geneid | 9798 |
---|---|
ensemblid | ENSG00000182149.21 |
hgncid | 28977 |
symbol | IST1 |
name | IST1 factor associated with ESCRT-III |
refseq_nuc | NM_001270975.2 |
refseq_prot | NP_001257904.1 |
ensembl_nuc | ENST00000378799.11 |
ensembl_prot | ENSP00000368076.6 |
mane_status | MANE Select |
chr | chr16 |
start | 71895531 |
end | 71931199 |
strand | + |
ver | v1.2 |
region | chr16:71895531-71931199 |
region5000 | chr16:71890531-71936199 |
regionname0 | IST1_chr16_71895531_71931199 |
regionname5000 | IST1_chr16_71890531_71936199 |
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 | 1/0 | 366 | 218 | 58 | 53 | 77 | 11 | 18 | 61 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002 | 0/1 | 364 | 119 | 18 | 19 | 55 | 5 | 21 | 47 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0003 | 0/0 | 368 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0004 | 0/0 | 364 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0005 | 0/0 | 366 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
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 | 1/0 | 1101 | 215 | 57 | 51 | 77 | 11 | 18 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0002 | 0/0 | 1095 | 80 | 4 | 6 | 52 | 2 | 16 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0003 | 0/1 | 1095 | 34 | 14 | 10 | 3 | 1 | 5 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0004 | 0/0 | 1107 | 12 | 12 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0005 | 0/0 | 1095 | 5 | 0 | 3 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0006 | 0/0 | 1095 | 2 | 0 | 0 | 0 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0007 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0008 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0009 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
c0010 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
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 | 1/0 | 3461 | 129 | 24 | 29 | 58 | 5 | 12 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0002 | 0/0 | 3455 | 82 | 4 | 9 | 49 | 4 | 16 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0003 | 0/0 | 3461 | 38 | 36 | 2 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0004 | 0/0 | 3461 | 22 | 0 | 13 | 4 | 1 | 4 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0005 | 0/0 | 3461 | 20 | 1 | 7 | 6 | 2 | 4 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0006 | 0/0 | 3453 | 11 | 11 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0007 | 0/1 | 3461 | 10 | 2 | 4 | 0 | 1 | 2 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0008 | 0/0 | 3461 | 9 | 0 | 0 | 8 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0009 | 0/0 | 3461 | 4 | 0 | 4 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0010 | 0/0 | 3461 | 3 | 0 | 1 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0011 | 0/0 | 3461 | 3 | 2 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0012 | 0/0 | 3461 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0013 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0014 | 0/0 | 3461 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0015 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0016 | 0/0 | 3455 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0017 | 0/0 | 3455 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0018 | 0/0 | 3455 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0019 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0020 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0021 | 0/0 | 3461 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0022 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0023 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0024 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0025 | 0/0 | 3461 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0026 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0027 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0028 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0029 | 0/0 | 3461 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0030 | 0/0 | 3461 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
t0031 | 0/0 | 3455 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
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 | 10 | 1 | 3 | 6 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
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 | 1/0 | 1101 | 215 | 57 | 51 | 77 | 11 | 18 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0007 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0009 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0010 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0002 | 0/0 | 1095 | 80 | 4 | 6 | 52 | 2 | 16 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003 | 0/1 | 1095 | 34 | 14 | 10 | 3 | 1 | 5 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0005 | 0/0 | 1095 | 5 | 0 | 3 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0003c0004 | 0/0 | 1107 | 12 | 12 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0004c0006 | 0/0 | 1095 | 2 | 0 | 0 | 0 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0005c0008 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4561 | 114 | 18 | 24 | 58 | 5 | 8 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0003 | 0/0 | 4561 | 31 | 29 | 2 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0004 | 0/0 | 4561 | 21 | 0 | 13 | 3 | 1 | 4 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0005 | 0/0 | 4561 | 18 | 1 | 6 | 5 | 2 | 4 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0007 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0008 | 0/0 | 4561 | 8 | 0 | 0 | 7 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0009 | 0/0 | 4561 | 4 | 0 | 4 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0010 | 0/0 | 4561 | 2 | 0 | 0 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0011 | 0/0 | 4561 | 3 | 2 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0012 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0013 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0014 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0015 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0019 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0022 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0023 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0024 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0025 | 0/0 | 4561 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0026 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0001t0030 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0007t0001 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0009t0005 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0001c0010t0001 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0002t0002 | 0/0 | 4549 | 76 | 4 | 6 | 49 | 2 | 15 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0002t0016 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0002t0017 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0002t0018 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0002t0031 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0001 | 0/0 | 4555 | 12 | 5 | 4 | 0 | 0 | 3 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0002 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0003 | 0/0 | 4555 | 7 | 7 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0004 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0005 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0007 | 0/1 | 4555 | 7 | 0 | 4 | 0 | 1 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0008 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0010 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0020 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0028 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0003t0029 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0002c0005t0002 | 0/0 | 4549 | 5 | 0 | 3 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0003c0004t0006 | 0/0 | 4559 | 11 | 11 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0003c0004t0027 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0004c0006t0007 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0004c0006t0021 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
a0005c0008t0001 | 0/0 | 4561 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | copy fasta | chr16 | 71890531 | 71936199 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0008g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0013g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0014g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0019g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0022g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0023g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0024g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0025g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0026g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0001t0030g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0007t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0009t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0001c0010t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0016g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0018g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0002t0031g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0007g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0007g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0008g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0010g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0020g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0028g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0003t0029g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0005t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0005t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0002c0005t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0003c0004t0027g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0004c0006t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0004c0006t0021g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
a0005c0008t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0052 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0019 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00323 | hp1 | a0002 | c0005 | t0002 | g0017 | EUR | FIN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0107 | EUR | FIN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00609 | hp1 | a0001 | c0001 | t0024 | g0152 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0252 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00733 | hp1 | a0002 | c0003 | t0029 | g0082 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00741 | hp1 | a0001 | c0001 | t0014 | g0046 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01069 | hp2 | a0002 | c0005 | t0002 | g0112 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01071 | hp2 | a0002 | c0005 | t0002 | g0017 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01074 | hp1 | a0002 | c0003 | t0007 | g0008 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01074 | hp2 | a0002 | c0003 | t0007 | g0081 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0170 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0160 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0157 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01175 | hp1 | a0002 | c0003 | t0007 | g0083 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0260 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0235 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0149 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01256 | hp2 | a0001 | c0009 | t0005 | g0183 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0159 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01346 | hp1 | a0002 | c0005 | t0002 | g0101 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01346 | hp2 | a0001 | c0010 | t0001 | g0220 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01358 | hp1 | a0002 | c0003 | t0010 | g0020 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01361 | hp2 | a0002 | c0003 | t0007 | g0180 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01433 | hp2 | a0001 | c0001 | t0030 | g0013 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01515 | hp1 | a0001 | c0001 | t0011 | g0072 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01516 | hp1 | a0001 | c0001 | t0010 | g0155 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0165 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01517 | hp2 | a0001 | c0001 | t0010 | g0020 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01884 | hp1 | a0002 | c0003 | t0003 | g0016 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01891 | hp1 | a0003 | c0004 | t0006 | g0076 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01891 | hp2 | a0001 | c0001 | t0023 | g0168 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01981 | hp2 | a0001 | c0001 | t0009 | g0051 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01993 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01993 | hp2 | a0002 | c0003 | t0001 | g0256 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02027 | hp1 | a0001 | c0001 | t0019 | g0201 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02132 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02145 | hp2 | a0002 | c0003 | t0003 | g0099 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | CDX | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0044 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02258 | hp2 | a0003 | c0004 | t0006 | g0066 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02280 | hp1 | a0002 | c0003 | t0003 | g0016 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02280 | hp2 | a0002 | c0003 | t0001 | g0192 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02293 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02300 | hp1 | a0001 | c0001 | t0009 | g0037 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02451 | hp1 | a0002 | c0003 | t0003 | g0095 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02451 | hp2 | a0002 | c0003 | t0028 | g0030 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02602 | hp1 | a0002 | c0003 | t0002 | g0146 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02602 | hp2 | a0002 | c0003 | t0007 | g0008 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0217 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02683 | hp2 | a0004 | c0006 | t0021 | g0078 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0122 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0230 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02717 | hp2 | a0002 | c0003 | t0003 | g0096 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0174 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0263 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02809 | hp1 | a0002 | c0003 | t0003 | g0093 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0161 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0074 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0073 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02896 | hp2 | a0003 | c0004 | t0006 | g0071 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0065 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02922 | hp1 | a0001 | c0007 | t0001 | g0053 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02965 | hp2 | a0003 | c0004 | t0006 | g0007 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02970 | hp2 | a0003 | c0004 | t0006 | g0069 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03130 | hp1 | a0003 | c0004 | t0027 | g0077 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03139 | hp1 | a0002 | c0003 | t0003 | g0097 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03225 | hp1 | a0002 | c0003 | t0020 | g0063 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0186 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03239 | hp1 | a0004 | c0006 | t0007 | g0008 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0181 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0185 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0184 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0019 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0277 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03540 | hp1 | a0002 | c0003 | t0001 | g0219 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03540 | hp2 | a0003 | c0004 | t0006 | g0070 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0116 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0119 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03831 | hp2 | a0005 | c0008 | t0001 | g0243 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0117 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0205 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0278 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0172 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0120 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04199 | hp2 | a0002 | c0002 | t0018 | g0104 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04204 | hp1 | a0001 | c0001 | t0025 | g0154 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0163 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18906 | hp2 | a0003 | c0004 | t0006 | g0007 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0215 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18953 | hp2 | a0001 | c0001 | t0026 | g0158 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18957 | hp2 | a0002 | c0002 | t0016 | g0139 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18965 | hp2 | a0001 | c0001 | t0013 | g0209 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18966 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18968 | hp2 | a0002 | c0003 | t0008 | g0225 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18971 | hp2 | a0002 | c0003 | t0005 | g0153 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18975 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18979 | hp2 | a0002 | c0002 | t0031 | g0018 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0276 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18990 | hp1 | a0002 | c0003 | t0004 | g0054 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19011 | hp1 | a0002 | c0002 | t0017 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19030 | hp2 | a0001 | c0001 | t0011 | g0075 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19043 | hp1 | a0003 | c0004 | t0006 | g0007 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19240 | hp1 | a0003 | c0004 | t0006 | g0068 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | ASW | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ASW | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20752 | hp1 | a0002 | c0003 | t0007 | g0080 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0106 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20805 | hp1 | a0002 | c0005 | t0002 | g0102 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0284 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02109 | hp2 | a0003 | c0004 | t0006 | g0067 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0188 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG06807 | hp1 | a0001 | c0001 | t0022 | g0148 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
HG06807 | hp2 | a0003 | c0004 | t0006 | g0064 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0127 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0007 | g0079 | REF | REF | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0033 | REF | REF | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71921367
|
G | A | 1 | a0004 | 2 | HG02683.hp2 HG03239.hp1 |
missense_variant | MODERATE | c.466G>A | p.Ala156Thr | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/10 | 540/4561 | 466/1101 | 156/366 | chr16 | 71921367 | ||
chr16:71922608
|
A | AATGCCC | 1 | a0003 | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
disruptive_inframe_insertion | MODERATE | c.705_710dupCATGCC | p.Pro237_Met238insMe others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 785/4561 | 711/1101 | 237/366 | INFO_REALIGN_3_PRIME | chr16 | 71922608 | |
chr16:71922608
|
AATGCCC | A | 2 | a0002a0004 | 121 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
disruptive_inframe_deletion | MODERATE | c.705_710delCATGCC | p.Met236_Pro237del | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 779/4561 | 705/1101 | 235/366 | INFO_REALIGN_3_PRIME | chr16 | 71922608 | |
chr16:71927632
|
A | C | 1 | a0005 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.920A>C | p.Glu307Ala | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 994/4561 | 920/1101 | 307/366 | chr16 | 71927632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71916547
|
C | T | 3 | a0001c0010a0002c0002a0002c0005 | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
synonymous_variant | LOW | c.174C>T | p.His58His | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 3/10 | 248/4561 | 174/1101 | 58/366 | chr16 | 71916547 | ||
chr16:71921411
|
A | G | 1 | a0001c0009 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.510A>G | p.Ala170Ala | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/10 | 584/4561 | 510/1101 | 170/366 | chr16 | 71921411 | ||
chr16:71922602
|
G | A | 1 | a0002c0005 | 5 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
synonymous_variant | LOW | c.681G>A | p.Thr227Thr | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 755/4561 | 681/1101 | 227/366 | chr16 | 71922602 | ||
chr16:71922662
|
T | C | 1 | a0001c0007 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.741T>C | p.Tyr247Tyr | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 815/4561 | 741/1101 | 247/366 | chr16 | 71922662 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71895555
|
C | T | 2 | a0001c0001t0030a0002c0002t0031 | 2 | HG01433.hp2 NA18979.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-50C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/10 | chr16 | 71895555 | ||||||
chr16:71895574
|
G | A | 3 | a0001c0001t0008a0001c0001t0013a0002c0003t0008 | 10 | HG00609.hp2 HG02083.hp1 HG02132.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-31G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/10 | 20067 | chr16 | 71895574 | |||||
chr16:71895585
|
G | A | 1 | a0001c0001t0014 | 1 | HG00741.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/10 | 20056 | chr16 | 71895585 | |||||
chr16:71927862
|
A | T | 2 | a0001c0001t0011a0001c0001t0012 | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 49 | chr16 | 71927862 | |||||
chr16:71928003
|
A | G | 21 | a0001c0001t0005a0001c0001t0007a0001c0001t0010others(18): Show | 59 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*190A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 190 | chr16 | 71928003 | |||||
chr16:71928053
|
T | C | 1 | a0001c0001t0015 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 240 | chr16 | 71928053 | |||||
chr16:71928368
|
A | G | 1 | a0002c0003t0029 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 555 | chr16 | 71928368 | |||||
chr16:71928416
|
G | A | 1 | a0002c0002t0016 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*603G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 603 | chr16 | 71928416 | |||||
chr16:71928522
|
G | A | 1 | a0002c0003t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 709 | chr16 | 71928522 | |||||
chr16:71928688
|
G | C | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0014others(3): Show | 29 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*875G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 875 | chr16 | 71928688 | |||||
chr16:71928823
|
A | G | 1 | a0002c0003t0028 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1010A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1010 | chr16 | 71928823 | |||||
chr16:71928966
|
C | T | 1 | a0001c0001t0015 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1153 | chr16 | 71928966 | |||||
chr16:71928967
|
TGTAGCTC others(1): Show |
T | 2 | a0003c0004t0006a0003c0004t0027 | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1161_*1168delCAGT others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1161 | INFO_REALIGN_3_PRIME | chr16 | 71928967 | ||||
chr16:71929000
|
C | T | 1 | a0001c0001t0026 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1187C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1187 | chr16 | 71929000 | |||||
chr16:71929173
|
G | C | 3 | a0001c0001t0022a0001c0001t0023a0002c0003t0028 | 3 | HG01891.hp2 HG02451.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1360G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1360 | chr16 | 71929173 | |||||
chr16:71929283
|
C | T | 15 | a0001c0001t0005a0001c0001t0007a0001c0001t0010others(12): Show | 40 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1470C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1470 | chr16 | 71929283 | |||||
chr16:71929563
|
G | A | 1 | a0001c0001t0013 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1750G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1750 | chr16 | 71929563 | |||||
chr16:71929579
|
C | T | 2 | a0001c0001t0023a0002c0003t0028 | 2 | HG01891.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1766C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1766 | chr16 | 71929579 | |||||
chr16:71929584
|
G | A | 2 | a0003c0004t0006a0003c0004t0027 | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1771G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1771 | chr16 | 71929584 | |||||
chr16:71929620
|
C | A | 1 | a0002c0003t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1807C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1807 | chr16 | 71929620 | |||||
chr16:71929788
|
A | G | 1 | a0001c0001t0009 | 4 | HG01981.hp2 HG01993.hp1 HG02293.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1975A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1975 | chr16 | 71929788 | |||||
chr16:71930018
|
T | C | 1 | a0002c0002t0017 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2205T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2205 | chr16 | 71930018 | |||||
chr16:71930021
|
C | T | 15 | a0001c0001t0005a0001c0001t0007a0001c0001t0010others(12): Show | 40 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2208C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2208 | chr16 | 71930021 | |||||
chr16:71930025
|
A | G | 2 | a0001c0001t0003a0002c0003t0003 | 38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2212A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2212 | chr16 | 71930025 | |||||
chr16:71930188
|
G | A | 1 | a0001c0001t0025 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2375 | chr16 | 71930188 | |||||
chr16:71930272
|
T | C | 2 | a0001c0001t0003a0002c0003t0003 | 38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2459T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2459 | chr16 | 71930272 | |||||
chr16:71930399
|
C | T | 7 | a0001c0001t0005a0001c0001t0010a0001c0001t0025others(4): Show | 25 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2586C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2586 | chr16 | 71930399 | |||||
chr16:71930409
|
A | C | 1 | a0001c0001t0019 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2596A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2596 | chr16 | 71930409 | |||||
chr16:71930412
|
A | G | 1 | a0001c0001t0012 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2599A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2599 | chr16 | 71930412 | |||||
chr16:71930458
|
CAT | C | 7 | a0002c0002t0002a0002c0002t0016a0002c0002t0017others(4): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2646_*2647delAT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2646 | chr16 | 71930458 | |||||
chr16:71930535
|
A | T | 1 | a0002c0002t0018 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2722A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2722 | chr16 | 71930535 | |||||
chr16:71930725
|
A | G | 1 | a0003c0004t0027 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2912A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2912 | chr16 | 71930725 | |||||
chr16:71930902
|
C | T | 18 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(15): Show | 55 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3089C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 3089 | chr16 | 71930902 | |||||
chr16:71930969
|
G | T | 1 | a0001c0001t0022 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3156G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 3156 | chr16 | 71930969 | |||||
chr16:71931072
|
GTTTA | G | 7 | a0002c0002t0002a0002c0002t0016a0002c0002t0017others(4): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3263_*3266delATTT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 3263 | INFO_REALIGN_3_PRIME | chr16 | 71931072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71895675
|
G | C | 1 | a0002c0003t0028g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+86G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895675 | ||||||
chr16:71895729
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-16+140G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895729 | ||||||
chr16:71895748
|
C | T | 13 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(10): Show | 15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+159C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895748 | ||||||
chr16:71895860
|
C | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.-16+271C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895860 | ||||||
chr16:71895956
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-16+367C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895956 | ||||||
chr16:71895992
|
A | T | 2 | a0002c0002t0002g0186a0002c0002t0002g0187 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-16+403A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895992 | ||||||
chr16:71896094
|
G | C | 16 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(13): Show | 18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+505G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896094 | ||||||
chr16:71896137
|
G | T | 1 | a0003c0004t0027g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-16+548G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896137 | ||||||
chr16:71896202
|
C | A | 8 | a0002c0003t0007g0008a0002c0003t0007g0079a0002c0003t0007g0080others(5): Show | 9 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+613C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896202 | ||||||
chr16:71896230
|
G | T | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-16+641G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896230 | ||||||
chr16:71896579
|
C | G | 1 | a0001c0001t0005g0282 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+990C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896579 | ||||||
chr16:71896904
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.-16+1315A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896904 | ||||||
chr16:71896975
|
G | GA | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(256): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.-16+1397dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71896975 | |||||
chr16:71897008
|
T | C | 6 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(3): Show | 8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+1419T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897008 | ||||||
chr16:71897129
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(227): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.-16+1540C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897129 | ||||||
chr16:71897172
|
C | CT | 11 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0279others(8): Show | 11 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+1603dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71897172 | |||||
chr16:71897172
|
CT | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(201): Show | 247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.-16+1603delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71897172 | |||||
chr16:71897185
|
T | C | 1 | a0001c0001t0015g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+1596T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897185 | ||||||
chr16:71897204
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-16+1615G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897204 | ||||||
chr16:71897223
|
T | A | 1 | a0002c0005t0002g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-16+1634T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897223 | ||||||
chr16:71897223
|
T | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(172): Show | 211 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-16+1634T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897223 | ||||||
chr16:71897316
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(227): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.-16+1727G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897316 | ||||||
chr16:71897324
|
G | C | 1 | a0001c0001t0001g0023 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-16+1735G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897324 | ||||||
chr16:71897330
|
C | T | 1 | a0001c0001t0005g0282 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+1741C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897330 | ||||||
chr16:71897382
|
T | C | 1 | a0001c0001t0015g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+1793T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897382 | ||||||
chr16:71897632
|
G | A | 33 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0028others(30): Show | 38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+2043G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897632 | ||||||
chr16:71897674
|
G | A | 1 | a0001c0001t0004g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-16+2085G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897674 | ||||||
chr16:71897701
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-16+2112T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897701 | ||||||
chr16:71897903
|
C | T | 4 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057others(1): Show | 4 | HG02071.hp2 NA18941.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2314C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897903 | ||||||
chr16:71897940
|
A | G | 1 | a0001c0001t0023g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-16+2351A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897940 | ||||||
chr16:71898092
|
T | C | 18 | a0002c0002t0002g0009a0002c0002t0002g0103a0002c0002t0002g0105others(15): Show | 21 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16+2503T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898092 | ||||||
chr16:71898143
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-16+2554G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898143 | ||||||
chr16:71898152
|
A | G | 1 | a0002c0003t0028g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+2563A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898152 | ||||||
chr16:71898314
|
T | A | 1 | a0001c0001t0003g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-16+2725T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898314 | ||||||
chr16:71898370
|
G | GA | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(166): Show | 205 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.-16+2799dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898370 | |||||
chr16:71898370
|
G | GAA | 6 | a0001c0001t0003g0088a0002c0002t0002g0173a0002c0002t0002g0174others(3): Show | 6 | HG01175.hp2 HG02738.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+2798_-16+2799d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898370 | |||||
chr16:71898432
|
C | G | 16 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(13): Show | 18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+2843C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898432 | ||||||
chr16:71898441
|
T | C | 1 | a0001c0001t0022g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-16+2852T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898441 | ||||||
chr16:71898534
|
A | G | 1 | a0002c0003t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-16+2945A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898534 | ||||||
chr16:71898626
|
A | G | 8 | a0002c0003t0007g0008a0002c0003t0007g0079a0002c0003t0007g0080others(5): Show | 9 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+3037A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898626 | ||||||
chr16:71898662
|
TA | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(252): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-16+3089delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898662 | |||||
chr16:71898674
|
A | C | 1 | a0002c0003t0028g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+3085A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898674 | ||||||
chr16:71898681
|
A | T | 1 | a0002c0003t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-16+3092A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898681 | ||||||
chr16:71898736
|
T | A | 1 | a0003c0004t0006g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-16+3147T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898736 | ||||||
chr16:71898771
|
G | A | 6 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(3): Show | 6 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+3182G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898771 | ||||||
chr16:71898808
|
C | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG03017.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-16+3219C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898808 | ||||||
chr16:71898834
|
G | A | 1 | a0001c0001t0015g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+3245G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898834 | ||||||
chr16:71898897
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-16+3308G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898897 | ||||||
chr16:71898964
|
CA | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(263): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-16+3394delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898964 | |||||
chr16:71898964
|
CAA | C | 7 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0259others(4): Show | 7 | HG01256.hp1 HG01891.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+3393_-16+3394d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898964 | |||||
chr16:71898980
|
A | C | 2 | a0001c0001t0001g0255a0001c0001t0015g0188 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+3391A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898980 | ||||||
chr16:71899084
|
C | A | 1 | a0002c0003t0028g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+3495C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899084 | ||||||
chr16:71899188
|
T | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(231): Show | 278 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.-16+3599T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899188 | ||||||
chr16:71899310
|
G | A | 1 | a0003c0004t0027g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-16+3721G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899310 | ||||||
chr16:71899349
|
C | T | 1 | a0002c0002t0002g0145 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-16+3760C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899349 | ||||||
chr16:71899542
|
A | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(297): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-16+3953A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899542 | ||||||
chr16:71899744
|
C | G | 3 | a0001c0001t0004g0013a0001c0001t0004g0052a0001c0001t0030g0013 | 3 | HG00099.hp1 HG00639.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-16+4155C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899744 | ||||||
chr16:71899913
|
C | T | 2 | a0002c0003t0001g0263a0002c0003t0001g0278 | 2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-16+4324C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899913 | ||||||
chr16:71899915
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-16+4326C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899915 | ||||||
chr16:71899938
|
A | G | 1 | a0002c0003t0001g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-16+4349A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899938 | ||||||
chr16:71899980
|
G | C | 1 | a0002c0003t0020g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-16+4391G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899980 | ||||||
chr16:71899996
|
C | CA | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.-16+4427dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71899996 | |||||
chr16:71899996
|
C | CAA | 16 | a0001c0001t0001g0191a0001c0001t0001g0199a0001c0001t0001g0200others(13): Show | 16 | HG01175.hp1 HG02027.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-16+4426_-16+4427d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71899996 | |||||
chr16:71900166
|
C | CA | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(167): Show | 206 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.-16+4592dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900166 | |||||
chr16:71900166
|
CA | C | 19 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(16): Show | 21 | HG01109.hp1 HG01515.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-16+4592delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900166 | |||||
chr16:71900202
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.-16+4613C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900202 | ||||||
chr16:71900230
|
G | A | 5 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+4641G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900230 | ||||||
chr16:71900327
|
C | CT | 78 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0031others(75): Show | 92 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-16+4761dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | |||||
chr16:71900327
|
C | CTT | 27 | a0001c0001t0001g0189a0001c0001t0001g0198a0001c0001t0001g0247others(24): Show | 31 | HG00438.hp1 HG00738.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.-16+4760_-16+4761d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | |||||
chr16:71900327
|
CT | C | 60 | a0001c0001t0001g0124a0001c0001t0001g0204a0001c0001t0001g0264others(57): Show | 75 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-16+4761delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | |||||
chr16:71900327
|
CTTTTTTT others(5): Show |
C | 38 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(35): Show | 41 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.-16+4750_-16+4761d others(14): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | |||||
chr16:71900516
|
A | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.-16+4927A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900516 | ||||||
chr16:71900524
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-16+4935G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900524 | ||||||
chr16:71900566
|
G | C | 6 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(3): Show | 8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+4977G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900566 | ||||||
chr16:71900673
|
A | ATT | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(259): Show | 308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-16+5085_-16+5086i others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900673 | |||||
chr16:71900673
|
A | T | 1 | a0001c0001t0015g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+5084A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900673 | ||||||
chr16:71900695
|
G | A | 1 | a0002c0002t0002g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-16+5106G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900695 | ||||||
chr16:71900748
|
T | C | 1 | a0001c0001t0005g0282 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+5159T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900748 | ||||||
chr16:71900790
|
C | T | 5 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+5201C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900790 | ||||||
chr16:71901307
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(226): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.-16+5718G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901307 | ||||||
chr16:71901434
|
C | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0195a0001c0001t0001g0196others(5): Show | 9 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+5845C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901434 | ||||||
chr16:71901435
|
G | T | 1 | a0001c0001t0001g0198 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-16+5846G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901435 | ||||||
chr16:71901511
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-16+5922C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901511 | ||||||
chr16:71901529
|
A | T | 6 | a0002c0003t0003g0016a0002c0003t0003g0093a0002c0003t0003g0095others(3): Show | 7 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+5940A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901529 | ||||||
chr16:71901562
|
G | C | 20 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(17): Show | 23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-16+5973G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901562 | ||||||
chr16:71901636
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-16+6047C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901636 | ||||||
chr16:71901691
|
T | C | 3 | a0001c0001t0022g0148a0001c0001t0023g0168a0002c0003t0028g0030 | 3 | HG01891.hp2 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-16+6102T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901691 | ||||||
chr16:71901698
|
G | T | 1 | a0002c0003t0028g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+6109G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901698 | ||||||
chr16:71901919
|
A | G | 1 | a0001c0001t0011g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+6330A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901919 | ||||||
chr16:71902126
|
A | G | 2 | a0002c0002t0002g0009a0002c0002t0002g0108 | 4 | HG02523.hp1 NA18948.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+6537A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902126 | ||||||
chr16:71902246
|
T | C | 1 | a0002c0002t0002g0116 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-16+6657T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902246 | ||||||
chr16:71902271
|
T | G | 3 | a0001c0001t0005g0150a0001c0001t0005g0151a0001c0001t0024g0152 | 3 | HG00609.hp1 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-16+6682T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902271 | ||||||
chr16:71902339
|
G | A | 4 | a0001c0001t0003g0285a0001c0001t0003g0286a0001c0001t0003g0289others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+6750G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902339 | ||||||
chr16:71902350
|
A | G | 70 | a0001c0001t0001g0124a0002c0002t0002g0002a0002c0002t0002g0003others(67): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-16+6761A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902350 | ||||||
chr16:71902476
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+6887G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902476 | ||||||
chr16:71902540
|
G | T | 1 | a0003c0004t0027g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-16+6951G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902540 | ||||||
chr16:71902559
|
C | T | 1 | a0001c0001t0005g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-16+6970C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902559 | ||||||
chr16:71902571
|
A | T | 4 | a0001c0001t0005g0150a0001c0001t0005g0151a0001c0001t0005g0166others(1): Show | 4 | HG00609.hp1 NA18964.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+6982A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902571 | ||||||
chr16:71902578
|
A | G | 16 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(13): Show | 18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+6989A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902578 | ||||||
chr16:71902678
|
G | T | 1 | a0001c0001t0005g0282 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+7089G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902678 | ||||||
chr16:71902743
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0226 | 3 | HG00741.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-16+7154C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902743 | ||||||
chr16:71902830
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(173): Show | 212 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-16+7241A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902830 | ||||||
chr16:71903028
|
T | A | 10 | a0003c0004t0006g0007a0003c0004t0006g0064a0003c0004t0006g0066others(7): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-16+7439T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903028 | ||||||
chr16:71903332
|
C | T | 2 | a0002c0003t0007g0081a0002c0003t0029g0082 | 2 | HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-16+7743C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903332 | ||||||
chr16:71903370
|
T | A | 146 | a0001c0001t0001g0124a0001c0001t0003g0014a0001c0001t0003g0015others(143): Show | 171 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-16+7781T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903370 | ||||||
chr16:71903372
|
T | A | 1 | a0002c0002t0002g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-16+7783T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903372 | ||||||
chr16:71903381
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-16+7792G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903381 | ||||||
chr16:71903593
|
C | T | 1 | a0002c0002t0002g0108 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-16+8004C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903593 | ||||||
chr16:71903652
|
G | A | 1 | a0002c0002t0002g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-16+8063G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903652 | ||||||
chr16:71903819
|
G | C | 1 | a0002c0003t0001g0230 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-16+8230G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903819 | ||||||
chr16:71904014
|
T | A | 3 | a0001c0001t0005g0167a0001c0001t0025g0154a0002c0003t0005g0153 | 3 | HG04204.hp1 NA18971.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-16+8425T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904014 | ||||||
chr16:71904211
|
C | T | 1 | a0002c0002t0002g0135 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-16+8622C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904211 | ||||||
chr16:71904421
|
C | T | 1 | a0001c0001t0025g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-16+8832C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904421 | ||||||
chr16:71904423
|
G | A | 1 | a0002c0002t0002g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-16+8834G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904423 | ||||||
chr16:71904438
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-16+8849G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904438 | ||||||
chr16:71904469
|
C | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-16+8880C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904469 | ||||||
chr16:71904539
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(225): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-16+8950G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904539 | ||||||
chr16:71904684
|
C | T | 2 | a0001c0001t0003g0292a0001c0001t0003g0293 | 2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+9095C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904684 | ||||||
chr16:71904743
|
C | G | 1 | a0001c0001t0004g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-16+9154C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904743 | ||||||
chr16:71904926
|
T | C | 1 | a0002c0002t0002g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-16+9337T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904926 | ||||||
chr16:71904936
|
G | A | 1 | a0002c0003t0005g0153 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-16+9347G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904936 | ||||||
chr16:71905007
|
T | A | 3 | a0001c0001t0001g0208a0002c0003t0001g0263a0002c0003t0001g0278 | 3 | HG01981.hp1 HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-16+9418T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905007 | ||||||
chr16:71905163
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-16+9574G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905163 | ||||||
chr16:71905251
|
G | T | 5 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+9662G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905251 | ||||||
chr16:71905292
|
C | T | 5 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(2): Show | 5 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+9703C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905292 | ||||||
chr16:71905333
|
C | T | 1 | a0002c0002t0002g0135 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-16+9744C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905333 | ||||||
chr16:71905402
|
C | CAG | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.-16+9814_-16+9815d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71905402 | |||||
chr16:71905410
|
C | G | 1 | a0002c0003t0005g0153 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-16+9821C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905410 | ||||||
chr16:71905417
|
T | A | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-16+9828T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905417 | ||||||
chr16:71905610
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-15-10016C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905610 | ||||||
chr16:71905778
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-15-9848C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905778 | ||||||
chr16:71905892
|
A | T | 1 | a0001c0001t0005g0165 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-15-9734A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905892 | ||||||
chr16:71905958
|
C | G | 1 | a0002c0003t0028g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15-9668C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905958 | ||||||
chr16:71906002
|
C | CT | 11 | a0001c0001t0001g0036a0001c0001t0001g0249a0001c0001t0003g0014others(8): Show | 13 | HG00738.hp1 HG01496.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15-9606dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71906002 | |||||
chr16:71906002
|
C | CTT | 70 | a0001c0001t0001g0124a0001c0001t0001g0245a0002c0002t0002g0002others(67): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15-9607_-15-9606d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71906002 | |||||
chr16:71906053
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-15-9573G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906053 | ||||||
chr16:71906108
|
A | T | 1 | a0001c0001t0003g0087 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-15-9518A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906108 | ||||||
chr16:71906128
|
C | G | 1 | a0002c0003t0008g0225 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-15-9498C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906128 | ||||||
chr16:71906128
|
C | T | 1 | a0002c0002t0002g0135 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-15-9498C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906128 | ||||||
chr16:71906144
|
C | T | 1 | a0001c0001t0022g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15-9482C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906144 | ||||||
chr16:71906161
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-15-9465G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906161 | ||||||
chr16:71906193
|
C | T | 2 | a0002c0002t0002g0186a0002c0002t0002g0187 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-15-9433C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906193 | ||||||
chr16:71906348
|
C | T | 6 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(3): Show | 8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-9278C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906348 | ||||||
chr16:71906411
|
G | C | 2 | a0002c0002t0002g0121a0002c0002t0002g0176 | 2 | NA18983.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-15-9215G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906411 | ||||||
chr16:71906922
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(259): Show | 308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-15-8704T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906922 | ||||||
chr16:71907037
|
A | T | 1 | a0002c0003t0001g0044 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-15-8589A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907037 | ||||||
chr16:71907187
|
CT | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(199): Show | 243 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-15-8425delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71907187 | |||||
chr16:71907187
|
CTT | C | 6 | a0001c0001t0001g0210a0001c0001t0001g0231a0001c0001t0001g0280others(3): Show | 6 | HG03490.hp2 NA18950.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-8426_-15-8425d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71907187 | |||||
chr16:71907280
|
A | AT | 38 | a0001c0001t0001g0062a0001c0001t0001g0244a0001c0001t0003g0014others(35): Show | 43 | HG00738.hp1 HG01081.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.-15-8331dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71907280 | |||||
chr16:71907356
|
C | T | 54 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(51): Show | 59 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.-15-8270C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907356 | ||||||
chr16:71907379
|
G | A | 6 | a0002c0002t0002g0115a0002c0002t0002g0120a0002c0002t0002g0122others(3): Show | 6 | HG02698.hp1 HG02735.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-8247G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907379 | ||||||
chr16:71907523
|
C | T | 4 | a0001c0001t0003g0029a0001c0001t0003g0284a0001c0001t0003g0287others(1): Show | 5 | HG02109.hp1 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-8103C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907523 | ||||||
chr16:71907554
|
G | T | 3 | a0001c0001t0004g0013a0001c0001t0004g0052a0001c0001t0030g0013 | 3 | HG00099.hp1 HG00639.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-15-8072G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907554 | ||||||
chr16:71907563
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-15-8063C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907563 | ||||||
chr16:71907733
|
T | A | 6 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(3): Show | 6 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-7893T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907733 | ||||||
chr16:71907795
|
A | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-7831A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907795 | ||||||
chr16:71907847
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-15-7779C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907847 | ||||||
chr16:71907883
|
G | A | 16 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(13): Show | 18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15-7743G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907883 | ||||||
chr16:71907896
|
C | G | 16 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(13): Show | 18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15-7730C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907896 | ||||||
chr16:71907965
|
A | T | 1 | a0002c0003t0007g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15-7661A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907965 | ||||||
chr16:71907966
|
G | T | 1 | a0002c0003t0007g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15-7660G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907966 | ||||||
chr16:71907994
|
G | A | 1 | a0002c0002t0002g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-15-7632G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907994 | ||||||
chr16:71908005
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-15-7621T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908005 | ||||||
chr16:71908009
|
A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(205): Show | 249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.-15-7617A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908009 | ||||||
chr16:71908027
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-15-7599G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908027 | ||||||
chr16:71908051
|
T | G | 1 | a0002c0003t0020g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-7575T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908051 | ||||||
chr16:71908126
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15-7500T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908126 | ||||||
chr16:71908158
|
G | A | 1 | a0002c0003t0020g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-7468G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908158 | ||||||
chr16:71908296
|
C | CT | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(65): Show | 87 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-15-7308dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | |||||
chr16:71908296
|
C | CTT | 138 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0124others(135): Show | 163 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-15-7309_-15-7308d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | |||||
chr16:71908296
|
C | CTTT | 20 | a0001c0001t0001g0194a0001c0001t0001g0223a0001c0001t0001g0224others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-7310_-15-7308d others(5): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | |||||
chr16:71908296
|
C | CTTTT | 32 | a0001c0001t0001g0241a0001c0001t0005g0019a0001c0001t0005g0021others(29): Show | 35 | HG00140.hp1 HG00423.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-15-7311_-15-7308d others(6): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | |||||
chr16:71908296
|
C | CTTTTT | 7 | a0001c0001t0005g0151a0001c0001t0005g0163a0001c0001t0005g0164others(4): Show | 7 | HG00609.hp1 HG00733.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-7312_-15-7308d others(7): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | |||||
chr16:71908296
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0007t0001g0053 | 4 | HG02055.hp2 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-7318_-15-7308d others(13): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | |||||
chr16:71908328
|
C | G | 1 | a0002c0003t0007g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15-7298C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908328 | ||||||
chr16:71908373
|
C | A | 1 | a0001c0001t0022g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15-7253C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908373 | ||||||
chr16:71908403
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-15-7223G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908403 | ||||||
chr16:71908527
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-15-7099C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908527 | ||||||
chr16:71908536
|
C | T | 33 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0028others(30): Show | 38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-7090C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908536 | ||||||
chr16:71908685
|
A | C | 13 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(10): Show | 15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15-6941A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908685 | ||||||
chr16:71908711
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15-6915T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908711 | ||||||
chr16:71908746
|
G | T | 7 | a0002c0002t0002g0003a0002c0002t0002g0113a0002c0002t0002g0114others(4): Show | 11 | NA18949.hp2 NA18951.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-6880G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908746 | ||||||
chr16:71909095
|
C | CT | 40 | a0001c0001t0001g0062a0001c0001t0001g0255a0001c0001t0003g0028others(37): Show | 44 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-15-6511dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | |||||
chr16:71909095
|
C | CTT | 25 | a0001c0001t0001g0023a0001c0001t0001g0191a0001c0001t0001g0203others(22): Show | 28 | HG00738.hp1 HG01433.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.-15-6512_-15-6511d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | |||||
chr16:71909095
|
C | CTTTT | 71 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(68): Show | 90 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-15-6514_-15-6511d others(6): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | |||||
chr16:71909095
|
C | CTTTTT | 15 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0001g0206others(12): Show | 15 | HG00609.hp2 HG00741.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15-6515_-15-6511d others(7): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | |||||
chr16:71909204
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-6422T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909204 | ||||||
chr16:71909266
|
G | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-6360G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909266 | ||||||
chr16:71909355
|
C | T | 2 | a0002c0002t0002g0131a0002c0002t0002g0182 | 2 | NA18946.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-15-6271C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909355 | ||||||
chr16:71909406
|
C | T | 36 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(33): Show | 39 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15-6220C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909406 | ||||||
chr16:71909511
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(259): Show | 308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-15-6115C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909511 | ||||||
chr16:71909608
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-6018A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909608 | ||||||
chr16:71909653
|
A | G | 69 | a0001c0001t0001g0124a0002c0002t0002g0002a0002c0002t0002g0003others(66): Show | 85 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-15-5973A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909653 | ||||||
chr16:71909691
|
C | T | 33 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0028others(30): Show | 38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-5935C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909691 | ||||||
chr16:71909878
|
C | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-15-5748C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909878 | ||||||
chr16:71909965
|
C | T | 7 | a0002c0002t0002g0115a0002c0002t0002g0120a0002c0002t0002g0122others(4): Show | 7 | HG02165.hp1 HG02698.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-5661C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909965 | ||||||
chr16:71910037
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-5589T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910037 | ||||||
chr16:71910044
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-15-5582A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910044 | ||||||
chr16:71910094
|
T | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0191a0001c0001t0001g0203others(12): Show | 16 | HG01433.hp1 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15-5532T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910094 | ||||||
chr16:71910124
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-15-5502G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910124 | ||||||
chr16:71910168
|
G | A | 10 | a0003c0004t0006g0007a0003c0004t0006g0064a0003c0004t0006g0066others(7): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15-5458G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910168 | ||||||
chr16:71910322
|
A | G | 3 | a0003c0004t0006g0064a0003c0004t0006g0068a0003c0004t0027g0077 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15-5304A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910322 | ||||||
chr16:71910377
|
C | T | 1 | a0001c0001t0022g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15-5249C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910377 | ||||||
chr16:71910561
|
G | T | 1 | a0002c0002t0002g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-15-5065G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910561 | ||||||
chr16:71910565
|
C | T | 1 | a0002c0003t0007g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-15-5061C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910565 | ||||||
chr16:71910605
|
C | CA | 35 | a0001c0001t0003g0285a0001c0001t0005g0019a0001c0001t0005g0021others(32): Show | 38 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-5008dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71910605 | |||||
chr16:71910763
|
A | T | 10 | a0003c0004t0006g0007a0003c0004t0006g0064a0003c0004t0006g0066others(7): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15-4863A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910763 | ||||||
chr16:71910828
|
GA | G | 20 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(17): Show | 23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-4794delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71910828 | |||||
chr16:71910943
|
T | G | 1 | a0002c0002t0002g0147 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-15-4683T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910943 | ||||||
chr16:71910989
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-4637A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910989 | ||||||
chr16:71911008
|
G | A | 3 | a0001c0001t0004g0032a0001c0001t0004g0045a0001c0001t0004g0060 | 3 | HG00642.hp1 HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-15-4618G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911008 | ||||||
chr16:71911045
|
G | T | 1 | a0001c0001t0001g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15-4581G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911045 | ||||||
chr16:71911069
|
G | A | 4 | a0001c0001t0001g0062a0002c0002t0002g0022a0002c0002t0002g0140others(1): Show | 5 | HG03098.hp1 NA18943.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-4557G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911069 | ||||||
chr16:71911089
|
A | G | 1 | a0003c0004t0006g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15-4537A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911089 | ||||||
chr16:71911219
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15-4407T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911219 | ||||||
chr16:71911264
|
C | T | 1 | a0002c0003t0020g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-4362C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911264 | ||||||
chr16:71911344
|
A | T | 1 | a0001c0001t0005g0164 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-15-4282A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911344 | ||||||
chr16:71911358
|
T | A | 2 | a0002c0002t0002g0142a0002c0002t0002g0173 | 2 | NA19072.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-15-4268T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911358 | ||||||
chr16:71911358
|
T | TA | 249 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(246): Show | 295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.-15-4260dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911358 | |||||
chr16:71911366
|
A | AC | 6 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(3): Show | 6 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-4259dupC | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911366 | |||||
chr16:71911375
|
A | G | 38 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(35): Show | 41 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.-15-4251A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911375 | ||||||
chr16:71911438
|
C | G | 20 | a0001c0001t0004g0005a0001c0001t0004g0012a0001c0001t0004g0032others(17): Show | 23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-4188C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911438 | ||||||
chr16:71911710
|
A | AT | 8 | a0001c0001t0001g0036a0001c0001t0003g0085a0001c0001t0003g0089others(5): Show | 8 | HG00735.hp1 HG01361.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-3892dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | |||||
chr16:71911710
|
AT | A | 31 | a0001c0001t0001g0062a0001c0001t0001g0237a0001c0001t0001g0255others(28): Show | 35 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15-3892delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | |||||
chr16:71911710
|
ATT | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(197): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.-15-3893_-15-3892d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | |||||
chr16:71911710
|
ATTT | A | 6 | a0001c0001t0001g0254a0001c0001t0001g0259a0001c0001t0005g0157others(3): Show | 6 | HG00639.hp1 HG01169.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3894_-15-3892d others(5): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | |||||
chr16:71911874
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-15-3752G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911874 | ||||||
chr16:71911944
|
G | C | 53 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(50): Show | 58 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15-3682G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911944 | ||||||
chr16:71912000
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-15-3626C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912000 | ||||||
chr16:71912214
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-15-3412T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912214 | ||||||
chr16:71912486
|
C | G | 20 | a0001c0001t0004g0005a0001c0001t0004g0012a0001c0001t0004g0032others(17): Show | 23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-3140C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912486 | ||||||
chr16:71912526
|
C | T | 5 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-3100C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912526 | ||||||
chr16:71912635
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-15-2991A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912635 | ||||||
chr16:71912647
|
G | A | 4 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057others(1): Show | 4 | HG02071.hp2 NA18941.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-2979G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912647 | ||||||
chr16:71912775
|
G | A | 1 | a0002c0002t0002g0116 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-15-2851G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912775 | ||||||
chr16:71913278
|
C | CT | 17 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(14): Show | 19 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15-2337dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71913278 | |||||
chr16:71913388
|
T | C | 1 | a0001c0001t0004g0060 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-15-2238T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913388 | ||||||
chr16:71913435
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15-2191C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913435 | ||||||
chr16:71913777
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-15-1849A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913777 | ||||||
chr16:71913831
|
G | A | 37 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(34): Show | 40 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-15-1795G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913831 | ||||||
chr16:71913894
|
C | T | 3 | a0001c0001t0022g0148a0001c0001t0023g0168a0002c0003t0028g0030 | 3 | HG01891.hp2 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-15-1732C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913894 | ||||||
chr16:71913965
|
C | T | 20 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(17): Show | 23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-1661C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913965 | ||||||
chr16:71914100
|
G | A | 70 | a0001c0010t0001g0220a0002c0002t0002g0002a0002c0002t0002g0003others(67): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15-1526G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914100 | ||||||
chr16:71914115
|
G | GTTGT | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-1505_-15-1502d others(6): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71914115 | |||||
chr16:71914138
|
A | G | 20 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(17): Show | 23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-1488A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914138 | ||||||
chr16:71914140
|
T | C | 70 | a0001c0010t0001g0220a0002c0002t0002g0002a0002c0002t0002g0003others(67): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15-1486T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914140 | ||||||
chr16:71914170
|
C | CT | 18 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(15): Show | 20 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1440dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71914170 | |||||
chr16:71914392
|
C | T | 1 | a0001c0001t0004g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15-1234C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914392 | ||||||
chr16:71914452
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-1174A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914452 | ||||||
chr16:71914582
|
G | C | 1 | a0001c0001t0004g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15-1044G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914582 | ||||||
chr16:71914731
|
T | C | 1 | a0002c0002t0002g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-15-895T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914731 | ||||||
chr16:71914990
|
T | C | 5 | a0002c0002t0002g0106a0002c0005t0002g0017a0002c0005t0002g0101others(2): Show | 6 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-636T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914990 | ||||||
chr16:71915260
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(102): Show | 125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-15-366C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915260 | ||||||
chr16:71915363
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(172): Show | 211 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-15-263C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915363 | ||||||
chr16:71915387
|
C | G | 1 | a0002c0002t0002g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-15-239C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915387 | ||||||
chr16:71915538
|
T | A | 6 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(3): Show | 6 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-88T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915538 | ||||||
chr16:71915951
|
C | T | 1 | a0001c0001t0008g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.88+223C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71915951 | ||||||
chr16:71916127
|
C | T | 1 | a0002c0002t0002g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.89-335C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916127 | ||||||
chr16:71916298
|
A | G | 25 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(22): Show | 27 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-164A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916298 | ||||||
chr16:71916390
|
G | A | 32 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(29): Show | 35 | HG00140.hp1 HG01074.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.89-72G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916390 | ||||||
chr16:71916390
|
G | C | 1 | a0002c0003t0001g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.89-72G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916390 | ||||||
chr16:71916419
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.89-43A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916419 | ||||||
chr16:71916736
|
C | CCCAA | 6 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(3): Show | 6 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+95_269+98dupCC others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 71916736 | |||||
chr16:71916989
|
G | A | 13 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(10): Show | 15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.270-58G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 3/9 | chr16 | 71916989 | ||||||
chr16:71917191
|
G | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(98): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.357+57G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917191 | ||||||
chr16:71917194
|
A | G | 1 | a0002c0002t0002g0187 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.357+60A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917194 | ||||||
chr16:71917205
|
C | A | 1 | a0002c0002t0002g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.357+71C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917205 | ||||||
chr16:71917303
|
T | TAGAAC | 3 | a0001c0001t0001g0212a0001c0001t0001g0233a0001c0001t0001g0254 | 3 | HG00140.hp2 HG02735.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.357+172_357+176dup others(5): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 71917303 | |||||
chr16:71917345
|
A | C | 13 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(10): Show | 15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.357+211A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917345 | ||||||
chr16:71917454
|
G | C | 5 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.357+320G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917454 | ||||||
chr16:71917454
|
G | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0191a0001c0001t0001g0203others(11): Show | 15 | HG01433.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.357+320G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917454 | ||||||
chr16:71917638
|
G | C | 1 | a0001c0001t0001g0234 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.357+504G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917638 | ||||||
chr16:71917942
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(189): Show | 230 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.357+808A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917942 | ||||||
chr16:71917969
|
T | C | 4 | a0002c0003t0001g0230a0002c0003t0001g0235a0002c0003t0001g0263others(1): Show | 4 | HG01243.hp1 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+835T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917969 | ||||||
chr16:71918014
|
G | A | 4 | a0001c0001t0004g0012a0001c0001t0004g0043a0001c0001t0004g0049others(1): Show | 5 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+880G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918014 | ||||||
chr16:71918041
|
G | C | 1 | a0005c0008t0001g0243 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.357+907G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918041 | ||||||
chr16:71918214
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.357+1080A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918214 | ||||||
chr16:71918340
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0222a0001c0001t0019g0201 | 4 | HG00408.hp1 HG02027.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+1206A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918340 | ||||||
chr16:71918417
|
CT | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.357+1300delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 71918417 | |||||
chr16:71918451
|
G | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(225): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.357+1317G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918451 | ||||||
chr16:71918606
|
C | T | 23 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(20): Show | 25 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.357+1472C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918606 | ||||||
chr16:71918668
|
G | A | 1 | a0001c0001t0004g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.357+1534G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918668 | ||||||
chr16:71918711
|
G | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(253): Show | 302 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.357+1577G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918711 | ||||||
chr16:71918828
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.357+1694C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918828 | ||||||
chr16:71919119
|
G | A | 50 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(47): Show | 55 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.358-1620G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919119 | ||||||
chr16:71919153
|
G | C | 1 | a0001c0001t0023g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1586G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919153 | ||||||
chr16:71919226
|
T | G | 1 | a0001c0001t0001g0244 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.358-1513T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919226 | ||||||
chr16:71919334
|
GTTTTC | G | 37 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(34): Show | 40 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.358-1399_358-1395d others(7): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 71919334 | |||||
chr16:71919404
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-1335G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919404 | ||||||
chr16:71919446
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358-1293C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919446 | ||||||
chr16:71919468
|
C | T | 1 | a0002c0002t0002g0107 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.358-1271C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919468 | ||||||
chr16:71919722
|
C | T | 2 | a0001c0001t0012g0065a0001c0001t0012g0073 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.358-1017C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919722 | ||||||
chr16:71919819
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.358-920T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919819 | ||||||
chr16:71919938
|
T | G | 13 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(10): Show | 15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.358-801T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919938 | ||||||
chr16:71919981
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.358-758G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919981 | ||||||
chr16:71920257
|
A | C | 1 | a0001c0001t0003g0015 | 2 | HG00738.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.358-482A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920257 | ||||||
chr16:71920310
|
A | G | 1 | a0002c0002t0002g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.358-429A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920310 | ||||||
chr16:71920416
|
CAA | C | 13 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(10): Show | 15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.358-322_358-321del others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920416 | ||||||
chr16:71920433
|
A | G | 2 | a0001c0001t0005g0157a0001c0001t0005g0160 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.358-306A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920433 | ||||||
chr16:71920545
|
C | A | 2 | a0001c0001t0003g0094a0001c0001t0003g0100 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.358-194C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920545 | ||||||
chr16:71920547
|
C | T | 5 | a0001c0001t0011g0072a0001c0001t0011g0074a0001c0001t0011g0075others(2): Show | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-192C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920547 | ||||||
chr16:71920630
|
G | A | 1 | a0001c0001t0023g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-109G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920630 | ||||||
chr16:71920880
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.441+58C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71920880 | ||||||
chr16:71920922
|
G | T | 9 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(6): Show | 12 | HG00738.hp1 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+100G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71920922 | ||||||
chr16:71920978
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0202others(1): Show | 4 | HG02071.hp1 HG02165.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+156C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71920978 | ||||||
chr16:71921182
|
C | T | 70 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0009others(67): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.442-161C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71921182 | ||||||
chr16:71921336
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19086.hp1 | splice_region_variant&intron_variant | LOW | c.442-7C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71921336 | ||||||
chr16:71921497
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(189): Show | 230 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.552+44T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921497 | ||||||
chr16:71921523
|
C | CAT | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.552+71_552+72dupAT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 71921523 | |||||
chr16:71921769
|
C | G | 1 | a0001c0001t0022g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.552+316C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921769 | ||||||
chr16:71921892
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.552+439C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921892 | ||||||
chr16:71921954
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.552+501G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921954 | ||||||
chr16:71921980
|
A | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0202others(1): Show | 4 | HG02071.hp1 HG02165.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-494A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921980 | ||||||
chr16:71922187
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.553-287G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71922187 | ||||||
chr16:71922685
|
GTATA | G | 73 | a0001c0001t0001g0255a0001c0001t0015g0188a0002c0002t0002g0002others(70): Show | 89 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+10_759+13delTA others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr16 | 71922685 | |||||
chr16:71922689
|
A | AAGTGTG | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(101): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+9_759+10insAGT others(3): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922689 | ||||||
chr16:71922690
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(101): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+10T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922690 | ||||||
chr16:71922693
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(101): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+13A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922693 | ||||||
chr16:71922694
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(101): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+14A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922694 | ||||||
chr16:71922800
|
A | G | 1 | a0002c0002t0002g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.759+120A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922800 | ||||||
chr16:71922831
|
C | G | 3 | a0001c0001t0010g0020a0001c0001t0010g0155a0002c0003t0010g0020 | 3 | HG01358.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.759+151C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922831 | ||||||
chr16:71923068
|
G | T | 1 | a0001c0001t0023g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.760-220G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71923068 | ||||||
chr16:71923578
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.852+198A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923578 | ||||||
chr16:71923784
|
AGATT | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0218 | 3 | HG02615.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.852+408_852+411del others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 71923784 | |||||
chr16:71923821
|
G | A | 1 | a0005c0008t0001g0243 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.852+441G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923821 | ||||||
chr16:71923822
|
C | A | 1 | a0005c0008t0001g0243 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.852+442C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923822 | ||||||
chr16:71923823
|
C | T | 2 | a0002c0002t0002g0105a0002c0002t0002g0111 | 2 | NA18959.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.852+443C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923823 | ||||||
chr16:71923850
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.852+470T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923850 | ||||||
chr16:71924020
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.852+640A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924020 | ||||||
chr16:71924040
|
T | G | 6 | a0002c0003t0003g0016a0002c0003t0003g0093a0002c0003t0003g0095others(3): Show | 7 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+660T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924040 | ||||||
chr16:71924122
|
C | G | 18 | a0001c0001t0004g0005a0001c0001t0004g0012a0001c0001t0004g0032others(15): Show | 21 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.853-647C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924122 | ||||||
chr16:71924149
|
A | G | 54 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(51): Show | 59 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.853-620A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924149 | ||||||
chr16:71924205
|
C | T | 6 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0084others(3): Show | 8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-564C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924205 | ||||||
chr16:71924336
|
G | A | 13 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(10): Show | 15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.853-433G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924336 | ||||||
chr16:71924543
|
A | G | 1 | a0001c0001t0023g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.853-226A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924543 | ||||||
chr16:71924662
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.853-107G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924662 | ||||||
chr16:71924861
|
C | G | 1 | a0001c0001t0004g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.901+44C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924861 | ||||||
chr16:71924863
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.901+46T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924863 | ||||||
chr16:71924877
|
A | G | 1 | a0001c0001t0004g0045 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.901+60A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924877 | ||||||
chr16:71924942
|
T | C | 1 | a0002c0002t0002g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.901+125T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924942 | ||||||
chr16:71925011
|
A | AT | 37 | a0001c0001t0001g0031a0001c0001t0001g0200a0001c0001t0001g0261others(34): Show | 40 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.901+213dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925011 | |||||
chr16:71925011
|
AT | A | 10 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(7): Show | 10 | HG00099.hp2 HG01496.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.901+213delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925011 | |||||
chr16:71925052
|
G | T | 1 | a0001c0001t0001g0266 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.901+235G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925052 | ||||||
chr16:71925059
|
C | T | 1 | a0002c0003t0028g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.901+242C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925059 | ||||||
chr16:71925096
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.901+279T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925096 | ||||||
chr16:71925097
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.901+280C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925097 | ||||||
chr16:71925111
|
C | T | 1 | a0002c0002t0002g0281 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.901+294C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925111 | ||||||
chr16:71925175
|
G | C | 35 | a0001c0001t0005g0019a0001c0001t0005g0021a0001c0001t0005g0149others(32): Show | 38 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.901+358G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925175 | ||||||
chr16:71925215
|
G | A | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.901+398G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925215 | ||||||
chr16:71925284
|
G | T | 1 | a0002c0002t0002g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.901+467G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925284 | ||||||
chr16:71925316
|
A | AT | 15 | a0001c0001t0001g0272a0001c0001t0003g0291a0001c0001t0004g0034others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.901+517dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925316 | |||||
chr16:71925316
|
A | ATT | 14 | a0001c0001t0001g0023a0001c0001t0001g0191a0001c0001t0001g0203others(11): Show | 15 | HG01433.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.901+516_901+517dup others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925316 | |||||
chr16:71925339
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.901+522C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925339 | ||||||
chr16:71925410
|
G | A | 1 | a0002c0003t0001g0252 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901+593G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925410 | ||||||
chr16:71925497
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.901+680G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925497 | ||||||
chr16:71925699
|
TGTA | T | 33 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0028others(30): Show | 38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.901+883_901+885del others(3): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925699 | ||||||
chr16:71925748
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.901+931A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925748 | ||||||
chr16:71925758
|
G | A | 9 | a0002c0003t0007g0008a0002c0003t0007g0079a0002c0003t0007g0080others(6): Show | 10 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.901+941G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925758 | ||||||
chr16:71925776
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.901+959C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925776 | ||||||
chr16:71925824
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(230): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.901+1007A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925824 | ||||||
chr16:71925830
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.901+1013T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925830 | ||||||
chr16:71925845
|
C | T | 73 | a0001c0001t0004g0056a0001c0001t0004g0057a0002c0002t0002g0002others(70): Show | 89 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.901+1028C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925845 | ||||||
chr16:71925907
|
T | C | 1 | a0001c0010t0001g0220 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.901+1090T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925907 | ||||||
chr16:71925908
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.901+1091G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925908 | ||||||
chr16:71925948
|
A | T | 1 | a0002c0002t0002g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.901+1131A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925948 | ||||||
chr16:71926154
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.901+1337C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926154 | ||||||
chr16:71926214
|
G | A | 1 | a0002c0003t0020g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.901+1397G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926214 | ||||||
chr16:71926329
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0200a0001c0001t0001g0261others(1): Show | 4 | HG00438.hp2 NA18955.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-1285T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926329 | ||||||
chr16:71926346
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.902-1268C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926346 | ||||||
chr16:71926347
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.902-1267A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926347 | ||||||
chr16:71926348
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.902-1266T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926348 | ||||||
chr16:71926415
|
C | G | 1 | a0002c0002t0002g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.902-1199C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926415 | ||||||
chr16:71926539
|
G | A | 3 | a0002c0002t0002g0009a0002c0002t0002g0108a0002c0002t0002g0169 | 5 | HG02083.hp2 HG02523.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.902-1075G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926539 | ||||||
chr16:71926710
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.902-904T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926710 | ||||||
chr16:71926927
|
C | T | 1 | a0002c0002t0002g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.902-687C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926927 | ||||||
chr16:71926983
|
T | G | 1 | a0001c0001t0001g0273 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.902-631T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926983 | ||||||
chr16:71927343
|
G | C | 24 | a0001c0001t0004g0005a0001c0001t0004g0012a0001c0001t0004g0013others(21): Show | 27 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.902-271G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71927343 | ||||||
chr16:71927436
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(263): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.902-178T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71927436 | ||||||
chr16:71927486
|
C | CA | 95 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0003g0289others(92): Show | 113 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.902-112dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71927486 | |||||
chr16:71927486
|
C | CAA | 12 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0283others(9): Show | 14 | HG01109.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.902-113_902-112dup others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71927486 | |||||
chr16:71927486
|
CA | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(88): Show | 110 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.902-112delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71927486 | |||||
chr16:71927591
|
G | A | 1 | a0001c0001t0026g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.902-23G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71927591 |