geneid | 85462 |
---|---|
ensemblid | ENSG00000137460.10 |
hgncid | 29363 |
symbol | FHDC1 |
name | FH2 domain containing 1 |
refseq_nuc | NM_001371116.1 |
refseq_prot | NP_001358045.1 |
ensembl_nuc | ENST00000511601.6 |
ensembl_prot | ENSP00000427567.1 |
mane_status | MANE Select |
chr | chr4 |
start | 152936323 |
end | 152979671 |
strand | + |
ver | v1.2 |
region | chr4:152936323-152979671 |
region5000 | chr4:152931323-152984671 |
regionname0 | FHDC1_chr4_152936323_152979671 |
regionname5000 | FHDC1_chr4_152931323_152984671 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1143 | 170 | 57 | 30 | 57 | 1 | 23 | 41 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002 | 0/0 | 1143 | 156 | 8 | 38 | 75 | 16 | 19 | 53 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003 | 0/0 | 1143 | 30 | 8 | 2 | 19 | 0 | 1 | 16 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0004 | 0/0 | 1143 | 26 | 0 | 2 | 24 | 0 | 0 | 21 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0005 | 0/0 | 1143 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0006 | 0/0 | 1143 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0007 | 0/0 | 1143 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0008 | 0/0 | 1143 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0009 | 0/0 | 1143 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0010 | 0/0 | 1143 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0011 | 0/0 | 1143 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0012 | 0/0 | 1143 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0013 | 0/0 | 1143 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0014 | 0/0 | 1143 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0015 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0016 | 0/0 | 1147 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0017 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0018 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0019 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0020 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0021 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0022 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0023 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0024 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0025 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0026 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0027 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0028 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0029 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0030 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0031 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0032 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0033 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0034 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0035 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3432 | 145 | 7 | 35 | 74 | 13 | 16 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0002 | 1/0 | 3432 | 135 | 39 | 25 | 51 | 0 | 19 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0003 | 0/0 | 3432 | 25 | 0 | 2 | 23 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0004 | 0/0 | 3432 | 24 | 2 | 2 | 19 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0005 | 0/1 | 3432 | 20 | 4 | 5 | 6 | 1 | 3 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0006 | 0/0 | 3432 | 9 | 0 | 0 | 9 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0007 | 0/0 | 3432 | 6 | 6 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0008 | 0/0 | 3432 | 5 | 0 | 2 | 0 | 3 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0009 | 0/0 | 3432 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0010 | 0/0 | 3432 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0011 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0012 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0013 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0014 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0015 | 0/0 | 3432 | 3 | 0 | 0 | 3 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0016 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0017 | 0/0 | 3432 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0018 | 0/0 | 3432 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0019 | 0/0 | 3432 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0020 | 0/0 | 3432 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0021 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0022 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0023 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0024 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0025 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0026 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0027 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0028 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0029 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0030 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0031 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0032 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0033 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0034 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0035 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0036 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0037 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0038 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0039 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0040 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0041 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0042 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0043 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0044 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0045 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0046 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0047 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0048 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0049 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0050 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0051 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0052 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0053 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0054 | 0/0 | 3444 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
c0055 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3163 | 180 | 14 | 37 | 101 | 12 | 16 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0002 | 0/1 | 3165 | 98 | 2 | 22 | 55 | 0 | 18 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0003 | 0/0 | 3163 | 36 | 24 | 1 | 11 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0004 | 0/0 | 3165 | 16 | 3 | 4 | 7 | 1 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0005 | 0/0 | 3165 | 9 | 1 | 0 | 3 | 0 | 5 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0006 | 1/0 | 3166 | 8 | 7 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0007 | 0/0 | 3166 | 7 | 6 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0008 | 0/0 | 3163 | 5 | 5 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0009 | 0/0 | 3165 | 5 | 0 | 2 | 0 | 3 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0010 | 0/0 | 3163 | 4 | 0 | 0 | 4 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0011 | 0/0 | 3165 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0012 | 0/0 | 3163 | 3 | 1 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0013 | 0/0 | 3166 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0014 | 0/0 | 3163 | 3 | 0 | 0 | 3 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0015 | 0/0 | 3166 | 3 | 1 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0016 | 0/0 | 3166 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0017 | 0/0 | 3163 | 3 | 0 | 0 | 1 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0018 | 0/0 | 3163 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0019 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0020 | 0/0 | 3163 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0021 | 0/0 | 3163 | 2 | 0 | 0 | 0 | 1 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0022 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0023 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0024 | 0/0 | 3164 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0025 | 0/0 | 3165 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0026 | 0/0 | 3163 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0027 | 0/0 | 3165 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0028 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0029 | 0/0 | 3166 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0030 | 0/0 | 3166 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0031 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0032 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0033 | 0/0 | 3162 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0034 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0035 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0036 | 0/0 | 3163 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0037 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0038 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0039 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0040 | 0/0 | 3166 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0041 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0042 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0043 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0044 | 0/0 | 3164 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0045 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0046 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0047 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0048 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0049 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0050 | 0/0 | 3166 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0051 | 0/0 | 3166 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0052 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0053 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0054 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
t0055 | 0/0 | 3165 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0403 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0411 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0412 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0414 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0417 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0418 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0419 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0420 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0421 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
g0422 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 3432 | 135 | 39 | 25 | 51 | 0 | 19 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0005 | 0/1 | 3432 | 20 | 4 | 5 | 6 | 1 | 3 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0007 | 0/0 | 3432 | 6 | 6 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0010 | 0/0 | 3432 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0013 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0040 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0051 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001 | 0/0 | 3432 | 145 | 7 | 35 | 74 | 13 | 16 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0008 | 0/0 | 3432 | 5 | 0 | 2 | 0 | 3 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0018 | 0/0 | 3432 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0030 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0042 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0044 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0052 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004 | 0/0 | 3432 | 24 | 2 | 2 | 19 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0011 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0023 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0025 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0027 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0004c0003 | 0/0 | 3432 | 25 | 0 | 2 | 23 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0004c0028 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0005c0006 | 0/0 | 3432 | 9 | 0 | 0 | 9 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0006c0016 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0006c0039 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0007c0009 | 0/0 | 3432 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0008c0012 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0008c0033 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0009c0015 | 0/0 | 3432 | 3 | 0 | 0 | 3 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0010c0014 | 0/0 | 3432 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0011c0017 | 0/0 | 3432 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0012c0019 | 0/0 | 3432 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0013c0046 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0013c0047 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0014c0020 | 0/0 | 3432 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0015c0055 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0016c0054 | 0/0 | 3444 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0017c0050 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0018c0029 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0019c0031 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0020c0032 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0021c0045 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0022c0041 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0023c0043 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0024c0034 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0025c0036 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0026c0038 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0027c0037 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0028c0035 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0029c0048 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0030c0049 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0031c0026 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0032c0024 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0033c0022 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0034c0021 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0035c0053 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 6594 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0002 | 0/0 | 6596 | 66 | 0 | 17 | 38 | 0 | 11 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0003 | 0/0 | 6594 | 20 | 15 | 1 | 4 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0004 | 0/0 | 6596 | 4 | 1 | 1 | 1 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0005 | 0/0 | 6596 | 8 | 0 | 0 | 3 | 0 | 5 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0006 | 1/0 | 6597 | 7 | 6 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0007 | 0/0 | 6597 | 5 | 5 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0012 | 0/0 | 6594 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0015 | 0/0 | 6597 | 3 | 1 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0018 | 0/0 | 6594 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0020 | 0/0 | 6594 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0025 | 0/0 | 6596 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0026 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0029 | 0/0 | 6597 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0039 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0044 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0045 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0049 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0050 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0053 | 0/0 | 6596 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0054 | 0/0 | 6581 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0002t0055 | 0/0 | 6596 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0005t0002 | 0/1 | 6596 | 14 | 2 | 2 | 6 | 0 | 3 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0005t0004 | 0/0 | 6596 | 4 | 0 | 3 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0005t0022 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0007t0008 | 0/0 | 6594 | 5 | 5 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0007t0028 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0010t0003 | 0/0 | 6594 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0010t0023 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0013t0003 | 0/0 | 6594 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0040t0003 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0001c0051t0002 | 0/0 | 6596 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0001 | 0/0 | 6594 | 128 | 6 | 34 | 65 | 11 | 12 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0010 | 0/0 | 6594 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0012 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0014 | 0/0 | 6594 | 3 | 0 | 0 | 3 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0017 | 0/0 | 6594 | 3 | 0 | 0 | 1 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0021 | 0/0 | 6594 | 2 | 0 | 0 | 0 | 1 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0033 | 0/0 | 6593 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0034 | 0/0 | 6593 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0035 | 0/0 | 6594 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0036 | 0/0 | 6594 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0038 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0001t0041 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0008t0009 | 0/0 | 6596 | 5 | 0 | 2 | 0 | 3 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0018t0001 | 0/0 | 6594 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0030t0001 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0042t0001 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0044t0037 | 0/0 | 6594 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0002c0052t0001 | 0/0 | 6594 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0001 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0002 | 0/0 | 6596 | 12 | 0 | 1 | 10 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0003 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0004 | 0/0 | 6596 | 6 | 0 | 0 | 6 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0006 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0007 | 0/0 | 6597 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0026 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0004t0031 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0011t0003 | 0/0 | 6594 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0011t0048 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0023t0005 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0025t0047 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0003c0027t0043 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0004c0003t0001 | 0/0 | 6594 | 23 | 0 | 2 | 21 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0004c0003t0010 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0004c0003t0032 | 0/0 | 6593 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0004c0028t0001 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0005c0006t0001 | 0/0 | 6594 | 9 | 0 | 0 | 9 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0006c0016t0011 | 0/0 | 6596 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0006c0039t0046 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0007c0009t0016 | 0/0 | 6597 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0007c0009t0030 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0008c0012t0004 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0008c0012t0019 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0008c0033t0004 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0009c0015t0003 | 0/0 | 6594 | 3 | 0 | 0 | 3 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0010c0014t0013 | 0/0 | 6597 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0011c0017t0002 | 0/0 | 6596 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0012c0019t0027 | 0/0 | 6596 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0013c0046t0024 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0013c0047t0024 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0014c0020t0002 | 0/0 | 6596 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0015c0055t0042 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0016c0054t0001 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0017c0050t0040 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0018c0029t0011 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0019c0031t0001 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0020c0032t0001 | 0/0 | 6594 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0021c0045t0003 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0022c0041t0001 | 0/0 | 6594 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0023c0043t0010 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0024c0034t0003 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0025c0036t0002 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0026c0038t0007 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0027c0037t0003 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0028c0035t0001 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0029c0048t0001 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0030c0049t0001 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0031c0026t0052 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0032c0024t0003 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0033c0022t0051 | 0/0 | 6597 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0034c0021t0001 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
a0035c0053t0001 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | copy fasta | chr4 | 152931323 | 152984671 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0420 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0421 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0007g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0012g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0015g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0018g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0018g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0020g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0020g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0025g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0025g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0026g0417 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0029g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0039g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0044g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0045g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0049g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0050g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0053g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0054g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0055g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0022g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0008g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0028g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0023g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0023g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0013t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0013t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0013t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0040t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0051t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0412 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0418 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0010g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0012g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0014g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0014g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0014g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0017g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0017g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0017g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0021g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0021g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0033g0422 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0034g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0035g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0036g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0038g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0041g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0009g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0009g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0009g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0009g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0009g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0018t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0030t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0042t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0044t0037g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0052t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0001g0414 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0403 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0003g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0004g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0004g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0007g0411 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0026g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0031g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0011t0003g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0011t0003g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0011t0048g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0023t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0025t0047g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0027t0043g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0419 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0010g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0032g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0028t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0016t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0016t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0016t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0039t0046g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0016g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0016g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0030g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0012t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0012t0019g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0012t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0033t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0009c0015t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0009c0015t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0009c0015t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0010c0014t0013g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0010c0014t0013g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0010c0014t0013g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0011c0017t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0012c0019t0027g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0012c0019t0027g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0013c0046t0024g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0013c0047t0024g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0014c0020t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0014c0020t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0015c0055t0042g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0016c0054t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0017c0050t0040g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0018c0029t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0019c0031t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0020c0032t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0021c0045t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0022c0041t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0023c0043t0010g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0024c0034t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0025c0036t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0026c0038t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0027c0037t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0028c0035t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0029c0048t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0030c0049t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0031c0026t0052g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0032c0024t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0033c0022t0051g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0034c0021t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0035c0053t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0335 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00099 | hp2 | a0002 | c0001 | t0021 | g0075 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00140 | hp1 | a0001 | c0005 | t0004 | g0126 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00140 | hp2 | a0020 | c0032 | t0001 | g0062 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00280 | hp1 | a0002 | c0001 | t0001 | g0331 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00280 | hp2 | a0002 | c0008 | t0009 | g0102 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00323 | hp1 | a0002 | c0001 | t0001 | g0253 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00323 | hp2 | a0002 | c0008 | t0009 | g0284 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0316 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00423 | hp1 | a0002 | c0042 | t0001 | g0356 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0387 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0394 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0261 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0229 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00558 | hp1 | a0025 | c0036 | t0002 | g0290 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00558 | hp2 | a0004 | c0003 | t0001 | g0407 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00597 | hp1 | a0001 | c0002 | t0026 | g0417 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00597 | hp2 | a0002 | c0001 | t0001 | g0418 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0277 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0296 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00621 | hp2 | a0001 | c0002 | t0004 | g0072 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0266 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0294 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00642 | hp1 | a0002 | c0001 | t0001 | g0309 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00642 | hp2 | a0022 | c0041 | t0001 | g0264 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00735 | hp1 | a0002 | c0001 | t0001 | g0114 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00735 | hp2 | a0002 | c0001 | t0001 | g0208 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00741 | hp1 | a0002 | c0001 | t0001 | g0311 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0323 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01069 | hp1 | a0001 | c0005 | t0004 | g0019 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0292 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01070 | hp1 | a0001 | c0002 | t0015 | g0005 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01070 | hp2 | a0004 | c0003 | t0001 | g0415 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01071 | hp1 | a0001 | c0005 | t0004 | g0020 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01071 | hp2 | a0001 | c0002 | t0015 | g0005 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0367 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0100 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0124 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0276 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01099 | hp1 | a0002 | c0001 | t0001 | g0211 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01099 | hp2 | a0002 | c0001 | t0001 | g0313 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01106 | hp1 | a0002 | c0001 | t0001 | g0187 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01106 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01109 | hp1 | a0002 | c0044 | t0037 | g0115 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01109 | hp2 | a0002 | c0008 | t0009 | g0085 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01167 | hp1 | a0002 | c0001 | t0001 | g0199 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01167 | hp2 | a0001 | c0002 | t0012 | g0013 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01168 | hp1 | a0001 | c0002 | t0004 | g0198 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01168 | hp2 | a0001 | c0005 | t0002 | g0328 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01169 | hp1 | a0001 | c0002 | t0012 | g0013 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01169 | hp2 | a0001 | c0005 | t0002 | g0327 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01175 | hp1 | a0002 | c0001 | t0001 | g0318 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01175 | hp2 | a0003 | c0004 | t0007 | g0411 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01192 | hp1 | a0001 | c0005 | t0004 | g0332 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0196 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0082 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01243 | hp2 | a0033 | c0022 | t0051 | g0026 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01256 | hp1 | a0011 | c0017 | t0002 | g0003 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0087 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0058 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01258 | hp2 | a0011 | c0017 | t0002 | g0003 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01261 | hp1 | a0002 | c0001 | t0001 | g0326 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0218 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0330 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0212 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01358 | hp2 | a0002 | c0001 | t0001 | g0050 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0293 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0083 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01433 | hp1 | a0002 | c0001 | t0001 | g0305 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01496 | hp2 | a0002 | c0001 | t0001 | g0195 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01515 | hp1 | a0002 | c0001 | t0033 | g0422 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01515 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01516 | hp1 | a0002 | c0001 | t0001 | g0122 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0004 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01517 | hp2 | a0002 | c0001 | t0001 | g0004 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0165 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01884 | hp2 | a0001 | c0002 | t0006 | g0337 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01891 | hp1 | a0001 | c0002 | t0003 | g0247 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01891 | hp2 | a0001 | c0007 | t0008 | g0405 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0213 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01934 | hp1 | a0002 | c0001 | t0001 | g0257 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0420 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0295 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01978 | hp1 | a0002 | c0001 | t0001 | g0043 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01978 | hp2 | a0001 | c0002 | t0044 | g0216 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01981 | hp1 | a0001 | c0002 | t0055 | g0225 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0300 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0121 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02004 | hp1 | a0002 | c0001 | t0001 | g0314 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0239 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02027 | hp1 | a0001 | c0005 | t0002 | g0185 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0103 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02055 | hp1 | a0001 | c0005 | t0002 | g0164 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02055 | hp2 | a0026 | c0038 | t0007 | g0048 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0061 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0214 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02071 | hp1 | a0009 | c0015 | t0003 | g0056 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02071 | hp2 | a0004 | c0003 | t0001 | g0002 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0285 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02080 | hp1 | a0030 | c0049 | t0001 | g0298 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02080 | hp2 | a0024 | c0034 | t0003 | g0111 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0059 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02083 | hp2 | a0003 | c0004 | t0026 | g0325 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02129 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02129 | hp2 | a0002 | c0001 | t0001 | g0060 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0153 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0302 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02145 | hp1 | a0001 | c0013 | t0003 | g0131 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02145 | hp2 | a0006 | c0016 | t0011 | g0167 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0067 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02155 | hp1 | a0001 | c0005 | t0002 | g0279 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02155 | hp2 | a0003 | c0004 | t0002 | g0044 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0088 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0066 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02258 | hp1 | a0007 | c0009 | t0016 | g0169 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02258 | hp2 | a0028 | c0035 | t0001 | g0341 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02273 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02273 | hp2 | a0004 | c0003 | t0001 | g0399 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02280 | hp1 | a0015 | c0055 | t0042 | g0242 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0338 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02293 | hp1 | a0003 | c0004 | t0002 | g0403 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0235 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0097 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0260 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02523 | hp1 | a0001 | c0002 | t0005 | g0035 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02572 | hp1 | a0001 | c0005 | t0002 | g0162 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0052 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02615 | hp1 | a0001 | c0007 | t0008 | g0163 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02615 | hp2 | a0010 | c0014 | t0013 | g0379 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0340 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02622 | hp2 | a0001 | c0040 | t0003 | g0191 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02630 | hp1 | a0007 | c0009 | t0016 | g0135 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02630 | hp2 | a0001 | c0010 | t0023 | g0136 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0267 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02647 | hp2 | a0001 | c0010 | t0023 | g0184 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02683 | hp1 | a0002 | c0001 | t0001 | g0188 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0421 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0130 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0287 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02717 | hp2 | a0001 | c0002 | t0018 | g0381 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02723 | hp1 | a0001 | c0010 | t0003 | g0315 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0144 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02735 | hp1 | a0002 | c0001 | t0017 | g0022 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02735 | hp2 | a0002 | c0001 | t0001 | g0273 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02738 | hp1 | a0001 | c0002 | t0004 | g0283 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0333 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02809 | hp1 | a0001 | c0002 | t0006 | g0254 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02809 | hp2 | a0003 | c0027 | t0043 | g0186 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02818 | hp1 | a0001 | c0007 | t0008 | g0168 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0137 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02886 | hp1 | a0003 | c0023 | t0005 | g0027 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02886 | hp2 | a0002 | c0001 | t0001 | g0268 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02895 | hp1 | a0008 | c0012 | t0019 | g0146 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02895 | hp2 | a0001 | c0002 | t0007 | g0207 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0271 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02896 | hp2 | a0010 | c0014 | t0013 | g0209 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02897 | hp1 | a0001 | c0002 | t0003 | g0270 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02897 | hp2 | a0008 | c0012 | t0019 | g0147 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02922 | hp1 | a0006 | c0039 | t0046 | g0138 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02922 | hp2 | a0008 | c0012 | t0004 | g0177 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02965 | hp1 | a0013 | c0047 | t0024 | g0149 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02965 | hp2 | a0001 | c0013 | t0003 | g0133 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02970 | hp1 | a0001 | c0002 | t0020 | g0183 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02970 | hp2 | a0001 | c0002 | t0007 | g0404 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02976 | hp1 | a0003 | c0011 | t0048 | g0029 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02976 | hp2 | a0002 | c0001 | t0001 | g0173 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03017 | hp1 | a0002 | c0052 | t0001 | g0152 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03041 | hp1 | a0001 | c0002 | t0007 | g0342 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03041 | hp2 | a0013 | c0046 | t0024 | g0096 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03098 | hp1 | a0001 | c0010 | t0003 | g0286 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03098 | hp2 | a0003 | c0004 | t0006 | g0193 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03130 | hp2 | a0003 | c0025 | t0047 | g0025 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03139 | hp1 | a0006 | c0016 | t0011 | g0166 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03139 | hp2 | a0003 | c0004 | t0001 | g0414 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0339 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03195 | hp2 | a0001 | c0007 | t0008 | g0150 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0145 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0308 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03225 | hp1 | a0017 | c0050 | t0040 | g0141 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03225 | hp2 | a0021 | c0045 | t0003 | g0157 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0246 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03239 | hp2 | a0001 | c0002 | t0053 | g0039 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03453 | hp1 | a0001 | c0002 | t0007 | g0155 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03453 | hp2 | a0001 | c0007 | t0008 | g0047 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03486 | hp2 | a0001 | c0007 | t0028 | g0383 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03490 | hp1 | a0016 | c0054 | t0001 | g0101 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03490 | hp2 | a0002 | c0018 | t0001 | g0010 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03491 | hp1 | a0001 | c0002 | t0005 | g0023 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03491 | hp2 | a0001 | c0002 | t0005 | g0038 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03492 | hp1 | a0001 | c0002 | t0005 | g0024 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03492 | hp2 | a0002 | c0018 | t0001 | g0010 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03516 | hp1 | a0001 | c0002 | t0049 | g0030 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03516 | hp2 | a0007 | c0009 | t0030 | g0384 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0148 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03540 | hp2 | a0001 | c0002 | t0006 | g0140 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03579 | hp1 | a0001 | c0002 | t0006 | g0255 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03579 | hp2 | a0003 | c0011 | t0003 | g0406 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03654 | hp1 | a0002 | c0001 | t0021 | g0202 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0040 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03669 | hp1 | a0001 | c0005 | t0002 | g0192 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0312 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0125 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03688 | hp2 | a0001 | c0005 | t0002 | g0182 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03704 | hp1 | a0012 | c0019 | t0027 | g0036 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03704 | hp2 | a0001 | c0051 | t0002 | g0151 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0051 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03710 | hp2 | a0012 | c0019 | t0027 | g0042 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0249 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03831 | hp2 | a0003 | c0004 | t0002 | g0086 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03834 | hp1 | a0002 | c0001 | t0001 | g0064 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0127 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03927 | hp1 | a0002 | c0001 | t0001 | g0129 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0263 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03942 | hp1 | a0001 | c0002 | t0029 | g0386 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0275 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0201 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04115 | hp2 | a0001 | c0005 | t0002 | g0304 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04184 | hp1 | a0002 | c0001 | t0036 | g0156 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04184 | hp2 | a0001 | c0002 | t0005 | g0037 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04199 | hp1 | a0002 | c0001 | t0017 | g0041 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04199 | hp2 | a0002 | c0001 | t0001 | g0412 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04204 | hp1 | a0014 | c0020 | t0002 | g0110 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0251 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04228 | hp2 | a0014 | c0020 | t0002 | g0334 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18522 | hp1 | a0031 | c0026 | t0052 | g0028 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0170 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18612 | hp1 | a0003 | c0004 | t0031 | g0016 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18612 | hp2 | a0004 | c0003 | t0010 | g0401 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0280 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18906 | hp2 | a0001 | c0002 | t0006 | g0045 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18939 | hp1 | a0003 | c0004 | t0002 | g0410 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18940 | hp1 | a0005 | c0006 | t0001 | g0120 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18941 | hp1 | a0003 | c0004 | t0004 | g0409 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18941 | hp2 | a0004 | c0003 | t0001 | g0306 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0243 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0388 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18943 | hp1 | a0002 | c0001 | t0001 | g0230 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18943 | hp2 | a0003 | c0004 | t0002 | g0112 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0392 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18944 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18945 | hp1 | a0004 | c0003 | t0001 | g0348 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18945 | hp2 | a0005 | c0006 | t0001 | g0116 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18946 | hp1 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18946 | hp2 | a0002 | c0001 | t0001 | g0180 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18947 | hp1 | a0005 | c0006 | t0001 | g0008 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18947 | hp2 | a0002 | c0001 | t0017 | g0032 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18948 | hp1 | a0005 | c0006 | t0001 | g0288 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18948 | hp2 | a0002 | c0001 | t0001 | g0396 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18949 | hp1 | a0005 | c0006 | t0001 | g0377 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18949 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18950 | hp1 | a0003 | c0004 | t0004 | g0343 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18950 | hp2 | a0002 | c0001 | t0010 | g0078 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18952 | hp2 | a0002 | c0001 | t0001 | g0063 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18953 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18954 | hp1 | a0001 | c0002 | t0045 | g0014 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18954 | hp2 | a0002 | c0001 | t0034 | g0204 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18956 | hp1 | a0003 | c0004 | t0004 | g0351 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18956 | hp2 | a0003 | c0004 | t0002 | g0018 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18960 | hp2 | a0009 | c0015 | t0003 | g0074 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18961 | hp1 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0174 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18962 | hp1 | a0001 | c0002 | t0025 | g0014 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18962 | hp2 | a0004 | c0003 | t0001 | g0011 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18964 | hp1 | a0003 | c0004 | t0003 | g0413 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18964 | hp2 | a0003 | c0004 | t0002 | g0017 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0391 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18968 | hp1 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0390 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18969 | hp2 | a0002 | c0001 | t0001 | g0359 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18970 | hp1 | a0002 | c0001 | t0014 | g0371 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0375 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18971 | hp2 | a0004 | c0003 | t0001 | g0345 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18973 | hp1 | a0004 | c0003 | t0001 | g0349 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18973 | hp2 | a0004 | c0003 | t0001 | g0002 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18974 | hp1 | a0002 | c0001 | t0010 | g0093 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18975 | hp1 | a0004 | c0003 | t0001 | g0395 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18975 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18977 | hp1 | a0005 | c0006 | t0001 | g0237 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18977 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0373 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18979 | hp2 | a0002 | c0001 | t0001 | g0289 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18980 | hp1 | a0002 | c0001 | t0001 | g0369 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18981 | hp2 | a0002 | c0001 | t0038 | g0321 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18982 | hp1 | a0029 | c0048 | t0001 | g0262 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0393 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18983 | hp1 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18983 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18984 | hp1 | a0002 | c0001 | t0001 | g0358 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18984 | hp2 | a0004 | c0003 | t0001 | g0353 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18985 | hp2 | a0002 | c0001 | t0014 | g0361 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18987 | hp2 | a0001 | c0005 | t0002 | g0113 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18990 | hp1 | a0032 | c0024 | t0003 | g0065 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18991 | hp1 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18993 | hp1 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18993 | hp2 | a0023 | c0043 | t0010 | g0408 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18997 | hp1 | a0027 | c0037 | t0003 | g0217 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18997 | hp2 | a0005 | c0006 | t0001 | g0073 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19000 | hp1 | a0004 | c0003 | t0001 | g0307 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19000 | hp2 | a0002 | c0001 | t0001 | g0282 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19001 | hp1 | a0034 | c0021 | t0001 | g0374 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19002 | hp1 | a0004 | c0003 | t0032 | g0291 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0397 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19003 | hp2 | a0004 | c0028 | t0001 | g0344 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19004 | hp1 | a0003 | c0004 | t0004 | g0352 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19005 | hp1 | a0002 | c0001 | t0001 | g0259 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19005 | hp2 | a0004 | c0003 | t0001 | g0011 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19007 | hp1 | a0001 | c0005 | t0002 | g0370 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19007 | hp2 | a0004 | c0003 | t0001 | g0317 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19009 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19009 | hp2 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19010 | hp1 | a0004 | c0003 | t0001 | g0354 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0364 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19011 | hp1 | a0003 | c0004 | t0004 | g0398 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19030 | hp1 | a0001 | c0002 | t0007 | g0336 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19030 | hp2 | a0018 | c0029 | t0011 | g0172 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19043 | hp1 | a0001 | c0005 | t0022 | g0046 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19043 | hp2 | a0001 | c0002 | t0006 | g0070 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19054 | hp1 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19054 | hp2 | a0004 | c0003 | t0001 | g0355 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19056 | hp1 | a0001 | c0002 | t0025 | g0319 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19056 | hp2 | a0002 | c0001 | t0001 | g0368 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19062 | hp1 | a0004 | c0003 | t0001 | g0329 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19062 | hp2 | a0009 | c0015 | t0003 | g0224 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19063 | hp1 | a0001 | c0002 | t0054 | g0031 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0362 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19064 | hp2 | a0004 | c0003 | t0001 | g0400 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19065 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19065 | hp2 | a0003 | c0004 | t0002 | g0322 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19066 | hp1 | a0004 | c0003 | t0001 | g0347 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19066 | hp2 | a0003 | c0004 | t0004 | g0350 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0363 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19068 | hp2 | a0004 | c0003 | t0001 | g0346 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19070 | hp1 | a0004 | c0003 | t0001 | g0419 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0389 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19074 | hp1 | a0002 | c0001 | t0041 | g0365 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19074 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19076 | hp1 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19076 | hp2 | a0003 | c0004 | t0002 | g0049 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19077 | hp1 | a0002 | c0001 | t0001 | g0108 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19078 | hp1 | a0002 | c0001 | t0001 | g0366 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19079 | hp1 | a0005 | c0006 | t0001 | g0175 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19080 | hp1 | a0001 | c0005 | t0002 | g0265 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19080 | hp2 | a0003 | c0004 | t0002 | g0071 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19081 | hp1 | a0001 | c0002 | t0005 | g0034 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19081 | hp2 | a0002 | c0001 | t0001 | g0372 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19082 | hp1 | a0004 | c0003 | t0001 | g0402 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19082 | hp2 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0360 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19085 | hp2 | a0002 | c0001 | t0014 | g0219 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19086 | hp1 | a0002 | c0001 | t0001 | g0118 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19086 | hp2 | a0035 | c0053 | t0001 | g0222 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19087 | hp1 | a0005 | c0006 | t0001 | g0357 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0303 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19088 | hp2 | a0001 | c0005 | t0002 | g0310 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19240 | hp1 | a0001 | c0013 | t0003 | g0134 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19240 | hp2 | a0002 | c0001 | t0012 | g0385 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20129 | hp1 | a0001 | c0002 | t0018 | g0380 | AFR | ASW | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20129 | hp2 | a0019 | c0031 | t0001 | g0159 | AFR | ASW | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0299 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0258 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20805 | hp1 | a0002 | c0008 | t0009 | g0117 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0378 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01123 | hp1 | a0002 | c0008 | t0009 | g0098 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01123 | hp2 | a0002 | c0001 | t0035 | g0203 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02109 | hp1 | a0003 | c0011 | t0003 | g0416 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02109 | hp2 | a0001 | c0005 | t0022 | g0158 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02486 | hp1 | a0001 | c0002 | t0039 | g0171 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02486 | hp2 | a0001 | c0002 | t0050 | g0021 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02559 | hp1 | a0002 | c0001 | t0001 | g0252 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02559 | hp2 | a0008 | c0033 | t0004 | g0272 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03471 | hp1 | a0010 | c0014 | t0013 | g0382 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03471 | hp2 | a0007 | c0009 | t0016 | g0161 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG06807 | hp1 | a0002 | c0030 | t0001 | g0189 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG06807 | hp2 | a0006 | c0016 | t0011 | g0210 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20300 | hp1 | a0001 | c0002 | t0015 | g0241 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0139 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA21309 | hp1 | a0001 | c0002 | t0020 | g0132 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA21309 | hp2 | a0002 | c0001 | t0001 | g0376 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0002 | g0057 | REF | REF | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0006 | g0143 | REF | REF | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152943167
|
C | T | 1 | a0015 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.110C>T | p.Pro37Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 327/6597 | 110/3432 | 37/1143 | chr4 | 152943167 | ||
chr4:152943168
|
T | TCCTCCTC others(5): Show |
1 | a0016 | 1 | HG03490.hp1 | disruptive_inframe_insertion | MODERATE | c.117_128dupTCCACCCC others(4): Show |
p.Pro40_Pro43dup | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 346/6597 | 129/3432 | 43/1143 | INFO_REALIGN_3_PRIME | chr4 | 152943168 | |
chr4:152943271
|
A | G | 1 | a0035 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.214A>G | p.Ile72Val | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 431/6597 | 214/3432 | 72/1143 | chr4 | 152943271 | ||
chr4:152943325
|
C | A | 1 | a0034 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.268C>A | p.His90Asn | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 485/6597 | 268/3432 | 90/1143 | chr4 | 152943325 | ||
chr4:152953514
|
G | A | 5 | a0003a0004a0031others(2): Show | 59 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(56): Show |
missense_variant | MODERATE | c.514G>A | p.Ala172Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 3/12 | 731/6597 | 514/3432 | 172/1143 | chr4 | 152953514 | ||
chr4:152954224
|
C | G | 1 | a0017 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.568C>G | p.Arg190Gly | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/12 | 785/6597 | 568/3432 | 190/1143 | chr4 | 152954224 | ||
chr4:152954225
|
G | A | 1 | a0018 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.569G>A | p.Arg190Gln | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/12 | 786/6597 | 569/3432 | 190/1143 | chr4 | 152954225 | ||
chr4:152960754
|
C | T | 1 | a0030 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.760C>T | p.Arg254Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/12 | 977/6597 | 760/3432 | 254/1143 | chr4 | 152960754 | ||
chr4:152974687
|
C | T | 2 | a0014a0029 | 3 | HG04204.hp1 HG04228.hp2 NA18982.hp1 |
missense_variant | MODERATE | c.1396C>T | p.Arg466Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1613/6597 | 1396/3432 | 466/1143 | chr4 | 152974687 | ||
chr4:152974745
|
G | A | 1 | a0019 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1454G>A | p.Arg485His | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1671/6597 | 1454/3432 | 485/1143 | chr4 | 152974745 | ||
chr4:152974760
|
G | A | 1 | a0020 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1469G>A | p.Gly490Glu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1686/6597 | 1469/3432 | 490/1143 | chr4 | 152974760 | ||
chr4:152974834
|
C | A | 1 | a0008 | 4 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.1543C>A | p.Leu515Met | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1760/6597 | 1543/3432 | 515/1143 | chr4 | 152974834 | ||
chr4:152974901
|
G | A | 1 | a0011 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.1610G>A | p.Arg537His | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1827/6597 | 1610/3432 | 537/1143 | chr4 | 152974901 | ||
chr4:152975008
|
C | T | 2 | a0005a0029 | 10 | NA18940.hp1 NA18945.hp2 NA18947.hp1 others(7): Show |
missense_variant | MODERATE | c.1717C>T | p.Arg573Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1934/6597 | 1717/3432 | 573/1143 | chr4 | 152975008 | ||
chr4:152975020
|
C | T | 1 | a0013 | 2 | HG02965.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.1729C>T | p.Arg577Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1946/6597 | 1729/3432 | 577/1143 | chr4 | 152975020 | ||
chr4:152975105
|
C | T | 3 | a0012a0015a0031 | 4 | HG02280.hp1 HG03704.hp1 HG03710.hp2 others(1): Show |
missense_variant | MODERATE | c.1814C>T | p.Ser605Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2031/6597 | 1814/3432 | 605/1143 | chr4 | 152975105 | ||
chr4:152975144
|
A | T | 1 | a0021 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1853A>T | p.Gln618Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2070/6597 | 1853/3432 | 618/1143 | chr4 | 152975144 | ||
chr4:152975147
|
C | A | 2 | a0007a0033 | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.1856C>A | p.Ala619Glu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2073/6597 | 1856/3432 | 619/1143 | chr4 | 152975147 | ||
chr4:152975206
|
C | T | 11 | a0002a0004a0005others(8): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
missense_variant | MODERATE | c.1915C>T | p.Arg639Cys | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2132/6597 | 1915/3432 | 639/1143 | chr4 | 152975206 | ||
chr4:152975215
|
G | A | 1 | a0015 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1924G>A | p.Val642Ile | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2141/6597 | 1924/3432 | 642/1143 | chr4 | 152975215 | ||
chr4:152975228
|
G | A | 1 | a0024 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1937G>A | p.Arg646Gln | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2154/6597 | 1937/3432 | 646/1143 | chr4 | 152975228 | ||
chr4:152975294
|
T | C | 1 | a0028 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.2003T>C | p.Leu668Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2220/6597 | 2003/3432 | 668/1143 | chr4 | 152975294 | ||
chr4:152975491
|
A | T | 3 | a0007a0017a0033 | 6 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
missense_variant | MODERATE | c.2200A>T | p.Ser734Cys | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2417/6597 | 2200/3432 | 734/1143 | chr4 | 152975491 | ||
chr4:152975539
|
G | A | 1 | a0017 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2248G>A | p.Gly750Arg | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2465/6597 | 2248/3432 | 750/1143 | chr4 | 152975539 | ||
chr4:152975830
|
G | A | 1 | a0010 | 3 | HG02615.hp2 HG02896.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.2539G>A | p.Gly847Ser | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2756/6597 | 2539/3432 | 847/1143 | chr4 | 152975830 | ||
chr4:152975965
|
C | T | 1 | a0023 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.2674C>T | p.Arg892Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2891/6597 | 2674/3432 | 892/1143 | chr4 | 152975965 | ||
chr4:152976009
|
G | A | 1 | a0025 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.2718G>A | p.Met906Ile | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2935/6597 | 2718/3432 | 906/1143 | chr4 | 152976009 | ||
chr4:152976160
|
C | A | 1 | a0027 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.2869C>A | p.Leu957Met | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3086/6597 | 2869/3432 | 957/1143 | chr4 | 152976160 | ||
chr4:152976373
|
G | C | 1 | a0026 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.3082G>C | p.Glu1028Gln | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3299/6597 | 3082/3432 | 1028/1143 | chr4 | 152976373 | ||
chr4:152976538
|
A | G | 2 | a0006a0018 | 5 | HG02145.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.3247A>G | p.Ser1083Gly | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3464/6597 | 3247/3432 | 1083/1143 | chr4 | 152976538 | ||
chr4:152976608
|
G | A | 2 | a0009a0032 | 4 | HG02071.hp1 NA18960.hp2 NA18990.hp1 others(1): Show |
missense_variant | MODERATE | c.3317G>A | p.Ser1106Asn | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3534/6597 | 3317/3432 | 1106/1143 | chr4 | 152976608 | ||
chr4:152976623
|
C | A | 1 | a0022 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.3332C>A | p.Ala1111Asp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3549/6597 | 3332/3432 | 1111/1143 | chr4 | 152976623 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152943300
|
A | C | 2 | a0001c0051a0002c0052 | 2 | HG03017.hp1 HG03704.hp2 |
synonymous_variant | LOW | c.243A>C | p.Pro81Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 460/6597 | 243/3432 | 81/1143 | chr4 | 152943300 | ||
chr4:152964952
|
G | A | 1 | a0002c0030 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1077G>A | p.Leu359Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/12 | 1294/6597 | 1077/3432 | 359/1143 | chr4 | 152964952 | ||
chr4:152972475
|
C | G | 1 | a0004c0028 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1317C>G | p.Thr439Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/12 | 1534/6597 | 1317/3432 | 439/1143 | chr4 | 152972475 | ||
chr4:152974683
|
C | T | 1 | a0003c0027 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1392C>T | p.His464His | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1609/6597 | 1392/3432 | 464/1143 | chr4 | 152974683 | ||
chr4:152974893
|
G | A | 2 | a0001c0013a0003c0011 | 6 | HG02109.hp1 HG02145.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.1602G>A | p.Pro534Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1819/6597 | 1602/3432 | 534/1143 | chr4 | 152974893 | ||
chr4:152975163
|
C | T | 3 | a0001c0010a0006c0016a0018c0029 | 8 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.1872C>T | p.Ala624Ala | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2089/6597 | 1872/3432 | 624/1143 | chr4 | 152975163 | ||
chr4:152975214
|
C | T | 1 | a0018c0029 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1923C>T | p.Gly641Gly | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2140/6597 | 1923/3432 | 641/1143 | chr4 | 152975214 | ||
chr4:152975286
|
A | C | 1 | a0001c0040 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1995A>C | p.Pro665Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2212/6597 | 1995/3432 | 665/1143 | chr4 | 152975286 | ||
chr4:152975286
|
A | G | 1 | a0002c0044 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1995A>G | p.Pro665Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2212/6597 | 1995/3432 | 665/1143 | chr4 | 152975286 | ||
chr4:152975286
|
A | T | 2 | a0001c0007a0003c0025 | 7 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(4): Show |
synonymous_variant | LOW | c.1995A>T | p.Pro665Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2212/6597 | 1995/3432 | 665/1143 | chr4 | 152975286 | ||
chr4:152975505
|
G | A | 2 | a0013c0046a0013c0047 | 2 | HG02965.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.2214G>A | p.Ala738Ala | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2431/6597 | 2214/3432 | 738/1143 | chr4 | 152975505 | ||
chr4:152975529
|
C | G | 1 | a0002c0018 | 2 | HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.2238C>G | p.Pro746Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2455/6597 | 2238/3432 | 746/1143 | chr4 | 152975529 | ||
chr4:152975613
|
G | C | 2 | a0001c0005a0003c0023 | 21 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
synonymous_variant | LOW | c.2322G>C | p.Ser774Ser | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2539/6597 | 2322/3432 | 774/1143 | chr4 | 152975613 | ||
chr4:152976018
|
C | G | 1 | a0002c0042 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.2727C>G | p.Thr909Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2944/6597 | 2727/3432 | 909/1143 | chr4 | 152976018 | ||
chr4:152976525
|
C | T | 1 | a0008c0033 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.3234C>T | p.Ala1078Ala | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3451/6597 | 3234/3432 | 1078/1143 | chr4 | 152976525 | ||
chr4:152976618
|
G | A | 17 | a0002c0001a0002c0018a0002c0030others(14): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
synonymous_variant | LOW | c.3327G>A | p.Thr1109Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3544/6597 | 3327/3432 | 1109/1143 | chr4 | 152976618 | ||
chr4:152976720
|
G | A | 1 | a0013c0046 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.3429G>A | p.Lys1143Lys | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3646/6597 | 3429/3432 | 1143/1143 | chr4 | 152976720 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152936340
|
G | T | 1 | a0001c0002t0055 | 1 | HG01981.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-200G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/12 | chr4 | 152936340 | ||||||
chr4:152936344
|
A | G | 12 | a0001c0002t0005a0001c0002t0049a0001c0002t0050others(9): Show | 22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-196A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/12 | chr4 | 152936344 | ||||||
chr4:152936385
|
G | C | 7 | a0001c0002t0012a0001c0002t0018a0001c0002t0029others(4): Show | 11 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-155G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/12 | 6673 | chr4 | 152936385 | |||||
chr4:152943022
|
G | A | 12 | a0001c0002t0005a0001c0002t0049a0001c0002t0050others(9): Show | 22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 36 | chr4 | 152943022 | |||||
chr4:152976732
|
T | C | 3 | a0001c0007t0008a0001c0007t0028a0003c0025t0047 | 7 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 9 | chr4 | 152976732 | |||||
chr4:152976772
|
A | G | 2 | a0001c0002t0026a0003c0004t0026 | 2 | HG00597.hp1 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 49 | chr4 | 152976772 | |||||
chr4:152976841
|
T | C | 1 | a0008c0012t0019 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*118T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 118 | chr4 | 152976841 | |||||
chr4:152976867
|
A | G | 1 | a0006c0039t0046 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 144 | chr4 | 152976867 | |||||
chr4:152976980
|
CCT | C | 55 | a0001c0002t0001a0001c0002t0003a0001c0002t0012others(52): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*259_*260delTC | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 259 | INFO_REALIGN_3_PRIME | chr4 | 152976980 | ||||
chr4:152977014
|
G | A | 18 | a0001c0002t0003a0001c0002t0018a0001c0002t0020others(15): Show | 45 | HG00597.hp1 HG01081.hp1 HG01891.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*291G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 291 | chr4 | 152977014 | |||||
chr4:152977026
|
A | G | 89 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(86): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
3_prime_UTR_variant | MODIFIER | c.*303A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 303 | chr4 | 152977026 | |||||
chr4:152977053
|
A | G | 1 | a0001c0002t0045 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 330 | chr4 | 152977053 | |||||
chr4:152977110
|
T | G | 1 | a0001c0005t0022 | 2 | HG02109.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 387 | chr4 | 152977110 | |||||
chr4:152977157
|
T | C | 2 | a0006c0016t0011a0018c0029t0011 | 4 | HG02145.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*434T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 434 | chr4 | 152977157 | |||||
chr4:152977182
|
A | G | 16 | a0001c0002t0002a0001c0002t0005a0001c0002t0025others(13): Show | 116 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 459 | chr4 | 152977182 | |||||
chr4:152977187
|
T | C | 1 | a0006c0039t0046 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*464T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 464 | chr4 | 152977187 | |||||
chr4:152977290
|
G | T | 18 | a0001c0002t0002a0001c0002t0005a0001c0002t0025others(15): Show | 119 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*567G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 567 | chr4 | 152977290 | |||||
chr4:152977404
|
G | T | 1 | a0006c0039t0046 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*681G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 681 | chr4 | 152977404 | |||||
chr4:152977449
|
T | C | 1 | a0002c0008t0009 | 5 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 726 | chr4 | 152977449 | |||||
chr4:152977540
|
C | T | 4 | a0007c0009t0016a0007c0009t0030a0017c0050t0040others(1): Show | 6 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*817C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 817 | chr4 | 152977540 | |||||
chr4:152977673
|
G | A | 1 | a0001c0002t0053 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*950G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 950 | chr4 | 152977673 | |||||
chr4:152977685
|
T | A | 3 | a0002c0001t0014a0002c0001t0041a0004c0003t0032 | 5 | NA18970.hp1 NA18985.hp2 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*962T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 962 | chr4 | 152977685 | |||||
chr4:152977876
|
T | C | 1 | a0001c0002t0025 | 2 | NA18962.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1153 | chr4 | 152977876 | |||||
chr4:152977912
|
A | G | 3 | a0008c0012t0019a0013c0046t0024a0013c0047t0024 | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1189A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1189 | chr4 | 152977912 | |||||
chr4:152977920
|
G | A | 4 | a0002c0001t0021a0002c0001t0033a0013c0046t0024others(1): Show | 5 | HG00099.hp2 HG01515.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1197G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1197 | chr4 | 152977920 | |||||
chr4:152977949
|
G | A | 1 | a0017c0050t0040 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1226G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1226 | chr4 | 152977949 | |||||
chr4:152978029
|
T | C | 2 | a0015c0055t0042a0031c0026t0052 | 2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1306 | chr4 | 152978029 | |||||
chr4:152978166
|
C | T | 1 | a0001c0002t0050 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1443C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1443 | chr4 | 152978166 | |||||
chr4:152978352
|
C | G | 1 | a0002c0001t0038 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1629C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1629 | chr4 | 152978352 | |||||
chr4:152978421
|
A | C | 88 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(85): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
3_prime_UTR_variant | MODIFIER | c.*1698A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1698 | chr4 | 152978421 | |||||
chr4:152978506
|
C | T | 90 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(87): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
3_prime_UTR_variant | MODIFIER | c.*1783C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1783 | chr4 | 152978506 | |||||
chr4:152978519
|
G | T | 1 | a0002c0044t0037 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1796G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1796 | chr4 | 152978519 | |||||
chr4:152978558
|
TG | T | 90 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(87): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
3_prime_UTR_variant | MODIFIER | c.*1838delG | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1838 | INFO_REALIGN_3_PRIME | chr4 | 152978558 | ||||
chr4:152978630
|
AT | A | 6 | a0001c0002t0044a0002c0001t0033a0002c0001t0034others(3): Show | 6 | HG01515.hp1 HG01978.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1917delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1917 | INFO_REALIGN_3_PRIME | chr4 | 152978630 | ||||
chr4:152978759
|
C | T | 1 | a0002c0001t0036 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2036C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2036 | chr4 | 152978759 | |||||
chr4:152978769
|
G | A | 1 | a0002c0001t0035 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2046G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2046 | chr4 | 152978769 | |||||
chr4:152978788
|
A | C | 3 | a0012c0019t0027a0015c0055t0042a0031c0026t0052 | 4 | HG02280.hp1 HG03704.hp1 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2065A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2065 | chr4 | 152978788 | |||||
chr4:152978843
|
T | C | 3 | a0002c0001t0010a0004c0003t0010a0023c0043t0010 | 4 | NA18612.hp2 NA18950.hp2 NA18974.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2120T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2120 | chr4 | 152978843 | |||||
chr4:152978873
|
A | G | 101 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(98): Show | 430 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(427): Show |
3_prime_UTR_variant | MODIFIER | c.*2150A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2150 | chr4 | 152978873 | |||||
chr4:152979096
|
C | G | 1 | a0008c0012t0019 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2373C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2373 | chr4 | 152979096 | |||||
chr4:152979122
|
A | G | 2 | a0001c0002t0020a0001c0002t0049 | 3 | HG02970.hp1 HG03516.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2399A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2399 | chr4 | 152979122 | |||||
chr4:152979249
|
C | G | 1 | a0006c0039t0046 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2526C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2526 | chr4 | 152979249 | |||||
chr4:152979342
|
ATCTCTAA others(8): Show |
A | 1 | a0001c0002t0054 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2620_*2634delTCTC others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2620 | chr4 | 152979342 | |||||
chr4:152979438
|
G | A | 2 | a0001c0002t0015a0001c0002t0029 | 4 | HG01070.hp1 HG01071.hp2 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2715G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2715 | chr4 | 152979438 | |||||
chr4:152979522
|
G | A | 1 | a0003c0004t0031 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2799G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2799 | chr4 | 152979522 | |||||
chr4:152979666
|
A | G | 1 | a0006c0039t0046 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2943A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2943 | chr4 | 152979666 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152936487
|
G | A | 3 | a0003c0004t0002g0017a0003c0004t0002g0018a0003c0004t0031g0016 | 3 | NA18612.hp1 NA18956.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-131+78G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936487 | ||||||
chr4:152936525
|
G | A | 2 | a0001c0005t0004g0019a0001c0005t0004g0020 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-131+116G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936525 | ||||||
chr4:152936606
|
T | C | 22 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(19): Show | 22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-131+197T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936606 | ||||||
chr4:152936852
|
A | T | 1 | a0002c0001t0033g0422 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-131+443A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936852 | ||||||
chr4:152936881
|
C | T | 21 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(18): Show | 21 | HG01243.hp2 HG02523.hp1 HG02735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-131+472C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936881 | ||||||
chr4:152936949
|
G | T | 1 | a0001c0002t0002g0421 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-131+540G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936949 | ||||||
chr4:152937048
|
G | C | 1 | a0002c0001t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-131+639G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937048 | ||||||
chr4:152937222
|
G | A | 3 | a0001c0002t0005g0023a0001c0002t0005g0024a0002c0001t0017g0022 | 3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-131+813G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937222 | ||||||
chr4:152937330
|
C | A | 1 | a0003c0004t0002g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-131+921C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937330 | ||||||
chr4:152937447
|
A | G | 291 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(288): Show | 300 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-131+1038A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937447 | ||||||
chr4:152937496
|
A | G | 1 | a0001c0002t0002g0420 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-131+1087A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937496 | ||||||
chr4:152937590
|
G | A | 1 | a0001c0002t0006g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-131+1181G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937590 | ||||||
chr4:152937713
|
G | T | 1 | a0004c0003t0001g0419 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-131+1304G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937713 | ||||||
chr4:152937945
|
G | T | 1 | a0001c0002t0050g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-131+1536G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937945 | ||||||
chr4:152938070
|
G | A | 3 | a0001c0005t0022g0046a0001c0007t0008g0047a0026c0038t0007g0048 | 3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-131+1661G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938070 | ||||||
chr4:152938109
|
A | T | 311 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(308): Show | 320 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.-131+1700A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938109 | ||||||
chr4:152938135
|
A | G | 37 | a0001c0002t0002g0388a0001c0002t0002g0390a0001c0002t0002g0392others(34): Show | 38 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-131+1726A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938135 | ||||||
chr4:152938137
|
G | T | 1 | a0002c0001t0001g0387 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-131+1728G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938137 | ||||||
chr4:152938183
|
G | C | 1 | a0001c0002t0050g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-131+1774G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938183 | ||||||
chr4:152938190
|
C | CT | 185 | a0001c0002t0001g0269a0001c0002t0002g0006a0001c0002t0002g0007others(182): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-131+1797dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | |||||
chr4:152938190
|
C | CTT | 9 | a0001c0002t0018g0380a0001c0002t0018g0381a0001c0002t0054g0031others(6): Show | 9 | HG02615.hp2 HG02717.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.-131+1796_-131+179 others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | |||||
chr4:152938190
|
C | CTTT | 19 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(16): Show | 20 | HG01167.hp2 HG01169.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.-131+1795_-131+179 others(7): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | |||||
chr4:152938190
|
CT | C | 6 | a0001c0002t0001g0160a0001c0002t0002g0388a0001c0002t0050g0021others(3): Show | 6 | HG02109.hp2 HG02486.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-131+1797delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | |||||
chr4:152938302
|
A | T | 38 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0002g0179others(35): Show | 39 | HG00408.hp1 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.-131+1893A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938302 | ||||||
chr4:152938313
|
G | A | 1 | a0010c0014t0013g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-131+1904G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938313 | ||||||
chr4:152938319
|
G | T | 3 | a0001c0005t0022g0046a0001c0007t0008g0047a0026c0038t0007g0048 | 3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-131+1910G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938319 | ||||||
chr4:152938409
|
G | A | 2 | a0001c0002t0005g0033a0002c0001t0017g0032 | 2 | NA18947.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-131+2000G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938409 | ||||||
chr4:152938437
|
G | C | 1 | a0003c0004t0002g0049 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-131+2028G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938437 | ||||||
chr4:152938503
|
C | G | 3 | a0001c0005t0022g0046a0001c0007t0008g0047a0026c0038t0007g0048 | 3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-131+2094C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938503 | ||||||
chr4:152938744
|
G | A | 1 | a0003c0004t0002g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-131+2335G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938744 | ||||||
chr4:152938766
|
A | G | 3 | a0001c0002t0001g0160a0001c0005t0022g0158a0019c0031t0001g0159 | 3 | HG02109.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-131+2357A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938766 | ||||||
chr4:152938778
|
C | G | 19 | a0001c0002t0002g0012a0001c0002t0002g0362a0001c0002t0002g0363others(16): Show | 20 | HG01074.hp1 NA18939.hp2 NA18940.hp2 others(17): Show |
intron_variant | MODIFIER | c.-131+2369C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938778 | ||||||
chr4:152938951
|
G | A | 1 | a0006c0016t0011g0210 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-131+2542G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938951 | ||||||
chr4:152938954
|
C | G | 6 | a0001c0002t0049g0030a0003c0011t0048g0029a0003c0023t0005g0027others(3): Show | 6 | HG01243.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-131+2545C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938954 | ||||||
chr4:152938982
|
G | T | 289 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(286): Show | 298 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.-131+2573G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938982 | ||||||
chr4:152939020
|
G | A | 183 | a0001c0002t0001g0269a0001c0002t0002g0006a0001c0002t0002g0007others(180): Show | 189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-131+2611G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939020 | ||||||
chr4:152939113
|
C | T | 1 | a0002c0001t0001g0418 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-131+2704C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939113 | ||||||
chr4:152939152
|
T | C | 15 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(12): Show | 15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.-131+2743T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939152 | ||||||
chr4:152939210
|
G | T | 1 | a0001c0002t0007g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131+2801G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939210 | ||||||
chr4:152939261
|
AGT | A | 13 | a0003c0004t0004g0343a0003c0004t0004g0350a0003c0004t0004g0351others(10): Show | 13 | NA18945.hp1 NA18950.hp1 NA18956.hp1 others(10): Show |
intron_variant | MODIFIER | c.-131+2861_-131+286 others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152939261 | |||||
chr4:152939274
|
C | G | 1 | a0002c0042t0001g0356 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-131+2865C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939274 | ||||||
chr4:152939313
|
T | C | 33 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0212others(30): Show | 35 | HG00544.hp2 HG01099.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.-131+2904T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939313 | ||||||
chr4:152939497
|
G | A | 22 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(19): Show | 22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-131+3088G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939497 | ||||||
chr4:152939510
|
G | A | 3 | a0002c0001t0001g0174a0002c0001t0001g0176a0005c0006t0001g0175 | 3 | NA18961.hp2 NA18991.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-131+3101G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939510 | ||||||
chr4:152939521
|
G | A | 3 | a0001c0002t0012g0013a0001c0007t0028g0383a0010c0014t0013g0379 | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+3112G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939521 | ||||||
chr4:152939550
|
T | C | 3 | a0001c0002t0001g0160a0001c0005t0022g0158a0019c0031t0001g0159 | 3 | HG02109.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-131+3141T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939550 | ||||||
chr4:152939605
|
C | T | 307 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(304): Show | 316 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.-131+3196C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939605 | ||||||
chr4:152939607
|
T | C | 12 | a0001c0002t0002g0388a0001c0002t0002g0390a0001c0002t0002g0392others(9): Show | 12 | HG00438.hp2 HG00597.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.-131+3198T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939607 | ||||||
chr4:152939740
|
G | A | 1 | a0008c0012t0004g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130-3188G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939740 | ||||||
chr4:152939915
|
G | A | 5 | a0001c0002t0005g0033a0001c0002t0005g0034a0001c0002t0005g0035others(2): Show | 5 | HG02523.hp1 NA18947.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130-3013G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939915 | ||||||
chr4:152940042
|
A | G | 183 | a0001c0002t0001g0269a0001c0002t0002g0006a0001c0002t0002g0007others(180): Show | 189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-130-2886A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940042 | ||||||
chr4:152940046
|
C | T | 8 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0340others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-130-2882C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940046 | ||||||
chr4:152940049
|
G | A | 1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-130-2879G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940049 | ||||||
chr4:152940071
|
G | A | 3 | a0001c0002t0001g0160a0001c0005t0022g0158a0019c0031t0001g0159 | 3 | HG02109.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-130-2857G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940071 | ||||||
chr4:152940142
|
C | G | 1 | a0001c0002t0050g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-130-2786C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940142 | ||||||
chr4:152940167
|
G | A | 1 | a0002c0001t0001g0211 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-130-2761G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940167 | ||||||
chr4:152940278
|
G | A | 5 | a0001c0002t0002g0053a0002c0001t0001g0050a0002c0001t0001g0051others(2): Show | 5 | HG01358.hp2 HG02602.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130-2650G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940278 | ||||||
chr4:152940752
|
A | G | 2 | a0001c0002t0005g0033a0002c0001t0017g0032 | 2 | NA18947.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-130-2176A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940752 | ||||||
chr4:152940816
|
C | T | 3 | a0001c0005t0022g0046a0001c0007t0008g0047a0026c0038t0007g0048 | 3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-130-2112C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940816 | ||||||
chr4:152940941
|
CT | C | 3 | a0001c0002t0005g0023a0001c0002t0005g0024a0002c0001t0017g0022 | 3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-130-1986delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940941 | ||||||
chr4:152940944
|
T | C | 3 | a0001c0002t0005g0023a0001c0002t0005g0024a0002c0001t0017g0022 | 3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-130-1984T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940944 | ||||||
chr4:152940970
|
T | G | 1 | a0002c0001t0001g0174 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-130-1958T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940970 | ||||||
chr4:152940978
|
A | G | 2 | a0002c0001t0001g0153a0002c0001t0001g0154 | 2 | HG02132.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-130-1950A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940978 | ||||||
chr4:152941101
|
T | C | 1 | a0002c0001t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-130-1827T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941101 | ||||||
chr4:152941198
|
T | C | 3 | a0001c0005t0022g0046a0001c0007t0008g0047a0026c0038t0007g0048 | 3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-130-1730T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941198 | ||||||
chr4:152941721
|
G | A | 1 | a0002c0001t0001g0178 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-130-1207G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941721 | ||||||
chr4:152941801
|
A | T | 22 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(19): Show | 22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-130-1127A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941801 | ||||||
chr4:152941813
|
G | A | 22 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(19): Show | 22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-130-1115G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941813 | ||||||
chr4:152941903
|
A | G | 1 | a0001c0002t0026g0417 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-130-1025A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941903 | ||||||
chr4:152941922
|
G | A | 1 | a0001c0002t0002g0212 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-130-1006G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941922 | ||||||
chr4:152942062
|
T | G | 38 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0002g0179others(35): Show | 39 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-130-866T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942062 | ||||||
chr4:152942094
|
T | A | 1 | a0001c0002t0002g0054 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-130-834T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942094 | ||||||
chr4:152942278
|
C | T | 37 | a0001c0002t0002g0388a0001c0002t0002g0390a0001c0002t0002g0392others(34): Show | 38 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-130-650C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942278 | ||||||
chr4:152942600
|
C | T | 1 | a0002c0001t0001g0335 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-130-328C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942600 | ||||||
chr4:152942673
|
A | G | 12 | a0001c0002t0002g0388a0001c0002t0002g0390a0001c0002t0002g0392others(9): Show | 12 | HG00438.hp2 HG00597.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.-130-255A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942673 | ||||||
chr4:152942708
|
A | G | 2 | a0001c0051t0002g0151a0002c0052t0001g0152 | 2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-130-220A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942708 | ||||||
chr4:152943747
|
C | T | 2 | a0001c0002t0002g0053a0001c0002t0002g0239 | 2 | HG02004.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.498+192C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152943747 | ||||||
chr4:152943875
|
C | CA | 96 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0002g0179others(93): Show | 99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.498+320_498+321ins others(1): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152943875 | ||||||
chr4:152943903
|
A | C | 1 | a0034c0021t0001g0374 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.498+348A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152943903 | ||||||
chr4:152944047
|
T | G | 402 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(399): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.498+492T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944047 | ||||||
chr4:152944160
|
T | G | 1 | a0021c0045t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.498+605T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944160 | ||||||
chr4:152944187
|
A | T | 267 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(264): Show | 277 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.498+632A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944187 | ||||||
chr4:152944336
|
G | GA | 191 | a0001c0002t0001g0269a0001c0002t0002g0006a0001c0002t0002g0007others(188): Show | 198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.498+787dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152944336 | |||||
chr4:152944383
|
T | C | 307 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(304): Show | 317 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.498+828T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944383 | ||||||
chr4:152944396
|
CACA | C | 6 | a0001c0002t0049g0030a0003c0011t0048g0029a0003c0023t0005g0027others(3): Show | 6 | HG01243.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.498+861_498+863del others(3): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152944396 | |||||
chr4:152944429
|
G | A | 1 | a0008c0012t0004g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.498+874G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944429 | ||||||
chr4:152944778
|
G | A | 181 | a0001c0002t0001g0269a0001c0002t0002g0006a0001c0002t0002g0007others(178): Show | 187 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.498+1223G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944778 | ||||||
chr4:152944873
|
C | A | 1 | a0001c0002t0002g0055 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.498+1318C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944873 | ||||||
chr4:152944946
|
C | G | 1 | a0014c0020t0002g0334 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.498+1391C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944946 | ||||||
chr4:152945000
|
GGTGGACC others(3): Show |
G | 3 | a0002c0001t0001g0243a0002c0001t0001g0244a0002c0001t0001g0245 | 3 | NA18942.hp1 NA18966.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.498+1451_498+1460d others(12): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152945000 | |||||
chr4:152945194
|
CAG | C | 9 | a0001c0002t0003g0170a0001c0002t0006g0045a0001c0005t0022g0046others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.498+1652_498+1653d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152945194 | |||||
chr4:152945194
|
CAGAG | C | 4 | a0001c0002t0001g0160a0001c0005t0022g0158a0019c0031t0001g0159others(1): Show | 4 | HG02109.hp2 HG03225.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1650_498+1653d others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152945194 | |||||
chr4:152945367
|
T | A | 4 | a0001c0002t0020g0132a0001c0013t0003g0131a0001c0013t0003g0133others(1): Show | 4 | HG02145.hp1 HG02965.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1812T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945367 | ||||||
chr4:152945411
|
A | G | 1 | a0002c0001t0001g0208 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.498+1856A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945411 | ||||||
chr4:152945520
|
A | G | 3 | a0001c0005t0022g0046a0001c0007t0008g0047a0026c0038t0007g0048 | 3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.498+1965A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945520 | ||||||
chr4:152945602
|
G | C | 268 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(265): Show | 278 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.498+2047G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945602 | ||||||
chr4:152945675
|
T | C | 1 | a0003c0004t0002g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.498+2120T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945675 | ||||||
chr4:152946097
|
T | C | 1 | a0002c0042t0001g0356 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.498+2542T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946097 | ||||||
chr4:152946179
|
G | A | 1 | a0007c0009t0016g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498+2624G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946179 | ||||||
chr4:152946421
|
G | A | 1 | a0001c0002t0002g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498+2866G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946421 | ||||||
chr4:152946529
|
C | T | 1 | a0001c0002t0007g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.498+2974C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946529 | ||||||
chr4:152946703
|
G | A | 1 | a0001c0002t0003g0247 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.498+3148G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946703 | ||||||
chr4:152946955
|
G | A | 5 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0006g0337others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+3400G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946955 | ||||||
chr4:152947177
|
C | T | 1 | a0001c0002t0029g0386 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.498+3622C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947177 | ||||||
chr4:152947216
|
C | CA | 9 | a0001c0002t0002g0179a0001c0002t0007g0342a0001c0002t0012g0013others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.498+3676dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152947216 | |||||
chr4:152947216
|
CA | C | 6 | a0001c0002t0002g0373a0001c0002t0007g0207a0002c0001t0001g0130others(3): Show | 6 | HG02698.hp2 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.498+3676delA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152947216 | |||||
chr4:152947293
|
T | A | 1 | a0001c0002t0002g0397 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.498+3738T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947293 | ||||||
chr4:152947465
|
T | G | 1 | a0001c0002t0002g0397 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.498+3910T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947465 | ||||||
chr4:152947660
|
T | G | 1 | a0002c0001t0001g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.498+4105T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947660 | ||||||
chr4:152947810
|
AAGAG | A | 286 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(283): Show | 296 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.498+4277_498+4280d others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152947810 | |||||
chr4:152948157
|
T | C | 30 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0002g0179others(27): Show | 31 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+4602T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948157 | ||||||
chr4:152948357
|
C | A | 15 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(12): Show | 15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.498+4802C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948357 | ||||||
chr4:152948371
|
A | AC | 15 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(12): Show | 15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.498+4817dupC | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152948371 | |||||
chr4:152948374
|
T | A | 15 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0033others(12): Show | 15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.498+4819T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948374 | ||||||
chr4:152948439
|
G | A | 10 | a0001c0002t0012g0013a0001c0002t0018g0380a0001c0002t0018g0381others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.498+4884G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948439 | ||||||
chr4:152948523
|
A | G | 1 | a0001c0002t0002g0333 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.498+4968A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948523 | ||||||
chr4:152948630
|
T | A | 1 | a0001c0002t0002g0397 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-4869T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948630 | ||||||
chr4:152948717
|
A | G | 1 | a0002c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.499-4782A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948717 | ||||||
chr4:152948842
|
A | G | 6 | a0001c0005t0002g0164a0001c0005t0022g0046a0001c0007t0008g0047others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4657A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948842 | ||||||
chr4:152948950
|
A | T | 1 | a0002c0001t0001g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-4549A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948950 | ||||||
chr4:152949090
|
G | GTAA | 7 | a0001c0005t0004g0126a0002c0001t0001g0125a0002c0001t0001g0378others(4): Show | 8 | HG00140.hp1 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.499-4375_499-4373d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
G | GTAATAA | 3 | a0001c0002t0002g0055a0001c0002t0003g0124a0001c0002t0003g0148 | 3 | HG01081.hp1 HG01261.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.499-4378_499-4373d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
G | GTAATAAT others(2): Show |
3 | a0001c0007t0008g0150a0002c0001t0035g0203a0013c0047t0024g0149 | 3 | HG01123.hp2 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.499-4381_499-4373d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
GTAA | G | 12 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0007g0155others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-4375_499-4373d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
GTAATAA | G | 4 | a0001c0002t0007g0207a0001c0002t0018g0380a0001c0005t0002g0182others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4378_499-4373d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
GTAATAAT others(2): Show |
G | 3 | a0001c0002t0002g0179a0006c0016t0011g0166a0006c0016t0011g0167 | 3 | HG02145.hp2 HG02698.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.499-4381_499-4373d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
GTAATAAT others(8): Show |
G | 1 | a0002c0001t0001g0389 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.499-4387_499-4373d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
GTAATAAT others(11): Show |
G | 8 | a0001c0002t0002g0388a0001c0002t0002g0390a0001c0002t0002g0392others(5): Show | 8 | NA18942.hp2 NA18944.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-4390_499-4373d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949090
|
GTAATAAT others(14): Show |
G | 2 | a0003c0004t0004g0398a0004c0003t0001g0399 | 2 | HG02273.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.499-4393_499-4373d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | |||||
chr4:152949100
|
T | C | 1 | a0001c0005t0002g0057 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.499-4399T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949100 | ||||||
chr4:152949106
|
TAATAATA others(14): Show |
T | 1 | a0001c0002t0002g0397 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-4390_499-4370d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949106 | |||||
chr4:152949106
|
TAATAATA others(17): Show |
T | 1 | a0002c0001t0001g0248 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.499-4390_499-4367d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949106 | |||||
chr4:152949106
|
TAATAATA others(32): Show |
T | 1 | a0021c0045t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.499-4390_499-4352d others(41): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949106 | |||||
chr4:152949109
|
TAATAATA others(11): Show |
T | 4 | a0002c0001t0001g0394a0002c0001t0001g0418a0004c0003t0001g0395others(1): Show | 4 | HG00438.hp2 HG00597.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4387_499-4370d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949109 | |||||
chr4:152949109
|
TAATAATA others(14): Show |
T | 7 | a0001c0002t0002g0213a0001c0002t0007g0404a0001c0007t0008g0405others(4): Show | 7 | HG01891.hp2 HG01928.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.499-4387_499-4367d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949109 | |||||
chr4:152949109
|
TAATAATA others(17): Show |
T | 4 | a0001c0002t0002g0250a0002c0001t0001g0205a0002c0001t0001g0358others(1): Show | 4 | HG02129.hp1 NA18953.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4387_499-4364d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949109 | |||||
chr4:152949110
|
A | G | 1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4389A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949110 | ||||||
chr4:152949112
|
T | G | 2 | a0001c0002t0003g0059a0002c0001t0001g0058 | 2 | HG01258.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.499-4387T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949112 | ||||||
chr4:152949112
|
TAATAATA others(8): Show |
T | 1 | a0004c0003t0001g0407 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.499-4384_499-4370d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | |||||
chr4:152949112
|
TAATAATA others(11): Show |
T | 4 | a0001c0002t0029g0386a0001c0007t0008g0168a0002c0001t0001g0251others(1): Show | 4 | HG02818.hp1 HG03942.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-4384_499-4367d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | |||||
chr4:152949112
|
TAATAATA others(14): Show |
T | 9 | a0001c0002t0002g0239a0001c0005t0004g0019a0001c0005t0004g0020others(6): Show | 10 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.499-4384_499-4364d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | |||||
chr4:152949112
|
TAATAATA others(17): Show |
T | 31 | a0001c0002t0002g0006a0001c0002t0002g0012a0001c0002t0002g0212others(28): Show | 33 | HG00423.hp2 HG00544.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.499-4384_499-4361d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | |||||
chr4:152949112
|
TAATAATA others(20): Show |
T | 1 | a0022c0041t0001g0264 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.499-4384_499-4358d others(29): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | |||||
chr4:152949113
|
A | G | 1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4386A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949113 | ||||||
chr4:152949115
|
T | G | 7 | a0001c0002t0001g0181a0001c0002t0003g0059a0002c0001t0001g0058others(4): Show | 7 | HG00140.hp2 HG01258.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.499-4384T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949115 | ||||||
chr4:152949115
|
T | TAAGAAGA others(5): Show |
2 | a0002c0001t0001g0064a0032c0024t0003g0065 | 2 | HG03834.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.499-4382_499-4381i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | |||||
chr4:152949115
|
T | TAAGAAGA others(8): Show |
1 | a0002c0001t0001g0063 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.499-4382_499-4381i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | |||||
chr4:152949115
|
TAATAATA others(8): Show |
T | 1 | a0001c0007t0008g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.499-4381_499-4367d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | |||||
chr4:152949115
|
TAATAATA others(11): Show |
T | 3 | a0001c0002t0050g0021a0003c0004t0007g0411a0007c0009t0016g0169 | 3 | HG01175.hp2 HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.499-4381_499-4364d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | |||||
chr4:152949115
|
TAATAATA others(14): Show |
T | 7 | a0001c0002t0012g0013a0001c0005t0002g0265a0002c0001t0001g0165others(4): Show | 8 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-4381_499-4361d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | |||||
chr4:152949115
|
TAATAATA others(17): Show |
T | 40 | a0001c0002t0001g0269a0001c0002t0002g0007a0001c0002t0002g0009others(37): Show | 42 | HG00323.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.499-4381_499-4358d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | |||||
chr4:152949115
|
TAATAATA others(20): Show |
T | 3 | a0002c0001t0001g0180a0003c0004t0002g0018a0004c0003t0001g0002 | 4 | HG02071.hp2 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4381_499-4355d others(29): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | |||||
chr4:152949116
|
A | G | 1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4383A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949116 | ||||||
chr4:152949118
|
T | G | 15 | a0001c0002t0001g0181a0001c0002t0003g0059a0001c0002t0020g0183others(12): Show | 15 | HG00140.hp2 HG01258.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.499-4381T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949118 | ||||||
chr4:152949118
|
T | TAAGAAG | 3 | a0001c0002t0004g0072a0005c0006t0001g0073a0009c0015t0003g0074 | 3 | HG00621.hp2 NA18960.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.499-4379_499-4378i others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949118
|
T | TAAGAAGA others(2): Show |
4 | a0001c0002t0006g0070a0002c0001t0001g0068a0002c0001t0001g0069others(1): Show | 4 | NA19003.hp1 NA19043.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-4379_499-4378i others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949118
|
T | TAAGAAGA others(58): Show |
1 | a0007c0009t0016g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.499-4379_499-4378i others(67): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949118
|
T | TAAGAAGA others(67): Show |
1 | a0001c0005t0002g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.499-4379_499-4378i others(76): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949118
|
TAATAATA others(8): Show |
T | 1 | a0001c0007t0028g0383 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.499-4378_499-4364d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949118
|
TAATAATA others(11): Show |
T | 5 | a0001c0002t0003g0170a0001c0002t0026g0417a0001c0005t0002g0164others(2): Show | 5 | HG00597.hp1 HG01070.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-4378_499-4361d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949118
|
TAATAATA others(14): Show |
T | 7 | a0002c0001t0001g0285a0002c0018t0001g0010a0003c0004t0004g0343others(4): Show | 8 | HG02074.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.499-4378_499-4358d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949118
|
TAATAATA others(17): Show |
T | 53 | a0001c0002t0002g0228a0001c0002t0002g0231a0001c0002t0002g0232others(50): Show | 53 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.499-4378_499-4355d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | |||||
chr4:152949119
|
A | G | 1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4380A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949119 | ||||||
chr4:152949121
|
T | G | 29 | a0001c0002t0001g0181a0001c0002t0003g0059a0001c0002t0004g0072others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.499-4378T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949121 | ||||||
chr4:152949121
|
T | TAAG | 5 | a0001c0002t0002g0421a0002c0001t0001g0082a0002c0001t0001g0083others(2): Show | 5 | HG01243.hp1 HG01361.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-4376_499-4375i others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949121
|
T | TAAGAAG | 4 | a0001c0002t0002g0080a0001c0002t0002g0081a0001c0002t0004g0137others(1): Show | 4 | HG02818.hp2 NA18981.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4376_499-4375i others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949121
|
T | TAAGAAGA others(5): Show |
5 | a0001c0002t0002g0079a0001c0010t0023g0136a0002c0001t0001g0129others(2): Show | 5 | HG02071.hp1 HG02630.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-4376_499-4375i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949121
|
T | TAAGAAGA others(14): Show |
1 | a0001c0002t0003g0077 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.499-4376_499-4375i others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949121
|
T | TAAGAAGA others(17): Show |
1 | a0001c0002t0002g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.499-4376_499-4375i others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949121
|
TAATAAGA others(11): Show |
T | 2 | a0001c0005t0022g0046a0001c0007t0008g0047 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.499-4375_499-4358d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949121
|
TAATAAGA others(14): Show |
T | 4 | a0001c0002t0002g0312a0001c0005t0002g0310a0002c0001t0001g0311others(1): Show | 4 | HG00741.hp1 HG01099.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4375_499-4355d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949121
|
TAATAAGA others(17): Show |
T | 23 | a0001c0002t0002g0234a0001c0002t0002g0320a0001c0002t0002g0333others(20): Show | 24 | HG00408.hp2 HG00741.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.499-4375_499-4352d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | |||||
chr4:152949122
|
A | G | 1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4377A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949122 | ||||||
chr4:152949124
|
T | G | 66 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0002g0076others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.499-4375T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949124 | ||||||
chr4:152949124
|
T | TAAGAAG | 7 | a0001c0002t0002g0099a0001c0002t0003g0142a0002c0001t0001g0001others(4): Show | 9 | HG01074.hp2 HG01106.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-4332_499-4327d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAAGAAGA others(2): Show |
7 | a0001c0002t0002g0092a0001c0002t0002g0095a0001c0005t0002g0192others(4): Show | 7 | HG03041.hp2 HG03669.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-4335_499-4327d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAAGAAGA others(5): Show |
10 | a0001c0002t0006g0140a0002c0001t0001g0052a0002c0001t0001g0087others(7): Show | 10 | HG00609.hp1 HG01256.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.499-4338_499-4327d others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAAGAAGA others(8): Show |
2 | a0001c0002t0003g0139a0003c0004t0002g0086 | 2 | HG03831.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.499-4341_499-4327d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAAG | 4 | a0001c0002t0002g0053a0001c0005t0002g0113a0002c0001t0001g0114others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4373_499-4372i others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAAGA others(2): Show |
11 | a0001c0051t0002g0151a0002c0001t0001g0107a0002c0001t0001g0108others(8): Show | 11 | HG00735.hp2 HG01496.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.499-4373_499-4372i others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAAGA others(5): Show |
2 | a0001c0002t0002g0106a0002c0001t0001g0103 | 2 | HG02040.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAAGA others(8): Show |
2 | a0001c0002t0002g0054a0001c0002t0002g0105 | 2 | HG02165.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAAGA others(20): Show |
1 | a0001c0002t0002g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.499-4373_499-4372i others(29): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAATA others(2): Show |
5 | a0001c0002t0003g0145a0002c0001t0001g0122a0002c0001t0001g0123others(2): Show | 5 | HG01516.hp1 HG02074.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-4373_499-4372i others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAATA others(5): Show |
2 | a0002c0001t0001g0121a0003c0004t0002g0049 | 2 | HG01993.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAATA others(8): Show |
2 | a0002c0001t0001g0119a0005c0006t0001g0120 | 2 | NA18940.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAATA others(14): Show |
2 | a0001c0002t0003g0144a0002c0001t0001g0118 | 2 | HG02723.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TAATAATA others(11): Show |
2 | a0002c0001t0001g0128a0007c0009t0016g0135 | 2 | HG02630.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
T | TGATGATG others(6): Show |
1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4375_499-4374i others(15): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949124 | ||||||
chr4:152949124
|
TAAG | T | 14 | a0001c0002t0004g0198a0001c0002t0005g0023a0001c0002t0005g0024others(11): Show | 14 | HG00423.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-4329_499-4327d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
TAAGAAG | T | 4 | a0001c0002t0049g0030a0002c0001t0001g0178a0002c0001t0001g0200others(1): Show | 4 | HG03516.hp1 NA18946.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4332_499-4327d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
TAAGAAGA others(2): Show |
T | 6 | a0001c0002t0002g0194a0001c0002t0002g0197a0001c0002t0002g0201others(3): Show | 6 | HG00408.hp1 HG02976.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4335_499-4327d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
TAAGAAGA others(5): Show |
T | 1 | a0012c0019t0027g0042 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.499-4338_499-4327d others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
TAAGAAGA others(11): Show |
T | 4 | a0001c0002t0006g0045a0002c0001t0001g0330a0002c0001t0001g0331others(1): Show | 4 | HG00280.hp1 HG01346.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4344_499-4327d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
TAAGAAGA others(14): Show |
T | 1 | a0004c0003t0001g0355 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.499-4347_499-4327d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949124
|
TAAGAAGA others(17): Show |
T | 14 | a0001c0002t0002g0235a0001c0002t0002g0236a0001c0002t0002g0324others(11): Show | 14 | HG00099.hp1 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.499-4350_499-4327d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | |||||
chr4:152949127
|
G | T | 11 | a0001c0002t0020g0132a0001c0005t0004g0126a0001c0007t0008g0150others(8): Show | 12 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-4372G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949127 | ||||||
chr4:152949130
|
G | T | 15 | a0001c0002t0004g0198a0001c0002t0005g0040a0001c0002t0020g0132others(12): Show | 15 | HG00423.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.499-4369G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949130 | ||||||
chr4:152949133
|
G | T | 14 | a0001c0002t0004g0198a0001c0002t0005g0040a0001c0002t0020g0132others(11): Show | 14 | HG00423.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-4366G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949133 | ||||||
chr4:152949136
|
G | T | 9 | a0001c0002t0002g0197a0001c0002t0002g0201a0001c0002t0005g0040others(6): Show | 9 | HG02976.hp1 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-4363G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949136 | ||||||
chr4:152949139
|
G | T | 6 | a0001c0002t0002g0201a0002c0001t0021g0202a0002c0001t0034g0204others(3): Show | 6 | HG02976.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4360G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949139 | ||||||
chr4:152949140
|
A | T | 1 | a0001c0002t0002g0397 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-4359A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949140 | ||||||
chr4:152949142
|
G | T | 2 | a0003c0011t0048g0029a0012c0019t0027g0042 | 2 | HG02976.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.499-4357G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949142 | ||||||
chr4:152949145
|
G | T | 3 | a0002c0001t0001g0330a0002c0001t0001g0331a0012c0019t0027g0042 | 3 | HG00280.hp1 HG01346.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.499-4354G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949145 | ||||||
chr4:152949148
|
G | T | 3 | a0002c0001t0001g0330a0002c0001t0001g0331a0004c0003t0001g0355 | 3 | HG00280.hp1 HG01346.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.499-4351G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949148 | ||||||
chr4:152949151
|
G | T | 3 | a0001c0005t0004g0332a0002c0001t0001g0331a0004c0003t0001g0329 | 3 | HG00280.hp1 HG01192.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.499-4348G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949151 | ||||||
chr4:152949154
|
G | T | 1 | a0001c0005t0004g0332 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.499-4345G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949154 | ||||||
chr4:152949157
|
G | GAAGAAGA others(26): Show |
1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4334_499-4333i others(35): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949157 | |||||
chr4:152949157
|
G | T | 1 | a0001c0005t0004g0332 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.499-4342G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949157 | ||||||
chr4:152949167
|
A | C | 1 | a0002c0001t0035g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.499-4332A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949167 | ||||||
chr4:152949170
|
A | AAGAAGAA others(8): Show |
1 | a0002c0001t0036g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.499-4327_499-4326i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949170 | |||||
chr4:152949170
|
A | AAGAAGAA others(5): Show |
1 | a0002c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.499-4327_499-4326i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949170 | |||||
chr4:152949170
|
A | C | 30 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0002g0179others(27): Show | 31 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.499-4329A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949170 | ||||||
chr4:152949173
|
C | A | 4 | a0001c0002t0039g0171a0001c0005t0002g0162a0002c0001t0001g0103others(1): Show | 4 | HG02040.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-4326C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949173 | ||||||
chr4:152949203
|
T | C | 283 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(280): Show | 293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.499-4296T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949203 | ||||||
chr4:152949204
|
G | A | 1 | a0001c0010t0023g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.499-4295G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949204 | ||||||
chr4:152949351
|
G | A | 1 | a0002c0001t0001g0314 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.499-4148G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949351 | ||||||
chr4:152949493
|
AAATAAAA others(7): Show |
A | 1 | a0001c0002t0039g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4004_499-3991d others(16): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949493 | |||||
chr4:152949502
|
G | A | 196 | a0001c0002t0001g0269a0001c0002t0002g0006a0001c0002t0002g0007others(193): Show | 203 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.499-3997G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949502 | ||||||
chr4:152949643
|
G | A | 2 | a0001c0002t0003g0139a0001c0002t0003g0144 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.499-3856G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949643 | ||||||
chr4:152949657
|
G | A | 2 | a0008c0012t0004g0177a0015c0055t0042g0242 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.499-3842G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949657 | ||||||
chr4:152949693
|
C | G | 11 | a0001c0005t0002g0327a0001c0005t0002g0328a0001c0005t0004g0332others(8): Show | 11 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-3806C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949693 | ||||||
chr4:152949695
|
G | A | 1 | a0002c0001t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.499-3804G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949695 | ||||||
chr4:152949755
|
G | A | 5 | a0002c0001t0001g0004a0002c0001t0001g0187a0002c0001t0001g0195others(2): Show | 6 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-3744G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949755 | ||||||
chr4:152949836
|
G | GCGTTAAT others(9): Show |
1 | a0001c0002t0002g0397 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-3662_499-3647d others(18): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949836 | |||||
chr4:152949837
|
C | T | 1 | a0002c0001t0001g0200 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.499-3662C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949837 | ||||||
chr4:152949963
|
G | A | 35 | a0001c0002t0002g0388a0001c0002t0002g0390a0001c0002t0002g0392others(32): Show | 37 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.499-3536G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949963 | ||||||
chr4:152950147
|
A | G | 2 | a0001c0002t0003g0308a0021c0045t0003g0157 | 2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.499-3352A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950147 | ||||||
chr4:152950188
|
C | T | 164 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0009others(161): Show | 171 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.499-3311C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950188 | ||||||
chr4:152950232
|
C | T | 1 | a0004c0003t0001g0354 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.499-3267C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950232 | ||||||
chr4:152950252
|
C | G | 2 | a0002c0001t0001g0200a0002c0001t0034g0204 | 2 | NA18954.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.499-3247C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950252 | ||||||
chr4:152950726
|
C | T | 3 | a0002c0001t0001g0118a0002c0001t0001g0127a0002c0001t0001g0128 | 3 | HG03834.hp2 NA19065.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.499-2773C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950726 | ||||||
chr4:152950785
|
T | G | 1 | a0001c0002t0012g0013 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.499-2714T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950785 | ||||||
chr4:152950798
|
C | T | 4 | a0001c0002t0007g0404a0001c0007t0008g0405a0003c0011t0003g0406others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-2701C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950798 | ||||||
chr4:152950807
|
C | T | 5 | a0001c0005t0002g0164a0001c0005t0022g0046a0001c0007t0008g0047others(2): Show | 5 | HG02055.hp1 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-2692C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950807 | ||||||
chr4:152950876
|
AG | A | 6 | a0001c0002t0003g0170a0001c0002t0006g0045a0001c0007t0008g0168others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.499-2621delG | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152950876 | |||||
chr4:152951007
|
C | T | 1 | a0001c0002t0002g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-2492C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951007 | ||||||
chr4:152951200
|
C | T | 1 | a0013c0046t0024g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.499-2299C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951200 | ||||||
chr4:152951291
|
C | T | 238 | a0001c0002t0001g0160a0001c0002t0001g0269a0001c0002t0002g0006others(235): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.499-2208C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951291 | ||||||
chr4:152951388
|
C | G | 1 | a0002c0001t0001g0318 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.499-2111C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951388 | ||||||
chr4:152951555
|
T | C | 1 | a0021c0045t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.499-1944T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951555 | ||||||
chr4:152951561
|
A | G | 5 | a0001c0005t0022g0046a0001c0007t0008g0047a0002c0001t0001g0196others(2): Show | 5 | HG01167.hp1 HG01192.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-1938A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951561 | ||||||
chr4:152951602
|
AAC | A | 8 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0034others(5): Show | 8 | HG02523.hp1 HG02735.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-1895_499-1894d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152951602 | |||||
chr4:152951696
|
T | C | 2 | a0001c0002t0007g0155a0001c0002t0049g0030 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.499-1803T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951696 | ||||||
chr4:152951699
|
A | G | 2 | a0008c0012t0019g0146a0008c0012t0019g0147 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.499-1800A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951699 | ||||||
chr4:152951814
|
G | A | 7 | a0001c0002t0005g0037a0001c0002t0005g0038a0001c0002t0005g0040others(4): Show | 7 | HG03239.hp2 HG03491.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-1685G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951814 | ||||||
chr4:152951962
|
A | G | 1 | a0002c0001t0001g0130 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.499-1537A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951962 | ||||||
chr4:152952119
|
C | T | 260 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(257): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.499-1380C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952119 | ||||||
chr4:152952288
|
T | C | 2 | a0001c0010t0023g0184a0008c0033t0004g0272 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.499-1211T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952288 | ||||||
chr4:152952297
|
AGTTGTTT others(144): Show |
A | 2 | a0004c0003t0001g0402a0004c0003t0032g0291 | 2 | NA19002.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.499-1201_499-1051d others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952297 | ||||||
chr4:152952703
|
G | A | 1 | a0017c0050t0040g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.499-796G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952703 | ||||||
chr4:152952731
|
G | C | 1 | a0013c0046t0024g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.499-768G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952731 | ||||||
chr4:152952989
|
G | A | 2 | a0001c0005t0002g0164a0001c0007t0008g0163 | 2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.499-510G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952989 | ||||||
chr4:152953003
|
A | T | 1 | a0002c0001t0001g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.499-496A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953003 | ||||||
chr4:152953027
|
G | A | 1 | a0001c0002t0002g0421 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.499-472G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953027 | ||||||
chr4:152953038
|
G | A | 3 | a0002c0001t0001g0180a0002c0001t0001g0205a0002c0001t0001g0285 | 3 | HG02074.hp2 HG02129.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.499-461G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953038 | ||||||
chr4:152953070
|
G | A | 9 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0005g0034others(6): Show | 9 | HG02486.hp2 HG02523.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-429G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953070 | ||||||
chr4:152953086
|
A | G | 3 | a0001c0005t0022g0046a0001c0007t0008g0047a0026c0038t0007g0048 | 3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.499-413A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953086 | ||||||
chr4:152953121
|
G | A | 3 | a0001c0002t0005g0037a0002c0001t0001g0125a0002c0001t0017g0041 | 3 | HG03688.hp1 HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.499-378G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953121 | ||||||
chr4:152953157
|
C | T | 56 | a0003c0004t0001g0414a0003c0004t0002g0015a0003c0004t0002g0017others(53): Show | 59 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.499-342C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953157 | ||||||
chr4:152953181
|
A | G | 1 | a0013c0046t0024g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.499-318A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953181 | ||||||
chr4:152953420
|
A | C | 1 | a0002c0001t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.499-79A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953420 | ||||||
chr4:152953424
|
G | T | 2 | a0002c0001t0012g0385a0007c0009t0030g0384 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.499-75G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953424 | ||||||
chr4:152953487
|
T | G | 1 | a0002c0001t0001g0257 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.499-12T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953487 | ||||||
chr4:152953618
|
C | A | 5 | a0001c0007t0028g0383a0002c0001t0012g0385a0007c0009t0030g0384others(2): Show | 5 | HG02615.hp2 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+58C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 3/11 | chr4 | 152953618 | ||||||
chr4:152953964
|
A | C | 60 | a0001c0007t0008g0150a0001c0010t0023g0184a0003c0004t0001g0414others(57): Show | 63 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(60): Show |
intron_variant | MODIFIER | c.561-253A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 3/11 | chr4 | 152953964 | ||||||
chr4:152954669
|
AGAGT | A | 56 | a0003c0004t0001g0414a0003c0004t0002g0015a0003c0004t0002g0017others(53): Show | 59 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.663+354_663+357del others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152954669 | |||||
chr4:152954694
|
A | G | 189 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(186): Show | 195 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.663+375A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954694 | ||||||
chr4:152954705
|
A | G | 7 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0006g0337others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+386A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954705 | ||||||
chr4:152954861
|
A | T | 1 | a0001c0002t0003g0308 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.663+542A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954861 | ||||||
chr4:152954919
|
A | G | 21 | a0001c0002t0003g0170a0001c0002t0003g0338a0001c0002t0003g0339others(18): Show | 22 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.663+600A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954919 | ||||||
chr4:152954977
|
A | C | 1 | a0001c0007t0008g0150 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.663+658A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954977 | ||||||
chr4:152955025
|
C | A | 250 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(247): Show | 259 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.663+706C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955025 | ||||||
chr4:152955050
|
C | G | 414 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(411): Show | 428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.663+731C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955050 | ||||||
chr4:152955051
|
A | T | 1 | a0004c0003t0001g0317 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.663+732A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955051 | ||||||
chr4:152955104
|
T | A | 58 | a0001c0002t0002g0275a0001c0007t0008g0150a0003c0004t0001g0414others(55): Show | 61 | HG01070.hp2 HG01175.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.663+785T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955104 | ||||||
chr4:152955104
|
T | TA | 6 | a0001c0002t0005g0037a0001c0002t0005g0038a0001c0002t0005g0040others(3): Show | 6 | HG03239.hp2 HG03491.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.663+794dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152955104 | |||||
chr4:152955105
|
A | T | 1 | a0002c0001t0001g0305 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.663+786A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955105 | ||||||
chr4:152955141
|
A | C | 1 | a0001c0002t0002g0079 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.663+822A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955141 | ||||||
chr4:152955321
|
A | C | 7 | a0001c0002t0005g0038a0001c0002t0005g0040a0001c0002t0053g0039others(4): Show | 7 | HG02071.hp1 HG02080.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+1002A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955321 | ||||||
chr4:152955587
|
C | T | 1 | a0021c0045t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.663+1268C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955587 | ||||||
chr4:152955760
|
G | A | 1 | a0026c0038t0007g0048 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.663+1441G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955760 | ||||||
chr4:152955798
|
A | G | 1 | a0001c0002t0002g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.663+1479A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955798 | ||||||
chr4:152955821
|
C | G | 1 | a0002c0008t0009g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.663+1502C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955821 | ||||||
chr4:152955850
|
T | G | 65 | a0001c0002t0003g0148a0001c0002t0005g0037a0001c0010t0023g0184others(62): Show | 68 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(65): Show |
intron_variant | MODIFIER | c.663+1531T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955850 | ||||||
chr4:152955868
|
T | C | 4 | a0001c0002t0020g0132a0001c0007t0008g0168a0007c0009t0016g0169others(1): Show | 4 | HG02258.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+1549T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955868 | ||||||
chr4:152955947
|
C | T | 1 | a0002c0001t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.663+1628C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955947 | ||||||
chr4:152956131
|
A | C | 7 | a0001c0002t0003g0148a0001c0002t0005g0038a0001c0002t0005g0040others(4): Show | 7 | HG02145.hp2 HG03139.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+1812A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956131 | ||||||
chr4:152956391
|
C | A | 2 | a0003c0004t0026g0325a0004c0003t0001g0317 | 2 | HG02083.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.663+2072C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956391 | ||||||
chr4:152956416
|
C | A | 2 | a0002c0001t0001g0196a0002c0001t0001g0199 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.663+2097C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956416 | ||||||
chr4:152956869
|
C | T | 2 | a0001c0005t0004g0126a0001c0005t0004g0332 | 2 | HG00140.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.663+2550C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956869 | ||||||
chr4:152956884
|
C | T | 1 | a0001c0002t0007g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.663+2565C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956884 | ||||||
chr4:152957236
|
T | C | 4 | a0001c0002t0005g0038a0001c0002t0005g0040a0001c0002t0053g0039others(1): Show | 4 | HG03239.hp2 HG03491.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+2917T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957236 | ||||||
chr4:152957328
|
A | G | 199 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(196): Show | 205 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.663+3009A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957328 | ||||||
chr4:152957463
|
G | A | 3 | a0001c0002t0002g0276a0001c0002t0002g0292a0001c0002t0002g0293 | 3 | HG01069.hp2 HG01081.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.664-3102G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957463 | ||||||
chr4:152957876
|
G | A | 1 | a0003c0004t0001g0414 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.664-2689G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957876 | ||||||
chr4:152957918
|
A | AC | 10 | a0001c0002t0003g0139a0001c0002t0003g0144a0001c0002t0003g0267others(7): Show | 10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2646dupC | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152957918 | |||||
chr4:152957920
|
A | C | 298 | a0001c0002t0001g0160a0001c0002t0001g0190a0001c0002t0001g0269others(295): Show | 308 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.664-2645A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957920 | ||||||
chr4:152957929
|
A | G | 220 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(217): Show | 226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.664-2636A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957929 | ||||||
chr4:152958002
|
T | C | 221 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(218): Show | 227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.664-2563T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958002 | ||||||
chr4:152958027
|
G | A | 1 | a0004c0003t0001g0349 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.664-2538G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958027 | ||||||
chr4:152958030
|
G | A | 1 | a0013c0046t0024g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.664-2535G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958030 | ||||||
chr4:152958048
|
C | T | 1 | a0001c0002t0002g0373 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.664-2517C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958048 | ||||||
chr4:152958113
|
T | C | 1 | a0002c0001t0001g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.664-2452T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958113 | ||||||
chr4:152958222
|
G | C | 10 | a0001c0002t0003g0139a0001c0002t0003g0144a0001c0002t0003g0267others(7): Show | 10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2343G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958222 | ||||||
chr4:152958370
|
C | T | 5 | a0003c0004t0002g0017a0003c0004t0002g0018a0003c0004t0003g0413others(2): Show | 6 | HG02071.hp2 NA18612.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-2195C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958370 | ||||||
chr4:152958466
|
G | A | 10 | a0001c0002t0003g0139a0001c0002t0003g0144a0001c0002t0003g0267others(7): Show | 10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2099G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958466 | ||||||
chr4:152958500
|
A | AT | 216 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(213): Show | 222 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.664-2057dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152958500 | |||||
chr4:152958556
|
T | C | 10 | a0001c0002t0003g0139a0001c0002t0003g0144a0001c0002t0003g0267others(7): Show | 10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2009T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958556 | ||||||
chr4:152958607
|
C | G | 2 | a0001c0007t0028g0383a0010c0014t0013g0379 | 2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.664-1958C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958607 | ||||||
chr4:152958726
|
C | T | 217 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(214): Show | 223 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.664-1839C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958726 | ||||||
chr4:152958728
|
C | G | 200 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(197): Show | 206 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.664-1837C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958728 | ||||||
chr4:152958886
|
A | C | 4 | a0001c0007t0008g0150a0001c0010t0023g0184a0008c0033t0004g0272others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1679A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958886 | ||||||
chr4:152958945
|
T | G | 5 | a0001c0002t0002g0421a0001c0002t0005g0038a0001c0002t0005g0040others(2): Show | 5 | HG02683.hp2 HG03239.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1620T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958945 | ||||||
chr4:152958959
|
G | A | 2 | a0001c0002t0001g0160a0001c0005t0022g0158 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.664-1606G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958959 | ||||||
chr4:152958997
|
A | T | 197 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(194): Show | 203 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.664-1568A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958997 | ||||||
chr4:152958999
|
G | C | 10 | a0001c0002t0003g0139a0001c0002t0003g0144a0001c0002t0003g0267others(7): Show | 10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-1566G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958999 | ||||||
chr4:152959037
|
A | G | 3 | a0001c0002t0003g0148a0006c0016t0011g0166a0006c0016t0011g0167 | 3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.664-1528A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959037 | ||||||
chr4:152959405
|
T | C | 4 | a0001c0007t0008g0150a0001c0010t0023g0184a0008c0033t0004g0272others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1160T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959405 | ||||||
chr4:152959439
|
T | C | 2 | a0001c0005t0002g0162a0007c0009t0016g0161 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.664-1126T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959439 | ||||||
chr4:152959503
|
T | C | 205 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(202): Show | 211 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.664-1062T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959503 | ||||||
chr4:152959585
|
G | C | 1 | a0001c0002t0001g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.664-980G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959585 | ||||||
chr4:152959594
|
C | T | 205 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(202): Show | 211 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.664-971C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959594 | ||||||
chr4:152959619
|
T | G | 216 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(213): Show | 222 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.664-946T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959619 | ||||||
chr4:152959627
|
C | T | 3 | a0001c0002t0003g0148a0006c0016t0011g0166a0006c0016t0011g0167 | 3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.664-938C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959627 | ||||||
chr4:152959679
|
G | A | 1 | a0004c0003t0001g0306 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.664-886G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959679 | ||||||
chr4:152959723
|
C | T | 274 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(271): Show | 283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.664-842C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959723 | ||||||
chr4:152959780
|
A | C | 2 | a0001c0002t0018g0380a0021c0045t0003g0157 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.664-785A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959780 | ||||||
chr4:152959800
|
C | T | 260 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(257): Show | 269 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.664-765C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959800 | ||||||
chr4:152959941
|
A | ACATCGGT | 276 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0006others(273): Show | 285 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.664-623_664-622ins others(7): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152959941 | |||||
chr4:152959947
|
C | T | 1 | a0001c0002t0006g0337 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.664-618C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959947 | ||||||
chr4:152959948
|
G | A | 68 | a0001c0002t0002g0223a0001c0002t0002g0276a0001c0002t0003g0139others(65): Show | 70 | HG00558.hp2 HG00609.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.664-617G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959948 | ||||||
chr4:152960036
|
A | G | 1 | a0002c0001t0001g0376 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664-529A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960036 | ||||||
chr4:152960139
|
G | A | 1 | a0001c0002t0002g0234 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.664-426G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960139 | ||||||
chr4:152960151
|
A | T | 3 | a0001c0002t0003g0148a0006c0016t0011g0166a0006c0016t0011g0167 | 3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.664-414A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960151 | ||||||
chr4:152960318
|
C | T | 1 | a0001c0002t0007g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.664-247C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960318 | ||||||
chr4:152960319
|
G | A | 1 | a0001c0007t0008g0150 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.664-246G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960319 | ||||||
chr4:152960683
|
C | T | 148 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0009others(145): Show | 156 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.749+33C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 5/11 | chr4 | 152960683 | ||||||
chr4:152960719
|
A | G | 2 | a0002c0001t0001g0196a0002c0001t0001g0199 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.750-25A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 5/11 | chr4 | 152960719 | ||||||
chr4:152960728
|
C | CT | 4 | a0001c0002t0004g0137a0001c0002t0006g0337a0003c0011t0003g0406others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.750-10dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 152960728 | |||||
chr4:152960850
|
T | C | 4 | a0002c0001t0001g0066a0002c0001t0001g0083a0002c0001t0001g0121others(1): Show | 4 | HG01361.hp2 HG01993.hp2 HG02257.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.850+6T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960850 | ||||||
chr4:152960867
|
G | A | 2 | a0001c0010t0023g0184a0008c0033t0004g0272 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.850+23G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960867 | ||||||
chr4:152960905
|
A | T | 288 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(285): Show | 298 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.850+61A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960905 | ||||||
chr4:152960906
|
A | T | 1 | a0002c0001t0001g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.850+62A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960906 | ||||||
chr4:152960995
|
G | C | 1 | a0001c0002t0002g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.850+151G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960995 | ||||||
chr4:152961028
|
G | T | 3 | a0001c0002t0003g0077a0005c0006t0001g0288a0005c0006t0001g0377 | 3 | NA18948.hp1 NA18949.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.850+184G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961028 | ||||||
chr4:152961130
|
G | A | 14 | a0001c0002t0005g0034a0001c0002t0005g0035a0001c0002t0054g0031others(11): Show | 15 | HG00639.hp2 HG01243.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.850+286G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961130 | ||||||
chr4:152961191
|
G | A | 1 | a0002c0001t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.850+347G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961191 | ||||||
chr4:152961246
|
C | CTG | 395 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(392): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.850+403_850+404ins others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 152961246 | |||||
chr4:152961301
|
C | G | 13 | a0001c0002t0005g0034a0001c0002t0005g0035a0001c0002t0054g0031others(10): Show | 14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.850+457C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961301 | ||||||
chr4:152961315
|
G | C | 1 | a0001c0002t0002g0275 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.850+471G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961315 | ||||||
chr4:152961413
|
C | T | 2 | a0005c0006t0001g0288a0005c0006t0001g0377 | 2 | NA18948.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.850+569C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961413 | ||||||
chr4:152961431
|
A | G | 65 | a0001c0002t0002g0095a0001c0002t0002g0223a0001c0002t0002g0234others(62): Show | 67 | HG00544.hp2 HG00597.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.850+587A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961431 | ||||||
chr4:152961459
|
T | C | 197 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(194): Show | 205 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.850+615T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961459 | ||||||
chr4:152961466
|
G | A | 1 | a0029c0048t0001g0262 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.850+622G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961466 | ||||||
chr4:152961490
|
G | A | 2 | a0001c0010t0023g0184a0008c0033t0004g0272 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.850+646G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961490 | ||||||
chr4:152961717
|
T | C | 5 | a0004c0003t0001g0347a0004c0003t0001g0348a0004c0003t0001g0349others(2): Show | 5 | NA18945.hp1 NA18973.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+873T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961717 | ||||||
chr4:152961855
|
A | G | 2 | a0003c0011t0003g0406a0008c0012t0004g0177 | 2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.851-959A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961855 | ||||||
chr4:152961967
|
C | T | 1 | a0003c0011t0003g0406 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.851-847C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961967 | ||||||
chr4:152962306
|
G | T | 186 | a0001c0002t0001g0181a0001c0002t0002g0006a0001c0002t0002g0007others(183): Show | 193 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.851-508G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962306 | ||||||
chr4:152962427
|
G | T | 1 | a0003c0011t0003g0406 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.851-387G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962427 | ||||||
chr4:152962498
|
A | G | 2 | a0003c0011t0003g0406a0008c0012t0004g0177 | 2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.851-316A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962498 | ||||||
chr4:152962710
|
C | T | 1 | a0002c0001t0001g0214 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.851-104C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962710 | ||||||
chr4:152962940
|
G | GGT | 218 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0002g0006others(215): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.922-42_922-41dupGT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
G | GGTGT | 58 | a0001c0002t0002g0053a0001c0002t0002g0054a0001c0002t0002g0095others(55): Show | 61 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.922-44_922-41dupGT others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
G | GGTGTGT | 19 | a0001c0002t0002g0388a0001c0002t0002g0390a0001c0002t0006g0337others(16): Show | 20 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.922-46_922-41dupGT others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
G | GGTGTGTG others(1): Show |
12 | a0001c0002t0001g0269a0001c0002t0002g0099a0001c0002t0004g0137others(9): Show | 12 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.922-48_922-41dupGT others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
G | GGTGTGTG others(3): Show |
1 | a0002c0001t0001g0127 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.922-50_922-41dupGT others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
GGT | G | 30 | a0001c0002t0001g0160a0001c0002t0002g0055a0001c0002t0002g0234others(27): Show | 30 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.922-42_922-41delGT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
GGTGT | G | 3 | a0001c0002t0002g0263a0003c0027t0043g0186a0014c0020t0002g0334 | 3 | HG02809.hp2 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.922-44_922-41delGT others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
GGTGTGT | G | 3 | a0002c0001t0001g0125a0013c0046t0024g0096a0013c0047t0024g0149 | 3 | HG02965.hp1 HG03041.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.922-46_922-41delGT others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
GGTGTGTG others(1): Show |
G | 13 | a0001c0002t0005g0034a0001c0002t0005g0035a0001c0002t0054g0031others(10): Show | 14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.922-48_922-41delGT others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
GGTGTGTG others(3): Show |
G | 4 | a0001c0002t0002g0079a0001c0002t0003g0148a0006c0016t0011g0166others(1): Show | 4 | HG02145.hp2 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.922-50_922-41delGT others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962940
|
GGTGTGTG others(11): Show |
G | 1 | a0002c0001t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.922-58_922-41delGT others(16): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | |||||
chr4:152962947
|
G | T | 2 | a0001c0002t0001g0160a0001c0002t0003g0247 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.921+63G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962947 | ||||||
chr4:152962951
|
G | T | 1 | a0002c0001t0001g0125 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.921+67G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962951 | ||||||
chr4:152962953
|
G | T | 12 | a0001c0002t0005g0034a0001c0002t0005g0035a0001c0002t0054g0031others(9): Show | 13 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.921+69G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962953 | ||||||
chr4:152962967
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0010t0023g0184a0008c0033t0004g0272 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.922-52_922-37delGT others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962967 | |||||
chr4:152962983
|
A | G | 1 | a0002c0001t0001g0316 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.922-40A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962983 | ||||||
chr4:152963012
|
G | C | 2 | a0003c0011t0003g0406a0008c0012t0004g0177 | 2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.922-11G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152963012 | ||||||
chr4:152963479
|
T | C | 5 | a0001c0002t0003g0338a0003c0011t0003g0406a0008c0012t0004g0177others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+349T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963479 | ||||||
chr4:152963489
|
A | G | 1 | a0004c0003t0001g0317 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1029+359A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963489 | ||||||
chr4:152963582
|
AGG | A | 18 | a0001c0002t0001g0160a0001c0002t0003g0247a0001c0002t0005g0034others(15): Show | 19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1029+456_1029+457d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963582 | |||||
chr4:152963589
|
G | GGGTAATG others(69): Show |
1 | a0001c0002t0012g0013 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1029+460_1029+535d others(78): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963589 | |||||
chr4:152963634
|
T | TA | 18 | a0001c0002t0001g0160a0001c0002t0003g0247a0001c0002t0005g0034others(15): Show | 19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1029+504_1029+505i others(3): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963634 | ||||||
chr4:152963675
|
G | A | 6 | a0001c0002t0002g0312a0002c0001t0001g0051a0002c0001t0001g0299others(3): Show | 7 | HG00741.hp1 HG01099.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029+545G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963675 | ||||||
chr4:152963742
|
T | A | 5 | a0001c0002t0001g0160a0001c0002t0003g0247a0003c0027t0043g0186others(2): Show | 5 | HG01891.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029+612T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963742 | ||||||
chr4:152963745
|
G | T | 1 | a0004c0003t0001g0348 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1029+615G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963745 | ||||||
chr4:152963769
|
G | GT | 40 | a0001c0002t0002g0054a0001c0002t0002g0080a0001c0002t0002g0081others(37): Show | 41 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1029+673dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
G | GTT | 15 | a0001c0002t0002g0201a0001c0002t0006g0140a0001c0002t0006g0254others(12): Show | 15 | HG01109.hp2 HG02027.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029+672_1029+673d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
G | GTTT | 9 | a0001c0002t0018g0381a0001c0005t0002g0162a0001c0005t0002g0310others(6): Show | 9 | HG00423.hp2 HG01074.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1029+671_1029+673d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
G | GTTTTTTT others(9): Show |
2 | a0001c0002t0003g0340a0028c0035t0001g0341 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1029+658_1029+673d others(18): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GT | G | 19 | a0001c0002t0002g0250a0001c0002t0003g0124a0001c0002t0003g0148others(16): Show | 19 | HG01081.hp1 HG01123.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1029+673delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTT | G | 10 | a0001c0002t0020g0132a0001c0005t0004g0019a0001c0007t0008g0047others(7): Show | 10 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+672_1029+673d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTT | G | 20 | a0001c0002t0002g0099a0001c0002t0002g0221a0001c0002t0002g0256others(17): Show | 20 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1029+669_1029+673d others(7): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTTT | G | 156 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0002g0006others(153): Show | 163 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1029+668_1029+673d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTTTT | G | 19 | a0001c0002t0002g0076a0001c0002t0002g0292a0001c0002t0005g0034others(16): Show | 20 | HG00323.hp2 HG00639.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1029+667_1029+673d others(9): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTTTT others(5): Show |
G | 13 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0393others(10): Show | 14 | HG00597.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1029+662_1029+673d others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTTTT others(6): Show |
G | 55 | a0001c0002t0002g0095a0001c0002t0002g0223a0001c0002t0002g0234others(52): Show | 57 | HG00544.hp2 HG01243.hp2 HG01433.hp1 others(54): Show |
intron_variant | MODIFIER | c.1029+661_1029+673d others(15): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0002t0004g0137a0001c0002t0006g0337a0006c0039t0046g0138 | 3 | HG01884.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1029+660_1029+673d others(16): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTTTT others(12): Show |
G | 2 | a0001c0005t0022g0158a0002c0001t0001g0214 | 2 | HG02056.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1029+655_1029+673d others(21): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963769
|
GTTTTTTT others(15): Show |
G | 1 | a0006c0016t0011g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1029+652_1029+673d others(24): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | |||||
chr4:152963780
|
T | G | 1 | a0005c0006t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1029+650T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963780 | ||||||
chr4:152963783
|
T | G | 2 | a0001c0005t0002g0113a0001c0010t0023g0136 | 2 | HG02630.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1029+653T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963783 | ||||||
chr4:152963784
|
T | G | 4 | a0001c0002t0020g0132a0001c0007t0008g0047a0001c0007t0008g0150others(1): Show | 4 | HG02258.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1029+654T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963784 | ||||||
chr4:152963785
|
T | G | 1 | a0001c0002t0002g0392 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1029+655T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963785 | ||||||
chr4:152963786
|
T | G | 1 | a0017c0050t0040g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1029+656T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963786 | ||||||
chr4:152963787
|
T | G | 1 | a0004c0003t0001g0345 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1029+657T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963787 | ||||||
chr4:152963788
|
T | G | 2 | a0001c0005t0002g0113a0003c0004t0026g0325 | 2 | HG02083.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1029+658T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963788 | ||||||
chr4:152963913
|
C | T | 13 | a0001c0002t0005g0034a0001c0002t0005g0035a0001c0002t0054g0031others(10): Show | 14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1029+783C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963913 | ||||||
chr4:152963986
|
A | C | 24 | a0001c0002t0002g0095a0001c0002t0002g0234a0001c0002t0002g0392others(21): Show | 24 | HG00597.hp2 HG01433.hp1 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.1029+856A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963986 | ||||||
chr4:152963999
|
A | T | 3 | a0003c0027t0043g0186a0013c0046t0024g0096a0013c0047t0024g0149 | 3 | HG02809.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1029+869A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963999 | ||||||
chr4:152964066
|
G | A | 1 | a0002c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1030-839G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964066 | ||||||
chr4:152964089
|
C | T | 1 | a0004c0003t0001g0329 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1030-816C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964089 | ||||||
chr4:152964203
|
G | A | 1 | a0002c0001t0001g0188 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1030-702G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964203 | ||||||
chr4:152964240
|
C | T | 15 | a0001c0002t0001g0160a0001c0002t0003g0247a0001c0002t0005g0034others(12): Show | 16 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1030-665C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964240 | ||||||
chr4:152964506
|
ATGGCTCC others(1): Show |
A | 3 | a0002c0001t0001g0064a0002c0001t0001g0121a0002c0001t0001g0130 | 3 | HG01993.hp2 HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1030-398_1030-391d others(10): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964506 | ||||||
chr4:152964647
|
T | G | 2 | a0001c0002t0001g0160a0001c0002t0003g0247 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1030-258T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964647 | ||||||
chr4:152965236
|
T | G | 322 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(319): Show | 333 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.1100+261T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965236 | ||||||
chr4:152965254
|
C | T | 4 | a0002c0001t0012g0385a0006c0016t0011g0210a0007c0009t0030g0384others(1): Show | 4 | HG03516.hp2 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1100+279C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965254 | ||||||
chr4:152965397
|
T | G | 18 | a0001c0002t0001g0160a0001c0002t0003g0247a0001c0002t0005g0034others(15): Show | 19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1100+422T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965397 | ||||||
chr4:152965402
|
G | A | 2 | a0002c0001t0001g0004a0002c0001t0017g0022 | 3 | HG01516.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1100+427G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965402 | ||||||
chr4:152965414
|
G | T | 1 | a0002c0001t0001g0364 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1100+439G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965414 | ||||||
chr4:152965546
|
T | C | 1 | a0010c0014t0013g0382 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1100+571T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965546 | ||||||
chr4:152965587
|
A | G | 2 | a0001c0010t0023g0184a0008c0033t0004g0272 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1100+612A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965587 | ||||||
chr4:152965767
|
A | G | 19 | a0001c0002t0001g0160a0001c0002t0001g0269a0001c0002t0003g0247others(16): Show | 20 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1100+792A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965767 | ||||||
chr4:152965799
|
G | A | 1 | a0001c0002t0002g0194 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1100+824G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965799 | ||||||
chr4:152965893
|
C | T | 1 | a0001c0005t0022g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1100+918C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965893 | ||||||
chr4:152965918
|
C | T | 3 | a0001c0002t0044g0216a0002c0001t0001g0305a0004c0003t0001g0400 | 3 | HG01433.hp1 HG01978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1100+943C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965918 | ||||||
chr4:152965936
|
C | A | 3 | a0003c0027t0043g0186a0013c0046t0024g0096a0013c0047t0024g0149 | 3 | HG02809.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1100+961C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965936 | ||||||
chr4:152966324
|
G | A | 1 | a0002c0001t0001g0125 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1100+1349G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966324 | ||||||
chr4:152966536
|
T | A | 2 | a0001c0002t0003g0142a0001c0040t0003g0191 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1101-1444T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966536 | ||||||
chr4:152966576
|
C | T | 1 | a0003c0004t0031g0016 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1101-1404C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966576 | ||||||
chr4:152966665
|
C | T | 18 | a0001c0002t0001g0160a0001c0002t0003g0247a0001c0002t0005g0034others(15): Show | 19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1101-1315C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966665 | ||||||
chr4:152966989
|
G | A | 1 | a0035c0053t0001g0222 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1101-991G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966989 | ||||||
chr4:152967007
|
T | C | 307 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(304): Show | 317 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.1101-973T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967007 | ||||||
chr4:152967054
|
G | T | 1 | a0002c0001t0038g0321 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1101-926G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967054 | ||||||
chr4:152967069
|
A | G | 1 | a0002c0001t0001g0125 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1101-911A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967069 | ||||||
chr4:152967104
|
A | G | 3 | a0002c0001t0001g0258a0002c0001t0001g0294a0002c0008t0009g0284 | 3 | HG00323.hp2 HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1101-876A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967104 | ||||||
chr4:152967155
|
G | A | 13 | a0001c0002t0005g0034a0001c0002t0005g0035a0001c0002t0054g0031others(10): Show | 14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1101-825G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967155 | ||||||
chr4:152967254
|
C | T | 29 | a0001c0002t0002g0055a0001c0002t0002g0397a0001c0002t0004g0283others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1101-726C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967254 | ||||||
chr4:152967426
|
C | CA | 15 | a0001c0002t0005g0034a0001c0002t0005g0035a0001c0002t0054g0031others(12): Show | 16 | HG00639.hp2 HG01243.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1101-542dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 152967426 | |||||
chr4:152967488
|
C | T | 305 | a0001c0002t0001g0181a0001c0002t0001g0190a0001c0002t0001g0269others(302): Show | 315 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.1101-492C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967488 | ||||||
chr4:152967697
|
C | G | 2 | a0001c0002t0003g0340a0028c0035t0001g0341 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1101-283C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967697 | ||||||
chr4:152967711
|
C | A | 3 | a0001c0005t0002g0162a0010c0014t0013g0209a0010c0014t0013g0382 | 3 | HG02572.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1101-269C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967711 | ||||||
chr4:152967711
|
C | T | 1 | a0002c0001t0001g0305 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1101-269C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967711 | ||||||
chr4:152967734
|
T | A | 105 | a0001c0002t0001g0190a0001c0002t0001g0269a0001c0002t0002g0055others(102): Show | 106 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1101-246T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967734 | ||||||
chr4:152967734
|
T | C | 1 | a0001c0007t0008g0405 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1101-246T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967734 | ||||||
chr4:152967755
|
C | G | 1 | a0002c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1101-225C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967755 | ||||||
chr4:152967827
|
A | G | 3 | a0001c0002t0003g0148a0006c0016t0011g0166a0006c0016t0011g0167 | 3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1101-153A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967827 | ||||||
chr4:152967943
|
T | C | 42 | a0001c0002t0002g0104a0001c0002t0002g0106a0001c0002t0002g0250others(39): Show | 43 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1101-37T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967943 | ||||||
chr4:152968113
|
A | G | 57 | a0001c0002t0001g0269a0001c0002t0002g0053a0001c0002t0002g0223others(54): Show | 59 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1218+16A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968113 | ||||||
chr4:152968158
|
G | C | 3 | a0001c0007t0028g0383a0008c0033t0004g0272a0019c0031t0001g0159 | 3 | HG02559.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1218+61G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968158 | ||||||
chr4:152968259
|
G | A | 1 | a0003c0004t0001g0414 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1218+162G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968259 | ||||||
chr4:152968293
|
A | AT | 15 | a0001c0002t0004g0283a0001c0002t0015g0005a0001c0002t0015g0241others(12): Show | 16 | HG01070.hp1 HG01071.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1218+208dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 152968293 | |||||
chr4:152968295
|
T | A | 2 | a0012c0019t0027g0036a0012c0019t0027g0042 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1218+198T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968295 | ||||||
chr4:152968310
|
C | T | 315 | a0001c0002t0001g0269a0001c0002t0002g0006a0001c0002t0002g0007others(312): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.1218+213C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968310 | ||||||
chr4:152968388
|
C | T | 19 | a0001c0002t0002g0055a0001c0002t0002g0179a0001c0002t0003g0077others(16): Show | 19 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1218+291C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968388 | ||||||
chr4:152968454
|
T | G | 239 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1218+357T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968454 | ||||||
chr4:152968517
|
C | T | 1 | a0024c0034t0003g0111 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1218+420C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968517 | ||||||
chr4:152968519
|
C | T | 1 | a0015c0055t0042g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218+422C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968519 | ||||||
chr4:152968520
|
G | A | 394 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0269others(391): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1218+423G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968520 | ||||||
chr4:152968622
|
G | A | 1 | a0001c0002t0002g0232 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1218+525G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968622 | ||||||
chr4:152968741
|
G | T | 2 | a0002c0001t0001g0109a0004c0003t0001g0353 | 2 | NA18984.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1218+644G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968741 | ||||||
chr4:152968794
|
T | C | 1 | a0002c0001t0001g0195 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1218+697T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968794 | ||||||
chr4:152968796
|
G | A | 7 | a0003c0025t0047g0025a0007c0009t0016g0135a0007c0009t0016g0161others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+699G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968796 | ||||||
chr4:152968954
|
G | A | 267 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1218+857G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968954 | ||||||
chr4:152968975
|
G | A | 58 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0012others(55): Show | 62 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1218+878G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968975 | ||||||
chr4:152969039
|
T | C | 2 | a0002c0001t0001g0094a0002c0001t0017g0032 | 2 | NA18947.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1218+942T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969039 | ||||||
chr4:152969051
|
C | T | 1 | a0001c0002t0002g0397 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1218+954C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969051 | ||||||
chr4:152969052
|
G | A | 1 | a0002c0001t0033g0422 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1218+955G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969052 | ||||||
chr4:152969066
|
A | G | 1 | a0003c0004t0002g0112 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1218+969A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969066 | ||||||
chr4:152969086
|
TA | T | 31 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0269others(28): Show | 32 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1218+1004delA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 152969086 | |||||
chr4:152969120
|
T | G | 1 | a0001c0005t0002g0279 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1218+1023T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969120 | ||||||
chr4:152969369
|
C | A | 13 | a0001c0010t0003g0286a0001c0010t0003g0315a0001c0010t0023g0136others(10): Show | 13 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+1272C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969369 | ||||||
chr4:152969494
|
C | T | 280 | a0001c0002t0001g0190a0001c0002t0002g0055a0001c0002t0002g0179others(277): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1218+1397C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969494 | ||||||
chr4:152969641
|
C | T | 219 | a0001c0002t0002g0055a0001c0002t0002g0179a0001c0005t0002g0057others(216): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1218+1544C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969641 | ||||||
chr4:152969665
|
G | GT | 61 | a0001c0002t0002g0012a0001c0002t0002g0079a0001c0002t0002g0081others(58): Show | 62 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1218+1587dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 152969665 | |||||
chr4:152969665
|
G | T | 3 | a0002c0001t0001g0088a0002c0001t0001g0230a0004c0003t0001g0419 | 3 | HG02165.hp1 NA18943.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1218+1568G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969665 | ||||||
chr4:152969672
|
T | C | 9 | a0001c0002t0004g0198a0001c0002t0004g0283a0003c0004t0002g0410others(6): Show | 9 | HG01168.hp1 HG02738.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+1575T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969672 | ||||||
chr4:152969684
|
T | C | 1 | a0001c0002t0006g0337 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1218+1587T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969684 | ||||||
chr4:152969732
|
C | T | 40 | a0001c0002t0003g0059a0001c0002t0003g0077a0001c0002t0003g0124others(37): Show | 40 | HG00597.hp1 HG01081.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.1218+1635C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969732 | ||||||
chr4:152969870
|
C | T | 194 | a0001c0007t0028g0383a0002c0001t0001g0001a0002c0001t0001g0004others(191): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1218+1773C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969870 | ||||||
chr4:152969871
|
G | A | 8 | a0001c0010t0003g0286a0001c0010t0003g0315a0001c0010t0023g0136others(5): Show | 8 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218+1774G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969871 | ||||||
chr4:152969916
|
A | G | 416 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0190others(413): Show | 430 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(427): Show |
intron_variant | MODIFIER | c.1218+1819A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969916 | ||||||
chr4:152969989
|
C | T | 1 | a0019c0031t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1218+1892C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969989 | ||||||
chr4:152970120
|
A | T | 2 | a0002c0001t0001g0004a0002c0001t0017g0022 | 3 | HG01516.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1218+2023A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970120 | ||||||
chr4:152970171
|
T | C | 6 | a0001c0002t0001g0190a0001c0007t0008g0047a0001c0007t0008g0150others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+2074T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970171 | ||||||
chr4:152970502
|
C | T | 1 | a0001c0007t0028g0383 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1219-1875C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970502 | ||||||
chr4:152970541
|
G | C | 1 | a0001c0002t0003g0226 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1219-1836G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970541 | ||||||
chr4:152970632
|
A | G | 2 | a0001c0013t0003g0133a0001c0013t0003g0134 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1219-1745A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970632 | ||||||
chr4:152970789
|
G | A | 1 | a0001c0002t0003g0059 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1219-1588G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970789 | ||||||
chr4:152971150
|
G | T | 38 | a0001c0002t0003g0059a0001c0002t0003g0077a0001c0002t0003g0139others(35): Show | 38 | HG00597.hp1 HG01891.hp1 HG02083.hp1 others(35): Show |
intron_variant | MODIFIER | c.1219-1227G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971150 | ||||||
chr4:152971152
|
G | A | 1 | a0019c0031t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1219-1225G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971152 | ||||||
chr4:152971209
|
A | C | 1 | a0004c0003t0001g0355 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1219-1168A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971209 | ||||||
chr4:152971273
|
T | C | 7 | a0001c0002t0004g0072a0001c0002t0004g0137a0006c0039t0046g0138others(4): Show | 7 | HG00621.hp2 HG02559.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1219-1104T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971273 | ||||||
chr4:152971519
|
C | T | 2 | a0002c0001t0001g0109a0004c0003t0001g0353 | 2 | NA18984.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1219-858C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971519 | ||||||
chr4:152971532
|
C | T | 1 | a0001c0002t0004g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1219-845C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971532 | ||||||
chr4:152971543
|
T | C | 2 | a0013c0046t0024g0096a0013c0047t0024g0149 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1219-834T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971543 | ||||||
chr4:152971704
|
A | G | 198 | a0001c0002t0003g0124a0002c0001t0001g0001a0002c0001t0001g0004others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1219-673A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971704 | ||||||
chr4:152971786
|
C | T | 2 | a0002c0001t0001g0004a0002c0001t0017g0022 | 3 | HG01516.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1219-591C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971786 | ||||||
chr4:152971850
|
G | C | 1 | a0002c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1219-527G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971850 | ||||||
chr4:152971920
|
A | G | 130 | a0001c0002t0001g0160a0001c0002t0001g0181a0001c0002t0001g0269others(127): Show | 138 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.1219-457A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971920 | ||||||
chr4:152971945
|
A | G | 21 | a0001c0005t0002g0057a0001c0005t0002g0113a0001c0005t0002g0162others(18): Show | 21 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1219-432A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971945 | ||||||
chr4:152972113
|
G | A | 258 | a0001c0002t0003g0059a0001c0002t0003g0077a0001c0002t0003g0124others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1219-264G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972113 | ||||||
chr4:152972190
|
G | T | 1 | a0001c0002t0006g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1219-187G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972190 | ||||||
chr4:152972202
|
G | A | 189 | a0002c0001t0001g0001a0002c0001t0001g0004a0002c0001t0001g0008others(186): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1219-175G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972202 | ||||||
chr4:152972317
|
C | G | 1 | a0006c0039t0046g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1219-60C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972317 | ||||||
chr4:152972325
|
C | T | 1 | a0006c0039t0046g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1219-52C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972325 | ||||||
chr4:152972706
|
T | C | 8 | a0001c0010t0003g0286a0001c0010t0003g0315a0001c0010t0023g0136others(5): Show | 8 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1383+165T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152972706 | ||||||
chr4:152972957
|
C | T | 3 | a0001c0002t0005g0023a0001c0002t0005g0024a0001c0002t0053g0039 | 3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1383+416C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152972957 | ||||||
chr4:152972990
|
G | C | 1 | a0001c0002t0003g0340 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1383+449G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152972990 | ||||||
chr4:152973047
|
C | T | 22 | a0001c0005t0002g0057a0001c0005t0002g0113a0001c0005t0002g0162others(19): Show | 23 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1383+506C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973047 | ||||||
chr4:152973091
|
G | A | 265 | a0001c0002t0003g0059a0001c0002t0003g0077a0001c0002t0003g0124others(262): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1383+550G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973091 | ||||||
chr4:152973229
|
T | C | 50 | a0001c0002t0003g0059a0001c0002t0003g0077a0001c0002t0003g0124others(47): Show | 50 | HG00597.hp1 HG01081.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1383+688T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973229 | ||||||
chr4:152973282
|
C | T | 1 | a0001c0002t0001g0269 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1383+741C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973282 | ||||||
chr4:152973727
|
A | G | 2 | a0001c0002t0039g0171a0003c0027t0043g0186 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1384-948A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973727 | ||||||
chr4:152973852
|
T | G | 3 | a0006c0039t0046g0138a0013c0046t0024g0096a0013c0047t0024g0149 | 3 | HG02922.hp1 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1384-823T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973852 | ||||||
chr4:152974126
|
T | C | 2 | a0001c0002t0001g0181a0028c0035t0001g0341 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1384-549T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974126 | ||||||
chr4:152974206
|
T | C | 1 | a0002c0001t0001g0257 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1384-469T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974206 | ||||||
chr4:152974393
|
T | C | 21 | a0001c0005t0002g0057a0001c0005t0002g0113a0001c0005t0002g0162others(18): Show | 21 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1384-282T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974393 | ||||||
chr4:152974393
|
TAAA | T | 189 | a0002c0001t0001g0001a0002c0001t0001g0004a0002c0001t0001g0008others(186): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1384-279_1384-277d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 152974393 | |||||
chr4:152974460
|
G | A | 3 | a0001c0002t0020g0132a0001c0002t0020g0183a0001c0002t0049g0030 | 3 | HG02970.hp1 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1384-215G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974460 | ||||||
chr4:152974517
|
T | G | 1 | a0001c0002t0002g0320 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1384-158T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974517 |