+8035G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487407 | ||||||
chr1:11487526
|
A | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(333): Show | 349 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.-4+8154A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487526 | ||||||
chr1:11487548
|
C | A | 1 | a0004c0028t0012g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-4+8176C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487548 | ||||||
chr1:11487578
|
A | G | 2 | a0001c0001t0003g0107a0002c0002t0002g0108 | 2 | HG02056.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-4+8206A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487578 | ||||||
chr1:11487632
|
C | T | 1 | a0005c0006t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-4+8260C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487632 | ||||||
chr1:11487691
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0001t0003g0045others(2): Show | 7 | NA18612.hp1 NA18951.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+8319A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487691 | ||||||
chr1:11487721
|
G | A | 1 | a0002c0039t0002g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4+8349G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487721 | ||||||
chr1:11487722
|
T | C | 1 | a0002c0041t0004g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-4+8350T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487722 | ||||||
chr1:11487762
|
A | C | 1 | a0002c0002t0002g0203 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-4+8390A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487762 | ||||||
chr1:11487979
|
G | A | 7 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+8607G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11487979 | ||||||
chr1:11488037
|
C | T | 7 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+8665C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488037 | ||||||
chr1:11488054
|
G | A | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-4+8682G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488054 | ||||||
chr1:11488344
|
C | G | 260 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(257): Show | 270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.-4+8972C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488344 | ||||||
chr1:11488406
|
C | T | 1 | a0019c0052t0002g0135 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-4+9034C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488406 | ||||||
chr1:11488414
|
C | T | 30 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(27): Show | 32 | HG00438.hp1 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-4+9042C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488414 | ||||||
chr1:11488440
|
C | T | 1 | a0004c0026t0004g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-4+9068C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488440 | ||||||
chr1:11488444
|
C | A | 7 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+9072C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488444 | ||||||
chr1:11488493
|
C | T | 1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-4+9121C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488493 | ||||||
chr1:11488523
|
G | T | 1 | a0002c0002t0002g0339 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-4+9151G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488523 | ||||||
chr1:11488635
|
CTCTGTG | C | 4 | a0004c0010t0007g0335a0004c0010t0007g0336a0004c0010t0007g0337others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+9265_-4+9270del others(6): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488635 | |||||
chr1:11488637
|
C | CTG | 205 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0002g0103others(202): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-4+9295_-4+9296dup others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
C | CTGTG | 14 | a0001c0005t0004g0020a0002c0002t0002g0048a0002c0002t0002g0049others(11): Show | 14 | HG00642.hp1 HG00741.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4+9293_-4+9296dup others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
C | CTGTGTG | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0021others(30): Show | 37 | HG00323.hp1 HG00408.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4+9291_-4+9296dup others(6): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
C | CTGTGTGT others(1): Show |
26 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0001t0003g0044others(23): Show | 28 | HG00423.hp2 HG00673.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.-4+9289_-4+9296dup others(8): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
C | CTGTGTGT others(3): Show |
5 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0043others(2): Show | 5 | HG00544.hp1 HG00544.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+9287_-4+9296dup others(10): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
C | CTGTGTGT others(5): Show |
3 | a0001c0001t0003g0040a0001c0001t0003g0109a0001c0005t0004g0059 | 3 | HG04115.hp1 NA18959.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-4+9285_-4+9296dup others(12): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
C | CTGTGTGT others(15): Show |
1 | a0001c0001t0003g0039 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-4+9275_-4+9296dup others(22): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
CTG | C | 15 | a0002c0011t0001g0201a0004c0004t0004g0213a0004c0004t0004g0214others(12): Show | 15 | HG00741.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-4+9295_-4+9296del others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488637
|
CTGTG | C | 25 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(22): Show | 27 | HG00438.hp1 HG02055.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-4+9293_-4+9296del others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11488637 | |||||
chr1:11488741
|
G | A | 1 | a0024c0023t0003g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-4+9369G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488741 | ||||||
chr1:11488893
|
C | T | 4 | a0001c0001t0003g0236a0002c0002t0002g0134a0002c0002t0002g0234others(1): Show | 4 | HG02602.hp2 HG03239.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+9521C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11488893 | ||||||
chr1:11489182
|
G | C | 4 | a0001c0001t0003g0236a0001c0001t0011g0233a0002c0002t0002g0234others(1): Show | 4 | HG02165.hp2 HG02602.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+9810G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11489182 | ||||||
chr1:11489219
|
G | A | 1 | a0004c0004t0006g0025 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-4+9847G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11489219 | ||||||
chr1:11489315
|
G | A | 1 | a0003c0003t0001g0278 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-4+9943G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11489315 | ||||||
chr1:11489329
|
G | A | 1 | a0001c0021t0008g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-4+9957G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11489329 | ||||||
chr1:11489444
|
G | A | 341 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(338): Show | 355 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.-4+10072G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11489444 | ||||||
chr1:11489876
|
A | G | 30 | a0001c0005t0004g0020a0001c0005t0005g0118a0001c0005t0006g0038others(27): Show | 32 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(29): Show |
intron_variant | MODIFIER | c.-4+10504A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11489876 | ||||||
chr1:11490004
|
C | T | 4 | a0004c0004t0004g0341a0004c0010t0004g0290a0004c0010t0014g0291others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+10632C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490004 | ||||||
chr1:11490124
|
C | T | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-4+10752C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490124 | ||||||
chr1:11490136
|
T | C | 246 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(243): Show | 256 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-4+10764T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490136 | ||||||
chr1:11490255
|
T | TTTTTTG | 7 | a0004c0004t0004g0319a0004c0004t0004g0320a0004c0004t0004g0329others(4): Show | 7 | HG00735.hp2 HG01257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-10710_-3-10705d others(8): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11490255 | |||||
chr1:11490441
|
G | A | 1 | a0004c0004t0004g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-3-10549G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490441 | ||||||
chr1:11490575
|
G | C | 336 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(333): Show | 349 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.-3-10415G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490575 | ||||||
chr1:11490590
|
T | G | 58 | a0001c0050t0001g0314a0004c0004t0004g0012a0004c0004t0004g0139others(55): Show | 59 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.-3-10400T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490590 | ||||||
chr1:11490824
|
G | A | 98 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(95): Show | 99 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-3-10166G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490824 | ||||||
chr1:11490954
|
G | A | 3 | a0004c0004t0006g0032a0004c0004t0006g0033a0004c0004t0006g0034 | 3 | NA18948.hp1 NA19054.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-3-10036G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11490954 | ||||||
chr1:11491008
|
C | G | 1 | a0001c0050t0001g0314 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-3-9982C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491008 | ||||||
chr1:11491250
|
G | A | 336 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(333): Show | 349 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.-3-9740G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491250 | ||||||
chr1:11491261
|
A | G | 1 | a0001c0007t0005g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3-9729A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491261 | ||||||
chr1:11491428
|
C | T | 2 | a0002c0002t0002g0192a0002c0002t0002g0193 | 2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-3-9562C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491428 | ||||||
chr1:11491512
|
G | A | 1 | a0002c0002t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-3-9478G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491512 | ||||||
chr1:11491516
|
G | A | 67 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(64): Show | 73 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-3-9474G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491516 | ||||||
chr1:11491535
|
C | G | 6 | a0001c0001t0003g0072a0001c0001t0003g0073a0001c0001t0003g0074others(3): Show | 6 | HG00423.hp2 HG02165.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-9455C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491535 | ||||||
chr1:11491588
|
G | T | 10 | a0001c0005t0005g0118a0001c0007t0005g0005a0001c0007t0005g0006others(7): Show | 12 | HG02055.hp2 HG02647.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3-9402G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491588 | ||||||
chr1:11491602
|
T | C | 336 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(333): Show | 349 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.-3-9388T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491602 | ||||||
chr1:11491759
|
G | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-9231G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491759 | ||||||
chr1:11491839
|
T | A | 13 | a0001c0001t0003g0002a0001c0001t0003g0055a0001c0001t0003g0077others(10): Show | 13 | HG01106.hp1 HG01256.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3-9151T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491839 | ||||||
chr1:11491840
|
T | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-9150T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491840 | ||||||
chr1:11491893
|
C | T | 1 | a0004c0004t0004g0329 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-3-9097C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491893 | ||||||
chr1:11491979
|
G | A | 3 | a0001c0005t0004g0020a0001c0005t0015g0342a0001c0005t0015g0343 | 3 | HG02572.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-3-9011G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491979 | ||||||
chr1:11491983
|
G | A | 1 | a0003c0003t0003g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-3-9007G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11491983 | ||||||
chr1:11492091
|
C | T | 1 | a0002c0002t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-3-8899C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11492091 | ||||||
chr1:11492109
|
G | A | 3 | a0004c0004t0004g0320a0004c0004t0004g0329a0004c0017t0001g0328 | 3 | HG00735.hp2 HG01257.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-3-8881G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11492109 | ||||||
chr1:11492116
|
C | A | 1 | a0001c0005t0006g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-3-8874C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11492116 | ||||||
chr1:11492121
|
C | CA | 62 | a0001c0005t0004g0298a0001c0005t0006g0038a0001c0007t0005g0046others(59): Show | 63 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.-3-8846dupA | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11492121 | |||||
chr1:11492121
|
C | CAA | 104 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(101): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-3-8847_-3-8846dup others(2): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11492121 | |||||
chr1:11492121
|
C | CAAA | 12 | a0001c0007t0005g0005a0002c0002t0002g0050a0002c0002t0002g0122others(9): Show | 13 | HG00438.hp1 HG02055.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-3-8848_-3-8846dup others(3): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11492121 | |||||
chr1:11492121
|
CA | C | 67 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(64): Show | 73 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-3-8846delA | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11492121 | |||||
chr1:11492121
|
CAAAAAAA others(4): Show |
C | 4 | a0004c0010t0007g0335a0004c0010t0007g0336a0004c0010t0007g0337others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-8856_-3-8846del others(11): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11492121 | |||||
chr1:11492421
|
G | A | 2 | a0001c0001t0003g0236a0001c0005t0004g0059 | 2 | HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-3-8569G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11492421 | ||||||
chr1:11492511
|
G | T | 1 | a0001c0005t0004g0097 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-3-8479G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11492511 | ||||||
chr1:11492642
|
C | T | 2 | a0004c0010t0014g0291a0004c0010t0014g0292 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-3-8348C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11492642 | ||||||
chr1:11492751
|
G | A | 2 | a0002c0002t0002g0146a0002c0002t0002g0147 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-3-8239G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11492751 | ||||||
chr1:11493250
|
C | T | 7 | a0004c0010t0004g0290a0004c0010t0007g0335a0004c0010t0007g0336others(4): Show | 7 | HG02615.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-7740C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493250 | ||||||
chr1:11493255
|
A | G | 8 | a0001c0007t0005g0046a0004c0010t0004g0290a0004c0010t0007g0335others(5): Show | 8 | HG02109.hp2 HG02615.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-7735A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493255 | ||||||
chr1:11493325
|
A | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-7665A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493325 | ||||||
chr1:11493332
|
T | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-7658T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493332 | ||||||
chr1:11493343
|
T | C | 1 | a0002c0011t0011g0137 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3-7647T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493343 | ||||||
chr1:11493399
|
A | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-7591A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493399 | ||||||
chr1:11493435
|
T | C | 2 | a0001c0001t0003g0088a0001c0005t0004g0097 | 2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-3-7555T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493435 | ||||||
chr1:11493490
|
G | T | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-7500G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493490 | ||||||
chr1:11493499
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-3-7491C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493499 | ||||||
chr1:11493703
|
A | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-7287A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493703 | ||||||
chr1:11493723
|
C | CA | 13 | a0001c0005t0015g0342a0003c0003t0001g0254a0004c0004t0004g0145others(10): Show | 13 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3-7254dupA | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11493723 | |||||
chr1:11493772
|
C | T | 113 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(110): Show | 116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-3-7218C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493772 | ||||||
chr1:11493885
|
G | T | 1 | a0007c0013t0009g0333 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-3-7105G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493885 | ||||||
chr1:11493950
|
C | T | 1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-3-7040C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11493950 | ||||||
chr1:11494506
|
C | T | 1 | a0005c0006t0001g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-3-6484C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494506 | ||||||
chr1:11494507
|
G | A | 66 | a0001c0007t0005g0046a0001c0021t0008g0194a0001c0021t0008g0212others(63): Show | 67 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.-3-6483G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494507 | ||||||
chr1:11494538
|
G | A | 65 | a0001c0007t0005g0046a0001c0021t0008g0194a0001c0021t0008g0212others(62): Show | 66 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.-3-6452G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494538 | ||||||
chr1:11494630
|
T | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-6360T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494630 | ||||||
chr1:11494775
|
A | C | 1 | a0001c0001t0003g0096 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-3-6215A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494775 | ||||||
chr1:11494780
|
C | T | 3 | a0008c0014t0002g0187a0008c0014t0002g0188a0008c0054t0011g0189 | 3 | HG00438.hp2 NA18971.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-3-6210C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494780 | ||||||
chr1:11494820
|
T | A | 14 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3-6170T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494820 | ||||||
chr1:11494860
|
A | T | 1 | a0001c0001t0003g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-3-6130A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494860 | ||||||
chr1:11494867
|
G | A | 1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3-6123G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494867 | ||||||
chr1:11494905
|
C | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-6085C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11494905 | ||||||
chr1:11495091
|
A | G | 2 | a0002c0011t0001g0144a0005c0006t0001g0143 | 2 | HG00741.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-3-5899A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495091 | ||||||
chr1:11495109
|
C | T | 2 | a0001c0005t0006g0038a0001c0050t0001g0314 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-3-5881C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495109 | ||||||
chr1:11495197
|
C | T | 1 | a0001c0007t0005g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3-5793C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495197 | ||||||
chr1:11495273
|
C | T | 1 | a0002c0011t0001g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-3-5717C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495273 | ||||||
chr1:11495316
|
G | A | 81 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0098others(78): Show | 84 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-3-5674G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495316 | ||||||
chr1:11495319
|
A | T | 1 | a0002c0002t0002g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-3-5671A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495319 | ||||||
chr1:11495347
|
C | T | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-5643C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495347 | ||||||
chr1:11495464
|
C | T | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-3-5526C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495464 | ||||||
chr1:11495724
|
A | C | 1 | a0004c0004t0006g0029 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-3-5266A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495724 | ||||||
chr1:11495805
|
C | T | 98 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(95): Show | 99 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-3-5185C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495805 | ||||||
chr1:11495999
|
C | G | 1 | a0004c0004t0006g0037 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-3-4991C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11495999 | ||||||
chr1:11496015
|
G | T | 1 | a0001c0007t0005g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-4975G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496015 | ||||||
chr1:11496111
|
G | T | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-4879G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496111 | ||||||
chr1:11496112
|
T | G | 1 | a0003c0032t0001g0279 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-3-4878T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496112 | ||||||
chr1:11496174
|
C | T | 1 | a0003c0003t0001g0334 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-3-4816C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496174 | ||||||
chr1:11496187
|
T | C | 65 | a0001c0007t0005g0046a0001c0021t0008g0194a0001c0021t0008g0212others(62): Show | 66 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.-3-4803T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496187 | ||||||
chr1:11496225
|
T | A | 14 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3-4765T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496225 | ||||||
chr1:11496291
|
A | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3-4699A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496291 | ||||||
chr1:11496323
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-3-4667C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496323 | ||||||
chr1:11496361
|
T | C | 88 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0098others(85): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-3-4629T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496361 | ||||||
chr1:11496395
|
A | G | 1 | a0004c0004t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-3-4595A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496395 | ||||||
chr1:11496510
|
C | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(227): Show | 238 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-3-4480C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496510 | ||||||
chr1:11496540
|
A | G | 244 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(241): Show | 254 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-3-4450A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496540 | ||||||
chr1:11496744
|
C | T | 1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3-4246C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496744 | ||||||
chr1:11496942
|
G | A | 1 | a0003c0003t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-3-4048G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496942 | ||||||
chr1:11496996
|
G | C | 1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3-3994G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11496996 | ||||||
chr1:11497046
|
G | A | 1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3-3944G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497046 | ||||||
chr1:11497113
|
C | G | 64 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(61): Show | 70 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.-3-3877C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497113 | ||||||
chr1:11497113
|
C | T | 2 | a0001c0001t0001g0007a0023c0029t0001g0140 | 3 | HG01123.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-3-3877C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497113 | ||||||
chr1:11497341
|
T | A | 1 | a0001c0050t0001g0314 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-3-3649T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497341 | ||||||
chr1:11497377
|
C | T | 1 | a0004c0004t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-3-3613C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497377 | ||||||
chr1:11497508
|
C | T | 59 | a0001c0007t0005g0046a0004c0004t0004g0012a0004c0004t0004g0139others(56): Show | 60 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.-3-3482C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497508 | ||||||
chr1:11497630
|
C | T | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-3-3360C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497630 | ||||||
chr1:11497869
|
T | G | 81 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0098others(78): Show | 84 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-3-3121T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497869 | ||||||
chr1:11497884
|
G | A | 1 | a0001c0050t0001g0314 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-3-3106G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497884 | ||||||
chr1:11497913
|
A | G | 58 | a0001c0007t0005g0046a0004c0004t0004g0012a0004c0004t0004g0139others(55): Show | 59 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.-3-3077A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497913 | ||||||
chr1:11497931
|
C | T | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-3-3059C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11497931 | ||||||
chr1:11498117
|
A | G | 1 | a0004c0004t0004g0324 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-3-2873A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11498117 | ||||||
chr1:11498144
|
G | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(95): Show | 99 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-3-2846G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11498144 | ||||||
chr1:11498213
|
C | T | 1 | a0004c0004t0004g0341 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-3-2777C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11498213 | ||||||
chr1:11498233
|
G | A | 9 | a0001c0005t0005g0118a0001c0007t0005g0005a0001c0007t0005g0006others(6): Show | 11 | HG02055.hp2 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3-2757G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11498233 | ||||||
chr1:11498336
|
C | T | 2 | a0004c0004t0004g0139a0004c0004t0006g0036 | 2 | NA18940.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-3-2654C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11498336 | ||||||
chr1:11498359
|
A | G | 1 | a0001c0021t0008g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3-2631A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11498359 | ||||||
chr1:11498866
|
C | G | 1 | a0014c0035t0001g0230 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-3-2124C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11498866 | ||||||
chr1:11499034
|
T | C | 7 | a0007c0013t0009g0316a0007c0013t0009g0331a0007c0013t0009g0332others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-1956T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499034 | ||||||
chr1:11499228
|
A | T | 2 | a0001c0021t0008g0194a0001c0021t0008g0212 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-3-1762A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499228 | ||||||
chr1:11499246
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0001t0003g0045others(3): Show | 8 | NA18612.hp1 NA18940.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-1744C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499246 | ||||||
chr1:11499306
|
A | G | 4 | a0001c0021t0008g0194a0001c0021t0008g0212a0012c0045t0004g0018others(1): Show | 4 | HG02559.hp1 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-1684A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499306 | ||||||
chr1:11499459
|
C | T | 1 | a0001c0007t0005g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-1531C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499459 | ||||||
chr1:11499729
|
GTCTC | G | 58 | a0001c0007t0005g0046a0004c0004t0004g0012a0004c0004t0004g0139others(55): Show | 59 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.-3-1256_-3-1253del others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11499729 | |||||
chr1:11499776
|
G | A | 1 | a0004c0004t0004g0329 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-3-1214G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499776 | ||||||
chr1:11499906
|
A | G | 1 | a0002c0002t0002g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-3-1084A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499906 | ||||||
chr1:11499999
|
G | A | 1 | a0001c0001t0003g0064 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-3-991G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11499999 | ||||||
chr1:11500176
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-3-814C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11500176 | ||||||
chr1:11500237
|
G | T | 4 | a0009c0019t0008g0014a0009c0019t0010g0112a0009c0042t0001g0015others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-753G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11500237 | ||||||
chr1:11500278
|
A | T | 3 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085 | 3 | HG01106.hp1 NA20300.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-3-712A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11500278 | ||||||
chr1:11500340
|
G | A | 6 | a0004c0004t0004g0319a0004c0004t0004g0320a0004c0004t0004g0329others(3): Show | 6 | HG00735.hp2 HG01257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-650G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11500340 | ||||||
chr1:11500673
|
A | AT | 20 | a0001c0001t0011g0233a0001c0005t0005g0118a0001c0005t0006g0038others(17): Show | 22 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.-3-307dupT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11500673 | |||||
chr1:11500795
|
A | T | 1 | a0002c0002t0002g0123 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-3-195A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11500795 | ||||||
chr1:11500897
|
A | C | 14 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3-93A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | chr1 | 11500897 | ||||||
chr1:11500902
|
GT | G | 4 | a0007c0013t0009g0331a0007c0013t0009g0332a0007c0037t0004g0330others(1): Show | 4 | HG01243.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-86delT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11500902 | |||||
chr1:11502180
|
C | T | 14 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1096+92C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/20 | chr1 | 11502180 | ||||||
chr1:11502219
|
C | T | 96 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(93): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1096+131C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/20 | chr1 | 11502219 | ||||||
chr1:11502349
|
C | T | 1 | a0001c0007t0005g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1096+261C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/20 | chr1 | 11502349 | ||||||
chr1:11502355
|
G | A | 7 | a0004c0004t0004g0302a0004c0004t0004g0319a0004c0004t0004g0320others(4): Show | 7 | HG00735.hp2 HG01257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096+267G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/20 | chr1 | 11502355 | ||||||
chr1:11502433
|
G | A | 243 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(240): Show | 248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1097-245G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/20 | chr1 | 11502433 | ||||||
chr1:11502498
|
G | A | 2 | a0001c0001t0001g0007a0023c0029t0001g0140 | 3 | HG01123.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1097-180G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 2/20 | chr1 | 11502498 | ||||||
chr1:11503069
|
C | T | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1316+172C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503069 | ||||||
chr1:11503115
|
G | A | 58 | a0001c0007t0005g0046a0004c0004t0004g0012a0004c0004t0004g0139others(55): Show | 59 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.1316+218G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503115 | ||||||
chr1:11503119
|
A | C | 2 | a0001c0021t0008g0194a0001c0021t0008g0212 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1316+222A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503119 | ||||||
chr1:11503217
|
A | G | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | NA18952.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1316+320A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503217 | ||||||
chr1:11503523
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1316+626C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503523 | ||||||
chr1:11503551
|
G | A | 1 | a0023c0029t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1316+654G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503551 | ||||||
chr1:11503570
|
G | GGAAAAAG others(12): Show |
1 | a0023c0029t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1316+674_1316+675i others(21): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11503570 | |||||
chr1:11503602
|
G | T | 1 | a0001c0005t0005g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1316+705G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503602 | ||||||
chr1:11503633
|
T | C | 14 | a0001c0007t0005g0046a0004c0010t0004g0290a0004c0010t0004g0312others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1316+736T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503633 | ||||||
chr1:11503693
|
C | G | 2 | a0012c0045t0004g0018a0012c0046t0021g0016 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1316+796C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503693 | ||||||
chr1:11503840
|
C | T | 7 | a0007c0013t0009g0316a0007c0013t0009g0331a0007c0013t0009g0332others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+943C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503840 | ||||||
chr1:11503907
|
C | T | 5 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0130others(2): Show | 5 | HG00423.hp1 HG02129.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1316+1010C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11503907 | ||||||
chr1:11504175
|
G | A | 3 | a0009c0019t0008g0014a0009c0042t0001g0015a0009c0049t0001g0013 | 3 | HG01891.hp2 HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1316+1278G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504175 | ||||||
chr1:11504187
|
A | G | 1 | a0001c0007t0005g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1316+1290A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504187 | ||||||
chr1:11504450
|
G | A | 265 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0011g0233others(262): Show | 272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1316+1553G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504450 | ||||||
chr1:11504532
|
G | T | 1 | a0023c0029t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1316+1635G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504532 | ||||||
chr1:11504533
|
T | G | 1 | a0023c0029t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1316+1636T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504533 | ||||||
chr1:11504687
|
C | T | 8 | a0004c0004t0004g0012a0004c0004t0004g0213a0004c0004t0004g0214others(5): Show | 9 | HG01069.hp1 HG01070.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1316+1790C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504687 | ||||||
chr1:11504762
|
C | G | 1 | a0003c0003t0001g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1316+1865C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504762 | ||||||
chr1:11504768
|
C | A | 2 | a0001c0001t0003g0003a0001c0001t0003g0045 | 3 | NA18951.hp2 NA18957.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1316+1871C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504768 | ||||||
chr1:11504899
|
A | T | 1 | a0004c0004t0004g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1316+2002A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504899 | ||||||
chr1:11504975
|
G | A | 1 | a0002c0002t0002g0149 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1316+2078G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11504975 | ||||||
chr1:11505378
|
G | A | 6 | a0001c0001t0001g0150a0005c0006t0001g0051a0005c0006t0001g0151others(3): Show | 6 | HG01081.hp2 HG01433.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316+2481G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11505378 | ||||||
chr1:11505431
|
G | A | 4 | a0001c0001t0003g0063a0001c0001t0003g0065a0001c0001t0003g0066others(1): Show | 4 | NA18946.hp2 NA18960.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316+2534G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11505431 | ||||||
chr1:11505482
|
G | C | 1 | a0023c0029t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1316+2585G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11505482 | ||||||
chr1:11505483
|
C | G | 1 | a0023c0029t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1316+2586C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11505483 | ||||||
chr1:11505725
|
A | C | 1 | a0006c0009t0001g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1316+2828A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11505725 | ||||||
chr1:11506007
|
G | A | 1 | a0003c0003t0003g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1316+3110G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506007 | ||||||
chr1:11506027
|
A | G | 3 | a0001c0001t0003g0064a0001c0001t0003g0107a0002c0002t0002g0108 | 3 | HG02056.hp1 NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1316+3130A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506027 | ||||||
chr1:11506127
|
T | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(111): Show | 117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1316+3230T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506127 | ||||||
chr1:11506532
|
G | T | 261 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1316+3635G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506532 | ||||||
chr1:11506655
|
T | G | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1316+3758T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506655 | ||||||
chr1:11506710
|
T | C | 1 | a0005c0006t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1316+3813T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506710 | ||||||
chr1:11506790
|
G | A | 1 | a0001c0005t0004g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1316+3893G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506790 | ||||||
chr1:11506808
|
A | T | 1 | a0005c0006t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1316+3911A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506808 | ||||||
chr1:11506892
|
C | T | 1 | a0002c0002t0002g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1316+3995C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11506892 | ||||||
chr1:11507111
|
C | A | 11 | a0001c0001t0007g0011a0001c0005t0004g0020a0001c0005t0004g0294others(8): Show | 12 | HG02572.hp1 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1316+4214C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11507111 | ||||||
chr1:11507133
|
C | T | 90 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0098others(87): Show | 93 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1316+4236C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11507133 | ||||||
chr1:11507541
|
C | T | 4 | a0001c0005t0004g0294a0001c0005t0004g0295a0001c0005t0004g0296others(1): Show | 4 | HG02630.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316+4644C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11507541 | ||||||
chr1:11507729
|
T | C | 1 | a0003c0003t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1316+4832T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11507729 | ||||||
chr1:11508089
|
CAT | C | 4 | a0001c0021t0008g0194a0001c0021t0008g0212a0012c0045t0004g0018others(1): Show | 4 | HG02559.hp1 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316+5193_1316+519 others(6): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508089 | ||||||
chr1:11508101
|
C | T | 1 | a0001c0001t0007g0011 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1316+5204C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508101 | ||||||
chr1:11508287
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0001t0003g0045others(2): Show | 7 | NA18612.hp1 NA18951.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+5390A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508287 | ||||||
chr1:11508381
|
G | A | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1316+5484G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508381 | ||||||
chr1:11508405
|
A | G | 279 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0007g0011others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1316+5508A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508405 | ||||||
chr1:11508419
|
T | TA | 14 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1316+5534dupA | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11508419 | |||||
chr1:11508475
|
C | G | 1 | a0003c0003t0024g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1316+5578C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508475 | ||||||
chr1:11508575
|
T | G | 166 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(163): Show | 172 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1316+5678T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508575 | ||||||
chr1:11508579
|
G | C | 262 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(259): Show | 269 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1316+5682G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508579 | ||||||
chr1:11508666
|
G | A | 7 | a0007c0013t0009g0316a0007c0013t0009g0331a0007c0013t0009g0332others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317-5724G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508666 | ||||||
chr1:11508740
|
G | A | 1 | a0017c0038t0017g0153 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1317-5650G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508740 | ||||||
chr1:11508775
|
T | C | 90 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0098others(87): Show | 93 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1317-5615T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508775 | ||||||
chr1:11508948
|
C | T | 261 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1317-5442C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11508948 | ||||||
chr1:11509000
|
C | T | 1 | a0001c0007t0005g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1317-5390C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11509000 | ||||||
chr1:11509022
|
A | G | 90 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0098others(87): Show | 93 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1317-5368A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11509022 | ||||||
chr1:11509028
|
A | G | 261 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1317-5362A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11509028 | ||||||
chr1:11509038
|
G | A | 1 | a0004c0028t0012g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1317-5352G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11509038 | ||||||
chr1:11509063
|
C | G | 57 | a0004c0004t0004g0012a0004c0004t0004g0139a0004c0004t0004g0145others(54): Show | 58 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.1317-5327C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11509063 | ||||||
chr1:11509191
|
G | A | 1 | a0024c0023t0003g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1317-5199G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11509191 | ||||||
chr1:11509764
|
G | A | 3 | a0001c0001t0003g0068a0004c0016t0020g0017a0004c0025t0008g0053 | 3 | HG00673.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1317-4626G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11509764 | ||||||
chr1:11510021
|
C | T | 96 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(93): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1317-4369C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11510021 | ||||||
chr1:11510023
|
C | T | 10 | a0002c0002t0002g0052a0002c0002t0002g0123a0002c0002t0002g0128others(7): Show | 10 | HG00621.hp1 HG00621.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1317-4367C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11510023 | ||||||
chr1:11510084
|
G | A | 1 | a0004c0004t0004g0139 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1317-4306G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11510084 | ||||||
chr1:11510463
|
G | A | 4 | a0004c0010t0007g0335a0004c0010t0007g0336a0004c0010t0007g0337others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-3927G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11510463 | ||||||
chr1:11510601
|
A | T | 57 | a0004c0004t0004g0012a0004c0004t0004g0139a0004c0004t0004g0145others(54): Show | 58 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.1317-3789A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11510601 | ||||||
chr1:11510609
|
T | TTTCAGTG others(11): Show |
261 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1317-3779_1317-377 others(22): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11510609 | |||||
chr1:11510693
|
C | T | 2 | a0004c0016t0020g0017a0004c0025t0008g0053 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1317-3697C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11510693 | ||||||
chr1:11510880
|
T | A | 261 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1317-3510T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11510880 | ||||||
chr1:11511118
|
T | G | 4 | a0001c0005t0004g0294a0001c0005t0004g0295a0001c0005t0004g0296others(1): Show | 4 | HG02630.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317-3272T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511118 | ||||||
chr1:11511137
|
C | T | 4 | a0009c0019t0008g0014a0009c0019t0010g0112a0009c0042t0001g0015others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-3253C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511137 | ||||||
chr1:11511256
|
C | A | 1 | a0008c0014t0002g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1317-3134C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511256 | ||||||
chr1:11511274
|
A | G | 1 | a0004c0004t0004g0012 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1317-3116A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511274 | ||||||
chr1:11511340
|
T | A | 1 | a0001c0001t0007g0011 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1317-3050T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511340 | ||||||
chr1:11511373
|
C | T | 4 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0215others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317-3017C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511373 | ||||||
chr1:11511635
|
A | G | 279 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0007g0011others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1317-2755A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511635 | ||||||
chr1:11511725
|
C | T | 1 | a0003c0003t0001g0287 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1317-2665C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11511725 | ||||||
chr1:11512102
|
G | A | 90 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0098others(87): Show | 93 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1317-2288G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512102 | ||||||
chr1:11512194
|
A | C | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1317-2196A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512194 | ||||||
chr1:11512257
|
G | GT | 19 | a0001c0001t0003g0070a0001c0001t0003g0082a0001c0001t0003g0087others(16): Show | 19 | HG00642.hp2 HG01106.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1317-2123dupT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11512257 | |||||
chr1:11512356
|
C | G | 1 | a0002c0002t0026g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1317-2034C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512356 | ||||||
chr1:11512395
|
A | G | 1 | a0004c0004t0004g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1317-1995A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512395 | ||||||
chr1:11512588
|
C | T | 3 | a0004c0004t0004g0214a0004c0004t0004g0215a0004c0004t0004g0217 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1317-1802C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512588 | ||||||
chr1:11512671
|
G | T | 1 | a0001c0021t0008g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1317-1719G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512671 | ||||||
chr1:11512702
|
A | G | 2 | a0001c0001t0003g0021a0001c0001t0003g0094 | 2 | HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1317-1688A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512702 | ||||||
chr1:11512727
|
C | A | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1317-1663C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512727 | ||||||
chr1:11512769
|
A | T | 2 | a0001c0021t0008g0194a0001c0021t0008g0212 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1317-1621A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512769 | ||||||
chr1:11512874
|
A | G | 1 | a0002c0002t0002g0203 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1317-1516A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512874 | ||||||
chr1:11512888
|
T | G | 1 | a0002c0002t0002g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1317-1502T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512888 | ||||||
chr1:11512899
|
G | A | 261 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1317-1491G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512899 | ||||||
chr1:11512970
|
A | G | 1 | a0004c0010t0004g0312 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1317-1420A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512970 | ||||||
chr1:11512972
|
C | G | 1 | a0001c0007t0005g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1317-1418C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11512972 | ||||||
chr1:11513068
|
G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(111): Show | 117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1317-1322G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513068 | ||||||
chr1:11513108
|
C | T | 9 | a0001c0005t0005g0118a0001c0007t0005g0005a0001c0007t0005g0006others(6): Show | 11 | HG02055.hp2 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1317-1282C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513108 | ||||||
chr1:11513137
|
C | T | 3 | a0003c0003t0001g0253a0003c0003t0001g0268a0003c0003t0001g0269 | 3 | HG00558.hp1 NA18953.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1317-1253C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513137 | ||||||
chr1:11513220
|
G | T | 1 | a0004c0004t0004g0313 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1317-1170G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513220 | ||||||
chr1:11513264
|
AC | A | 14 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1317-1125delC | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513264 | ||||||
chr1:11513385
|
T | C | 1 | a0010c0012t0001g0221 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1317-1005T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513385 | ||||||
chr1:11513543
|
TGCTTTTT others(2): Show |
T | 57 | a0004c0004t0004g0012a0004c0004t0004g0139a0004c0004t0004g0145others(54): Show | 58 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.1317-845_1317-837d others(11): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11513543 | |||||
chr1:11513605
|
G | GT | 15 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(12): Show | 17 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1317-778dupT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11513605 | |||||
chr1:11513706
|
T | C | 7 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(4): Show | 8 | HG02622.hp2 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1317-684T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513706 | ||||||
chr1:11513799
|
G | T | 1 | a0001c0001t0003g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1317-591G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513799 | ||||||
chr1:11513861
|
T | C | 1 | a0001c0007t0005g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1317-529T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513861 | ||||||
chr1:11513899
|
A | T | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1317-491A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513899 | ||||||
chr1:11513948
|
G | GT | 10 | a0001c0001t0003g0109a0004c0004t0004g0319a0004c0010t0004g0290others(7): Show | 10 | HG02615.hp2 HG02717.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1317-427dupT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11513948 | |||||
chr1:11513948
|
GT | G | 132 | a0001c0001t0002g0103a0001c0001t0003g0076a0001c0001t0003g0089others(129): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1317-427delT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11513948 | |||||
chr1:11513948
|
GTT | G | 121 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(118): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1317-428_1317-427d others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr1 | 11513948 | |||||
chr1:11513952
|
T | G | 96 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(93): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1317-438T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11513952 | ||||||
chr1:11514102
|
A | G | 1 | a0010c0012t0003g0232 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1317-288A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11514102 | ||||||
chr1:11514309
|
C | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(112): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1317-81C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 3/20 | chr1 | 11514309 | ||||||
chr1:11514630
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1453+104G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11514630 | ||||||
chr1:11514863
|
T | A | 2 | a0002c0002t0002g0048a0002c0002t0002g0049 | 2 | HG00642.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1453+337T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11514863 | ||||||
chr1:11514885
|
C | T | 109 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(106): Show | 114 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1453+359C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11514885 | ||||||
chr1:11514918
|
G | A | 1 | a0004c0010t0014g0291 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1453+392G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11514918 | ||||||
chr1:11514948
|
A | G | 1 | a0003c0003t0024g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1454-421A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11514948 | ||||||
chr1:11514988
|
T | C | 1 | a0018c0047t0002g0202 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1454-381T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11514988 | ||||||
chr1:11515203
|
G | T | 95 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(92): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1454-166G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11515203 | ||||||
chr1:11515274
|
A | G | 95 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0005t0004g0155others(92): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1454-95A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11515274 | ||||||
chr1:11515300
|
G | A | 18 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(15): Show | 20 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1454-69G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11515300 | ||||||
chr1:11515318
|
T | A | 108 | a0001c0005t0005g0118a0001c0005t0006g0038a0001c0007t0005g0005others(105): Show | 113 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1454-51T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11515318 | ||||||
chr1:11515341
|
G | A | 43 | a0004c0004t0004g0012a0004c0004t0004g0139a0004c0004t0004g0145others(40): Show | 44 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1454-28G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 4/20 | chr1 | 11515341 | ||||||
chr1:11515663
|
C | A | 1 | a0001c0005t0004g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1588+160C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515663 | ||||||
chr1:11515676
|
T | C | 1 | a0003c0008t0002g0222 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1588+173T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515676 | ||||||
chr1:11515696
|
G | C | 19 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0005t0004g0020others(16): Show | 20 | HG01891.hp2 HG02109.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.1588+193G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515696 | ||||||
chr1:11515724
|
G | A | 1 | a0002c0002t0002g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1588+221G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515724 | ||||||
chr1:11515724
|
GGTGGGAA others(13): Show |
G | 3 | a0001c0001t0011g0233a0002c0002t0002g0234a0002c0002t0002g0235 | 3 | HG02165.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1588+229_1588+248d others(22): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 11515724 | |||||
chr1:11515775
|
C | G | 1 | a0004c0004t0004g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1589-226C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515775 | ||||||
chr1:11515877
|
A | T | 14 | a0001c0005t0006g0038a0001c0007t0005g0005a0001c0007t0005g0006others(11): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1589-124A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515877 | ||||||
chr1:11515890
|
C | G | 2 | a0002c0002t0002g0326a0002c0002t0002g0327 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1589-111C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515890 | ||||||
chr1:11515951
|
C | A | 2 | a0001c0021t0008g0194a0001c0021t0008g0212 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1589-50C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 5/20 | chr1 | 11515951 | ||||||
chr1:11516461
|
C | T | 1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1749+300C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11516461 | ||||||
chr1:11516897
|
A | G | 4 | a0004c0016t0012g0054a0004c0016t0020g0017a0004c0025t0008g0053others(1): Show | 4 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1750-566A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11516897 | ||||||
chr1:11516979
|
C | T | 2 | a0001c0005t0005g0118a0004c0004t0008g0308 | 2 | HG01167.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1750-484C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11516979 | ||||||
chr1:11517036
|
C | A | 23 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0046others(20): Show | 25 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1750-427C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11517036 | ||||||
chr1:11517068
|
C | T | 85 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1750-395C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11517068 | ||||||
chr1:11517130
|
T | C | 23 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0046others(20): Show | 25 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1750-333T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11517130 | ||||||
chr1:11517142
|
TC | T | 85 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1750-316delC | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11517142 | |||||
chr1:11517156
|
G | A | 6 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(3): Show | 7 | HG02622.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1750-307G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11517156 | ||||||
chr1:11517244
|
G | GGGGACCC others(15): Show |
1 | a0003c0003t0001g0197 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1750-217_1750-196d others(24): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11517244 | |||||
chr1:11517282
|
C | A | 14 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0046others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1750-181C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11517282 | ||||||
chr1:11517457
|
C | T | 1 | a0002c0002t0002g0185 | 1 | NA18952.hp2 | splice_region_variant&intron_variant | LOW | c.1750-6C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 6/20 | chr1 | 11517457 | ||||||
chr1:11517774
|
A | G | 23 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0046others(20): Show | 25 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1889+172A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11517774 | ||||||
chr1:11518062
|
G | A | 1 | a0004c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1889+460G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518062 | ||||||
chr1:11518275
|
T | C | 1 | a0004c0004t0006g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1889+673T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518275 | ||||||
chr1:11518323
|
G | A | 1 | a0001c0005t0004g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1889+721G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518323 | ||||||
chr1:11518381
|
C | A | 2 | a0001c0001t0007g0011a0015c0053t0007g0300 | 3 | HG02622.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1889+779C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518381 | ||||||
chr1:11518522
|
A | G | 4 | a0001c0005t0004g0294a0001c0005t0004g0295a0001c0005t0004g0296others(1): Show | 4 | HG02630.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-833A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518522 | ||||||
chr1:11518578
|
C | T | 1 | a0001c0043t0002g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1890-777C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518578 | ||||||
chr1:11518836
|
C | T | 1 | a0005c0006t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1890-519C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518836 | ||||||
chr1:11518848
|
A | G | 3 | a0004c0015t0004g0317a0004c0015t0004g0318a0004c0015t0004g0321 | 3 | HG03041.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1890-507A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518848 | ||||||
chr1:11518916
|
T | C | 86 | a0001c0001t0001g0150a0002c0002t0001g0121a0002c0002t0002g0048others(83): Show | 86 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1890-439T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11518916 | ||||||
chr1:11519238
|
T | G | 1 | a0004c0004t0016g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1890-117T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11519238 | ||||||
chr1:11519287
|
G | A | 85 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1890-68G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 7/20 | chr1 | 11519287 | ||||||
chr1:11519539
|
G | A | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2038+36G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/20 | chr1 | 11519539 | ||||||
chr1:11519547
|
C | T | 3 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058 | 3 | HG00544.hp2 NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2038+44C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/20 | chr1 | 11519547 | ||||||
chr1:11519551
|
G | A | 3 | a0003c0003t0001g0100a0003c0003t0001g0256a0003c0003t0001g0257 | 3 | HG00323.hp1 HG01109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2038+48G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/20 | chr1 | 11519551 | ||||||
chr1:11519649
|
C | T | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2039-70C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/20 | chr1 | 11519649 | ||||||
chr1:11519662
|
G | A | 1 | a0020c0036t0008g0315 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2039-57G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 8/20 | chr1 | 11519662 | ||||||
chr1:11519941
|
A | T | 3 | a0002c0002t0002g0108a0002c0002t0002g0174a0008c0014t0002g0188 | 3 | NA18957.hp1 NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2200+61A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11519941 | ||||||
chr1:11520015
|
C | G | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2200+135C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520015 | ||||||
chr1:11520016
|
C | G | 14 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0046others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2200+136C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520016 | ||||||
chr1:11520019
|
C | G | 7 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0113others(4): Show | 9 | HG02055.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.2200+139C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520019 | ||||||
chr1:11520119
|
CATGGGCC others(6): Show |
C | 1 | a0001c0005t0006g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2200+240_2200+252d others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520119 | ||||||
chr1:11520130
|
G | C | 1 | a0002c0002t0002g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2200+250G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520130 | ||||||
chr1:11520152
|
AGTCCCAG others(9): Show |
A | 4 | a0001c0001t0003g0072a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG00423.hp2 NA18941.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.2200+277_2200+292d others(18): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 11520152 | |||||
chr1:11520309
|
G | A | 1 | a0002c0002t0002g0123 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2201-378G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520309 | ||||||
chr1:11520422
|
A | G | 23 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0046others(20): Show | 25 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2201-265A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520422 | ||||||
chr1:11520587
|
C | A | 1 | a0007c0037t0004g0330 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2201-100C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520587 | ||||||
chr1:11520599
|
G | T | 3 | a0001c0001t0007g0011a0001c0001t0011g0233a0015c0053t0007g0300 | 4 | HG02165.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2201-88G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 9/20 | chr1 | 11520599 | ||||||
chr1:11520879
|
C | T | 1 | a0004c0004t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2362+31C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11520879 | ||||||
chr1:11521059
|
G | T | 1 | a0001c0001t0007g0011 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2362+211G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521059 | ||||||
chr1:11521075
|
C | T | 1 | a0001c0001t0007g0011 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2362+227C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521075 | ||||||
chr1:11521202
|
G | T | 1 | a0004c0004t0016g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2362+354G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521202 | ||||||
chr1:11521225
|
T | A | 1 | a0002c0002t0002g0211 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2362+377T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521225 | ||||||
chr1:11521279
|
C | A | 3 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0002g0177 | 3 | NA18943.hp1 NA18951.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2362+431C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521279 | ||||||
chr1:11521335
|
G | C | 7 | a0007c0013t0009g0316a0007c0013t0009g0331a0007c0013t0009g0332others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2362+487G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521335 | ||||||
chr1:11521519
|
G | A | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2362+671G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521519 | ||||||
chr1:11521551
|
C | T | 1 | a0002c0002t0002g0134 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2362+703C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521551 | ||||||
chr1:11521588
|
G | T | 1 | a0002c0002t0002g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2362+740G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521588 | ||||||
chr1:11521752
|
G | C | 1 | a0003c0003t0001g0231 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2362+904G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521752 | ||||||
chr1:11521785
|
T | C | 2 | a0001c0005t0005g0118a0004c0004t0008g0308 | 2 | HG01167.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2362+937T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521785 | ||||||
chr1:11521798
|
T | G | 34 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0005t0004g0294others(31): Show | 37 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.2362+950T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521798 | ||||||
chr1:11521888
|
TAAGTGGA others(4): Show |
T | 1 | a0003c0003t0001g0254 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2362+1041_2362+105 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521888 | ||||||
chr1:11521936
|
G | A | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2362+1088G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521936 | ||||||
chr1:11521941
|
A | G | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2362+1093A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521941 | ||||||
chr1:11521978
|
C | T | 83 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2362+1130C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521978 | ||||||
chr1:11521989
|
G | C | 1 | a0001c0001t0003g0087 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2362+1141G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11521989 | ||||||
chr1:11522075
|
C | A | 1 | a0007c0013t0009g0333 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2362+1227C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522075 | ||||||
chr1:11522075
|
C | T | 1 | a0001c0044t0005g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2362+1227C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522075 | ||||||
chr1:11522161
|
C | T | 1 | a0008c0014t0002g0173 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2362+1313C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522161 | ||||||
chr1:11522185
|
C | T | 85 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2362+1337C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522185 | ||||||
chr1:11522285
|
T | C | 1 | a0003c0003t0003g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2362+1437T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522285 | ||||||
chr1:11522426
|
C | G | 1 | a0003c0003t0024g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2363-1516C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522426 | ||||||
chr1:11522429
|
C | A | 1 | a0003c0003t0024g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2363-1513C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522429 | ||||||
chr1:11522523
|
G | GGCCAGGA others(147): Show |
1 | a0001c0021t0008g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2363-1382_2363-138 others(158): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522523 | |||||
chr1:11522530
|
A | ACCCAGCC others(92): Show |
1 | a0002c0002t0002g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522530 | |||||
chr1:11522552
|
A | ACCCAGCC others(59): Show |
1 | a0001c0021t0008g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2363-1382_2363-138 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522552 | |||||
chr1:11522561
|
G | A | 5 | a0001c0001t0011g0233a0001c0005t0004g0020a0001c0050t0001g0314others(2): Show | 5 | HG01243.hp1 HG01433.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.2363-1381G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522561 | ||||||
chr1:11522562
|
A | AGCCCAGC others(92): Show |
2 | a0002c0002t0002g0129a0002c0002t0002g0207 | 2 | HG00621.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2363-1360_2363-135 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522562 | |||||
chr1:11522562
|
A | G | 13 | a0001c0001t0011g0233a0001c0005t0004g0020a0001c0021t0008g0194others(10): Show | 13 | HG00558.hp2 HG01175.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2363-1380A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522562 | ||||||
chr1:11522563
|
G | A | 5 | a0001c0001t0011g0233a0001c0005t0004g0020a0001c0050t0001g0314others(2): Show | 5 | HG01243.hp1 HG01433.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.2363-1379G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522563 | ||||||
chr1:11522563
|
G | GCCCAGCC others(807): Show |
1 | a0003c0003t0024g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2363-1370_2363-136 others(818): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522563 | |||||
chr1:11522563
|
G | GCCCAGCC others(158): Show |
1 | a0002c0002t0002g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(169): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522563 | |||||
chr1:11522563
|
G | GCCCAGCC others(180): Show |
1 | a0002c0002t0002g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522563 | |||||
chr1:11522573
|
G | A | 2 | a0001c0021t0008g0194a0003c0003t0001g0255 | 2 | HG01175.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2363-1369G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522573 | ||||||
chr1:11522574
|
A | ACCCAGCC others(81): Show |
2 | a0002c0002t0002g0122a0002c0002t0002g0126 | 2 | NA18949.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2363-1360_2363-135 others(92): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(147): Show |
1 | a0002c0002t0002g0158 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(158): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(70): Show |
1 | a0001c0005t0004g0297 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(81): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(202): Show |
1 | a0002c0002t0002g0108 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(213): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(202): Show |
1 | a0002c0002t0002g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(213): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(213): Show |
5 | a0002c0002t0002g0174a0002c0002t0002g0184a0002c0002t0002g0185others(2): Show | 5 | NA18952.hp2 NA18963.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.2363-1360_2363-135 others(224): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0002c0002t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0002c0002t0002g0161 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(213): Show |
1 | a0008c0054t0011g0189 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(224): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0002c0002t0002g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0002c0002t0002g0289 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0002c0002t0002g0162 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(213): Show |
1 | a0002c0002t0002g0163 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(224): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(213): Show |
1 | a0008c0014t0002g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(224): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(224): Show |
1 | a0002c0011t0001g0164 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(235): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(191): Show |
1 | a0002c0002t0002g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(202): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(169): Show |
2 | a0002c0002t0002g0127a0002c0002t0002g0130 | 2 | NA18946.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.2363-1360_2363-135 others(180): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(224): Show |
2 | a0002c0002t0002g0165a0002c0011t0011g0137 | 2 | HG04228.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2363-1360_2363-135 others(235): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(147): Show |
1 | a0002c0039t0002g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(158): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(202): Show |
1 | a0018c0047t0002g0202 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(213): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(59): Show |
1 | a0002c0002t0002g0049 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0014c0035t0001g0230 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(169): Show |
1 | a0016c0030t0002g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(180): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0002c0002t0022g0168 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(213): Show |
1 | a0002c0011t0001g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(224): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(213): Show |
1 | a0002c0002t0002g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(224): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(202): Show |
1 | a0002c0002t0002g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(213): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(224): Show |
1 | a0002c0002t0002g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(235): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(224): Show |
1 | a0002c0048t0002g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(235): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(125): Show |
1 | a0002c0002t0002g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(136): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(81): Show |
1 | a0002c0002t0002g0182 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(92): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(180): Show |
1 | a0019c0052t0002g0135 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(59): Show |
1 | a0002c0002t0002g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | ACCCAGCC others(92): Show |
1 | a0002c0011t0003g0131 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522574 | |||||
chr1:11522574
|
A | G | 3 | a0001c0021t0008g0194a0001c0021t0008g0212a0003c0003t0001g0255 | 3 | HG01175.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2363-1368A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522574 | ||||||
chr1:11522582
|
A | AGAGCCCA others(58): Show |
1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(69): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522582 | ||||||
chr1:11522582
|
A | AGGGCCCA others(190): Show |
1 | a0002c0002t0002g0339 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2363-1360_2363-135 others(201): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522582 | ||||||
chr1:11522583
|
A | AGACCCAG others(4): Show |
1 | a0003c0003t0001g0267 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2363-1347_2363-133 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522583 | |||||
chr1:11522583
|
A | G | 94 | a0001c0005t0004g0020a0001c0005t0004g0297a0001c0021t0008g0194others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2363-1359A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522583 | ||||||
chr1:11522584
|
G | A | 5 | a0001c0005t0004g0020a0001c0050t0001g0314a0004c0010t0007g0338others(2): Show | 5 | HG01243.hp1 HG01433.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2363-1358G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522584 | ||||||
chr1:11522585
|
A | ACCCAGCC others(15): Show |
16 | a0001c0005t0004g0298a0001c0007t0005g0005a0001c0007t0005g0006others(13): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2363-1325_2363-130 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522585 | |||||
chr1:11522585
|
A | G | 48 | a0001c0005t0004g0020a0001c0050t0001g0314a0002c0002t0002g0048others(45): Show | 48 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2363-1357A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522585 | ||||||
chr1:11522595
|
G | A | 2 | a0001c0021t0008g0212a0003c0003t0001g0255 | 2 | HG01175.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2363-1347G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522595 | ||||||
chr1:11522596
|
A | ACCCAGCC others(191): Show |
1 | a0002c0040t0002g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2363-1337_2363-133 others(202): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522596 | |||||
chr1:11522596
|
A | ACCCAGCC others(191): Show |
1 | a0002c0011t0001g0201 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2363-1337_2363-133 others(202): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522596 | |||||
chr1:11522596
|
A | G | 47 | a0001c0021t0008g0212a0002c0002t0001g0121a0002c0002t0002g0049others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.2363-1346A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522596 | ||||||
chr1:11522606
|
A | AGCCCAGC others(114): Show |
1 | a0002c0002t0002g0062 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2363-1325_2363-132 others(125): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522606 | |||||
chr1:11522606
|
A | AGCCCAGC others(180): Show |
1 | a0002c0002t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2363-1325_2363-132 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522606 | |||||
chr1:11522606
|
A | AGCCCAGC others(180): Show |
1 | a0002c0002t0002g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2363-1325_2363-132 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522606 | |||||
chr1:11522606
|
A | AGCCCAGC others(158): Show |
1 | a0002c0002t0002g0326 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2363-1325_2363-132 others(169): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522606 | |||||
chr1:11522606
|
A | AGCCCAGC others(158): Show |
1 | a0002c0002t0002g0327 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2363-1325_2363-132 others(169): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522606 | |||||
chr1:11522606
|
A | G | 27 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0052others(24): Show | 27 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2363-1336A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522606 | ||||||
chr1:11522607
|
G | GCCCAGCC others(521): Show |
1 | a0004c0010t0007g0337 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(532): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522607 | |||||
chr1:11522607
|
G | GCCCAGCC others(521): Show |
2 | a0003c0003t0001g0245a0005c0006t0001g0143 | 2 | HG00741.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(532): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522607 | |||||
chr1:11522607
|
G | GCCCAGCC others(554): Show |
2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(565): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522607 | |||||
chr1:11522607
|
G | GCCCAGCC others(510): Show |
1 | a0003c0003t0001g0275 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(521): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522607 | |||||
chr1:11522607
|
G | GCCCAGCC others(554): Show |
1 | a0005c0006t0001g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(565): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522607 | |||||
chr1:11522607
|
G | GCCCAGCC others(202): Show |
1 | a0002c0002t0002g0170 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2363-1325_2363-132 others(213): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522607 | |||||
chr1:11522618
|
A | G | 34 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0050others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.2363-1324A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522618 | ||||||
chr1:11522628
|
A | G | 47 | a0001c0021t0008g0212a0002c0002t0002g0048a0002c0002t0002g0049others(44): Show | 47 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2363-1314A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522628 | ||||||
chr1:11522629
|
G | A | 5 | a0001c0021t0008g0212a0002c0002t0002g0052a0002c0002t0002g0210others(2): Show | 5 | HG01175.hp2 HG02083.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2363-1313G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522629 | ||||||
chr1:11522629
|
G | GCCCAGCC others(4): Show |
44 | a0001c0001t0001g0007a0001c0005t0004g0020a0001c0005t0004g0059others(41): Show | 46 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(301): Show |
1 | a0001c0005t0005g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(312): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(532): Show |
2 | a0004c0004t0006g0035a0004c0004t0006g0037 | 2 | NA18985.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(543): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(576): Show |
2 | a0004c0004t0004g0320a0004c0017t0001g0328 | 2 | HG00735.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(587): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(598): Show |
1 | a0001c0043t0002g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(609): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(554): Show |
1 | a0004c0004t0004g0329 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(565): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(565): Show |
5 | a0004c0010t0004g0290a0004c0010t0004g0312a0004c0010t0014g0291others(2): Show | 5 | HG02615.hp2 HG02717.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(576): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(92): Show |
72 | a0001c0001t0001g0150a0003c0003t0001g0009a0003c0003t0001g0098others(69): Show | 74 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(587): Show |
1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(598): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(92): Show |
1 | a0001c0007t0005g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(576): Show |
1 | a0004c0015t0004g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(587): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(15): Show |
2 | a0002c0002t0002g0157a0008c0014t0002g0154 | 2 | HG00609.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.2363-1304_2363-130 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(191): Show |
1 | a0002c0002t0002g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(202): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522629
|
G | GCCCAGCC others(147): Show |
1 | a0002c0002t0002g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(158): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522629 | |||||
chr1:11522636
|
C | CAGGACCC others(455): Show |
1 | a0003c0008t0013g0244 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(466): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522636 | |||||
chr1:11522636
|
C | CAGGGCCC others(576): Show |
1 | a0004c0015t0004g0321 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(587): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522636 | |||||
chr1:11522636
|
C | CAGGGCCC others(576): Show |
1 | a0004c0015t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2363-1304_2363-130 others(587): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522636 | |||||
chr1:11522639
|
A | G | 129 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0005t0004g0294others(126): Show | 133 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.2363-1303A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522639 | ||||||
chr1:11522640
|
G | A | 57 | a0001c0005t0004g0297a0001c0021t0008g0194a0002c0002t0001g0121others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.2363-1302G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522640 | ||||||
chr1:11522640
|
G | GCCCAGCC others(4): Show |
1 | a0002c0002t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522640 | |||||
chr1:11522640
|
G | GCCCAGCC others(180): Show |
1 | a0002c0002t0026g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522640 | |||||
chr1:11522640
|
G | GCCCAGCC others(169): Show |
1 | a0002c0002t0002g0123 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(180): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522640 | |||||
chr1:11522640
|
G | GCCCAGCC others(191): Show |
1 | a0002c0002t0002g0211 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(202): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522640 | |||||
chr1:11522640
|
G | GCCCAGCC others(158): Show |
1 | a0002c0018t0002g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(169): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522640 | |||||
chr1:11522640
|
G | GCCCAGCC others(26): Show |
1 | a0001c0005t0004g0296 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2363-1292_2363-126 others(37): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522640 | |||||
chr1:11522640
|
G | GCCCAGCC others(37): Show |
1 | a0002c0002t0002g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2363-1282_2363-128 others(48): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522640 | |||||
chr1:11522650
|
G | A | 55 | a0001c0005t0004g0297a0001c0021t0008g0194a0002c0002t0001g0121others(52): Show | 56 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.2363-1292G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522650 | ||||||
chr1:11522650
|
G | GACCCAGC others(4): Show |
1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522650 | ||||||
chr1:11522650
|
G | GACCCAGC others(114): Show |
1 | a0002c0002t0002g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(125): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522650 | ||||||
chr1:11522650
|
G | GACCCAGC others(147): Show |
1 | a0002c0011t0001g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(158): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522650 | ||||||
chr1:11522650
|
G | GACCCAGC others(224): Show |
1 | a0002c0002t0002g0149 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(235): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522650 | ||||||
chr1:11522650
|
G | GACCCAGC others(92): Show |
1 | a0002c0002t0002g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2363-1292_2363-129 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522650 | ||||||
chr1:11522650
|
G | GGCCCAGC others(147): Show |
1 | a0002c0002t0002g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2363-1282_2363-128 others(158): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522650 | |||||
chr1:11522651
|
G | A | 22 | a0001c0021t0008g0212a0002c0002t0002g0048a0002c0002t0002g0124others(19): Show | 22 | HG00621.hp1 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2363-1291G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522651 | ||||||
chr1:11522651
|
G | GCCCAGCC others(950): Show |
2 | a0001c0001t0003g0081a0001c0001t0003g0082 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2363-1270_2363-126 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522651 | |||||
chr1:11522651
|
G | GCCCAGCC others(37): Show |
1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2363-1282_2363-128 others(48): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522651 | |||||
chr1:11522658
|
C | G | 11 | a0001c0005t0005g0118a0001c0043t0002g0102a0003c0008t0013g0244others(8): Show | 11 | HG00735.hp2 HG01257.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2363-1284C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522658 | ||||||
chr1:11522661
|
A | G | 46 | a0001c0005t0004g0297a0001c0021t0008g0194a0002c0002t0002g0048others(43): Show | 47 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2363-1281A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522661 | ||||||
chr1:11522662
|
G | A | 4 | a0002c0002t0002g0170a0002c0002t0002g0235a0002c0002t0026g0030others(1): Show | 4 | HG00438.hp1 HG03239.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2363-1280G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522662 | ||||||
chr1:11522672
|
G | A | 46 | a0002c0002t0001g0121a0002c0002t0002g0108a0002c0002t0002g0128others(43): Show | 46 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2363-1270G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522672 | ||||||
chr1:11522672
|
G | GGCCCAGC others(158): Show |
1 | a0002c0002t0002g0235 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2363-1270_2363-126 others(169): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522672 | ||||||
chr1:11522672
|
G | T | 1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2363-1270G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522672 | ||||||
chr1:11522673
|
A | G | 83 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0050others(80): Show | 84 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2363-1269A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522673 | ||||||
chr1:11522682
|
G | A | 1 | a0001c0021t0008g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2363-1260G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522682 | ||||||
chr1:11522682
|
G | GGACCCAG others(112): Show |
1 | a0002c0041t0004g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2363-1260_2363-125 others(123): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522682 | ||||||
chr1:11522682
|
G | GGACCCAG others(145): Show |
1 | a0002c0051t0004g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2363-1260_2363-125 others(156): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522682 | ||||||
chr1:11522683
|
A | G | 109 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(106): Show | 112 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.2363-1259A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522683 | ||||||
chr1:11522684
|
G | A | 84 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(81): Show | 87 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.2363-1258G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522684 | ||||||
chr1:11522684
|
G | GCCCAGCC others(26): Show |
3 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0181 | 3 | HG00423.hp1 HG00621.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2363-1249_2363-124 others(37): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(92): Show |
1 | a0002c0002t0002g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2363-1249_2363-124 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(15): Show |
1 | a0002c0002t0002g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2363-1249_2363-124 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(191): Show |
1 | a0002c0002t0002g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2363-1249_2363-124 others(202): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(4): Show |
4 | a0002c0002t0002g0129a0002c0002t0002g0171a0002c0002t0002g0182others(1): Show | 4 | HG00621.hp1 HG02027.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2363-1248_2363-124 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(180): Show |
1 | a0002c0002t0002g0050 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2363-1248_2363-124 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(59): Show |
1 | a0008c0014t0002g0173 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2363-1238_2363-123 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(26): Show |
1 | a0002c0002t0002g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2363-1238_2363-123 others(37): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522684
|
G | GCCCAGCC others(92): Show |
2 | a0002c0002t0002g0052a0002c0002t0002g0210 | 2 | NA18947.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2363-1216_2363-121 others(103): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522684 | |||||
chr1:11522693
|
G | A | 2 | a0002c0002t0002g0192a0002c0002t0002g0193 | 2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.2363-1249G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522693 | ||||||
chr1:11522694
|
G | A | 19 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0005t0004g0294others(16): Show | 20 | HG00438.hp1 HG01175.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.2363-1248G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522694 | ||||||
chr1:11522694
|
G | GACCCAGC others(103): Show |
1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2363-1248_2363-124 others(114): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522694 | ||||||
chr1:11522694
|
G | GGCCCAGC others(708): Show |
1 | a0001c0001t0003g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(719): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522694 | |||||
chr1:11522694
|
G | GGCCCAGC others(708): Show |
1 | a0001c0001t0003g0043 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(719): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522694 | |||||
chr1:11522695
|
G | A | 23 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0005t0004g0296others(20): Show | 24 | HG00099.hp2 HG00609.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.2363-1247G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522695 | ||||||
chr1:11522695
|
G | GCCCAGCC others(961): Show |
1 | a0001c0001t0003g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522695 | |||||
chr1:11522705
|
G | A | 2 | a0001c0005t0004g0296a0001c0021t0008g0212 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2363-1237G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522705 | ||||||
chr1:11522706
|
A | ACCCAGCC others(1236): Show |
1 | a0003c0003t0001g0243 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1247): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522706 | |||||
chr1:11522706
|
A | ACCCAGCC others(191): Show |
1 | a0002c0002t0002g0124 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(202): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522706 | |||||
chr1:11522706
|
A | G | 21 | a0001c0005t0004g0296a0001c0021t0008g0212a0002c0002t0002g0048others(18): Show | 21 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.2363-1236A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522706 | ||||||
chr1:11522716
|
G | A | 36 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0090others(33): Show | 39 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.2363-1226G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(565): Show |
2 | a0004c0016t0020g0017a0004c0025t0008g0053 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(576): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0003c0003t0001g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0003c0003t0001g0276 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0003c0003t0001g0258 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1203): Show |
1 | a0003c0003t0001g0259 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1214): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1170): Show |
1 | a0003c0003t0001g0260 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1181): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1181): Show |
1 | a0003c0003t0001g0261 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1192): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1159): Show |
1 | a0010c0012t0001g0221 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1170): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1203): Show |
1 | a0003c0003t0001g0228 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1214): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1148): Show |
3 | a0003c0003t0001g0216a0003c0003t0001g0218a0003c0003t0001g0223 | 3 | HG01070.hp2 HG01099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(1159): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
5 | a0003c0003t0001g0252a0003c0003t0001g0262a0003c0003t0001g0268others(2): Show | 5 | HG00558.hp1 HG00609.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1236): Show |
1 | a0003c0003t0001g0253 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1247): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0003c0003t0001g0269 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0003c0008t0002g0240 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1225): Show |
1 | a0003c0003t0001g0280 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1236): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0003c0003t0001g0224 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1181): Show |
1 | a0003c0003t0001g0256 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1192): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1137): Show |
1 | a0003c0003t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1148): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0005c0006t0018g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1181): Show |
1 | a0003c0003t0001g0257 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1192): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1181): Show |
2 | a0010c0012t0001g0220a0010c0012t0001g0225 | 2 | HG01123.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(1192): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1148): Show |
1 | a0003c0003t0001g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1159): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1137): Show |
1 | a0003c0003t0001g0229 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1148): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1159): Show |
1 | a0003c0003t0001g0148 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1170): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1159): Show |
1 | a0003c0003t0001g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1170): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1181): Show |
1 | a0003c0003t0001g0231 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1192): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1181): Show |
1 | a0003c0008t0002g0222 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1192): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1225): Show |
7 | a0001c0001t0001g0150a0003c0003t0001g0098a0003c0003t0001g0195others(4): Show | 7 | HG01255.hp1 HG02027.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(1236): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1236): Show |
1 | a0003c0008t0002g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1247): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1225): Show |
1 | a0003c0003t0001g0099 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1236): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1247): Show |
1 | a0003c0008t0023g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1258): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1247): Show |
1 | a0005c0006t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1258): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0003c0032t0001g0279 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1181): Show |
1 | a0003c0003t0001g0286 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1192): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
2 | a0003c0003t0001g0287a0003c0008t0002g0277 | 2 | NA18962.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0003c0003t0001g0009 | 2 | NA18950.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0005c0006t0001g0133 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1203): Show |
1 | a0003c0008t0013g0272 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1214): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0006c0009t0001g0263 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1203): Show |
1 | a0006c0009t0001g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1214): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1203): Show |
1 | a0006c0009t0001g0264 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1214): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
2 | a0006c0009t0001g0010a0006c0009t0001g0265 | 3 | HG01175.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0006c0009t0001g0250 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0017c0038t0017g0153 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1203): Show |
1 | a0003c0003t0001g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1214): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1192): Show |
1 | a0006c0009t0001g0288 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1203): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1247): Show |
1 | a0005c0006t0001g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1258): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1209): Show |
1 | a0003c0003t0001g0254 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1220): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0021c0033t0001g0283 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(873): Show |
1 | a0004c0004t0004g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(884): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(928): Show |
1 | a0004c0004t0004g0303 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(917): Show |
1 | a0004c0004t0004g0012 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(928): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(961): Show |
2 | a0004c0004t0004g0304a0004c0004t0004g0306 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
2 | a0001c0001t0001g0007a0023c0029t0001g0140 | 3 | HG01123.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(807): Show |
1 | a0001c0005t0004g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(818): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(917): Show |
6 | a0001c0005t0004g0155a0001c0005t0004g0208a0001c0005t0004g0209others(3): Show | 6 | HG02602.hp1 NA18948.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(928): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(917): Show |
1 | a0004c0004t0006g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(928): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(917): Show |
2 | a0004c0004t0006g0026a0004c0004t0006g0027 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(928): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(917): Show |
1 | a0004c0004t0006g0029 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(928): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(961): Show |
3 | a0004c0004t0004g0213a0004c0004t0004g0214a0004c0004t0004g0217 | 3 | HG02145.hp2 HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0004c0004t0004g0215 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(928): Show |
1 | a0004c0004t0004g0340 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(928): Show |
1 | a0004c0004t0004g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(983): Show |
1 | a0004c0004t0004g0313 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(994): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
1 | a0004c0004t0006g0033 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(983): Show |
1 | a0004c0004t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(994): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
1 | a0004c0004t0006g0036 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(917): Show |
1 | a0004c0004t0004g0139 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(928): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(961): Show |
1 | a0004c0004t0004g0341 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
1 | a0004c0004t0008g0308 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
3 | a0001c0005t0004g0020a0001c0005t0015g0342a0001c0005t0015g0343 | 3 | HG02572.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(983): Show |
1 | a0004c0004t0004g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(994): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
1 | a0004c0004t0004g0322 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
2 | a0004c0004t0004g0323a0004c0004t0004g0324 | 2 | HG01952.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
1 | a0004c0004t0004g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
1 | a0004c0026t0004g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(928): Show |
5 | a0001c0001t0003g0001a0001c0001t0003g0069a0001c0001t0003g0087others(2): Show | 9 | HG02135.hp2 NA18977.hp2 NA18999.hp2 others(6): Show |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(928): Show |
1 | a0001c0001t0003g0078 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(971): Show |
1 | a0001c0001t0003g0236 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(982): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(928): Show |
1 | a0001c0001t0003g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
10 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0001t0003g0039others(7): Show | 12 | HG02056.hp1 HG02165.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(972): Show |
1 | a0001c0001t0003g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(983): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0001c0001t0003g0076 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
1 | a0001c0001t0003g0074 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
1 | a0001c0001t0003g0044 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(961): Show |
1 | a0001c0001t0003g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1863): Show |
1 | a0001c0001t0003g0083 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1874): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(961): Show |
2 | a0010c0012t0003g0232a0013c0020t0003g0079 | 2 | HG01168.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(972): Show |
5 | a0001c0001t0003g0002a0001c0001t0003g0055a0001c0001t0003g0080others(2): Show | 5 | HG01433.hp1 HG01515.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(983): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0004c0017t0025g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
3 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058 | 3 | HG00544.hp2 NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
1 | a0001c0001t0003g0075 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
1 | a0001c0005t0004g0097 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
1 | a0001c0001t0003g0088 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
3 | a0001c0001t0003g0060a0001c0001t0003g0086a0001c0001t0003g0095 | 3 | HG00544.hp1 HG02080.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0001c0001t0003g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(928): Show |
1 | a0001c0001t0003g0070 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(917): Show |
1 | a0001c0001t0003g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(928): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0001c0001t0003g0096 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1038): Show |
1 | a0001c0001t0003g0093 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1049): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1005): Show |
1 | a0001c0001t0003g0065 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1016): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1005): Show |
1 | a0001c0001t0003g0066 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1016): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1005): Show |
1 | a0001c0001t0003g0067 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1016): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1005): Show |
1 | a0001c0001t0003g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1016): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(906): Show |
1 | a0004c0004t0016g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(917): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0001c0001t0003g0094 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0022c0031t0001g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0005c0006t0001g0071 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(961): Show |
1 | a0001c0001t0002g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(961): Show |
1 | a0001c0001t0003g0089 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(972): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0004c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(620): Show |
1 | a0001c0005t0005g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(631): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(939): Show |
1 | a0001c0001t0003g0068 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(950): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1137): Show |
1 | a0003c0003t0001g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1148): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1214): Show |
1 | a0003c0003t0001g0100 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(950): Show |
1 | a0024c0023t0003g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(356): Show |
1 | a0004c0017t0001g0328 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(367): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(367): Show |
7 | a0001c0043t0002g0102a0004c0004t0004g0320a0004c0004t0004g0329others(4): Show | 7 | HG01257.hp2 HG02083.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2363-1226_2363-122 others(378): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GACCCAGC others(1159): Show |
1 | a0003c0003t0001g0334 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2363-1226_2363-122 others(1170): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522716 | ||||||
chr1:11522716
|
G | GGCCCAGC others(1214): Show |
1 | a0005c0006t0001g0152 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2363-1216_2363-121 others(1225): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522716 | |||||
chr1:11522716
|
G | GGCCCAGC others(664): Show |
1 | a0004c0016t0012g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(675): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522716 | |||||
chr1:11522716
|
G | GGCCCAGC others(1236): Show |
1 | a0003c0003t0001g0238 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(1247): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522716 | |||||
chr1:11522716
|
G | GGCCCAGC others(1280): Show |
1 | a0003c0003t0001g0249 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(1291): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522716 | |||||
chr1:11522716
|
G | GGCCCAGC others(1324): Show |
1 | a0003c0003t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(1335): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522716 | |||||
chr1:11522716
|
G | GGCCCAGC others(1247): Show |
1 | a0005c0006t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(1258): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522716 | |||||
chr1:11522716
|
G | GGCCCAGC others(1280): Show |
1 | a0003c0003t0001g0008 | 2 | NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2363-1215_2363-121 others(1291): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522716 | |||||
chr1:11522717
|
G | A | 8 | a0001c0001t0003g0077a0001c0005t0004g0297a0001c0005t0006g0038others(5): Show | 8 | HG00099.hp2 HG00609.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.2363-1225G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522717 | ||||||
chr1:11522717
|
G | GCCCAGCC others(125): Show |
1 | a0002c0002t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2363-1204_2363-120 others(136): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522717 | |||||
chr1:11522727
|
G | A | 8 | a0001c0001t0003g0077a0001c0001t0003g0090a0001c0005t0004g0297others(5): Show | 8 | HG02647.hp1 HG02976.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2363-1215G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522727 | ||||||
chr1:11522727
|
G | GACCCAGC others(653): Show |
1 | a0004c0028t0012g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(664): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522727 | ||||||
chr1:11522727
|
G | GACCCAGC others(1313): Show |
1 | a0003c0003t0001g0198 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2363-1215_2363-121 others(1324): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522727 | ||||||
chr1:11522728
|
G | A | 225 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(222): Show | 237 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.2363-1214G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522728 | ||||||
chr1:11522728
|
G | GCCCAGCC others(477): Show |
2 | a0009c0019t0008g0014a0020c0036t0008g0315 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2363-1205_2363-120 others(488): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522728 | |||||
chr1:11522728
|
G | GCCCAGCC others(466): Show |
2 | a0009c0042t0001g0015a0009c0049t0001g0013 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2363-1205_2363-120 others(477): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522728 | |||||
chr1:11522728
|
G | GCCCAGCC others(1104): Show |
1 | a0004c0010t0007g0335 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2363-1205_2363-120 others(1115): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522728 | |||||
chr1:11522728
|
G | GCCCAGCC others(1093): Show |
1 | a0004c0010t0007g0336 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2363-1205_2363-120 others(1104): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522728 | |||||
chr1:11522738
|
G | A | 225 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(222): Show | 239 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.2363-1204G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522738 | ||||||
chr1:11522738
|
G | GACCCAGC others(1082): Show |
1 | a0004c0010t0007g0338 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2363-1204_2363-120 others(1093): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522738 | ||||||
chr1:11522738
|
G | GACCCAGC others(719): Show |
1 | a0005c0006t0001g0143 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2363-1204_2363-120 others(730): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522738 | ||||||
chr1:11522738
|
G | GACCCAGC others(1159): Show |
1 | a0003c0003t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2363-1204_2363-120 others(1170): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522738 | ||||||
chr1:11522738
|
G | GACCCAGC others(367): Show |
1 | a0004c0015t0004g0321 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2363-1204_2363-120 others(378): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522738 | ||||||
chr1:11522738
|
G | GGCCCAGC others(1291): Show |
1 | a0003c0003t0001g0266 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2363-1193_2363-119 others(1302): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522738
|
G | GGCCCAGC others(1302): Show |
1 | a0006c0009t0001g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2363-1193_2363-119 others(1313): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522738
|
G | GGCCCAGC others(554): Show |
1 | a0004c0010t0004g0312 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2363-1193_2363-119 others(565): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522738
|
G | GGCCCAGC others(554): Show |
2 | a0004c0010t0014g0291a0004c0010t0014g0292 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2363-1193_2363-119 others(565): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522738
|
G | GGCCCAGC others(1313): Show |
1 | a0003c0003t0001g0278 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2363-1193_2363-119 others(1324): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522738
|
G | GGCCCAGC others(576): Show |
1 | a0004c0010t0004g0290 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2363-1193_2363-119 others(587): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522738
|
G | GGCCCAGC others(565): Show |
1 | a0004c0024t0019g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2363-1193_2363-119 others(576): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522738
|
G | GGCCCAGC others(576): Show |
1 | a0004c0010t0007g0337 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2363-1193_2363-119 others(587): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522738 | |||||
chr1:11522739
|
G | A | 17 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0005t0004g0297others(14): Show | 17 | HG00099.hp2 HG01168.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.2363-1203G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522739 | ||||||
chr1:11522744
|
G | A | 1 | a0001c0005t0004g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2363-1198G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522744 | ||||||
chr1:11522749
|
G | A | 6 | a0001c0001t0003g0077a0001c0005t0004g0296a0001c0005t0006g0038others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2363-1193G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522749 | ||||||
chr1:11522750
|
A | ACCCAGCC others(543): Show |
3 | a0001c0007t0005g0113a0001c0007t0005g0114a0001c0007t0005g0115 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2363-1183_2363-118 others(554): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(1225): Show |
1 | a0003c0003t0001g0267 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(1236): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(1247): Show |
1 | a0005c0006t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(1258): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(1291): Show |
1 | a0003c0003t0001g0199 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(1302): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(1280): Show |
1 | a0005c0006t0001g0180 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(1291): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(444): Show |
1 | a0001c0005t0004g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(455): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(1288): Show |
1 | a0003c0003t0001g0200 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(1299): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(840): Show |
1 | a0003c0008t0013g0244 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(851): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(730): Show |
2 | a0003c0003t0001g0245a0003c0003t0001g0275 | 2 | HG01069.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2363-1172_2363-117 others(741): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(180): Show |
1 | a0003c0003t0024g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2363-1172_2363-117 others(191): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(928): Show |
1 | a0001c0001t0003g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2363-1171_2363-117 others(939): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(70): Show |
1 | a0019c0052t0002g0135 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2363-1182_2363-118 others(81): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | ACCCAGCC others(774): Show |
1 | a0005c0006t0001g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2363-1182_2363-118 others(785): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522750 | |||||
chr1:11522750
|
A | G | 242 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(239): Show | 254 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.2363-1192A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522750 | ||||||
chr1:11522757
|
C | G | 1 | a0002c0002t0002g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2363-1185C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522757 | ||||||
chr1:11522759
|
G | A | 1 | a0001c0007t0005g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2363-1183G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522759 | ||||||
chr1:11522759
|
G | GAGCCCAG others(542): Show |
1 | a0011c0022t0010g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(553): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522759 | ||||||
chr1:11522759
|
G | GAGCCCAG others(520): Show |
1 | a0011c0022t0010g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(531): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522759 | ||||||
chr1:11522759
|
G | GAGCCCAG others(575): Show |
5 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0116others(2): Show | 7 | HG02055.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2363-1183_2363-118 others(586): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522759 | ||||||
chr1:11522759
|
G | GAGCCCAG others(564): Show |
3 | a0001c0007t0005g0046a0001c0050t0001g0314a0004c0027t0001g0310 | 3 | HG01243.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2363-1183_2363-118 others(575): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522759 | ||||||
chr1:11522759
|
G | GAGCCCAG others(278): Show |
1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2363-1183_2363-118 others(289): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522759 | ||||||
chr1:11522760
|
G | A | 1 | a0002c0002t0002g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2363-1182G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522760 | ||||||
chr1:11522760
|
G | GGCCCAGC others(257): Show |
1 | a0008c0014t0002g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2363-1182_2363-118 others(268): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522760 | ||||||
chr1:11522760
|
G | GGCCCAGC others(59): Show |
1 | a0002c0011t0003g0131 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2363-1182_2363-118 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522760 | ||||||
chr1:11522760
|
G | GGCCCAGC others(235): Show |
1 | a0014c0034t0002g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2363-1182_2363-118 others(246): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522760 | ||||||
chr1:11522760
|
G | GGCCCAGC others(246): Show |
1 | a0002c0002t0002g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2363-1182_2363-118 others(257): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522760 | ||||||
chr1:11522761
|
A | ACCCAGCC others(411): Show |
1 | a0012c0046t0021g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2363-1172_2363-117 others(422): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(444): Show |
4 | a0007c0013t0009g0316a0007c0013t0009g0331a0007c0013t0009g0333others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2363-1172_2363-117 others(455): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(411): Show |
1 | a0012c0045t0004g0018 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2363-1172_2363-117 others(422): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(444): Show |
1 | a0007c0013t0009g0332 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2363-1172_2363-117 others(455): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(466): Show |
3 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295 | 4 | HG02622.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2363-1172_2363-117 others(477): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(48): Show |
1 | a0002c0002t0002g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2363-1172_2363-117 others(59): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(81): Show |
2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1172_2363-117 others(92): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(48): Show |
1 | a0002c0002t0002g0182 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2363-1172_2363-117 others(59): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(499): Show |
1 | a0001c0007t0005g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2363-1161_2363-116 others(510): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(59): Show |
1 | a0002c0002t0002g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2363-1161_2363-116 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(950): Show |
1 | a0001c0001t0003g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2363-1150_2363-114 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCC others(279): Show |
1 | a0002c0002t0002g0203 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2363-1171_2363-117 others(290): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | ACCCAGCG others(48): Show |
2 | a0002c0002t0002g0156a0002c0002t0002g0177 | 2 | NA18951.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2363-1175_2363-117 others(59): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522761 | |||||
chr1:11522761
|
A | AG | 11 | a0001c0007t0005g0005a0001c0007t0005g0006a0001c0007t0005g0046others(8): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2363-1181_2363-118 others(5): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522761 | ||||||
chr1:11522761
|
A | G | 63 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0021t0008g0212others(60): Show | 63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2363-1181A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522761 | ||||||
chr1:11522770
|
G | GAGCCCAG others(58): Show |
5 | a0002c0002t0002g0052a0002c0002t0002g0129a0002c0002t0002g0183others(2): Show | 5 | HG00621.hp1 NA18747.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2363-1172_2363-117 others(69): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522770 | ||||||
chr1:11522771
|
G | A | 16 | a0001c0001t0011g0233a0001c0005t0004g0297a0001c0007t0005g0113others(13): Show | 16 | HG00639.hp2 HG02083.hp2 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.2363-1171G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522771 | ||||||
chr1:11522772
|
A | ACCCAGCC others(70): Show |
2 | a0002c0002t0002g0049a0002c0002t0002g0146 | 2 | HG01168.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2363-1161_2363-116 others(81): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522772 | |||||
chr1:11522772
|
A | ACCCAGCC others(730): Show |
1 | a0003c0003t0001g0196 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2363-1160_2363-115 others(741): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522772 | |||||
chr1:11522772
|
A | ACCCAGCC others(708): Show |
1 | a0003c0003t0001g0197 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2363-1160_2363-115 others(719): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522772 | |||||
chr1:11522772
|
A | ACCCAGCC others(290): Show |
1 | a0002c0002t0002g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2363-1160_2363-115 others(301): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522772 | |||||
chr1:11522772
|
A | AG | 5 | a0002c0002t0002g0052a0002c0002t0002g0129a0002c0002t0002g0183others(2): Show | 5 | HG00621.hp1 NA18747.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2363-1170_2363-116 others(5): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522772 | ||||||
chr1:11522772
|
A | G | 20 | a0001c0001t0011g0233a0001c0005t0004g0297a0001c0005t0004g0298others(17): Show | 20 | HG00639.hp2 HG02083.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.2363-1170A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522772 | ||||||
chr1:11522779
|
C | CAGAGCCC others(433): Show |
1 | a0001c0005t0004g0296 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2363-1161_2363-116 others(444): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522779 | |||||
chr1:11522779
|
C | G | 10 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(7): Show | 11 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2363-1163C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522779 | ||||||
chr1:11522782
|
G | A | 33 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(30): Show | 36 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2363-1160G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522782 | ||||||
chr1:11522782
|
G | GACCCAGC others(70): Show |
2 | a0002c0002t0002g0289a0016c0030t0002g0167 | 2 | HG00408.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2363-1160_2363-115 others(81): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522782 | ||||||
chr1:11522782
|
G | GACCCAGC others(70): Show |
1 | a0002c0041t0004g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2363-1160_2363-115 others(81): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522782 | ||||||
chr1:11522782
|
G | GACCCAGC others(268): Show |
1 | a0002c0002t0002g0134 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2363-1160_2363-115 others(279): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522782 | ||||||
chr1:11522782
|
G | GACCCAGC others(268): Show |
1 | a0002c0002t0002g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2363-1160_2363-115 others(279): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522782 | ||||||
chr1:11522782
|
G | GGCCCAGC others(257): Show |
1 | a0002c0018t0002g0160 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2363-1150_2363-114 others(268): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522782 | |||||
chr1:11522783
|
G | A | 55 | a0001c0001t0011g0233a0001c0005t0004g0297a0001c0021t0008g0194others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2363-1159G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522783 | ||||||
chr1:11522783
|
G | GCCCAGCC others(15): Show |
2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2363-1150_2363-114 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522783 | |||||
chr1:11522783
|
G | GCCCAGCC others(994): Show |
1 | a0004c0004t0004g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2363-1150_2363-114 others(1005): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522783 | |||||
chr1:11522790
|
C | CAGGACCC others(59): Show |
1 | a0002c0002t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2363-1150_2363-114 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522790 | |||||
chr1:11522790
|
C | CAGGACCC others(81): Show |
1 | a0002c0002t0002g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2363-1150_2363-114 others(92): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522790 | |||||
chr1:11522790
|
C | G | 3 | a0001c0007t0005g0113a0001c0007t0005g0114a0001c0007t0005g0115 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2363-1152C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522790 | ||||||
chr1:11522793
|
A | G | 58 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0005t0004g0294others(55): Show | 61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2363-1149A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522793 | ||||||
chr1:11522794
|
G | A | 12 | a0001c0005t0006g0038a0002c0002t0002g0049a0002c0002t0002g0052others(9): Show | 12 | HG00621.hp1 HG01168.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2363-1148G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522794 | ||||||
chr1:11522794
|
G | GCCCAGCC others(59): Show |
10 | a0002c0002t0002g0050a0002c0002t0002g0108a0002c0002t0002g0174others(7): Show | 10 | HG00639.hp2 HG02083.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2363-1138_2363-113 others(70): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522794 | |||||
chr1:11522804
|
G | A | 2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1138G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522804 | ||||||
chr1:11522805
|
A | ACCCAGCC others(268): Show |
1 | a0002c0002t0002g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2363-1128_2363-112 others(279): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522805 | |||||
chr1:11522805
|
A | ACCCAGCC others(81): Show |
2 | a0002c0002t0002g0122a0002c0002t0002g0126 | 2 | NA18949.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2363-1128_2363-112 others(92): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522805 | |||||
chr1:11522805
|
A | ACCCAGCC others(125): Show |
1 | a0002c0048t0002g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2363-1128_2363-112 others(136): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522805 | |||||
chr1:11522805
|
A | ACCCAGCC others(950): Show |
1 | a0001c0005t0006g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2363-1127_2363-112 others(961): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522805 | |||||
chr1:11522805
|
A | G | 4 | a0001c0021t0008g0194a0002c0002t0002g0124a0002c0002t0002g0125others(1): Show | 4 | HG03579.hp1 NA18942.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.2363-1137A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522805 | ||||||
chr1:11522814
|
G | GAGCCCAG others(102): Show |
2 | a0002c0002t0002g0123a0002c0018t0002g0166 | 2 | NA18974.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.2363-1128_2363-112 others(113): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522814 | ||||||
chr1:11522814
|
G | GAGCCCAG others(102): Show |
1 | a0002c0002t0002g0062 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2363-1128_2363-112 others(113): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522814 | ||||||
chr1:11522814
|
G | GAGCCCAG others(80): Show |
34 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0130others(31): Show | 34 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2363-1128_2363-112 others(91): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522814 | ||||||
chr1:11522814
|
G | GAGCCCAG others(80): Show |
1 | a0002c0002t0002g0127 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2363-1128_2363-112 others(91): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522814 | ||||||
chr1:11522814
|
G | GAGCCCAG others(80): Show |
1 | a0002c0002t0002g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2363-1128_2363-112 others(91): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522814 | ||||||
chr1:11522815
|
G | A | 21 | a0001c0007t0005g0113a0001c0007t0005g0114a0001c0007t0005g0115others(18): Show | 21 | HG00621.hp1 HG00639.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.2363-1127G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522815 | ||||||
chr1:11522815
|
G | GGCCCAGC others(81): Show |
4 | a0002c0002t0001g0121a0002c0002t0002g0186a0002c0002t0002g0193others(1): Show | 4 | HG00438.hp1 HG00558.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2363-1127_2363-112 others(92): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522815 | ||||||
chr1:11522816
|
A | ACCCAGCC others(4): Show |
18 | a0001c0001t0011g0233a0002c0002t0002g0048a0002c0002t0002g0134others(15): Show | 18 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.2363-1116_2363-110 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522816 | |||||
chr1:11522816
|
A | ACCCAGCC others(15): Show |
1 | a0002c0002t0002g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2363-1117_2363-111 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522816 | |||||
chr1:11522816
|
A | AG | 39 | a0002c0002t0002g0062a0002c0002t0002g0110a0002c0002t0002g0111others(36): Show | 39 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2363-1126_2363-112 others(5): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522816 | ||||||
chr1:11522816
|
A | G | 25 | a0001c0007t0005g0113a0001c0007t0005g0114a0001c0007t0005g0115others(22): Show | 25 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.2363-1126A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522816 | ||||||
chr1:11522826
|
A | G | 8 | a0001c0007t0005g0113a0001c0007t0005g0114a0001c0007t0005g0115others(5): Show | 8 | HG01891.hp2 HG02135.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2363-1116A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522826 | ||||||
chr1:11522827
|
G | A | 3 | a0001c0007t0005g0113a0001c0007t0005g0114a0001c0007t0005g0115 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2363-1115G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522827 | ||||||
chr1:11522827
|
G | GCCCAGCC others(15): Show |
21 | a0001c0001t0007g0011a0001c0005t0004g0294a0001c0005t0004g0295others(18): Show | 24 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2363-1106_2363-110 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522827 | |||||
chr1:11522827
|
G | GCCCAGCC others(290): Show |
1 | a0001c0021t0008g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2363-1106_2363-110 others(301): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522827 | |||||
chr1:11522827
|
G | GCCCAGCC others(224): Show |
2 | a0001c0001t0003g0042a0001c0001t0003g0043 | 2 | NA18949.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2363-1106_2363-110 others(235): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522827 | |||||
chr1:11522827
|
G | GCCCAGCC others(400): Show |
1 | a0001c0005t0004g0297 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2363-1095_2363-109 others(411): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522827 | |||||
chr1:11522827
|
G | GCCCAGCC others(378): Show |
1 | a0001c0021t0008g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2363-1095_2363-109 others(389): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522827 | |||||
chr1:11522837
|
G | A | 6 | a0002c0002t0002g0122a0002c0002t0002g0126a0002c0002t0002g0157others(3): Show | 6 | HG02145.hp1 HG03195.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2363-1105G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522837 | ||||||
chr1:11522838
|
A | G | 6 | a0002c0002t0002g0122a0002c0002t0002g0126a0002c0002t0002g0157others(3): Show | 6 | HG02145.hp1 HG03195.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2363-1104A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522838 | ||||||
chr1:11522848
|
A | G | 5 | a0009c0019t0008g0014a0009c0042t0001g0015a0009c0049t0001g0013others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2363-1094A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522848 | ||||||
chr1:11522849
|
G | A | 2 | a0011c0022t0010g0023a0011c0022t0010g0024 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2363-1093G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522849 | ||||||
chr1:11522859
|
G | A | 2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1083G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522859 | ||||||
chr1:11522860
|
A | ACCCAGCC others(4): Show |
222 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0007g0011others(219): Show | 230 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.2363-1061_2363-105 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522860 | |||||
chr1:11522860
|
A | ACCCAGCC others(15): Show |
1 | a0001c0007t0005g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2363-1072_2363-105 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522860 | |||||
chr1:11522860
|
A | ACCCCAGC others(5): Show |
1 | a0003c0003t0001g0254 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2363-1079_2363-107 others(16): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522860 | |||||
chr1:11522860
|
A | G | 2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1082A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522860 | ||||||
chr1:11522871
|
G | GCCCAGCC others(70): Show |
1 | a0004c0004t0004g0322 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2363-1051_2363-105 others(81): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522871 | |||||
chr1:11522871
|
G | GCCCAGCC others(4): Show |
2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1062_2363-106 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522871 | |||||
chr1:11522871
|
G | GCCCAGCC others(48): Show |
2 | a0011c0022t0010g0023a0011c0022t0010g0024 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2363-1062_2363-106 others(59): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522871 | |||||
chr1:11522880
|
G | GGACCCAG others(2): Show |
3 | a0002c0002t0002g0122a0002c0002t0002g0126a0002c0002t0002g0157 | 3 | NA18943.hp1 NA18949.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2363-1062_2363-106 others(13): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522880 | ||||||
chr1:11522881
|
A | G | 1 | a0002c0048t0002g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2363-1061A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522881 | ||||||
chr1:11522882
|
G | A | 1 | a0002c0048t0002g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2363-1060G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522882 | ||||||
chr1:11522882
|
G | GCCCAGCC others(48): Show |
20 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0132others(17): Show | 20 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.2363-1051_2363-105 others(59): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522882 | |||||
chr1:11522882
|
G | GGA | 3 | a0002c0002t0002g0122a0002c0002t0002g0126a0002c0002t0002g0157 | 3 | NA18943.hp1 NA18949.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2363-1060_2363-105 others(6): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522882 | ||||||
chr1:11522892
|
G | A | 2 | a0001c0007t0005g0114a0001c0007t0005g0115 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2363-1050G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522892 | ||||||
chr1:11522893
|
A | G | 2 | a0001c0007t0005g0114a0001c0007t0005g0115 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2363-1049A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522893 | ||||||
chr1:11522900
|
C | A | 2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1042C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522900 | ||||||
chr1:11522903
|
A | G | 2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1039A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522903 | ||||||
chr1:11522904
|
G | ACCCAGCC others(15): Show |
2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2363-1039_2363-103 others(26): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522904 | ||||||
chr1:11522922
|
A | C | 29 | a0001c0001t0011g0233a0001c0007t0005g0114a0001c0007t0005g0115others(26): Show | 29 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.2363-1020A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522922 | ||||||
chr1:11522924
|
G | GAGCCCAG others(36): Show |
2 | a0001c0007t0005g0114a0001c0007t0005g0115 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2363-1018_2363-101 others(47): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522924 | ||||||
chr1:11522925
|
G | A | 26 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0122others(23): Show | 26 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.2363-1017G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522925 | ||||||
chr1:11522926
|
A | ACCCAGCC others(4): Show |
2 | a0001c0001t0011g0233a0001c0007t0005g0113 | 2 | HG02165.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2363-1007_2363-100 others(15): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522926 | |||||
chr1:11522926
|
A | ACCCAGCC others(15): Show |
183 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0007g0011others(180): Show | 191 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.2363-1011_2363-990 others(25): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522926 | |||||
chr1:11522926
|
A | ACCCAGCC others(37): Show |
58 | a0002c0002t0001g0121a0002c0002t0002g0050a0002c0002t0002g0052others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.2363-990_2363-989i others(46): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522926 | |||||
chr1:11522926
|
A | G | 26 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0122others(23): Show | 26 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.2363-1016A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522926 | ||||||
chr1:11522937
|
A | ACCCAGCC others(4): Show |
1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2363-1000_2363-990 others(14): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522937 | |||||
chr1:11522953
|
A | G | 281 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0007g0011others(278): Show | 289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.2363-989A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522953 | ||||||
chr1:11522959
|
A | ACCCAGCC others(4): Show |
8 | a0005c0006t0001g0051a0007c0013t0009g0316a0007c0013t0009g0331others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2363-974_2363-973i others(13): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522959 | |||||
chr1:11522959
|
A | ACCCAGCC others(26): Show |
1 | a0008c0054t0011g0189 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2363-974_2363-973i others(35): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11522959 | |||||
chr1:11522972
|
C | A | 1 | a0006c0009t0001g0288 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2363-970C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11522972 | ||||||
chr1:11523014
|
C | A | 1 | a0003c0003t0001g0200 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2363-928C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523014 | ||||||
chr1:11523071
|
C | T | 93 | a0001c0001t0001g0150a0003c0003t0001g0008a0003c0003t0001g0009others(90): Show | 96 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.2363-871C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523071 | ||||||
chr1:11523125
|
C | T | 1 | a0003c0003t0001g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2363-817C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523125 | ||||||
chr1:11523129
|
G | A | 2 | a0002c0002t0002g0192a0002c0002t0002g0193 | 2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.2363-813G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523129 | ||||||
chr1:11523169
|
G | T | 85 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2363-773G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523169 | ||||||
chr1:11523352
|
T | A | 1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2363-590T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523352 | ||||||
chr1:11523387
|
G | A | 1 | a0002c0002t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2363-555G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523387 | ||||||
chr1:11523423
|
G | T | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | NA18941.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2363-519G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523423 | ||||||
chr1:11523477
|
A | C | 1 | a0001c0001t0003g0068 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2363-465A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523477 | ||||||
chr1:11523479
|
C | T | 2 | a0002c0002t0002g0161a0002c0002t0002g0191 | 2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2363-463C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523479 | ||||||
chr1:11523507
|
G | C | 1 | a0004c0004t0004g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2363-435G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523507 | ||||||
chr1:11523564
|
C | T | 1 | a0001c0007t0005g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2363-378C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523564 | ||||||
chr1:11523565
|
GAGCAGGG others(23): Show |
G | 1 | a0003c0003t0001g0199 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2363-351_2363-322d others(32): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11523565 | |||||
chr1:11523625
|
GAGCAGGG others(23): Show |
G | 1 | a0003c0003t0003g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2363-291_2363-262d others(32): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11523625 | |||||
chr1:11523652
|
A | G | 105 | a0001c0001t0001g0150a0003c0003t0001g0008a0003c0003t0001g0009others(102): Show | 108 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2363-290A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523652 | ||||||
chr1:11523655
|
A | G | 105 | a0001c0001t0001g0150a0003c0003t0001g0008a0003c0003t0001g0009others(102): Show | 108 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2363-287A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523655 | ||||||
chr1:11523661
|
G | A | 4 | a0009c0019t0008g0014a0009c0042t0001g0015a0009c0049t0001g0013others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2363-281G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523661 | ||||||
chr1:11523883
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2363-59C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 10/20 | chr1 | 11523883 | ||||||
chr1:11524087
|
C | G | 2 | a0002c0002t0002g0134a0002c0002t0002g0158 | 2 | NA19000.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2476+32C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524087 | ||||||
chr1:11524107
|
A | G | 114 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0005t0004g0020others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.2476+52A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524107 | ||||||
chr1:11524261
|
T | A | 4 | a0001c0043t0002g0102a0004c0004t0004g0320a0004c0004t0004g0329others(1): Show | 4 | HG00735.hp2 HG01257.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2476+206T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524261 | ||||||
chr1:11524473
|
C | T | 1 | a0001c0001t0003g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2476+418C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524473 | ||||||
chr1:11524554
|
C | T | 1 | a0012c0045t0004g0018 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2476+499C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524554 | ||||||
chr1:11524571
|
C | T | 108 | a0001c0001t0001g0150a0003c0003t0001g0008a0003c0003t0001g0009others(105): Show | 111 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.2476+516C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524571 | ||||||
chr1:11524595
|
C | T | 2 | a0011c0022t0010g0023a0011c0022t0010g0024 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2476+540C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524595 | ||||||
chr1:11524661
|
GCCCACCA others(34): Show |
G | 1 | a0003c0032t0001g0279 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2477-489_2477-449d others(43): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | 11524661 | |||||
chr1:11524705
|
C | T | 1 | a0003c0003t0001g0224 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2477-471C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524705 | ||||||
chr1:11524748
|
CCATCCCT others(34): Show |
C | 11 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0003others(8): Show | 13 | NA18612.hp1 NA18946.hp2 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.2477-358_2477-318d others(43): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | 11524748 | |||||
chr1:11524800
|
A | C | 1 | a0001c0001t0011g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2477-376A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524800 | ||||||
chr1:11524852
|
G | A | 85 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2477-324G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11524852 | ||||||
chr1:11524855
|
C | CCTATCTC others(75): Show |
1 | a0003c0003t0003g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2477-249_2477-248i others(84): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | 11524855 | |||||
chr1:11524900
|
T | TCTCCCCC others(46): Show |
1 | a0001c0005t0004g0297 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2477-248_2477-196d others(55): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | 11524900 | |||||
chr1:11524928
|
TCTGTGCC others(45): Show |
T | 1 | a0002c0002t0002g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2477-237_2477-186d others(54): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | 11524928 | |||||
chr1:11525082
|
G | T | 13 | a0003c0003t0001g0098a0003c0003t0001g0099a0003c0003t0001g0195others(10): Show | 13 | HG01934.hp2 HG02071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.2477-94G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11525082 | ||||||
chr1:11525172
|
G | A | 1 | a0004c0004t0004g0293 | 1 | HG02622.hp1 | splice_region_variant&intron_variant | LOW | c.2477-4G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 11/20 | chr1 | 11525172 | ||||||
chr1:11525356
|
G | A | 1 | a0009c0019t0010g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2613+44G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11525356 | ||||||
chr1:11525384
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2613+72G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11525384 | ||||||
chr1:11525440
|
C | T | 1 | a0003c0003t0001g0334 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2613+128C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11525440 | ||||||
chr1:11525544
|
CTG | C | 95 | a0001c0001t0001g0150a0001c0001t0003g0055a0001c0001t0003g0085others(92): Show | 98 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.2613+238_2613+239d others(4): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 11525544 | |||||
chr1:11525675
|
G | A | 1 | a0012c0045t0004g0018 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2613+363G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11525675 | ||||||
chr1:11525738
|
G | A | 8 | a0001c0005t0004g0020a0001c0005t0015g0342a0001c0005t0015g0343others(5): Show | 8 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2613+426G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11525738 | ||||||
chr1:11525777
|
C | T | 2 | a0009c0019t0008g0014a0020c0036t0008g0315 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2613+465C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11525777 | ||||||
chr1:11525968
|
C | T | 79 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(76): Show | 79 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2613+656C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11525968 | ||||||
chr1:11526256
|
A | G | 3 | a0001c0001t0007g0011a0001c0021t0008g0194a0001c0021t0008g0212 | 4 | HG02622.hp2 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2614-395A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526256 | ||||||
chr1:11526359
|
G | C | 1 | a0002c0002t0002g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2614-292G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526359 | ||||||
chr1:11526475
|
A | G | 15 | a0001c0005t0004g0296a0001c0007t0005g0005a0001c0007t0005g0006others(12): Show | 17 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2614-176A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526475 | ||||||
chr1:11526528
|
C | G | 80 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(77): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2614-123C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526528 | ||||||
chr1:11526530
|
A | G | 3 | a0002c0002t0002g0146a0002c0002t0002g0147a0014c0034t0002g0019 | 3 | HG02630.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2614-121A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526530 | ||||||
chr1:11526543
|
G | A | 1 | a0003c0003t0001g0278 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2614-108G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526543 | ||||||
chr1:11526599
|
C | T | 1 | a0005c0006t0001g0152 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2614-52C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526599 | ||||||
chr1:11526620
|
T | C | 82 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(79): Show | 82 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2614-31T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 12/20 | chr1 | 11526620 | ||||||
chr1:11526904
|
C | A | 3 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058 | 3 | HG00544.hp2 NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2798+69C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11526904 | ||||||
chr1:11526939
|
C | T | 62 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(59): Show | 68 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2798+104C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11526939 | ||||||
chr1:11526944
|
CT | C | 12 | a0001c0001t0003g0082a0001c0001t0011g0233a0001c0005t0004g0208others(9): Show | 12 | HG00438.hp2 HG01256.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.2798+123delT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11526944 | |||||
chr1:11526976
|
G | T | 2 | a0003c0003t0001g0227a0004c0004t0006g0029 | 2 | HG03491.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2798+141G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11526976 | ||||||
chr1:11527061
|
G | A | 82 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(79): Show | 82 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2798+226G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527061 | ||||||
chr1:11527074
|
A | G | 85 | a0002c0002t0001g0121a0002c0002t0002g0048a0002c0002t0002g0049others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2798+239A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527074 | ||||||
chr1:11527187
|
G | A | 73 | a0001c0001t0003g0077a0001c0005t0004g0020a0001c0005t0004g0059others(70): Show | 74 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.2798+352G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527187 | ||||||
chr1:11527290
|
T | C | 1 | a0004c0004t0004g0341 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2798+455T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527290 | ||||||
chr1:11527341
|
C | T | 65 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(62): Show | 71 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2798+506C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527341 | ||||||
chr1:11527346
|
G | C | 6 | a0004c0004t0004g0301a0004c0004t0004g0303a0004c0004t0004g0304others(3): Show | 6 | HG02818.hp2 HG03098.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798+511G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527346 | ||||||
chr1:11527353
|
T | G | 30 | a0001c0005t0004g0020a0001c0005t0005g0118a0001c0005t0015g0342others(27): Show | 30 | HG00438.hp2 HG01167.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.2798+518T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527353 | ||||||
chr1:11527410
|
A | G | 1 | a0004c0024t0019g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2798+575A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527410 | ||||||
chr1:11527417
|
C | T | 4 | a0001c0050t0001g0314a0004c0027t0001g0310a0009c0042t0001g0015others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2798+582C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527417 | ||||||
chr1:11527418
|
A | G | 4 | a0001c0050t0001g0314a0004c0027t0001g0310a0009c0042t0001g0015others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2798+583A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527418 | ||||||
chr1:11527419
|
C | T | 4 | a0001c0050t0001g0314a0004c0027t0001g0310a0009c0042t0001g0015others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2798+584C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527419 | ||||||
chr1:11527429
|
A | G | 90 | a0001c0005t0004g0155a0001c0005t0004g0208a0001c0043t0002g0102others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.2798+594A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527429 | ||||||
chr1:11527509
|
C | T | 112 | a0001c0001t0001g0004a0001c0001t0002g0103a0001c0001t0003g0001others(109): Show | 119 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2798+674C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527509 | ||||||
chr1:11527545
|
C | A | 1 | a0002c0002t0022g0168 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2798+710C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527545 | ||||||
chr1:11527547
|
C | CA | 80 | a0001c0043t0002g0102a0002c0002t0001g0121a0002c0002t0002g0048others(77): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2798+727dupA | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11527547 | |||||
chr1:11527547
|
CA | C | 14 | a0001c0001t0003g0040a0001c0001t0003g0075a0001c0001t0003g0078others(11): Show | 14 | HG00323.hp1 HG00323.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.2798+727delA | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11527547 | |||||
chr1:11527698
|
G | A | 5 | a0001c0001t0007g0011a0004c0010t0007g0335a0004c0010t0007g0336others(2): Show | 6 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798+863G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527698 | ||||||
chr1:11527866
|
C | T | 61 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(58): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2798+1031C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527866 | ||||||
chr1:11527907
|
T | G | 81 | a0001c0043t0002g0102a0002c0002t0001g0121a0002c0002t0002g0048others(78): Show | 81 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2798+1072T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11527907 | ||||||
chr1:11528050
|
G | A | 61 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(58): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2798+1215G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528050 | ||||||
chr1:11528159
|
T | C | 1 | a0004c0016t0012g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2798+1324T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528159 | ||||||
chr1:11528174
|
T | C | 113 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0005t0004g0298others(110): Show | 116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2798+1339T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528174 | ||||||
chr1:11528320
|
C | T | 1 | a0001c0007t0005g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2799-1236C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528320 | ||||||
chr1:11528374
|
C | A | 1 | a0004c0010t0014g0291 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2799-1182C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528374 | ||||||
chr1:11528571
|
C | A | 3 | a0001c0007t0005g0046a0001c0007t0005g0119a0004c0004t0016g0307 | 3 | HG02109.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2799-985C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528571 | ||||||
chr1:11528689
|
C | T | 5 | a0001c0001t0007g0011a0004c0010t0007g0335a0004c0010t0007g0336others(2): Show | 6 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2799-867C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528689 | ||||||
chr1:11528709
|
G | A | 84 | a0001c0043t0002g0102a0002c0002t0001g0121a0002c0002t0002g0048others(81): Show | 84 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.2799-847G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528709 | ||||||
chr1:11528762
|
G | A | 2 | a0001c0005t0005g0118a0004c0004t0008g0308 | 2 | HG01167.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2799-794G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528762 | ||||||
chr1:11528778
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2799-778G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528778 | ||||||
chr1:11528810
|
C | T | 85 | a0001c0043t0002g0102a0002c0002t0001g0121a0002c0002t0002g0048others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2799-746C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528810 | ||||||
chr1:11528867
|
G | C | 3 | a0001c0005t0004g0155a0001c0005t0004g0208a0001c0005t0004g0209 | 3 | NA18962.hp1 NA19003.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2799-689G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528867 | ||||||
chr1:11528946
|
G | A | 2 | a0002c0011t0001g0138a0009c0019t0010g0112 | 2 | HG02071.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2799-610G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528946 | ||||||
chr1:11528950
|
G | A | 1 | a0002c0002t0002g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2799-606G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11528950 | ||||||
chr1:11529122
|
T | C | 1 | a0012c0046t0021g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2799-434T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11529122 | ||||||
chr1:11529392
|
A | T | 85 | a0001c0043t0002g0102a0002c0002t0001g0121a0002c0002t0002g0048others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2799-164A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11529392 | ||||||
chr1:11529429
|
C | T | 3 | a0002c0002t0001g0121a0002c0048t0002g0136a0003c0008t0002g0277 | 3 | NA18964.hp2 NA18994.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2799-127C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 13/20 | chr1 | 11529429 | ||||||
chr1:11529973
|
G | A | 1 | a0012c0046t0021g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3102+14G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11529973 | ||||||
chr1:11530057
|
C | A | 1 | a0003c0003t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3102+98C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530057 | ||||||
chr1:11530118
|
C | T | 80 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(77): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.3102+159C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530118 | ||||||
chr1:11530200
|
G | A | 2 | a0002c0002t0002g0326a0002c0002t0002g0327 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3102+241G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530200 | ||||||
chr1:11530203
|
G | A | 1 | a0003c0003t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3102+244G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530203 | ||||||
chr1:11530225
|
A | G | 4 | a0004c0015t0004g0317a0004c0015t0004g0318a0004c0015t0004g0321others(1): Show | 4 | HG03041.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3102+266A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530225 | ||||||
chr1:11530340
|
T | C | 3 | a0001c0001t0011g0233a0002c0011t0011g0137a0008c0054t0011g0189 | 3 | HG02165.hp2 HG04228.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3102+381T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530340 | ||||||
chr1:11530417
|
G | A | 85 | a0001c0043t0002g0102a0002c0002t0001g0121a0002c0002t0002g0048others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.3102+458G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530417 | ||||||
chr1:11530423
|
G | C | 1 | a0003c0003t0001g0266 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3102+464G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530423 | ||||||
chr1:11530510
|
G | A | 1 | a0004c0004t0004g0341 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3103-397G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530510 | ||||||
chr1:11530530
|
G | A | 1 | a0001c0050t0001g0314 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3103-377G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530530 | ||||||
chr1:11530620
|
G | A | 1 | a0002c0002t0002g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3103-287G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530620 | ||||||
chr1:11530719
|
T | A | 167 | a0001c0001t0003g0088a0001c0001t0007g0011a0001c0001t0011g0233others(164): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.3103-188T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530719 | ||||||
chr1:11530721
|
T | A | 167 | a0001c0001t0003g0088a0001c0001t0007g0011a0001c0001t0011g0233others(164): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.3103-186T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530721 | ||||||
chr1:11530759
|
G | C | 1 | a0002c0011t0011g0137 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3103-148G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530759 | ||||||
chr1:11530851
|
G | A | 1 | a0001c0001t0003g0070 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3103-56G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530851 | ||||||
chr1:11530862
|
C | A | 85 | a0001c0043t0002g0102a0002c0002t0001g0121a0002c0002t0002g0048others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.3103-45C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 15/20 | chr1 | 11530862 | ||||||
chr1:11531176
|
A | G | 7 | a0001c0005t0004g0298a0004c0010t0004g0290a0004c0010t0004g0312others(4): Show | 7 | HG02559.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3229+143A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 16/20 | chr1 | 11531176 | ||||||
chr1:11531293
|
G | A | 3 | a0003c0003t0001g0224a0003c0003t0001g0237a0003c0003t0001g0258 | 3 | HG02293.hp2 NA18747.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.3229+260G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 16/20 | chr1 | 11531293 | ||||||
chr1:11531320
|
C | T | 1 | a0010c0012t0001g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3230-245C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 16/20 | chr1 | 11531320 | ||||||
chr1:11531366
|
C | T | 9 | a0004c0025t0008g0053a0007c0013t0009g0316a0007c0013t0009g0331others(6): Show | 9 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3230-199C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 16/20 | chr1 | 11531366 | ||||||
chr1:11531437
|
A | G | 1 | a0020c0036t0008g0315 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3230-128A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 16/20 | chr1 | 11531437 | ||||||
chr1:11531747
|
T | A | 10 | a0001c0001t0007g0011a0001c0007t0005g0046a0001c0007t0005g0119others(7): Show | 11 | HG02109.hp2 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.3375+37T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11531747 | ||||||
chr1:11531794
|
C | A | 1 | a0004c0004t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3375+84C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11531794 | ||||||
chr1:11531804
|
A | T | 1 | a0001c0001t0003g0093 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3375+94A>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11531804 | ||||||
chr1:11531824
|
G | A | 1 | a0003c0003t0001g0257 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3375+114G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11531824 | ||||||
chr1:11531884
|
C | T | 1 | a0004c0004t0004g0012 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.3375+174C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11531884 | ||||||
chr1:11531885
|
G | A | 2 | a0011c0022t0010g0023a0011c0022t0010g0024 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3375+175G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11531885 | ||||||
chr1:11531971
|
C | A | 1 | a0024c0023t0003g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3375+261C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11531971 | ||||||
chr1:11532072
|
C | T | 1 | a0004c0004t0004g0341 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3375+362C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532072 | ||||||
chr1:11532119
|
C | G | 3 | a0001c0001t0011g0233a0002c0011t0011g0137a0008c0054t0011g0189 | 3 | HG02165.hp2 HG04228.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3375+409C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532119 | ||||||
chr1:11532155
|
G | A | 5 | a0004c0004t0004g0145a0004c0004t0004g0205a0004c0004t0004g0322others(2): Show | 5 | HG00099.hp1 HG01081.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3375+445G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532155 | ||||||
chr1:11532228
|
G | A | 2 | a0001c0050t0001g0314a0009c0049t0001g0013 | 2 | HG01243.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.3375+518G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532228 | ||||||
chr1:11532455
|
C | A | 1 | a0003c0003t0001g0284 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3375+745C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532455 | ||||||
chr1:11532538
|
C | A | 6 | a0001c0001t0007g0011a0004c0010t0007g0335a0004c0010t0007g0336others(3): Show | 7 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3375+828C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532538 | ||||||
chr1:11532894
|
C | T | 3 | a0004c0016t0012g0054a0004c0016t0020g0017a0004c0028t0012g0047 | 3 | HG01891.hp1 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3375+1184C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532894 | ||||||
chr1:11532909
|
T | A | 1 | a0002c0002t0002g0170 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3375+1199T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532909 | ||||||
chr1:11532958
|
G | A | 4 | a0003c0008t0002g0239a0003c0008t0002g0240a0003c0008t0002g0241others(1): Show | 4 | HG00639.hp1 HG01255.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3375+1248G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532958 | ||||||
chr1:11532960
|
C | T | 1 | a0011c0022t0010g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3375+1250C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11532960 | ||||||
chr1:11533025
|
C | T | 1 | a0004c0024t0019g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3375+1315C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533025 | ||||||
chr1:11533059
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3376-1322T>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533059 | ||||||
chr1:11533134
|
C | G | 1 | a0010c0012t0001g0225 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3376-1247C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533134 | ||||||
chr1:11533144
|
C | A | 6 | a0001c0005t0006g0038a0004c0004t0004g0213a0004c0004t0004g0214others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.3376-1237C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533144 | ||||||
chr1:11533184
|
A | G | 1 | a0004c0024t0019g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3376-1197A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533184 | ||||||
chr1:11533202
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3376-1179G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533202 | ||||||
chr1:11533207
|
C | T | 83 | a0001c0043t0002g0102a0002c0002t0002g0048a0002c0002t0002g0049others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3376-1174C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533207 | ||||||
chr1:11533221
|
A | C | 1 | a0003c0008t0013g0272 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3376-1160A>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533221 | ||||||
chr1:11533248
|
T | G | 1 | a0004c0004t0016g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3376-1133T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533248 | ||||||
chr1:11533248
|
TGTTTC | T | 3 | a0001c0001t0011g0233a0002c0011t0011g0137a0008c0054t0011g0189 | 3 | HG02165.hp2 HG04228.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3376-1132_3376-112 others(9): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533248 | ||||||
chr1:11533252
|
T | G | 1 | a0002c0002t0002g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3376-1129T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533252 | ||||||
chr1:11533253
|
C | CT | 12 | a0001c0001t0003g0068a0001c0001t0003g0083a0001c0001t0003g0084others(9): Show | 12 | HG00609.hp1 HG00673.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.3376-1106dupT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 11533253 | |||||
chr1:11533253
|
CT | C | 21 | a0001c0001t0003g0040a0001c0001t0003g0057a0001c0001t0003g0091others(18): Show | 21 | HG01099.hp2 HG01168.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.3376-1106delT | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 11533253 | |||||
chr1:11533302
|
C | T | 3 | a0001c0001t0011g0233a0002c0011t0011g0137a0008c0054t0011g0189 | 3 | HG02165.hp2 HG04228.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3376-1079C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533302 | ||||||
chr1:11533329
|
C | G | 5 | a0001c0005t0005g0118a0001c0007t0005g0120a0002c0051t0004g0172others(2): Show | 5 | HG01167.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3376-1052C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533329 | ||||||
chr1:11533500
|
G | A | 2 | a0004c0004t0006g0032a0004c0004t0006g0034 | 2 | NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.3376-881G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533500 | ||||||
chr1:11533548
|
C | T | 2 | a0001c0001t0003g0075a0001c0001t0003g0076 | 2 | NA18941.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3376-833C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533548 | ||||||
chr1:11533582
|
C | T | 3 | a0004c0025t0008g0053a0009c0019t0008g0014a0020c0036t0008g0315 | 3 | HG02559.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3376-799C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533582 | ||||||
chr1:11533583
|
A | G | 334 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0002g0103others(331): Show | 348 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.3376-798A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533583 | ||||||
chr1:11533619
|
C | T | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG01106.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3376-762C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533619 | ||||||
chr1:11533689
|
G | A | 3 | a0001c0007t0005g0046a0001c0007t0005g0119a0004c0004t0016g0307 | 3 | HG02109.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3376-692G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533689 | ||||||
chr1:11533736
|
T | TGCACACA others(5): Show |
335 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0150others(332): Show | 348 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.3376-637_3376-636i others(14): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 11533736 | |||||
chr1:11533736
|
T | TGCACACA others(9): Show |
8 | a0001c0001t0007g0011a0001c0044t0005g0117a0004c0010t0007g0335others(5): Show | 9 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3376-637_3376-636i others(18): Show |
DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 11533736 | |||||
chr1:11533878
|
G | T | 2 | a0011c0022t0010g0023a0011c0022t0010g0024 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3376-503G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533878 | ||||||
chr1:11533960
|
A | G | 1 | a0001c0007t0005g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3376-421A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11533960 | ||||||
chr1:11534101
|
G | C | 1 | a0001c0007t0005g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3376-280G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11534101 | ||||||
chr1:11534229
|
G | C | 1 | a0002c0002t0002g0123 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3376-152G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11534229 | ||||||
chr1:11534284
|
A | G | 1 | a0004c0028t0012g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3376-97A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11534284 | ||||||
chr1:11534343
|
T | C | 250 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(247): Show | 259 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.3376-38T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 17/20 | chr1 | 11534343 | ||||||
chr1:11534624
|
C | T | 83 | a0001c0043t0002g0102a0002c0002t0002g0048a0002c0002t0002g0049others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3535+84C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11534624 | ||||||
chr1:11534873
|
G | A | 1 | a0001c0044t0005g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3536-138G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11534873 | ||||||
chr1:11534885
|
C | T | 1 | a0002c0002t0002g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3536-126C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11534885 | ||||||
chr1:11534915
|
G | A | 11 | a0001c0001t0007g0011a0001c0001t0011g0233a0001c0044t0005g0117others(8): Show | 12 | HG02165.hp2 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.3536-96G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11534915 | ||||||
chr1:11534944
|
C | A | 7 | a0001c0001t0001g0150a0002c0011t0001g0201a0005c0006t0001g0051others(4): Show | 7 | HG01081.hp2 HG01433.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.3536-67C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11534944 | ||||||
chr1:11534965
|
C | T | 1 | a0004c0004t0004g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3536-46C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11534965 | ||||||
chr1:11534981
|
A | G | 64 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(61): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.3536-30A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11534981 | ||||||
chr1:11535004
|
C | T | 2 | a0001c0001t0003g0081a0001c0001t0003g0082 | 2 | HG03490.hp2 HG03492.hp1 |
splice_region_variant&intron_variant | LOW | c.3536-7C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 18/20 | chr1 | 11535004 | ||||||
chr1:11535146
|
A | G | 74 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(71): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.3649+22A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535146 | ||||||
chr1:11535174
|
G | C | 2 | a0004c0004t0004g0320a0004c0004t0004g0329 | 2 | HG01257.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.3649+50G>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535174 | ||||||
chr1:11535175
|
A | G | 7 | a0001c0001t0007g0011a0001c0044t0005g0117a0004c0010t0007g0335others(4): Show | 8 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.3649+51A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535175 | ||||||
chr1:11535185
|
C | T | 1 | a0015c0053t0007g0300 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3649+61C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535185 | ||||||
chr1:11535236
|
A | G | 74 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(71): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.3649+112A>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535236 | ||||||
chr1:11535238
|
C | G | 73 | a0001c0005t0004g0020a0001c0005t0004g0059a0001c0005t0004g0097others(70): Show | 76 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.3649+114C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535238 | ||||||
chr1:11535274
|
G | A | 74 | a0001c0001t0002g0103a0001c0001t0003g0001a0001c0001t0003g0002others(71): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.3649+150G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535274 | ||||||
chr1:11535282
|
G | T | 1 | a0004c0024t0019g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3649+158G>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535282 | ||||||
chr1:11535283
|
C | G | 5 | a0001c0001t0007g0011a0004c0010t0007g0335a0004c0010t0007g0336others(2): Show | 6 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3649+159C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535283 | ||||||
chr1:11535333
|
C | T | 47 | a0001c0005t0004g0020a0001c0005t0004g0294a0001c0005t0004g0295others(44): Show | 50 | HG01069.hp1 HG01070.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.3650-145C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535333 | ||||||
chr1:11535356
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3650-122C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535356 | ||||||
chr1:11535460
|
C | G | 1 | a0004c0017t0001g0328 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3650-18C>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 19/20 | chr1 | 11535460 | ||||||
chr1:11535745
|
C | T | 83 | a0001c0043t0002g0102a0002c0002t0002g0048a0002c0002t0002g0049others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3816+101C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11535745 | ||||||
chr1:11535761
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3816+117G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11535761 | ||||||
chr1:11535776
|
C | A | 1 | a0001c0001t0003g0076 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3816+132C>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11535776 | ||||||
chr1:11536068
|
G | A | 1 | a0001c0001t0003g0093 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3817-256G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11536068 | ||||||
chr1:11536070
|
G | A | 1 | a0001c0005t0005g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3817-254G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11536070 | ||||||
chr1:11536097
|
T | C | 1 | a0010c0012t0003g0232 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3817-227T>C | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11536097 | ||||||
chr1:11536167
|
C | T | 3 | a0001c0007t0005g0046a0001c0007t0005g0119a0004c0004t0016g0307 | 3 | HG02109.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3817-157C>T | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11536167 | ||||||
chr1:11536244
|
T | G | 1 | a0001c0001t0003g0094 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3817-80T>G | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11536244 | ||||||
chr1:11536253
|
G | A | 1 | a0001c0044t0005g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3817-71G>A | DISP3 | ENSG00000204624.8 | transcript | ENST00000294484.7 | protein_coding | 20/20 | chr1 | 11536253 |