geneid | 221937 |
---|---|
ensemblid | ENSG00000164916.11 |
hgncid | 23480 |
symbol | FOXK1 |
name | forkhead box K1 |
refseq_nuc | NM_001037165.2 |
refseq_prot | NP_001032242.1 |
ensembl_nuc | ENST00000328914.5 |
ensembl_prot | ENSP00000328720.4 |
mane_status | MANE Select |
chr | chr7 |
start | 4682295 |
end | 4771442 |
strand | + |
ver | v1.2 |
region | chr7:4682295-4771442 |
region5000 | chr7:4677295-4776442 |
regionname0 | FOXK1_chr7_4682295_4771442 |
regionname5000 | FOXK1_chr7_4677295_4776442 |
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 | 733 | 283 | 89 | 50 | 95 | 9 | 38 | 58 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002 | 0/0 | 733 | 5 | 3 | 1 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0003 | 0/0 | 733 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0004 | 0/0 | 733 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0005 | 0/0 | 733 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0006 | 0/0 | 733 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
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 | 2202 | 103 | 7 | 15 | 61 | 3 | 16 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0002 | 0/0 | 2202 | 61 | 20 | 14 | 13 | 4 | 10 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0003 | 0/0 | 2202 | 50 | 41 | 4 | 2 | 0 | 3 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0004 | 0/0 | 2202 | 28 | 7 | 3 | 10 | 0 | 8 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0005 | 0/0 | 2202 | 7 | 1 | 5 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0006 | 0/0 | 2202 | 5 | 3 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0007 | 0/0 | 2202 | 5 | 5 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0008 | 0/0 | 2202 | 4 | 0 | 0 | 4 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0009 | 0/0 | 2202 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0010 | 1/0 | 2202 | 3 | 0 | 1 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0011 | 0/0 | 2202 | 3 | 1 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0012 | 0/0 | 2202 | 2 | 1 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0013 | 0/0 | 2202 | 2 | 1 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0014 | 0/0 | 2202 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0015 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0016 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0017 | 0/0 | 2202 | 2 | 0 | 1 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0018 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0019 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0020 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0021 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0022 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0023 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0024 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0025 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0026 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
c0027 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
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 | 0/0 | 8989 | 58 | 3 | 15 | 29 | 1 | 10 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0002 | 1/0 | 8993 | 21 | 0 | 8 | 10 | 2 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0003 | 0/0 | 8990 | 12 | 2 | 2 | 5 | 0 | 3 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0004 | 0/0 | 8997 | 9 | 9 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0005 | 0/0 | 8991 | 9 | 0 | 4 | 3 | 0 | 2 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0006 | 0/0 | 8673 | 7 | 5 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0007 | 0/0 | 8986 | 5 | 5 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0008 | 0/0 | 8992 | 4 | 0 | 0 | 0 | 0 | 4 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0009 | 0/0 | 8995 | 4 | 0 | 0 | 4 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0010 | 0/0 | 8670 | 4 | 4 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0011 | 0/0 | 8988 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0012 | 0/0 | 8983 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0013 | 0/0 | 8993 | 3 | 0 | 0 | 0 | 2 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0014 | 0/0 | 8989 | 3 | 3 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0015 | 0/0 | 8990 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0016 | 0/0 | 8670 | 2 | 1 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0017 | 0/0 | 8989 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0018 | 0/0 | 8999 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0019 | 0/0 | 8998 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0020 | 0/0 | 8989 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0021 | 0/0 | 8989 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0022 | 0/0 | 8989 | 2 | 1 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0023 | 0/0 | 8995 | 2 | 0 | 0 | 1 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0024 | 0/0 | 8993 | 2 | 0 | 1 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0025 | 0/0 | 8990 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0026 | 0/0 | 8986 | 2 | 1 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0027 | 0/0 | 8989 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0028 | 0/0 | 9000 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0029 | 0/0 | 8995 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0030 | 0/0 | 8999 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0031 | 0/0 | 8997 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0032 | 0/0 | 8993 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0033 | 0/0 | 8990 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0034 | 0/0 | 8989 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0035 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0036 | 0/0 | 8996 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0037 | 0/0 | 8986 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0038 | 0/0 | 8987 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0039 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0040 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0041 | 0/0 | 8670 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0042 | 0/0 | 8991 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0043 | 0/0 | 8983 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0044 | 0/0 | 8989 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0045 | 0/0 | 8991 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0046 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0047 | 0/0 | 8990 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0048 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0049 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0050 | 0/0 | 8989 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0051 | 0/0 | 8993 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0052 | 0/0 | 8996 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0053 | 0/0 | 8995 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0054 | 0/0 | 8997 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0055 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0056 | 0/0 | 8993 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0057 | 0/0 | 8990 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0058 | 0/0 | 8670 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0059 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0060 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0061 | 0/0 | 8990 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0062 | 0/0 | 8990 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0063 | 0/0 | 8987 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0064 | 0/0 | 8984 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0065 | 0/0 | 8992 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0066 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0067 | 0/0 | 8990 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0068 | 0/0 | 8990 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0069 | 0/0 | 8991 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0070 | 0/0 | 8985 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0071 | 0/0 | 8993 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0072 | 0/0 | 8989 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0073 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0074 | 0/1 | 8997 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0075 | 0/0 | 8989 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0076 | 0/0 | 8993 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0077 | 0/0 | 8989 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0078 | 0/0 | 8989 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0079 | 0/0 | 8993 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0080 | 0/0 | 8991 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0081 | 0/0 | 8994 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0082 | 0/0 | 8994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0083 | 0/0 | 8994 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0084 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0085 | 0/0 | 8989 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0086 | 0/0 | 8993 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0087 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0088 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0089 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0090 | 0/0 | 8993 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0091 | 0/0 | 8995 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0092 | 0/0 | 8997 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0093 | 0/0 | 8998 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0094 | 0/0 | 8999 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0095 | 0/0 | 8990 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0096 | 0/0 | 8990 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0097 | 0/0 | 8990 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0098 | 0/0 | 8993 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0099 | 0/0 | 8998 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0100 | 0/0 | 8987 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0101 | 0/0 | 8985 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0102 | 0/0 | 8988 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0103 | 0/0 | 8987 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0104 | 0/0 | 8984 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0105 | 0/0 | 8989 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0106 | 0/0 | 8998 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0107 | 0/0 | 8975 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0108 | 0/0 | 8983 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0109 | 0/0 | 8673 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0110 | 0/0 | 8993 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0111 | 0/0 | 8990 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0112 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0113 | 0/0 | 8993 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0114 | 0/0 | 8990 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0115 | 0/0 | 8992 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0116 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0117 | 0/0 | 8994 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0118 | 0/0 | 8994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0119 | 0/0 | 8992 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0120 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0121 | 0/0 | 8998 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0122 | 0/0 | 8998 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0123 | 0/0 | 8999 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0124 | 0/0 | 8999 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0125 | 0/0 | 8994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0126 | 0/0 | 8997 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0127 | 0/0 | 8996 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0128 | 0/0 | 8990 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0129 | 0/0 | 8989 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0130 | 0/0 | 8989 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0131 | 0/0 | 8990 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0132 | 0/0 | 8992 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0133 | 0/0 | 8998 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0134 | 0/0 | 8990 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0135 | 0/0 | 8674 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0136 | 0/0 | 8676 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0137 | 0/0 | 8679 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0138 | 0/0 | 8666 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0139 | 0/0 | 8985 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0140 | 0/0 | 8984 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0141 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0142 | 0/0 | 8996 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0143 | 0/0 | 8997 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0144 | 0/0 | 8995 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0145 | 0/0 | 8997 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
t0146 | 0/0 | 8999 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
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 | 2 | 0 | 0 | 0 | 0 | 2 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
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 | 2202 | 103 | 7 | 15 | 61 | 3 | 16 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002 | 0/0 | 2202 | 61 | 20 | 14 | 13 | 4 | 10 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003 | 0/0 | 2202 | 50 | 41 | 4 | 2 | 0 | 3 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004 | 0/0 | 2202 | 28 | 7 | 3 | 10 | 0 | 8 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0005 | 0/0 | 2202 | 7 | 1 | 5 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0006 | 0/0 | 2202 | 5 | 3 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0007 | 0/0 | 2202 | 5 | 5 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0008 | 0/0 | 2202 | 4 | 0 | 0 | 4 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0009 | 0/0 | 2202 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0010 | 1/0 | 2202 | 3 | 0 | 1 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0011 | 0/0 | 2202 | 3 | 1 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0015 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0017 | 0/0 | 2202 | 2 | 0 | 1 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0019 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0021 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0022 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0023 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0024 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0026 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0027 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0012 | 0/0 | 2202 | 2 | 1 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0013 | 0/0 | 2202 | 2 | 1 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0018 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0003c0014 | 0/0 | 2202 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0004c0016 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0005c0020 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0006c0025 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11190 | 36 | 2 | 5 | 22 | 0 | 7 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0002 | 0/0 | 11194 | 13 | 0 | 4 | 8 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0003 | 0/0 | 11191 | 7 | 1 | 1 | 4 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0005 | 0/0 | 11192 | 3 | 0 | 0 | 2 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0011 | 0/0 | 11189 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0012 | 0/0 | 11184 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0013 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0016 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0017 | 0/0 | 11190 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0020 | 0/0 | 11190 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0021 | 0/0 | 11190 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0023 | 0/0 | 11196 | 2 | 0 | 0 | 1 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0024 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0035 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0050 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0051 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0058 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0059 | 0/0 | 11192 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0060 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0062 | 0/0 | 11191 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0063 | 0/0 | 11188 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0065 | 0/0 | 11193 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0066 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0068 | 0/0 | 11191 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0071 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0072 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0073 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0074 | 0/1 | 11198 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0075 | 0/0 | 11190 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0076 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0077 | 0/0 | 11190 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0078 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0079 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0080 | 0/0 | 11192 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0081 | 0/0 | 11195 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0082 | 0/0 | 11195 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0084 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0086 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0089 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0090 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0096 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0097 | 0/0 | 11191 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0001t0108 | 0/0 | 11184 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0001 | 0/0 | 11190 | 16 | 1 | 4 | 7 | 1 | 3 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0002 | 0/0 | 11194 | 4 | 0 | 2 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0003 | 0/0 | 11191 | 4 | 1 | 0 | 1 | 0 | 2 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0004 | 0/0 | 11198 | 8 | 8 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0005 | 0/0 | 11192 | 5 | 0 | 3 | 1 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0012 | 0/0 | 11184 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0013 | 0/0 | 11194 | 2 | 0 | 0 | 0 | 2 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0017 | 0/0 | 11190 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0018 | 0/0 | 11200 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0019 | 0/0 | 11199 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0024 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0025 | 0/0 | 11191 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0032 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0041 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0042 | 0/0 | 11192 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0044 | 0/0 | 11190 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0055 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0057 | 0/0 | 11191 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0061 | 0/0 | 11191 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0067 | 0/0 | 11191 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0083 | 0/0 | 11195 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0085 | 0/0 | 11190 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0088 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0095 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0098 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0002t0105 | 0/0 | 11190 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0005 | 0/0 | 11192 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0007 | 0/0 | 11187 | 3 | 3 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0010 | 0/0 | 10871 | 3 | 3 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0014 | 0/0 | 11190 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0015 | 0/0 | 11191 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0019 | 0/0 | 11199 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0026 | 0/0 | 11187 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0031 | 0/0 | 11198 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0036 | 0/0 | 11197 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0037 | 0/0 | 11187 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0038 | 0/0 | 11188 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0039 | 0/0 | 11192 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0040 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0047 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0087 | 0/0 | 11192 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0099 | 0/0 | 11199 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0100 | 0/0 | 11188 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0101 | 0/0 | 11186 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0102 | 0/0 | 11189 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0103 | 0/0 | 11188 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0104 | 0/0 | 11185 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0111 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0112 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0113 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0120 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0123 | 0/0 | 11200 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0124 | 0/0 | 11200 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0129 | 0/0 | 11190 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0130 | 0/0 | 11190 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0131 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0132 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0134 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0135 | 0/0 | 10875 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0136 | 0/0 | 10877 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0137 | 0/0 | 10880 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0138 | 0/0 | 10867 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0139 | 0/0 | 11186 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0140 | 0/0 | 11185 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0142 | 0/0 | 11197 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0143 | 0/0 | 11198 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0144 | 0/0 | 11196 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0145 | 0/0 | 11198 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0003t0146 | 0/0 | 11200 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0001 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0007 | 0/0 | 11187 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0008 | 0/0 | 11193 | 4 | 0 | 0 | 0 | 0 | 4 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0009 | 0/0 | 11196 | 4 | 0 | 0 | 4 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0014 | 0/0 | 11190 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0029 | 0/0 | 11196 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0033 | 0/0 | 11191 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0034 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0043 | 0/0 | 11184 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0046 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0048 | 0/0 | 11192 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0056 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0115 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0116 | 0/0 | 11189 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0117 | 0/0 | 11195 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0121 | 0/0 | 11199 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0125 | 0/0 | 11195 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0126 | 0/0 | 11198 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0127 | 0/0 | 11197 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0133 | 0/0 | 11199 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0004t0141 | 0/0 | 11192 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0005t0001 | 0/0 | 11190 | 3 | 0 | 3 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0005t0003 | 0/0 | 11191 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0005t0011 | 0/0 | 11189 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0005t0022 | 0/0 | 11190 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0005t0069 | 0/0 | 11192 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0006t0052 | 0/0 | 11197 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0006t0053 | 0/0 | 11196 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0006t0054 | 0/0 | 11198 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0006t0092 | 0/0 | 11198 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0006t0093 | 0/0 | 11199 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0007t0006 | 0/0 | 10874 | 4 | 4 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0007t0109 | 0/0 | 10874 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0008t0028 | 0/0 | 11201 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0008t0118 | 0/0 | 11195 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0008t0122 | 0/0 | 11199 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0009t0030 | 0/0 | 11200 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0009t0119 | 0/0 | 11193 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0010t0002 | 1/0 | 11194 | 2 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0010t0110 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0011t0006 | 0/0 | 10874 | 3 | 1 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0015t0091 | 0/0 | 11196 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0015t0094 | 0/0 | 11200 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0017t0027 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0017t0114 | 0/0 | 11191 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0019t0128 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0021t0027 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0022t0070 | 0/0 | 11186 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0023t0049 | 0/0 | 11192 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0024t0002 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0026t0001 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0001c0027t0064 | 0/0 | 11185 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0012t0004 | 0/0 | 11198 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0012t0016 | 0/0 | 10871 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0013t0010 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0013t0026 | 0/0 | 11187 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0002c0018t0007 | 0/0 | 11187 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0003c0014t0001 | 0/0 | 11190 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0003c0014t0002 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0004c0016t0106 | 0/0 | 11199 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0004c0016t0107 | 0/0 | 11176 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0005c0020t0045 | 0/0 | 11192 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
a0006c0025t0022 | 0/0 | 11190 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | copy fasta | chr7 | 4677295 | 4776442 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0017g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0020g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0020g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0021g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0021g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0023g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0023g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0024g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0035g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0050g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0051g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0058g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0059g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0060g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0062g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0063g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0065g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0066g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0068g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0071g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0072g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0073g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0074g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0075g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0076g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0077g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0078g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0079g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0080g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0081g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0082g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0084g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0086g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0089g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0090g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0096g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0097g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0001t0108g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0012g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0013g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0013g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0017g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0018g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0024g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0025g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0025g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0032g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0041g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0042g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0044g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0055g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0057g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0061g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0067g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0083g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0085g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0088g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0095g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0098g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0002t0105g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0015g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0026g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0031g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0031g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0036g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0037g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0038g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0039g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0040g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0047g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0087g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0099g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0100g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0101g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0102g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0103g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0104g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0111g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0112g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0113g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0120g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0123g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0124g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0129g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0130g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0131g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0132g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0134g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0135g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0136g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0137g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0138g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0139g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0140g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0142g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0143g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0144g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0145g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0003t0146g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0008g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0008g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0009g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0029g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0029g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0033g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0034g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0043g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0046g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0048g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0056g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0115g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0116g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0117g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0121g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0125g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0126g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0127g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0133g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0004t0141g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0005t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0005t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0005t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0005t0022g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0005t0069g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0006t0052g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0006t0053g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0006t0054g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0006t0092g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0006t0093g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0007t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0007t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0007t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0007t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0007t0109g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0008t0028g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0008t0028g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0008t0118g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0008t0122g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0009t0030g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0009t0030g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0009t0119g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0010t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0010t0002g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0010t0110g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0011t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0011t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0011t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0015t0091g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0015t0094g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0017t0027g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0017t0114g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0019t0128g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0021t0027g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0022t0070g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0023t0049g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0024t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0026t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0001c0027t0064g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0002c0012t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0002c0012t0016g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0002c0013t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0002c0013t0026g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0002c0018t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0003c0014t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0003c0014t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0004c0016t0106g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0004c0016t0107g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0005c0020t0045g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
a0006c0025t0022g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0130 | EUR | GBR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00140 | hp2 | a0001 | c0001 | t0079 | g0060 | EUR | GBR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00323 | hp1 | a0001 | c0002 | t0013 | g0216 | EUR | FIN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00323 | hp2 | a0001 | c0027 | t0064 | g0217 | EUR | FIN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00408 | hp1 | a0001 | c0001 | t0059 | g0121 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00408 | hp2 | a0001 | c0002 | t0005 | g0198 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00597 | hp1 | a0001 | c0008 | t0028 | g0264 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00621 | hp2 | a0006 | c0025 | t0022 | g0032 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00639 | hp2 | a0001 | c0005 | t0001 | g0167 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00673 | hp2 | a0001 | c0001 | t0035 | g0064 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00735 | hp2 | a0001 | c0002 | t0025 | g0277 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00738 | hp1 | a0001 | c0024 | t0002 | g0212 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG00738 | hp2 | a0001 | c0004 | t0034 | g0028 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01070 | hp1 | a0001 | c0003 | t0005 | g0112 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01070 | hp2 | a0001 | c0006 | t0092 | g0002 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01071 | hp1 | a0001 | c0006 | t0093 | g0002 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0158 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01074 | hp1 | a0001 | c0003 | t0031 | g0155 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01074 | hp2 | a0003 | c0014 | t0001 | g0057 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01081 | hp1 | a0001 | c0003 | t0145 | g0172 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01081 | hp2 | a0001 | c0011 | t0006 | g0082 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01099 | hp2 | a0001 | c0002 | t0025 | g0222 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0113 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01106 | hp2 | a0001 | c0001 | t0078 | g0019 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01109 | hp1 | a0002 | c0012 | t0016 | g0291 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01109 | hp2 | a0001 | c0010 | t0110 | g0274 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01175 | hp1 | a0001 | c0001 | t0050 | g0137 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01175 | hp2 | a0001 | c0001 | t0080 | g0023 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01192 | hp2 | a0001 | c0002 | t0024 | g0046 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01256 | hp2 | a0001 | c0001 | t0065 | g0011 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01258 | hp2 | a0001 | c0017 | t0027 | g0105 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01261 | hp1 | a0001 | c0021 | t0027 | g0271 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01346 | hp1 | a0001 | c0002 | t0042 | g0156 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01361 | hp1 | a0001 | c0003 | t0031 | g0171 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0257 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01496 | hp1 | a0001 | c0002 | t0057 | g0244 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01496 | hp2 | a0001 | c0011 | t0006 | g0281 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01515 | hp1 | a0001 | c0002 | t0013 | g0050 | EUR | IBS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01515 | hp2 | a0001 | c0001 | t0068 | g0010 | EUR | IBS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01884 | hp2 | a0001 | c0011 | t0006 | g0249 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01891 | hp1 | a0001 | c0001 | t0096 | g0093 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01891 | hp2 | a0001 | c0003 | t0112 | g0006 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01928 | hp1 | a0001 | c0001 | t0072 | g0015 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01928 | hp2 | a0001 | c0002 | t0005 | g0098 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01934 | hp1 | a0003 | c0014 | t0002 | g0163 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01978 | hp1 | a0001 | c0004 | t0033 | g0027 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01978 | hp2 | a0001 | c0005 | t0003 | g0223 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01981 | hp1 | a0001 | c0005 | t0069 | g0166 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02004 | hp1 | a0001 | c0026 | t0001 | g0099 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02004 | hp2 | a0001 | c0005 | t0001 | g0153 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02055 | hp1 | a0001 | c0002 | t0041 | g0102 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02055 | hp2 | a0001 | c0003 | t0134 | g0285 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02056 | hp1 | a0001 | c0001 | t0060 | g0038 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02056 | hp2 | a0001 | c0002 | t0012 | g0127 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02074 | hp2 | a0001 | c0001 | t0063 | g0258 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02080 | hp1 | a0001 | c0001 | t0012 | g0005 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02080 | hp2 | a0001 | c0001 | t0051 | g0051 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02132 | hp2 | a0001 | c0002 | t0067 | g0195 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02135 | hp2 | a0001 | c0001 | t0108 | g0123 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02145 | hp2 | a0001 | c0007 | t0006 | g0085 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02155 | hp1 | a0001 | c0001 | t0086 | g0181 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02257 | hp1 | a0001 | c0003 | t0015 | g0094 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0240 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02258 | hp1 | a0001 | c0002 | t0004 | g0227 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02258 | hp2 | a0001 | c0004 | t0048 | g0183 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02273 | hp1 | a0001 | c0005 | t0001 | g0173 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02280 | hp1 | a0001 | c0003 | t0014 | g0081 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02280 | hp2 | a0002 | c0012 | t0004 | g0292 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02451 | hp1 | a0001 | c0003 | t0139 | g0074 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02451 | hp2 | a0001 | c0002 | t0018 | g0243 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02523 | hp1 | a0001 | c0001 | t0011 | g0040 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02572 | hp1 | a0001 | c0003 | t0014 | g0236 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02572 | hp2 | a0001 | c0002 | t0004 | g0067 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02602 | hp2 | a0001 | c0001 | t0013 | g0041 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02615 | hp1 | a0001 | c0006 | t0052 | g0078 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02615 | hp2 | a0001 | c0004 | t0014 | g0256 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02622 | hp1 | a0001 | c0003 | t0019 | g0238 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02622 | hp2 | a0001 | c0003 | t0087 | g0071 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02630 | hp1 | a0001 | c0007 | t0006 | g0235 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02630 | hp2 | a0001 | c0002 | t0004 | g0252 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02647 | hp1 | a0001 | c0003 | t0039 | g0229 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02647 | hp2 | a0001 | c0003 | t0102 | g0086 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02698 | hp1 | a0001 | c0001 | t0024 | g0013 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02698 | hp2 | a0001 | c0003 | t0132 | g0160 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02717 | hp1 | a0001 | c0003 | t0103 | g0209 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02717 | hp2 | a0001 | c0003 | t0010 | g0100 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02723 | hp1 | a0001 | c0001 | t0058 | g0251 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02723 | hp2 | a0001 | c0003 | t0010 | g0077 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02738 | hp1 | a0001 | c0002 | t0005 | g0278 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02738 | hp2 | a0001 | c0002 | t0083 | g0008 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02809 | hp1 | a0001 | c0003 | t0138 | g0262 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02809 | hp2 | a0001 | c0003 | t0007 | g0226 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02818 | hp1 | a0001 | c0003 | t0111 | g0059 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02818 | hp2 | a0001 | c0003 | t0010 | g0231 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02895 | hp1 | a0001 | c0003 | t0037 | g0284 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02895 | hp2 | a0001 | c0002 | t0019 | g0125 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02896 | hp1 | a0004 | c0016 | t0106 | g0146 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02896 | hp2 | a0001 | c0003 | t0131 | g0070 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02897 | hp1 | a0004 | c0016 | t0107 | g0147 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0126 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02922 | hp1 | a0001 | c0004 | t0056 | g0233 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02922 | hp2 | a0001 | c0003 | t0146 | g0174 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02965 | hp1 | a0001 | c0003 | t0140 | g0003 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02965 | hp2 | a0001 | c0001 | t0016 | g0241 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02970 | hp1 | a0001 | c0003 | t0036 | g0004 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02970 | hp2 | a0001 | c0003 | t0099 | g0282 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02976 | hp1 | a0001 | c0003 | t0101 | g0242 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02976 | hp2 | a0001 | c0004 | t0043 | g0091 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03017 | hp1 | a0001 | c0001 | t0075 | g0128 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03041 | hp1 | a0001 | c0003 | t0038 | g0208 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03041 | hp2 | a0001 | c0002 | t0055 | g0087 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03098 | hp1 | a0001 | c0003 | t0137 | g0287 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03098 | hp2 | a0001 | c0003 | t0007 | g0250 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03130 | hp1 | a0001 | c0002 | t0098 | g0268 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03130 | hp2 | a0001 | c0006 | t0054 | g0075 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03139 | hp1 | a0001 | c0003 | t0104 | g0092 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03139 | hp2 | a0001 | c0003 | t0129 | g0279 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03209 | hp1 | a0001 | c0003 | t0100 | g0248 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03209 | hp2 | a0001 | c0007 | t0109 | g0073 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03225 | hp1 | a0001 | c0002 | t0088 | g0254 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03225 | hp2 | a0001 | c0003 | t0015 | g0066 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03239 | hp1 | a0001 | c0004 | t0115 | g0108 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03453 | hp1 | a0001 | c0019 | t0128 | g0218 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03453 | hp2 | a0001 | c0003 | t0026 | g0246 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03486 | hp1 | a0001 | c0002 | t0004 | g0239 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03486 | hp2 | a0001 | c0004 | t0141 | g0247 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03491 | hp1 | a0001 | c0004 | t0008 | g0001 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03491 | hp2 | a0001 | c0003 | t0144 | g0142 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03492 | hp1 | a0001 | c0004 | t0008 | g0001 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03516 | hp1 | a0001 | c0007 | t0006 | g0089 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03516 | hp2 | a0002 | c0018 | t0007 | g0290 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03540 | hp1 | a0001 | c0004 | t0007 | g0263 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03540 | hp2 | a0001 | c0002 | t0095 | g0207 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03579 | hp1 | a0001 | c0003 | t0136 | g0210 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03579 | hp2 | a0001 | c0003 | t0130 | g0088 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03654 | hp1 | a0001 | c0004 | t0121 | g0031 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0162 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03669 | hp2 | a0001 | c0002 | t0061 | g0133 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0111 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03688 | hp2 | a0001 | c0003 | t0123 | g0197 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03704 | hp1 | a0001 | c0001 | t0077 | g0024 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03710 | hp1 | a0001 | c0004 | t0008 | g0180 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03710 | hp2 | a0001 | c0004 | t0117 | g0048 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03927 | hp1 | a0001 | c0017 | t0114 | g0122 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03927 | hp2 | a0001 | c0002 | t0044 | g0154 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04115 | hp1 | a0001 | c0004 | t0008 | g0136 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04184 | hp1 | a0001 | c0001 | t0081 | g0042 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04184 | hp2 | a0001 | c0004 | t0133 | g0275 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04199 | hp2 | a0001 | c0002 | t0032 | g0018 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04228 | hp1 | a0001 | c0002 | t0003 | g0055 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18522 | hp1 | a0001 | c0003 | t0143 | g0079 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18522 | hp2 | a0001 | c0002 | t0017 | g0286 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18747 | hp2 | a0001 | c0003 | t0124 | g0150 | EAS | CHB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18906 | hp1 | a0001 | c0002 | t0018 | g0283 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0224 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18940 | hp2 | a0001 | c0004 | t0029 | g0228 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18942 | hp2 | a0001 | c0008 | t0028 | g0206 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18944 | hp1 | a0001 | c0001 | t0020 | g0110 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18950 | hp1 | a0001 | c0001 | t0084 | g0232 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18950 | hp2 | a0001 | c0001 | t0090 | g0201 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18951 | hp2 | a0001 | c0004 | t0116 | g0139 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18954 | hp1 | a0001 | c0001 | t0066 | g0120 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18954 | hp2 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18959 | hp2 | a0001 | c0022 | t0070 | g0211 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18960 | hp1 | a0001 | c0005 | t0011 | g0168 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18962 | hp1 | a0001 | c0004 | t0126 | g0196 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18962 | hp2 | a0001 | c0004 | t0029 | g0119 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18964 | hp1 | a0001 | c0001 | t0076 | g0026 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18969 | hp2 | a0001 | c0009 | t0030 | g0169 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18980 | hp1 | a0001 | c0001 | t0021 | g0203 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18980 | hp2 | a0001 | c0001 | t0023 | g0175 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18984 | hp2 | a0001 | c0001 | t0012 | g0014 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18985 | hp1 | a0001 | c0008 | t0122 | g0272 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18985 | hp2 | a0001 | c0001 | t0020 | g0124 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18995 | hp2 | a0001 | c0004 | t0127 | g0178 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA18999 | hp2 | a0001 | c0001 | t0097 | g0052 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19000 | hp1 | a0001 | c0002 | t0003 | g0151 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19002 | hp1 | a0001 | c0001 | t0089 | g0044 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19002 | hp2 | a0001 | c0004 | t0009 | g0140 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19030 | hp1 | a0001 | c0004 | t0046 | g0009 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19043 | hp1 | a0001 | c0002 | t0105 | g0237 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19043 | hp2 | a0001 | c0007 | t0006 | g0084 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19056 | hp2 | a0001 | c0004 | t0009 | g0007 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19058 | hp1 | a0001 | c0004 | t0009 | g0234 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19058 | hp2 | a0001 | c0001 | t0073 | g0145 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19060 | hp1 | a0001 | c0001 | t0021 | g0219 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19060 | hp2 | a0001 | c0003 | t0120 | g0213 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19062 | hp1 | a0001 | c0004 | t0125 | g0273 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19066 | hp1 | a0001 | c0001 | t0082 | g0063 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19066 | hp2 | a0001 | c0009 | t0119 | g0141 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19070 | hp1 | a0001 | c0001 | t0062 | g0186 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19070 | hp2 | a0001 | c0009 | t0030 | g0170 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19082 | hp2 | a0001 | c0004 | t0009 | g0143 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19085 | hp1 | a0001 | c0008 | t0118 | g0095 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20129 | hp1 | a0001 | c0015 | t0091 | g0225 | AFR | ASW | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0068 | AFR | ASW | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20752 | hp1 | a0001 | c0010 | t0002 | g0159 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20752 | hp2 | a0001 | c0002 | t0085 | g0103 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20805 | hp1 | a0002 | c0013 | t0026 | g0288 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20905 | hp1 | a0001 | c0001 | t0071 | g0021 | SAS | GIH | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20905 | hp2 | a0001 | c0001 | t0023 | g0107 | SAS | GIH | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01123 | hp1 | a0001 | c0002 | t0005 | g0045 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG01123 | hp2 | a0005 | c0020 | t0045 | g0221 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02109 | hp1 | a0001 | c0003 | t0047 | g0072 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02109 | hp2 | a0001 | c0003 | t0040 | g0083 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02486 | hp1 | a0001 | c0006 | t0053 | g0076 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02486 | hp2 | a0001 | c0023 | t0049 | g0104 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02559 | hp1 | a0001 | c0002 | t0004 | g0245 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG02559 | hp2 | a0002 | c0013 | t0010 | g0289 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03471 | hp1 | a0001 | c0003 | t0113 | g0276 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG03471 | hp2 | a0001 | c0015 | t0094 | g0280 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0065 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20300 | hp1 | a0001 | c0005 | t0022 | g0165 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA20300 | hp2 | a0001 | c0003 | t0142 | g0080 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA21309 | hp1 | a0001 | c0003 | t0135 | g0255 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
NA21309 | hp2 | a0001 | c0003 | t0007 | g0090 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0074 | g0016 | REF | REF | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
homoSapiens_grch38 | hp1 | a0001 | c0010 | t0002 | g0269 | REF | REF | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4682510
|
G | A | 1 | a0002 | 5 | HG01109.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
missense_variant | MODERATE | c.202G>A | p.Ala68Thr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/9 | 216/11194 | 202/2202 | 68/733 | chr7 | 4682510 | ||
chr7:4759469
|
A | G | 1 | a0006 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1570A>G | p.Met524Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/9 | 1584/11194 | 1570/2202 | 524/733 | chr7 | 4759469 | ||
chr7:4761084
|
A | G | 1 | a0004 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1717A>G | p.Ile573Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/9 | 1731/11194 | 1717/2202 | 573/733 | chr7 | 4761084 | ||
chr7:4762301
|
C | T | 1 | a0005 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2039C>T | p.Ala680Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2053/11194 | 2039/2202 | 680/733 | chr7 | 4762301 | ||
chr7:4762342
|
G | A | 1 | a0003 | 2 | HG01074.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.2080G>A | p.Ala694Thr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2094/11194 | 2080/2202 | 694/733 | chr7 | 4762342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4682746
|
G | A | 2 | a0001c0005a0001c0009 | 10 | HG00639.hp2 HG01978.hp2 HG01981.hp1 others(7): Show |
synonymous_variant | LOW | c.438G>A | p.Arg146Arg | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/9 | 452/11194 | 438/2202 | 146/733 | chr7 | 4682746 | ||
chr7:4740883
|
G | T | 15 | a0001c0001a0001c0004a0001c0005others(12): Show | 160 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
synonymous_variant | LOW | c.606G>T | p.Thr202Thr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/9 | 620/11194 | 606/2202 | 202/733 | chr7 | 4740883 | ||
chr7:4755263
|
C | T | 1 | a0001c0027 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.930C>T | p.Tyr310Tyr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/9 | 944/11194 | 930/2202 | 310/733 | chr7 | 4755263 | ||
chr7:4759099
|
C | T | 2 | a0001c0007a0001c0011 | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
synonymous_variant | LOW | c.1293C>T | p.Ser431Ser | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/9 | 1307/11194 | 1293/2202 | 431/733 | chr7 | 4759099 | ||
chr7:4759126
|
G | A | 1 | a0001c0019 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1320G>A | p.Leu440Leu | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/9 | 1334/11194 | 1320/2202 | 440/733 | chr7 | 4759126 | ||
chr7:4759144
|
C | T | 1 | a0001c0026 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.1338C>T | p.Pro446Pro | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/9 | 1352/11194 | 1338/2202 | 446/733 | chr7 | 4759144 | ||
chr7:4759504
|
C | T | 1 | a0001c0024 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.1605C>T | p.Ala535Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/9 | 1619/11194 | 1605/2202 | 535/733 | chr7 | 4759504 | ||
chr7:4759510
|
A | T | 3 | a0001c0017a0001c0021a0001c0023 | 4 | HG01258.hp2 HG01261.hp1 HG02486.hp2 others(1): Show |
synonymous_variant | LOW | c.1611A>T | p.Gly537Gly | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/9 | 1625/11194 | 1611/2202 | 537/733 | chr7 | 4759510 | ||
chr7:4761089
|
G | A | 1 | a0001c0024 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.1722G>A | p.Ala574Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/9 | 1736/11194 | 1722/2202 | 574/733 | chr7 | 4761089 | ||
chr7:4762194
|
C | T | 3 | a0001c0006a0001c0015a0004c0016 | 9 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(6): Show |
synonymous_variant | LOW | c.1932C>T | p.Ser644Ser | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1946/11194 | 1932/2202 | 644/733 | chr7 | 4762194 | ||
chr7:4762221
|
G | A | 1 | a0006c0025 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1959G>A | p.Ala653Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1973/11194 | 1959/2202 | 653/733 | chr7 | 4762221 | ||
chr7:4762293
|
G | A | 1 | a0001c0022 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.2031G>A | p.Ala677Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2045/11194 | 2031/2202 | 677/733 | chr7 | 4762293 | ||
chr7:4762398
|
T | G | 26 | a0001c0001a0001c0002a0001c0003others(23): Show | 291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
synonymous_variant | LOW | c.2136T>G | p.Gly712Gly | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2150/11194 | 2136/2202 | 712/733 | chr7 | 4762398 | ||
chr7:4762401
|
T | C | 1 | a0001c0008 | 4 | HG00597.hp1 NA18942.hp2 NA18985.hp1 others(1): Show |
synonymous_variant | LOW | c.2139T>C | p.Ala713Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2153/11194 | 2139/2202 | 713/733 | chr7 | 4762401 | ||
chr7:4762404
|
A | G | 14 | a0001c0003a0001c0004a0001c0006others(11): Show | 109 | HG00597.hp1 HG00738.hp2 HG01070.hp1 others(106): Show |
synonymous_variant | LOW | c.2142A>G | p.Val714Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2156/11194 | 2142/2202 | 714/733 | chr7 | 4762404 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4762567
|
C | A | 1 | a0001c0002t0032 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 103 | chr7 | 4762567 | |||||
chr7:4762570
|
C | T | 1 | a0001c0003t0146 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 106 | chr7 | 4762570 | |||||
chr7:4762682
|
T | G | 2 | a0001c0004t0033a0001c0004t0034 | 2 | HG00738.hp2 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*218T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 218 | chr7 | 4762682 | |||||
chr7:4762811
|
C | T | 45 | a0001c0003t0010a0001c0003t0014a0001c0003t0031others(42): Show | 58 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*347C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 347 | chr7 | 4762811 | |||||
chr7:4762816
|
C | T | 1 | a0001c0003t0113 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 352 | chr7 | 4762816 | |||||
chr7:4762834
|
G | A | 1 | a0001c0001t0035 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 370 | chr7 | 4762834 | |||||
chr7:4762843
|
C | T | 1 | a0001c0003t0112 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 379 | chr7 | 4762843 | |||||
chr7:4762844
|
G | A | 6 | a0001c0003t0015a0001c0003t0036a0001c0003t0037others(3): Show | 7 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*380G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 380 | chr7 | 4762844 | |||||
chr7:4762888
|
G | A | 3 | a0001c0001t0016a0001c0002t0041a0002c0012t0016 | 3 | HG01109.hp1 HG02055.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*424G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 424 | chr7 | 4762888 | |||||
chr7:4762965
|
C | T | 1 | a0001c0003t0111 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 501 | chr7 | 4762965 | |||||
chr7:4762969
|
C | T | 3 | a0001c0003t0031a0001c0003t0144a0001c0003t0145 | 4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*505C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 505 | chr7 | 4762969 | |||||
chr7:4763292
|
C | T | 1 | a0001c0003t0113 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 828 | chr7 | 4763292 | |||||
chr7:4763296
|
C | T | 1 | a0001c0010t0110 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 832 | chr7 | 4763296 | |||||
chr7:4763306
|
G | T | 1 | a0001c0007t0109 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*842G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 842 | chr7 | 4763306 | |||||
chr7:4763308
|
G | T | 1 | a0001c0001t0108 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*844G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 844 | chr7 | 4763308 | |||||
chr7:4763363
|
C | T | 2 | a0004c0016t0106a0004c0016t0107 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*899C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 899 | chr7 | 4763363 | |||||
chr7:4763372
|
G | A | 1 | a0001c0002t0042 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*908G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 908 | chr7 | 4763372 | |||||
chr7:4763388
|
C | T | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 924 | chr7 | 4763388 | |||||
chr7:4763394
|
C | T | 2 | a0001c0003t0142a0001c0003t0143 | 2 | NA18522.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*930C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 930 | chr7 | 4763394 | |||||
chr7:4763444
|
C | A | 1 | a0001c0004t0043 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 980 | chr7 | 4763444 | |||||
chr7:4763454
|
A | G | 18 | a0001c0003t0007a0001c0003t0015a0001c0003t0026others(15): Show | 21 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*990A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 990 | chr7 | 4763454 | |||||
chr7:4763526
|
C | T | 1 | a0001c0002t0098 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1062C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1062 | chr7 | 4763526 | |||||
chr7:4763592
|
C | T | 1 | a0001c0001t0097 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1128C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1128 | chr7 | 4763592 | |||||
chr7:4763606
|
G | A | 7 | a0001c0003t0015a0001c0003t0036a0001c0003t0037others(4): Show | 8 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1142G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1142 | chr7 | 4763606 | |||||
chr7:4763634
|
C | T | 2 | a0001c0001t0096a0001c0002t0095 | 2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1170C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1170 | chr7 | 4763634 | |||||
chr7:4763644
|
C | T | 4 | a0001c0006t0092a0001c0006t0093a0001c0015t0091others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1180C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1180 | chr7 | 4763644 | |||||
chr7:4763844
|
G | A | 3 | a0001c0003t0031a0001c0003t0144a0001c0003t0145 | 4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1380G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1380 | chr7 | 4763844 | |||||
chr7:4763899
|
G | A | 1 | a0001c0004t0043 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1435G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1435 | chr7 | 4763899 | |||||
chr7:4763984
|
C | T | 7 | a0001c0002t0105a0001c0003t0139a0001c0003t0140others(4): Show | 7 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1520C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1520 | chr7 | 4763984 | |||||
chr7:4763994
|
C | T | 1 | a0001c0004t0034 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1530 | chr7 | 4763994 | |||||
chr7:4764127
|
A | G | 1 | a0001c0001t0090 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1663 | chr7 | 4764127 | |||||
chr7:4764158
|
G | C | 6 | a0001c0003t0015a0001c0003t0036a0001c0003t0037others(3): Show | 7 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1694G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1694 | chr7 | 4764158 | |||||
chr7:4764249
|
C | T | 1 | a0001c0001t0089 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1785C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1785 | chr7 | 4764249 | |||||
chr7:4764292
|
C | T | 14 | a0001c0002t0088a0001c0002t0105a0001c0003t0015others(11): Show | 15 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1828C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1828 | chr7 | 4764292 | |||||
chr7:4764315
|
G | A | 13 | a0001c0002t0088a0001c0003t0015a0001c0003t0036others(10): Show | 14 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1851G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1851 | chr7 | 4764315 | |||||
chr7:4764452
|
G | A | 1 | a0001c0002t0044 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1988G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1988 | chr7 | 4764452 | |||||
chr7:4764454
|
C | T | 6 | a0001c0003t0010a0001c0003t0135a0001c0003t0136others(3): Show | 8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1990C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1990 | chr7 | 4764454 | |||||
chr7:4764473
|
G | T | 15 | a0001c0002t0105a0001c0003t0015a0001c0003t0036others(12): Show | 16 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2009G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2009 | chr7 | 4764473 | |||||
chr7:4764498
|
C | T | 15 | a0001c0002t0088a0001c0002t0105a0001c0003t0015others(12): Show | 16 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2034C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2034 | chr7 | 4764498 | |||||
chr7:4764506
|
G | A | 1 | a0001c0004t0008 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2042G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2042 | chr7 | 4764506 | |||||
chr7:4764572
|
G | C | 7 | a0001c0003t0015a0001c0003t0036a0001c0003t0037others(4): Show | 8 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2108G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2108 | chr7 | 4764572 | |||||
chr7:4764630
|
G | A | 1 | a0005c0020t0045 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2166G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2166 | chr7 | 4764630 | |||||
chr7:4764639
|
C | T | 4 | a0001c0003t0014a0001c0003t0134a0001c0004t0014others(1): Show | 5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2175C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2175 | chr7 | 4764639 | |||||
chr7:4764697
|
G | A | 5 | a0001c0003t0047a0001c0003t0111a0001c0003t0112others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2233G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2233 | chr7 | 4764697 | |||||
chr7:4764734
|
C | A | 2 | a0001c0003t0142a0001c0003t0143 | 2 | NA18522.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2270C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2270 | chr7 | 4764734 | |||||
chr7:4764752
|
C | T | 2 | a0001c0003t0112a0001c0003t0113 | 2 | HG01891.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2288C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2288 | chr7 | 4764752 | |||||
chr7:4764831
|
C | G | 1 | a0001c0002t0098 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2367 | chr7 | 4764831 | |||||
chr7:4764866
|
G | C | 1 | a0001c0023t0049 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2402G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2402 | chr7 | 4764866 | |||||
chr7:4764906
|
A | G | 5 | a0001c0003t0047a0001c0003t0087a0001c0003t0111others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2442A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2442 | chr7 | 4764906 | |||||
chr7:4764920
|
G | T | 7 | a0001c0002t0105a0001c0003t0139a0001c0003t0140others(4): Show | 7 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2456G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2456 | chr7 | 4764920 | |||||
chr7:4764965
|
G | A | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2501G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2501 | chr7 | 4764965 | |||||
chr7:4764976
|
G | A | 1 | a0001c0001t0050 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2512G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2512 | chr7 | 4764976 | |||||
chr7:4765007
|
A | G | 4 | a0001c0003t0031a0001c0003t0132a0001c0003t0144others(1): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2543 | chr7 | 4765007 | |||||
chr7:4765031
|
G | A | 1 | a0001c0001t0051 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2567G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2567 | chr7 | 4765031 | |||||
chr7:4765089
|
T | C | 48 | a0001c0001t0017a0001c0001t0058a0001c0001t0096others(45): Show | 65 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2625T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2625 | chr7 | 4765089 | |||||
chr7:4765103
|
G | C | 32 | a0001c0002t0088a0001c0002t0105a0001c0003t0007others(29): Show | 35 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2639G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2639 | chr7 | 4765103 | |||||
chr7:4765113
|
C | T | 2 | a0001c0001t0058a0001c0002t0057 | 2 | HG01496.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2649C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2649 | chr7 | 4765113 | |||||
chr7:4765114
|
G | A | 1 | a0001c0003t0099 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2650 | chr7 | 4765114 | |||||
chr7:4765173
|
T | C | 4 | a0001c0003t0031a0001c0003t0132a0001c0003t0144others(1): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2709T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2709 | chr7 | 4765173 | |||||
chr7:4765261
|
G | A | 16 | a0001c0001t0016a0001c0002t0041a0001c0003t0010others(13): Show | 19 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2797G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2797 | chr7 | 4765261 | |||||
chr7:4765378
|
A | G | 22 | a0001c0003t0007a0001c0003t0015a0001c0003t0026others(19): Show | 26 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2914A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2914 | chr7 | 4765378 | |||||
chr7:4765382
|
G | C | 1 | a0001c0001t0059 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2918G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2918 | chr7 | 4765382 | |||||
chr7:4765433
|
G | A | 7 | a0001c0003t0014a0001c0003t0129a0001c0003t0130others(4): Show | 8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2969G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2969 | chr7 | 4765433 | |||||
chr7:4765506
|
G | A | 52 | a0001c0002t0088a0001c0002t0105a0001c0003t0007others(49): Show | 57 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3042 | chr7 | 4765506 | |||||
chr7:4765619
|
G | A | 7 | a0001c0003t0047a0001c0003t0087a0001c0003t0111others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3155G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3155 | chr7 | 4765619 | |||||
chr7:4765737
|
T | C | 9 | a0001c0001t0016a0001c0002t0041a0001c0003t0010others(6): Show | 11 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3273T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3273 | chr7 | 4765737 | |||||
chr7:4765745
|
C | T | 53 | a0001c0001t0016a0001c0002t0041a0001c0002t0088others(50): Show | 63 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3281C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3281 | chr7 | 4765745 | |||||
chr7:4765850
|
C | T | 7 | a0001c0003t0047a0001c0003t0087a0001c0003t0111others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3386C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3386 | chr7 | 4765850 | |||||
chr7:4766038
|
C | T | 3 | a0001c0007t0006a0001c0007t0109a0001c0011t0006 | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3574C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3574 | chr7 | 4766038 | |||||
chr7:4766039
|
G | A | 1 | a0001c0003t0100 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3575G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3575 | chr7 | 4766039 | |||||
chr7:4766055
|
C | T | 8 | a0001c0002t0088a0001c0002t0105a0001c0003t0139others(5): Show | 8 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3591C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3591 | chr7 | 4766055 | |||||
chr7:4766094
|
G | A | 1 | a0001c0004t0046 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3630G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3630 | chr7 | 4766094 | |||||
chr7:4766181
|
T | A | 10 | a0001c0003t0036a0001c0006t0052a0001c0006t0053others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3717T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3717 | chr7 | 4766181 | |||||
chr7:4766219
|
CG | C | 7 | a0001c0003t0014a0001c0003t0129a0001c0003t0130others(4): Show | 8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3758delG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3758 | INFO_REALIGN_3_PRIME | chr7 | 4766219 | ||||
chr7:4766369
|
G | C | 8 | a0001c0003t0007a0001c0003t0026a0001c0003t0101others(5): Show | 10 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3905G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3905 | chr7 | 4766369 | |||||
chr7:4766401
|
A | C | 20 | a0001c0003t0120a0001c0003t0123a0001c0003t0124others(17): Show | 29 | HG00597.hp1 HG02698.hp2 HG03239.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3937A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3937 | chr7 | 4766401 | |||||
chr7:4766567
|
T | C | 12 | a0001c0003t0014a0001c0003t0015a0001c0003t0039others(9): Show | 14 | HG00738.hp2 HG01978.hp1 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4103T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4103 | chr7 | 4766567 | |||||
chr7:4766587
|
G | A | 3 | a0001c0003t0015a0001c0003t0039a0001c0003t0040 | 4 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4123G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4123 | chr7 | 4766587 | |||||
chr7:4766591
|
C | T | 1 | a0005c0020t0045 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4127C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4127 | chr7 | 4766591 | |||||
chr7:4766592
|
A | G | 67 | a0001c0001t0016a0001c0001t0058a0001c0002t0041others(64): Show | 79 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4128A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4128 | chr7 | 4766592 | |||||
chr7:4766756
|
A | G | 1 | a0001c0003t0040 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4292A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4292 | chr7 | 4766756 | |||||
chr7:4766783
|
T | C | 10 | a0001c0001t0016a0001c0001t0058a0001c0002t0041others(7): Show | 12 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4319T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4319 | chr7 | 4766783 | |||||
chr7:4766809
|
T | A | 3 | a0001c0003t0031a0001c0003t0144a0001c0003t0145 | 4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4345T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4345 | chr7 | 4766809 | |||||
chr7:4766853
|
G | A | 3 | a0001c0003t0015a0001c0003t0039a0001c0003t0040 | 4 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4389G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4389 | chr7 | 4766853 | |||||
chr7:4766870
|
TGA | T | 7 | a0001c0003t0014a0001c0003t0129a0001c0003t0130others(4): Show | 8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4417_*4418delGA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4417 | INFO_REALIGN_3_PRIME | chr7 | 4766870 | ||||
chr7:4766899
|
G | T | 1 | a0001c0001t0086 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4435G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4435 | chr7 | 4766899 | |||||
chr7:4766900
|
A | G | 13 | a0001c0001t0016a0001c0001t0058a0001c0002t0041others(10): Show | 15 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4436A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4436 | chr7 | 4766900 | |||||
chr7:4766951
|
T | C | 1 | a0001c0003t0113 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4487T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4487 | chr7 | 4766951 | |||||
chr7:4767044
|
C | T | 1 | a0001c0002t0085 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4580C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4580 | chr7 | 4767044 | |||||
chr7:4767095
|
A | G | 10 | a0001c0002t0105a0001c0003t0047a0001c0003t0087others(7): Show | 10 | HG00738.hp2 HG01891.hp2 HG01978.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4631A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4631 | chr7 | 4767095 | |||||
chr7:4767130
|
G | A | 1 | a0001c0002t0088 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4666G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4666 | chr7 | 4767130 | |||||
chr7:4767211
|
A | G | 12 | a0001c0003t0036a0001c0003t0099a0001c0003t0111others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4747A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4747 | chr7 | 4767211 | |||||
chr7:4767240
|
C | T | 6 | a0001c0003t0014a0001c0003t0129a0001c0003t0130others(3): Show | 7 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4776C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4776 | chr7 | 4767240 | |||||
chr7:4767267
|
C | T | 5 | a0001c0003t0037a0001c0003t0038a0001c0003t0100others(2): Show | 5 | HG02895.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4803C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4803 | chr7 | 4767267 | |||||
chr7:4767268
|
T | C | 12 | a0001c0002t0055a0001c0002t0105a0001c0003t0015others(9): Show | 13 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4804T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4804 | chr7 | 4767268 | |||||
chr7:4767327
|
C | G | 4 | a0001c0004t0009a0001c0004t0125a0001c0004t0126others(1): Show | 7 | NA18962.hp1 NA18995.hp2 NA19002.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4863C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4863 | chr7 | 4767327 | |||||
chr7:4767331
|
A | C | 10 | a0001c0003t0099a0001c0006t0052a0001c0006t0053others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4867A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4867 | chr7 | 4767331 | |||||
chr7:4767334
|
G | A | 1 | a0001c0001t0060 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4870G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4870 | chr7 | 4767334 | |||||
chr7:4767544
|
T | C | 1 | a0001c0002t0061 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5080T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5080 | chr7 | 4767544 | |||||
chr7:4767578
|
C | T | 1 | a0001c0001t0084 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5114C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5114 | chr7 | 4767578 | |||||
chr7:4767592
|
G | T | 11 | a0001c0002t0105a0001c0003t0015a0001c0003t0039others(8): Show | 12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5128G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5128 | chr7 | 4767592 | |||||
chr7:4767620
|
G | A | 19 | a0001c0001t0016a0001c0002t0041a0001c0003t0010others(16): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5156G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5156 | chr7 | 4767620 | |||||
chr7:4767692
|
CCTTTT | C | 3 | a0001c0003t0139a0001c0003t0140a0001c0004t0141 | 3 | HG02451.hp1 HG02965.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5235_*5239delTTTT others(1): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5235 | INFO_REALIGN_3_PRIME | chr7 | 4767692 | ||||
chr7:4767790
|
C | T | 1 | a0001c0004t0056 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5326C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5326 | chr7 | 4767790 | |||||
chr7:4767814
|
C | G | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5350C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5350 | chr7 | 4767814 | |||||
chr7:4767865
|
C | T | 9 | a0001c0001t0016a0001c0002t0041a0001c0003t0010others(6): Show | 11 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5401C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5401 | chr7 | 4767865 | |||||
chr7:4768111
|
TCACTGAC others(313): Show |
T | 13 | a0001c0001t0016a0001c0001t0058a0001c0002t0041others(10): Show | 20 | HG01081.hp2 HG01109.hp1 HG01496.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5661_*5980del | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5661 | INFO_REALIGN_3_PRIME | chr7 | 4768111 | ||||
chr7:4768121
|
C | CT | 31 | a0001c0001t0003a0001c0001t0050a0001c0001t0080others(28): Show | 49 | HG00597.hp2 HG00735.hp2 HG01099.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*5686dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768121
|
C | CTT | 6 | a0001c0002t0019a0001c0002t0098a0001c0003t0019others(3): Show | 6 | HG01123.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5685_*5686dupTT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768121
|
C | CTTTTTT | 7 | a0001c0004t0009a0001c0004t0121a0001c0004t0125others(4): Show | 11 | HG00597.hp1 HG03654.hp1 HG04184.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5681_*5686dupTTTT others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768121
|
C | CTTTTTTT | 5 | a0001c0003t0123a0001c0003t0124a0001c0004t0029others(2): Show | 7 | HG03688.hp2 NA18747.hp2 NA18940.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5680_*5686dupTTTT others(3): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768121
|
C | CTTTTTTT others(4): Show |
1 | a0001c0003t0142 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5676_*5686dupTTTT others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768121
|
C | CTTTTTTT others(5): Show |
1 | a0001c0003t0143 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5675_*5686dupTTTT others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768121
|
CT | C | 14 | a0001c0001t0062a0001c0001t0063a0001c0001t0065others(11): Show | 15 | HG00323.hp2 HG01070.hp2 HG01256.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5686delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5686 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768121
|
CTT | C | 5 | a0001c0003t0015a0001c0003t0040a0001c0003t0047others(2): Show | 6 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5685_*5686delTT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5685 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | ||||
chr7:4768155
|
C | T | 9 | a0001c0002t0105a0001c0003t0015a0001c0003t0039others(6): Show | 10 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5691C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5691 | chr7 | 4768155 | |||||
chr7:4768172
|
G | A | 7 | a0001c0003t0014a0001c0003t0129a0001c0003t0130others(4): Show | 8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5708G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5708 | chr7 | 4768172 | |||||
chr7:4768195
|
T | C | 9 | a0001c0002t0105a0001c0003t0014a0001c0003t0099others(6): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5731T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5731 | chr7 | 4768195 | |||||
chr7:4768199
|
C | T | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5735C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5735 | chr7 | 4768199 | |||||
chr7:4768201
|
C | T | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5737C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5737 | chr7 | 4768201 | |||||
chr7:4768202
|
G | A | 7 | a0001c0003t0014a0001c0003t0129a0001c0003t0130others(4): Show | 8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5738G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5738 | chr7 | 4768202 | |||||
chr7:4768210
|
G | T | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5746G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5746 | chr7 | 4768210 | |||||
chr7:4768220
|
C | T | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5756C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5756 | chr7 | 4768220 | |||||
chr7:4768222
|
T | C | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5758T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5758 | chr7 | 4768222 | |||||
chr7:4768233
|
C | T | 1 | a0001c0019t0128 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5769C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5769 | chr7 | 4768233 | |||||
chr7:4768277
|
C | T | 4 | a0001c0003t0120a0001c0003t0124a0001c0009t0030others(1): Show | 5 | NA18747.hp2 NA18969.hp2 NA19060.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5813C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5813 | chr7 | 4768277 | |||||
chr7:4768282
|
G | A | 1 | a0001c0001t0066 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5818G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5818 | chr7 | 4768282 | |||||
chr7:4768284
|
T | C | 3 | a0001c0001t0020a0001c0001t0062a0001c0001t0066 | 4 | NA18944.hp1 NA18954.hp1 NA18985.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5820T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5820 | chr7 | 4768284 | |||||
chr7:4768293
|
C | A | 1 | a0001c0002t0025 | 2 | HG00735.hp2 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5829C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5829 | chr7 | 4768293 | |||||
chr7:4768322
|
C | T | 1 | a0001c0001t0079 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5858C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5858 | chr7 | 4768322 | |||||
chr7:4768356
|
T | C | 1 | a0001c0003t0144 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5892T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5892 | chr7 | 4768356 | |||||
chr7:4768368
|
G | A | 1 | a0001c0019t0128 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5904G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5904 | chr7 | 4768368 | |||||
chr7:4768379
|
G | A | 5 | a0001c0003t0047a0001c0003t0087a0001c0003t0111others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5915G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5915 | chr7 | 4768379 | |||||
chr7:4768423
|
C | T | 3 | a0001c0001t0013a0001c0002t0013a0001c0002t0083 | 4 | HG00323.hp1 HG01515.hp1 HG02602.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5959C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5959 | chr7 | 4768423 | |||||
chr7:4768427
|
C | T | 3 | a0001c0001t0013a0001c0002t0013a0001c0002t0083 | 4 | HG00323.hp1 HG01515.hp1 HG02602.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5963C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5963 | chr7 | 4768427 | |||||
chr7:4768428
|
G | A | 5 | a0001c0001t0011a0001c0001t0063a0001c0002t0044others(2): Show | 6 | HG02074.hp2 HG02132.hp2 HG02523.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5964G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5964 | chr7 | 4768428 | |||||
chr7:4768467
|
G | A | 1 | a0001c0003t0111 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6003G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6003 | chr7 | 4768467 | |||||
chr7:4768538
|
C | T | 4 | a0001c0004t0056a0001c0007t0006a0001c0007t0109others(1): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6074C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6074 | chr7 | 4768538 | |||||
chr7:4768563
|
C | T | 10 | a0001c0001t0016a0001c0001t0058a0001c0002t0041others(7): Show | 12 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6099C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6099 | chr7 | 4768563 | |||||
chr7:4768715
|
C | T | 1 | a0001c0001t0082 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6251C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6251 | chr7 | 4768715 | |||||
chr7:4768738
|
A | G | 4 | a0001c0003t0031a0001c0003t0132a0001c0003t0144others(1): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6274A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6274 | chr7 | 4768738 | |||||
chr7:4768772
|
C | T | 1 | a0001c0003t0111 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6308C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6308 | chr7 | 4768772 | |||||
chr7:4768773
|
G | A | 11 | a0001c0001t0016a0001c0003t0010a0001c0003t0135others(8): Show | 18 | HG01081.hp2 HG01109.hp1 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*6309G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6309 | chr7 | 4768773 | |||||
chr7:4768936
|
G | T | 5 | a0001c0001t0017a0001c0001t0096a0001c0002t0017others(2): Show | 5 | HG01891.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6472G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6472 | chr7 | 4768936 | |||||
chr7:4769047
|
A | T | 57 | a0001c0001t0016a0001c0001t0058a0001c0001t0078others(54): Show | 72 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*6583A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6583 | chr7 | 4769047 | |||||
chr7:4769054
|
G | A | 1 | a0001c0002t0105 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6590G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6590 | chr7 | 4769054 | |||||
chr7:4769061
|
C | T | 55 | a0001c0001t0016a0001c0001t0058a0001c0001t0078others(52): Show | 70 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*6597C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6597 | chr7 | 4769061 | |||||
chr7:4769317
|
C | G | 8 | a0001c0003t0007a0001c0003t0026a0001c0003t0101others(5): Show | 10 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6853C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6853 | chr7 | 4769317 | |||||
chr7:4769318
|
C | T | 4 | a0001c0002t0088a0001c0007t0006a0001c0007t0109others(1): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6854C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6854 | chr7 | 4769318 | |||||
chr7:4769322
|
C | G | 36 | a0001c0001t0016a0001c0001t0058a0001c0002t0004others(33): Show | 47 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*6858C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6858 | chr7 | 4769322 | |||||
chr7:4769355
|
G | C | 3 | a0001c0007t0006a0001c0007t0109a0001c0011t0006 | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6891G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6891 | chr7 | 4769355 | |||||
chr7:4769372
|
A | G | 71 | a0001c0001t0016a0001c0001t0024a0001c0001t0058others(68): Show | 95 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*6908A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6908 | chr7 | 4769372 | |||||
chr7:4769401
|
G | A | 2 | a0001c0001t0058a0001c0002t0041 | 2 | HG02055.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6937G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6937 | chr7 | 4769401 | |||||
chr7:4769419
|
G | A | 10 | a0001c0001t0016a0001c0001t0058a0001c0002t0041others(7): Show | 12 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6955G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6955 | chr7 | 4769419 | |||||
chr7:4769443
|
CT | C | 7 | a0001c0001t0011a0001c0001t0050a0001c0001t0063others(4): Show | 8 | HG01175.hp1 HG02074.hp2 HG02132.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6992delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6992 | INFO_REALIGN_3_PRIME | chr7 | 4769443 | ||||
chr7:4769465
|
G | A | 2 | a0001c0003t0113a0001c0003t0146 | 2 | HG02922.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7001G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7001 | chr7 | 4769465 | |||||
chr7:4769592
|
A | C | 36 | a0001c0001t0016a0001c0001t0058a0001c0002t0004others(33): Show | 47 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*7128A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7128 | chr7 | 4769592 | |||||
chr7:4769686
|
C | T | 1 | a0001c0008t0122 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7222C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7222 | chr7 | 4769686 | |||||
chr7:4769705
|
T | C | 29 | a0001c0001t0068a0001c0001t0080a0001c0002t0088others(26): Show | 40 | HG00597.hp1 HG01081.hp2 HG01175.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*7241T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7241 | chr7 | 4769705 | |||||
chr7:4769732
|
C | T | 1 | a0001c0001t0076 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7268C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7268 | chr7 | 4769732 | |||||
chr7:4769806
|
T | G | 83 | a0001c0001t0016a0001c0001t0058a0001c0001t0068others(80): Show | 109 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*7342T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7342 | chr7 | 4769806 | |||||
chr7:4769876
|
T | G | 4 | a0001c0006t0092a0001c0006t0093a0001c0015t0091others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7412T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7412 | chr7 | 4769876 | |||||
chr7:4769911
|
G | A | 1 | a0001c0001t0076 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7447G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7447 | chr7 | 4769911 | |||||
chr7:4769918
|
A | AGAGTGCA others(16): Show |
1 | a0004c0016t0106 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7456_*7478dupAGTG others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7479 | INFO_REALIGN_3_PRIME | chr7 | 4769918 | ||||
chr7:4770029
|
G | T | 78 | a0001c0001t0016a0001c0001t0058a0001c0001t0068others(75): Show | 103 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*7565G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7565 | chr7 | 4770029 | |||||
chr7:4770066
|
A | G | 3 | a0001c0007t0006a0001c0007t0109a0001c0011t0006 | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7602A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7602 | chr7 | 4770066 | |||||
chr7:4770222
|
A | C | 1 | a0001c0001t0075 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7758A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7758 | chr7 | 4770222 | |||||
chr7:4770301
|
G | A | 7 | a0001c0003t0014a0001c0003t0129a0001c0003t0130others(4): Show | 8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7837G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7837 | chr7 | 4770301 | |||||
chr7:4770316
|
C | T | 5 | a0001c0002t0055a0001c0003t0111a0001c0003t0112others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7852C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7852 | chr7 | 4770316 | |||||
chr7:4770319
|
G | C | 5 | a0001c0002t0055a0001c0003t0111a0001c0003t0112others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7855G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7855 | chr7 | 4770319 | |||||
chr7:4770389
|
G | C | 3 | a0001c0003t0135a0001c0003t0136a0001c0003t0137 | 3 | HG03098.hp1 HG03579.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7925G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7925 | chr7 | 4770389 | |||||
chr7:4770391
|
C | G | 1 | a0001c0001t0077 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7927C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7927 | chr7 | 4770391 | |||||
chr7:4770392
|
G | A | 1 | a0001c0003t0113 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7928G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7928 | chr7 | 4770392 | |||||
chr7:4770479
|
C | T | 2 | a0001c0001t0068a0001c0001t0080 | 2 | HG01175.hp2 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8015C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8015 | chr7 | 4770479 | |||||
chr7:4770566
|
CTCT | C | 16 | a0001c0001t0068a0001c0001t0080a0001c0003t0007others(13): Show | 18 | HG01175.hp2 HG01515.hp2 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8107_*8109delCTT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8107 | INFO_REALIGN_3_PRIME | chr7 | 4770566 | ||||
chr7:4770569
|
T | C | 5 | a0001c0002t0004a0001c0002t0018a0001c0002t0019others(2): Show | 13 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8105T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8105 | chr7 | 4770569 | |||||
chr7:4770593
|
T | C | 28 | a0001c0001t0016a0001c0001t0058a0001c0001t0068others(25): Show | 32 | HG01109.hp1 HG01175.hp2 HG01515.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*8129T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8129 | chr7 | 4770593 | |||||
chr7:4770652
|
G | A | 1 | a0001c0001t0021 | 2 | NA18980.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8188G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8188 | chr7 | 4770652 | |||||
chr7:4770685
|
G | A | 1 | a0001c0001t0077 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8221G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8221 | chr7 | 4770685 | |||||
chr7:4770795
|
T | C | 3 | a0001c0005t0022a0001c0005t0069a0006c0025t0022 | 3 | HG00621.hp2 HG01981.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8331T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8331 | chr7 | 4770795 | |||||
chr7:4770831
|
G | A | 1 | a0001c0003t0145 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8367G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8367 | chr7 | 4770831 | |||||
chr7:4770864
|
G | GGT | 7 | a0001c0001t0023a0001c0003t0040a0001c0003t0144others(4): Show | 9 | HG00597.hp1 HG02109.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8437_*8438dupGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770864
|
G | GGTGT | 13 | a0001c0001t0074a0001c0002t0004a0001c0002t0019others(10): Show | 21 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*8435_*8438dupGTGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770864
|
G | GGTGTGT | 8 | a0001c0002t0018a0001c0003t0099a0001c0003t0136others(5): Show | 9 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8433_*8438dupGTGT others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770864
|
GGT | G | 16 | a0001c0001t0005a0001c0001t0059a0001c0001t0062others(13): Show | 22 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*8437_*8438delGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8437 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770864
|
GGTGT | G | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(59): Show | 133 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*8435_*8438delGTGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8435 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770864
|
GGTGTGTG others(1): Show |
G | 6 | a0001c0003t0104a0001c0003t0142a0001c0003t0143others(3): Show | 6 | HG00323.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8431_*8438delGTGT others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8431 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770864
|
GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0012a0001c0001t0108a0001c0002t0012 | 4 | HG02056.hp2 HG02080.hp1 HG02135.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8429_*8438delGTGT others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8429 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770864
|
GGTGTGTG others(11): Show |
G | 2 | a0004c0016t0106a0004c0016t0107 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8421_*8438delGTGT others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8421 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | ||||
chr7:4770884
|
T | G | 2 | a0004c0016t0106a0004c0016t0107 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8420T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8420 | chr7 | 4770884 | |||||
chr7:4770895
|
G | A | 1 | a0001c0003t0129 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8431G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8431 | chr7 | 4770895 | |||||
chr7:4770899
|
G | A | 1 | a0001c0001t0071 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8435G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8435 | chr7 | 4770899 | |||||
chr7:4770903
|
A | G | 3 | a0001c0003t0031a0001c0003t0144a0001c0003t0145 | 4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8439A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | chr7 | 4770903 | |||||
chr7:4770903
|
A | T | 2 | a0001c0003t0130a0001c0019t0128 | 2 | HG03453.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8439A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | chr7 | 4770903 | |||||
chr7:4770905
|
T | A | 3 | a0001c0003t0031a0001c0003t0144a0001c0003t0145 | 4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8441T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8441 | chr7 | 4770905 | |||||
chr7:4770923
|
G | A | 1 | a0001c0001t0072 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8459G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8459 | chr7 | 4770923 | |||||
chr7:4770927
|
G | A | 1 | a0001c0003t0103 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8463G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8463 | chr7 | 4770927 | |||||
chr7:4770936
|
AT | A | 37 | a0001c0002t0004a0001c0002t0018a0001c0002t0019others(34): Show | 52 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*8477delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8477 | INFO_REALIGN_3_PRIME | chr7 | 4770936 | ||||
chr7:4770978
|
C | T | 1 | a0001c0001t0073 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8514C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8514 | chr7 | 4770978 | |||||
chr7:4771081
|
G | A | 3 | a0001c0003t0015a0001c0003t0039a0001c0003t0040 | 4 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8617G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8617 | chr7 | 4771081 | |||||
chr7:4771103
|
C | G | 1 | a0001c0023t0049 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8639C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8639 | chr7 | 4771103 | |||||
chr7:4771170
|
A | G | 83 | a0001c0001t0016a0001c0001t0058a0001c0001t0068others(80): Show | 109 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*8706A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8706 | chr7 | 4771170 | |||||
chr7:4771208
|
TTAA | T | 9 | a0001c0001t0016a0001c0001t0058a0001c0002t0041others(6): Show | 11 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8748_*8750delTAA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8748 | INFO_REALIGN_3_PRIME | chr7 | 4771208 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4682884
|
A | AC | 5 | a0001c0001t0012g0005a0001c0002t0083g0008a0001c0003t0112g0006others(2): Show | 5 | HG01891.hp2 HG02080.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+21dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4682884 | |||||
chr7:4682885
|
C | A | 2 | a0001c0003t0036g0004a0001c0003t0140g0003 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.560+17C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4682885 | ||||||
chr7:4682979
|
C | A | 57 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(54): Show | 58 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.560+111C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4682979 | ||||||
chr7:4682991
|
C | T | 5 | a0002c0012t0004g0292a0002c0012t0016g0291a0002c0013t0010g0289others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+123C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4682991 | ||||||
chr7:4683059
|
A | G | 3 | a0001c0002t0017g0286a0001c0003t0134g0285a0001c0003t0137g0287 | 3 | HG02055.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+191A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683059 | ||||||
chr7:4683076
|
C | T | 8 | a0001c0002t0017g0286a0001c0003t0134g0285a0001c0003t0137g0287others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+208C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683076 | ||||||
chr7:4683098
|
T | A | 1 | a0001c0002t0003g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+230T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683098 | ||||||
chr7:4683142
|
C | G | 3 | a0001c0002t0017g0286a0001c0003t0134g0285a0001c0003t0137g0287 | 3 | HG02055.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+274C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683142 | ||||||
chr7:4683181
|
C | T | 1 | a0001c0003t0037g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+313C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683181 | ||||||
chr7:4683198
|
C | T | 4 | a0001c0002t0018g0283a0001c0003t0099g0282a0001c0004t0046g0009others(1): Show | 4 | HG01496.hp2 HG02970.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+330C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683198 | ||||||
chr7:4683259
|
C | T | 1 | a0002c0012t0004g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.560+391C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683259 | ||||||
chr7:4683291
|
C | G | 1 | a0001c0015t0094g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.560+423C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683291 | ||||||
chr7:4683293
|
C | T | 2 | a0001c0003t0036g0004a0001c0003t0140g0003 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.560+425C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683293 | ||||||
chr7:4683300
|
T | C | 8 | a0001c0002t0017g0286a0001c0003t0134g0285a0001c0003t0137g0287others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+432T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683300 | ||||||
chr7:4683311
|
C | T | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.560+443C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683311 | ||||||
chr7:4683410
|
A | AC | 12 | a0001c0001t0003g0270a0001c0001t0012g0005a0001c0002t0005g0278others(9): Show | 12 | HG00735.hp2 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.560+547dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4683410 | |||||
chr7:4683449
|
G | A | 49 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0002g0097others(46): Show | 49 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.560+581G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683449 | ||||||
chr7:4683522
|
T | C | 54 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0002g0097others(51): Show | 54 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.560+654T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683522 | ||||||
chr7:4683710
|
G | C | 48 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.560+842G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683710 | ||||||
chr7:4683712
|
T | C | 48 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(45): Show | 49 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.560+844T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683712 | ||||||
chr7:4683903
|
G | A | 16 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0062others(13): Show | 16 | HG00140.hp2 HG01074.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.560+1035G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683903 | ||||||
chr7:4683976
|
G | A | 2 | a0001c0003t0005g0112a0001c0004t0001g0113 | 2 | HG01070.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.560+1108G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683976 | ||||||
chr7:4684046
|
G | C | 292 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(289): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.560+1178G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684046 | ||||||
chr7:4684056
|
C | T | 3 | a0001c0003t0037g0284a0001c0006t0092g0002a0001c0006t0093g0002 | 3 | HG01070.hp2 HG01071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.560+1188C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684056 | ||||||
chr7:4684410
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.560+1542T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684410 | ||||||
chr7:4684578
|
A | C | 2 | a0001c0002t0017g0286a0001c0003t0137g0287 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+1710A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684578 | ||||||
chr7:4684623
|
G | C | 3 | a0001c0002t0004g0067a0001c0002t0004g0068a0001c0003t0015g0066 | 3 | HG02572.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.560+1755G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684623 | ||||||
chr7:4684670
|
C | T | 1 | a0001c0002t0098g0268 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.560+1802C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684670 | ||||||
chr7:4684726
|
C | T | 1 | a0001c0002t0003g0111 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.560+1858C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684726 | ||||||
chr7:4684742
|
G | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0002g0114others(1): Show | 4 | HG00735.hp1 HG01261.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+1874G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684742 | ||||||
chr7:4684766
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.560+1898G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684766 | ||||||
chr7:4684876
|
G | T | 1 | a0001c0004t0117g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.560+2008G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684876 | ||||||
chr7:4684962
|
C | T | 1 | a0001c0001t0082g0063 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.560+2094C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684962 | ||||||
chr7:4684976
|
G | T | 1 | a0001c0002t0041g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+2108G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684976 | ||||||
chr7:4685107
|
G | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0002g0097others(6): Show | 9 | HG01192.hp1 HG01928.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+2239G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685107 | ||||||
chr7:4685133
|
T | G | 4 | a0001c0002t0004g0067a0001c0002t0004g0068a0001c0003t0015g0066others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+2265T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685133 | ||||||
chr7:4685171
|
A | G | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0002t0005g0278 | 3 | HG02145.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.560+2303A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685171 | ||||||
chr7:4685208
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.560+2340A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685208 | ||||||
chr7:4685221
|
C | CT | 15 | a0001c0001t0001g0062a0001c0001t0002g0101a0001c0001t0003g0117others(12): Show | 15 | HG00597.hp1 HG00673.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.560+2373dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685221 | |||||
chr7:4685221
|
CT | C | 147 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(144): Show | 147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.560+2373delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685221 | |||||
chr7:4685301
|
A | G | 1 | a0001c0003t0134g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+2433A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685301 | ||||||
chr7:4685349
|
G | A | 1 | a0001c0002t0041g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+2481G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685349 | ||||||
chr7:4685399
|
A | G | 3 | a0001c0002t0004g0067a0001c0002t0004g0068a0001c0003t0015g0066 | 3 | HG02572.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.560+2531A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685399 | ||||||
chr7:4685517
|
C | T | 1 | a0001c0002t0041g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+2649C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685517 | ||||||
chr7:4685525
|
CT | C | 26 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0062others(23): Show | 26 | HG00140.hp2 HG01070.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.560+2676delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685525 | |||||
chr7:4685600
|
C | CTTTTTTG others(10): Show |
1 | a0001c0004t0009g0007 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.560+2733_560+2749d others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685600 | |||||
chr7:4685675
|
CCTCACGC others(14): Show |
C | 1 | a0001c0004t0007g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.560+2810_560+2830d others(23): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685675 | |||||
chr7:4685680
|
C | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0002g0097others(30): Show | 33 | HG01192.hp1 HG01496.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.560+2812C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685680 | ||||||
chr7:4685681
|
G | A | 1 | a0001c0001t0059g0121 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+2813G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685681 | ||||||
chr7:4685867
|
C | T | 1 | a0001c0001t0003g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.560+2999C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685867 | ||||||
chr7:4685958
|
G | GA | 9 | a0001c0001t0003g0012a0001c0001t0003g0253a0001c0001t0024g0013others(6): Show | 9 | HG00597.hp2 HG02135.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+3102dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685958 | |||||
chr7:4685972
|
C | CA | 3 | a0001c0001t0020g0124a0001c0003t0014g0236a0001c0008t0122g0272 | 3 | HG02572.hp1 NA18985.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.560+3110dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685972 | |||||
chr7:4685979
|
C | T | 4 | a0001c0002t0004g0067a0001c0002t0004g0068a0001c0003t0015g0066others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+3111C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685979 | ||||||
chr7:4686071
|
T | A | 36 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0002g0097others(33): Show | 36 | HG01192.hp1 HG01496.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.560+3203T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686071 | ||||||
chr7:4686289
|
G | A | 24 | a0001c0001t0003g0270a0001c0002t0055g0087a0001c0002t0088g0254others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.560+3421G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686289 | ||||||
chr7:4686393
|
G | A | 39 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(36): Show | 40 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.560+3525G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686393 | ||||||
chr7:4686418
|
T | G | 1 | a0001c0004t0009g0007 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.560+3550T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686418 | ||||||
chr7:4686492
|
A | G | 1 | a0001c0001t0084g0232 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.560+3624A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686492 | ||||||
chr7:4686593
|
G | A | 1 | a0001c0002t0004g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.560+3725G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686593 | ||||||
chr7:4686601
|
G | A | 21 | a0001c0001t0002g0109a0001c0001t0016g0241a0001c0001t0058g0251others(18): Show | 21 | HG01496.hp1 HG01884.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+3733G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686601 | ||||||
chr7:4686767
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.560+3899A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686767 | ||||||
chr7:4686778
|
G | A | 3 | a0001c0003t0037g0284a0001c0006t0092g0002a0001c0006t0093g0002 | 3 | HG01070.hp2 HG01071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.560+3910G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686778 | ||||||
chr7:4686936
|
TC | T | 42 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0001g0267others(39): Show | 42 | HG01192.hp1 HG01496.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+4069delC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686936 | ||||||
chr7:4686937
|
C | T | 21 | a0001c0001t0003g0270a0001c0001t0058g0251a0001c0002t0004g0067others(18): Show | 21 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+4069C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686937 | ||||||
chr7:4686975
|
G | C | 62 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0001g0267others(59): Show | 62 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.560+4107G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686975 | ||||||
chr7:4686996
|
G | A | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+4128G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686996 | ||||||
chr7:4687026
|
G | A | 1 | a0001c0001t0082g0063 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.560+4158G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687026 | ||||||
chr7:4687135
|
T | C | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.560+4267T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687135 | ||||||
chr7:4687183
|
C | T | 1 | a0001c0002t0041g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+4315C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687183 | ||||||
chr7:4687194
|
A | G | 7 | a0001c0002t0041g0102a0001c0011t0006g0249a0002c0012t0004g0292others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+4326A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687194 | ||||||
chr7:4687222
|
A | G | 1 | a0001c0026t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.560+4354A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687222 | ||||||
chr7:4687224
|
G | A | 1 | a0001c0026t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.560+4356G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687224 | ||||||
chr7:4687337
|
G | T | 1 | a0001c0008t0122g0272 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.560+4469G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687337 | ||||||
chr7:4687438
|
G | A | 3 | a0002c0012t0016g0291a0002c0013t0010g0289a0002c0013t0026g0288 | 3 | HG01109.hp1 HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.560+4570G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687438 | ||||||
chr7:4687440
|
A | C | 3 | a0002c0012t0016g0291a0002c0013t0010g0289a0002c0013t0026g0288 | 3 | HG01109.hp1 HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.560+4572A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687440 | ||||||
chr7:4687443
|
T | C | 3 | a0002c0012t0016g0291a0002c0013t0010g0289a0002c0013t0026g0288 | 3 | HG01109.hp1 HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.560+4575T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687443 | ||||||
chr7:4687500
|
C | T | 1 | a0001c0001t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.560+4632C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687500 | ||||||
chr7:4687638
|
C | T | 13 | a0001c0001t0003g0270a0001c0002t0055g0087a0001c0003t0037g0284others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.560+4770C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687638 | ||||||
chr7:4687718
|
C | G | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+4850C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687718 | ||||||
chr7:4687750
|
A | C | 9 | a0001c0002t0055g0087a0001c0003t0039g0229a0001c0003t0087g0071others(6): Show | 9 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+4882A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687750 | ||||||
chr7:4687923
|
G | T | 1 | a0001c0004t0043g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+5055G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687923 | ||||||
chr7:4687974
|
C | T | 1 | a0001c0004t0029g0228 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.560+5106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687974 | ||||||
chr7:4688159
|
C | G | 4 | a0001c0001t0013g0041a0001c0001t0081g0042a0001c0004t0008g0001others(1): Show | 5 | HG02602.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+5291C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688159 | ||||||
chr7:4688237
|
A | C | 2 | a0001c0003t0014g0081a0001c0003t0134g0285 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.560+5369A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688237 | ||||||
chr7:4688266
|
T | TA | 7 | a0001c0001t0012g0014a0001c0002t0002g0106a0001c0003t0112g0006others(4): Show | 7 | HG01261.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+5414dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688266 | |||||
chr7:4688266
|
TA | T | 87 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0062others(84): Show | 88 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.560+5414delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688266 | |||||
chr7:4688310
|
A | G | 1 | a0001c0001t0079g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.560+5442A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688310 | ||||||
chr7:4688311
|
T | C | 16 | a0001c0002t0004g0126a0001c0002t0004g0245a0001c0002t0018g0283others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.560+5443T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688311 | ||||||
chr7:4688349
|
A | G | 143 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0069others(140): Show | 143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.560+5481A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688349 | ||||||
chr7:4688409
|
A | AT | 13 | a0001c0001t0058g0251a0001c0002t0004g0067a0001c0002t0004g0227others(10): Show | 13 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.560+5550dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688409 | |||||
chr7:4688465
|
A | G | 60 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0001g0116others(57): Show | 60 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.560+5597A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688465 | ||||||
chr7:4688550
|
G | A | 1 | a0001c0001t0003g0253 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.560+5682G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688550 | ||||||
chr7:4688633
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.560+5765C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688633 | ||||||
chr7:4688672
|
G | A | 5 | a0001c0001t0011g0040a0001c0002t0017g0286a0001c0002t0018g0243others(2): Show | 5 | HG01081.hp2 HG02451.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+5804G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688672 | ||||||
chr7:4688693
|
T | C | 1 | a0001c0003t0015g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+5825T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688693 | ||||||
chr7:4688713
|
T | A | 1 | a0001c0003t0015g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+5845T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688713 | ||||||
chr7:4688714
|
G | A | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+5846G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688714 | ||||||
chr7:4688812
|
C | T | 1 | a0001c0007t0006g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.560+5944C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688812 | ||||||
chr7:4688835
|
GT | G | 4 | a0001c0002t0004g0068a0001c0004t0046g0009a0001c0007t0006g0235others(1): Show | 4 | HG01496.hp2 HG02630.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+5971delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688835 | |||||
chr7:4688944
|
A | G | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.560+6076A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688944 | ||||||
chr7:4688978
|
A | C | 28 | a0001c0001t0001g0037a0001c0001t0001g0054a0001c0001t0001g0062others(25): Show | 28 | HG00140.hp2 HG00558.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.560+6110A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688978 | ||||||
chr7:4688979
|
C | CT | 7 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0060g0038others(4): Show | 7 | HG01258.hp2 HG02056.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+6125dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688979 | |||||
chr7:4688980
|
T | C | 1 | a0001c0002t0013g0050 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.560+6112T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688980 | ||||||
chr7:4689137
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+6269C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689137 | ||||||
chr7:4689186
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.560+6318C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689186 | ||||||
chr7:4689317
|
G | C | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+6449G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689317 | ||||||
chr7:4689640
|
A | G | 2 | a0001c0002t0025g0222a0001c0002t0025g0277 | 2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.560+6772A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689640 | ||||||
chr7:4689772
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.560+6904C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689772 | ||||||
chr7:4689821
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.560+6953C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689821 | ||||||
chr7:4689892
|
C | T | 2 | a0001c0003t0100g0248a0001c0003t0137g0287 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.560+7024C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689892 | ||||||
chr7:4690002
|
G | T | 1 | a0001c0002t0001g0188 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.560+7134G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690002 | ||||||
chr7:4690052
|
G | A | 1 | a0001c0002t0003g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+7184G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690052 | ||||||
chr7:4690121
|
G | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0002t0005g0278 | 3 | HG02145.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.560+7253G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690121 | ||||||
chr7:4690232
|
G | C | 1 | a0001c0001t0059g0121 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+7364G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690232 | ||||||
chr7:4690314
|
G | A | 2 | a0001c0002t0001g0188a0001c0002t0012g0127 | 2 | HG02056.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.560+7446G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690314 | ||||||
chr7:4690570
|
A | G | 4 | a0001c0003t0130g0088a0001c0003t0131g0070a0001c0004t0014g0256others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+7702A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690570 | ||||||
chr7:4690620
|
T | C | 1 | a0001c0001t0097g0052 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.560+7752T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690620 | ||||||
chr7:4690646
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.560+7778G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690646 | ||||||
chr7:4690713
|
T | TA | 13 | a0001c0002t0004g0068a0001c0002t0017g0286a0001c0002t0041g0102others(10): Show | 13 | HG01081.hp2 HG01109.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.560+7845_560+7846i others(3): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690713 | ||||||
chr7:4690904
|
T | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0075g0128others(8): Show | 11 | HG00140.hp1 HG01070.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.560+8036T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690904 | ||||||
chr7:4691077
|
T | C | 1 | a0001c0004t0141g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+8209T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691077 | ||||||
chr7:4691164
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.560+8296G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691164 | ||||||
chr7:4691239
|
TTTTGCTT others(6): Show |
T | 1 | a0001c0001t0035g0064 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.560+8372_560+8384d others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691239 | ||||||
chr7:4691351
|
C | T | 10 | a0001c0001t0016g0241a0001c0002t0004g0227a0001c0002t0004g0239others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+8483C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691351 | ||||||
chr7:4691352
|
A | G | 40 | a0001c0001t0016g0241a0001c0001t0065g0011a0001c0001t0096g0093others(37): Show | 40 | HG01081.hp2 HG01109.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.560+8484A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691352 | ||||||
chr7:4691446
|
T | A | 1 | a0001c0003t0019g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+8578T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691446 | ||||||
chr7:4691482
|
CTGCCACC others(1055): Show |
C | 1 | a0001c0004t0008g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560+8638_560+9699d others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4691482 | |||||
chr7:4691483
|
T | C | 50 | a0001c0001t0016g0241a0001c0001t0065g0011a0001c0001t0096g0093others(47): Show | 50 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.560+8615T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691483 | ||||||
chr7:4691523
|
C | T | 4 | a0001c0002t0017g0286a0001c0003t0087g0071a0001c0003t0129g0279others(1): Show | 4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+8655C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691523 | ||||||
chr7:4691540
|
C | T | 1 | a0001c0002t0024g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.560+8672C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691540 | ||||||
chr7:4691745
|
G | A | 1 | a0001c0001t0084g0232 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.560+8877G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691745 | ||||||
chr7:4691763
|
T | C | 17 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0098g0268others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+8895T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691763 | ||||||
chr7:4691818
|
G | A | 3 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0004t0007g0263 | 3 | HG02257.hp1 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.560+8950G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691818 | ||||||
chr7:4692049
|
G | A | 3 | a0001c0001t0072g0015a0001c0001t0074g0016a0001c0002t0002g0257 | 3 | HG01433.hp2 HG01928.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.560+9181G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692049 | ||||||
chr7:4692068
|
G | A | 64 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(61): Show | 64 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.560+9200G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692068 | ||||||
chr7:4692080
|
A | G | 10 | a0001c0002t0018g0283a0001c0003t0026g0246a0001c0003t0100g0248others(7): Show | 10 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+9212A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692080 | ||||||
chr7:4692115
|
A | C | 12 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0098g0268others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+9247A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692115 | ||||||
chr7:4692275
|
A | G | 1 | a0001c0003t0037g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+9407A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692275 | ||||||
chr7:4692346
|
G | A | 7 | a0001c0002t0018g0283a0001c0003t0026g0246a0001c0006t0052g0078others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+9478G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692346 | ||||||
chr7:4692364
|
C | T | 2 | a0001c0003t0039g0229a0001c0003t0139g0074 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+9496C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692364 | ||||||
chr7:4692623
|
A | G | 21 | a0001c0002t0017g0286a0001c0002t0018g0283a0001c0002t0041g0102others(18): Show | 21 | HG01081.hp2 HG01109.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+9755A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692623 | ||||||
chr7:4692704
|
G | A | 2 | a0001c0001t0003g0138a0001c0001t0050g0137 | 2 | HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.560+9836G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692704 | ||||||
chr7:4692752
|
T | C | 67 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(64): Show | 67 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.560+9884T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692752 | ||||||
chr7:4692766
|
A | T | 1 | a0001c0004t0009g0234 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.560+9898A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692766 | ||||||
chr7:4692809
|
C | G | 9 | a0001c0002t0018g0283a0001c0003t0026g0246a0001c0003t0037g0284others(6): Show | 9 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+9941C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692809 | ||||||
chr7:4692811
|
T | C | 1 | a0001c0003t0036g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.560+9943T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692811 | ||||||
chr7:4692829
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.560+9961C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692829 | ||||||
chr7:4692938
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.560+10070C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692938 | ||||||
chr7:4692940
|
C | G | 2 | a0001c0001t0003g0138a0001c0001t0050g0137 | 2 | HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.560+10072C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692940 | ||||||
chr7:4692953
|
G | A | 4 | a0001c0002t0017g0286a0001c0003t0087g0071a0001c0003t0129g0279others(1): Show | 4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+10085G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692953 | ||||||
chr7:4692955
|
T | G | 2 | a0001c0004t0009g0140a0001c0004t0116g0139 | 2 | NA18951.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.560+10087T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692955 | ||||||
chr7:4693120
|
G | T | 1 | a0001c0001t0063g0258 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.560+10252G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693120 | ||||||
chr7:4693277
|
A | G | 1 | a0001c0002t0041g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+10409A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693277 | ||||||
chr7:4693387
|
T | C | 1 | a0001c0009t0119g0141 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.560+10519T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693387 | ||||||
chr7:4693443
|
A | G | 65 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0034others(62): Show | 66 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.560+10575A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693443 | ||||||
chr7:4693564
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.560+10696T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693564 | ||||||
chr7:4693582
|
C | T | 2 | a0001c0003t0037g0284a0001c0003t0136g0210 | 2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+10714C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693582 | ||||||
chr7:4693585
|
C | T | 1 | a0001c0017t0114g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.560+10717C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693585 | ||||||
chr7:4693927
|
C | T | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.560+11059C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693927 | ||||||
chr7:4694286
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.560+11418T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694286 | ||||||
chr7:4694390
|
C | G | 4 | a0001c0002t0017g0286a0001c0003t0087g0071a0001c0003t0129g0279others(1): Show | 4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+11522C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694390 | ||||||
chr7:4694479
|
C | T | 2 | a0001c0003t0100g0248a0001c0004t0141g0247 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+11611C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694479 | ||||||
chr7:4694711
|
G | A | 1 | a0001c0001t0003g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.560+11843G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694711 | ||||||
chr7:4694828
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0039 | 3 | HG00544.hp2 NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.560+11960C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694828 | ||||||
chr7:4694863
|
T | G | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+11995T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694863 | ||||||
chr7:4695097
|
G | A | 1 | a0001c0003t0039g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.560+12229G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695097 | ||||||
chr7:4695216
|
C | T | 4 | a0001c0002t0001g0056a0001c0002t0001g0058a0001c0002t0003g0055others(1): Show | 4 | HG01074.hp2 HG03017.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+12348C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695216 | ||||||
chr7:4695441
|
G | A | 1 | a0001c0003t0019g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+12573G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695441 | ||||||
chr7:4695475
|
G | C | 2 | a0001c0003t0019g0238a0001c0003t0039g0229 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+12607G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695475 | ||||||
chr7:4695498
|
G | T | 24 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0004g0227others(21): Show | 24 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.560+12630G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695498 | ||||||
chr7:4695525
|
C | T | 45 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(42): Show | 45 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.560+12657C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695525 | ||||||
chr7:4695691
|
C | G | 14 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0098g0268others(11): Show | 14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.560+12823C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695691 | ||||||
chr7:4695758
|
G | A | 2 | a0001c0003t0100g0248a0001c0004t0141g0247 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+12890G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695758 | ||||||
chr7:4695843
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.560+12975G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695843 | ||||||
chr7:4695876
|
C | T | 2 | a0001c0002t0013g0216a0001c0002t0083g0008 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.560+13008C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695876 | ||||||
chr7:4695877
|
G | A | 21 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0004g0227others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+13009G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695877 | ||||||
chr7:4695936
|
C | CA | 113 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0034others(110): Show | 114 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.560+13086dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4695936 | |||||
chr7:4695974
|
G | T | 2 | a0001c0003t0039g0229a0001c0003t0139g0074 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+13106G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695974 | ||||||
chr7:4695985
|
G | A | 1 | a0001c0004t0043g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+13117G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695985 | ||||||
chr7:4695998
|
C | T | 1 | a0001c0011t0006g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.560+13130C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695998 | ||||||
chr7:4696002
|
A | G | 59 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(56): Show | 59 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.560+13134A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696002 | ||||||
chr7:4696019
|
G | A | 1 | a0001c0002t0085g0103 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.560+13151G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696019 | ||||||
chr7:4696094
|
C | A | 11 | a0001c0001t0096g0093a0001c0003t0014g0236a0001c0003t0102g0086others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.560+13226C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696094 | ||||||
chr7:4696115
|
CA | C | 59 | a0001c0001t0001g0182a0001c0001t0002g0033a0001c0001t0005g0191others(56): Show | 59 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.560+13266delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4696115 | |||||
chr7:4696186
|
A | G | 1 | a0001c0004t0008g0180 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.560+13318A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696186 | ||||||
chr7:4696202
|
A | T | 1 | a0001c0003t0134g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+13334A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696202 | ||||||
chr7:4696303
|
G | T | 4 | a0001c0002t0001g0260a0001c0002t0025g0222a0001c0002t0025g0277others(1): Show | 4 | HG00735.hp2 HG01099.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+13435G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696303 | ||||||
chr7:4696306
|
G | A | 1 | a0001c0002t0041g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+13438G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696306 | ||||||
chr7:4696341
|
G | C | 1 | a0001c0003t0040g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+13473G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696341 | ||||||
chr7:4696442
|
G | T | 1 | a0001c0003t0136g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+13574G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696442 | ||||||
chr7:4696496
|
C | A | 1 | a0001c0002t0005g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.560+13628C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696496 | ||||||
chr7:4696532
|
G | T | 2 | a0001c0003t0100g0248a0001c0004t0141g0247 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+13664G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696532 | ||||||
chr7:4696573
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.560+13705G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696573 | ||||||
chr7:4696598
|
G | A | 2 | a0001c0002t0105g0237a0001c0007t0109g0073 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560+13730G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696598 | ||||||
chr7:4696687
|
A | G | 2 | a0001c0003t0100g0248a0001c0004t0141g0247 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+13819A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696687 | ||||||
chr7:4696830
|
G | C | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+13962G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696830 | ||||||
chr7:4696924
|
C | T | 25 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(22): Show | 25 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.560+14056C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696924 | ||||||
chr7:4696942
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.560+14074C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696942 | ||||||
chr7:4696960
|
C | T | 3 | a0001c0002t0055g0087a0001c0003t0099g0282a0001c0019t0128g0218 | 3 | HG02970.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.560+14092C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696960 | ||||||
chr7:4697079
|
A | G | 55 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(52): Show | 55 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.560+14211A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697079 | ||||||
chr7:4697130
|
G | T | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.560+14262G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697130 | ||||||
chr7:4697145
|
G | A | 1 | a0001c0002t0003g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+14277G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697145 | ||||||
chr7:4697267
|
A | G | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+14399A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697267 | ||||||
chr7:4697294
|
A | G | 3 | a0001c0002t0055g0087a0001c0003t0099g0282a0001c0019t0128g0218 | 3 | HG02970.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.560+14426A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697294 | ||||||
chr7:4697336
|
G | C | 2 | a0001c0003t0039g0229a0001c0003t0139g0074 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+14468G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697336 | ||||||
chr7:4697343
|
T | C | 2 | a0001c0001t0001g0062a0001c0002t0013g0050 | 2 | HG01515.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.560+14475T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697343 | ||||||
chr7:4697390
|
C | G | 4 | a0001c0002t0017g0286a0001c0003t0087g0071a0001c0003t0129g0279others(1): Show | 4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+14522C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697390 | ||||||
chr7:4697544
|
G | A | 2 | a0001c0003t0039g0229a0001c0003t0139g0074 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+14676G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697544 | ||||||
chr7:4697605
|
G | C | 55 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(52): Show | 55 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.560+14737G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697605 | ||||||
chr7:4697685
|
G | A | 1 | a0001c0004t0048g0183 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560+14817G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697685 | ||||||
chr7:4697696
|
CTTA | C | 3 | a0001c0003t0100g0248a0001c0004t0008g0136a0001c0004t0141g0247 | 3 | HG03209.hp1 HG03486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.560+14834_560+1483 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697696 | |||||
chr7:4697729
|
AG | A | 5 | a0001c0001t0013g0041a0001c0001t0081g0042a0001c0003t0144g0142others(2): Show | 6 | HG02602.hp2 HG03491.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+14863delG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697729 | |||||
chr7:4697741
|
C | CTG | 3 | a0001c0001t0001g0118a0001c0001t0086g0181a0001c0002t0001g0144 | 3 | HG02135.hp1 HG02155.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.560+14921_560+1492 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTG | C | 74 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0061others(71): Show | 74 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.560+14921_560+1492 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTG | C | 77 | a0001c0001t0001g0017a0001c0001t0001g0115a0001c0001t0001g0129others(74): Show | 78 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.560+14919_560+1492 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTGTG | C | 42 | a0001c0001t0001g0030a0001c0001t0001g0205a0001c0001t0002g0053others(39): Show | 42 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.560+14917_560+1492 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTGTGT others(1): Show |
C | 33 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0062others(30): Show | 33 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.560+14915_560+1492 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0058g0251a0001c0002t0003g0111a0001c0003t0039g0229others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+14913_560+1492 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTGTGT others(5): Show |
C | 5 | a0001c0002t0001g0134a0001c0002t0061g0133a0001c0003t0047g0072others(2): Show | 5 | HG02109.hp1 HG03209.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+14911_560+1492 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0002g0179a0001c0004t0141g0247 | 2 | HG01099.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+14909_560+1492 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTGTGT others(9): Show |
C | 15 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0098g0268others(12): Show | 15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.560+14907_560+1492 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697741
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0002t0001g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.560+14905_560+1492 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | |||||
chr7:4697785
|
GTGTGT | G | 3 | a0001c0001t0001g0037a0001c0001t0003g0138a0001c0003t0132g0160 | 3 | HG01981.hp2 HG02698.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.560+14919_560+1492 others(9): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697785 | |||||
chr7:4697821
|
T | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+14953T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697821 | ||||||
chr7:4697860
|
T | C | 1 | a0001c0004t0009g0143 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.560+14992T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697860 | ||||||
chr7:4697886
|
G | A | 1 | a0001c0002t0002g0106 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.560+15018G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697886 | ||||||
chr7:4697985
|
T | C | 70 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(67): Show | 70 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.560+15117T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697985 | ||||||
chr7:4698195
|
A | C | 1 | a0001c0006t0053g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.560+15327A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698195 | ||||||
chr7:4698304
|
A | ATG | 15 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0098g0268others(12): Show | 15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.560+15444_560+1544 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698304 | |||||
chr7:4698312
|
G | GTA | 9 | a0001c0001t0001g0266a0001c0001t0002g0053a0001c0001t0002g0230others(6): Show | 9 | HG02083.hp2 HG02738.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+15462_560+1546 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | |||||
chr7:4698312
|
G | GTGTA | 3 | a0001c0002t0105g0237a0001c0003t0037g0284a0001c0003t0136g0210 | 3 | HG02895.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.560+15445_560+1544 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | |||||
chr7:4698312
|
G | GTGTATA | 3 | a0001c0002t0018g0283a0001c0003t0026g0246a0002c0013t0010g0289 | 3 | HG02559.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.560+15445_560+1544 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | |||||
chr7:4698312
|
G | GTGTATAT others(1): Show |
4 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+15445_560+1544 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | |||||
chr7:4698314
|
A | G | 7 | a0001c0001t0001g0192a0001c0002t0001g0157a0001c0002t0005g0158others(4): Show | 7 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+15446A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698314 | ||||||
chr7:4698320
|
A | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+15452A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698320 | ||||||
chr7:4698393
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.560+15525G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698393 | ||||||
chr7:4698822
|
G | A | 1 | a0001c0004t0043g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+15954G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698822 | ||||||
chr7:4698905
|
C | G | 1 | a0001c0002t0003g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+16037C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698905 | ||||||
chr7:4699041
|
C | T | 1 | a0001c0002t0001g0215 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.560+16173C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699041 | ||||||
chr7:4699129
|
T | C | 1 | a0001c0007t0109g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+16261T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699129 | ||||||
chr7:4699141
|
C | T | 29 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0135others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.560+16273C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699141 | ||||||
chr7:4699285
|
GT | G | 22 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0004g0227others(19): Show | 22 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.560+16434delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4699285 | |||||
chr7:4699286
|
T | TTTTTTTT others(82): Show |
1 | a0001c0002t0001g0043 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.560+16419_560+1650 others(93): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4699286 | |||||
chr7:4699306
|
A | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+16438A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699306 | ||||||
chr7:4699345
|
C | T | 20 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0095g0207others(17): Show | 20 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.560+16477C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699345 | ||||||
chr7:4699376
|
G | GT | 75 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(72): Show | 76 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.560+16521dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4699376 | |||||
chr7:4699429
|
C | G | 26 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(23): Show | 26 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.560+16561C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699429 | ||||||
chr7:4699492
|
C | T | 1 | a0001c0001t0059g0121 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+16624C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699492 | ||||||
chr7:4699512
|
T | C | 17 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0098g0268others(14): Show | 17 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+16644T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699512 | ||||||
chr7:4699584
|
T | G | 1 | a0001c0001t0003g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+16716T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699584 | ||||||
chr7:4699616
|
C | G | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+16748C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699616 | ||||||
chr7:4700015
|
G | T | 1 | a0001c0003t0039g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.560+17147G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700015 | ||||||
chr7:4700020
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.560+17152G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700020 | ||||||
chr7:4700091
|
G | A | 1 | a0001c0003t0010g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560+17223G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700091 | ||||||
chr7:4700169
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.560+17301G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700169 | ||||||
chr7:4700179
|
A | G | 1 | a0001c0003t0037g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+17311A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700179 | ||||||
chr7:4700233
|
A | G | 3 | a0001c0002t0095g0207a0001c0003t0036g0004a0001c0003t0111g0059 | 3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+17365A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700233 | ||||||
chr7:4700322
|
T | G | 27 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(24): Show | 27 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.560+17454T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700322 | ||||||
chr7:4700328
|
C | T | 1 | a0001c0001t0003g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.560+17460C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700328 | ||||||
chr7:4700366
|
A | G | 3 | a0001c0002t0095g0207a0001c0003t0036g0004a0001c0003t0111g0059 | 3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+17498A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700366 | ||||||
chr7:4700581
|
C | T | 1 | a0001c0004t0008g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560+17713C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700581 | ||||||
chr7:4700604
|
C | CCAGGTGT others(6): Show |
1 | a0001c0003t0019g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+17738_560+1775 others(17): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4700604 | |||||
chr7:4700798
|
C | T | 1 | a0001c0004t0008g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560+17930C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700798 | ||||||
chr7:4700858
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0023g0175 | 2 | NA18980.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.560+17990T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700858 | ||||||
chr7:4700962
|
G | A | 1 | a0001c0023t0049g0104 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.560+18094G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700962 | ||||||
chr7:4700990
|
A | G | 64 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(61): Show | 64 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.560+18122A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700990 | ||||||
chr7:4701094
|
C | A | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+18226C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701094 | ||||||
chr7:4701176
|
G | A | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+18308G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701176 | ||||||
chr7:4701189
|
C | T | 1 | a0001c0003t0146g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.560+18321C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701189 | ||||||
chr7:4701197
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.560+18329G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701197 | ||||||
chr7:4701253
|
C | CG | 8 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0001t0002g0033others(5): Show | 8 | HG00408.hp2 HG02071.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+18391dupG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4701253 | |||||
chr7:4701303
|
A | G | 3 | a0001c0001t0002g0109a0001c0001t0003g0117a0001c0001t0020g0110 | 3 | HG02071.hp2 NA18944.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.560+18435A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701303 | ||||||
chr7:4701394
|
C | A | 1 | a0001c0002t0013g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.560+18526C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701394 | ||||||
chr7:4701656
|
G | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0135others(24): Show | 27 | HG00323.hp2 HG00621.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.560+18788G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701656 | ||||||
chr7:4701698
|
C | T | 1 | a0001c0003t0015g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.560+18830C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701698 | ||||||
chr7:4701786
|
G | A | 2 | a0001c0001t0017g0224a0001c0004t0048g0183 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.560+18918G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701786 | ||||||
chr7:4701790
|
G | A | 1 | a0001c0002t0018g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.560+18922G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701790 | ||||||
chr7:4701812
|
G | C | 3 | a0001c0002t0095g0207a0001c0003t0036g0004a0001c0003t0111g0059 | 3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+18944G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701812 | ||||||
chr7:4701817
|
T | C | 1 | a0001c0003t0037g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+18949T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701817 | ||||||
chr7:4701818
|
G | A | 1 | a0001c0003t0037g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+18950G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701818 | ||||||
chr7:4701850
|
G | A | 2 | a0001c0001t0001g0020a0001c0003t0136g0210 | 2 | HG03579.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.560+18982G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701850 | ||||||
chr7:4701872
|
G | A | 1 | a0001c0007t0109g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+19004G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701872 | ||||||
chr7:4701886
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0039 | 2 | NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.560+19018C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701886 | ||||||
chr7:4701942
|
G | A | 4 | a0001c0001t0001g0259a0001c0002t0001g0193a0001c0002t0001g0194others(1): Show | 4 | HG02071.hp1 HG02132.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+19074G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701942 | ||||||
chr7:4702031
|
T | C | 57 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0002g0106others(54): Show | 57 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.560+19163T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702031 | ||||||
chr7:4702041
|
C | G | 1 | a0001c0003t0136g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+19173C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702041 | ||||||
chr7:4702101
|
A | G | 29 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(26): Show | 29 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.560+19233A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702101 | ||||||
chr7:4702229
|
G | A | 3 | a0001c0003t0037g0284a0001c0003t0113g0276a0001c0003t0136g0210 | 3 | HG02895.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+19361G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702229 | ||||||
chr7:4702285
|
C | T | 2 | a0001c0001t0001g0062a0001c0002t0013g0050 | 2 | HG01515.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.560+19417C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702285 | ||||||
chr7:4702356
|
T | A | 4 | a0001c0001t0024g0013a0001c0001t0073g0145a0001c0004t0009g0234others(1): Show | 4 | HG02698.hp1 NA18962.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+19488T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702356 | ||||||
chr7:4702360
|
T | G | 9 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0252others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+19492T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702360 | ||||||
chr7:4702373
|
C | T | 1 | a0001c0003t0102g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.560+19505C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702373 | ||||||
chr7:4702416
|
C | T | 1 | a0001c0002t0013g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.560+19548C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702416 | ||||||
chr7:4702672
|
T | A | 32 | a0001c0001t0096g0093a0001c0002t0003g0065a0001c0002t0004g0227others(29): Show | 32 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.560+19804T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702672 | ||||||
chr7:4702793
|
G | A | 1 | a0001c0001t0096g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.560+19925G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702793 | ||||||
chr7:4702821
|
A | T | 3 | a0001c0002t0095g0207a0001c0003t0036g0004a0001c0003t0111g0059 | 3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+19953A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702821 | ||||||
chr7:4702861
|
C | T | 31 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(28): Show | 31 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.560+19993C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702861 | ||||||
chr7:4702983
|
C | T | 2 | a0001c0003t0037g0284a0001c0003t0136g0210 | 2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+20115C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702983 | ||||||
chr7:4703053
|
G | T | 3 | a0001c0003t0010g0100a0001c0003t0010g0231a0001c0003t0104g0092 | 3 | HG02717.hp2 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.560+20185G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703053 | ||||||
chr7:4703091
|
T | C | 73 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(70): Show | 73 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.560+20223T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703091 | ||||||
chr7:4703092
|
G | A | 1 | a0001c0003t0037g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+20224G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703092 | ||||||
chr7:4703179
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.560+20311G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703179 | ||||||
chr7:4703318
|
A | G | 4 | a0001c0002t0017g0286a0001c0003t0087g0071a0001c0003t0129g0279others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+20450A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703318 | ||||||
chr7:4703414
|
C | T | 1 | a0001c0007t0109g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+20546C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703414 | ||||||
chr7:4703471
|
C | A | 7 | a0001c0002t0105g0237a0001c0003t0099g0282a0001c0003t0138g0262others(4): Show | 7 | HG02809.hp1 HG02970.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+20603C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703471 | ||||||
chr7:4703503
|
G | A | 3 | a0001c0002t0095g0207a0001c0003t0036g0004a0001c0003t0111g0059 | 3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+20635G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703503 | ||||||
chr7:4703512
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.560+20644G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703512 | ||||||
chr7:4703690
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.560+20822G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703690 | ||||||
chr7:4703715
|
C | T | 2 | a0001c0003t0037g0284a0001c0003t0136g0210 | 2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+20847C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703715 | ||||||
chr7:4703743
|
C | A | 64 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(61): Show | 64 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.560+20875C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703743 | ||||||
chr7:4703743
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.560+20875C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703743 | ||||||
chr7:4704084
|
G | A | 4 | a0001c0002t0017g0286a0001c0003t0087g0071a0001c0003t0129g0279others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+21216G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704084 | ||||||
chr7:4704311
|
C | T | 1 | a0001c0007t0109g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+21443C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704311 | ||||||
chr7:4704450
|
C | CA | 25 | a0001c0001t0001g0054a0001c0001t0001g0118a0001c0001t0002g0109others(22): Show | 25 | HG01099.hp1 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.560+21600dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704450 | |||||
chr7:4704450
|
C | CAA | 12 | a0001c0002t0002g0106a0001c0002t0004g0068a0001c0002t0098g0268others(9): Show | 12 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+21599_560+2160 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704450 | |||||
chr7:4704463
|
A | G | 8 | a0001c0002t0018g0283a0001c0003t0026g0246a0001c0006t0052g0078others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+21595A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704463 | ||||||
chr7:4704464
|
A | G | 7 | a0001c0002t0105g0237a0001c0003t0099g0282a0001c0003t0138g0262others(4): Show | 7 | HG02809.hp1 HG02970.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+21596A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704464 | ||||||
chr7:4704601
|
A | C | 1 | a0001c0001t0020g0124 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.560+21733A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704601 | ||||||
chr7:4704621
|
C | T | 21 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0004g0227others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+21753C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704621 | ||||||
chr7:4704676
|
C | T | 34 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(31): Show | 34 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.560+21808C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704676 | ||||||
chr7:4704690
|
C | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+21822C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704690 | ||||||
chr7:4704745
|
T | C | 1 | a0001c0002t0017g0286 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560+21877T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704745 | ||||||
chr7:4704830
|
C | T | 45 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(42): Show | 45 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.560+21962C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704830 | ||||||
chr7:4704834
|
C | CTTTTTTT others(2): Show |
7 | a0001c0002t0098g0268a0001c0003t0038g0208a0001c0004t0046g0009others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+21973_560+2198 others(13): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(3): Show |
8 | a0001c0002t0002g0106a0001c0003t0005g0112a0001c0003t0010g0077others(5): Show | 8 | HG01070.hp1 HG01106.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+21972_560+2198 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(4): Show |
3 | a0001c0002t0003g0065a0001c0003t0047g0072a0001c0004t0043g0091 | 3 | HG02109.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+21971_560+2198 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(5): Show |
22 | a0001c0001t0016g0241a0001c0002t0004g0227a0001c0002t0004g0239others(19): Show | 22 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.560+21970_560+2198 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(6): Show |
13 | a0001c0001t0096g0093a0001c0002t0004g0245a0001c0002t0057g0244others(10): Show | 13 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.560+21969_560+2198 others(17): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0058g0251a0001c0003t0113g0276a0002c0012t0016g0291 | 3 | HG01109.hp1 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.560+21968_560+2198 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(8): Show |
9 | a0001c0002t0018g0283a0001c0002t0041g0102a0001c0003t0026g0246others(6): Show | 9 | HG01081.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+21967_560+2198 others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(9): Show |
1 | a0001c0004t0141g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+21981_560+2198 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(12): Show |
1 | a0001c0003t0019g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+21981_560+2198 others(23): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(17): Show |
2 | a0001c0003t0036g0004a0001c0003t0111g0059 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.560+21981_560+2198 others(28): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4704834
|
C | CTTTTTTT others(18): Show |
1 | a0001c0002t0095g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.560+21981_560+2198 others(29): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | |||||
chr7:4705165
|
A | G | 4 | a0001c0002t0017g0286a0001c0003t0087g0071a0001c0003t0129g0279others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+22297A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705165 | ||||||
chr7:4705313
|
C | T | 1 | a0001c0002t0017g0286 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560+22445C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705313 | ||||||
chr7:4705511
|
TTCTCTTT others(3): Show |
T | 2 | a0001c0003t0037g0284a0002c0012t0016g0291 | 2 | HG01109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705511 | |||||
chr7:4705513
|
CTCTT | C | 3 | a0001c0002t0041g0102a0001c0002t0057g0244a0002c0013t0026g0288 | 3 | HG01496.hp1 HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705513 | |||||
chr7:4705515
|
CT | C | 4 | a0001c0001t0002g0199a0001c0001t0021g0219a0001c0002t0003g0055others(1): Show | 4 | HG01123.hp1 HG04228.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+22650delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705515 | |||||
chr7:4705516
|
TTTCTCTC others(4): Show |
T | 1 | a0001c0001t0005g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.560+22650_560+2266 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705516 | |||||
chr7:4705517
|
T | C | 19 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(16): Show | 19 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.560+22649T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | ||||||
chr7:4705517
|
T | TC | 5 | a0001c0001t0002g0053a0001c0001t0003g0253a0001c0002t0083g0008others(2): Show | 5 | HG02083.hp2 HG02738.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22649_560+2265 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | ||||||
chr7:4705517
|
T | TCTC | 6 | a0001c0001t0005g0047a0001c0001t0082g0063a0001c0002t0044g0154others(3): Show | 6 | HG00738.hp1 HG02074.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+22649_560+2265 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | ||||||
chr7:4705517
|
T | TCTCTC | 3 | a0001c0002t0002g0257a0001c0007t0006g0085a0001c0009t0119g0141 | 3 | HG01433.hp2 HG02145.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(9): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | ||||||
chr7:4705517
|
T | TCTCTCTC others(4): Show |
3 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0103g0209 | 3 | HG02717.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | ||||||
chr7:4705517
|
T | TTC | 37 | a0001c0001t0001g0034a0001c0001t0001g0115a0001c0001t0001g0118others(34): Show | 37 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+22690_560+2269 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
T | TTCTC | 23 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0072g0015others(20): Show | 23 | HG01891.hp1 HG01928.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.560+22688_560+2269 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
T | TTCTCTC | 15 | a0001c0001t0001g0017a0001c0001t0002g0097a0001c0001t0002g0109others(12): Show | 15 | HG00621.hp1 HG01192.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.560+22686_560+2269 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
T | TTCTCTCT others(1): Show |
16 | a0001c0001t0001g0030a0001c0001t0001g0054a0001c0001t0001g0204others(13): Show | 16 | HG02155.hp2 HG02523.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.560+22684_560+2269 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
T | TTCTCTCT others(3): Show |
6 | a0001c0001t0001g0265a0001c0001t0012g0005a0001c0001t0023g0175others(3): Show | 6 | HG01346.hp2 HG02004.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+22682_560+2269 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
T | TTCTCTCT others(5): Show |
2 | a0001c0001t0060g0038a0001c0002t0004g0067 | 2 | HG02056.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.560+22680_560+2269 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
T | TTCTCTCT others(7): Show |
4 | a0001c0002t0001g0188a0001c0002t0067g0195a0001c0003t0101g0242others(1): Show | 4 | HG02132.hp2 HG02165.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+22678_560+2269 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
T | TTCTCTCT others(11): Show |
1 | a0001c0001t0001g0259 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.560+22674_560+2269 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
TTC | T | 40 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0039others(37): Show | 41 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.560+22690_560+2269 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
TTCTC | T | 6 | a0001c0001t0001g0061a0001c0001t0005g0191a0001c0002t0001g0134others(3): Show | 6 | HG00558.hp2 HG01361.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+22688_560+2269 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
TTCTCTCT others(5): Show |
T | 1 | a0001c0002t0004g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.560+22680_560+2269 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705517
|
TTCTCTCT others(7): Show |
T | 9 | a0001c0001t0016g0241a0001c0002t0004g0227a0001c0002t0004g0239others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+22678_560+2269 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | |||||
chr7:4705525
|
C | T | 1 | a0001c0010t0110g0274 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.560+22657C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705525 | ||||||
chr7:4705534
|
T | TCTCTCGC others(11): Show |
1 | a0001c0003t0015g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+22671_560+2267 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705534 | |||||
chr7:4705540
|
T | G | 1 | a0001c0003t0015g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+22672T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705540 | ||||||
chr7:4705540
|
T | TCTCTCGC others(5): Show |
1 | a0001c0003t0036g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.560+22677_560+2267 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705540 | |||||
chr7:4705546
|
T | G | 4 | a0001c0003t0015g0066a0001c0003t0019g0238a0001c0003t0036g0004others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+22678T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705546 | ||||||
chr7:4705546
|
T | TCGCTCTC others(7): Show |
1 | a0001c0003t0038g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.560+22679_560+2268 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | |||||
chr7:4705546
|
T | TCTCGCTC others(9): Show |
1 | a0001c0021t0027g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.560+22681_560+2268 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | |||||
chr7:4705546
|
T | TCTCTCGC others(5): Show |
2 | a0001c0004t0046g0009a0001c0011t0006g0281 | 2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.560+22683_560+2268 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | |||||
chr7:4705546
|
T | TCTCTCGC others(11): Show |
5 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(2): Show | 5 | HG01433.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22683_560+2268 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | |||||
chr7:4705552
|
T | G | 14 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(11): Show | 14 | HG01261.hp1 HG01433.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.560+22684T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705552 | ||||||
chr7:4705552
|
T | TCGCTCTC others(7): Show |
1 | a0001c0004t0001g0113 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.560+22685_560+2268 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | |||||
chr7:4705552
|
T | TCGCTCTC others(13): Show |
1 | a0001c0003t0015g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.560+22685_560+2268 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | |||||
chr7:4705552
|
T | TCTCGCTC others(9): Show |
1 | a0001c0003t0005g0112 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.560+22687_560+2268 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | |||||
chr7:4705552
|
T | TCTCGCTC others(15): Show |
2 | a0001c0006t0092g0002a0001c0006t0093g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.560+22687_560+2268 others(26): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | |||||
chr7:4705554
|
T | TCGCTCTC others(1): Show |
7 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+22687_560+2268 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | |||||
chr7:4705554
|
T | TCTCGCTC others(3): Show |
1 | a0001c0011t0006g0082 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.560+22689_560+2269 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | |||||
chr7:4705554
|
T | TCTCTCG | 30 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0004g0227others(27): Show | 30 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.560+22698_560+2270 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | |||||
chr7:4705554
|
T | TCTCTCGC others(5): Show |
5 | a0001c0002t0041g0102a0001c0002t0057g0244a0001c0003t0047g0072others(2): Show | 5 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22692_560+2270 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | |||||
chr7:4705554
|
T | TCTCTCGC others(11): Show |
3 | a0001c0003t0037g0284a0001c0003t0136g0210a0002c0012t0016g0291 | 3 | HG01109.hp1 HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+22703_560+2270 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | |||||
chr7:4705554
|
T | TCTCTCTC others(13): Show |
1 | a0001c0002t0003g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+22691_560+2269 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | |||||
chr7:4705556
|
T | G | 1 | a0001c0004t0121g0031 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.560+22688T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705556 | ||||||
chr7:4705556
|
TCTCG | T | 5 | a0001c0001t0001g0182a0001c0001t0002g0164a0001c0001t0063g0258others(2): Show | 5 | HG00558.hp1 HG02074.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22692_560+2269 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705556 | |||||
chr7:4705558
|
TCG | T | 4 | a0001c0001t0001g0161a0001c0004t0009g0140a0001c0004t0116g0139others(1): Show | 4 | HG04115.hp2 NA18951.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+22692_560+2269 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705558 | |||||
chr7:4705560
|
G | T | 51 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0037others(48): Show | 51 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.560+22692G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705560 | ||||||
chr7:4705587
|
A | G | 2 | a0001c0001t0065g0011a0001c0002t0024g0046 | 2 | HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.560+22719A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705587 | ||||||
chr7:4705588
|
G | A | 19 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(16): Show | 19 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.560+22720G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705588 | ||||||
chr7:4705629
|
C | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0001t0002g0033others(5): Show | 8 | HG00408.hp2 HG02071.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+22761C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705629 | ||||||
chr7:4705656
|
C | G | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.560+22788C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705656 | ||||||
chr7:4705688
|
G | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+22820G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705688 | ||||||
chr7:4705689
|
C | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+22821C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705689 | ||||||
chr7:4705767
|
A | G | 71 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(68): Show | 71 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.560+22899A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705767 | ||||||
chr7:4705776
|
A | AC | 40 | a0001c0001t0001g0149a0001c0001t0001g0259a0001c0001t0002g0114others(37): Show | 40 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.560+22917dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705776 | |||||
chr7:4705778
|
C | CA | 9 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(6): Show | 9 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+22910_560+2291 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705778 | ||||||
chr7:4705780
|
C | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0220a0001c0008t0028g0206 | 3 | HG02129.hp2 NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.560+22912C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705780 | ||||||
chr7:4705783
|
C | CG | 3 | a0001c0003t0047g0072a0001c0004t0014g0256a0001c0004t0043g0091 | 3 | HG02109.hp1 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.560+22915_560+2291 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705783 | ||||||
chr7:4705792
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0220a0001c0008t0028g0206 | 3 | HG02129.hp2 NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.560+22924G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705792 | ||||||
chr7:4705959
|
T | C | 7 | a0001c0002t0041g0102a0001c0002t0057g0244a0001c0003t0138g0262others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+23091T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705959 | ||||||
chr7:4705959
|
T | TGTATATA others(37): Show |
1 | a0001c0001t0012g0005 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.560+23101_560+2314 others(48): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705959 | |||||
chr7:4705960
|
GTA | G | 37 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0003g0065others(34): Show | 37 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+23103_560+2310 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705960 | |||||
chr7:4705960
|
GTATATAT others(39): Show |
G | 6 | a0001c0001t0001g0192a0001c0002t0001g0157a0001c0002t0005g0158others(3): Show | 6 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+23099_560+2314 others(50): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705960 | |||||
chr7:4705962
|
A | G | 1 | a0001c0004t0048g0183 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560+23094A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705962 | ||||||
chr7:4705962
|
ATATATAT others(35): Show |
A | 8 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+23103_560+2314 others(46): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705962 | |||||
chr7:4705964
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0005g0162a0001c0002t0017g0286 | 2 | HG03669.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+23148_560+2315 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | |||||
chr7:4705964
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0035g0064a0001c0002t0004g0252a0001c0003t0007g0090others(2): Show | 5 | HG00673.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+23138_560+2315 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | |||||
chr7:4705964
|
A | ATATATAT others(43): Show |
1 | a0001c0002t0004g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.560+23108_560+2315 others(54): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | |||||
chr7:4705964
|
ATATATAT others(3): Show |
A | 26 | a0001c0001t0001g0020a0001c0001t0001g0062a0001c0001t0001g0115others(23): Show | 27 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.560+23148_560+2315 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | |||||
chr7:4705964
|
ATATATAT others(13): Show |
A | 6 | a0001c0001t0001g0152a0001c0001t0002g0179a0001c0001t0005g0047others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+23138_560+2315 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | |||||
chr7:4705964
|
ATATATAT others(23): Show |
A | 2 | a0004c0016t0106g0146a0004c0016t0107g0147 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.560+23128_560+2315 others(34): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | |||||
chr7:4705964
|
ATATATAT others(33): Show |
A | 3 | a0001c0002t0001g0131a0001c0002t0001g0132a0001c0003t0120g0213 | 3 | HG01256.hp1 HG01258.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.560+23118_560+2315 others(44): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | |||||
chr7:4705970
|
A | ATG | 4 | a0001c0002t0002g0106a0001c0002t0098g0268a0001c0006t0092g0002others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23103_560+2310 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705970 | |||||
chr7:4705970
|
A | ATGTATAT others(39): Show |
1 | a0001c0007t0006g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.560+23103_560+2310 others(50): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705970 | |||||
chr7:4705971
|
T | C | 2 | a0001c0001t0089g0044a0006c0025t0022g0032 | 2 | HG00621.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.560+23103T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705971 | ||||||
chr7:4705972
|
A | G | 12 | a0001c0002t0095g0207a0001c0003t0015g0066a0001c0003t0015g0094others(9): Show | 12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23104A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705972 | ||||||
chr7:4705973
|
C | T | 16 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23105C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705973 | ||||||
chr7:4705974
|
G | A | 16 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23106G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705974 | ||||||
chr7:4705974
|
GTATATAT others(25): Show |
G | 1 | a0001c0008t0122g0272 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.560+23113_560+2314 others(36): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705974 | |||||
chr7:4705981
|
T | C | 2 | a0001c0001t0003g0012a0001c0001t0003g0200 | 2 | HG00597.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.560+23113T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705981 | ||||||
chr7:4705983
|
C | CATATATA others(45): Show |
4 | a0001c0002t0002g0106a0001c0002t0098g0268a0001c0006t0092g0002others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23115_560+2311 others(56): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705983 | ||||||
chr7:4705983
|
C | T | 12 | a0001c0002t0095g0207a0001c0003t0015g0066a0001c0003t0015g0094others(9): Show | 12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23115C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705983 | ||||||
chr7:4705984
|
G | A | 12 | a0001c0002t0095g0207a0001c0003t0015g0066a0001c0003t0015g0094others(9): Show | 12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23116G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705984 | ||||||
chr7:4705984
|
G | GTATATAT others(45): Show |
1 | a0001c0002t0057g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.560+23124_560+2312 others(56): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705984 | |||||
chr7:4705984
|
G | GTATATAT others(69): Show |
1 | a0001c0002t0041g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+23124_560+2312 others(80): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705984 | |||||
chr7:4705985
|
T | C | 12 | a0001c0002t0095g0207a0001c0003t0015g0066a0001c0003t0015g0094others(9): Show | 12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23117T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705985 | ||||||
chr7:4705988
|
ATATACGT others(51): Show |
A | 5 | a0001c0002t0105g0237a0001c0003t0100g0248a0001c0003t0113g0276others(2): Show | 5 | HG03209.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23125_560+2318 others(62): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705988 | |||||
chr7:4705990
|
ATACGTAT others(49): Show |
A | 5 | a0001c0003t0099g0282a0001c0003t0138g0262a0001c0003t0142g0080others(2): Show | 5 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23125_560+2318 others(60): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705990 | |||||
chr7:4705992
|
ACG | A | 3 | a0001c0002t0003g0065a0001c0004t0014g0256a0001c0004t0043g0091 | 3 | HG02615.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+23125_560+2312 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705992 | ||||||
chr7:4705993
|
C | T | 16 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23125C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705993 | ||||||
chr7:4705993
|
CGTATATA others(51): Show |
C | 23 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0004g0227others(20): Show | 23 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.560+23126_560+2318 others(62): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705993 | ||||||
chr7:4705994
|
G | A | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+23126G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705994 | ||||||
chr7:4705994
|
G | GTATGTA | 5 | a0001c0002t0002g0106a0001c0002t0098g0268a0001c0006t0092g0002others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23129_560+2313 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705994 | |||||
chr7:4705996
|
A | ATATATAC others(23): Show |
2 | a0001c0001t0001g0069a0001c0003t0087g0071 | 2 | HG02622.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.560+23138_560+2316 others(34): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705996 | |||||
chr7:4705998
|
A | G | 3 | a0001c0002t0003g0065a0001c0004t0014g0256a0001c0004t0043g0091 | 3 | HG02615.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+23130A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705998 | ||||||
chr7:4706001
|
T | C | 1 | a0001c0005t0001g0153 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.560+23133T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706001 | ||||||
chr7:4706002
|
A | T | 3 | a0001c0001t0001g0204a0001c0001t0021g0203a0001c0001t0021g0219 | 3 | NA18980.hp1 NA19060.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.560+23134A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706002 | ||||||
chr7:4706002
|
ACGTATAT others(17): Show |
A | 3 | a0001c0002t0003g0065a0001c0004t0014g0256a0001c0004t0043g0091 | 3 | HG02615.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+23135_560+2315 others(28): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706002 | ||||||
chr7:4706003
|
C | T | 9 | a0001c0002t0095g0207a0001c0003t0015g0066a0001c0003t0015g0094others(6): Show | 9 | HG02257.hp1 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+23135C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706003 | ||||||
chr7:4706004
|
G | GTATATAT others(87): Show |
1 | a0001c0021t0027g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.560+23144_560+2314 others(98): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706004 | |||||
chr7:4706004
|
G | GTATGTA | 4 | a0001c0002t0095g0207a0001c0003t0019g0238a0001c0003t0036g0004others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23139_560+2314 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706004 | |||||
chr7:4706006
|
A | ATATATAC others(13): Show |
8 | a0001c0001t0001g0152a0001c0001t0002g0179a0001c0001t0003g0138others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+23148_560+2316 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706006 | |||||
chr7:4706006
|
A | G | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+23138A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706006 | ||||||
chr7:4706013
|
C | T | 5 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0038g0208others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23145C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706013 | ||||||
chr7:4706013
|
CGT | C | 5 | a0001c0002t0002g0106a0001c0002t0098g0268a0001c0006t0092g0002others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23146_560+2314 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706013 | ||||||
chr7:4706015
|
T | TATATATA others(93): Show |
4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0038g0208others(1): Show | 4 | HG02257.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+23154_560+2315 others(104): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706015 | |||||
chr7:4706015
|
T | TATATATA others(49): Show |
1 | a0001c0003t0039g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.560+23154_560+2315 others(60): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706015 | |||||
chr7:4706016
|
A | ATATATAC others(3): Show |
1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+23175_560+2318 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706016 | |||||
chr7:4706016
|
ATATATAC others(13): Show |
A | 17 | a0001c0001t0001g0192a0001c0002t0001g0131a0001c0002t0001g0132others(14): Show | 17 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23165_560+2318 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706016 | |||||
chr7:4706023
|
C | CATATATA others(1): Show |
5 | a0001c0002t0095g0207a0001c0003t0019g0238a0001c0003t0036g0004others(2): Show | 5 | HG01261.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23155_560+2315 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706023 | ||||||
chr7:4706023
|
C | CATATATA others(45): Show |
2 | a0001c0004t0046g0009a0001c0011t0006g0281 | 2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.560+23155_560+2315 others(56): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706023 | ||||||
chr7:4706023
|
C | T | 10 | a0001c0002t0002g0106a0001c0002t0098g0268a0001c0003t0015g0066others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.560+23155C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706023 | ||||||
chr7:4706026
|
G | A | 12 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(9): Show | 12 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23158G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706026 | ||||||
chr7:4706033
|
C | CGTATATA others(23): Show |
4 | a0001c0002t0041g0102a0001c0002t0057g0244a0002c0012t0016g0291others(1): Show | 4 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23167_560+2316 others(34): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706033 | |||||
chr7:4706033
|
C | T | 27 | a0001c0001t0058g0251a0001c0002t0002g0106a0001c0002t0018g0283others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.560+23165C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706033 | ||||||
chr7:4706034
|
G | A | 8 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+23166G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706034 | ||||||
chr7:4706036
|
G | A | 225 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(222): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.560+23168G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706036 | ||||||
chr7:4706036
|
G | GTATATAC others(3): Show |
1 | a0001c0003t0010g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560+23177_560+2317 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706036 | |||||
chr7:4706043
|
C | T | 25 | a0001c0001t0058g0251a0001c0002t0002g0106a0001c0002t0018g0283others(22): Show | 25 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.560+23175C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706043 | ||||||
chr7:4706044
|
G | A | 8 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+23176G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706044 | ||||||
chr7:4706046
|
G | A | 27 | a0001c0002t0002g0106a0001c0002t0003g0065a0001c0002t0041g0102others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.560+23178G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706046 | ||||||
chr7:4706053
|
T | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0187a0001c0001t0035g0064others(8): Show | 11 | HG00673.hp2 HG01109.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.560+23185T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706053 | ||||||
chr7:4706054
|
G | A | 16 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0003t0015g0066others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23186G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706054 | ||||||
chr7:4706056
|
A | G | 17 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23188A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706056 | ||||||
chr7:4706062
|
ATG | A | 45 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(42): Show | 45 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.560+23198_560+2319 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706062 | |||||
chr7:4706064
|
G | A | 17 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23196G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706064 | ||||||
chr7:4706065
|
T | C | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+23197T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706065 | ||||||
chr7:4706204
|
A | G | 17 | a0001c0002t0002g0106a0001c0002t0095g0207a0001c0002t0098g0268others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23336A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706204 | ||||||
chr7:4706343
|
G | A | 2 | a0001c0004t0014g0256a0001c0004t0043g0091 | 2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.560+23475G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706343 | ||||||
chr7:4706366
|
TTAG | T | 10 | a0001c0001t0016g0241a0001c0002t0004g0227a0001c0002t0004g0239others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+23499_560+2350 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706366 | ||||||
chr7:4706367
|
T | G | 36 | a0001c0001t0058g0251a0001c0001t0096g0093a0001c0002t0003g0065others(33): Show | 36 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.560+23499T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706367 | ||||||
chr7:4706473
|
T | C | 62 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(59): Show | 62 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.560+23605T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706473 | ||||||
chr7:4706883
|
C | T | 1 | a0001c0002t0013g0050 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.560+24015C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706883 | ||||||
chr7:4706908
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0002g0049a0001c0004t0033g0027others(1): Show | 4 | HG00738.hp2 HG01361.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+24040C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706908 | ||||||
chr7:4706916
|
T | A | 1 | a0001c0007t0006g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.560+24048T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706916 | ||||||
chr7:4706981
|
G | C | 65 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(62): Show | 65 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.560+24113G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706981 | ||||||
chr7:4707120
|
C | T | 41 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(38): Show | 41 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.560+24252C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707120 | ||||||
chr7:4707238
|
G | A | 2 | a0001c0002t0003g0111a0001c0002t0018g0283 | 2 | HG03688.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.560+24370G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707238 | ||||||
chr7:4707414
|
A | C | 3 | a0001c0003t0037g0284a0001c0003t0136g0210a0001c0007t0109g0073 | 3 | HG02895.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.560+24546A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707414 | ||||||
chr7:4707506
|
G | T | 6 | a0001c0002t0105g0237a0001c0003t0099g0282a0001c0003t0138g0262others(3): Show | 6 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+24638G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707506 | ||||||
chr7:4707573
|
C | G | 8 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+24705C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707573 | ||||||
chr7:4707586
|
G | C | 1 | a0001c0003t0031g0155 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.560+24718G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707586 | ||||||
chr7:4707598
|
A | G | 8 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+24730A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707598 | ||||||
chr7:4707643
|
G | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+24775G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707643 | ||||||
chr7:4707649
|
C | G | 4 | a0001c0002t0105g0237a0001c0003t0138g0262a0001c0003t0142g0080others(1): Show | 4 | HG02809.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+24781C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707649 | ||||||
chr7:4707689
|
C | CT | 65 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0001t0096g0093others(62): Show | 65 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.560+24834dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4707689 | |||||
chr7:4707717
|
C | G | 3 | a0001c0003t0100g0248a0001c0003t0113g0276a0001c0004t0141g0247 | 3 | HG03209.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+24849C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707717 | ||||||
chr7:4707717
|
C | T | 32 | a0001c0001t0016g0241a0001c0001t0096g0093a0001c0002t0004g0227others(29): Show | 32 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.560+24849C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707717 | ||||||
chr7:4707720
|
C | T | 2 | a0001c0003t0136g0210a0001c0007t0109g0073 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.560+24852C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707720 | ||||||
chr7:4707765
|
A | G | 19 | a0001c0002t0002g0106a0001c0002t0003g0065a0001c0002t0095g0207others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.560+24897A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707765 | ||||||
chr7:4707954
|
A | T | 8 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0003t0026g0246others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+25086A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707954 | ||||||
chr7:4707984
|
G | T | 10 | a0001c0002t0002g0106a0001c0002t0098g0268a0001c0003t0015g0066others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.560+25116G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707984 | ||||||
chr7:4708075
|
T | TGGAA | 8 | a0001c0002t0003g0065a0001c0002t0095g0207a0001c0003t0019g0238others(5): Show | 8 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+25211_560+2521 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4708075 | |||||
chr7:4708116
|
C | T | 1 | a0001c0002t0002g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.560+25248C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708116 | ||||||
chr7:4708413
|
A | T | 16 | a0001c0002t0002g0106a0001c0002t0041g0102a0001c0002t0057g0244others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+25545A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708413 | ||||||
chr7:4708452
|
T | C | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.560+25584T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708452 | ||||||
chr7:4708611
|
G | T | 8 | a0001c0001t0001g0129a0001c0001t0075g0128a0001c0002t0001g0130others(5): Show | 8 | HG00140.hp1 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+25743G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708611 | ||||||
chr7:4708659
|
A | G | 58 | a0001c0001t0016g0241a0001c0001t0024g0013a0001c0001t0058g0251others(55): Show | 58 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.560+25791A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708659 | ||||||
chr7:4708694
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.560+25826C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708694 | ||||||
chr7:4708719
|
C | T | 1 | a0001c0001t0079g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.560+25851C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708719 | ||||||
chr7:4708779
|
G | T | 1 | a0001c0001t0059g0121 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+25911G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708779 | ||||||
chr7:4708802
|
C | T | 1 | a0001c0005t0069g0166 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.560+25934C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708802 | ||||||
chr7:4708835
|
C | T | 7 | a0001c0002t0018g0283a0001c0003t0026g0246a0001c0006t0052g0078others(4): Show | 7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+25967C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708835 | ||||||
chr7:4708874
|
G | C | 31 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0002t0002g0106others(28): Show | 31 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.560+26006G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708874 | ||||||
chr7:4708958
|
G | A | 2 | a0001c0001t0073g0145a0001c0004t0009g0234 | 2 | NA19058.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.560+26090G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708958 | ||||||
chr7:4709020
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.560+26152G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709020 | ||||||
chr7:4709055
|
C | T | 7 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0102g0086others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+26187C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709055 | ||||||
chr7:4709063
|
C | CA | 40 | a0001c0001t0003g0036a0001c0001t0024g0013a0001c0001t0058g0251others(37): Show | 40 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.560+26211dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4709063 | |||||
chr7:4709075
|
A | G | 1 | a0001c0001t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.560+26207A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709075 | ||||||
chr7:4709198
|
C | T | 6 | a0001c0002t0105g0237a0001c0003t0099g0282a0001c0003t0138g0262others(3): Show | 6 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+26330C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709198 | ||||||
chr7:4709199
|
C | T | 6 | a0001c0002t0105g0237a0001c0003t0099g0282a0001c0003t0138g0262others(3): Show | 6 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+26331C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709199 | ||||||
chr7:4709203
|
G | A | 1 | a0001c0027t0064g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.560+26335G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709203 | ||||||
chr7:4709231
|
G | GCATCCCC others(7): Show |
1 | a0001c0001t0003g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+26370_560+2638 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4709231 | |||||
chr7:4709278
|
T | C | 41 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0002t0002g0106others(38): Show | 41 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.560+26410T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709278 | ||||||
chr7:4709318
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.560+26450C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709318 | ||||||
chr7:4709347
|
C | T | 1 | a0001c0003t0144g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.560+26479C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709347 | ||||||
chr7:4709705
|
G | A | 3 | a0001c0001t0002g0109a0001c0001t0003g0117a0001c0001t0020g0110 | 3 | HG02071.hp2 NA18944.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.560+26837G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709705 | ||||||
chr7:4709726
|
G | A | 16 | a0001c0001t0024g0013a0001c0002t0002g0106a0001c0002t0005g0045others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+26858G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709726 | ||||||
chr7:4709777
|
G | A | 1 | a0001c0002t0005g0098 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.560+26909G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709777 | ||||||
chr7:4709788
|
C | G | 33 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0002t0002g0106others(30): Show | 33 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.560+26920C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709788 | ||||||
chr7:4709896
|
C | T | 27 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0002t0002g0106others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.560+27028C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709896 | ||||||
chr7:4709897
|
G | A | 1 | a0001c0003t0136g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+27029G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709897 | ||||||
chr7:4709924
|
G | T | 1 | a0001c0003t0136g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+27056G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709924 | ||||||
chr7:4710047
|
C | T | 3 | a0001c0002t0098g0268a0001c0006t0092g0002a0001c0006t0093g0002 | 3 | HG01070.hp2 HG01071.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.560+27179C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710047 | ||||||
chr7:4710468
|
C | T | 21 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0002t0002g0106others(18): Show | 21 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+27600C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710468 | ||||||
chr7:4710527
|
A | G | 7 | a0001c0002t0018g0283a0001c0003t0026g0246a0001c0006t0052g0078others(4): Show | 7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+27659A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710527 | ||||||
chr7:4710529
|
C | T | 1 | a0001c0001t0005g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.560+27661C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710529 | ||||||
chr7:4710718
|
G | T | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+27850G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710718 | ||||||
chr7:4710727
|
C | T | 2 | a0001c0003t0146g0174a0001c0004t0056g0233 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.560+27859C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710727 | ||||||
chr7:4710776
|
C | T | 4 | a0001c0003t0087g0071a0001c0003t0129g0279a0001c0003t0139g0074others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+27908C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710776 | ||||||
chr7:4710787
|
A | G | 54 | a0001c0001t0001g0020a0001c0001t0001g0096a0001c0001t0001g0116others(51): Show | 54 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.560+27919A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710787 | ||||||
chr7:4710854
|
C | T | 12 | a0001c0001t0058g0251a0001c0002t0004g0068a0001c0002t0018g0283others(9): Show | 12 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+27986C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710854 | ||||||
chr7:4710961
|
G | A | 3 | a0001c0003t0031g0171a0001c0003t0144g0142a0001c0003t0145g0172 | 3 | HG01081.hp1 HG01361.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.560+28093G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710961 | ||||||
chr7:4711038
|
TTTAGAGA others(4): Show |
T | 5 | a0001c0002t0041g0102a0001c0002t0057g0244a0001c0003t0019g0238others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+28179_560+2818 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4711038 | |||||
chr7:4711134
|
ACTT | A | 12 | a0001c0002t0004g0227a0001c0002t0004g0240a0001c0002t0004g0245others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.560+28272_560+2827 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4711134 | |||||
chr7:4711159
|
C | T | 8 | a0001c0002t0018g0283a0001c0003t0026g0246a0001c0003t0136g0210others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+28291C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711159 | ||||||
chr7:4711178
|
C | T | 2 | a0001c0003t0135g0255a0001c0004t0043g0091 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.560+28310C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711178 | ||||||
chr7:4711199
|
T | G | 93 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0189others(90): Show | 93 | HG00558.hp2 HG00735.hp2 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.560+28331T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711199 | ||||||
chr7:4711256
|
T | G | 98 | a0001c0001t0001g0062a0001c0001t0001g0189a0001c0001t0002g0053others(95): Show | 98 | HG00140.hp2 HG00558.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.560+28388T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711256 | ||||||
chr7:4711276
|
G | C | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+28408G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711276 | ||||||
chr7:4711358
|
T | A | 1 | a0003c0014t0002g0163 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.560+28490T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711358 | ||||||
chr7:4711408
|
T | C | 1 | a0001c0001t0077g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.560+28540T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711408 | ||||||
chr7:4711490
|
C | T | 1 | a0001c0002t0003g0151 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.560+28622C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711490 | ||||||
chr7:4711527
|
C | T | 1 | a0001c0004t0034g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.560+28659C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711527 | ||||||
chr7:4711528
|
C | T | 5 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+28660C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711528 | ||||||
chr7:4711620
|
G | A | 10 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+28752G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711620 | ||||||
chr7:4711656
|
T | C | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+28788T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711656 | ||||||
chr7:4711812
|
G | A | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+28944G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711812 | ||||||
chr7:4711833
|
T | G | 1 | a0001c0002t0095g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.560+28965T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711833 | ||||||
chr7:4711840
|
G | A | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.560+28972G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711840 | ||||||
chr7:4711844
|
G | A | 2 | a0001c0002t0055g0087a0001c0003t0100g0248 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.560+28976G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711844 | ||||||
chr7:4711851
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.560+28983A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711851 | ||||||
chr7:4711893
|
T | C | 3 | a0001c0002t0001g0134a0001c0002t0005g0278a0001c0002t0061g0133 | 3 | HG02738.hp1 HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.561-28945T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711893 | ||||||
chr7:4711910
|
A | C | 7 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(4): Show | 7 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-28928A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711910 | ||||||
chr7:4711913
|
G | A | 12 | a0001c0002t0105g0237a0001c0003t0007g0250a0001c0003t0014g0081others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-28925G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711913 | ||||||
chr7:4711918
|
G | T | 12 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-28920G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711918 | ||||||
chr7:4711935
|
G | A | 7 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0113g0276others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-28903G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711935 | ||||||
chr7:4712034
|
T | C | 1 | a0001c0004t0001g0113 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561-28804T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712034 | ||||||
chr7:4712055
|
C | CT | 14 | a0001c0002t0002g0106a0001c0002t0004g0227a0001c0002t0004g0239others(11): Show | 14 | HG01433.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.561-28771dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4712055 | |||||
chr7:4712202
|
C | T | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-28636C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712202 | ||||||
chr7:4712209
|
C | T | 109 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(106): Show | 109 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.561-28629C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712209 | ||||||
chr7:4712388
|
G | A | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-28450G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712388 | ||||||
chr7:4712397
|
A | G | 1 | a0001c0002t0002g0148 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.561-28441A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712397 | ||||||
chr7:4712401
|
A | C | 12 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0189others(9): Show | 12 | HG00558.hp2 HG00597.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-28437A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712401 | ||||||
chr7:4712543
|
C | T | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-28295C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712543 | ||||||
chr7:4712813
|
G | A | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.561-28025G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712813 | ||||||
chr7:4712981
|
T | C | 2 | a0001c0002t0001g0131a0001c0002t0001g0132 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.561-27857T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712981 | ||||||
chr7:4713004
|
G | A | 104 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(101): Show | 104 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.561-27834G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713004 | ||||||
chr7:4713009
|
A | G | 110 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(107): Show | 110 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(107): Show |
intron_variant | MODIFIER | c.561-27829A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713009 | ||||||
chr7:4713062
|
T | C | 1 | a0001c0002t0067g0195 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.561-27776T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713062 | ||||||
chr7:4713130
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.561-27708C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713130 | ||||||
chr7:4713141
|
C | T | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-27697C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713141 | ||||||
chr7:4713163
|
C | G | 1 | a0001c0001t0058g0251 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.561-27675C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713163 | ||||||
chr7:4713182
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.561-27656A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713182 | ||||||
chr7:4713202
|
A | C | 11 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-27636A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713202 | ||||||
chr7:4713298
|
G | A | 1 | a0001c0001t0096g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561-27540G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713298 | ||||||
chr7:4713329
|
A | AGATTCCC others(9): Show |
1 | a0001c0003t0036g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.561-27491_561-2747 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713329 | |||||
chr7:4713334
|
C | CCCGCTCA others(9): Show |
14 | a0001c0002t0105g0237a0001c0003t0007g0250a0001c0003t0014g0081others(11): Show | 14 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.561-27489_561-2748 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713334 | |||||
chr7:4713359
|
T | C | 11 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-27479T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713359 | ||||||
chr7:4713382
|
C | T | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-27456C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713382 | ||||||
chr7:4713434
|
G | A | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-27404G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713434 | ||||||
chr7:4713488
|
GT | G | 98 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(95): Show | 98 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(95): Show |
intron_variant | MODIFIER | c.561-27339delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713488 | |||||
chr7:4713490
|
T | G | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-27348T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713490 | ||||||
chr7:4713499
|
T | G | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.561-27339T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713499 | ||||||
chr7:4713500
|
G | GT | 9 | a0001c0002t0018g0283a0001c0002t0041g0102a0001c0002t0083g0008others(6): Show | 9 | HG01081.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-27328dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713500 | |||||
chr7:4713500
|
G | T | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.561-27338G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713500 | ||||||
chr7:4713615
|
C | T | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-27223C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713615 | ||||||
chr7:4713736
|
C | T | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-27102C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713736 | ||||||
chr7:4713737
|
G | A | 4 | a0001c0001t0058g0251a0001c0002t0095g0207a0001c0003t0019g0238others(1): Show | 4 | HG02622.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-27101G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713737 | ||||||
chr7:4713788
|
C | T | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-27050C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713788 | ||||||
chr7:4713791
|
C | T | 9 | a0001c0001t0001g0192a0001c0002t0001g0157a0001c0002t0005g0158others(6): Show | 9 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-27047C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713791 | ||||||
chr7:4713824
|
T | C | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-27014T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713824 | ||||||
chr7:4713919
|
G | A | 1 | a0001c0003t0111g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.561-26919G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713919 | ||||||
chr7:4714059
|
C | T | 1 | a0001c0001t0066g0120 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.561-26779C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714059 | ||||||
chr7:4714105
|
T | G | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-26733T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714105 | ||||||
chr7:4714106
|
G | T | 5 | a0001c0001t0016g0241a0001c0003t0146g0174a0001c0004t0014g0256others(2): Show | 5 | HG02615.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-26732G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714106 | ||||||
chr7:4714276
|
C | G | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-26562C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714276 | ||||||
chr7:4714284
|
G | T | 1 | a0001c0022t0070g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.561-26554G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714284 | ||||||
chr7:4714335
|
A | G | 4 | a0001c0001t0058g0251a0001c0002t0095g0207a0001c0003t0019g0238others(1): Show | 4 | HG02622.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-26503A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714335 | ||||||
chr7:4714484
|
A | C | 7 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0113g0276others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-26354A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714484 | ||||||
chr7:4714671
|
C | T | 3 | a0001c0002t0004g0068a0001c0003t0135g0255a0001c0004t0043g0091 | 3 | HG02976.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.561-26167C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714671 | ||||||
chr7:4714695
|
G | A | 1 | a0001c0001t0005g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.561-26143G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714695 | ||||||
chr7:4714714
|
T | TA | 5 | a0001c0001t0001g0017a0001c0001t0020g0124a0001c0001t0084g0232others(2): Show | 5 | HG00621.hp1 HG00621.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-26123dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4714714 | |||||
chr7:4714725
|
G | A | 1 | a0001c0001t0023g0175 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.561-26113G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714725 | ||||||
chr7:4714822
|
G | A | 2 | a0001c0001t0068g0010a0001c0001t0080g0023 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-26016G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714822 | ||||||
chr7:4714879
|
C | G | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-25959C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714879 | ||||||
chr7:4715098
|
T | A | 2 | a0001c0001t0001g0205a0001c0008t0028g0206 | 2 | NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.561-25740T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715098 | ||||||
chr7:4715121
|
T | C | 18 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(15): Show | 18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-25717T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715121 | ||||||
chr7:4715136
|
G | C | 2 | a0001c0003t0037g0284a0001c0003t0038g0208 | 2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.561-25702G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715136 | ||||||
chr7:4715143
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.561-25695T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715143 | ||||||
chr7:4715151
|
C | T | 1 | a0001c0002t0003g0111 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.561-25687C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715151 | ||||||
chr7:4715171
|
A | ACGATACG others(19): Show |
38 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0001t0074g0016others(35): Show | 38 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.561-25641_561-2561 others(30): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4715171 | |||||
chr7:4715182
|
C | CACGGTGG others(19): Show |
1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-25631_561-2563 others(30): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4715182 | |||||
chr7:4715226
|
A | C | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-25612A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715226 | ||||||
chr7:4715244
|
T | C | 1 | a0001c0003t0140g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.561-25594T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715244 | ||||||
chr7:4715252
|
C | T | 2 | a0001c0001t0068g0010a0001c0001t0080g0023 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-25586C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715252 | ||||||
chr7:4715281
|
A | C | 1 | a0001c0001t0066g0120 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.561-25557A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715281 | ||||||
chr7:4715333
|
G | A | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-25505G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715333 | ||||||
chr7:4715807
|
T | A | 37 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0002t0002g0106others(34): Show | 37 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-25031T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715807 | ||||||
chr7:4715853
|
C | A | 2 | a0001c0003t0087g0071a0001c0003t0139g0074 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.561-24985C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715853 | ||||||
chr7:4715863
|
A | C | 37 | a0001c0001t0024g0013a0001c0001t0058g0251a0001c0002t0002g0106others(34): Show | 37 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-24975A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715863 | ||||||
chr7:4715924
|
C | T | 18 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(15): Show | 18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-24914C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715924 | ||||||
chr7:4716018
|
G | C | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-24820G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716018 | ||||||
chr7:4716157
|
G | A | 1 | a0001c0017t0114g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.561-24681G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716157 | ||||||
chr7:4716202
|
C | T | 7 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0113g0276others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-24636C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716202 | ||||||
chr7:4716230
|
C | CA | 6 | a0001c0001t0058g0251a0001c0002t0001g0215a0001c0002t0017g0286others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-24594dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4716230 | |||||
chr7:4716508
|
A | C | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-24330A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716508 | ||||||
chr7:4716646
|
C | T | 12 | a0001c0002t0041g0102a0001c0002t0057g0244a0001c0002t0088g0254others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-24192C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716646 | ||||||
chr7:4716671
|
C | T | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-24167C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716671 | ||||||
chr7:4716674
|
G | C | 7 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(4): Show | 7 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-24164G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716674 | ||||||
chr7:4716792
|
G | A | 18 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(15): Show | 18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-24046G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716792 | ||||||
chr7:4716957
|
G | A | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.561-23881G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716957 | ||||||
chr7:4717042
|
G | A | 41 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(38): Show | 41 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.561-23796G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717042 | ||||||
chr7:4717181
|
G | C | 11 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-23657G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717181 | ||||||
chr7:4717305
|
A | G | 10 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-23533A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717305 | ||||||
chr7:4717325
|
G | A | 2 | a0001c0003t0037g0284a0001c0003t0038g0208 | 2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.561-23513G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717325 | ||||||
chr7:4717416
|
A | G | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-23422A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717416 | ||||||
chr7:4717440
|
A | C | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-23398A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717440 | ||||||
chr7:4717453
|
GTGTGGCT others(8): Show |
G | 111 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(108): Show | 111 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(108): Show |
intron_variant | MODIFIER | c.561-23355_561-2334 others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4717453 | |||||
chr7:4717473
|
G | A | 12 | a0001c0002t0041g0102a0001c0002t0057g0244a0001c0002t0088g0254others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-23365G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717473 | ||||||
chr7:4717497
|
C | T | 29 | a0001c0002t0004g0068a0001c0002t0041g0102a0001c0002t0057g0244others(26): Show | 29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-23341C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717497 | ||||||
chr7:4717503
|
G | A | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-23335G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717503 | ||||||
chr7:4717553
|
C | G | 110 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(107): Show | 110 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(107): Show |
intron_variant | MODIFIER | c.561-23285C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717553 | ||||||
chr7:4717585
|
C | T | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-23253C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717585 | ||||||
chr7:4717760
|
A | G | 39 | a0001c0001t0058g0251a0001c0001t0074g0016a0001c0002t0002g0257others(36): Show | 39 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.561-23078A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717760 | ||||||
chr7:4717792
|
G | A | 7 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0113g0276others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-23046G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717792 | ||||||
chr7:4718213
|
TGC | T | 29 | a0001c0002t0004g0068a0001c0002t0041g0102a0001c0002t0057g0244others(26): Show | 29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-22622_561-2262 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4718213 | |||||
chr7:4718227
|
T | C | 29 | a0001c0002t0004g0068a0001c0002t0041g0102a0001c0002t0057g0244others(26): Show | 29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-22611T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718227 | ||||||
chr7:4718243
|
C | T | 11 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-22595C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718243 | ||||||
chr7:4718255
|
C | T | 10 | a0001c0003t0007g0250a0001c0003t0014g0081a0001c0003t0014g0236others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-22583C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718255 | ||||||
chr7:4718268
|
G | A | 1 | a0001c0004t0008g0180 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.561-22570G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718268 | ||||||
chr7:4718324
|
A | C | 6 | a0001c0002t0003g0065a0001c0002t0018g0283a0001c0003t0026g0246others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-22514A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718324 | ||||||
chr7:4718584
|
C | A | 28 | a0001c0002t0004g0068a0001c0002t0041g0102a0001c0002t0057g0244others(25): Show | 28 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.561-22254C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718584 | ||||||
chr7:4718597
|
C | T | 29 | a0001c0002t0004g0068a0001c0002t0004g0227a0001c0002t0004g0239others(26): Show | 29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-22241C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718597 | ||||||
chr7:4718598
|
G | A | 8 | a0001c0003t0007g0250a0001c0003t0014g0081a0001c0003t0014g0236others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.561-22240G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718598 | ||||||
chr7:4718626
|
C | T | 2 | a0001c0003t0132g0160a0001c0003t0144g0142 | 2 | HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.561-22212C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718626 | ||||||
chr7:4718678
|
G | A | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-22160G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718678 | ||||||
chr7:4718750
|
A | T | 19 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(16): Show | 19 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-22088A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718750 | ||||||
chr7:4718852
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0002g0049 | 2 | HG01361.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.561-21986C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718852 | ||||||
chr7:4718925
|
C | T | 103 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(100): Show | 103 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(100): Show |
intron_variant | MODIFIER | c.561-21913C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718925 | ||||||
chr7:4718960
|
C | T | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-21878C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718960 | ||||||
chr7:4718982
|
T | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0215a0001c0002t0012g0127 | 3 | HG02056.hp2 HG02165.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.561-21856T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718982 | ||||||
chr7:4719029
|
G | A | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-21809G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719029 | ||||||
chr7:4719040
|
C | T | 7 | a0001c0001t0001g0214a0001c0004t0009g0007a0001c0004t0009g0140others(4): Show | 7 | NA18962.hp2 NA18995.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-21798C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719040 | ||||||
chr7:4719089
|
A | G | 3 | a0001c0003t0138g0262a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-21749A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719089 | ||||||
chr7:4719120
|
GT | G | 16 | a0001c0002t0018g0283a0001c0003t0007g0250a0001c0003t0014g0081others(13): Show | 16 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.561-21708delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4719120 | |||||
chr7:4719122
|
T | G | 1 | a0001c0011t0006g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.561-21716T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719122 | ||||||
chr7:4719128
|
TTTG | T | 56 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(53): Show | 56 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-21707_561-2170 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4719128 | |||||
chr7:4719130
|
TG | T | 5 | a0001c0002t0105g0237a0001c0003t0047g0072a0001c0003t0087g0071others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-21707delG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719130 | ||||||
chr7:4719139
|
T | G | 78 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(75): Show | 78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21699T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719139 | ||||||
chr7:4719140
|
G | T | 78 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(75): Show | 78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21698G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719140 | ||||||
chr7:4719170
|
C | G | 1 | a0001c0001t0060g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.561-21668C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719170 | ||||||
chr7:4719179
|
A | G | 86 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(83): Show | 86 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.561-21659A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719179 | ||||||
chr7:4719189
|
C | T | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-21649C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719189 | ||||||
chr7:4719260
|
G | A | 7 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(4): Show | 7 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-21578G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719260 | ||||||
chr7:4719382
|
C | T | 48 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(45): Show | 48 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.561-21456C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719382 | ||||||
chr7:4719494
|
A | T | 78 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(75): Show | 78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21344A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719494 | ||||||
chr7:4719543
|
G | A | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-21295G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719543 | ||||||
chr7:4719592
|
C | G | 1 | a0005c0020t0045g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.561-21246C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719592 | ||||||
chr7:4719698
|
T | TC | 47 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(44): Show | 47 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.561-21139dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4719698 | |||||
chr7:4719725
|
A | G | 78 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(75): Show | 78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21113A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719725 | ||||||
chr7:4719851
|
T | C | 1 | a0001c0003t0037g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.561-20987T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719851 | ||||||
chr7:4719911
|
G | A | 78 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(75): Show | 78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-20927G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719911 | ||||||
chr7:4720088
|
C | A | 14 | a0001c0002t0105g0237a0001c0003t0007g0250a0001c0003t0014g0081others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.561-20750C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720088 | ||||||
chr7:4720266
|
T | G | 1 | a0001c0003t0036g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.561-20572T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720266 | ||||||
chr7:4720276
|
G | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-20562G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720276 | ||||||
chr7:4720322
|
A | AC | 78 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(75): Show | 78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-20515dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4720322 | |||||
chr7:4720381
|
T | C | 1 | a0001c0023t0049g0104 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561-20457T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720381 | ||||||
chr7:4720420
|
T | G | 1 | a0001c0017t0114g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.561-20418T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720420 | ||||||
chr7:4720471
|
T | G | 10 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-20367T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720471 | ||||||
chr7:4720493
|
A | G | 119 | a0001c0001t0001g0020a0001c0001t0001g0054a0001c0001t0001g0061others(116): Show | 120 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.561-20345A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720493 | ||||||
chr7:4720600
|
G | A | 7 | a0001c0001t0074g0016a0001c0002t0002g0257a0001c0003t0031g0171others(4): Show | 7 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-20238G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720600 | ||||||
chr7:4720631
|
C | G | 4 | a0001c0002t0041g0102a0001c0002t0057g0244a0002c0012t0016g0291others(1): Show | 4 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-20207C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720631 | ||||||
chr7:4720638
|
G | C | 7 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0113g0276others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-20200G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720638 | ||||||
chr7:4720669
|
T | C | 2 | a0001c0002t0018g0283a0001c0003t0026g0246 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-20169T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720669 | ||||||
chr7:4720692
|
C | T | 10 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-20146C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720692 | ||||||
chr7:4720708
|
CT | C | 42 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(39): Show | 42 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.561-20117delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4720708 | |||||
chr7:4720763
|
G | A | 10 | a0001c0002t0105g0237a0001c0003t0007g0250a0001c0003t0014g0081others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-20075G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720763 | ||||||
chr7:4720768
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.561-20070C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720768 | ||||||
chr7:4720828
|
C | A | 2 | a0001c0002t0018g0283a0001c0003t0026g0246 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-20010C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720828 | ||||||
chr7:4720849
|
C | G | 78 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0266others(75): Show | 78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-19989C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720849 | ||||||
chr7:4720922
|
G | GA | 8 | a0001c0001t0017g0224a0001c0001t0074g0016a0001c0002t0002g0257others(5): Show | 8 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-19906dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4720922 | |||||
chr7:4720970
|
T | A | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-19868T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720970 | ||||||
chr7:4721018
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.561-19820C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721018 | ||||||
chr7:4721052
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.561-19786A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721052 | ||||||
chr7:4721065
|
C | T | 162 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0037others(159): Show | 163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.561-19773C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721065 | ||||||
chr7:4721082
|
G | A | 1 | a0001c0002t0088g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.561-19756G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721082 | ||||||
chr7:4721094
|
C | G | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-19744C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721094 | ||||||
chr7:4721114
|
C | T | 18 | a0001c0002t0004g0227a0001c0002t0004g0239a0001c0002t0004g0240others(15): Show | 18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-19724C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721114 | ||||||
chr7:4721161
|
C | T | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-19677C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721161 | ||||||
chr7:4721190
|
G | T | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-19648G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721190 | ||||||
chr7:4721237
|
C | T | 6 | a0001c0002t0002g0257a0001c0003t0031g0171a0001c0003t0132g0160others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-19601C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721237 | ||||||
chr7:4721313
|
G | A | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-19525G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721313 | ||||||
chr7:4721328
|
C | T | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-19510C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721328 | ||||||
chr7:4721329
|
G | A | 1 | a0001c0003t0019g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.561-19509G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721329 | ||||||
chr7:4721367
|
G | T | 1 | a0001c0004t0115g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.561-19471G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721367 | ||||||
chr7:4721389
|
G | A | 25 | a0001c0001t0058g0251a0001c0002t0002g0257a0001c0002t0004g0227others(22): Show | 25 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.561-19449G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721389 | ||||||
chr7:4721572
|
T | C | 1 | a0001c0007t0109g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.561-19266T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721572 | ||||||
chr7:4721580
|
C | T | 1 | a0001c0001t0011g0040 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.561-19258C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721580 | ||||||
chr7:4721581
|
TTTTTTTT others(1): Show |
T | 26 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(23): Show | 26 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.561-19249_561-1924 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721581 | |||||
chr7:4721589
|
C | CT | 50 | a0001c0001t0001g0161a0001c0001t0002g0199a0001c0001t0003g0138others(47): Show | 50 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.561-19230dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721589 | |||||
chr7:4721589
|
C | T | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.561-19249C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721589 | ||||||
chr7:4721589
|
CT | C | 31 | a0001c0001t0001g0062a0001c0001t0001g0192a0001c0001t0024g0013others(28): Show | 31 | HG00544.hp1 HG01123.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.561-19230delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721589 | |||||
chr7:4721589
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0005t0069g0166 | 3 | HG00673.hp1 HG01981.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.561-19240_561-1923 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721589 | |||||
chr7:4721604
|
T | G | 1 | a0001c0001t0078g0019 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.561-19234T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721604 | ||||||
chr7:4721621
|
T | G | 1 | a0001c0003t0143g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.561-19217T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721621 | ||||||
chr7:4721659
|
T | C | 3 | a0001c0001t0068g0010a0001c0001t0080g0023a0001c0004t0033g0027 | 3 | HG01175.hp2 HG01515.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.561-19179T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721659 | ||||||
chr7:4721725
|
GGATTACA others(128): Show |
G | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.561-19097_561-1896 others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721725 | |||||
chr7:4721825
|
A | T | 1 | a0001c0001t0073g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.561-19013A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721825 | ||||||
chr7:4721843
|
G | C | 2 | a0001c0001t0002g0164a0001c0024t0002g0212 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.561-18995G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721843 | ||||||
chr7:4721871
|
G | T | 1 | a0001c0002t0005g0158 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.561-18967G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721871 | ||||||
chr7:4721982
|
C | T | 176 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(173): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.561-18856C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721982 | ||||||
chr7:4721985
|
A | C | 7 | a0001c0002t0017g0286a0001c0003t0019g0238a0001c0003t0039g0229others(4): Show | 7 | HG01496.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-18853A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721985 | ||||||
chr7:4721991
|
G | C | 7 | a0001c0001t0001g0214a0001c0004t0009g0007a0001c0004t0009g0140others(4): Show | 7 | NA18962.hp2 NA18995.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-18847G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721991 | ||||||
chr7:4722007
|
A | T | 2 | a0001c0001t0096g0093a0001c0003t0087g0071 | 2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.561-18831A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722007 | ||||||
chr7:4722076
|
A | G | 36 | a0001c0001t0096g0093a0001c0002t0004g0068a0001c0002t0004g0240others(33): Show | 36 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.561-18762A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722076 | ||||||
chr7:4722215
|
G | A | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-18623G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722215 | ||||||
chr7:4722215
|
G | T | 1 | a0001c0001t0003g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.561-18623G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722215 | ||||||
chr7:4722266
|
TTCCCGAG others(2): Show |
T | 9 | a0001c0001t0001g0054a0001c0001t0001g0266a0001c0001t0001g0267others(6): Show | 9 | HG00140.hp2 HG01106.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-18567_561-1855 others(13): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4722266 | |||||
chr7:4722512
|
A | G | 251 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(248): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.561-18326A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722512 | ||||||
chr7:4722541
|
G | A | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-18297G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722541 | ||||||
chr7:4722564
|
G | A | 2 | a0001c0003t0113g0276a0001c0003t0136g0210 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.561-18274G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722564 | ||||||
chr7:4722606
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.561-18232G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722606 | ||||||
chr7:4722621
|
A | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0215a0001c0002t0012g0127 | 3 | HG02056.hp2 HG02165.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.561-18217A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722621 | ||||||
chr7:4722699
|
C | T | 19 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-18139C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722699 | ||||||
chr7:4722771
|
C | T | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-18067C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722771 | ||||||
chr7:4722789
|
C | T | 37 | a0001c0002t0004g0067a0001c0002t0004g0068a0001c0002t0004g0126others(34): Show | 37 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.561-18049C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722789 | ||||||
chr7:4722914
|
G | C | 3 | a0001c0003t0137g0287a0001c0004t0141g0247a0001c0011t0006g0281 | 3 | HG01496.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.561-17924G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722914 | ||||||
chr7:4722921
|
G | A | 2 | a0001c0001t0068g0010a0001c0001t0080g0023 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-17917G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722921 | ||||||
chr7:4723018
|
G | A | 4 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0142g0080others(1): Show | 4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-17820G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723018 | ||||||
chr7:4723025
|
T | C | 5 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(2): Show | 5 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-17813T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723025 | ||||||
chr7:4723027
|
A | G | 2 | a0001c0003t0087g0071a0001c0003t0139g0074 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.561-17811A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723027 | ||||||
chr7:4723223
|
G | A | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-17615G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723223 | ||||||
chr7:4723390
|
G | T | 3 | a0001c0003t0137g0287a0001c0004t0141g0247a0001c0011t0006g0281 | 3 | HG01496.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.561-17448G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723390 | ||||||
chr7:4723526
|
A | C | 258 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.561-17312A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723526 | ||||||
chr7:4723541
|
C | T | 1 | a0001c0004t0115g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.561-17297C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723541 | ||||||
chr7:4723568
|
C | A | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-17270C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723568 | ||||||
chr7:4723584
|
G | A | 1 | a0001c0007t0109g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.561-17254G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723584 | ||||||
chr7:4723594
|
C | T | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-17244C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723594 | ||||||
chr7:4723599
|
C | T | 2 | a0001c0001t0068g0010a0001c0001t0080g0023 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-17239C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723599 | ||||||
chr7:4723611
|
G | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-17227G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723611 | ||||||
chr7:4723863
|
A | G | 254 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(251): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.561-16975A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723863 | ||||||
chr7:4723884
|
C | T | 1 | a0001c0003t0132g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.561-16954C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723884 | ||||||
chr7:4723911
|
T | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-16927T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723911 | ||||||
chr7:4723988
|
CT | C | 25 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0018g0283others(22): Show | 25 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.561-16848delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4723988 | |||||
chr7:4724079
|
C | G | 5 | a0001c0002t0095g0207a0001c0003t0111g0059a0001c0003t0137g0287others(2): Show | 5 | HG01496.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-16759C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724079 | ||||||
chr7:4724114
|
C | T | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-16724C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724114 | ||||||
chr7:4724190
|
G | T | 198 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(195): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.561-16648G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724190 | ||||||
chr7:4724194
|
G | A | 9 | a0001c0001t0016g0241a0001c0001t0058g0251a0001c0003t0140g0003others(6): Show | 9 | HG02615.hp2 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-16644G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724194 | ||||||
chr7:4724230
|
C | T | 2 | a0001c0001t0068g0010a0001c0001t0080g0023 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-16608C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724230 | ||||||
chr7:4724283
|
T | C | 254 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(251): Show | 255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.561-16555T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724283 | ||||||
chr7:4724320
|
C | G | 1 | a0001c0002t0017g0286 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.561-16518C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724320 | ||||||
chr7:4724329
|
G | A | 183 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(180): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.561-16509G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724329 | ||||||
chr7:4724421
|
C | G | 2 | a0001c0003t0132g0160a0001c0003t0144g0142 | 2 | HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.561-16417C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724421 | ||||||
chr7:4724428
|
T | C | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-16410T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724428 | ||||||
chr7:4724475
|
C | T | 1 | a0001c0002t0018g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.561-16363C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724475 | ||||||
chr7:4724580
|
A | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-16258A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724580 | ||||||
chr7:4724582
|
CAG | C | 3 | a0001c0002t0003g0065a0001c0004t0046g0009a0001c0007t0006g0235 | 3 | HG02630.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.561-16255_561-1625 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724582 | ||||||
chr7:4724612
|
C | T | 56 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0062others(53): Show | 57 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-16226C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724612 | ||||||
chr7:4724613
|
G | A | 3 | a0001c0001t0001g0187a0001c0002t0017g0286a0001c0003t0039g0229 | 3 | HG02015.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-16225G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724613 | ||||||
chr7:4724627
|
C | T | 3 | a0001c0001t0001g0184a0001c0003t0120g0213a0001c0005t0069g0166 | 3 | HG00673.hp1 HG01981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.561-16211C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724627 | ||||||
chr7:4724628
|
G | A | 19 | a0001c0002t0018g0283a0001c0002t0041g0102a0001c0002t0057g0244others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.561-16210G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724628 | ||||||
chr7:4724663
|
C | G | 1 | a0001c0002t0003g0151 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.561-16175C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724663 | ||||||
chr7:4724691
|
C | A | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-16147C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724691 | ||||||
chr7:4724810
|
G | C | 1 | a0001c0004t0014g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.561-16028G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724810 | ||||||
chr7:4724831
|
T | C | 2 | a0001c0003t0019g0238a0001c0003t0026g0246 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.561-16007T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724831 | ||||||
chr7:4724835
|
T | C | 1 | a0001c0002t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.561-16003T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724835 | ||||||
chr7:4724859
|
C | T | 1 | a0001c0001t0023g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.561-15979C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724859 | ||||||
chr7:4725079
|
C | G | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-15759C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725079 | ||||||
chr7:4725136
|
T | G | 257 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(254): Show | 257 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.561-15702T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725136 | ||||||
chr7:4725137
|
C | T | 2 | a0001c0015t0091g0225a0001c0015t0094g0280 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.561-15701C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725137 | ||||||
chr7:4725140
|
G | A | 4 | a0001c0002t0017g0286a0001c0002t0095g0207a0001c0003t0039g0229others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-15698G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725140 | ||||||
chr7:4725191
|
G | A | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-15647G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725191 | ||||||
chr7:4725230
|
G | A | 165 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.561-15608G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725230 | ||||||
chr7:4725257
|
G | A | 58 | a0001c0002t0003g0065a0001c0002t0004g0067a0001c0002t0004g0126others(55): Show | 58 | HG01081.hp2 HG01109.hp1 HG01496.hp1 others(55): Show |
intron_variant | MODIFIER | c.561-15581G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725257 | ||||||
chr7:4725264
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.561-15574G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725264 | ||||||
chr7:4725272
|
C | G | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-15566C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725272 | ||||||
chr7:4725292
|
C | T | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-15546C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725292 | ||||||
chr7:4725347
|
G | T | 2 | a0001c0003t0036g0004a0001c0003t0047g0072 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.561-15491G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725347 | ||||||
chr7:4725387
|
A | G | 162 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(159): Show | 163 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.561-15451A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725387 | ||||||
chr7:4725387
|
A | T | 1 | a0001c0003t0120g0213 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.561-15451A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725387 | ||||||
chr7:4725460
|
G | T | 2 | a0001c0003t0015g0066a0001c0003t0015g0094 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.561-15378G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725460 | ||||||
chr7:4725616
|
C | T | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-15222C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725616 | ||||||
chr7:4725621
|
G | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0004t0009g0143 | 3 | NA18969.hp1 NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.561-15217G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725621 | ||||||
chr7:4725700
|
C | T | 1 | a0001c0002t0003g0111 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.561-15138C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725700 | ||||||
chr7:4725794
|
G | T | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-15044G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725794 | ||||||
chr7:4725858
|
G | A | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-14980G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725858 | ||||||
chr7:4725916
|
A | T | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-14922A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725916 | ||||||
chr7:4725938
|
G | A | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-14900G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725938 | ||||||
chr7:4726009
|
A | G | 5 | a0001c0002t0018g0283a0001c0003t0087g0071a0001c0003t0140g0003others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-14829A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726009 | ||||||
chr7:4726015
|
C | CT | 169 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(166): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.561-14810dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4726015 | |||||
chr7:4726015
|
C | T | 2 | a0001c0003t0130g0088a0001c0003t0131g0070 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.561-14823C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726015 | ||||||
chr7:4726015
|
CT | C | 6 | a0001c0003t0007g0250a0001c0003t0014g0081a0001c0003t0014g0236others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-14810delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4726015 | |||||
chr7:4726115
|
G | A | 2 | a0001c0004t0033g0027a0001c0004t0034g0028 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.561-14723G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726115 | ||||||
chr7:4726146
|
A | G | 19 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-14692A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726146 | ||||||
chr7:4726180
|
T | C | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-14658T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726180 | ||||||
chr7:4726293
|
C | T | 1 | a0001c0002t0013g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.561-14545C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726293 | ||||||
chr7:4726479
|
G | A | 1 | a0001c0027t0064g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.561-14359G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726479 | ||||||
chr7:4726621
|
C | CA | 24 | a0001c0001t0001g0034a0001c0001t0002g0025a0001c0001t0078g0019others(21): Show | 24 | HG00544.hp2 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.561-14204dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4726621 | |||||
chr7:4726752
|
A | T | 238 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(235): Show | 239 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.561-14086A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726752 | ||||||
chr7:4726764
|
G | A | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-14074G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726764 | ||||||
chr7:4726771
|
C | A | 1 | a0001c0001t0011g0040 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.561-14067C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726771 | ||||||
chr7:4727019
|
A | C | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-13819A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727019 | ||||||
chr7:4727045
|
A | G | 160 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(157): Show | 161 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.561-13793A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727045 | ||||||
chr7:4727207
|
C | G | 1 | a0001c0002t0004g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.561-13631C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727207 | ||||||
chr7:4727231
|
C | T | 1 | a0001c0004t0008g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.561-13607C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727231 | ||||||
chr7:4727292
|
T | C | 11 | a0001c0002t0041g0102a0001c0002t0057g0244a0001c0002t0088g0254others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.561-13546T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727292 | ||||||
chr7:4727412
|
T | G | 203 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(200): Show | 204 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.561-13426T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727412 | ||||||
chr7:4727481
|
A | T | 202 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(199): Show | 203 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.561-13357A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727481 | ||||||
chr7:4727511
|
C | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-13327C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727511 | ||||||
chr7:4727514
|
C | T | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-13324C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727514 | ||||||
chr7:4727609
|
C | T | 10 | a0001c0003t0007g0250a0001c0003t0014g0081a0001c0003t0014g0236others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-13229C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727609 | ||||||
chr7:4727610
|
G | A | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-13228G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727610 | ||||||
chr7:4727653
|
T | C | 1 | a0001c0004t0008g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.561-13185T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727653 | ||||||
chr7:4727658
|
C | T | 5 | a0001c0002t0017g0286a0001c0002t0095g0207a0001c0003t0039g0229others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-13180C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727658 | ||||||
chr7:4727663
|
G | C | 1 | a0001c0003t0111g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.561-13175G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727663 | ||||||
chr7:4727700
|
C | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-13138C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727700 | ||||||
chr7:4727869
|
G | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-12969G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727869 | ||||||
chr7:4728115
|
C | T | 1 | a0001c0001t0096g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561-12723C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728115 | ||||||
chr7:4728302
|
C | T | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-12536C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728302 | ||||||
chr7:4728359
|
G | C | 1 | a0001c0001t0058g0251 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.561-12479G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728359 | ||||||
chr7:4728374
|
C | T | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-12464C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728374 | ||||||
chr7:4728379
|
C | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-12459C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728379 | ||||||
chr7:4728407
|
T | C | 23 | a0001c0001t0024g0013a0001c0002t0002g0106a0001c0002t0005g0045others(20): Show | 23 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.561-12431T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728407 | ||||||
chr7:4728426
|
C | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-12412C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728426 | ||||||
chr7:4728458
|
C | A | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-12380C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728458 | ||||||
chr7:4728632
|
T | A | 1 | a0001c0002t0085g0103 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.561-12206T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728632 | ||||||
chr7:4728683
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.561-12155G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728683 | ||||||
chr7:4728730
|
G | GA | 208 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(205): Show | 209 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.561-12087dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4728730 | |||||
chr7:4728730
|
G | GAA | 7 | a0001c0001t0001g0161a0001c0001t0021g0219a0001c0001t0075g0128others(4): Show | 7 | HG01106.hp1 HG01258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-12088_561-1208 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4728730 | |||||
chr7:4728746
|
A | G | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-12092A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728746 | ||||||
chr7:4728748
|
A | AG | 7 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0105g0237others(4): Show | 7 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-12090_561-1208 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728748 | ||||||
chr7:4728772
|
T | C | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-12066T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728772 | ||||||
chr7:4728835
|
G | A | 16 | a0001c0001t0024g0013a0001c0002t0002g0106a0001c0002t0005g0045others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.561-12003G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728835 | ||||||
chr7:4728850
|
G | T | 1 | a0001c0001t0051g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.561-11988G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728850 | ||||||
chr7:4729010
|
C | T | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-11828C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729010 | ||||||
chr7:4729034
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.561-11804A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729034 | ||||||
chr7:4729183
|
G | A | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-11655G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729183 | ||||||
chr7:4729198
|
G | A | 2 | a0001c0002t0018g0283a0001c0003t0087g0071 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-11640G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729198 | ||||||
chr7:4729208
|
C | T | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-11630C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729208 | ||||||
chr7:4729359
|
C | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-11479C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729359 | ||||||
chr7:4729373
|
G | A | 2 | a0001c0002t0018g0283a0001c0003t0087g0071 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-11465G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729373 | ||||||
chr7:4729398
|
T | G | 246 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(243): Show | 247 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.561-11440T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729398 | ||||||
chr7:4729399
|
T | C | 242 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(239): Show | 243 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.561-11439T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729399 | ||||||
chr7:4729536
|
C | T | 161 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(158): Show | 162 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.561-11302C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729536 | ||||||
chr7:4729663
|
C | G | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-11175C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729663 | ||||||
chr7:4729712
|
G | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-11126G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729712 | ||||||
chr7:4729772
|
C | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-11066C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729772 | ||||||
chr7:4729835
|
C | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-11003C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729835 | ||||||
chr7:4729981
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0078g0019 | 2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.561-10857C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729981 | ||||||
chr7:4730150
|
A | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-10688A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730150 | ||||||
chr7:4730208
|
T | C | 2 | a0001c0002t0001g0131a0001c0002t0001g0132 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.561-10630T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730208 | ||||||
chr7:4730276
|
C | T | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-10562C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730276 | ||||||
chr7:4730443
|
C | T | 1 | a0001c0001t0066g0120 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.561-10395C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730443 | ||||||
chr7:4730508
|
G | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-10330G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730508 | ||||||
chr7:4730537
|
G | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-10301G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730537 | ||||||
chr7:4730567
|
C | G | 2 | a0001c0002t0025g0222a0001c0002t0025g0277 | 2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.561-10271C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730567 | ||||||
chr7:4730627
|
G | A | 1 | a0001c0007t0109g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.561-10211G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730627 | ||||||
chr7:4730644
|
G | A | 4 | a0001c0003t0019g0238a0001c0003t0026g0246a0001c0003t0142g0080others(1): Show | 4 | HG02622.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-10194G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730644 | ||||||
chr7:4730723
|
C | T | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-10115C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730723 | ||||||
chr7:4730900
|
C | T | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-9938C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730900 | ||||||
chr7:4730917
|
A | G | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-9921A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730917 | ||||||
chr7:4730932
|
C | T | 19 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-9906C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730932 | ||||||
chr7:4730947
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0021g0203a0001c0001t0021g0219 | 3 | NA18980.hp1 NA19060.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.561-9891C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730947 | ||||||
chr7:4731073
|
C | T | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-9765C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731073 | ||||||
chr7:4731124
|
C | T | 1 | a0001c0004t0009g0234 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.561-9714C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731124 | ||||||
chr7:4731140
|
T | C | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-9698T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731140 | ||||||
chr7:4731263
|
C | T | 7 | a0001c0002t0017g0286a0001c0003t0015g0066a0001c0003t0015g0094others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-9575C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731263 | ||||||
chr7:4731315
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0109 | 2 | HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.561-9523G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731315 | ||||||
chr7:4731384
|
A | G | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-9454A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731384 | ||||||
chr7:4731414
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.561-9424G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731414 | ||||||
chr7:4731589
|
A | G | 23 | a0001c0001t0058g0251a0001c0002t0002g0257a0001c0002t0005g0098others(20): Show | 23 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.561-9249A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731589 | ||||||
chr7:4731647
|
C | G | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-9191C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731647 | ||||||
chr7:4731746
|
G | A | 1 | a0001c0001t0077g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.561-9092G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731746 | ||||||
chr7:4731758
|
C | CA | 21 | a0001c0001t0003g0200a0001c0001t0021g0219a0001c0001t0060g0038others(18): Show | 21 | HG00735.hp2 HG02055.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.561-9061dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4731758 | |||||
chr7:4731758
|
CAA | C | 13 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0095g0207others(10): Show | 13 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.561-9062_561-9061d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4731758 | |||||
chr7:4731780
|
A | G | 10 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0002g0114others(7): Show | 10 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-9058A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731780 | ||||||
chr7:4731791
|
C | T | 3 | a0001c0002t0095g0207a0001c0003t0111g0059a0001c0003t0129g0279 | 3 | HG02818.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.561-9047C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731791 | ||||||
chr7:4731814
|
C | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-9024C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731814 | ||||||
chr7:4731904
|
C | T | 6 | a0001c0002t0017g0286a0001c0002t0105g0237a0001c0003t0039g0229others(3): Show | 6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-8934C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731904 | ||||||
chr7:4731950
|
C | T | 1 | a0001c0007t0006g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561-8888C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731950 | ||||||
chr7:4731958
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.561-8880G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731958 | ||||||
chr7:4732006
|
C | T | 5 | a0001c0002t0017g0286a0001c0002t0105g0237a0001c0003t0039g0229others(2): Show | 5 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-8832C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732006 | ||||||
chr7:4732015
|
T | C | 12 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0017g0286others(9): Show | 12 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-8823T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732015 | ||||||
chr7:4732071
|
G | A | 1 | a0001c0003t0130g0088 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.561-8767G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732071 | ||||||
chr7:4732154
|
C | T | 1 | a0001c0004t0133g0275 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.561-8684C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732154 | ||||||
chr7:4732188
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG00544.hp2 NA18944.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-8650G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732188 | ||||||
chr7:4732212
|
T | C | 4 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0142g0080others(1): Show | 4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-8626T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732212 | ||||||
chr7:4732233
|
C | G | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8605C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732233 | ||||||
chr7:4732234
|
T | C | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8604T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732234 | ||||||
chr7:4732235
|
G | A | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8603G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732235 | ||||||
chr7:4732236
|
A | C | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8602A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732236 | ||||||
chr7:4732238
|
T | C | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8600T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732238 | ||||||
chr7:4732239
|
A | C | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8599A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732239 | ||||||
chr7:4732240
|
T | A | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8598T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732240 | ||||||
chr7:4732244
|
C | T | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-8594C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732244 | ||||||
chr7:4732256
|
C | T | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-8582C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732256 | ||||||
chr7:4732330
|
A | G | 2 | a0001c0001t0068g0010a0001c0001t0080g0023 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-8508A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732330 | ||||||
chr7:4732347
|
T | G | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-8491T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732347 | ||||||
chr7:4732378
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.561-8460C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732378 | ||||||
chr7:4732379
|
G | A | 1 | a0001c0001t0090g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.561-8459G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732379 | ||||||
chr7:4732386
|
A | G | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-8452A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732386 | ||||||
chr7:4732441
|
C | T | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-8397C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732441 | ||||||
chr7:4732524
|
G | T | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-8314G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732524 | ||||||
chr7:4732594
|
G | A | 1 | a0001c0001t0035g0064 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.561-8244G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732594 | ||||||
chr7:4732606
|
C | T | 1 | a0001c0001t0073g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.561-8232C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732606 | ||||||
chr7:4732754
|
T | G | 1 | a0001c0001t0074g0016 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.561-8084T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732754 | ||||||
chr7:4732872
|
C | T | 7 | a0001c0002t0095g0207a0001c0003t0015g0066a0001c0003t0015g0094others(4): Show | 7 | HG02257.hp1 HG02818.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-7966C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732872 | ||||||
chr7:4732900
|
C | T | 1 | a0001c0002t0055g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.561-7938C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732900 | ||||||
chr7:4732917
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.561-7921G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732917 | ||||||
chr7:4733071
|
G | C | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7767G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733071 | ||||||
chr7:4733085
|
C | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7753C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733085 | ||||||
chr7:4733096
|
C | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7742C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733096 | ||||||
chr7:4733179
|
C | CT | 6 | a0001c0002t0018g0283a0001c0003t0087g0071a0001c0003t0120g0213others(3): Show | 6 | HG02622.hp2 NA18906.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-7648dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4733179 | |||||
chr7:4733190
|
T | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-7648T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733190 | ||||||
chr7:4733368
|
C | G | 2 | a0001c0003t0137g0287a0001c0011t0006g0281 | 2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-7470C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733368 | ||||||
chr7:4733386
|
G | A | 9 | a0001c0001t0001g0054a0001c0001t0001g0266a0001c0001t0001g0267others(6): Show | 9 | HG00140.hp2 HG01106.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-7452G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733386 | ||||||
chr7:4733520
|
C | G | 7 | a0001c0001t0001g0214a0001c0004t0009g0007a0001c0004t0009g0140others(4): Show | 7 | NA18962.hp2 NA18995.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-7318C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733520 | ||||||
chr7:4733722
|
C | G | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7116C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733722 | ||||||
chr7:4733723
|
G | T | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7115G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733723 | ||||||
chr7:4733775
|
C | G | 1 | a0001c0002t0088g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.561-7063C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733775 | ||||||
chr7:4733947
|
C | T | 1 | a0001c0003t0039g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.561-6891C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733947 | ||||||
chr7:4733971
|
G | GCTGGCCA others(16): Show |
13 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(10): Show | 13 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.561-6865_561-6843d others(25): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4733971 | |||||
chr7:4733979
|
C | T | 2 | a0001c0001t0001g0259a0001c0022t0070g0211 | 2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.561-6859C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733979 | ||||||
chr7:4734040
|
G | C | 1 | a0001c0001t0024g0013 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.561-6798G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734040 | ||||||
chr7:4734139
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.561-6699C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734139 | ||||||
chr7:4734390
|
G | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0205a0001c0001t0001g0220 | 3 | HG02129.hp2 NA18942.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.561-6448G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734390 | ||||||
chr7:4734469
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.561-6369T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734469 | ||||||
chr7:4734603
|
G | A | 32 | a0001c0002t0004g0067a0001c0002t0004g0068a0001c0002t0004g0126others(29): Show | 32 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.561-6235G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734603 | ||||||
chr7:4734619
|
G | C | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-6219G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734619 | ||||||
chr7:4734624
|
C | T | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-6214C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734624 | ||||||
chr7:4734625
|
A | G | 1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-6213A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734625 | ||||||
chr7:4734765
|
C | T | 1 | a0003c0014t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.561-6073C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734765 | ||||||
chr7:4734854
|
G | A | 4 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0142g0080others(1): Show | 4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-5984G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734854 | ||||||
chr7:4734972
|
A | T | 21 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0017g0286others(18): Show | 21 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.561-5866A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734972 | ||||||
chr7:4735373
|
C | T | 6 | a0001c0002t0017g0286a0001c0002t0105g0237a0001c0003t0039g0229others(3): Show | 6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-5465C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735373 | ||||||
chr7:4735418
|
G | A | 2 | a0001c0003t0015g0066a0001c0003t0015g0094 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.561-5420G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735418 | ||||||
chr7:4735511
|
C | G | 1 | a0001c0004t0043g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.561-5327C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735511 | ||||||
chr7:4735544
|
C | T | 2 | a0001c0003t0113g0276a0001c0003t0136g0210 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.561-5294C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735544 | ||||||
chr7:4735648
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.561-5190G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735648 | ||||||
chr7:4735735
|
C | T | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-5103C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735735 | ||||||
chr7:4735736
|
G | A | 1 | a0001c0004t0126g0196 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.561-5102G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735736 | ||||||
chr7:4735750
|
C | T | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-5088C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735750 | ||||||
chr7:4735766
|
C | T | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-5072C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735766 | ||||||
chr7:4735835
|
C | G | 1 | a0001c0007t0006g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561-5003C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735835 | ||||||
chr7:4735839
|
G | A | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-4999G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735839 | ||||||
chr7:4735844
|
T | C | 22 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0017g0286others(19): Show | 22 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.561-4994T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735844 | ||||||
chr7:4735860
|
A | G | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-4978A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735860 | ||||||
chr7:4735876
|
A | G | 238 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(235): Show | 239 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.561-4962A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735876 | ||||||
chr7:4736414
|
G | GT | 18 | a0001c0001t0002g0230a0001c0001t0050g0137a0001c0001t0060g0038others(15): Show | 18 | HG01081.hp1 HG01175.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.561-4408dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4736414 | |||||
chr7:4736414
|
G | T | 10 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-4424G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736414 | ||||||
chr7:4736767
|
A | G | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-4071A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736767 | ||||||
chr7:4736849
|
G | T | 19 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-3989G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736849 | ||||||
chr7:4736916
|
A | G | 234 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(231): Show | 235 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.561-3922A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736916 | ||||||
chr7:4737425
|
GGTGTGTG others(7): Show |
G | 4 | a0001c0002t0095g0207a0001c0003t0111g0059a0001c0003t0129g0279others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-3402_561-3389d others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737425 | |||||
chr7:4737439
|
CGT | C | 66 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0054others(63): Show | 66 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.561-3391_561-3390d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737439 | |||||
chr7:4737447
|
T | C | 1 | a0001c0004t0029g0119 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.561-3391T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737447 | ||||||
chr7:4737462
|
ATG | A | 5 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-3365_561-3364d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737462 | |||||
chr7:4737471
|
T | C | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.561-3367T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737471 | ||||||
chr7:4737475
|
C | T | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-3363C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737475 | ||||||
chr7:4737484
|
G | A | 1 | a0001c0010t0110g0274 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.561-3354G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737484 | ||||||
chr7:4737530
|
A | G | 242 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(239): Show | 243 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.561-3308A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737530 | ||||||
chr7:4737540
|
G | A | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-3298G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737540 | ||||||
chr7:4737551
|
C | CGTGTGTG others(3): Show |
2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-3287_561-3286i others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737551 | ||||||
chr7:4737551
|
C | CGTGTGTG others(17): Show |
2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-3287_561-3286i others(26): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737551 | ||||||
chr7:4737552
|
C | CTG | 15 | a0001c0001t0002g0101a0001c0001t0090g0201a0001c0002t0001g0215others(12): Show | 15 | HG02055.hp2 HG02056.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.561-3265_561-3264d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | |||||
chr7:4737552
|
C | CTGTG | 181 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(178): Show | 182 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.561-3267_561-3264d others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | |||||
chr7:4737552
|
C | CTGTGTG | 13 | a0001c0001t0001g0192a0001c0001t0001g0265a0001c0001t0002g0230others(10): Show | 13 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.561-3269_561-3264d others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | |||||
chr7:4737552
|
C | CTGTGTGT others(1): Show |
6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-3271_561-3264d others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | |||||
chr7:4737552
|
C | CTGTGTGT others(3): Show |
2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-3273_561-3264d others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | |||||
chr7:4737552
|
C | CTGTGTGT others(5): Show |
3 | a0001c0003t0137g0287a0001c0003t0139g0074a0001c0011t0006g0281 | 3 | HG01496.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.561-3275_561-3264d others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | |||||
chr7:4737552
|
C | CTGTGTGT others(9): Show |
1 | a0001c0002t0105g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-3279_561-3264d others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | |||||
chr7:4737552
|
C | G | 4 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0142g0080others(1): Show | 4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-3286C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737552 | ||||||
chr7:4737569
|
T | TGTGTGTG others(3): Show |
10 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0002g0114others(7): Show | 10 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-3264_561-3263i others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737569 | |||||
chr7:4737573
|
T | TGTGTGTG others(9): Show |
1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-3264_561-3263i others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737573 | |||||
chr7:4737581
|
T | G | 1 | a0001c0001t0012g0005 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.561-3257T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737581 | ||||||
chr7:4737624
|
G | A | 1 | a0001c0003t0146g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.561-3214G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737624 | ||||||
chr7:4737808
|
A | T | 21 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0017g0286others(18): Show | 21 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.561-3030A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737808 | ||||||
chr7:4737861
|
G | A | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-2977G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737861 | ||||||
chr7:4737999
|
G | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-2839G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737999 | ||||||
chr7:4738130
|
GAA | G | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-2694_561-2693d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738130 | |||||
chr7:4738133
|
A | G | 6 | a0001c0002t0017g0286a0001c0002t0105g0237a0001c0003t0039g0229others(3): Show | 6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-2705A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738133 | ||||||
chr7:4738225
|
T | C | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-2613T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738225 | ||||||
chr7:4738246
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0075g0128 | 2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.561-2592G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738246 | ||||||
chr7:4738265
|
C | T | 10 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0002g0114others(7): Show | 10 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-2573C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738265 | ||||||
chr7:4738295
|
G | A | 42 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0135others(39): Show | 43 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.561-2543G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738295 | ||||||
chr7:4738322
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.561-2516A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738322 | ||||||
chr7:4738393
|
C | T | 1 | a0001c0004t0014g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.561-2445C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738393 | ||||||
chr7:4738436
|
CA | C | 16 | a0001c0001t0001g0118a0001c0002t0001g0215a0001c0002t0005g0198others(13): Show | 16 | HG00408.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.561-2388delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738436 | |||||
chr7:4738436
|
CAA | C | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-2389_561-2388d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738436 | |||||
chr7:4738664
|
C | T | 10 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0015g0066others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-2174C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738664 | ||||||
chr7:4738665
|
G | A | 1 | a0001c0001t0090g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.561-2173G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738665 | ||||||
chr7:4738949
|
G | GGGAAGAA others(3): Show |
3 | a0001c0003t0019g0238a0001c0003t0026g0246a0001c0003t0135g0255 | 3 | HG02622.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.561-1887_561-1878d others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738949 | |||||
chr7:4739416
|
T | C | 3 | a0001c0001t0058g0251a0001c0002t0095g0207a0001c0003t0111g0059 | 3 | HG02723.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-1422T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739416 | ||||||
chr7:4739420
|
TTTG | T | 7 | a0001c0002t0018g0283a0001c0003t0087g0071a0001c0006t0052g0078others(4): Show | 7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-1415_561-1413d others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4739420 | |||||
chr7:4739484
|
A | G | 3 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231 | 3 | HG02717.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.561-1354A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739484 | ||||||
chr7:4739652
|
G | C | 1 | a0001c0010t0002g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.561-1186G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739652 | ||||||
chr7:4739700
|
T | A | 19 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-1138T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739700 | ||||||
chr7:4739833
|
C | T | 1 | a0001c0002t0004g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.561-1005C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739833 | ||||||
chr7:4739980
|
T | C | 18 | a0001c0002t0017g0286a0001c0002t0018g0283a0001c0002t0095g0207others(15): Show | 18 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-858T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739980 | ||||||
chr7:4739987
|
TCA | T | 9 | a0001c0003t0007g0250a0001c0003t0014g0081a0001c0003t0014g0236others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-844_561-843del others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4739987 | |||||
chr7:4740043
|
C | G | 1 | a0001c0001t0073g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.561-795C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740043 | ||||||
chr7:4740059
|
C | T | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-779C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740059 | ||||||
chr7:4740168
|
C | T | 1 | a0001c0003t0112g0006 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.561-670C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740168 | ||||||
chr7:4740169
|
G | T | 12 | a0001c0002t0018g0283a0001c0002t0095g0207a0001c0003t0087g0071others(9): Show | 12 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-669G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740169 | ||||||
chr7:4740251
|
A | G | 6 | a0001c0002t0017g0286a0001c0002t0105g0237a0001c0003t0039g0229others(3): Show | 6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-587A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740251 | ||||||
chr7:4740262
|
C | G | 1 | a0001c0003t0140g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.561-576C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740262 | ||||||
chr7:4740274
|
T | C | 28 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0017g0286others(25): Show | 28 | HG01081.hp1 HG01081.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.561-564T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740274 | ||||||
chr7:4740292
|
T | C | 4 | a0001c0004t0007g0263a0001c0007t0006g0084a0001c0007t0006g0085others(1): Show | 4 | HG02145.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-546T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740292 | ||||||
chr7:4740322
|
C | T | 5 | a0001c0002t0017g0286a0001c0002t0105g0237a0001c0003t0039g0229others(2): Show | 5 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-516C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740322 | ||||||
chr7:4740371
|
A | G | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-467A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740371 | ||||||
chr7:4740388
|
T | C | 1 | a0001c0003t0031g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.561-450T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740388 | ||||||
chr7:4740390
|
C | A | 1 | a0001c0003t0031g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.561-448C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740390 | ||||||
chr7:4740408
|
C | T | 10 | a0001c0002t0018g0283a0001c0002t0095g0207a0001c0003t0087g0071others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-430C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740408 | ||||||
chr7:4740413
|
G | A | 8 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(5): Show | 8 | HG02109.hp1 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-425G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740413 | ||||||
chr7:4740438
|
A | T | 17 | a0001c0002t0018g0283a0001c0002t0095g0207a0001c0003t0015g0066others(14): Show | 17 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.561-400A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740438 | ||||||
chr7:4740483
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.561-355C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740483 | ||||||
chr7:4740484
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.561-354G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740484 | ||||||
chr7:4740572
|
T | A | 2 | a0001c0004t0009g0234a0001c0004t0029g0119 | 2 | NA18962.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.561-266T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740572 | ||||||
chr7:4740583
|
C | T | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-255C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740583 | ||||||
chr7:4740592
|
C | CAG | 28 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0002t0017g0286others(25): Show | 28 | HG01081.hp1 HG01081.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.561-245_561-244dup others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4740592 | |||||
chr7:4740596
|
G | A | 3 | a0001c0002t0003g0065a0001c0004t0046g0009a0001c0007t0006g0235 | 3 | HG02630.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.561-242G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740596 | ||||||
chr7:4740643
|
A | C | 1 | a0001c0011t0006g0082 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561-195A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740643 | ||||||
chr7:4740807
|
C | T | 1 | a0001c0002t0002g0148 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.561-31C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740807 | ||||||
chr7:4740819
|
GCTC | G | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.561-10_561-8delCCT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4740819 | |||||
chr7:4741036
|
C | G | 1 | a0001c0002t0004g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.746+13C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741036 | ||||||
chr7:4741100
|
C | T | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.746+77C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741100 | ||||||
chr7:4741301
|
T | C | 1 | a0001c0002t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.746+278T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741301 | ||||||
chr7:4741312
|
G | A | 231 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(228): Show | 232 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.746+289G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741312 | ||||||
chr7:4741323
|
GT | G | 43 | a0001c0002t0004g0067a0001c0002t0004g0068a0001c0002t0004g0126others(40): Show | 43 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.746+310delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4741323 | |||||
chr7:4741330
|
T | G | 173 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(170): Show | 174 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.746+307T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741330 | ||||||
chr7:4741389
|
C | T | 6 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0031g0171others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.746+366C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741389 | ||||||
chr7:4741485
|
C | G | 3 | a0001c0002t0105g0237a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+462C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741485 | ||||||
chr7:4741532
|
T | C | 14 | a0001c0001t0058g0251a0001c0002t0017g0286a0001c0002t0018g0283others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.746+509T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741532 | ||||||
chr7:4741561
|
C | T | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+538C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741561 | ||||||
chr7:4741580
|
C | T | 2 | a0001c0002t0025g0222a0001c0002t0025g0277 | 2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.746+557C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741580 | ||||||
chr7:4741622
|
C | T | 5 | a0001c0001t0016g0241a0001c0004t0014g0256a0002c0012t0016g0291others(2): Show | 5 | HG01109.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+599C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741622 | ||||||
chr7:4741734
|
A | G | 1 | a0001c0003t0140g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.746+711A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741734 | ||||||
chr7:4741846
|
G | A | 1 | a0001c0003t0129g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.746+823G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741846 | ||||||
chr7:4741928
|
T | G | 1 | a0001c0002t0001g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.746+905T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741928 | ||||||
chr7:4742003
|
C | T | 4 | a0001c0003t0019g0238a0001c0003t0026g0246a0001c0003t0137g0287others(1): Show | 4 | HG01496.hp2 HG02622.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+980C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742003 | ||||||
chr7:4742010
|
T | G | 3 | a0001c0002t0105g0237a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+987T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742010 | ||||||
chr7:4742045
|
C | T | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.746+1022C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742045 | ||||||
chr7:4742056
|
C | T | 1 | a0001c0004t0008g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.746+1033C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742056 | ||||||
chr7:4742073
|
C | T | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.746+1050C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742073 | ||||||
chr7:4742074
|
G | A | 2 | a0001c0002t0017g0286a0001c0003t0039g0229 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.746+1051G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742074 | ||||||
chr7:4742298
|
G | A | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.746+1275G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742298 | ||||||
chr7:4742340
|
C | T | 2 | a0001c0003t0015g0066a0001c0003t0015g0094 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.746+1317C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742340 | ||||||
chr7:4742455
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.746+1432C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742455 | ||||||
chr7:4742536
|
C | T | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+1513C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742536 | ||||||
chr7:4742600
|
A | G | 1 | a0001c0002t0005g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.746+1577A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742600 | ||||||
chr7:4742659
|
C | T | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.746+1636C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742659 | ||||||
chr7:4742722
|
A | G | 1 | a0001c0001t0079g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.746+1699A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742722 | ||||||
chr7:4742916
|
G | A | 1 | a0001c0008t0118g0095 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.746+1893G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742916 | ||||||
chr7:4742965
|
A | C | 11 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0015g0066others(8): Show | 11 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.746+1942A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742965 | ||||||
chr7:4742984
|
C | T | 10 | a0001c0002t0002g0257a0001c0002t0005g0098a0001c0003t0015g0066others(7): Show | 10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+1961C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742984 | ||||||
chr7:4743012
|
C | T | 1 | a0001c0003t0111g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.746+1989C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743012 | ||||||
chr7:4743292
|
C | G | 1 | a0001c0003t0104g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.746+2269C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743292 | ||||||
chr7:4743443
|
G | A | 9 | a0001c0003t0007g0250a0001c0003t0014g0081a0001c0003t0014g0236others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.746+2420G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743443 | ||||||
chr7:4743486
|
G | T | 4 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0113g0276others(1): Show | 4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+2463G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743486 | ||||||
chr7:4743512
|
T | G | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.746+2489T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743512 | ||||||
chr7:4743575
|
T | G | 231 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(228): Show | 232 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.746+2552T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743575 | ||||||
chr7:4743593
|
A | G | 164 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(161): Show | 165 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.746+2570A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743593 | ||||||
chr7:4743622
|
T | G | 1 | a0002c0013t0026g0288 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.746+2599T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743622 | ||||||
chr7:4743677
|
A | G | 7 | a0001c0002t0018g0283a0001c0003t0087g0071a0001c0006t0052g0078others(4): Show | 7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.746+2654A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743677 | ||||||
chr7:4743822
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0109 | 2 | HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.746+2799C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743822 | ||||||
chr7:4743823
|
G | A | 3 | a0001c0002t0105g0237a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+2800G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743823 | ||||||
chr7:4743878
|
G | GC | 4 | a0001c0001t0068g0010a0001c0001t0080g0023a0001c0027t0064g0217others(1): Show | 4 | HG00323.hp2 HG00621.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+2856dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4743878 | |||||
chr7:4743879
|
CT | C | 15 | a0001c0001t0001g0118a0001c0001t0001g0189a0001c0001t0016g0241others(12): Show | 15 | HG01070.hp1 HG01081.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.746+2871delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4743879 | |||||
chr7:4743880
|
T | C | 167 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(164): Show | 168 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.746+2857T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743880 | ||||||
chr7:4743881
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0189a0001c0001t0016g0241others(1): Show | 4 | HG01256.hp2 HG02965.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+2858T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743881 | ||||||
chr7:4743915
|
C | T | 1 | a0001c0021t0027g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.746+2892C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743915 | ||||||
chr7:4744038
|
G | A | 1 | a0001c0001t0020g0110 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.746+3015G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744038 | ||||||
chr7:4744079
|
G | T | 1 | a0002c0013t0026g0288 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.746+3056G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744079 | ||||||
chr7:4744092
|
G | C | 181 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(178): Show | 182 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.746+3069G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744092 | ||||||
chr7:4744135
|
A | G | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.746+3112A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744135 | ||||||
chr7:4744177
|
G | GTT | 13 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0002t0095g0207others(10): Show | 13 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.746+3154_746+3155i others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744177 | ||||||
chr7:4744196
|
T | C | 1 | a0001c0001t0024g0013 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.746+3173T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744196 | ||||||
chr7:4744231
|
T | C | 1 | a0001c0002t0057g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.746+3208T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744231 | ||||||
chr7:4744307
|
C | T | 9 | a0001c0003t0007g0250a0001c0003t0014g0081a0001c0003t0014g0236others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.746+3284C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744307 | ||||||
chr7:4744408
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.746+3385G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744408 | ||||||
chr7:4744600
|
G | C | 1 | a0001c0003t0010g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.746+3577G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744600 | ||||||
chr7:4744609
|
G | A | 1 | a0001c0008t0122g0272 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.746+3586G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744609 | ||||||
chr7:4744779
|
C | A | 3 | a0001c0002t0105g0237a0001c0003t0142g0080a0001c0003t0143g0079 | 3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+3756C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744779 | ||||||
chr7:4744999
|
C | T | 3 | a0001c0002t0017g0286a0001c0003t0039g0229a0001c0003t0129g0279 | 3 | HG02647.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.746+3976C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744999 | ||||||
chr7:4745021
|
T | C | 181 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(178): Show | 182 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.746+3998T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745021 | ||||||
chr7:4745135
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.746+4112G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745135 | ||||||
chr7:4745185
|
A | G | 184 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(181): Show | 185 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.746+4162A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745185 | ||||||
chr7:4745246
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0109 | 2 | HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.746+4223C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745246 | ||||||
chr7:4745378
|
G | A | 126 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0034others(123): Show | 126 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.746+4355G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745378 | ||||||
chr7:4745392
|
C | T | 119 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0034others(116): Show | 119 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.746+4369C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745392 | ||||||
chr7:4745472
|
T | TTG | 168 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(165): Show | 169 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.746+4465_746+4466d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4745472 | |||||
chr7:4745498
|
T | G | 183 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(180): Show | 184 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.746+4475T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745498 | ||||||
chr7:4745600
|
T | A | 4 | a0001c0002t0041g0102a0001c0002t0057g0244a0001c0003t0037g0284others(1): Show | 4 | HG01496.hp1 HG02055.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+4577T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745600 | ||||||
chr7:4745655
|
G | T | 1 | a0001c0002t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.746+4632G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745655 | ||||||
chr7:4745731
|
C | G | 1 | a0001c0003t0139g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.746+4708C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745731 | ||||||
chr7:4745756
|
G | T | 188 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(185): Show | 189 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.746+4733G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745756 | ||||||
chr7:4745773
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.746+4750C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745773 | ||||||
chr7:4745884
|
C | CA | 184 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(181): Show | 185 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.746+4871dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4745884 | |||||
chr7:4745899
|
T | C | 10 | a0001c0001t0058g0251a0001c0002t0018g0283a0001c0002t0095g0207others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.746+4876T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745899 | ||||||
chr7:4746129
|
C | T | 2 | a0001c0003t0015g0066a0001c0003t0015g0094 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.746+5106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746129 | ||||||
chr7:4746146
|
C | T | 1 | a0001c0003t0087g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.746+5123C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746146 | ||||||
chr7:4746152
|
A | G | 1 | a0001c0003t0135g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.746+5129A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746152 | ||||||
chr7:4746249
|
C | T | 1 | a0001c0002t0005g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.746+5226C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746249 | ||||||
chr7:4746430
|
C | T | 2 | a0001c0002t0095g0207a0001c0003t0111g0059 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.746+5407C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746430 | ||||||
chr7:4746439
|
G | A | 1 | a0001c0005t0001g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.746+5416G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746439 | ||||||
chr7:4746494
|
G | A | 252 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0034others(249): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.746+5471G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746494 | ||||||
chr7:4746503
|
G | C | 5 | a0001c0001t0058g0251a0001c0002t0041g0102a0001c0002t0057g0244others(2): Show | 5 | HG01496.hp1 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+5480G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746503 | ||||||
chr7:4746537
|
A | C | 1 | a0001c0003t0138g0262 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.746+5514A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746537 | ||||||
chr7:4747078
|
G | A | 4 | a0001c0002t0001g0130a0001c0002t0001g0157a0001c0017t0027g0105others(1): Show | 4 | HG00140.hp1 HG00639.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+6055G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747078 | ||||||
chr7:4747132
|
G | A | 1 | a0001c0001t0097g0052 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.746+6109G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747132 | ||||||
chr7:4747170
|
G | A | 1 | a0001c0003t0019g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.746+6147G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747170 | ||||||
chr7:4747241
|
C | T | 10 | a0001c0001t0001g0202a0001c0001t0024g0013a0001c0001t0075g0128others(7): Show | 10 | HG01074.hp1 HG01109.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+6218C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747241 | ||||||
chr7:4747252
|
C | T | 7 | a0001c0001t0096g0093a0001c0002t0018g0283a0001c0003t0037g0284others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.746+6229C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747252 | ||||||
chr7:4747253
|
G | A | 2 | a0001c0002t0041g0102a0001c0003t0129g0279 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.746+6230G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747253 | ||||||
chr7:4747268
|
C | T | 1 | a0001c0001t0063g0258 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.746+6245C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747268 | ||||||
chr7:4747333
|
C | T | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.746+6310C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747333 | ||||||
chr7:4747356
|
G | A | 1 | a0001c0007t0006g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.746+6333G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747356 | ||||||
chr7:4747368
|
A | G | 25 | a0001c0002t0004g0068a0001c0002t0004g0126a0001c0002t0019g0125others(22): Show | 25 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.746+6345A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747368 | ||||||
chr7:4747378
|
G | A | 16 | a0001c0001t0058g0251a0001c0001t0096g0093a0001c0002t0004g0068others(13): Show | 16 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+6355G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747378 | ||||||
chr7:4747387
|
A | G | 1 | a0001c0002t0088g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.746+6364A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747387 | ||||||
chr7:4747461
|
A | G | 104 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0035others(101): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.746+6438A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747461 | ||||||
chr7:4747629
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.746+6606G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747629 | ||||||
chr7:4747729
|
T | G | 1 | a0001c0002t0001g0043 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.746+6706T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747729 | ||||||
chr7:4747752
|
A | G | 3 | a0001c0009t0030g0169a0001c0009t0030g0170a0001c0009t0119g0141 | 3 | NA18969.hp2 NA19066.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.747-6707A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747752 | ||||||
chr7:4747779
|
C | T | 1 | a0001c0001t0012g0005 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.747-6680C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747779 | ||||||
chr7:4747799
|
A | C | 14 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(11): Show | 14 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.747-6660A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747799 | ||||||
chr7:4747877
|
G | A | 5 | a0001c0003t0031g0155a0001c0003t0031g0171a0001c0003t0132g0160others(2): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-6582G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747877 | ||||||
chr7:4747906
|
T | TC | 6 | a0001c0007t0006g0235a0001c0007t0109g0073a0001c0011t0006g0082others(3): Show | 6 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-6551dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4747906 | |||||
chr7:4747912
|
C | T | 5 | a0001c0003t0031g0155a0001c0003t0031g0171a0001c0003t0132g0160others(2): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-6547C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747912 | ||||||
chr7:4747919
|
C | A | 2 | a0001c0003t0039g0229a0001c0003t0112g0006 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.747-6540C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747919 | ||||||
chr7:4747930
|
C | G | 15 | a0001c0002t0003g0065a0001c0003t0019g0238a0001c0003t0031g0155others(12): Show | 15 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.747-6529C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747930 | ||||||
chr7:4747938
|
G | A | 9 | a0001c0001t0062g0186a0001c0003t0007g0090a0001c0003t0007g0226others(6): Show | 9 | HG02717.hp1 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.747-6521G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747938 | ||||||
chr7:4747949
|
G | A | 2 | a0001c0001t0005g0191a0001c0001t0076g0026 | 2 | HG00558.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.747-6510G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747949 | ||||||
chr7:4747981
|
A | G | 218 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0037others(215): Show | 219 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.747-6478A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747981 | ||||||
chr7:4748030
|
G | A | 7 | a0001c0001t0001g0017a0001c0007t0006g0235a0001c0007t0109g0073others(4): Show | 7 | HG00621.hp1 HG01081.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-6429G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748030 | ||||||
chr7:4748078
|
G | A | 15 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(12): Show | 15 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.747-6381G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748078 | ||||||
chr7:4748124
|
G | C | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.747-6335G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748124 | ||||||
chr7:4748130
|
G | A | 2 | a0001c0003t0099g0282a0001c0017t0027g0105 | 2 | HG01258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.747-6329G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748130 | ||||||
chr7:4748136
|
ACTAT | A | 9 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(6): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-6310_747-6307d others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4748136 | |||||
chr7:4748222
|
C | A | 3 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075 | 3 | HG02486.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.747-6237C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748222 | ||||||
chr7:4748252
|
C | T | 1 | a0001c0002t0003g0055 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.747-6207C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748252 | ||||||
chr7:4748284
|
C | T | 5 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0130g0088others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-6175C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748284 | ||||||
chr7:4748285
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.747-6174G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748285 | ||||||
chr7:4748466
|
G | A | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.747-5993G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748466 | ||||||
chr7:4748479
|
C | G | 1 | a0001c0003t0026g0246 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747-5980C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748479 | ||||||
chr7:4748584
|
C | T | 9 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(6): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-5875C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748584 | ||||||
chr7:4748680
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG00544.hp2 HG02074.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-5779G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748680 | ||||||
chr7:4748744
|
TCA | T | 5 | a0001c0003t0031g0155a0001c0003t0031g0171a0001c0003t0132g0160others(2): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-5713_747-5712d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4748744 | |||||
chr7:4748878
|
C | T | 8 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-5581C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748878 | ||||||
chr7:4748920
|
C | T | 4 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0004t0046g0009others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-5539C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748920 | ||||||
chr7:4749019
|
G | A | 1 | a0001c0003t0019g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.747-5440G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749019 | ||||||
chr7:4749204
|
T | G | 5 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-5255T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749204 | ||||||
chr7:4749255
|
A | C | 2 | a0001c0003t0039g0229a0001c0003t0112g0006 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.747-5204A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749255 | ||||||
chr7:4749255
|
A | G | 184 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0054others(181): Show | 185 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.747-5204A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749255 | ||||||
chr7:4749259
|
C | T | 9 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(6): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-5200C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749259 | ||||||
chr7:4749510
|
G | A | 34 | a0001c0003t0123g0197a0001c0003t0139g0074a0001c0003t0140g0003others(31): Show | 35 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.747-4949G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749510 | ||||||
chr7:4749555
|
C | T | 12 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(9): Show | 12 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.747-4904C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749555 | ||||||
chr7:4749669
|
G | A | 1 | a0001c0003t0112g0006 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747-4790G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749669 | ||||||
chr7:4749734
|
T | A | 9 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(6): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-4725T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749734 | ||||||
chr7:4749746
|
T | C | 2 | a0001c0004t0033g0027a0001c0004t0034g0028 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.747-4713T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749746 | ||||||
chr7:4749756
|
G | A | 1 | a0001c0003t0047g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.747-4703G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749756 | ||||||
chr7:4749849
|
T | G | 14 | a0001c0002t0105g0237a0001c0003t0010g0077a0001c0003t0010g0100others(11): Show | 14 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.747-4610T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749849 | ||||||
chr7:4749862
|
G | A | 13 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0031g0155others(10): Show | 13 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.747-4597G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749862 | ||||||
chr7:4749890
|
G | A | 44 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(41): Show | 44 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.747-4569G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749890 | ||||||
chr7:4749894
|
T | C | 77 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(74): Show | 78 | HG00597.hp1 HG01081.hp2 HG01258.hp2 others(75): Show |
intron_variant | MODIFIER | c.747-4565T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749894 | ||||||
chr7:4749900
|
T | C | 4 | a0001c0006t0092g0002a0001c0006t0093g0002a0001c0015t0091g0225others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-4559T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749900 | ||||||
chr7:4749910
|
C | A | 5 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-4549C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749910 | ||||||
chr7:4749911
|
G | A | 1 | a0001c0004t0126g0196 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.747-4548G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749911 | ||||||
chr7:4749914
|
C | T | 1 | a0001c0001t0072g0015 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.747-4545C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749914 | ||||||
chr7:4749928
|
C | T | 11 | a0001c0002t0004g0067a0001c0002t0004g0126a0001c0002t0004g0227others(8): Show | 11 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.747-4531C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749928 | ||||||
chr7:4750004
|
C | T | 5 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-4455C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750004 | ||||||
chr7:4750045
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0002g0053 | 2 | HG02083.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.747-4414C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750045 | ||||||
chr7:4750055
|
G | A | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.747-4404G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750055 | ||||||
chr7:4750213
|
G | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.747-4246G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750213 | ||||||
chr7:4750218
|
G | A | 1 | a0001c0003t0137g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.747-4241G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750218 | ||||||
chr7:4750253
|
A | T | 4 | a0001c0006t0092g0002a0001c0006t0093g0002a0001c0015t0091g0225others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-4206A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750253 | ||||||
chr7:4750258
|
T | C | 103 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(100): Show | 104 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.747-4201T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750258 | ||||||
chr7:4750292
|
G | T | 5 | a0001c0003t0039g0229a0001c0003t0112g0006a0001c0003t0113g0276others(2): Show | 5 | HG00738.hp2 HG01891.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-4167G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750292 | ||||||
chr7:4750296
|
G | C | 5 | a0001c0002t0001g0260a0001c0002t0003g0055a0001c0002t0025g0222others(2): Show | 5 | HG00735.hp2 HG01099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-4163G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750296 | ||||||
chr7:4750403
|
G | A | 4 | a0001c0006t0092g0002a0001c0006t0093g0002a0001c0015t0091g0225others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-4056G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750403 | ||||||
chr7:4750431
|
C | T | 23 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(20): Show | 23 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.747-4028C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750431 | ||||||
chr7:4750445
|
C | G | 1 | a0001c0001t0062g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.747-4014C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750445 | ||||||
chr7:4750474
|
G | A | 4 | a0001c0006t0092g0002a0001c0006t0093g0002a0001c0015t0091g0225others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-3985G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750474 | ||||||
chr7:4750477
|
C | G | 5 | a0001c0003t0031g0155a0001c0003t0031g0171a0001c0003t0132g0160others(2): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-3982C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750477 | ||||||
chr7:4750592
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.747-3867G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750592 | ||||||
chr7:4750650
|
G | A | 1 | a0001c0003t0111g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.747-3809G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750650 | ||||||
chr7:4750710
|
CT | C | 48 | a0001c0001t0001g0205a0001c0003t0007g0090a0001c0003t0007g0226others(45): Show | 48 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.747-3738delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4750710 | |||||
chr7:4750745
|
T | C | 46 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(43): Show | 46 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.747-3714T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750745 | ||||||
chr7:4750890
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.747-3569G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750890 | ||||||
chr7:4750985
|
G | A | 5 | a0001c0002t0001g0260a0001c0002t0003g0055a0001c0002t0025g0222others(2): Show | 5 | HG00735.hp2 HG01099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-3474G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750985 | ||||||
chr7:4751012
|
C | CT | 15 | a0001c0001t0001g0017a0001c0001t0001g0259a0001c0001t0002g0114others(12): Show | 15 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.747-3427dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4751012 | |||||
chr7:4751012
|
CT | C | 21 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0019g0238others(18): Show | 21 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.747-3427delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4751012 | |||||
chr7:4751014
|
T | TC | 44 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(41): Show | 44 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.747-3445_747-3444i others(3): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751014 | ||||||
chr7:4751076
|
G | A | 3 | a0001c0001t0051g0051a0001c0001t0084g0232a0001c0001t0086g0181 | 3 | HG02080.hp2 HG02155.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.747-3383G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751076 | ||||||
chr7:4751207
|
G | A | 4 | a0001c0006t0092g0002a0001c0006t0093g0002a0001c0015t0091g0225others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-3252G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751207 | ||||||
chr7:4751263
|
C | T | 32 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(29): Show | 32 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.747-3196C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751263 | ||||||
chr7:4751300
|
A | G | 10 | a0001c0001t0002g0049a0001c0001t0013g0041a0001c0001t0065g0011others(7): Show | 10 | HG00323.hp1 HG01071.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.747-3159A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751300 | ||||||
chr7:4751340
|
C | T | 4 | a0001c0006t0092g0002a0001c0006t0093g0002a0001c0015t0091g0225others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-3119C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751340 | ||||||
chr7:4751347
|
G | C | 3 | a0001c0003t0019g0238a0001c0003t0037g0284a0001c0003t0038g0208 | 3 | HG02622.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.747-3112G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751347 | ||||||
chr7:4751373
|
T | C | 5 | a0001c0003t0031g0155a0001c0003t0031g0171a0001c0003t0132g0160others(2): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-3086T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751373 | ||||||
chr7:4751388
|
C | T | 1 | a0002c0012t0016g0291 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.747-3071C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751388 | ||||||
chr7:4751400
|
A | G | 1 | a0001c0002t0088g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-3059A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751400 | ||||||
chr7:4751427
|
T | C | 291 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(288): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.747-3032T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751427 | ||||||
chr7:4751624
|
C | T | 1 | a0001c0004t0008g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.747-2835C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751624 | ||||||
chr7:4751644
|
G | A | 5 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-2815G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751644 | ||||||
chr7:4751702
|
A | C | 2 | a0001c0001t0058g0251a0001c0002t0057g0244 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.747-2757A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751702 | ||||||
chr7:4751718
|
G | A | 7 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(4): Show | 7 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-2741G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751718 | ||||||
chr7:4751760
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.747-2699G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751760 | ||||||
chr7:4751761
|
C | G | 37 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(34): Show | 37 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.747-2698C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751761 | ||||||
chr7:4751765
|
C | T | 1 | a0001c0001t0086g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.747-2694C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751765 | ||||||
chr7:4751836
|
G | A | 3 | a0001c0003t0031g0171a0001c0003t0132g0160a0001c0003t0144g0142 | 3 | HG01361.hp1 HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.747-2623G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751836 | ||||||
chr7:4751981
|
C | T | 3 | a0001c0003t0113g0276a0001c0004t0033g0027a0001c0004t0034g0028 | 3 | HG00738.hp2 HG01978.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.747-2478C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751981 | ||||||
chr7:4752092
|
G | T | 3 | a0001c0003t0019g0238a0001c0003t0037g0284a0001c0003t0038g0208 | 3 | HG02622.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.747-2367G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752092 | ||||||
chr7:4752109
|
C | T | 1 | a0001c0004t0116g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.747-2350C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752109 | ||||||
chr7:4752118
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.747-2341A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752118 | ||||||
chr7:4752143
|
T | G | 1 | a0001c0003t0100g0248 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747-2316T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752143 | ||||||
chr7:4752189
|
C | T | 5 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0130g0088others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-2270C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752189 | ||||||
chr7:4752227
|
C | A | 1 | a0001c0004t0141g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.747-2232C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752227 | ||||||
chr7:4752227
|
C | G | 15 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(12): Show | 15 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.747-2232C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752227 | ||||||
chr7:4752265
|
C | A | 24 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(21): Show | 24 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.747-2194C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752265 | ||||||
chr7:4752303
|
C | G | 1 | a0001c0023t0049g0104 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.747-2156C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752303 | ||||||
chr7:4752447
|
C | G | 5 | a0001c0003t0100g0248a0001c0003t0104g0092a0001c0003t0129g0279others(2): Show | 5 | HG02976.hp2 HG03139.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-2012C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752447 | ||||||
chr7:4752454
|
T | C | 16 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0019g0238others(13): Show | 16 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.747-2005T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752454 | ||||||
chr7:4752467
|
C | T | 7 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(4): Show | 7 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-1992C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752467 | ||||||
chr7:4752502
|
T | C | 4 | a0001c0002t0001g0134a0001c0002t0005g0278a0001c0002t0061g0133others(1): Show | 4 | HG02486.hp2 HG02738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-1957T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752502 | ||||||
chr7:4752515
|
G | A | 9 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(6): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-1944G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752515 | ||||||
chr7:4752585
|
C | T | 1 | a0001c0003t0038g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.747-1874C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752585 | ||||||
chr7:4752590
|
G | T | 9 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(6): Show | 9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-1869G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752590 | ||||||
chr7:4752598
|
A | G | 1 | a0001c0024t0002g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.747-1861A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752598 | ||||||
chr7:4752646
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.747-1813G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752646 | ||||||
chr7:4752682
|
G | A | 1 | a0001c0003t0099g0282 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.747-1777G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752682 | ||||||
chr7:4752716
|
G | A | 2 | a0001c0003t0146g0174a0001c0004t0056g0233 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.747-1743G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752716 | ||||||
chr7:4753118
|
G | A | 1 | a0001c0001t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.747-1341G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753118 | ||||||
chr7:4753131
|
C | T | 13 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0019g0238others(10): Show | 13 | HG00738.hp2 HG01978.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.747-1328C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753131 | ||||||
chr7:4753219
|
A | G | 1 | a0001c0003t0137g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.747-1240A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753219 | ||||||
chr7:4753220
|
T | C | 7 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0112g0006others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-1239T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753220 | ||||||
chr7:4753348
|
T | G | 1 | a0001c0002t0085g0103 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.747-1111T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753348 | ||||||
chr7:4753353
|
C | T | 1 | a0001c0001t0017g0224 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.747-1106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753353 | ||||||
chr7:4753389
|
A | C | 1 | a0001c0003t0112g0006 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747-1070A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753389 | ||||||
chr7:4753480
|
C | T | 2 | a0001c0003t0146g0174a0001c0004t0056g0233 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.747-979C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753480 | ||||||
chr7:4753570
|
G | A | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.747-889G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753570 | ||||||
chr7:4753635
|
T | C | 5 | a0001c0003t0100g0248a0001c0003t0104g0092a0001c0003t0129g0279others(2): Show | 5 | HG02976.hp2 HG03139.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-824T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753635 | ||||||
chr7:4753688
|
C | T | 2 | a0001c0003t0102g0086a0002c0013t0026g0288 | 2 | HG02647.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.747-771C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753688 | ||||||
chr7:4753693
|
T | A | 8 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(5): Show | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-766T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753693 | ||||||
chr7:4753821
|
C | T | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.747-638C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753821 | ||||||
chr7:4753952
|
C | T | 4 | a0001c0003t0142g0080a0001c0003t0143g0079a0001c0004t0008g0001others(1): Show | 5 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-507C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753952 | ||||||
chr7:4754022
|
A | C | 5 | a0001c0003t0112g0006a0001c0003t0113g0276a0001c0006t0052g0078others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-437A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754022 | ||||||
chr7:4754036
|
T | C | 1 | a0001c0001t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.747-423T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754036 | ||||||
chr7:4754059
|
C | T | 2 | a0004c0016t0106g0146a0004c0016t0107g0147 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.747-400C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754059 | ||||||
chr7:4754120
|
C | T | 1 | a0001c0002t0004g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.747-339C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754120 | ||||||
chr7:4754222
|
C | T | 5 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0130g0088others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-237C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754222 | ||||||
chr7:4754240
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.747-219C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754240 | ||||||
chr7:4754406
|
C | T | 1 | a0001c0002t0018g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.747-53C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754406 | ||||||
chr7:4754632
|
C | T | 8 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.903+17C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754632 | ||||||
chr7:4754720
|
G | C | 12 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(9): Show | 12 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+105G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754720 | ||||||
chr7:4754738
|
A | G | 4 | a0001c0008t0028g0206a0001c0008t0028g0264a0001c0008t0118g0095others(1): Show | 4 | HG00597.hp1 NA18942.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+123A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754738 | ||||||
chr7:4754760
|
G | A | 3 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089 | 3 | HG02145.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.903+145G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754760 | ||||||
chr7:4754796
|
A | T | 1 | a0001c0003t0112g0006 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.903+181A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754796 | ||||||
chr7:4754805
|
C | T | 24 | a0001c0001t0016g0241a0001c0001t0017g0224a0001c0001t0058g0251others(21): Show | 24 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.903+190C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754805 | ||||||
chr7:4754852
|
C | T | 2 | a0001c0003t0112g0006a0001c0003t0113g0276 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.903+237C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754852 | ||||||
chr7:4754989
|
C | G | 65 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(62): Show | 65 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.904-248C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754989 | ||||||
chr7:4755115
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0068g0010a0001c0001t0080g0023 | 3 | HG01175.hp2 HG01515.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.904-122C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4755115 | ||||||
chr7:4755186
|
A | G | 13 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0019g0238others(10): Show | 13 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.904-51A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4755186 | ||||||
chr7:4755489
|
C | A | 2 | a0004c0016t0106g0146a0004c0016t0107g0147 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1050+106C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755489 | ||||||
chr7:4755530
|
G | C | 7 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+147G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755530 | ||||||
chr7:4755689
|
C | T | 6 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0072g0015others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050+306C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755689 | ||||||
chr7:4755791
|
C | T | 6 | a0001c0001t0050g0137a0001c0003t0031g0155a0001c0003t0031g0171others(3): Show | 6 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050+408C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755791 | ||||||
chr7:4755824
|
C | T | 6 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0130g0088others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050+441C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755824 | ||||||
chr7:4755969
|
T | C | 56 | a0001c0001t0050g0137a0001c0003t0010g0077a0001c0003t0010g0100others(53): Show | 57 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.1050+586T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755969 | ||||||
chr7:4756004
|
G | A | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1050+621G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756004 | ||||||
chr7:4756079
|
T | A | 94 | a0001c0001t0050g0137a0001c0003t0010g0077a0001c0003t0010g0100others(91): Show | 95 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(92): Show |
intron_variant | MODIFIER | c.1050+696T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756079 | ||||||
chr7:4756110
|
TTTTG | T | 7 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+743_1050+746d others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 4756110 | |||||
chr7:4756146
|
G | A | 3 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075 | 3 | HG02486.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1050+763G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756146 | ||||||
chr7:4756169
|
T | C | 86 | a0001c0001t0050g0137a0001c0003t0010g0077a0001c0003t0010g0100others(83): Show | 87 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1050+786T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756169 | ||||||
chr7:4756170
|
G | A | 5 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050+787G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756170 | ||||||
chr7:4756217
|
C | T | 5 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0036g0004others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-777C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756217 | ||||||
chr7:4756222
|
C | G | 1 | a0001c0003t0137g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1051-772C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756222 | ||||||
chr7:4756297
|
T | C | 7 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051-697T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756297 | ||||||
chr7:4756316
|
T | C | 1 | a0001c0003t0099g0282 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1051-678T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756316 | ||||||
chr7:4756367
|
C | T | 8 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(5): Show | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1051-627C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756367 | ||||||
chr7:4756418
|
G | C | 1 | a0001c0002t0005g0098 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1051-576G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756418 | ||||||
chr7:4756523
|
T | C | 94 | a0001c0001t0050g0137a0001c0003t0010g0077a0001c0003t0010g0100others(91): Show | 95 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(92): Show |
intron_variant | MODIFIER | c.1051-471T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756523 | ||||||
chr7:4756655
|
G | C | 85 | a0001c0001t0050g0137a0001c0003t0010g0077a0001c0003t0010g0100others(82): Show | 86 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.1051-339G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756655 | ||||||
chr7:4756713
|
C | T | 8 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1051-281C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756713 | ||||||
chr7:4756730
|
A | T | 9 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-264A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756730 | ||||||
chr7:4756921
|
C | G | 1 | a0001c0002t0004g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1051-73C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756921 | ||||||
chr7:4756961
|
T | G | 2 | a0004c0016t0106g0146a0004c0016t0107g0147 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1051-33T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756961 | ||||||
chr7:4757261
|
G | A | 1 | a0001c0017t0114g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1244+74G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757261 | ||||||
chr7:4757292
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1244+105C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757292 | ||||||
chr7:4757311
|
A | G | 14 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+124A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757311 | ||||||
chr7:4757318
|
A | C | 2 | a0001c0004t0033g0027a0001c0004t0034g0028 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1244+131A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757318 | ||||||
chr7:4757351
|
G | A | 6 | a0001c0001t0050g0137a0001c0003t0031g0155a0001c0003t0031g0171others(3): Show | 6 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244+164G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757351 | ||||||
chr7:4757356
|
G | A | 8 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(5): Show | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1244+169G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757356 | ||||||
chr7:4757438
|
G | A | 3 | a0001c0003t0139g0074a0001c0003t0140g0003a0001c0004t0141g0247 | 3 | HG02451.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1244+251G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757438 | ||||||
chr7:4757463
|
T | C | 2 | a0001c0004t0033g0027a0001c0004t0034g0028 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1244+276T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757463 | ||||||
chr7:4757570
|
C | G | 18 | a0001c0001t0050g0137a0001c0003t0031g0155a0001c0003t0031g0171others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1244+383C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757570 | ||||||
chr7:4757602
|
G | C | 19 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0100g0248others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+415G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757602 | ||||||
chr7:4757634
|
C | CA | 30 | a0001c0001t0001g0129a0001c0001t0001g0205a0001c0001t0002g0049others(27): Show | 30 | HG00323.hp1 HG01175.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1244+477dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757634
|
CA | C | 26 | a0001c0001t0001g0039a0001c0001t0001g0118a0001c0001t0001g0214others(23): Show | 26 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1244+477delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757634
|
CAA | C | 14 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0104g0092others(11): Show | 14 | HG01496.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+476_1244+477d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757634
|
CAAA | C | 10 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244+475_1244+477d others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757634
|
CAAAAAAA others(1): Show |
C | 15 | a0001c0002t0004g0068a0001c0003t0010g0077a0001c0003t0010g0100others(12): Show | 15 | HG02109.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1244+470_1244+477d others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757634
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0215 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1244+468_1244+477d others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757634
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0004t0033g0027a0001c0004t0034g0028 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1244+466_1244+477d others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757634
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0003t0112g0006a0001c0003t0113g0276 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1244+463_1244+477d others(17): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | |||||
chr7:4757658
|
A | C | 19 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0100g0248others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+471A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757658 | ||||||
chr7:4757659
|
A | C | 19 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0100g0248others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+472A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757659 | ||||||
chr7:4757687
|
C | T | 19 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0100g0248others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+500C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757687 | ||||||
chr7:4757742
|
G | A | 8 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1244+555G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757742 | ||||||
chr7:4757866
|
G | A | 10 | a0001c0003t0014g0081a0001c0003t0014g0236a0001c0003t0100g0248others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1244+679G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757866 | ||||||
chr7:4758003
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1244+816T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758003 | ||||||
chr7:4758048
|
C | T | 1 | a0001c0002t0001g0043 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1244+861C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758048 | ||||||
chr7:4758215
|
C | T | 5 | a0001c0003t0031g0155a0001c0003t0031g0171a0001c0003t0132g0160others(2): Show | 5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245-836C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758215 | ||||||
chr7:4758374
|
C | A | 9 | a0001c0006t0052g0078a0001c0006t0053g0076a0001c0006t0054g0075others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1245-677C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758374 | ||||||
chr7:4758649
|
C | T | 30 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0019g0238others(27): Show | 30 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1245-402C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758649 | ||||||
chr7:4758669
|
G | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1245-382G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758669 | ||||||
chr7:4758702
|
C | A | 13 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(10): Show | 13 | HG02451.hp1 HG02559.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1245-349C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758702 | ||||||
chr7:4758721
|
T | G | 5 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245-330T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758721 | ||||||
chr7:4758769
|
G | A | 1 | a0001c0003t0111g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1245-282G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758769 | ||||||
chr7:4758796
|
C | A | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1245-255C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758796 | ||||||
chr7:4758902
|
G | C | 38 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(35): Show | 38 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.1245-149G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758902 | ||||||
chr7:4758965
|
C | T | 2 | a0001c0001t0011g0029a0001c0002t0001g0177 | 2 | HG00544.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1245-86C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758965 | ||||||
chr7:4759239
|
T | TGCGGGGC others(3): Show |
1 | a0001c0001t0001g0035 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1411+33_1411+42dup others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 4759239 | |||||
chr7:4759650
|
G | A | 1 | a0001c0003t0010g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1696+55G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759650 | ||||||
chr7:4759669
|
G | A | 5 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1696+74G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759669 | ||||||
chr7:4759701
|
T | C | 3 | a0001c0001t0003g0270a0001c0002t0003g0065a0001c0002t0088g0254 | 3 | HG03225.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1696+106T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759701 | ||||||
chr7:4759901
|
C | T | 26 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0118others(23): Show | 26 | HG00323.hp2 HG00597.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696+306C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759901 | ||||||
chr7:4759945
|
C | T | 7 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1696+350C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759945 | ||||||
chr7:4759954
|
C | T | 2 | a0001c0004t0033g0027a0001c0004t0034g0028 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1696+359C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759954 | ||||||
chr7:4759957
|
G | A | 1 | a0001c0003t0038g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1696+362G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759957 | ||||||
chr7:4760014
|
A | G | 1 | a0001c0001t0003g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1696+419A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760014 | ||||||
chr7:4760024
|
T | C | 41 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(38): Show | 42 | HG00597.hp1 HG01258.hp2 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.1696+429T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760024 | ||||||
chr7:4760029
|
C | CA | 6 | a0001c0001t0001g0062a0001c0001t0003g0036a0001c0002t0005g0278others(3): Show | 6 | HG00735.hp2 HG01361.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1696+447dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | |||||
chr7:4760029
|
C | CAA | 18 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0019g0238others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1696+446_1696+447d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | |||||
chr7:4760029
|
C | CAAA | 12 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(9): Show | 12 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1696+445_1696+447d others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | |||||
chr7:4760029
|
CA | C | 11 | a0001c0002t0001g0215a0001c0003t0014g0081a0001c0003t0014g0236others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1696+447delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | |||||
chr7:4760043
|
C | A | 13 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(10): Show | 13 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1696+448C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760043 | ||||||
chr7:4760056
|
G | A | 7 | a0001c0003t0047g0072a0001c0003t0087g0071a0001c0003t0111g0059others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1696+461G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760056 | ||||||
chr7:4760063
|
T | C | 100 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(97): Show | 101 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(98): Show |
intron_variant | MODIFIER | c.1696+468T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760063 | ||||||
chr7:4760064
|
G | A | 1 | a0001c0019t0128g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1696+469G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760064 | ||||||
chr7:4760248
|
A | G | 8 | a0001c0003t0015g0066a0001c0003t0015g0094a0001c0003t0019g0238others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1696+653A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760248 | ||||||
chr7:4760320
|
A | G | 67 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(64): Show | 68 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.1696+725A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760320 | ||||||
chr7:4760348
|
G | A | 1 | a0001c0001t0078g0019 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1697-716G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760348 | ||||||
chr7:4760352
|
C | T | 1 | a0001c0001t0086g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1697-712C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760352 | ||||||
chr7:4760379
|
G | C | 89 | a0001c0003t0010g0077a0001c0003t0010g0100a0001c0003t0010g0231others(86): Show | 90 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1697-685G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760379 | ||||||
chr7:4760425
|
A | G | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1697-639A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760425 | ||||||
chr7:4760573
|
G | A | 2 | a0001c0003t0037g0284a0001c0003t0038g0208 | 2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1697-491G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760573 | ||||||
chr7:4760720
|
A | G | 107 | a0001c0003t0007g0090a0001c0003t0007g0226a0001c0003t0007g0250others(104): Show | 108 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(105): Show |
intron_variant | MODIFIER | c.1697-344A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760720 | ||||||
chr7:4760773
|
C | T | 1 | a0001c0001t0081g0042 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1697-291C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760773 | ||||||
chr7:4760883
|
T | A | 1 | a0001c0003t0113g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1697-181T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760883 | ||||||
chr7:4761060
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.1697-4G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4761060 | ||||||
chr7:4761298
|
T | C | 8 | a0001c0007t0006g0084a0001c0007t0006g0085a0001c0007t0006g0089others(5): Show | 8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1921+10T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761298 | ||||||
chr7:4761321
|
C | T | 1 | a0002c0018t0007g0290 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1921+33C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761321 | ||||||
chr7:4761422
|
C | T | 1 | a0001c0001t0077g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1921+134C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761422 | ||||||
chr7:4761771
|
C | G | 1 | a0001c0003t0005g0112 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1922-413C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761771 | ||||||
chr7:4761816
|
G | C | 2 | a0001c0001t0096g0093a0001c0002t0095g0207 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1922-368G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761816 | ||||||
chr7:4761868
|
C | T | 2 | a0001c0004t0033g0027a0001c0004t0034g0028 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1922-316C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761868 | ||||||
chr7:4761955
|
T | C | 108 | a0001c0001t0002g0199a0001c0003t0007g0090a0001c0003t0007g0226others(105): Show | 109 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.1922-229T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761955 | ||||||
chr7:4762083
|
C | A | 2 | a0001c0003t0142g0080a0001c0003t0143g0079 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1922-101C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4762083 |