geneid | 1186 |
---|---|
ensemblid | ENSG00000103249.19 |
hgncid | 2025 |
symbol | CLCN7 |
name | chloride voltage-gated channel 7 |
refseq_nuc | NM_001287.6 |
refseq_prot | NP_001278.1 |
ensembl_nuc | ENST00000382745.9 |
ensembl_prot | ENSP00000372193.4 |
mane_status | MANE Select |
chr | chr16 |
start | 1444935 |
end | 1475028 |
strand | - |
ver | v1.2 |
region | chr16:1444935-1475028 |
region5000 | chr16:1439935-1480028 |
regionname0 | CLCN7_chr16_1444935_1475028 |
regionname5000 | CLCN7_chr16_1439935_1480028 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 805 | 363 | 74 | 62 | 162 | 15 | 48 | 118 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002 | 0/0 | 805 | 30 | 18 | 10 | 0 | 1 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003 | 0/0 | 802 | 5 | 2 | 2 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0004 | 0/0 | 805 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0005 | 0/0 | 254 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0006 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0007 | 0/0 | 805 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
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 | 0/1 | 2418 | 125 | 17 | 8 | 84 | 1 | 14 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0002 | 0/0 | 2418 | 78 | 24 | 11 | 31 | 5 | 7 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0003 | 1/0 | 2418 | 62 | 0 | 23 | 18 | 6 | 14 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0004 | 0/0 | 2418 | 55 | 9 | 13 | 24 | 2 | 7 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0005 | 0/0 | 2418 | 28 | 11 | 6 | 4 | 1 | 6 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0006 | 0/0 | 2418 | 13 | 3 | 9 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0007 | 0/0 | 2418 | 7 | 7 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0008 | 0/0 | 2418 | 5 | 4 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0009 | 0/0 | 2418 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0010 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0011 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0012 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0013 | 0/0 | 2409 | 2 | 0 | 1 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0014 | 0/0 | 2618 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0015 | 0/0 | 2418 | 2 | 1 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0016 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0017 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0018 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0019 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0020 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0021 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0022 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0023 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0024 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0025 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
c0026 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
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 | 0/1 | 1751 | 171 | 12 | 26 | 110 | 3 | 19 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0002 | 0/0 | 1751 | 65 | 13 | 20 | 12 | 8 | 12 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0003 | 0/0 | 1751 | 25 | 7 | 2 | 11 | 0 | 5 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0004 | 0/0 | 1752 | 23 | 11 | 5 | 5 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0005 | 0/0 | 1751 | 13 | 4 | 3 | 2 | 2 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0006 | 0/0 | 1751 | 7 | 6 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0007 | 0/0 | 1751 | 7 | 0 | 0 | 6 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0008 | 0/0 | 1751 | 7 | 5 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0009 | 0/0 | 1751 | 7 | 0 | 0 | 7 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0010 | 0/0 | 1751 | 6 | 1 | 4 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0011 | 0/0 | 1751 | 5 | 0 | 0 | 0 | 2 | 3 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0012 | 0/0 | 1751 | 4 | 0 | 0 | 3 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0013 | 0/0 | 1751 | 4 | 3 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0014 | 0/0 | 1751 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0015 | 0/0 | 1752 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0016 | 0/0 | 1752 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0017 | 0/0 | 1749 | 3 | 2 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0018 | 0/0 | 1751 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0019 | 1/0 | 1751 | 2 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0020 | 0/0 | 1751 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0021 | 0/0 | 1751 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0022 | 0/0 | 1751 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0023 | 0/0 | 1751 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0024 | 0/0 | 1752 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0025 | 0/0 | 1753 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0026 | 0/0 | 1753 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0027 | 0/0 | 1751 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0028 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0029 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0030 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0031 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0032 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0033 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0034 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0035 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0036 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0037 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0038 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0039 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0040 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0041 | 0/0 | 1751 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0042 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0043 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0044 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0045 | 0/0 | 1752 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0046 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0047 | 0/0 | 1751 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0048 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0049 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0050 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0051 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0052 | 0/0 | 1751 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0053 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
t0054 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
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 | 3 | 0 | 3 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0336 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
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 | 0/1 | 2418 | 125 | 17 | 8 | 84 | 1 | 14 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002 | 0/0 | 2418 | 78 | 24 | 11 | 31 | 5 | 7 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003 | 1/0 | 2418 | 62 | 0 | 23 | 18 | 6 | 14 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004 | 0/0 | 2418 | 55 | 9 | 13 | 24 | 2 | 7 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0005 | 0/0 | 2418 | 28 | 11 | 6 | 4 | 1 | 6 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0007 | 0/0 | 2418 | 7 | 7 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0010 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0015 | 0/0 | 2418 | 2 | 1 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0017 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0019 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0022 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0006 | 0/0 | 2418 | 13 | 3 | 9 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0008 | 0/0 | 2418 | 5 | 4 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0009 | 0/0 | 2418 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0011 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0012 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0026 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0013 | 0/0 | 2409 | 2 | 0 | 1 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0016 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0021 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0023 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0004c0018 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0004c0024 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0005c0014 | 0/0 | 2618 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0006c0020 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0007c0025 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4168 | 93 | 10 | 8 | 62 | 1 | 11 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0002 | 0/0 | 4168 | 3 | 1 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0004 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0005 | 0/0 | 4168 | 3 | 0 | 0 | 2 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0007 | 0/0 | 4168 | 5 | 0 | 0 | 5 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0008 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0009 | 0/0 | 4168 | 7 | 0 | 0 | 7 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0012 | 0/0 | 4168 | 3 | 0 | 0 | 3 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0021 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0031 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0032 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0033 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0035 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0039 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0045 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0001t0049 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0001 | 0/0 | 4168 | 21 | 0 | 2 | 18 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0002 | 0/0 | 4168 | 31 | 8 | 5 | 8 | 4 | 6 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0003 | 0/0 | 4168 | 8 | 5 | 0 | 3 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0007 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0008 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0011 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0013 | 0/0 | 4168 | 3 | 2 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0015 | 0/0 | 4169 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0020 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0023 | 0/0 | 4168 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0034 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0036 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0042 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0043 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0044 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0002t0054 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0001 | 0/0 | 4168 | 10 | 0 | 2 | 6 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0002 | 0/0 | 4168 | 23 | 0 | 13 | 2 | 4 | 4 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0003 | 0/0 | 4168 | 15 | 0 | 2 | 8 | 0 | 5 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0005 | 0/0 | 4168 | 3 | 0 | 2 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0008 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0011 | 0/0 | 4168 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0019 | 1/0 | 4168 | 2 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0020 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0022 | 0/0 | 4168 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0037 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0038 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0003t0047 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0001 | 0/0 | 4168 | 40 | 2 | 11 | 23 | 1 | 3 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0002 | 0/0 | 4168 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0004 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0005 | 0/0 | 4168 | 2 | 0 | 1 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0006 | 0/0 | 4168 | 7 | 6 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0007 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0012 | 0/0 | 4168 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0004t0030 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0005t0001 | 0/0 | 4168 | 3 | 0 | 1 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0005t0004 | 0/0 | 4169 | 20 | 9 | 5 | 4 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0005t0005 | 0/0 | 4168 | 3 | 2 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0005t0011 | 0/0 | 4168 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0007t0002 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0007t0003 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0007t0004 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0007t0040 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0010t0008 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0015t0028 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0015t0046 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0017t0041 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0019t0002 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0001c0022t0048 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0006t0010 | 0/0 | 4168 | 6 | 1 | 4 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0006t0024 | 0/0 | 4169 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0006t0025 | 0/0 | 4170 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0006t0026 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0006t0051 | 0/0 | 4169 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0006t0052 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0008t0017 | 0/0 | 4166 | 3 | 2 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0008t0027 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0009t0005 | 0/0 | 4168 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0009t0016 | 0/0 | 4169 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0011t0018 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0012t0014 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0002c0026t0024 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0013t0001 | 0/0 | 4159 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0013t0021 | 0/0 | 4159 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0016t0050 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0021t0013 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0003c0023t0002 | 0/0 | 4159 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0004c0018t0053 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0004c0024t0029 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0005c0014t0001 | 0/0 | 4368 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0006c0020t0001 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
a0007c0025t0002 | 0/0 | 4168 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | copy fasta | chr16 | 1439935 | 1480028 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0007g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0012g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0012g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0021g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0031g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0032g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0033g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0035g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0039g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0045g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0001t0049g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0011g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0013g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0015g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0020g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0023g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0023g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0034g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0036g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0042g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0043g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0044g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0002t0054g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0002g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0003g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0005g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0008g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0011g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0011g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0019g0336 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0019g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0020g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0022g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0022g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0037g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0038g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0003t0047g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0002g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0005g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0005g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0007g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0012g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0004t0030g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0005t0011g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0007t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0007t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0007t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0007t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0007t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0007t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0007t0040g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0010t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0010t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0010t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0015t0028g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0015t0046g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0017t0041g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0019t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0001c0022t0048g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0010g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0010g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0010g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0010g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0024g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0025g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0025g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0026g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0051g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0006t0052g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0008t0017g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0008t0017g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0008t0027g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0008t0027g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0009t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0009t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0009t0016g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0009t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0009t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0011t0018g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0011t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0011t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0012t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0012t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0012t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0002c0026t0024g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0003c0013t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0003c0013t0021g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0003c0016t0050g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0003c0021t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0003c0023t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0004c0018t0053g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0004c0024t0029g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0005c0014t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0005c0014t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0006c0020t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
a0007c0025t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0002 | g0318 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0382 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00140 | hp1 | a0001 | c0003 | t0002 | g0314 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00280 | hp1 | a0001 | c0005 | t0005 | g0102 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00280 | hp2 | a0001 | c0004 | t0005 | g0356 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0217 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0313 | EUR | FIN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00423 | hp2 | a0001 | c0004 | t0001 | g0307 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00544 | hp1 | a0001 | c0003 | t0002 | g0326 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00609 | hp1 | a0001 | c0001 | t0031 | g0243 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00609 | hp2 | a0001 | c0004 | t0001 | g0389 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00621 | hp1 | a0001 | c0004 | t0001 | g0345 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00621 | hp2 | a0001 | c0002 | t0003 | g0127 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00639 | hp1 | a0002 | c0006 | t0010 | g0258 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00639 | hp2 | a0001 | c0002 | t0013 | g0029 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00642 | hp2 | a0002 | c0006 | t0010 | g0010 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0335 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00733 | hp1 | a0001 | c0003 | t0019 | g0337 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00735 | hp1 | a0002 | c0006 | t0025 | g0266 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00738 | hp1 | a0001 | c0004 | t0005 | g0360 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00738 | hp2 | a0001 | c0003 | t0002 | g0329 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00741 | hp1 | a0001 | c0003 | t0005 | g0379 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0288 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01070 | hp2 | a0001 | c0003 | t0008 | g0384 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01071 | hp1 | a0001 | c0005 | t0004 | g0181 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01071 | hp2 | a0001 | c0004 | t0001 | g0350 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01074 | hp1 | a0002 | c0006 | t0025 | g0260 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01074 | hp2 | a0005 | c0014 | t0001 | g0116 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01081 | hp1 | a0001 | c0005 | t0004 | g0165 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01081 | hp2 | a0001 | c0003 | t0047 | g0319 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01099 | hp1 | a0002 | c0006 | t0010 | g0010 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01099 | hp2 | a0001 | c0017 | t0041 | g0163 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01106 | hp1 | a0001 | c0003 | t0022 | g0320 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01106 | hp2 | a0001 | c0005 | t0004 | g0182 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01109 | hp2 | a0001 | c0004 | t0006 | g0026 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0321 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01168 | hp1 | a0001 | c0005 | t0004 | g0193 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0324 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01192 | hp1 | a0002 | c0006 | t0024 | g0263 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01192 | hp2 | a0002 | c0006 | t0052 | g0264 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0331 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01243 | hp2 | a0002 | c0008 | t0017 | g0009 | AMR | PUR | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01255 | hp2 | a0001 | c0002 | t0023 | g0076 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0333 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01256 | hp2 | a0001 | c0003 | t0002 | g0312 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01257 | hp2 | a0001 | c0003 | t0003 | g0014 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0334 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01258 | hp2 | a0001 | c0003 | t0003 | g0014 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0370 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01261 | hp2 | a0001 | c0002 | t0023 | g0051 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01346 | hp2 | a0001 | c0004 | t0001 | g0298 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01433 | hp1 | a0001 | c0004 | t0001 | g0296 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01433 | hp2 | a0001 | c0004 | t0001 | g0339 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01496 | hp1 | a0001 | c0005 | t0001 | g0183 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0305 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0151 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0223 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01516 | hp1 | a0002 | c0006 | t0010 | g0257 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01516 | hp2 | a0001 | c0003 | t0011 | g0322 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01517 | hp1 | a0001 | c0003 | t0011 | g0325 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0152 | EUR | IBS | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01884 | hp1 | a0001 | c0004 | t0006 | g0022 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01884 | hp2 | a0001 | c0005 | t0005 | g0188 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01891 | hp1 | a0004 | c0024 | t0029 | g0024 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01891 | hp2 | a0001 | c0022 | t0048 | g0172 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01934 | hp2 | a0001 | c0003 | t0002 | g0330 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01952 | hp2 | a0001 | c0003 | t0002 | g0292 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01975 | hp1 | a0001 | c0003 | t0002 | g0293 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01978 | hp1 | a0002 | c0006 | t0051 | g0259 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01978 | hp2 | a0003 | c0013 | t0001 | g0109 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01981 | hp1 | a0001 | c0003 | t0002 | g0294 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01981 | hp2 | a0002 | c0006 | t0010 | g0255 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01993 | hp1 | a0003 | c0023 | t0002 | g0323 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0353 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02004 | hp1 | a0001 | c0004 | t0001 | g0354 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02004 | hp2 | a0001 | c0003 | t0005 | g0317 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0344 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02055 | hp1 | a0002 | c0009 | t0005 | g0284 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02055 | hp2 | a0001 | c0005 | t0004 | g0153 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02056 | hp2 | a0001 | c0004 | t0001 | g0343 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02080 | hp1 | a0001 | c0002 | t0020 | g0204 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02080 | hp2 | a0001 | c0003 | t0003 | g0373 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02129 | hp1 | a0001 | c0004 | t0001 | g0351 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0347 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02145 | hp1 | a0001 | c0010 | t0008 | g0241 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02148 | hp1 | a0001 | c0004 | t0001 | g0357 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02148 | hp2 | a0001 | c0002 | t0008 | g0049 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0341 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0310 | EAS | CDX | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02257 | hp2 | a0001 | c0004 | t0006 | g0025 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02258 | hp1 | a0002 | c0009 | t0016 | g0079 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02258 | hp2 | a0001 | c0004 | t0006 | g0019 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02273 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02273 | hp2 | a0007 | c0025 | t0002 | g0352 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0077 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02280 | hp2 | a0002 | c0008 | t0017 | g0160 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0328 | AMR | PEL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02451 | hp1 | a0001 | c0005 | t0004 | g0273 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02451 | hp2 | a0001 | c0007 | t0003 | g0191 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02572 | hp1 | a0001 | c0002 | t0036 | g0207 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02572 | hp2 | a0001 | c0007 | t0002 | g0170 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02602 | hp1 | a0001 | c0002 | t0011 | g0221 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02602 | hp2 | a0001 | c0004 | t0001 | g0355 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02615 | hp2 | a0001 | c0004 | t0006 | g0018 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02622 | hp1 | a0003 | c0021 | t0013 | g0189 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02622 | hp2 | a0003 | c0016 | t0050 | g0154 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02630 | hp1 | a0001 | c0002 | t0015 | g0275 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02647 | hp1 | a0001 | c0002 | t0054 | g0030 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0365 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02698 | hp1 | a0001 | c0001 | t0032 | g0119 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02698 | hp2 | a0002 | c0026 | t0024 | g0309 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02717 | hp1 | a0002 | c0008 | t0027 | g0253 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02717 | hp2 | a0001 | c0002 | t0015 | g0050 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02723 | hp1 | a0002 | c0009 | t0005 | g0031 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0229 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0232 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02735 | hp2 | a0001 | c0005 | t0001 | g0179 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02738 | hp1 | a0001 | c0004 | t0002 | g0348 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02738 | hp2 | a0001 | c0005 | t0004 | g0168 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0349 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02809 | hp2 | a0001 | c0015 | t0028 | g0021 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0201 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02886 | hp2 | a0001 | c0001 | t0039 | g0174 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02896 | hp1 | a0001 | c0005 | t0004 | g0280 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02896 | hp2 | a0001 | c0007 | t0002 | g0171 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02897 | hp1 | a0001 | c0002 | t0013 | g0032 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02897 | hp2 | a0001 | c0005 | t0004 | g0267 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02965 | hp1 | a0001 | c0002 | t0013 | g0028 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0300 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02976 | hp1 | a0001 | c0005 | t0004 | g0265 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02976 | hp2 | a0001 | c0007 | t0002 | g0169 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03017 | hp1 | a0001 | c0001 | t0045 | g0230 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0387 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0175 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03041 | hp2 | a0001 | c0005 | t0005 | g0187 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03098 | hp1 | a0001 | c0010 | t0008 | g0240 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03098 | hp2 | a0002 | c0011 | t0018 | g0270 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03130 | hp2 | a0001 | c0005 | t0004 | g0186 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03139 | hp1 | a0002 | c0008 | t0017 | g0009 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03195 | hp1 | a0004 | c0018 | t0053 | g0276 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03195 | hp2 | a0002 | c0006 | t0026 | g0262 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03209 | hp1 | a0002 | c0012 | t0014 | g0015 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03209 | hp2 | a0001 | c0002 | t0044 | g0071 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03225 | hp1 | a0001 | c0005 | t0004 | g0274 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03225 | hp2 | a0001 | c0002 | t0042 | g0269 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03239 | hp1 | a0005 | c0014 | t0001 | g0117 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03239 | hp2 | a0001 | c0004 | t0012 | g0338 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03453 | hp1 | a0001 | c0005 | t0004 | g0272 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03486 | hp1 | a0001 | c0004 | t0030 | g0371 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03486 | hp2 | a0001 | c0004 | t0006 | g0020 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03490 | hp2 | a0001 | c0005 | t0011 | g0008 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03491 | hp1 | a0001 | c0003 | t0003 | g0012 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0205 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03492 | hp1 | a0001 | c0003 | t0003 | g0012 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03492 | hp2 | a0001 | c0005 | t0011 | g0008 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03516 | hp1 | a0001 | c0002 | t0003 | g0202 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03516 | hp2 | a0001 | c0010 | t0008 | g0239 | AFR | ESN | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03540 | hp1 | a0001 | c0007 | t0004 | g0177 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03579 | hp1 | a0002 | c0012 | t0014 | g0016 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03579 | hp2 | a0002 | c0008 | t0027 | g0252 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0199 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0346 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0218 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0135 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03710 | hp2 | a0001 | c0003 | t0003 | g0289 | SAS | PJL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0197 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03831 | hp2 | a0001 | c0005 | t0001 | g0190 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0290 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03834 | hp2 | a0001 | c0003 | t0003 | g0377 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03927 | hp1 | a0001 | c0004 | t0002 | g0362 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03927 | hp2 | a0001 | c0003 | t0037 | g0359 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03942 | hp1 | a0001 | c0004 | t0001 | g0363 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03942 | hp2 | a0001 | c0004 | t0007 | g0297 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0295 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0369 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04199 | hp1 | a0001 | c0003 | t0005 | g0299 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04204 | hp2 | a0001 | c0003 | t0003 | g0380 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG04228 | hp2 | a0001 | c0003 | t0022 | g0291 | SAS | STU | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18522 | hp1 | a0002 | c0006 | t0026 | g0261 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0279 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18612 | hp2 | a0001 | c0001 | t0021 | g0063 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18906 | hp2 | a0001 | c0005 | t0004 | g0180 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18939 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18943 | hp2 | a0001 | c0004 | t0001 | g0358 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18945 | hp1 | a0006 | c0020 | t0001 | g0147 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18950 | hp1 | a0001 | c0004 | t0001 | g0388 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18953 | hp1 | a0001 | c0001 | t0009 | g0054 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18953 | hp2 | a0001 | c0003 | t0003 | g0304 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18954 | hp1 | a0001 | c0005 | t0004 | g0167 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18959 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18960 | hp1 | a0001 | c0004 | t0001 | g0367 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18962 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18962 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18964 | hp2 | a0001 | c0004 | t0004 | g0287 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18966 | hp1 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18970 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18974 | hp2 | a0001 | c0003 | t0002 | g0316 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18979 | hp1 | a0001 | c0001 | t0012 | g0066 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18979 | hp2 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18982 | hp2 | a0001 | c0001 | t0007 | g0158 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18983 | hp2 | a0001 | c0004 | t0001 | g0308 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18986 | hp2 | a0001 | c0001 | t0009 | g0100 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18987 | hp2 | a0001 | c0003 | t0003 | g0303 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18991 | hp2 | a0001 | c0005 | t0004 | g0164 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18993 | hp2 | a0001 | c0004 | t0001 | g0366 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18995 | hp1 | a0001 | c0004 | t0001 | g0311 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18995 | hp2 | a0001 | c0004 | t0001 | g0364 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18997 | hp2 | a0001 | c0003 | t0003 | g0386 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19000 | hp1 | a0001 | c0004 | t0001 | g0302 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19004 | hp1 | a0001 | c0001 | t0009 | g0099 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19005 | hp1 | a0001 | c0004 | t0001 | g0332 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19007 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19009 | hp1 | a0001 | c0004 | t0001 | g0301 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19010 | hp2 | a0001 | c0004 | t0001 | g0368 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19012 | hp1 | a0001 | c0003 | t0003 | g0378 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19043 | hp1 | a0001 | c0004 | t0006 | g0023 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19043 | hp2 | a0001 | c0001 | t0049 | g0238 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19054 | hp1 | a0001 | c0015 | t0046 | g0385 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19054 | hp2 | a0001 | c0004 | t0001 | g0372 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19056 | hp1 | a0001 | c0005 | t0004 | g0166 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0381 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19058 | hp2 | a0001 | c0003 | t0003 | g0375 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19063 | hp2 | a0001 | c0003 | t0003 | g0376 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19065 | hp2 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19067 | hp1 | a0001 | c0003 | t0038 | g0315 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19067 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19070 | hp2 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19074 | hp1 | a0001 | c0004 | t0001 | g0286 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19079 | hp1 | a0003 | c0013 | t0021 | g0055 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19081 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19081 | hp2 | a0001 | c0003 | t0020 | g0374 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19082 | hp1 | a0001 | c0002 | t0007 | g0132 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19082 | hp2 | a0001 | c0003 | t0003 | g0383 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0053 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19087 | hp1 | a0001 | c0004 | t0001 | g0340 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19087 | hp2 | a0001 | c0001 | t0033 | g0064 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0306 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA19240 | hp2 | a0002 | c0009 | t0016 | g0081 | AFR | YRI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ASW | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20129 | hp2 | a0001 | c0002 | t0015 | g0268 | AFR | ASW | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20805 | hp1 | a0001 | c0003 | t0002 | g0327 | EUR | TSI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0219 | EUR | TSI | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0342 | SAS | GIH | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20905 | hp2 | a0001 | c0005 | t0004 | g0185 | SAS | GIH | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01123 | hp1 | a0001 | c0004 | t0001 | g0361 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG01123 | hp2 | a0001 | c0005 | t0004 | g0184 | AMR | CLM | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0212 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02486 | hp1 | a0001 | c0019 | t0002 | g0173 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02486 | hp2 | a0001 | c0007 | t0003 | g0192 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG02559 | hp2 | a0001 | c0001 | t0035 | g0034 | AFR | ACB | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03471 | hp1 | a0001 | c0007 | t0040 | g0176 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG03471 | hp2 | a0002 | c0011 | t0018 | g0254 | AFR | MSL | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG06807 | hp1 | a0001 | c0002 | t0043 | g0036 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
HG06807 | hp2 | a0001 | c0002 | t0034 | g0277 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18955 | hp1 | a0001 | c0005 | t0004 | g0037 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20300 | hp1 | a0002 | c0006 | t0010 | g0256 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA20300 | hp2 | a0002 | c0011 | t0018 | g0271 | AFR | USA | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA21309 | hp1 | a0002 | c0009 | t0016 | g0080 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
NA21309 | hp2 | a0002 | c0012 | t0014 | g0017 | AFR | LWK | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0094 | REF | REF | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0019 | g0336 | REF | REF | CLCN7_chr16_1439935_1480028 | CLCN7 | chr16 | 1439935 | 1480028 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1448407
|
G | A | 1 | a0004 | 2 | HG01891.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.1961C>T | p.Thr654Met | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/25 | 2015/4168 | 1961/2418 | 654/805 | chr16 | 1448407 | ||
chr16:1450651
|
A | T | 1 | a0006 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.1463T>A | p.Leu488Gln | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/25 | 1517/4168 | 1463/2418 | 488/805 | chr16 | 1450651 | ||
chr16:1452856
|
C | T | 2 | a0002a0004 | 32 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(29): Show |
missense_variant | MODERATE | c.1252G>A | p.Val418Met | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/25 | 1306/4168 | 1252/2418 | 418/805 | chr16 | 1452856 | ||
chr16:1453892
|
C | T | 1 | a0007 | 1 | HG02273.hp2 | missense_variant&splice_region_variant | MODERATE | c.1156G>A | p.Gly386Ser | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/25 | 1210/4168 | 1156/2418 | 386/805 | chr16 | 1453892 | ||
chr16:1457328
|
T | TCGGCCCT others(193): Show |
1 | a0005 | 2 | HG01074.hp2 HG03239.hp1 |
frameshift_variant&stop_gained | HIGH | c.747_748insCGTCACGC others(192): Show |
p.Met250fs | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 747/2418 | 249/805 | chr16 | 1457328 | ||
chr16:1457328
|
TCGGCCCT others(93): Show |
T | 1 | a0003 | 1 | HG01993.hp1 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.739-91_747delCGTCA others(95): Show |
p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 | ||
chr16:1457328
|
TCGGCCCT others(143): Show |
T | 1 | a0003 | 2 | HG02622.hp1 HG02622.hp2 |
splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.739-141_747del | p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 | ||
chr16:1457328
|
TCGGCCCT others(193): Show |
T | 1 | a0003 | 1 | NA19079.hp1 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.738+166_747del | p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 | ||
chr16:1457328
|
TCGGCCCT others(243): Show |
T | 1 | a0003 | 1 | HG01978.hp2 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.738+116_747del | p.Glu247_Met250del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 801/4168 | 739/2418 | 247/805 | chr16 | 1457328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1448707
|
C | T | 1 | a0001c0010 | 3 | HG02145.hp1 HG03098.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1857G>A | p.Pro619Pro | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/25 | 1911/4168 | 1857/2418 | 619/805 | chr16 | 1448707 | ||
chr16:1449092
|
G | A | 2 | a0002c0011a0002c0012 | 6 | HG03098.hp2 HG03209.hp1 HG03471.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.1671C>T | p.Gly557Gly | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/25 | 1725/4168 | 1671/2418 | 557/805 | chr16 | 1449092 | ||
chr16:1449319
|
C | A | 1 | a0001c0022 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1626G>T | p.Ala542Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 18/25 | 1680/4168 | 1626/2418 | 542/805 | chr16 | 1449319 | ||
chr16:1450500
|
C | T | 2 | a0002c0006a0002c0026 | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
synonymous_variant | LOW | c.1614G>A | p.Ala538Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/25 | 1668/4168 | 1614/2418 | 538/805 | chr16 | 1450500 | ||
chr16:1450662
|
G | C | 1 | a0001c0019 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1452C>G | p.Ser484Ser | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/25 | 1506/4168 | 1452/2418 | 484/805 | chr16 | 1450662 | ||
chr16:1452863
|
A | G | 7 | a0002c0006a0002c0008a0002c0011others(4): Show | 27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
synonymous_variant | LOW | c.1245T>C | p.Ile415Ile | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/25 | 1299/4168 | 1245/2418 | 415/805 | chr16 | 1452863 | ||
chr16:1453878
|
T | A | 14 | a0001c0001a0001c0004a0001c0005others(11): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
synonymous_variant | LOW | c.1170A>T | p.Ala390Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/25 | 1224/4168 | 1170/2418 | 390/805 | chr16 | 1453878 | ||
chr16:1454436
|
C | T | 2 | a0002c0006a0002c0026 | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
synonymous_variant | LOW | c.1128G>A | p.Pro376Pro | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/25 | 1182/4168 | 1128/2418 | 376/805 | chr16 | 1454436 | ||
chr16:1455791
|
C | T | 3 | a0002c0008a0004c0018a0004c0024 | 7 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(4): Show |
synonymous_variant | LOW | c.921G>A | p.Gly307Gly | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/25 | 975/4168 | 921/2418 | 307/805 | chr16 | 1455791 | ||
chr16:1456129
|
C | T | 1 | a0005c0014 | 2 | HG01074.hp2 HG03239.hp1 |
synonymous_variant | LOW | c.900G>A | p.Ala300Ala | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/25 | 954/4168 | 900/2418 | 300/805 | chr16 | 1456129 | ||
chr16:1457275
|
C | T | 1 | a0001c0017 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.801G>A | p.Thr267Thr | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/25 | 855/4168 | 801/2418 | 267/805 | chr16 | 1457275 | ||
chr16:1459122
|
G | A | 7 | a0001c0005a0001c0007a0001c0015others(4): Show | 53 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
synonymous_variant | LOW | c.660C>T | p.His220His | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/25 | 714/4168 | 660/2418 | 220/805 | chr16 | 1459122 | ||
chr16:1474849
|
A | G | 18 | a0001c0001a0001c0002a0001c0005others(15): Show | 278 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(275): Show |
synonymous_variant | LOW | c.126T>C | p.Pro42Pro | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/25 | 180/4168 | 126/2418 | 42/805 | chr16 | 1474849 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1444986
|
C | G | 2 | a0001c0002t0015a0001c0002t0042 | 4 | HG02630.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1645G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1645 | chr16 | 1444986 | |||||
chr16:1445005
|
C | G | 61 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(58): Show | 289 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*1626G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1626 | chr16 | 1445005 | |||||
chr16:1445006
|
AACC | A | 3 | a0002c0008t0017a0004c0018t0053a0004c0024t0029 | 5 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1622_*1624delGGT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1622 | chr16 | 1445006 | |||||
chr16:1445033
|
G | A | 2 | a0001c0001t0049a0001c0002t0044 | 2 | HG03209.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1598C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1598 | chr16 | 1445033 | |||||
chr16:1445035
|
T | C | 2 | a0001c0001t0049a0001c0002t0044 | 2 | HG03209.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1596A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1596 | chr16 | 1445035 | |||||
chr16:1445105
|
C | T | 1 | a0001c0002t0043 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1526G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1526 | chr16 | 1445105 | |||||
chr16:1445133
|
G | GC | 3 | a0002c0006t0025a0002c0006t0026a0002c0006t0051 | 5 | HG00735.hp1 HG01074.hp1 HG01978.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1497dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1497 | chr16 | 1445133 | |||||
chr16:1445152
|
A | G | 3 | a0001c0002t0054a0002c0011t0018a0002c0012t0014 | 7 | HG02647.hp1 HG03098.hp2 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1479T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1479 | chr16 | 1445152 | |||||
chr16:1445242
|
T | G | 83 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(80): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*1389A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1389 | chr16 | 1445242 | |||||
chr16:1445264
|
G | A | 1 | a0001c0003t0038 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1367C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1367 | chr16 | 1445264 | |||||
chr16:1445299
|
G | A | 26 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(23): Show | 208 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*1332C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1332 | chr16 | 1445299 | |||||
chr16:1445451
|
C | G | 2 | a0001c0001t0021a0003c0013t0021 | 2 | NA18612.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1180G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1180 | chr16 | 1445451 | |||||
chr16:1445455
|
G | A | 1 | a0002c0006t0010 | 6 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1176C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1176 | chr16 | 1445455 | |||||
chr16:1445474
|
G | A | 14 | a0001c0001t0049a0001c0002t0013a0001c0002t0034others(11): Show | 21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1157C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1157 | chr16 | 1445474 | |||||
chr16:1445486
|
G | GC | 17 | a0001c0001t0004a0001c0001t0039a0001c0001t0045others(14): Show | 44 | HG00735.hp1 HG01071.hp1 HG01074.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1144dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1144 | chr16 | 1445486 | |||||
chr16:1445567
|
C | T | 1 | a0001c0002t0036 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1064G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1064 | chr16 | 1445567 | |||||
chr16:1445579
|
C | T | 1 | a0001c0007t0040 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1052G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 1052 | chr16 | 1445579 | |||||
chr16:1445641
|
G | A | 7 | a0001c0002t0013a0001c0002t0054a0002c0008t0027others(4): Show | 10 | HG00639.hp2 HG01891.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*990C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 990 | chr16 | 1445641 | |||||
chr16:1445744
|
G | A | 73 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(70): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*887C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 887 | chr16 | 1445744 | |||||
chr16:1445745
|
G | A | 73 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(70): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*886C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 886 | chr16 | 1445745 | |||||
chr16:1445896
|
G | A | 46 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(43): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*735C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 735 | chr16 | 1445896 | |||||
chr16:1446004
|
T | C | 18 | a0001c0002t0013a0001c0002t0054a0001c0003t0047others(15): Show | 34 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*627A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 627 | chr16 | 1446004 | |||||
chr16:1446101
|
C | T | 1 | a0001c0002t0034 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 530 | chr16 | 1446101 | |||||
chr16:1446135
|
A | G | 2 | a0001c0001t0035a0001c0002t0034 | 2 | HG02559.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*496T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 496 | chr16 | 1446135 | |||||
chr16:1446206
|
G | C | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*425C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 425 | chr16 | 1446206 | |||||
chr16:1446207
|
G | C | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*424C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 424 | chr16 | 1446207 | |||||
chr16:1446208
|
A | T | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*423T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 423 | chr16 | 1446208 | |||||
chr16:1446209
|
G | T | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*422C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 422 | chr16 | 1446209 | |||||
chr16:1446210
|
G | C | 1 | a0001c0002t0023 | 2 | HG01255.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*421C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 421 | chr16 | 1446210 | |||||
chr16:1446235
|
C | T | 1 | a0001c0001t0033 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*396G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 396 | chr16 | 1446235 | |||||
chr16:1446250
|
C | T | 1 | a0001c0001t0032 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 381 | chr16 | 1446250 | |||||
chr16:1446337
|
C | G | 1 | a0001c0001t0031 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 294 | chr16 | 1446337 | |||||
chr16:1446338
|
G | A | 1 | a0001c0001t0049 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 293 | chr16 | 1446338 | |||||
chr16:1446403
|
G | A | 1 | a0001c0001t0009 | 7 | NA18953.hp1 NA18962.hp2 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*228C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 228 | chr16 | 1446403 | |||||
chr16:1446568
|
C | T | 1 | a0001c0004t0030 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 63 | chr16 | 1446568 | |||||
chr16:1446612
|
T | C | 17 | a0001c0002t0013a0001c0002t0054a0002c0006t0010others(14): Show | 33 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*19A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 25/25 | 19 | chr16 | 1446612 | |||||
chr16:1474994
|
C | G | 4 | a0001c0004t0006a0001c0015t0028a0002c0012t0014others(1): Show | 12 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-20G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/25 | chr16 | 1474994 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:1446737
|
C | T | 1 | a0001c0022t0048g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2332-20G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446737 | ||||||
chr16:1446747
|
C | T | 1 | a0002c0011t0018g0270 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2332-30G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446747 | ||||||
chr16:1446754
|
C | T | 2 | a0001c0005t0004g0164a0001c0015t0046g0385 | 2 | NA18991.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2332-37G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446754 | ||||||
chr16:1446825
|
G | C | 10 | a0001c0002t0002g0011a0001c0002t0002g0281a0001c0002t0002g0282others(7): Show | 11 | HG00639.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2332-108C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446825 | ||||||
chr16:1446914
|
C | T | 1 | a0001c0001t0035g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2331+92G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446914 | ||||||
chr16:1446927
|
G | A | 9 | a0001c0005t0004g0153a0001c0005t0004g0180a0001c0005t0004g0181others(6): Show | 9 | HG01071.hp1 HG01106.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2331+79C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446927 | ||||||
chr16:1446964
|
A | C | 1 | a0001c0007t0003g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2331+42T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 24/24 | chr16 | 1446964 | ||||||
chr16:1447124
|
A | G | 36 | a0001c0001t0035g0034a0001c0001t0049g0238a0001c0002t0013g0028others(33): Show | 38 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2251-38T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447124 | ||||||
chr16:1447130
|
G | A | 1 | a0001c0004t0001g0358 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2251-44C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447130 | ||||||
chr16:1447136
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(200): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2251-50G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447136 | ||||||
chr16:1447208
|
C | T | 1 | a0001c0004t0001g0366 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2251-122G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447208 | ||||||
chr16:1447271
|
G | A | 2 | a0001c0001t0049g0238a0001c0002t0044g0071 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2250+121C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447271 | ||||||
chr16:1447319
|
C | A | 1 | a0001c0002t0002g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2250+73G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447319 | ||||||
chr16:1447344
|
T | C | 1 | a0001c0002t0002g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2250+48A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447344 | ||||||
chr16:1447372
|
T | C | 5 | a0001c0002t0013g0028a0001c0002t0013g0029a0001c0002t0013g0032others(2): Show | 5 | HG00639.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2250+20A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 23/24 | chr16 | 1447372 | ||||||
chr16:1447594
|
G | C | 1 | a0002c0011t0018g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2074-26C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 22/24 | chr16 | 1447594 | ||||||
chr16:1447622
|
C | T | 5 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0009t0016g0079others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2073+33G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 22/24 | chr16 | 1447622 | ||||||
chr16:1447639
|
G | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.2073+16C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 22/24 | chr16 | 1447639 | ||||||
chr16:1447731
|
C | A | 1 | a0001c0005t0004g0186 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2014-17G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447731 | ||||||
chr16:1447827
|
T | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0195a0001c0001t0001g0244others(3): Show | 6 | HG02523.hp1 NA18945.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2014-113A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447827 | ||||||
chr16:1447900
|
C | T | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2014-186G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447900 | ||||||
chr16:1447922
|
C | T | 1 | a0001c0003t0002g0331 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2014-208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1447922 | ||||||
chr16:1448196
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(197): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2013+159T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1448196 | ||||||
chr16:1448269
|
A | G | 36 | a0001c0001t0035g0034a0001c0002t0013g0028a0001c0002t0013g0029others(33): Show | 38 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2013+86T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1448269 | ||||||
chr16:1448303
|
G | A | 1 | a0001c0002t0001g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2013+52C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 21/24 | chr16 | 1448303 | ||||||
chr16:1448500
|
G | A | 1 | a0001c0003t0005g0379 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1884-16C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448500 | ||||||
chr16:1448509
|
T | C | 34 | a0001c0002t0013g0028a0001c0002t0013g0029a0001c0002t0013g0032others(31): Show | 36 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1884-25A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448509 | ||||||
chr16:1448519
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(240): Show | 253 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1884-35T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448519 | ||||||
chr16:1448571
|
T | C | 37 | a0001c0001t0035g0034a0001c0001t0049g0238a0001c0002t0013g0028others(34): Show | 39 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1884-87A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448571 | ||||||
chr16:1448578
|
G | A | 9 | a0001c0002t0013g0028a0001c0002t0013g0029a0001c0002t0013g0032others(6): Show | 9 | HG00639.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1884-94C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448578 | ||||||
chr16:1448596
|
G | A | 9 | a0001c0002t0013g0028a0001c0002t0013g0029a0001c0002t0013g0032others(6): Show | 9 | HG00639.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1883+85C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448596 | ||||||
chr16:1448602
|
G | A | 2 | a0001c0005t0004g0153a0001c0005t0004g0181 | 2 | HG01071.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1883+79C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448602 | ||||||
chr16:1448609
|
G | A | 1 | a0001c0002t0002g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1883+72C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 20/24 | chr16 | 1448609 | ||||||
chr16:1448774
|
C | T | 27 | a0001c0004t0001g0300a0001c0004t0030g0371a0002c0006t0010g0010others(24): Show | 29 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1798-8G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448774 | ||||||
chr16:1448776
|
G | A | 8 | a0002c0006t0024g0263a0002c0006t0025g0260a0002c0006t0025g0266others(5): Show | 8 | HG00735.hp1 HG01074.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1798-10C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448776 | ||||||
chr16:1448821
|
C | A | 1 | a0001c0003t0003g0380 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1798-55G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448821 | ||||||
chr16:1448823
|
C | T | 1 | a0001c0002t0001g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1798-57G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448823 | ||||||
chr16:1448824
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1798-58C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448824 | ||||||
chr16:1448851
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1798-85C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448851 | ||||||
chr16:1448873
|
C | A | 1 | a0001c0004t0005g0356 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1797+93G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448873 | ||||||
chr16:1448874
|
C | G | 7 | a0001c0001t0035g0034a0001c0002t0034g0277a0002c0009t0005g0031others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1797+92G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448874 | ||||||
chr16:1448885
|
G | A | 3 | a0002c0012t0014g0015a0002c0012t0014g0016a0002c0012t0014g0017 | 3 | HG03209.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1797+81C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448885 | ||||||
chr16:1448950
|
C | T | 25 | a0001c0007t0002g0170a0001c0007t0002g0171a0002c0006t0010g0010others(22): Show | 27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1797+16G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 19/24 | chr16 | 1448950 | ||||||
chr16:1449178
|
C | A | 1 | a0001c0002t0002g0083 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1670-85G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 18/24 | chr16 | 1449178 | ||||||
chr16:1449376
|
C | T | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(191): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1618-49G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449376 | ||||||
chr16:1449396
|
G | A | 1 | a0001c0002t0002g0227 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1618-69C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449396 | ||||||
chr16:1449407
|
G | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1618-80C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449407 | ||||||
chr16:1449411
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1618-84T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449411 | ||||||
chr16:1449426
|
A | G | 3 | a0001c0001t0035g0034a0003c0016t0050g0154a0003c0021t0013g0189 | 3 | HG02559.hp2 HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1618-99T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449426 | ||||||
chr16:1449434
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1618-107C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449434 | ||||||
chr16:1449452
|
C | T | 1 | a0001c0003t0002g0329 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1618-125G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449452 | ||||||
chr16:1449494
|
C | T | 2 | a0001c0007t0004g0177a0001c0022t0048g0172 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1618-167G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449494 | ||||||
chr16:1449585
|
C | T | 2 | a0001c0004t0001g0300a0001c0004t0030g0371 | 2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1618-258G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449585 | ||||||
chr16:1449616
|
T | C | 29 | a0001c0001t0001g0278a0001c0002t0015g0268a0001c0002t0015g0275others(26): Show | 31 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1618-289A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449616 | ||||||
chr16:1449663
|
G | A | 2 | a0001c0001t0049g0238a0001c0002t0044g0071 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1618-336C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449663 | ||||||
chr16:1449667
|
A | C | 3 | a0001c0002t0001g0128a0001c0003t0001g0310a0001c0003t0001g0341 | 3 | HG00558.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1618-340T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449667 | ||||||
chr16:1449703
|
T | C | 33 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0034g0277others(30): Show | 35 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1618-376A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449703 | ||||||
chr16:1449706
|
A | AGATGCTG others(80): Show |
29 | a0001c0007t0003g0191a0001c0007t0003g0192a0002c0006t0010g0010others(26): Show | 31 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1618-380_1618-379i others(89): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449706 | ||||||
chr16:1449738
|
G | A | 1 | a0001c0001t0007g0142 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1618-411C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449738 | ||||||
chr16:1449767
|
T | C | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1618-440A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449767 | ||||||
chr16:1449796
|
C | T | 1 | a0001c0005t0004g0164 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1618-469G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449796 | ||||||
chr16:1449836
|
C | T | 2 | a0001c0001t0049g0238a0001c0002t0044g0071 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1618-509G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449836 | ||||||
chr16:1449869
|
A | G | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1618-542T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449869 | ||||||
chr16:1449891
|
C | G | 2 | a0003c0016t0050g0154a0003c0021t0013g0189 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1618-564G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449891 | ||||||
chr16:1449907
|
T | C | 40 | a0001c0001t0035g0034a0001c0001t0049g0238a0001c0002t0002g0279others(37): Show | 42 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1618-580A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449907 | ||||||
chr16:1449919
|
A | C | 1 | a0001c0003t0022g0320 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1617+578T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1449919 | ||||||
chr16:1450050
|
G | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1617+447C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450050 | ||||||
chr16:1450160
|
C | T | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1617+337G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450160 | ||||||
chr16:1450174
|
C | T | 1 | a0001c0004t0001g0349 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617+323G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450174 | ||||||
chr16:1450240
|
A | G | 13 | a0001c0019t0002g0173a0002c0008t0017g0009a0002c0008t0017g0160others(10): Show | 14 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1617+257T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450240 | ||||||
chr16:1450299
|
C | T | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1617+198G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450299 | ||||||
chr16:1450317
|
T | C | 2 | a0002c0009t0005g0031a0002c0009t0005g0284 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1617+180A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450317 | ||||||
chr16:1450328
|
C | CAGGACAA others(24): Show |
19 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(16): Show | 20 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617+138_1617+168d others(33): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450328 | ||||||
chr16:1450367
|
C | T | 4 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1617+130G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450367 | ||||||
chr16:1450388
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1617+109C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450388 | ||||||
chr16:1450484
|
C | T | 3 | a0001c0002t0002g0011a0001c0002t0002g0281a0001c0002t0002g0282 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617+13G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 17/24 | chr16 | 1450484 | ||||||
chr16:1450687
|
ACGGGGCC others(231): Show |
A | 26 | a0001c0003t0001g0365a0002c0006t0010g0010a0002c0006t0010g0255others(23): Show | 28 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1448-259_1448-22de others(1): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450687 | ||||||
chr16:1450688
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1448-22G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450688 | ||||||
chr16:1450707
|
G | GC | 123 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0052others(120): Show | 129 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1448-42dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450707 | ||||||
chr16:1450743
|
C | T | 1 | a0001c0004t0001g0311 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1448-77G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450743 | ||||||
chr16:1450917
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0086a0001c0001t0001g0092others(9): Show | 13 | HG00438.hp1 NA18951.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.1448-251G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450917 | ||||||
chr16:1450939
|
C | A | 8 | a0002c0011t0018g0254a0002c0011t0018g0270a0002c0011t0018g0271others(5): Show | 8 | HG01891.hp1 HG03098.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1448-273G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1450939 | ||||||
chr16:1451011
|
A | G | 8 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG00735.hp2 HG01167.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1448-345T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451011 | ||||||
chr16:1451047
|
G | T | 2 | a0001c0001t0049g0238a0001c0002t0044g0071 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1448-381C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451047 | ||||||
chr16:1451135
|
G | T | 8 | a0001c0004t0004g0287a0001c0005t0004g0037a0001c0005t0004g0164others(5): Show | 8 | HG00280.hp1 HG01081.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1448-469C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451135 | ||||||
chr16:1451179
|
G | A | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1447+444C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451179 | ||||||
chr16:1451214
|
C | A | 2 | a0003c0016t0050g0154a0003c0021t0013g0189 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1447+409G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451214 | ||||||
chr16:1451240
|
C | T | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1447+383G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451240 | ||||||
chr16:1451320
|
G | A | 5 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447+303C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451320 | ||||||
chr16:1451374
|
G | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(221): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1447+249C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451374 | ||||||
chr16:1451464
|
C | A | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1447+159G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451464 | ||||||
chr16:1451575
|
C | T | 1 | a0001c0002t0043g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1447+48G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451575 | ||||||
chr16:1451605
|
G | A | 1 | a0001c0002t0036g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1447+18C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 16/24 | chr16 | 1451605 | ||||||
chr16:1451788
|
C | T | 12 | a0002c0008t0017g0009a0002c0008t0017g0160a0002c0008t0027g0252others(9): Show | 13 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-72G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1451788 | ||||||
chr16:1451957
|
C | T | 26 | a0001c0001t0004g0146a0001c0001t0045g0230a0001c0004t0004g0287others(23): Show | 26 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1354-241G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1451957 | ||||||
chr16:1451970
|
G | C | 1 | a0005c0014t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1354-254C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1451970 | ||||||
chr16:1452021
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0236 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1354-305G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452021 | ||||||
chr16:1452049
|
G | C | 1 | a0001c0001t0032g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1354-333C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452049 | ||||||
chr16:1452320
|
C | T | 1 | a0001c0005t0004g0272 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1353+435G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452320 | ||||||
chr16:1452324
|
TGGTTCCT others(23): Show |
T | 1 | a0001c0003t0001g0381 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1353+401_1353+430d others(32): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452324 | ||||||
chr16:1452337
|
C | T | 25 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(22): Show | 27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1353+418G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452337 | ||||||
chr16:1452338
|
G | A | 5 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+417C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452338 | ||||||
chr16:1452378
|
C | T | 8 | a0002c0006t0024g0263a0002c0006t0025g0260a0002c0006t0025g0266others(5): Show | 8 | HG00735.hp1 HG01074.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353+377G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452378 | ||||||
chr16:1452382
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1353+373G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452382 | ||||||
chr16:1452386
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1353+369G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452386 | ||||||
chr16:1452429
|
G | A | 1 | a0001c0004t0001g0353 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1353+326C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452429 | ||||||
chr16:1452611
|
T | C | 1 | a0001c0002t0002g0232 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1353+144A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452611 | ||||||
chr16:1452640
|
C | T | 1 | a0002c0006t0025g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1353+115G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452640 | ||||||
chr16:1452641
|
G | A | 1 | a0001c0002t0001g0237 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1353+114C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452641 | ||||||
chr16:1452672
|
C | T | 1 | a0001c0003t0002g0327 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1353+83G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452672 | ||||||
chr16:1452677
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1353+78G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452677 | ||||||
chr16:1452683
|
C | T | 2 | a0001c0001t0049g0238a0001c0002t0044g0071 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1353+72G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452683 | ||||||
chr16:1452705
|
G | T | 5 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+50C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452705 | ||||||
chr16:1452734
|
C | T | 12 | a0002c0008t0017g0009a0002c0008t0017g0160a0002c0008t0027g0252others(9): Show | 13 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1353+21G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 15/24 | chr16 | 1452734 | ||||||
chr16:1452930
|
G | A | 1 | a0001c0004t0001g0364 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1215-37C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1452930 | ||||||
chr16:1452941
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1215-48G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1452941 | ||||||
chr16:1452946
|
C | T | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1215-53G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1452946 | ||||||
chr16:1453019
|
G | T | 1 | a0001c0004t0012g0338 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1215-126C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453019 | ||||||
chr16:1453032
|
A | C | 5 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0009t0016g0079others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215-139T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453032 | ||||||
chr16:1453114
|
T | C | 3 | a0001c0002t0002g0011a0001c0002t0002g0281a0001c0002t0002g0282 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215-221A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453114 | ||||||
chr16:1453153
|
G | A | 6 | a0001c0002t0001g0216a0001c0004t0001g0343a0001c0004t0001g0351others(3): Show | 6 | HG01109.hp1 HG02056.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215-260C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453153 | ||||||
chr16:1453197
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1215-304C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453197 | ||||||
chr16:1453203
|
G | A | 1 | a0001c0002t0002g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1215-310C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453203 | ||||||
chr16:1453257
|
C | A | 1 | a0001c0002t0036g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1215-364G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453257 | ||||||
chr16:1453259
|
C | T | 2 | a0001c0001t0049g0238a0001c0002t0044g0071 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1215-366G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453259 | ||||||
chr16:1453260
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1215-367C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453260 | ||||||
chr16:1453265
|
G | A | 2 | a0001c0004t0006g0022a0001c0004t0006g0023 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1215-372C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453265 | ||||||
chr16:1453288
|
T | C | 33 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(30): Show | 35 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1215-395A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453288 | ||||||
chr16:1453309
|
G | A | 19 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(16): Show | 21 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1215-416C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453309 | ||||||
chr16:1453428
|
T | C | 34 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(31): Show | 36 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1214+406A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453428 | ||||||
chr16:1453429
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1214+405C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453429 | ||||||
chr16:1453433
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1214+401G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453433 | ||||||
chr16:1453443
|
C | T | 3 | a0002c0009t0016g0079a0002c0009t0016g0080a0002c0009t0016g0081 | 3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1214+391G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453443 | ||||||
chr16:1453650
|
C | T | 1 | a0002c0011t0018g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1214+184G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453650 | ||||||
chr16:1453662
|
G | A | 1 | a0001c0003t0003g0377 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1214+172C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453662 | ||||||
chr16:1453786
|
T | C | 1 | a0001c0003t0002g0295 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1214+48A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 14/24 | chr16 | 1453786 | ||||||
chr16:1453941
|
G | C | 1 | a0001c0001t0001g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1154-47C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1453941 | ||||||
chr16:1453948
|
C | T | 1 | a0001c0001t0039g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1154-54G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1453948 | ||||||
chr16:1453952
|
C | T | 1 | a0001c0002t0002g0039 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1154-58G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1453952 | ||||||
chr16:1454016
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(263): Show | 274 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1154-122T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454016 | ||||||
chr16:1454019
|
G | A | 2 | a0001c0003t0002g0318a0001c0003t0005g0317 | 2 | HG00099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1154-125C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454019 | ||||||
chr16:1454148
|
T | C | 116 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0087others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1154-254A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454148 | ||||||
chr16:1454214
|
G | A | 23 | a0001c0001t0039g0174a0001c0002t0002g0279a0001c0002t0015g0268others(20): Show | 24 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1153+197C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454214 | ||||||
chr16:1454229
|
C | T | 23 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(20): Show | 23 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1153+182G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454229 | ||||||
chr16:1454277
|
C | G | 1 | a0001c0019t0002g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+134G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454277 | ||||||
chr16:1454285
|
C | A | 1 | a0001c0005t0004g0037 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1153+126G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454285 | ||||||
chr16:1454300
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1153+111C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 13/24 | chr16 | 1454300 | ||||||
chr16:1454496
|
G | A | 3 | a0002c0009t0016g0079a0002c0009t0016g0080a0002c0009t0016g0081 | 3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1099-31C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454496 | ||||||
chr16:1454621
|
C | T | 1 | a0001c0004t0001g0301 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099-156G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454621 | ||||||
chr16:1454629
|
G | T | 1 | a0001c0001t0001g0033 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1099-164C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454629 | ||||||
chr16:1454632
|
C | T | 295 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(292): Show | 305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1099-167G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454632 | ||||||
chr16:1454659
|
G | A | 1 | a0001c0002t0001g0231 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1099-194C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454659 | ||||||
chr16:1454701
|
C | T | 118 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0002g0130others(115): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1099-236G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454701 | ||||||
chr16:1454709
|
G | A | 3 | a0001c0001t0032g0119a0001c0003t0002g0316a0001c0003t0038g0315 | 3 | HG02698.hp1 NA18974.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1099-244C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454709 | ||||||
chr16:1454733
|
CAT | C | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1099-270_1099-269d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454733 | ||||||
chr16:1454741
|
G | A | 2 | a0001c0004t0006g0022a0001c0004t0006g0023 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1099-276C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454741 | ||||||
chr16:1454770
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(185): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1099-305G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454770 | ||||||
chr16:1454850
|
G | A | 1 | a0001c0004t0001g0364 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1098+284C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454850 | ||||||
chr16:1454856
|
G | A | 1 | a0001c0001t0005g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1098+278C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454856 | ||||||
chr16:1454866
|
C | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0118 | 2 | NA18945.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1098+268G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454866 | ||||||
chr16:1454880
|
G | A | 30 | a0001c0001t0004g0146a0001c0004t0004g0287a0001c0005t0001g0190others(27): Show | 31 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1098+254C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454880 | ||||||
chr16:1454904
|
A | G | 1 | a0003c0013t0001g0109 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1098+230T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454904 | ||||||
chr16:1454933
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(225): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1098+201A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454933 | ||||||
chr16:1454935
|
A | T | 1 | a0001c0004t0001g0355 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1098+199T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1454935 | ||||||
chr16:1455003
|
C | T | 2 | a0002c0008t0017g0009a0002c0008t0017g0160 | 3 | HG01243.hp2 HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+131G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 12/24 | chr16 | 1455003 | ||||||
chr16:1455275
|
C | T | 1 | a0001c0003t0003g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.982-25G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455275 | ||||||
chr16:1455276
|
G | A | 3 | a0001c0001t0049g0238a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG03209.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.982-26C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455276 | ||||||
chr16:1455277
|
C | G | 2 | a0002c0012t0014g0015a0002c0012t0014g0016 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.982-27G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455277 | ||||||
chr16:1455307
|
CACGGACC others(4): Show |
C | 1 | a0001c0001t0001g0033 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.982-68_982-58delTG others(9): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455307 | ||||||
chr16:1455369
|
G | A | 25 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(22): Show | 27 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.982-119C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455369 | ||||||
chr16:1455418
|
G | A | 2 | a0003c0016t0050g0154a0003c0021t0013g0189 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.982-168C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455418 | ||||||
chr16:1455428
|
C | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(260): Show | 274 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.982-178G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455428 | ||||||
chr16:1455493
|
C | G | 1 | a0001c0005t0005g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.981+238G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455493 | ||||||
chr16:1455494
|
C | T | 3 | a0002c0009t0016g0079a0002c0009t0016g0080a0002c0009t0016g0081 | 3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.981+237G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455494 | ||||||
chr16:1455557
|
G | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.981+174C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455557 | ||||||
chr16:1455587
|
T | C | 37 | a0001c0001t0004g0146a0001c0004t0004g0287a0001c0005t0001g0179others(34): Show | 38 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.981+144A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455587 | ||||||
chr16:1455598
|
C | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(235): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.981+133G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 11/24 | chr16 | 1455598 | ||||||
chr16:1455825
|
A | G | 2 | a0003c0016t0050g0154a0003c0021t0013g0189 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.917-30T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455825 | ||||||
chr16:1455866
|
C | G | 11 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0108others(8): Show | 11 | HG00423.hp1 HG01934.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-71G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455866 | ||||||
chr16:1455891
|
G | A | 16 | a0001c0002t0002g0200a0001c0002t0013g0028a0001c0002t0013g0029others(13): Show | 17 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.917-96C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455891 | ||||||
chr16:1455910
|
G | A | 1 | a0001c0001t0012g0066 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.917-115C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455910 | ||||||
chr16:1455931
|
G | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.917-136C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455931 | ||||||
chr16:1455977
|
G | A | 8 | a0002c0008t0027g0252a0002c0008t0027g0253a0002c0011t0018g0254others(5): Show | 8 | HG02717.hp1 HG03098.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.916+136C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455977 | ||||||
chr16:1455979
|
C | T | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+134G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1455979 | ||||||
chr16:1456010
|
G | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+103C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1456010 | ||||||
chr16:1456033
|
C | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+80G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1456033 | ||||||
chr16:1456072
|
G | A | 5 | a0001c0001t0002g0228a0001c0002t0003g0201a0001c0002t0003g0202others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+41C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 10/24 | chr16 | 1456072 | ||||||
chr16:1456252
|
C | T | 5 | a0001c0001t0002g0228a0001c0002t0003g0201a0001c0002t0003g0202others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-46G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456252 | ||||||
chr16:1456317
|
A | G | 15 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(12): Show | 16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-111T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456317 | ||||||
chr16:1456389
|
C | T | 2 | a0003c0016t0050g0154a0003c0021t0013g0189 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.823-183G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456389 | ||||||
chr16:1456396
|
C | T | 1 | a0002c0026t0024g0309 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.823-190G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456396 | ||||||
chr16:1456406
|
G | C | 37 | a0001c0001t0004g0146a0001c0004t0004g0287a0001c0005t0001g0179others(34): Show | 38 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.823-200C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456406 | ||||||
chr16:1456462
|
A | G | 15 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(12): Show | 16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-256T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456462 | ||||||
chr16:1456488
|
C | A | 2 | a0001c0004t0006g0022a0001c0004t0006g0023 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.823-282G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456488 | ||||||
chr16:1456489
|
G | A | 127 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0002g0130others(124): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.823-283C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456489 | ||||||
chr16:1456541
|
C | T | 1 | a0001c0007t0004g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823-335G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456541 | ||||||
chr16:1456542
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(224): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.823-336G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456542 | ||||||
chr16:1456607
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.823-401C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456607 | ||||||
chr16:1456621
|
C | T | 6 | a0002c0008t0017g0009a0002c0008t0017g0160a0002c0008t0027g0252others(3): Show | 7 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-415G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456621 | ||||||
chr16:1456648
|
G | A | 2 | a0003c0016t0050g0154a0003c0021t0013g0189 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.823-442C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456648 | ||||||
chr16:1456701
|
C | T | 1 | a0001c0004t0001g0349 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.823-495G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456701 | ||||||
chr16:1456709
|
C | T | 1 | a0001c0002t0001g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.823-503G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456709 | ||||||
chr16:1456733
|
C | T | 1 | a0001c0002t0001g0231 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.822+521G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456733 | ||||||
chr16:1456773
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(180): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.822+481C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456773 | ||||||
chr16:1456795
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.822+459A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456795 | ||||||
chr16:1456812
|
G | A | 2 | a0001c0003t0002g0290a0001c0003t0003g0289 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.822+442C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456812 | ||||||
chr16:1456813
|
C | G | 1 | a0001c0004t0001g0345 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.822+441G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456813 | ||||||
chr16:1456815
|
T | C | 2 | a0001c0002t0002g0074a0001c0002t0002g0078 | 2 | HG01361.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.822+439A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456815 | ||||||
chr16:1456838
|
C | CAA | 14 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0257others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.822+414_822+415dup others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456838 | ||||||
chr16:1456838
|
CA | C | 8 | a0001c0001t0001g0091a0001c0001t0001g0245a0001c0001t0001g0247others(5): Show | 8 | HG01167.hp1 HG03225.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+415delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456838 | ||||||
chr16:1456919
|
T | C | 1 | a0002c0011t0018g0270 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.822+335A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456919 | ||||||
chr16:1456920
|
G | A | 1 | a0001c0004t0001g0013 | 2 | NA18939.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.822+334C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456920 | ||||||
chr16:1456999
|
T | C | 16 | a0001c0005t0004g0153a0002c0006t0010g0010a0002c0006t0010g0255others(13): Show | 17 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.822+255A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1456999 | ||||||
chr16:1457126
|
G | T | 5 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0009t0016g0079others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+128C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457126 | ||||||
chr16:1457148
|
C | A | 2 | a0002c0008t0027g0252a0002c0008t0027g0253 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.822+106G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457148 | ||||||
chr16:1457182
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.822+72G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457182 | ||||||
chr16:1457208
|
C | T | 3 | a0001c0002t0002g0088a0001c0003t0001g0346a0001c0004t0001g0382 | 3 | HG00099.hp2 HG03704.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.822+46G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457208 | ||||||
chr16:1457217
|
G | A | 1 | a0001c0002t0044g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.822+37C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457217 | ||||||
chr16:1457236
|
C | T | 1 | a0001c0002t0013g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.822+18G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457236 | ||||||
chr16:1457237
|
A | G | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.822+17T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 9/24 | chr16 | 1457237 | ||||||
chr16:1457357
|
G | GTGCTCAG others(43): Show |
4 | a0001c0001t0001g0094a0001c0002t0002g0199a0001c0004t0005g0356others(1): Show | 4 | HG00280.hp2 HG00738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-70_739-21dupTC others(48): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457357 | ||||||
chr16:1457357
|
GTGCTCAG others(43): Show |
G | 17 | a0001c0001t0001g0106a0001c0002t0001g0059a0001c0002t0001g0068others(14): Show | 17 | HG00558.hp2 HG02155.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.739-70_739-21delTC others(48): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457357 | ||||||
chr16:1457357
|
GTGCTCAG others(93): Show |
G | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0035g0034others(1): Show | 4 | HG02559.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-120_739-21delT others(99): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457357 | ||||||
chr16:1457407
|
A | G | 2 | a0001c0001t0001g0140a0001c0005t0004g0153 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.739-70T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457407 | ||||||
chr16:1457407
|
ATGCTCAG others(93): Show |
A | 34 | a0001c0002t0001g0007a0001c0002t0001g0150a0001c0002t0002g0151others(31): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.739-170_739-71delC others(99): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457407 | ||||||
chr16:1457430
|
G | T | 1 | a0001c0002t0044g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.739-93C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457430 | ||||||
chr16:1457455
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | NA18957.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.739-118G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457455 | ||||||
chr16:1457457
|
A | ATGCTCAG others(43): Show |
5 | a0001c0001t0001g0126a0001c0005t0004g0267a0001c0005t0004g0274others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-170_739-121dup others(50): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457457
|
A | ATGCTCAG others(93): Show |
1 | a0001c0001t0032g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.738+137_739-121dup others(100): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457457
|
A | ATGCTCAG others(143): Show |
2 | a0002c0009t0005g0031a0002c0009t0005g0284 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.738+87_739-121dupC others(149): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457457
|
A | ATGCTCAG others(293): Show |
1 | a0001c0004t0001g0364 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.739-121_739-120ins others(300): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457457
|
A | ATGCTCAG others(143): Show |
3 | a0002c0009t0016g0079a0002c0009t0016g0080a0002c0009t0016g0081 | 3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.739-121_739-120ins others(150): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457457
|
A | G | 20 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0140others(17): Show | 21 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-120T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457457
|
ATGCTCAG others(43): Show |
A | 16 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0008g0077others(13): Show | 17 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.739-170_739-121del others(50): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457457
|
ATGCTCAG others(93): Show |
A | 8 | a0001c0001t0001g0247a0001c0003t0003g0014a0002c0006t0010g0010others(5): Show | 10 | HG00642.hp2 HG01099.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.738+137_739-121del others(100): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457457 | ||||||
chr16:1457505
|
C | T | 1 | a0001c0003t0020g0374 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.739-168G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457505 | ||||||
chr16:1457507
|
G | A | 2 | a0002c0009t0016g0080a0002c0009t0016g0081 | 2 | NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.739-170C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457507 | ||||||
chr16:1457516
|
G | A | 3 | a0001c0002t0002g0211a0001c0002t0002g0217a0001c0002t0011g0221 | 3 | HG00323.hp1 HG01255.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.738+178C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457516 | ||||||
chr16:1457521
|
G | A | 2 | a0002c0008t0017g0009a0002c0008t0017g0160 | 3 | HG01243.hp2 HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.738+173C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457521 | ||||||
chr16:1457527
|
C | T | 1 | a0002c0006t0025g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.738+167G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457527 | ||||||
chr16:1457579
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0084 | 3 | HG03654.hp2 HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.738+115G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457579 | ||||||
chr16:1457605
|
C | T | 8 | a0001c0005t0004g0037a0001c0005t0004g0164a0001c0005t0004g0165others(5): Show | 8 | HG00280.hp1 HG01081.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.738+89G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457605 | ||||||
chr16:1457628
|
C | T | 1 | a0001c0017t0041g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.738+66G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 8/24 | chr16 | 1457628 | ||||||
chr16:1457777
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(212): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.676-21A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457777 | ||||||
chr16:1457813
|
C | G | 1 | a0001c0002t0002g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.676-57G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457813 | ||||||
chr16:1457819
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0203 | 3 | HG02015.hp1 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.676-63G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457819 | ||||||
chr16:1457841
|
C | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0111others(91): Show | 99 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.676-85G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457841 | ||||||
chr16:1457842
|
G | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0111others(80): Show | 88 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.676-86C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457842 | ||||||
chr16:1457934
|
A | T | 1 | a0001c0004t0001g0307 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.676-178T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457934 | ||||||
chr16:1457979
|
C | T | 1 | a0001c0002t0013g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.676-223G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457979 | ||||||
chr16:1457987
|
C | T | 245 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(242): Show | 256 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.676-231G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1457987 | ||||||
chr16:1458062
|
C | CA | 214 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0033others(211): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.676-307dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458062 | ||||||
chr16:1458239
|
T | C | 7 | a0001c0002t0002g0248a0001c0003t0002g0292a0001c0003t0002g0293others(4): Show | 7 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-483A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458239 | ||||||
chr16:1458262
|
T | C | 1 | a0001c0003t0002g0326 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.676-506A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458262 | ||||||
chr16:1458330
|
T | C | 11 | a0001c0001t0001g0161a0001c0007t0002g0169a0001c0007t0002g0170others(8): Show | 11 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-574A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458330 | ||||||
chr16:1458346
|
C | T | 7 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0004g0182others(4): Show | 8 | HG01106.hp2 HG01123.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-590G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458346 | ||||||
chr16:1458414
|
C | T | 3 | a0001c0002t0002g0011a0001c0002t0002g0281a0001c0002t0002g0282 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-658G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458414 | ||||||
chr16:1458520
|
C | T | 40 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0067others(37): Show | 41 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.675+587G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458520 | ||||||
chr16:1458543
|
A | C | 2 | a0001c0002t0002g0038a0001c0002t0002g0039 | 2 | NA18942.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.675+564T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458543 | ||||||
chr16:1458545
|
G | A | 8 | a0002c0006t0010g0010a0002c0006t0025g0260a0002c0006t0025g0266others(5): Show | 9 | HG00642.hp2 HG00735.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.675+562C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458545 | ||||||
chr16:1458559
|
G | A | 13 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0086others(10): Show | 14 | HG00438.hp1 NA18951.hp1 NA18953.hp1 others(11): Show |
intron_variant | MODIFIER | c.675+548C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458559 | ||||||
chr16:1458613
|
G | A | 1 | a0001c0003t0001g0365 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.675+494C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458613 | ||||||
chr16:1458643
|
G | A | 4 | a0001c0002t0002g0088a0001c0002t0020g0204a0001c0003t0020g0374others(1): Show | 4 | HG02080.hp1 HG03195.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+464C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458643 | ||||||
chr16:1458668
|
A | G | 207 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(204): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.675+439T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458668 | ||||||
chr16:1458673
|
G | A | 2 | a0001c0001t0045g0230a0001c0002t0002g0197 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.675+434C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458673 | ||||||
chr16:1458681
|
G | A | 2 | a0001c0001t0002g0224a0001c0002t0002g0222 | 2 | HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.675+426C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458681 | ||||||
chr16:1458735
|
T | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.675+372A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458735 | ||||||
chr16:1458899
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0140 | 3 | HG02970.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.675+208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458899 | ||||||
chr16:1458974
|
C | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.675+133G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458974 | ||||||
chr16:1458987
|
T | C | 45 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(42): Show | 47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.675+120A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458987 | ||||||
chr16:1458995
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0141a0001c0001t0007g0142 | 4 | NA18948.hp2 NA18959.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+112C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1458995 | ||||||
chr16:1459097
|
G | A | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.675+10C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 7/24 | chr16 | 1459097 | ||||||
chr16:1459215
|
G | A | 1 | a0001c0002t0002g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595-28C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459215 | ||||||
chr16:1459220
|
C | T | 1 | a0001c0005t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.595-33G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459220 | ||||||
chr16:1459245
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.595-58G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459245 | ||||||
chr16:1459270
|
T | C | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.595-83A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459270 | ||||||
chr16:1459277
|
A | G | 5 | a0001c0007t0002g0169a0001c0007t0002g0170a0001c0007t0002g0171others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-90T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459277 | ||||||
chr16:1459312
|
C | A | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-125G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459312 | ||||||
chr16:1459313
|
T | G | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-126A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459313 | ||||||
chr16:1459319
|
C | G | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-132G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459319 | ||||||
chr16:1459321
|
CAA | C | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-136_595-135del others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459321 | ||||||
chr16:1459335
|
C | T | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-148G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459335 | ||||||
chr16:1459346
|
A | G | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-159T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459346 | ||||||
chr16:1459349
|
A | C | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-162T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459349 | ||||||
chr16:1459350
|
G | T | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-163C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459350 | ||||||
chr16:1459354
|
C | A | 1 | a0001c0001t0009g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.595-167G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459354 | ||||||
chr16:1459358
|
C | CAA | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-172_595-171ins others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459358 | ||||||
chr16:1459360
|
C | T | 40 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0002g0224others(37): Show | 41 | HG00323.hp1 HG00544.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.595-173G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459360 | ||||||
chr16:1459364
|
A | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(198): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.595-177T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459364 | ||||||
chr16:1459368
|
C | G | 1 | a0001c0003t0003g0386 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.595-181G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459368 | ||||||
chr16:1459381
|
G | A | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-194C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459381 | ||||||
chr16:1459390
|
G | A | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-203C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459390 | ||||||
chr16:1459395
|
C | T | 3 | a0001c0001t0035g0034a0002c0008t0017g0009a0002c0008t0017g0160 | 4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459395 | ||||||
chr16:1459419
|
C | A | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-232G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459419 | ||||||
chr16:1459420
|
T | G | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-233A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459420 | ||||||
chr16:1459438
|
C | G | 1 | a0001c0002t0015g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.595-251G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459438 | ||||||
chr16:1459439
|
A | C | 139 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(136): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.595-252T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459439 | ||||||
chr16:1459440
|
T | C | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-253A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459440 | ||||||
chr16:1459454
|
A | C | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-267T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459454 | ||||||
chr16:1459455
|
G | T | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.595-268C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459455 | ||||||
chr16:1459464
|
G | A | 196 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(193): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.595-277C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459464 | ||||||
chr16:1459465
|
C | G | 19 | a0001c0001t0035g0034a0001c0001t0049g0238a0002c0008t0017g0009others(16): Show | 20 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.595-278G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459465 | ||||||
chr16:1459474
|
C | A | 118 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-287G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459474 | ||||||
chr16:1459490
|
GCAGCACA others(203): Show |
G | 19 | a0001c0001t0035g0034a0001c0001t0049g0238a0002c0008t0017g0009others(16): Show | 20 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.595-513_595-304del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459490 | ||||||
chr16:1459500
|
T | C | 116 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.595-313A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459500 | ||||||
chr16:1459500
|
T | G | 51 | a0001c0001t0008g0077a0001c0001t0045g0230a0001c0002t0002g0197others(48): Show | 53 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.595-313A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459500 | ||||||
chr16:1459509
|
C | A | 1 | a0001c0003t0001g0310 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.595-322G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459509 | ||||||
chr16:1459510
|
TCAGGGAA others(28): Show |
T | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.595-358_595-324del others(35): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459510 | ||||||
chr16:1459524
|
C | A | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-337G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459524 | ||||||
chr16:1459525
|
T | G | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-338A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459525 | ||||||
chr16:1459535
|
C | G | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-348G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459535 | ||||||
chr16:1459536
|
T | G | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-349A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459536 | ||||||
chr16:1459540
|
G | A | 5 | a0001c0001t0008g0077a0001c0001t0045g0230a0001c0002t0002g0197others(2): Show | 5 | HG01515.hp2 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-353C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459540 | ||||||
chr16:1459545
|
C | T | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-358G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459545 | ||||||
chr16:1459560
|
GCAGCACA others(133): Show |
G | 12 | a0001c0001t0001g0278a0001c0001t0005g0040a0001c0002t0001g0105others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-513_595-374del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459560 | ||||||
chr16:1459570
|
T | G | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-383A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459570 | ||||||
chr16:1459574
|
G | A | 49 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0247others(46): Show | 52 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.595-387C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459574 | ||||||
chr16:1459575
|
G | A | 116 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.595-388C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459575 | ||||||
chr16:1459585
|
G | A | 1 | a0001c0002t0002g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595-398C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459585 | ||||||
chr16:1459592
|
AGCTCAGC others(26): Show |
A | 3 | a0001c0001t0045g0230a0001c0002t0002g0197a0001c0002t0002g0223 | 3 | HG01515.hp2 HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.595-438_595-406del others(33): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459592 | ||||||
chr16:1459594
|
C | A | 118 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-407G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459594 | ||||||
chr16:1459595
|
T | G | 118 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-408A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459595 | ||||||
chr16:1459605
|
C | G | 118 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-418G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459605 | ||||||
chr16:1459606
|
T | G | 118 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-419A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459606 | ||||||
chr16:1459615
|
C | T | 118 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.595-428G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459615 | ||||||
chr16:1459628
|
GCT | G | 3 | a0001c0001t0045g0230a0001c0002t0002g0197a0001c0002t0002g0223 | 3 | HG01515.hp2 HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.595-443_595-442del others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459628 | ||||||
chr16:1459629
|
C | A | 119 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(116): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.595-442G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459629 | ||||||
chr16:1459630
|
T | G | 119 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(116): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.595-443A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459630 | ||||||
chr16:1459640
|
C | T | 1 | a0001c0002t0044g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.595-453G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459640 | ||||||
chr16:1459641
|
T | G | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-454A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459641 | ||||||
chr16:1459650
|
C | T | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-463G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459650 | ||||||
chr16:1459663
|
G | T | 2 | a0001c0005t0004g0182a0001c0005t0004g0193 | 2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.595-476C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459663 | ||||||
chr16:1459667
|
G | A | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-480C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459667 | ||||||
chr16:1459675
|
C | G | 121 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.595-488G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459675 | ||||||
chr16:1459685
|
T | TCAGGGAA others(63): Show |
1 | a0001c0002t0044g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.595-499_595-498ins others(70): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459685 | ||||||
chr16:1459685
|
TCAGGGAA others(273): Show |
T | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+453_595-499del | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459685 | ||||||
chr16:1459699
|
C | A | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-512G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459699 | ||||||
chr16:1459700
|
T | G | 122 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.595-513A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459700 | ||||||
chr16:1459704
|
C | A | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.595-517G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459704 | ||||||
chr16:1459928
|
C | A | 1 | a0001c0004t0001g0349 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.594+490G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459928 | ||||||
chr16:1459941
|
GAGAGCAG others(63): Show |
G | 3 | a0002c0008t0027g0252a0002c0008t0027g0253a0004c0018t0053g0276 | 3 | HG02717.hp1 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.594+407_594+476del others(70): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459941 | ||||||
chr16:1459994
|
G | A | 1 | a0001c0002t0013g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.594+424C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459994 | ||||||
chr16:1459997
|
G | A | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.594+421C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1459997 | ||||||
chr16:1460131
|
G | A | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.594+287C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460131 | ||||||
chr16:1460202
|
A | G | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+216T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460202 | ||||||
chr16:1460283
|
A | G | 197 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(194): Show | 204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.594+135T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460283 | ||||||
chr16:1460302
|
C | T | 1 | a0002c0009t0016g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.594+116G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460302 | ||||||
chr16:1460303
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0159 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.594+115C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460303 | ||||||
chr16:1460305
|
G | C | 8 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0078others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.594+113C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460305 | ||||||
chr16:1460401
|
G | A | 2 | a0002c0008t0027g0252a0002c0008t0027g0253 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.594+17C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 6/24 | chr16 | 1460401 | ||||||
chr16:1460537
|
A | G | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.485-10T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460537 | ||||||
chr16:1460561
|
C | T | 1 | a0001c0002t0043g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485-34G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460561 | ||||||
chr16:1460562
|
G | A | 2 | a0001c0002t0015g0275a0001c0002t0042g0269 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.485-35C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460562 | ||||||
chr16:1460566
|
T | G | 247 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0065others(244): Show | 255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.485-39A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460566 | ||||||
chr16:1460609
|
T | C | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485-82A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460609 | ||||||
chr16:1460633
|
G | A | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.485-106C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460633 | ||||||
chr16:1460665
|
G | A | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485-138C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460665 | ||||||
chr16:1460706
|
C | G | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.484+110G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460706 | ||||||
chr16:1460780
|
C | G | 3 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0011t0018g0254 | 3 | HG02055.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.484+36G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460780 | ||||||
chr16:1460784
|
C | T | 1 | a0001c0002t0044g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.484+32G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460784 | ||||||
chr16:1460799
|
C | T | 1 | a0001c0017t0041g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.484+17G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 5/24 | chr16 | 1460799 | ||||||
chr16:1461032
|
A | T | 1 | a0001c0001t0001g0110 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.352-84T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461032 | ||||||
chr16:1461099
|
C | T | 1 | a0001c0002t0003g0229 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.352-151G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461099 | ||||||
chr16:1461109
|
G | A | 5 | a0001c0007t0002g0169a0001c0007t0002g0170a0001c0007t0002g0171others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-161C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461109 | ||||||
chr16:1461111
|
C | T | 2 | a0001c0001t0008g0077a0001c0002t0015g0050 | 2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.352-163G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461111 | ||||||
chr16:1461118
|
G | A | 1 | a0001c0002t0044g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.352-170C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461118 | ||||||
chr16:1461138
|
G | C | 1 | a0001c0004t0001g0368 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.352-190C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461138 | ||||||
chr16:1461195
|
A | G | 1 | a0001c0005t0011g0008 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.351+210T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461195 | ||||||
chr16:1461197
|
C | T | 1 | a0002c0011t0018g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.351+208G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461197 | ||||||
chr16:1461228
|
C | T | 2 | a0002c0008t0017g0009a0002c0008t0017g0160 | 3 | HG01243.hp2 HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.351+177G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461228 | ||||||
chr16:1461236
|
G | A | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.351+169C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461236 | ||||||
chr16:1461371
|
C | T | 44 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(41): Show | 46 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.351+34G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 4/24 | chr16 | 1461371 | ||||||
chr16:1461538
|
C | T | 1 | a0003c0013t0001g0109 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.285+65G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461538 | ||||||
chr16:1461551
|
G | T | 196 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(193): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.285+52C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461551 | ||||||
chr16:1461567
|
C | T | 1 | a0007c0025t0002g0352 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.285+36G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461567 | ||||||
chr16:1461568
|
G | A | 1 | a0001c0001t0002g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.285+35C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 3/24 | chr16 | 1461568 | ||||||
chr16:1461757
|
A | G | 69 | a0001c0001t0035g0034a0001c0001t0049g0238a0001c0002t0002g0279others(66): Show | 72 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.214-83T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461757 | ||||||
chr16:1461810
|
C | T | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.214-136G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461810 | ||||||
chr16:1461812
|
C | T | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214-138G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461812 | ||||||
chr16:1461936
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.214-262A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461936 | ||||||
chr16:1461999
|
C | A | 1 | a0001c0003t0003g0383 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.214-325G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1461999 | ||||||
chr16:1462088
|
GA | G | 182 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0001g0198others(179): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.214-415delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462088 | ||||||
chr16:1462101
|
A | G | 135 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(132): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.214-427T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462101 | ||||||
chr16:1462251
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214-577C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462251 | ||||||
chr16:1462256
|
C | G | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.214-582G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462256 | ||||||
chr16:1462365
|
C | CT | 51 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0048others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.214-692dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | ||||||
chr16:1462365
|
CT | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(16): Show | 20 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.214-692delA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | ||||||
chr16:1462365
|
CTTTTT | C | 6 | a0001c0002t0003g0127a0001c0003t0002g0288a0001c0003t0002g0295others(3): Show | 7 | HG00621.hp2 HG00741.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-696_214-692del others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | ||||||
chr16:1462365
|
CTTTTTT | C | 103 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(100): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.214-697_214-692del others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | ||||||
chr16:1462365
|
CTTTTTTT | C | 27 | a0001c0001t0035g0034a0001c0001t0049g0238a0001c0002t0001g0128others(24): Show | 29 | HG00558.hp2 HG01070.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.214-698_214-692del others(7): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | ||||||
chr16:1462365
|
CTTTTTTT others(1): Show |
C | 44 | a0001c0003t0003g0303a0001c0005t0001g0179a0001c0005t0001g0183others(41): Show | 46 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.214-699_214-692del others(8): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462365 | ||||||
chr16:1462462
|
G | A | 15 | a0001c0001t0035g0034a0001c0001t0049g0238a0001c0002t0002g0279others(12): Show | 16 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.214-788C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462462 | ||||||
chr16:1462624
|
G | A | 1 | a0003c0016t0050g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214-950C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462624 | ||||||
chr16:1462665
|
C | CA | 28 | a0001c0001t0001g0043a0001c0001t0001g0101a0001c0001t0001g0133others(25): Show | 28 | HG00597.hp1 HG00621.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.214-992dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | ||||||
chr16:1462665
|
C | CAA | 8 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0003t0001g0347others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-993_214-992dup others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | ||||||
chr16:1462665
|
C | CAAAAAAA | 6 | a0001c0022t0048g0172a0002c0008t0027g0252a0002c0008t0027g0253others(3): Show | 6 | HG01891.hp2 HG02717.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-998_214-992dup others(7): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | ||||||
chr16:1462665
|
C | CAAAAAAA others(3): Show |
1 | a0003c0016t0050g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214-1001_214-992du others(11): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462665 | ||||||
chr16:1462666
|
A | AAAAAC | 120 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.214-993_214-992ins others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462666 | ||||||
chr16:1462671
|
A | C | 123 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(120): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.214-997T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462671 | ||||||
chr16:1462672
|
A | C | 1 | a0001c0003t0003g0303 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.214-998T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462672 | ||||||
chr16:1462675
|
A | C | 1 | a0001c0003t0005g0379 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.214-1001T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462675 | ||||||
chr16:1462676
|
A | C | 113 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0220others(110): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.214-1002T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462676 | ||||||
chr16:1462677
|
A | AAC | 45 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(42): Show | 47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.214-1004_214-1003i others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462677 | ||||||
chr16:1462677
|
A | C | 1 | a0001c0003t0003g0303 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.214-1003T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462677 | ||||||
chr16:1462723
|
G | A | 1 | a0002c0011t0018g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-1049C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462723 | ||||||
chr16:1462730
|
A | G | 46 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(43): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.214-1056T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462730 | ||||||
chr16:1462770
|
C | T | 7 | a0001c0001t0001g0278a0001c0002t0034g0277a0002c0009t0005g0031others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-1096G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462770 | ||||||
chr16:1462884
|
G | T | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214-1210C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462884 | ||||||
chr16:1462978
|
T | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.214-1304A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462978 | ||||||
chr16:1462984
|
G | T | 1 | a0002c0011t0018g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-1310C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1462984 | ||||||
chr16:1463167
|
C | T | 2 | a0001c0001t0001g0278a0001c0002t0034g0277 | 2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-1493G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463167 | ||||||
chr16:1463356
|
C | T | 5 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0009t0016g0079others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-1682G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463356 | ||||||
chr16:1463393
|
A | G | 154 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0278others(151): Show | 159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.214-1719T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463393 | ||||||
chr16:1463422
|
C | T | 138 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0002g0224others(135): Show | 143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.214-1748G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463422 | ||||||
chr16:1463440
|
C | T | 4 | a0001c0005t0004g0153a0001c0005t0004g0180a0001c0005t0004g0181others(1): Show | 4 | HG01071.hp1 HG02055.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-1766G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463440 | ||||||
chr16:1463505
|
C | T | 33 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(30): Show | 34 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.213+1762G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463505 | ||||||
chr16:1463515
|
G | A | 2 | a0001c0001t0008g0077a0001c0002t0015g0050 | 2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.213+1752C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463515 | ||||||
chr16:1463573
|
G | A | 124 | a0001c0001t0001g0198a0001c0001t0001g0208a0001c0001t0001g0220others(121): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.213+1694C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463573 | ||||||
chr16:1463646
|
G | A | 1 | a0001c0002t0001g0085 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.213+1621C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463646 | ||||||
chr16:1463684
|
G | A | 155 | a0001c0001t0001g0198a0001c0001t0001g0208a0001c0001t0001g0220others(152): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.213+1583C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463684 | ||||||
chr16:1463690
|
T | C | 155 | a0001c0001t0001g0198a0001c0001t0001g0208a0001c0001t0001g0220others(152): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.213+1577A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463690 | ||||||
chr16:1463704
|
C | G | 155 | a0001c0001t0001g0198a0001c0001t0001g0208a0001c0001t0001g0220others(152): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.213+1563G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463704 | ||||||
chr16:1463719
|
A | G | 3 | a0001c0001t0035g0034a0002c0008t0017g0009a0002c0008t0017g0160 | 4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1548T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463719 | ||||||
chr16:1463774
|
G | GA | 14 | a0001c0004t0002g0348a0002c0006t0010g0010a0002c0006t0010g0255others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.213+1492dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | ||||||
chr16:1463774
|
G | GAA | 32 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(29): Show | 33 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.213+1491_213+1492d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | ||||||
chr16:1463774
|
GA | G | 150 | a0001c0001t0001g0110a0001c0001t0001g0198a0001c0001t0001g0208others(147): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.213+1492delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | ||||||
chr16:1463774
|
GAA | G | 6 | a0001c0002t0044g0071a0001c0007t0002g0169a0001c0007t0002g0170others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+1491_213+1492d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463774 | ||||||
chr16:1463827
|
T | C | 5 | a0001c0007t0002g0169a0001c0007t0002g0170a0001c0007t0002g0171others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+1440A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463827 | ||||||
chr16:1463949
|
A | G | 5 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0009t0016g0079others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+1318T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1463949 | ||||||
chr16:1464105
|
G | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0004t0006g0025others(1): Show | 4 | HG01109.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1162C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464105 | ||||||
chr16:1464170
|
G | A | 3 | a0001c0002t0002g0011a0001c0002t0002g0281a0001c0002t0002g0282 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+1097C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464170 | ||||||
chr16:1464189
|
A | G | 1 | a0001c0002t0002g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.213+1078T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464189 | ||||||
chr16:1464260
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.213+1007C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464260 | ||||||
chr16:1464324
|
C | T | 58 | a0001c0001t0001g0278a0001c0001t0035g0034a0001c0001t0049g0238others(55): Show | 60 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.213+943G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464324 | ||||||
chr16:1464343
|
C | G | 25 | a0001c0001t0001g0278a0001c0001t0035g0034a0001c0001t0049g0238others(22): Show | 26 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.213+924G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464343 | ||||||
chr16:1464444
|
C | T | 1 | a0001c0003t0002g0314 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.213+823G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464444 | ||||||
chr16:1464445
|
G | A | 1 | a0001c0017t0041g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.213+822C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464445 | ||||||
chr16:1464463
|
G | C | 6 | a0001c0002t0044g0071a0001c0007t0002g0169a0001c0007t0002g0170others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+804C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464463 | ||||||
chr16:1464590
|
G | T | 2 | a0001c0001t0001g0278a0001c0002t0034g0277 | 2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.213+677C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464590 | ||||||
chr16:1464651
|
A | G | 203 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0208others(200): Show | 210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.213+616T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464651 | ||||||
chr16:1464673
|
G | A | 6 | a0002c0011t0018g0254a0002c0011t0018g0270a0002c0011t0018g0271others(3): Show | 6 | HG03098.hp2 HG03209.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+594C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464673 | ||||||
chr16:1464691
|
T | C | 8 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+576A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464691 | ||||||
chr16:1464721
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.213+546G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464721 | ||||||
chr16:1464724
|
G | A | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.213+543C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464724 | ||||||
chr16:1464746
|
G | A | 36 | a0001c0001t0001g0033a0001c0001t0001g0067a0001c0001t0001g0086others(33): Show | 37 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.213+521C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464746 | ||||||
chr16:1464798
|
G | C | 1 | a0001c0004t0001g0382 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.213+469C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464798 | ||||||
chr16:1464824
|
T | A | 1 | a0001c0002t0043g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.213+443A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464824 | ||||||
chr16:1464851
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.213+416G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464851 | ||||||
chr16:1464966
|
G | GC | 117 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0208others(114): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.213+300dupG | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1464966 | ||||||
chr16:1465004
|
C | T | 2 | a0001c0001t0001g0108a0003c0013t0001g0109 | 2 | HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.213+263G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465004 | ||||||
chr16:1465049
|
C | T | 1 | a0001c0001t0045g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.213+218G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465049 | ||||||
chr16:1465068
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.213+199G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465068 | ||||||
chr16:1465134
|
C | G | 7 | a0001c0005t0004g0037a0001c0005t0004g0164a0001c0005t0004g0165others(4): Show | 7 | HG00280.hp1 HG01081.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+133G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465134 | ||||||
chr16:1465158
|
G | A | 1 | a0001c0003t0002g0294 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.213+109C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465158 | ||||||
chr16:1465161
|
C | T | 129 | a0001c0001t0001g0106a0001c0001t0001g0198a0001c0001t0001g0208others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.213+106G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465161 | ||||||
chr16:1465195
|
G | A | 5 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0009t0016g0079others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+72C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465195 | ||||||
chr16:1465246
|
C | T | 3 | a0001c0002t0002g0011a0001c0002t0002g0281a0001c0002t0002g0282 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+21G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465246 | ||||||
chr16:1465247
|
G | T | 6 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0078others(3): Show | 6 | HG01255.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+20C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 2/24 | chr16 | 1465247 | ||||||
chr16:1465381
|
C | T | 1 | a0001c0003t0008g0384 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.142-43G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465381 | ||||||
chr16:1465391
|
C | T | 1 | a0001c0002t0003g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.142-53G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465391 | ||||||
chr16:1465413
|
C | T | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-75G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465413 | ||||||
chr16:1465414
|
G | T | 50 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(47): Show | 52 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-76C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465414 | ||||||
chr16:1465427
|
G | A | 3 | a0001c0001t0001g0060a0001c0004t0001g0285a0001c0004t0001g0286 | 3 | HG00423.hp1 NA18966.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.142-89C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465427 | ||||||
chr16:1465433
|
C | A | 3 | a0001c0002t0003g0201a0001c0002t0003g0202a0001c0002t0003g0212 | 3 | HG02109.hp2 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.142-95G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465433 | ||||||
chr16:1465502
|
G | A | 195 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0278others(192): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.142-164C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465502 | ||||||
chr16:1465514
|
G | A | 50 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(47): Show | 52 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-176C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465514 | ||||||
chr16:1465534
|
C | G | 3 | a0001c0001t0035g0034a0002c0008t0017g0009a0002c0008t0017g0160 | 4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-196G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465534 | ||||||
chr16:1465563
|
G | A | 1 | a0001c0004t0001g0349 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-225C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465563 | ||||||
chr16:1465580
|
G | A | 3 | a0001c0005t0005g0187a0001c0005t0005g0188a0003c0021t0013g0189 | 3 | HG01884.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142-242C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465580 | ||||||
chr16:1465643
|
G | A | 5 | a0001c0007t0002g0169a0001c0007t0002g0170a0001c0007t0002g0171others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-305C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465643 | ||||||
chr16:1465754
|
C | T | 1 | a0001c0005t0004g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.142-416G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465754 | ||||||
chr16:1465763
|
C | G | 1 | a0001c0002t0015g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-425G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465763 | ||||||
chr16:1465801
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.142-463G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465801 | ||||||
chr16:1465869
|
T | C | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-531A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465869 | ||||||
chr16:1465925
|
T | C | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-587A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465925 | ||||||
chr16:1465941
|
G | A | 1 | a0002c0006t0024g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142-603C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1465941 | ||||||
chr16:1466147
|
G | A | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-809C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466147 | ||||||
chr16:1466150
|
C | T | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-812G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466150 | ||||||
chr16:1466166
|
G | A | 3 | a0001c0001t0035g0034a0002c0008t0017g0009a0002c0008t0017g0160 | 4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-828C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466166 | ||||||
chr16:1466175
|
C | T | 2 | a0001c0001t0001g0278a0001c0002t0034g0277 | 2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.142-837G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466175 | ||||||
chr16:1466176
|
G | A | 117 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0002g0224others(114): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.142-838C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466176 | ||||||
chr16:1466197
|
G | A | 1 | a0001c0003t0001g0365 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.142-859C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466197 | ||||||
chr16:1466275
|
G | A | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-937C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466275 | ||||||
chr16:1466341
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0236a0001c0002t0001g0103others(1): Show | 4 | NA18948.hp1 NA18970.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1003G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466341 | ||||||
chr16:1466392
|
G | C | 1 | a0001c0003t0003g0380 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.142-1054C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466392 | ||||||
chr16:1466662
|
G | A | 1 | a0001c0003t0005g0299 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142-1324C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466662 | ||||||
chr16:1466685
|
G | A | 49 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(46): Show | 51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-1347C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466685 | ||||||
chr16:1466712
|
A | G | 196 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0249others(193): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.142-1374T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466712 | ||||||
chr16:1466723
|
C | T | 10 | a0001c0002t0002g0279a0002c0008t0027g0252a0002c0008t0027g0253others(7): Show | 10 | HG02717.hp1 HG03098.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-1385G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466723 | ||||||
chr16:1466810
|
G | A | 2 | a0002c0008t0027g0252a0002c0008t0027g0253 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142-1472C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466810 | ||||||
chr16:1466851
|
G | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-1513C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466851 | ||||||
chr16:1466923
|
C | CA | 49 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0043others(46): Show | 52 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-1586dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
C | CAA | 13 | a0001c0001t0001g0134a0001c0001t0001g0246a0001c0001t0005g0135others(10): Show | 13 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-1587_142-1586d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
CA | C | 66 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0067others(63): Show | 69 | HG00438.hp1 HG00544.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.142-1586delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
CAA | C | 102 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0198others(99): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.142-1587_142-1586d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
CAAA | C | 21 | a0001c0001t0001g0090a0001c0001t0049g0238a0001c0002t0002g0197others(18): Show | 21 | HG00735.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-1588_142-1586d others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-1597_142-1586d others(14): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
CAAAAAAA others(7): Show |
C | 30 | a0001c0005t0001g0183a0001c0005t0001g0190a0001c0005t0004g0153others(27): Show | 31 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.142-1599_142-1586d others(16): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0005t0001g0179a0001c0005t0004g0037 | 2 | HG02735.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.142-1600_142-1586d others(17): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1466923
|
CAAAAAAA others(9): Show |
C | 3 | a0002c0009t0016g0079a0002c0009t0016g0080a0002c0009t0016g0081 | 3 | HG02258.hp1 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.142-1601_142-1586d others(18): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1466923 | ||||||
chr16:1467024
|
G | A | 29 | a0001c0001t0001g0278a0001c0001t0035g0034a0001c0001t0049g0238others(26): Show | 30 | HG01081.hp1 HG01243.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-1686C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467024 | ||||||
chr16:1467049
|
G | A | 3 | a0001c0001t0035g0034a0001c0001t0049g0238a0002c0008t0017g0009 | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1711C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467049 | ||||||
chr16:1467076
|
A | C | 189 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0278others(186): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.142-1738T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467076 | ||||||
chr16:1467089
|
T | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-1751A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467089 | ||||||
chr16:1467103
|
T | TG | 15 | a0001c0002t0002g0279a0001c0007t0002g0169a0001c0007t0002g0170others(12): Show | 15 | HG01891.hp2 HG02572.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-1766dupC | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467103 | ||||||
chr16:1467113
|
C | T | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-1775G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467113 | ||||||
chr16:1467225
|
C | T | 49 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(46): Show | 51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-1887G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467225 | ||||||
chr16:1467297
|
C | G | 13 | a0001c0002t0002g0011a0001c0002t0002g0279a0001c0002t0002g0281others(10): Show | 14 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-1959G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467297 | ||||||
chr16:1467311
|
C | T | 3 | a0001c0004t0001g0366a0001c0004t0001g0367a0001c0004t0001g0372 | 3 | NA18960.hp1 NA18993.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.142-1973G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467311 | ||||||
chr16:1467373
|
C | T | 5 | a0002c0009t0005g0031a0002c0009t0005g0284a0002c0009t0016g0079others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-2035G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467373 | ||||||
chr16:1467409
|
C | T | 32 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(29): Show | 33 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-2071G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467409 | ||||||
chr16:1467412
|
G | A | 1 | a0001c0002t0001g0085 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.142-2074C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467412 | ||||||
chr16:1467454
|
G | A | 3 | a0001c0001t0035g0034a0002c0008t0017g0009a0002c0008t0017g0160 | 4 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2116C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467454 | ||||||
chr16:1467466
|
C | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-2128G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467466 | ||||||
chr16:1467556
|
G | A | 1 | a0002c0006t0010g0010 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.142-2218C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467556 | ||||||
chr16:1467678
|
T | C | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-2340A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467678 | ||||||
chr16:1467727
|
A | G | 191 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0249others(188): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.142-2389T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467727 | ||||||
chr16:1467760
|
G | A | 1 | a0002c0011t0018g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.142-2422C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467760 | ||||||
chr16:1467851
|
C | G | 53 | a0001c0001t0001g0278a0001c0002t0015g0268a0001c0002t0015g0275others(50): Show | 55 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-2513G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467851 | ||||||
chr16:1467864
|
C | T | 1 | a0001c0004t0001g0388 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.142-2526G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467864 | ||||||
chr16:1467999
|
C | T | 5 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(2): Show | 6 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2661G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1467999 | ||||||
chr16:1468008
|
G | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0136a0001c0001t0001g0137others(12): Show | 15 | HG01109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-2670C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468008 | ||||||
chr16:1468047
|
C | T | 4 | a0001c0001t0035g0034a0001c0004t0001g0335a0002c0008t0017g0009others(1): Show | 5 | HG00673.hp1 HG01243.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-2709G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468047 | ||||||
chr16:1468067
|
G | C | 2 | a0001c0004t0001g0363a0001c0004t0002g0362 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.142-2729C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468067 | ||||||
chr16:1468155
|
G | A | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-2817C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468155 | ||||||
chr16:1468285
|
G | A | 1 | a0001c0004t0001g0364 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.142-2947C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468285 | ||||||
chr16:1468300
|
C | G | 32 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(29): Show | 33 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-2962G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468300 | ||||||
chr16:1468389
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.142-3051G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468389 | ||||||
chr16:1468456
|
C | G | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-3118G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468456 | ||||||
chr16:1468578
|
C | T | 1 | a0001c0003t0002g0313 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.142-3240G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468578 | ||||||
chr16:1468668
|
G | C | 3 | a0002c0012t0014g0015a0002c0012t0014g0016a0002c0012t0014g0017 | 3 | HG03209.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.142-3330C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468668 | ||||||
chr16:1468673
|
G | A | 1 | a0003c0016t0050g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-3335C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468673 | ||||||
chr16:1468683
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0004t0001g0308 | 3 | NA18957.hp2 NA18983.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.142-3345C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468683 | ||||||
chr16:1468699
|
G | A | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-3361C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468699 | ||||||
chr16:1468751
|
G | A | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-3413C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468751 | ||||||
chr16:1468771
|
C | G | 114 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0249others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.142-3433G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468771 | ||||||
chr16:1468773
|
G | A | 1 | a0001c0017t0041g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.142-3435C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468773 | ||||||
chr16:1468795
|
T | C | 56 | a0001c0001t0001g0278a0001c0001t0007g0006a0001c0001t0007g0141others(53): Show | 59 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-3457A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468795 | ||||||
chr16:1468806
|
G | A | 47 | a0001c0005t0001g0179a0001c0005t0001g0183a0001c0005t0001g0190others(44): Show | 49 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-3468C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468806 | ||||||
chr16:1468826
|
G | A | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0044g0071 | 3 | HG02109.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.142-3488C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468826 | ||||||
chr16:1468869
|
T | A | 190 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0249others(187): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.142-3531A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468869 | ||||||
chr16:1468915
|
G | A | 50 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(47): Show | 52 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.142-3577C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468915 | ||||||
chr16:1468944
|
G | A | 53 | a0001c0001t0001g0278a0001c0002t0015g0268a0001c0002t0015g0275others(50): Show | 55 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-3606C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468944 | ||||||
chr16:1468964
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.142-3626C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1468964 | ||||||
chr16:1469019
|
C | T | 1 | a0003c0016t0050g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-3681G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469019 | ||||||
chr16:1469039
|
G | GA | 16 | a0001c0001t0001g0048a0001c0001t0001g0143a0001c0001t0001g0144others(13): Show | 16 | HG00438.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-3702dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469039 | ||||||
chr16:1469039
|
GA | G | 52 | a0001c0001t0001g0069a0001c0001t0002g0228a0001c0001t0049g0238others(49): Show | 54 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.142-3702delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469039 | ||||||
chr16:1469099
|
G | A | 1 | a0001c0001t0049g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-3761C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469099 | ||||||
chr16:1469099
|
G | C | 2 | a0001c0003t0002g0333a0001c0003t0002g0334 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.142-3761C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469099 | ||||||
chr16:1469125
|
G | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-3787C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469125 | ||||||
chr16:1469456
|
C | T | 189 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0249others(186): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.142-4118G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469456 | ||||||
chr16:1469501
|
T | C | 1 | a0001c0022t0048g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-4163A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469501 | ||||||
chr16:1469624
|
C | T | 112 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0249others(109): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.142-4286G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469624 | ||||||
chr16:1469673
|
G | A | 50 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(47): Show | 52 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.142-4335C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469673 | ||||||
chr16:1469706
|
A | C | 1 | a0002c0026t0024g0309 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142-4368T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469706 | ||||||
chr16:1469743
|
C | G | 1 | a0003c0016t0050g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-4405G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469743 | ||||||
chr16:1469743
|
C | T | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-4405G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469743 | ||||||
chr16:1469764
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.142-4426G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469764 | ||||||
chr16:1469805
|
G | A | 49 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(46): Show | 51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-4467C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469805 | ||||||
chr16:1469859
|
C | T | 2 | a0001c0001t0001g0052a0001c0002t0002g0083 | 2 | NA18939.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.142-4521G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469859 | ||||||
chr16:1469888
|
A | T | 4 | a0001c0001t0001g0278a0001c0002t0034g0277a0001c0002t0036g0207others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-4550T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469888 | ||||||
chr16:1469897
|
C | T | 1 | a0001c0004t0001g0311 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142-4559G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469897 | ||||||
chr16:1469914
|
C | T | 1 | a0001c0004t0001g0335 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.142-4576G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469914 | ||||||
chr16:1469926
|
G | C | 1 | a0003c0016t0050g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-4588C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469926 | ||||||
chr16:1469940
|
G | A | 58 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269others(55): Show | 60 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.142-4602C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469940 | ||||||
chr16:1469984
|
C | T | 1 | a0001c0002t0036g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.142-4646G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1469984 | ||||||
chr16:1470037
|
G | A | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142-4699C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470037 | ||||||
chr16:1470063
|
G | A | 1 | a0001c0003t0003g0378 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.142-4725C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470063 | ||||||
chr16:1470134
|
A | T | 146 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0161others(143): Show | 151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.141+4700T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470134 | ||||||
chr16:1470235
|
A | G | 201 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0082others(198): Show | 207 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.141+4599T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470235 | ||||||
chr16:1470250
|
G | A | 1 | a0001c0001t0039g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.141+4584C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470250 | ||||||
chr16:1470268
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4566T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470268 | ||||||
chr16:1470270
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4564C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470270 | ||||||
chr16:1470272
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4562C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470272 | ||||||
chr16:1470275
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4559C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470275 | ||||||
chr16:1470276
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4558G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470276 | ||||||
chr16:1470277
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4557C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470277 | ||||||
chr16:1470278
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4556A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470278 | ||||||
chr16:1470281
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4553T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470281 | ||||||
chr16:1470282
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4552G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470282 | ||||||
chr16:1470283
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4551G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470283 | ||||||
chr16:1470285
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4549G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470285 | ||||||
chr16:1470286
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4548G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470286 | ||||||
chr16:1470289
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4545C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470289 | ||||||
chr16:1470290
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4544G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470290 | ||||||
chr16:1470291
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4543G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470291 | ||||||
chr16:1470292
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4542A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470292 | ||||||
chr16:1470295
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4539G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470295 | ||||||
chr16:1470297
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4537G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470297 | ||||||
chr16:1470301
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4533T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470301 | ||||||
chr16:1470303
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4531C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470303 | ||||||
chr16:1470304
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4530C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470304 | ||||||
chr16:1470307
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4527T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470307 | ||||||
chr16:1470313
|
T | C | 35 | a0001c0001t0001g0178a0001c0001t0001g0278a0001c0002t0034g0277others(32): Show | 36 | HG01071.hp1 HG01081.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.141+4521A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470313 | ||||||
chr16:1470316
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4518A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470316 | ||||||
chr16:1470319
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4515C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470319 | ||||||
chr16:1470321
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4513C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470321 | ||||||
chr16:1470322
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4512A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470322 | ||||||
chr16:1470324
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4510G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470324 | ||||||
chr16:1470325
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4509A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470325 | ||||||
chr16:1470326
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4508A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470326 | ||||||
chr16:1470329
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4505G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470329 | ||||||
chr16:1470330
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4504G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470330 | ||||||
chr16:1470331
|
A | AAGGGGAT others(4): Show |
1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4502_141+4503i others(13): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470331 | ||||||
chr16:1470335
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4499A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470335 | ||||||
chr16:1470336
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4498A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470336 | ||||||
chr16:1470337
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4497A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470337 | ||||||
chr16:1470339
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4495A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470339 | ||||||
chr16:1470340
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4494A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470340 | ||||||
chr16:1470341
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4493A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470341 | ||||||
chr16:1470346
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4488T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470346 | ||||||
chr16:1470351
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4483T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470351 | ||||||
chr16:1470357
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4477C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470357 | ||||||
chr16:1470360
|
TAAAGACC others(14): Show |
T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.141+4453_141+4473d others(23): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470360 | ||||||
chr16:1470436
|
C | T | 3 | a0001c0004t0006g0025a0001c0004t0006g0026a0004c0024t0029g0024 | 3 | HG01109.hp2 HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.141+4398G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470436 | ||||||
chr16:1470467
|
G | A | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+4367C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470467 | ||||||
chr16:1470485
|
C | T | 1 | a0001c0002t0001g0231 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.141+4349G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470485 | ||||||
chr16:1470554
|
T | A | 1 | a0001c0001t0001g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.141+4280A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470554 | ||||||
chr16:1470592
|
A | C | 5 | a0001c0001t0001g0149a0001c0002t0002g0038a0001c0002t0002g0039others(2): Show | 5 | HG00558.hp1 HG02080.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+4242T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470592 | ||||||
chr16:1470738
|
C | T | 1 | a0001c0002t0020g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.141+4096G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470738 | ||||||
chr16:1470769
|
C | T | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+4065G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470769 | ||||||
chr16:1470794
|
G | A | 1 | a0001c0003t0001g0365 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.141+4040C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470794 | ||||||
chr16:1470893
|
A | G | 1 | a0001c0003t0001g0310 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.141+3941T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470893 | ||||||
chr16:1470999
|
C | T | 1 | a0004c0018t0053g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141+3835G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1470999 | ||||||
chr16:1471451
|
C | A | 139 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(136): Show | 143 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.141+3383G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471451 | ||||||
chr16:1471513
|
A | G | 1 | a0001c0003t0003g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.141+3321T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471513 | ||||||
chr16:1471555
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(249): Show | 262 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(259): Show |
intron_variant | MODIFIER | c.141+3279T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471555 | ||||||
chr16:1471576
|
C | T | 6 | a0001c0002t0013g0028a0001c0002t0013g0029a0001c0002t0013g0032others(3): Show | 6 | HG00639.hp2 HG02055.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+3258G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471576 | ||||||
chr16:1471577
|
G | A | 2 | a0002c0008t0027g0252a0002c0008t0027g0253 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.141+3257C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471577 | ||||||
chr16:1471581
|
C | A | 1 | a0002c0006t0052g0264 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.141+3253G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471581 | ||||||
chr16:1471612
|
G | A | 1 | a0001c0001t0045g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.141+3222C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471612 | ||||||
chr16:1471665
|
G | A | 5 | a0001c0001t0001g0244a0001c0004t0006g0025a0001c0004t0006g0026others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+3169C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471665 | ||||||
chr16:1471744
|
G | A | 184 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(181): Show | 190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.141+3090C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471744 | ||||||
chr16:1471761
|
C | T | 1 | a0001c0002t0003g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.141+3073G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471761 | ||||||
chr16:1471805
|
C | T | 2 | a0001c0001t0001g0278a0001c0002t0034g0277 | 2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+3029G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471805 | ||||||
chr16:1471815
|
G | C | 1 | a0001c0002t0020g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.141+3019C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471815 | ||||||
chr16:1471980
|
CG | C | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+2853delC | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1471980 | ||||||
chr16:1472013
|
G | A | 1 | a0001c0005t0001g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.141+2821C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472013 | ||||||
chr16:1472051
|
C | A | 1 | a0001c0003t0003g0303 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.141+2783G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472051 | ||||||
chr16:1472175
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(55): Show | 62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2659T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472175 | ||||||
chr16:1472223
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(55): Show | 62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2611A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472223 | ||||||
chr16:1472244
|
A | AT | 3 | a0001c0002t0015g0268a0001c0002t0015g0275a0001c0002t0042g0269 | 3 | HG02630.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141+2589dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472244 | ||||||
chr16:1472250
|
A | T | 58 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(55): Show | 62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2584T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472250 | ||||||
chr16:1472291
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(39): Show | 45 | HG00438.hp2 HG00741.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.141+2543G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472291 | ||||||
chr16:1472333
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+2501G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472333 | ||||||
chr16:1472354
|
C | T | 1 | a0001c0002t0044g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141+2480G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472354 | ||||||
chr16:1472369
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(55): Show | 62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2465A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472369 | ||||||
chr16:1472385
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(55): Show | 62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2449A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472385 | ||||||
chr16:1472387
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(249): Show | 262 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(259): Show |
intron_variant | MODIFIER | c.141+2447A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472387 | ||||||
chr16:1472403
|
C | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(55): Show | 62 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+2431G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472403 | ||||||
chr16:1472530
|
C | A | 15 | a0001c0001t0049g0238a0001c0002t0015g0268a0001c0002t0015g0275others(12): Show | 15 | HG02258.hp2 HG02615.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+2304G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472530 | ||||||
chr16:1472539
|
T | C | 3 | a0001c0002t0002g0011a0001c0002t0002g0281a0001c0002t0002g0282 | 4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2295A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472539 | ||||||
chr16:1472572
|
C | T | 5 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(2): Show | 6 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+2262G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472572 | ||||||
chr16:1472573
|
A | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(49): Show | 56 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.141+2261T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472573 | ||||||
chr16:1472669
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(193): Show | 205 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.141+2165T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472669 | ||||||
chr16:1472711
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.141+2123G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472711 | ||||||
chr16:1472744
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.141+2090T>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472744 | ||||||
chr16:1472745
|
T | A | 2 | a0001c0005t0004g0267a0001c0005t0004g0280 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.141+2089A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472745 | ||||||
chr16:1472813
|
G | GA | 14 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0002t0001g0068others(11): Show | 14 | HG01261.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+2020dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472813 | ||||||
chr16:1472813
|
GA | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0046others(25): Show | 31 | HG01081.hp1 HG01099.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.141+2020delT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472813 | ||||||
chr16:1472865
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0046others(28): Show | 34 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.141+1969G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472865 | ||||||
chr16:1472871
|
C | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(189): Show | 201 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.141+1963G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472871 | ||||||
chr16:1472938
|
G | GT | 15 | a0001c0003t0001g0306a0001c0003t0003g0373a0001c0003t0003g0386others(12): Show | 16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.141+1895dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1472938 | ||||||
chr16:1473009
|
C | CCTCCCCT others(1): Show |
12 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(9): Show | 13 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+1817_141+1824d others(10): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473009 | ||||||
chr16:1473023
|
G | C | 1 | a0001c0003t0003g0380 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.141+1811C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473023 | ||||||
chr16:1473068
|
C | CCTTA | 104 | a0001c0001t0001g0027a0001c0001t0001g0161a0001c0001t0001g0162others(101): Show | 109 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.141+1765_141+1766i others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473068 | ||||||
chr16:1473086
|
A | AAC | 4 | a0001c0001t0001g0045a0001c0003t0002g0290a0001c0003t0003g0289others(1): Show | 4 | HG02055.hp1 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+1746_141+1747d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473086 | ||||||
chr16:1473086
|
A | AACAC | 3 | a0001c0003t0002g0288a0001c0003t0002g0305a0001c0003t0002g0387 | 3 | HG00741.hp2 HG01496.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.141+1744_141+1747d others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473086 | ||||||
chr16:1473086
|
AAC | A | 64 | a0001c0001t0001g0027a0001c0001t0001g0161a0001c0001t0001g0162others(61): Show | 67 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.141+1746_141+1747d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473086 | ||||||
chr16:1473118
|
T | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1716A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473118 | ||||||
chr16:1473212
|
C | T | 1 | a0001c0002t0002g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.141+1622G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473212 | ||||||
chr16:1473299
|
G | A | 14 | a0001c0001t0001g0245a0001c0001t0001g0246a0002c0006t0010g0010others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+1535C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473299 | ||||||
chr16:1473370
|
C | CT | 74 | a0001c0001t0001g0027a0001c0001t0001g0156a0001c0001t0001g0159others(71): Show | 75 | HG00639.hp1 HG00741.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.141+1463dupA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | ||||||
chr16:1473370
|
C | CTT | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0033others(145): Show | 155 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.141+1462_141+1463d others(4): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | ||||||
chr16:1473370
|
C | CTTT | 40 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(37): Show | 40 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.141+1461_141+1463d others(5): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | ||||||
chr16:1473370
|
C | CTTTT | 8 | a0001c0002t0015g0268a0001c0002t0042g0269a0001c0005t0004g0265others(5): Show | 8 | HG02451.hp1 HG02976.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+1460_141+1463d others(6): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | ||||||
chr16:1473370
|
CT | C | 13 | a0001c0001t0001g0044a0001c0001t0049g0238a0001c0002t0002g0011others(10): Show | 15 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+1463delA | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473370 | ||||||
chr16:1473401
|
G | A | 1 | a0001c0003t0008g0384 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.141+1433C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473401 | ||||||
chr16:1473411
|
C | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(221): Show | 232 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.141+1423G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473411 | ||||||
chr16:1473414
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.141+1420G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473414 | ||||||
chr16:1473452
|
T | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1382A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473452 | ||||||
chr16:1473463
|
T | G | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1371A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473463 | ||||||
chr16:1473474
|
A | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1360T>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473474 | ||||||
chr16:1473475
|
T | G | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1359A>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473475 | ||||||
chr16:1473476
|
T | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1358A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473476 | ||||||
chr16:1473477
|
G | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1357C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473477 | ||||||
chr16:1473485
|
T | A | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1349A>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473485 | ||||||
chr16:1473522
|
C | A | 2 | a0001c0001t0001g0195a0001c0002t0001g0194 | 2 | HG02523.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.141+1312G>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473522 | ||||||
chr16:1473534
|
T | C | 13 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1300A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473534 | ||||||
chr16:1473619
|
C | T | 1 | a0001c0001t0005g0040 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.141+1215G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473619 | ||||||
chr16:1473672
|
C | T | 1 | a0001c0002t0002g0196 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.141+1162G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473672 | ||||||
chr16:1473808
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.141+1026C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473808 | ||||||
chr16:1473865
|
A | G | 12 | a0002c0006t0010g0010a0002c0006t0010g0255a0002c0006t0010g0256others(9): Show | 13 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+969T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473865 | ||||||
chr16:1473883
|
G | A | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0004c0018t0053g0276 | 3 | HG02109.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+951C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473883 | ||||||
chr16:1473886
|
G | A | 3 | a0001c0001t0001g0278a0001c0002t0034g0277a0004c0018t0053g0276 | 3 | HG02109.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+948C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473886 | ||||||
chr16:1473891
|
C | T | 7 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0004t0006g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+943G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1473891 | ||||||
chr16:1474045
|
T | C | 45 | a0001c0001t0001g0198a0001c0001t0001g0203a0001c0001t0001g0208others(42): Show | 45 | HG00323.hp1 HG00597.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.141+789A>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474045 | ||||||
chr16:1474084
|
C | CA | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(237): Show | 249 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.141+749dupT | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474084 | ||||||
chr16:1474084
|
C | CAA | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0002t0002g0011others(2): Show | 6 | HG00673.hp2 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+748_141+749dup others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474084 | ||||||
chr16:1474237
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.141+597T>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474237 | ||||||
chr16:1474260
|
G | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(260): Show | 273 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.141+574C>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474260 | ||||||
chr16:1474293
|
C | G | 5 | a0001c0002t0013g0028a0001c0002t0013g0029a0001c0002t0013g0032others(2): Show | 5 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+541G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474293 | ||||||
chr16:1474477
|
C | G | 2 | a0002c0008t0027g0252a0002c0008t0027g0253 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.141+357G>C | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474477 | ||||||
chr16:1474483
|
G | C | 5 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG00609.hp1 NA18957.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+351C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474483 | ||||||
chr16:1474521
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.141+313C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474521 | ||||||
chr16:1474580
|
G | A | 1 | a0001c0003t0002g0387 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.141+254C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474580 | ||||||
chr16:1474603
|
C | T | 276 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(273): Show | 286 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.141+231G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474603 | ||||||
chr16:1474695
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.141+139G>A | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474695 | ||||||
chr16:1474763
|
G | A | 2 | a0001c0004t0001g0388a0001c0004t0001g0389 | 2 | HG00609.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.141+71C>T | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474763 | ||||||
chr16:1474773
|
G | GGCGC | 34 | a0001c0001t0001g0278a0001c0002t0002g0011a0001c0002t0002g0279others(31): Show | 36 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.141+57_141+60dupGC others(2): Show |
CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474773 | ||||||
chr16:1474815
|
G | C | 1 | a0001c0002t0001g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.141+19C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474815 | ||||||
chr16:1474826
|
G | C | 1 | a0002c0009t0005g0284 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.141+8C>G | CLCN7 | ENSG00000103249.19 | transcript | ENST00000382745.9 | protein_coding | 1/24 | chr16 | 1474826 |