geneid | 10021 |
---|---|
ensemblid | ENSG00000138622.4 |
hgncid | 16882 |
symbol | HCN4 |
name | hyperpolarization activated cyclic nucleotide gated potassium channel 4 |
refseq_nuc | NM_005477.3 |
refseq_prot | NP_005468.1 |
ensembl_nuc | ENST00000261917.4 |
ensembl_prot | ENSP00000261917.3 |
mane_status | MANE Select |
chr | chr15 |
start | 73319859 |
end | 73368958 |
strand | - |
ver | v1.2 |
region | chr15:73319859-73368958 |
region5000 | chr15:73314859-73373958 |
regionname0 | HCN4_chr15_73319859_73368958 |
regionname5000 | HCN4_chr15_73314859_73373958 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1203 | 329 | 88 | 64 | 125 | 11 | 39 | 85 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0002 | 0/0 | 1203 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0003 | 0/0 | 1203 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0004 | 0/0 | 1203 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0005 | 0/0 | 1203 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0006 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0007 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0008 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0009 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3612 | 219 | 44 | 39 | 99 | 8 | 29 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0002 | 1/0 | 3612 | 48 | 19 | 4 | 19 | 1 | 4 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0003 | 0/0 | 3612 | 22 | 8 | 6 | 0 | 2 | 6 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0004 | 0/0 | 3612 | 10 | 0 | 5 | 5 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0005 | 0/1 | 3612 | 8 | 0 | 7 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0006 | 0/0 | 3612 | 7 | 6 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0007 | 0/0 | 3612 | 6 | 6 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0008 | 0/0 | 3612 | 5 | 0 | 3 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0009 | 0/0 | 3612 | 2 | 1 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0010 | 0/0 | 3612 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0011 | 0/0 | 3612 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0012 | 0/0 | 3612 | 2 | 0 | 1 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0013 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0014 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0015 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0016 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0017 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0018 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0019 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0020 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0021 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0022 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
c0023 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3311 | 104 | 15 | 27 | 40 | 4 | 18 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0002 | 0/0 | 3308 | 88 | 4 | 13 | 53 | 4 | 14 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0003 | 1/0 | 3311 | 63 | 35 | 6 | 17 | 0 | 4 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0004 | 0/0 | 3311 | 26 | 20 | 5 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0005 | 0/1 | 3311 | 11 | 1 | 9 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0006 | 0/0 | 3311 | 10 | 6 | 0 | 4 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0007 | 0/0 | 3311 | 8 | 4 | 0 | 4 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0008 | 0/0 | 3311 | 3 | 0 | 0 | 0 | 1 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0009 | 0/0 | 3311 | 3 | 0 | 2 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0010 | 0/0 | 3311 | 3 | 3 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0011 | 0/0 | 3308 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0012 | 0/0 | 3308 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0013 | 0/0 | 3301 | 2 | 0 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0014 | 0/0 | 3311 | 2 | 1 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0015 | 0/0 | 3308 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0016 | 0/0 | 3308 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0017 | 0/0 | 3311 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0018 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0019 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0020 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0021 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0022 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0023 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0024 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0025 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0026 | 0/0 | 3308 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0027 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0028 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
t0029 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0284 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3612 | 219 | 44 | 39 | 99 | 8 | 29 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0002 | 1/0 | 3612 | 48 | 19 | 4 | 19 | 1 | 4 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0003 | 0/0 | 3612 | 22 | 8 | 6 | 0 | 2 | 6 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0004 | 0/0 | 3612 | 10 | 0 | 5 | 5 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0005 | 0/1 | 3612 | 8 | 0 | 7 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0006 | 0/0 | 3612 | 7 | 6 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0007 | 0/0 | 3612 | 6 | 6 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0009 | 0/0 | 3612 | 2 | 1 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0013 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0014 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0016 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0017 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0020 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0022 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0023 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0002c0008 | 0/0 | 3612 | 5 | 0 | 3 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0003c0010 | 0/0 | 3612 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0004c0011 | 0/0 | 3612 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0005c0012 | 0/0 | 3612 | 2 | 0 | 1 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0006c0018 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0007c0019 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0008c0015 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0009c0021 | 0/0 | 3612 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6922 | 70 | 6 | 15 | 34 | 2 | 13 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0002 | 0/0 | 6919 | 82 | 3 | 10 | 53 | 4 | 12 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0003 | 0/0 | 6922 | 6 | 5 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0004 | 0/0 | 6922 | 23 | 17 | 5 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0005 | 0/0 | 6922 | 3 | 1 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0006 | 0/0 | 6922 | 9 | 6 | 0 | 3 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0007 | 0/0 | 6922 | 6 | 3 | 0 | 3 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0011 | 0/0 | 6919 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0012 | 0/0 | 6919 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0013 | 0/0 | 6912 | 2 | 0 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0015 | 0/0 | 6919 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0016 | 0/0 | 6919 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0017 | 0/0 | 6922 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0018 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0019 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0021 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0022 | 0/0 | 6922 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0023 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0026 | 0/0 | 6919 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0027 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0028 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0001t0029 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0002t0003 | 1/0 | 6922 | 40 | 16 | 4 | 17 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0002t0008 | 0/0 | 6922 | 3 | 0 | 0 | 0 | 1 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0002t0010 | 0/0 | 6922 | 3 | 3 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0002t0024 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0002t0025 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0003t0001 | 0/0 | 6922 | 18 | 8 | 4 | 0 | 1 | 5 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0003t0009 | 0/0 | 6922 | 3 | 0 | 2 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0003t0020 | 0/0 | 6922 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0004t0001 | 0/0 | 6922 | 10 | 0 | 5 | 5 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0005t0005 | 0/1 | 6922 | 8 | 0 | 7 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0006t0003 | 0/0 | 6922 | 7 | 6 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0007t0003 | 0/0 | 6922 | 6 | 6 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0009t0014 | 0/0 | 6922 | 2 | 1 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0013t0001 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0014t0003 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0016t0001 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0017t0004 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0020t0007 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0022t0002 | 0/0 | 6919 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0001c0023t0001 | 0/0 | 6922 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0002c0008t0002 | 0/0 | 6919 | 5 | 0 | 3 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0003c0010t0003 | 0/0 | 6922 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0004c0011t0004 | 0/0 | 6922 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0005c0012t0001 | 0/0 | 6922 | 2 | 0 | 1 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0006c0018t0003 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0007c0019t0001 | 0/0 | 6922 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0008c0015t0007 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
a0009c0021t0006 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | copy fasta | chr15 | 73314859 | 73373958 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0005g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0011g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0012g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0012g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0013g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0015g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0015g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0016g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0017g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0019g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0021g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0023g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0026g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0027g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0028g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0001t0029g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0003g0284 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0008g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0010g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0024g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0002t0025g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0009g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0009g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0003t0020g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0005t0005g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0005t0005g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0005t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0005t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0005t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0005t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0006t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0006t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0006t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0006t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0006t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0006t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0007t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0007t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0007t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0007t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0009t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0009t0014g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0013t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0014t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0016t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0017t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0020t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0022t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0001c0023t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0002c0008t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0002c0008t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0002c0008t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0002c0008t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0003c0010t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0003c0010t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0004c0011t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0004c0011t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0005c0012t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0005c0012t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0006c0018t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0007c0019t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0008c0015t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
a0009c0021t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | GBR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0235 | EUR | GBR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | FIN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00280 | hp2 | a0001 | c0003 | t0009 | g0238 | EUR | FIN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0217 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00558 | hp2 | a0001 | c0001 | t0029 | g0155 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0052 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00733 | hp1 | a0001 | c0004 | t0001 | g0028 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00733 | hp2 | a0001 | c0003 | t0009 | g0239 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0237 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0028 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01069 | hp2 | a0001 | c0001 | t0011 | g0004 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01070 | hp1 | a0002 | c0008 | t0002 | g0048 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0053 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01074 | hp2 | a0001 | c0005 | t0005 | g0290 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01081 | hp2 | a0002 | c0008 | t0002 | g0046 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0229 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01169 | hp2 | a0001 | c0023 | t0001 | g0296 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01175 | hp1 | a0001 | c0005 | t0005 | g0125 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01192 | hp1 | a0001 | c0001 | t0011 | g0004 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01192 | hp2 | a0001 | c0001 | t0016 | g0040 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01243 | hp1 | a0001 | c0001 | t0017 | g0043 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0094 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01255 | hp1 | a0001 | c0009 | t0014 | g0264 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01257 | hp2 | a0005 | c0012 | t0001 | g0152 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01346 | hp1 | a0001 | c0006 | t0003 | g0056 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01346 | hp2 | a0002 | c0008 | t0002 | g0047 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01358 | hp2 | a0001 | c0003 | t0009 | g0096 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01361 | hp1 | a0001 | c0005 | t0005 | g0005 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01433 | hp1 | a0003 | c0010 | t0003 | g0272 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0129 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0166 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01516 | hp1 | a0001 | c0001 | t0013 | g0006 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01516 | hp2 | a0001 | c0002 | t0008 | g0154 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01517 | hp2 | a0001 | c0001 | t0013 | g0006 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0236 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01891 | hp2 | a0001 | c0001 | t0021 | g0242 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01934 | hp2 | a0001 | c0001 | t0012 | g0041 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01943 | hp2 | a0001 | c0004 | t0001 | g0160 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01952 | hp1 | a0001 | c0005 | t0005 | g0232 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01981 | hp1 | a0001 | c0001 | t0012 | g0042 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01981 | hp2 | a0007 | c0019 | t0001 | g0100 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01993 | hp1 | a0001 | c0004 | t0001 | g0253 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01993 | hp2 | a0001 | c0005 | t0005 | g0005 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02004 | hp1 | a0001 | c0001 | t0011 | g0004 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02055 | hp1 | a0001 | c0002 | t0003 | g0265 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02071 | hp1 | a0001 | c0004 | t0001 | g0142 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02080 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02083 | hp2 | a0001 | c0004 | t0001 | g0293 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02129 | hp1 | a0001 | c0002 | t0024 | g0107 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0157 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02135 | hp2 | a0001 | c0001 | t0015 | g0095 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02145 | hp1 | a0001 | c0006 | t0003 | g0059 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02145 | hp2 | a0001 | c0007 | t0003 | g0017 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02155 | hp1 | a0001 | c0002 | t0003 | g0159 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02155 | hp2 | a0001 | c0002 | t0025 | g0140 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02258 | hp2 | a0006 | c0018 | t0003 | g0291 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02293 | hp1 | a0001 | c0005 | t0005 | g0005 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02293 | hp2 | a0001 | c0004 | t0001 | g0099 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02451 | hp1 | a0001 | c0009 | t0014 | g0263 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02572 | hp1 | a0001 | c0013 | t0001 | g0221 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02572 | hp2 | a0001 | c0007 | t0003 | g0015 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02622 | hp1 | a0001 | c0006 | t0003 | g0008 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02630 | hp1 | a0001 | c0001 | t0023 | g0067 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02683 | hp1 | a0001 | c0003 | t0020 | g0230 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0231 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02735 | hp1 | a0003 | c0010 | t0003 | g0153 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0119 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02818 | hp2 | a0001 | c0002 | t0010 | g0292 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0081 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0083 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02922 | hp1 | a0001 | c0007 | t0003 | g0015 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0163 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02965 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0269 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0286 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03098 | hp2 | a0001 | c0006 | t0003 | g0057 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0254 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0164 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0268 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0289 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03225 | hp1 | a0001 | c0007 | t0003 | g0078 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0086 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03491 | hp2 | a0002 | c0008 | t0002 | g0007 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03492 | hp1 | a0001 | c0001 | t0026 | g0190 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03492 | hp2 | a0002 | c0008 | t0002 | g0007 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03516 | hp1 | a0001 | c0017 | t0004 | g0176 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03516 | hp2 | a0008 | c0015 | t0007 | g0250 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03540 | hp1 | a0001 | c0014 | t0003 | g0082 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0114 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0074 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0098 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03834 | hp2 | a0001 | c0001 | t0022 | g0089 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03942 | hp2 | a0001 | c0002 | t0008 | g0146 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0138 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0245 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04228 | hp1 | a0001 | c0002 | t0008 | g0115 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18906 | hp2 | a0001 | c0007 | t0003 | g0017 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18944 | hp1 | a0001 | c0001 | t0028 | g0280 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18954 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18961 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18967 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18991 | hp1 | a0009 | c0021 | t0006 | g0294 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19000 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19003 | hp2 | a0001 | c0001 | t0007 | g0198 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19005 | hp2 | a0001 | c0001 | t0015 | g0204 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19009 | hp1 | a0001 | c0004 | t0001 | g0090 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19012 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19012 | hp2 | a0001 | c0001 | t0019 | g0045 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19030 | hp2 | a0001 | c0006 | t0003 | g0008 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19062 | hp1 | a0001 | c0001 | t0027 | g0278 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19068 | hp1 | a0001 | c0020 | t0007 | g0208 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19074 | hp1 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19074 | hp2 | a0001 | c0016 | t0001 | g0145 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19077 | hp1 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19083 | hp2 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19088 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19240 | hp1 | a0001 | c0002 | t0010 | g0013 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ASW | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20805 | hp2 | a0005 | c0012 | t0001 | g0151 | EUR | TSI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | GIH | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG01123 | hp2 | a0001 | c0005 | t0005 | g0234 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02109 | hp1 | a0001 | c0002 | t0003 | g0162 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02109 | hp2 | a0001 | c0002 | t0010 | g0013 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02486 | hp2 | a0001 | c0022 | t0002 | g0295 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0069 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03471 | hp1 | a0001 | c0001 | t0018 | g0044 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG03471 | hp2 | a0001 | c0007 | t0003 | g0156 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG06807 | hp1 | a0004 | c0011 | t0004 | g0073 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
HG06807 | hp2 | a0001 | c0006 | t0003 | g0058 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA20300 | hp2 | a0001 | c0006 | t0003 | g0060 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA21309 | hp1 | a0004 | c0011 | t0004 | g0084 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0005 | g0120 | REF | REF | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0284 | REF | REF | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73322756
|
T | C | 2 | a0003a0006 | 3 | HG01433.hp1 HG02258.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.3337A>G | p.Met1113Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 4025/6922 | 3337/3612 | 1113/1203 | chr15 | 73322756 | ||
chr15:73322788
|
C | T | 1 | a0007 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.3305G>A | p.Arg1102His | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3993/6922 | 3305/3612 | 1102/1203 | chr15 | 73322788 | ||
chr15:73323262
|
G | A | 1 | a0004 | 2 | HG06807.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.2831C>T | p.Ala944Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3519/6922 | 2831/3612 | 944/1203 | chr15 | 73323262 | ||
chr15:73323293
|
G | A | 1 | a0006 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.2800C>T | p.Arg934Cys | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3488/6922 | 2800/3612 | 934/1203 | chr15 | 73323293 | ||
chr15:73323436
|
G | A | 1 | a0008 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2657C>T | p.Ala886Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3345/6922 | 2657/3612 | 886/1203 | chr15 | 73323436 | ||
chr15:73323445
|
G | C | 1 | a0005 | 2 | HG01257.hp2 NA20805.hp2 |
missense_variant | MODERATE | c.2648C>G | p.Pro883Arg | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3336/6922 | 2648/3612 | 883/1203 | chr15 | 73323445 | ||
chr15:73367687
|
G | A | 1 | a0009 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.584C>T | p.Ala195Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 1272/6922 | 584/3612 | 195/1203 | chr15 | 73367687 | ||
chr15:73368164
|
C | T | 1 | a0002 | 5 | HG01070.hp1 HG01081.hp2 HG01346.hp2 others(2): Show |
missense_variant | MODERATE | c.107G>A | p.Gly36Glu | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 795/6922 | 107/3612 | 36/1203 | chr15 | 73368164 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73322493
|
T | C | 18 | a0001c0001a0001c0003a0001c0004others(15): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
synonymous_variant | LOW | c.3600A>G | p.Pro1200Pro | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 4288/6922 | 3600/3612 | 1200/1203 | chr15 | 73322493 | ||
chr15:73322805
|
G | A | 1 | a0001c0017 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.3288C>T | p.Asp1096Asp | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3976/6922 | 3288/3612 | 1096/1203 | chr15 | 73322805 | ||
chr15:73323060
|
A | C | 1 | a0001c0009 | 2 | HG01255.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.3033T>G | p.Ser1011Ser | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3721/6922 | 3033/3612 | 1011/1203 | chr15 | 73323060 | ||
chr15:73323114
|
C | T | 2 | a0001c0007a0001c0016 | 7 | HG02145.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.2979G>A | p.Thr993Thr | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3667/6922 | 2979/3612 | 993/1203 | chr15 | 73323114 | ||
chr15:73323420
|
C | T | 1 | a0001c0009 | 2 | HG01255.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.2673G>A | p.Ser891Ser | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3361/6922 | 2673/3612 | 891/1203 | chr15 | 73323420 | ||
chr15:73323492
|
G | T | 1 | a0008c0015 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.2601C>A | p.Ala867Ala | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3289/6922 | 2601/3612 | 867/1203 | chr15 | 73323492 | ||
chr15:73323537
|
C | T | 1 | a0001c0005 | 8 | HG01074.hp2 HG01123.hp2 HG01175.hp1 others(5): Show |
synonymous_variant | LOW | c.2556G>A | p.Pro852Pro | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3244/6922 | 2556/3612 | 852/1203 | chr15 | 73323537 | ||
chr15:73325094
|
G | A | 2 | a0001c0004a0007c0019 | 11 | HG00733.hp1 HG00735.hp2 HG01943.hp2 others(8): Show |
synonymous_variant | LOW | c.1839C>T | p.Phe613Phe | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/8 | 2527/6922 | 1839/3612 | 613/1203 | chr15 | 73325094 | ||
chr15:73325118
|
C | T | 1 | a0001c0014 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1815G>A | p.Thr605Thr | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/8 | 2503/6922 | 1815/3612 | 605/1203 | chr15 | 73325118 | ||
chr15:73325352
|
G | T | 1 | a0001c0006 | 7 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
synonymous_variant | LOW | c.1683C>A | p.Gly561Gly | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 5/8 | 2371/6922 | 1683/3612 | 561/1203 | chr15 | 73325352 | ||
chr15:73325382
|
G | T | 1 | a0001c0013 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1653C>A | p.Ile551Ile | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 5/8 | 2341/6922 | 1653/3612 | 551/1203 | chr15 | 73325382 | ||
chr15:73329600
|
G | A | 1 | a0001c0020 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.1563C>T | p.Asp521Asp | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/8 | 2251/6922 | 1563/3612 | 521/1203 | chr15 | 73329600 | ||
chr15:73329605
|
G | A | 1 | a0001c0003 | 22 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(19): Show |
synonymous_variant | LOW | c.1558C>T | p.Leu520Leu | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/8 | 2246/6922 | 1558/3612 | 520/1203 | chr15 | 73329605 | ||
chr15:73367743
|
G | A | 1 | a0001c0022 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.528C>T | p.Ser176Ser | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 1216/6922 | 528/3612 | 176/1203 | chr15 | 73367743 | ||
chr15:73368235
|
G | C | 1 | a0001c0023 | 1 | HG01169.hp2 | synonymous_variant | LOW | c.36C>G | p.Leu12Leu | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 724/6922 | 36/3612 | 12/1203 | chr15 | 73368235 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73319864
|
G | C | 1 | a0001c0001t0028 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2617C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2617 | chr15 | 73319864 | |||||
chr15:73320036
|
G | A | 3 | a0001c0001t0004a0001c0017t0004a0004c0011t0004 | 26 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2445C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2445 | chr15 | 73320036 | |||||
chr15:73320060
|
G | C | 1 | a0001c0001t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2421C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2421 | chr15 | 73320060 | |||||
chr15:73320088
|
G | C | 2 | a0001c0001t0005a0001c0005t0005 | 11 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2393C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2393 | chr15 | 73320088 | |||||
chr15:73320127
|
T | C | 1 | a0001c0001t0022 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2354A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2354 | chr15 | 73320127 | |||||
chr15:73320230
|
A | G | 1 | a0001c0001t0027 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2251T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2251 | chr15 | 73320230 | |||||
chr15:73320380
|
C | T | 1 | a0001c0001t0026 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2101G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2101 | chr15 | 73320380 | |||||
chr15:73320492
|
C | T | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1989G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1989 | chr15 | 73320492 | |||||
chr15:73320822
|
T | C | 5 | a0001c0001t0006a0001c0001t0017a0001c0001t0018others(2): Show | 13 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1659A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1659 | chr15 | 73320822 | |||||
chr15:73320999
|
T | C | 1 | a0001c0001t0011 | 3 | HG01069.hp2 HG01192.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1482A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1482 | chr15 | 73320999 | |||||
chr15:73321284
|
A | G | 1 | a0001c0003t0009 | 3 | HG00280.hp2 HG00733.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1197 | chr15 | 73321284 | |||||
chr15:73321309
|
T | C | 1 | a0001c0001t0029 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1172A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1172 | chr15 | 73321309 | |||||
chr15:73321341
|
C | T | 1 | a0001c0002t0008 | 3 | HG01516.hp2 HG03942.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1140G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1140 | chr15 | 73321341 | |||||
chr15:73321545
|
C | T | 1 | a0001c0009t0014 | 2 | HG01255.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*936G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 936 | chr15 | 73321545 | |||||
chr15:73321639
|
T | C | 1 | a0001c0009t0014 | 2 | HG01255.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 842 | chr15 | 73321639 | |||||
chr15:73321773
|
T | C | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(31): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*708A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 708 | chr15 | 73321773 | |||||
chr15:73321778
|
CA | C | 12 | a0001c0001t0002a0001c0001t0011a0001c0001t0012others(9): Show | 101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*702delT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 702 | chr15 | 73321778 | |||||
chr15:73321816
|
T | C | 1 | a0001c0002t0010 | 3 | HG02109.hp2 HG02818.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*665A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 665 | chr15 | 73321816 | |||||
chr15:73321839
|
C | T | 1 | a0001c0003t0020 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 642 | chr15 | 73321839 | |||||
chr15:73321876
|
T | C | 1 | a0001c0009t0014 | 2 | HG01255.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*605A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 605 | chr15 | 73321876 | |||||
chr15:73322014
|
G | A | 1 | a0001c0002t0024 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 467 | chr15 | 73322014 | |||||
chr15:73322022
|
C | A | 1 | a0001c0002t0025 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 459 | chr15 | 73322022 | |||||
chr15:73322067
|
G | T | 12 | a0001c0001t0002a0001c0001t0011a0001c0001t0012others(9): Show | 101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 414 | chr15 | 73322067 | |||||
chr15:73322361
|
GGT | G | 12 | a0001c0001t0002a0001c0001t0011a0001c0001t0012others(9): Show | 101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*118_*119delAC | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 118 | chr15 | 73322361 | |||||
chr15:73368304
|
G | A | 2 | a0001c0001t0017a0001c0001t0018 | 2 | HG01243.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-34C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 34 | chr15 | 73368304 | |||||
chr15:73368459
|
C | T | 2 | a0001c0001t0017a0001c0001t0018 | 2 | HG01243.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-189G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 189 | chr15 | 73368459 | |||||
chr15:73368537
|
TCCCTCTG others(3): Show |
T | 1 | a0001c0001t0013 | 2 | HG01516.hp1 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-277_-268delCGCCAG others(4): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 268 | chr15 | 73368537 | |||||
chr15:73368611
|
G | T | 1 | a0001c0001t0019 | 1 | NA19012.hp2 | 5_prime_UTR_variant | MODIFIER | c.-341C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 341 | chr15 | 73368611 | |||||
chr15:73368677
|
G | A | 1 | a0001c0001t0018 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-407C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 407 | chr15 | 73368677 | |||||
chr15:73368768
|
G | T | 2 | a0001c0001t0017a0001c0001t0018 | 2 | HG01243.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-498C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 498 | chr15 | 73368768 | |||||
chr15:73368852
|
A | G | 1 | a0001c0001t0012 | 2 | HG01934.hp2 HG01981.hp1 |
5_prime_UTR_variant | MODIFIER | c.-582T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 582 | chr15 | 73368852 | |||||
chr15:73368855
|
G | T | 1 | a0001c0001t0016 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-585C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 585 | chr15 | 73368855 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73324004
|
T | C | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2144-55A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 7/7 | chr15 | 73324004 | ||||||
chr15:73324055
|
C | A | 1 | a0001c0001t0001g0202 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2143+34G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 7/7 | chr15 | 73324055 | ||||||
chr15:73324294
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(213): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1979-41A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324294 | ||||||
chr15:73324403
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(79): Show | 94 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1979-150G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324403 | ||||||
chr15:73324460
|
G | A | 1 | a0001c0001t0004g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1979-207C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324460 | ||||||
chr15:73324605
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1978+350C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324605 | ||||||
chr15:73324694
|
A | G | 290 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(287): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1978+261T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324694 | ||||||
chr15:73324695
|
A | T | 9 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0007g0186others(6): Show | 9 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.1978+260T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324695 | ||||||
chr15:73324703
|
G | A | 57 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0022others(54): Show | 76 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1978+252C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324703 | ||||||
chr15:73324728
|
C | A | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1978+227G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324728 | ||||||
chr15:73324909
|
C | T | 1 | a0001c0001t0022g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1978+46G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324909 | ||||||
chr15:73325278
|
C | T | 4 | a0001c0007t0003g0015a0001c0007t0003g0017a0001c0007t0003g0078others(1): Show | 6 | HG02145.hp2 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+20G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 5/7 | chr15 | 73325278 | ||||||
chr15:73325458
|
AAGGGGGC others(17): Show |
A | 1 | a0001c0002t0003g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1591-38_1591-15del others(24): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325458 | ||||||
chr15:73325463
|
G | T | 2 | a0005c0012t0001g0151a0005c0012t0001g0152 | 2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1591-19C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325463 | ||||||
chr15:73325529
|
C | T | 1 | a0001c0001t0006g0072 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1591-85G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325529 | ||||||
chr15:73325681
|
G | A | 3 | a0001c0001t0004g0077a0001c0001t0004g0258a0001c0002t0003g0127 | 3 | HG02809.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1591-237C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325681 | ||||||
chr15:73325714
|
G | A | 1 | a0001c0002t0003g0091 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1591-270C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325714 | ||||||
chr15:73325790
|
T | C | 1 | a0001c0013t0001g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1591-346A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325790 | ||||||
chr15:73325897
|
C | T | 125 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0222others(122): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1591-453G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325897 | ||||||
chr15:73325950
|
G | A | 1 | a0001c0001t0004g0241 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1591-506C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325950 | ||||||
chr15:73325968
|
C | T | 126 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0222others(123): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1591-524G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325968 | ||||||
chr15:73325983
|
G | A | 5 | a0001c0003t0001g0009a0001c0003t0001g0050a0001c0003t0001g0051others(2): Show | 6 | HG02559.hp1 HG03225.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1591-539C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325983 | ||||||
chr15:73326141
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1591-697G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326141 | ||||||
chr15:73326227
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1591-783G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326227 | ||||||
chr15:73326280
|
C | T | 1 | a0001c0004t0001g0160 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1591-836G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326280 | ||||||
chr15:73326353
|
G | A | 2 | a0001c0002t0003g0001a0001c0002t0003g0163 | 6 | HG02257.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1591-909C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326353 | ||||||
chr15:73326402
|
C | T | 1 | a0001c0005t0005g0232 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1591-958G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326402 | ||||||
chr15:73326468
|
A | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(245): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1591-1024T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326468 | ||||||
chr15:73326717
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0181 | 3 | HG02056.hp1 NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1591-1273G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326717 | ||||||
chr15:73326744
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1591-1300C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326744 | ||||||
chr15:73326769
|
T | TTTTA | 5 | a0001c0001t0004g0257a0001c0001t0004g0260a0001c0001t0004g0266others(2): Show | 5 | HG02055.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1591-1329_1591-132 others(8): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326769 | ||||||
chr15:73326785
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1591-1341T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326785 | ||||||
chr15:73326789
|
A | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0092others(43): Show | 53 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1591-1345T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326789 | ||||||
chr15:73326790
|
T | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG01261.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1591-1346A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326790 | ||||||
chr15:73326792
|
T | A | 1 | a0008c0015t0007g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1591-1348A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326792 | ||||||
chr15:73326793
|
A | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(70): Show | 82 | HG00544.hp1 HG00673.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.1591-1349T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326793 | ||||||
chr15:73326797
|
T | A | 35 | a0001c0001t0003g0116a0001c0001t0004g0037a0001c0001t0004g0049others(32): Show | 36 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1591-1353A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326797 | ||||||
chr15:73326879
|
T | TG | 10 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0007g0186others(7): Show | 10 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1591-1436dupC | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326879 | ||||||
chr15:73326918
|
C | T | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1591-1474G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326918 | ||||||
chr15:73326984
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1591-1540C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326984 | ||||||
chr15:73327094
|
C | T | 1 | a0004c0011t0004g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1591-1650G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327094 | ||||||
chr15:73327108
|
C | CT | 11 | a0001c0001t0002g0200a0001c0001t0003g0075a0001c0001t0003g0076others(8): Show | 11 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.1591-1665dupA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327108 | ||||||
chr15:73327108
|
CT | C | 8 | a0001c0001t0001g0106a0001c0001t0001g0185a0001c0001t0001g0202others(5): Show | 8 | HG01070.hp2 HG01515.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1591-1665delA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327108 | ||||||
chr15:73327358
|
G | A | 129 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(126): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1591-1914C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327358 | ||||||
chr15:73327391
|
G | A | 25 | a0001c0001t0004g0037a0001c0001t0004g0049a0001c0001t0004g0077others(22): Show | 26 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1591-1947C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327391 | ||||||
chr15:73327415
|
A | G | 2 | a0001c0009t0014g0263a0001c0009t0014g0264 | 2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1591-1971T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327415 | ||||||
chr15:73327463
|
G | A | 2 | a0001c0009t0014g0263a0001c0009t0014g0264 | 2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1591-2019C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327463 | ||||||
chr15:73327631
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1590+1942C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327631 | ||||||
chr15:73327656
|
T | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(243): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1590+1917A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327656 | ||||||
chr15:73327830
|
T | C | 1 | a0001c0001t0006g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1590+1743A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327830 | ||||||
chr15:73327849
|
C | T | 2 | a0001c0009t0014g0263a0001c0009t0014g0264 | 2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1590+1724G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327849 | ||||||
chr15:73327969
|
C | T | 129 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(126): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1590+1604G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327969 | ||||||
chr15:73328057
|
G | A | 3 | a0001c0006t0003g0008a0001c0006t0003g0058a0001c0006t0003g0060 | 4 | HG02622.hp1 HG06807.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1590+1516C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328057 | ||||||
chr15:73328108
|
C | T | 131 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(128): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1590+1465G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328108 | ||||||
chr15:73328119
|
C | T | 129 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(126): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1590+1454G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328119 | ||||||
chr15:73328184
|
C | T | 131 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(128): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1590+1389G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328184 | ||||||
chr15:73328188
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1590+1385G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328188 | ||||||
chr15:73328231
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(80): Show | 95 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1590+1342C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328231 | ||||||
chr15:73328437
|
C | G | 7 | a0001c0001t0007g0186a0001c0001t0007g0198a0001c0001t0007g0203others(4): Show | 7 | HG02135.hp2 HG03130.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.1590+1136G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328437 | ||||||
chr15:73328495
|
C | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0110others(27): Show | 33 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1590+1078G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328495 | ||||||
chr15:73328694
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1590+879C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328694 | ||||||
chr15:73328791
|
G | C | 1 | a0001c0001t0002g0033 | 2 | NA18952.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1590+782C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328791 | ||||||
chr15:73328858
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(216): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1590+715G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328858 | ||||||
chr15:73329090
|
G | A | 24 | a0001c0001t0004g0037a0001c0001t0004g0049a0001c0001t0004g0077others(21): Show | 25 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1590+483C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329090 | ||||||
chr15:73329094
|
C | T | 104 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(101): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1590+479G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329094 | ||||||
chr15:73329176
|
T | G | 2 | a0001c0009t0014g0263a0001c0009t0014g0264 | 2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1590+397A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329176 | ||||||
chr15:73329191
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(79): Show | 94 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1590+382C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329191 | ||||||
chr15:73329208
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1590+365G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329208 | ||||||
chr15:73329270
|
C | T | 1 | a0001c0001t0004g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1590+303G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329270 | ||||||
chr15:73329513
|
G | A | 1 | a0001c0001t0006g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1590+60C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329513 | ||||||
chr15:73329818
|
A | G | 1 | a0001c0023t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1372-27T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73329818 | ||||||
chr15:73329940
|
T | G | 1 | a0001c0001t0007g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1372-149A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73329940 | ||||||
chr15:73330103
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(78): Show | 93 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1372-312C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330103 | ||||||
chr15:73330113
|
A | G | 5 | a0001c0001t0001g0062a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-322T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330113 | ||||||
chr15:73330180
|
C | G | 1 | a0001c0002t0003g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1372-389G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330180 | ||||||
chr15:73330183
|
A | C | 1 | a0001c0002t0003g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1372-392T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330183 | ||||||
chr15:73330184
|
T | A | 1 | a0001c0002t0003g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1372-393A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330184 | ||||||
chr15:73330852
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 60 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1372-1061G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330852 | ||||||
chr15:73330970
|
C | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | HG01934.hp1 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1371+1161G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330970 | ||||||
chr15:73331076
|
A | C | 290 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(287): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1371+1055T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331076 | ||||||
chr15:73331121
|
A | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 60 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1371+1010T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331121 | ||||||
chr15:73331163
|
T | G | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1371+968A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331163 | ||||||
chr15:73331196
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(79): Show | 94 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1371+935G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331196 | ||||||
chr15:73331348
|
C | G | 223 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(220): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1371+783G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331348 | ||||||
chr15:73331350
|
A | G | 256 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(253): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1371+781T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331350 | ||||||
chr15:73331441
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(78): Show | 93 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1371+690C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331441 | ||||||
chr15:73331577
|
C | A | 1 | a0003c0010t0003g0272 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1371+554G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331577 | ||||||
chr15:73331596
|
G | A | 131 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(128): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1371+535C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331596 | ||||||
chr15:73331749
|
G | C | 129 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(126): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1371+382C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331749 | ||||||
chr15:73331980
|
G | A | 2 | a0001c0001t0004g0257a0001c0001t0004g0260 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1371+151C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331980 | ||||||
chr15:73332067
|
C | T | 1 | a0001c0001t0007g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1371+64G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73332067 | ||||||
chr15:73332395
|
G | C | 7 | a0001c0002t0003g0081a0001c0002t0003g0083a0001c0002t0003g0094others(4): Show | 8 | HG01243.hp2 HG01496.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1210-103C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332395 | ||||||
chr15:73332508
|
C | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 60 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1210-216G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332508 | ||||||
chr15:73332549
|
T | A | 1 | a0001c0001t0007g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1210-257A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332549 | ||||||
chr15:73332559
|
G | T | 1 | a0001c0001t0002g0196 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1210-267C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332559 | ||||||
chr15:73333006
|
T | C | 1 | a0001c0009t0014g0264 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1210-714A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333006 | ||||||
chr15:73333178
|
C | T | 129 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(126): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1210-886G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333178 | ||||||
chr15:73333227
|
A | C | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1210-935T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333227 | ||||||
chr15:73333311
|
T | G | 10 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0007g0186others(7): Show | 10 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1210-1019A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333311 | ||||||
chr15:73333321
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1210-1029C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333321 | ||||||
chr15:73333554
|
G | A | 131 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(128): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1210-1262C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333554 | ||||||
chr15:73333565
|
C | A | 5 | a0001c0002t0003g0127a0001c0007t0003g0015a0001c0007t0003g0017others(2): Show | 7 | HG02145.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-1273G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333565 | ||||||
chr15:73333882
|
G | A | 130 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(127): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1210-1590C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333882 | ||||||
chr15:73334098
|
C | T | 78 | a0001c0001t0001g0104a0001c0001t0002g0002a0001c0001t0002g0010others(75): Show | 99 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1210-1806G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334098 | ||||||
chr15:73334104
|
C | T | 1 | a0001c0001t0017g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1210-1812G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334104 | ||||||
chr15:73334113
|
T | C | 26 | a0001c0001t0004g0037a0001c0001t0004g0049a0001c0001t0004g0077others(23): Show | 27 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.1210-1821A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334113 | ||||||
chr15:73334629
|
G | A | 76 | a0001c0001t0001g0104a0001c0001t0002g0002a0001c0001t0002g0010others(73): Show | 97 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1210-2337C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334629 | ||||||
chr15:73334652
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-2360C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334652 | ||||||
chr15:73334652
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1210-2360C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334652 | ||||||
chr15:73334693
|
C | T | 29 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0110others(26): Show | 32 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1210-2401G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334693 | ||||||
chr15:73334723
|
CCT | C | 28 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0110others(25): Show | 31 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1210-2433_1210-243 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334723 | ||||||
chr15:73334781
|
C | A | 129 | a0001c0001t0001g0062a0001c0001t0001g0104a0001c0001t0001g0222others(126): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1210-2489G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334781 | ||||||
chr15:73334782
|
G | A | 28 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0110others(25): Show | 31 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1210-2490C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334782 | ||||||
chr15:73334862
|
T | C | 225 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(222): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1210-2570A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334862 | ||||||
chr15:73334921
|
C | T | 1 | a0001c0003t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1210-2629G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334921 | ||||||
chr15:73335129
|
A | G | 4 | a0001c0001t0004g0086a0001c0001t0004g0226a0001c0001t0004g0248others(1): Show | 4 | HG00738.hp2 HG01175.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-2837T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335129 | ||||||
chr15:73335146
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1210-2854G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335146 | ||||||
chr15:73335190
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1210-2898A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335190 | ||||||
chr15:73335260
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0139a0001c0001t0001g0143 | 4 | HG02083.hp1 HG02132.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-2968C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335260 | ||||||
chr15:73335382
|
A | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(51): Show | 63 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1210-3090T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335382 | ||||||
chr15:73335421
|
C | T | 1 | a0001c0001t0006g0065 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1210-3129G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335421 | ||||||
chr15:73335429
|
A | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(95): Show | 108 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(105): Show |
intron_variant | MODIFIER | c.1210-3137T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335429 | ||||||
chr15:73335530
|
C | G | 236 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(233): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1210-3238G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335530 | ||||||
chr15:73335745
|
T | C | 140 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0080others(137): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1210-3453A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335745 | ||||||
chr15:73335781
|
A | G | 1 | a0001c0001t0002g0179 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1210-3489T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335781 | ||||||
chr15:73335827
|
T | C | 141 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0038others(138): Show | 168 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1210-3535A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335827 | ||||||
chr15:73335830
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1210-3538G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335830 | ||||||
chr15:73335873
|
C | A | 161 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0020others(158): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1210-3581G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335873 | ||||||
chr15:73335883
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0215 | 2 | HG01261.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1210-3591T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335883 | ||||||
chr15:73336068
|
G | C | 1 | a0001c0001t0002g0194 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1210-3776C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336068 | ||||||
chr15:73336159
|
G | C | 1 | a0001c0001t0004g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1210-3867C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336159 | ||||||
chr15:73336205
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1210-3913G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336205 | ||||||
chr15:73336373
|
T | C | 126 | a0001c0001t0001g0062a0001c0001t0001g0102a0001c0001t0001g0137others(123): Show | 150 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1210-4081A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336373 | ||||||
chr15:73336506
|
T | A | 16 | a0001c0001t0004g0241a0001c0001t0004g0285a0001c0001t0004g0286others(13): Show | 16 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1210-4214A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336506 | ||||||
chr15:73336534
|
A | G | 4 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0039others(1): Show | 7 | NA18939.hp1 NA18942.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-4242T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336534 | ||||||
chr15:73336591
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1210-4299C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336591 | ||||||
chr15:73336736
|
C | T | 7 | a0001c0003t0001g0074a0001c0003t0001g0229a0001c0003t0001g0231others(4): Show | 7 | HG00280.hp2 HG00733.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-4444G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336736 | ||||||
chr15:73336788
|
G | A | 2 | a0001c0001t0002g0173a0001c0022t0002g0295 | 2 | HG01358.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1210-4496C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336788 | ||||||
chr15:73336799
|
C | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0249 | 3 | NA18939.hp1 NA18942.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1210-4507G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336799 | ||||||
chr15:73336844
|
C | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1210-4552G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336844 | ||||||
chr15:73336937
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1210-4645G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336937 | ||||||
chr15:73336992
|
G | A | 1 | a0001c0002t0003g0083 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1210-4700C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336992 | ||||||
chr15:73337029
|
C | T | 28 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0003g0055others(25): Show | 31 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.1210-4737G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337029 | ||||||
chr15:73337400
|
A | G | 49 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0038others(46): Show | 55 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1210-5108T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337400 | ||||||
chr15:73337405
|
A | G | 123 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0093others(120): Show | 144 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1210-5113T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337405 | ||||||
chr15:73337741
|
C | G | 1 | a0001c0001t0001g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1210-5449G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337741 | ||||||
chr15:73337881
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1209+5504T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337881 | ||||||
chr15:73338007
|
G | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0134 | 3 | NA18957.hp2 NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1209+5378C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338007 | ||||||
chr15:73338067
|
TA | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(44): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1209+5317delT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338067 | ||||||
chr15:73338125
|
G | T | 1 | a0001c0001t0001g0018 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1209+5260C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338125 | ||||||
chr15:73338138
|
G | A | 1 | a0001c0001t0018g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1209+5247C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338138 | ||||||
chr15:73338345
|
G | A | 98 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(95): Show | 105 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1209+5040C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338345 | ||||||
chr15:73338352
|
G | A | 9 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0004g0049others(6): Show | 10 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+5033C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338352 | ||||||
chr15:73338462
|
C | T | 2 | a0001c0001t0003g0054a0001c0001t0022g0089 | 2 | HG02717.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1209+4923G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338462 | ||||||
chr15:73338602
|
A | C | 1 | a0001c0002t0008g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1209+4783T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338602 | ||||||
chr15:73338614
|
A | G | 1 | a0002c0008t0002g0007 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1209+4771T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338614 | ||||||
chr15:73338870
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1209+4515G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338870 | ||||||
chr15:73338934
|
A | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+4451T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338934 | ||||||
chr15:73338947
|
G | A | 14 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1209+4438C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338947 | ||||||
chr15:73339024
|
C | A | 1 | a0001c0001t0004g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1209+4361G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339024 | ||||||
chr15:73339045
|
C | T | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1209+4340G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339045 | ||||||
chr15:73339216
|
A | G | 48 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(45): Show | 53 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1209+4169T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339216 | ||||||
chr15:73339237
|
G | A | 74 | a0001c0001t0001g0093a0001c0001t0001g0137a0001c0001t0001g0182others(71): Show | 92 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1209+4148C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339237 | ||||||
chr15:73339257
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1209+4128C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339257 | ||||||
chr15:73339360
|
G | A | 13 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+4025C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339360 | ||||||
chr15:73339379
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1209+4006G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339379 | ||||||
chr15:73339381
|
G | C | 1 | a0001c0001t0004g0226 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1209+4004C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339381 | ||||||
chr15:73339393
|
A | G | 1 | a0001c0003t0001g0024 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1209+3992T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339393 | ||||||
chr15:73339489
|
G | A | 75 | a0001c0001t0001g0093a0001c0001t0001g0137a0001c0001t0001g0182others(72): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1209+3896C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339489 | ||||||
chr15:73339507
|
G | A | 1 | a0004c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209+3878C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339507 | ||||||
chr15:73339801
|
C | T | 62 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(59): Show | 67 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1209+3584G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339801 | ||||||
chr15:73339850
|
G | T | 13 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+3535C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339850 | ||||||
chr15:73340035
|
G | A | 74 | a0001c0001t0001g0093a0001c0001t0001g0137a0001c0001t0001g0182others(71): Show | 92 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1209+3350C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340035 | ||||||
chr15:73340528
|
C | T | 61 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(58): Show | 66 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1209+2857G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340528 | ||||||
chr15:73340571
|
G | A | 47 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(44): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1209+2814C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340571 | ||||||
chr15:73340704
|
C | T | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1209+2681G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340704 | ||||||
chr15:73340742
|
G | A | 1 | a0001c0001t0005g0019 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1209+2643C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340742 | ||||||
chr15:73341054
|
G | A | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1209+2331C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341054 | ||||||
chr15:73341069
|
G | GGGGTGTG others(29): Show |
1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1209+2315_1209+231 others(40): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGGTGTGT others(32): Show |
1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1209+2315_1209+231 others(43): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGT | 20 | a0001c0001t0001g0206a0001c0001t0001g0222a0001c0001t0001g0223others(17): Show | 21 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1209+2314_1209+231 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGT | 10 | a0001c0001t0002g0210a0001c0001t0004g0049a0001c0001t0007g0186others(7): Show | 11 | HG01346.hp1 HG02165.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1209+2312_1209+231 others(8): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGT | 10 | a0001c0001t0001g0202a0001c0001t0001g0207a0001c0001t0001g0209others(7): Show | 10 | HG00738.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+2310_1209+231 others(10): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGTG others(1): Show |
10 | a0001c0001t0004g0257a0001c0001t0004g0259a0001c0001t0004g0260others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+2308_1209+231 others(12): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGTG others(3): Show |
12 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0001t0001g0277others(9): Show | 14 | HG00558.hp2 HG01884.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1209+2306_1209+231 others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGTG others(5): Show |
19 | a0001c0001t0001g0085a0001c0001t0001g0143a0001c0001t0001g0147others(16): Show | 21 | HG00621.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1209+2304_1209+231 others(16): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGTG others(7): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0141a0001c0001t0001g0148others(13): Show | 17 | HG00423.hp2 HG01109.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1209+2302_1209+231 others(18): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGTG others(9): Show |
6 | a0001c0001t0001g0062a0001c0001t0001g0255a0001c0001t0002g0066others(3): Show | 6 | HG01109.hp2 HG02258.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209+2300_1209+231 others(20): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGTG others(11): Show |
1 | a0001c0001t0028g0280 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1209+2298_1209+231 others(22): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
G | GGTGTGTG others(13): Show |
1 | a0001c0001t0001g0038 | 2 | NA18993.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1209+2296_1209+231 others(24): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
GGT | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(91): Show | 111 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1209+2314_1209+231 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
GGTGT | G | 76 | a0001c0001t0001g0093a0001c0001t0001g0137a0001c0001t0001g0182others(73): Show | 94 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1209+2312_1209+231 others(8): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341069
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1209+2306_1209+231 others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | ||||||
chr15:73341265
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1209+2120G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341265 | ||||||
chr15:73341266
|
G | A | 1 | a0001c0003t0001g0024 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1209+2119C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341266 | ||||||
chr15:73341322
|
A | G | 1 | a0001c0002t0025g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1209+2063T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341322 | ||||||
chr15:73341328
|
G | GA | 15 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0006g0063others(12): Show | 16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1209+2056dupT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341328 | ||||||
chr15:73341331
|
G | A | 13 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+2054C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341331 | ||||||
chr15:73341343
|
C | T | 14 | a0001c0001t0001g0147a0001c0001t0001g0222a0001c0001t0001g0223others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1209+2042G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341343 | ||||||
chr15:73341394
|
G | A | 13 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+1991C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341394 | ||||||
chr15:73341430
|
C | T | 1 | a0001c0004t0001g0099 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1209+1955G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341430 | ||||||
chr15:73341587
|
T | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0004t0001g0253 | 3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1209+1798A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341587 | ||||||
chr15:73341806
|
C | T | 5 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0001t0004g0287others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209+1579G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341806 | ||||||
chr15:73341847
|
G | A | 1 | a0001c0001t0004g0226 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1209+1538C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341847 | ||||||
chr15:73341894
|
C | G | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1209+1491G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341894 | ||||||
chr15:73341965
|
G | T | 1 | a0001c0001t0002g0029 | 2 | NA18948.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1209+1420C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341965 | ||||||
chr15:73342012
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1209+1373C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342012 | ||||||
chr15:73342024
|
TCCATGGA others(12): Show |
T | 1 | a0001c0001t0002g0035 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1209+1342_1209+136 others(23): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342024 | ||||||
chr15:73342241
|
G | A | 13 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+1144C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342241 | ||||||
chr15:73342255
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1209+1130C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342255 | ||||||
chr15:73342392
|
C | T | 2 | a0001c0001t0004g0257a0001c0001t0004g0260 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1209+993G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342392 | ||||||
chr15:73342400
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1209+985C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342400 | ||||||
chr15:73342420
|
G | A | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1209+965C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342420 | ||||||
chr15:73342771
|
C | T | 2 | a0001c0003t0001g0050a0001c0003t0001g0051 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1209+614G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342771 | ||||||
chr15:73342829
|
C | A | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1209+556G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342829 | ||||||
chr15:73343011
|
A | G | 4 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0039others(1): Show | 7 | NA18939.hp1 NA18942.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209+374T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343011 | ||||||
chr15:73343020
|
T | C | 48 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(45): Show | 54 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1209+365A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343020 | ||||||
chr15:73343174
|
T | C | 1 | a0001c0003t0009g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1209+211A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343174 | ||||||
chr15:73343262
|
T | C | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+123A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343262 | ||||||
chr15:73343307
|
T | C | 1 | a0001c0004t0001g0160 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1209+78A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343307 | ||||||
chr15:73343321
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1209+64G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343321 | ||||||
chr15:73343900
|
A | G | 2 | a0001c0003t0001g0050a0001c0003t0001g0051 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786-92T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73343900 | ||||||
chr15:73344260
|
T | C | 1 | a0006c0018t0003g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786-452A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344260 | ||||||
chr15:73344311
|
G | A | 1 | a0001c0023t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.786-503C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344311 | ||||||
chr15:73344732
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.786-924C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344732 | ||||||
chr15:73344792
|
G | A | 47 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(44): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.786-984C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344792 | ||||||
chr15:73344810
|
A | C | 47 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(44): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.786-1002T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344810 | ||||||
chr15:73345103
|
G | A | 1 | a0001c0001t0017g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.786-1295C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345103 | ||||||
chr15:73345299
|
C | A | 1 | a0001c0007t0003g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.786-1491G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345299 | ||||||
chr15:73345315
|
A | T | 1 | a0001c0001t0004g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.786-1507T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345315 | ||||||
chr15:73345431
|
C | T | 13 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0233others(10): Show | 15 | HG01074.hp2 HG01123.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.786-1623G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345431 | ||||||
chr15:73345487
|
C | A | 1 | a0001c0001t0002g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.786-1679G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345487 | ||||||
chr15:73345559
|
C | G | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.786-1751G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345559 | ||||||
chr15:73345666
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0139others(24): Show | 30 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.786-1858G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345666 | ||||||
chr15:73345870
|
C | T | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.786-2062G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345870 | ||||||
chr15:73345881
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.786-2073G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345881 | ||||||
chr15:73345882
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.786-2074C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345882 | ||||||
chr15:73345903
|
C | T | 1 | a0002c0008t0002g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.786-2095G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345903 | ||||||
chr15:73346116
|
G | T | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.786-2308C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346116 | ||||||
chr15:73346321
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.786-2513T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346321 | ||||||
chr15:73346390
|
G | A | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-2582C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346390 | ||||||
chr15:73346410
|
G | T | 3 | a0001c0001t0002g0118a0001c0002t0003g0117a0001c0002t0003g0217 | 3 | HG00438.hp1 HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.786-2602C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346410 | ||||||
chr15:73346642
|
C | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-2834G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346642 | ||||||
chr15:73346785
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0135 | 2 | NA18942.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.786-2977C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346785 | ||||||
chr15:73346961
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.786-3153C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346961 | ||||||
chr15:73347010
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.786-3202G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347010 | ||||||
chr15:73347057
|
A | C | 1 | a0001c0001t0002g0224 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.786-3249T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347057 | ||||||
chr15:73347066
|
G | C | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-3258C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347066 | ||||||
chr15:73347150
|
C | G | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-3342G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347150 | ||||||
chr15:73347563
|
C | T | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.786-3755G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347563 | ||||||
chr15:73347805
|
C | T | 1 | a0001c0003t0001g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.786-3997G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347805 | ||||||
chr15:73347849
|
C | T | 3 | a0001c0003t0001g0229a0001c0003t0001g0231a0001c0003t0020g0230 | 3 | HG01167.hp1 HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.786-4041G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347849 | ||||||
chr15:73347885
|
C | T | 3 | a0001c0004t0001g0099a0001c0004t0001g0160a0007c0019t0001g0100 | 3 | HG01943.hp2 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.786-4077G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347885 | ||||||
chr15:73347984
|
G | A | 8 | a0001c0001t0006g0068a0001c0001t0006g0070a0001c0001t0006g0071others(5): Show | 9 | HG02451.hp2 HG02559.hp1 NA18522.hp1 others(6): Show |
intron_variant | MODIFIER | c.786-4176C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347984 | ||||||
chr15:73348030
|
G | T | 5 | a0001c0001t0003g0116a0001c0002t0008g0115a0001c0002t0008g0146others(2): Show | 5 | HG01516.hp2 HG03942.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.786-4222C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348030 | ||||||
chr15:73348389
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.786-4581G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348389 | ||||||
chr15:73348542
|
T | C | 1 | a0006c0018t0003g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786-4734A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348542 | ||||||
chr15:73348626
|
C | T | 1 | a0001c0001t0003g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.786-4818G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348626 | ||||||
chr15:73348963
|
G | A | 2 | a0001c0001t0003g0243a0001c0001t0021g0242 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.786-5155C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348963 | ||||||
chr15:73349143
|
G | A | 11 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0004g0049others(8): Show | 12 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-5335C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349143 | ||||||
chr15:73349345
|
T | C | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-5537A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349345 | ||||||
chr15:73349360
|
C | A | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.786-5552G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349360 | ||||||
chr15:73349551
|
T | C | 53 | a0001c0001t0001g0137a0001c0001t0001g0182a0001c0001t0002g0002others(50): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.786-5743A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349551 | ||||||
chr15:73349724
|
G | A | 1 | a0001c0001t0001g0020 | 2 | HG01081.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.786-5916C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349724 | ||||||
chr15:73350112
|
G | A | 1 | a0001c0003t0001g0237 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.786-6304C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350112 | ||||||
chr15:73350225
|
T | C | 1 | a0001c0001t0018g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-6417A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350225 | ||||||
chr15:73350256
|
C | T | 1 | a0002c0008t0002g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.786-6448G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350256 | ||||||
chr15:73350414
|
A | G | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.786-6606T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350414 | ||||||
chr15:73350516
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.786-6708C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350516 | ||||||
chr15:73350782
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.786-6974G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350782 | ||||||
chr15:73350853
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.786-7045T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350853 | ||||||
chr15:73350888
|
C | G | 1 | a0001c0001t0002g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.786-7080G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350888 | ||||||
chr15:73350949
|
C | T | 1 | a0001c0002t0003g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.786-7141G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350949 | ||||||
chr15:73351222
|
G | A | 1 | a0003c0010t0003g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786-7414C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351222 | ||||||
chr15:73351222
|
G | C | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-7414C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351222 | ||||||
chr15:73351223
|
G | A | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-7415C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351223 | ||||||
chr15:73351270
|
G | A | 1 | a0001c0001t0004g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786-7462C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351270 | ||||||
chr15:73351506
|
T | G | 9 | a0001c0003t0001g0074a0001c0003t0001g0229a0001c0003t0001g0231others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-7698A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351506 | ||||||
chr15:73351706
|
C | T | 15 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0006g0063others(12): Show | 16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.786-7898G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351706 | ||||||
chr15:73351959
|
C | T | 1 | a0001c0002t0003g0199 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.786-8151G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351959 | ||||||
chr15:73352055
|
C | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(44): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.786-8247G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352055 | ||||||
chr15:73352170
|
T | C | 2 | a0001c0002t0003g0268a0001c0002t0003g0269 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786-8362A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352170 | ||||||
chr15:73352237
|
ATGCCATG others(17): Show |
A | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-8453_786-8430d others(26): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352237 | ||||||
chr15:73352632
|
C | T | 1 | a0001c0002t0003g0036 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.786-8824G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352632 | ||||||
chr15:73352641
|
C | T | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-8833G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352641 | ||||||
chr15:73352655
|
C | A | 1 | a0001c0001t0002g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.786-8847G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352655 | ||||||
chr15:73352729
|
G | A | 1 | a0001c0002t0003g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.786-8921C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352729 | ||||||
chr15:73352996
|
G | GGATGGAC others(1): Show |
37 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0085others(34): Show | 42 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.786-9196_786-9189d others(10): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352996 | ||||||
chr15:73353004
|
A | AGATG | 33 | a0001c0001t0001g0062a0001c0001t0001g0097a0001c0001t0001g0182others(30): Show | 37 | HG00438.hp2 HG00733.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.786-9200_786-9197d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | ||||||
chr15:73353004
|
A | AGATGGAC others(5): Show |
3 | a0001c0001t0004g0257a0001c0001t0004g0258a0001c0001t0004g0259 | 3 | HG02486.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.786-9197_786-9196i others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | ||||||
chr15:73353004
|
A | AGATGGAT others(1): Show |
3 | a0001c0001t0006g0070a0001c0001t0006g0071a0009c0021t0006g0294 | 3 | NA18991.hp1 NA19007.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.786-9204_786-9197d others(10): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | ||||||
chr15:73353004
|
AGATG | A | 22 | a0001c0001t0001g0080a0001c0001t0002g0079a0001c0001t0002g0228others(19): Show | 23 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.786-9200_786-9197d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | ||||||
chr15:73353004
|
AGATGGAT others(5): Show |
A | 1 | a0001c0002t0003g0083 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.786-9208_786-9197d others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | ||||||
chr15:73353004
|
AGATGGAT others(9): Show |
A | 3 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0007g0198 | 3 | NA18979.hp1 NA18990.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.786-9212_786-9197d others(18): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | ||||||
chr15:73353008
|
G | GGACA | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0158others(3): Show | 6 | HG00423.hp2 HG01109.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.786-9201_786-9200i others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353008 | ||||||
chr15:73353011
|
T | C | 1 | a0001c0001t0004g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.786-9203A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353011 | ||||||
chr15:73353012
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.786-9204C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353012 | ||||||
chr15:73353015
|
T | C | 1 | a0001c0001t0002g0220 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.786-9207A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353015 | ||||||
chr15:73353026
|
A | G | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.786-9218T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353026 | ||||||
chr15:73353043
|
T | C | 3 | a0001c0003t0001g0009a0001c0003t0001g0061a0001c0003t0001g0069 | 4 | HG02559.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-9235A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353043 | ||||||
chr15:73353047
|
T | C | 1 | a0003c0010t0003g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786-9239A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353047 | ||||||
chr15:73353047
|
TGGAC | T | 3 | a0001c0003t0001g0009a0001c0003t0001g0061a0001c0003t0001g0069 | 4 | HG02559.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-9243_786-9240d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353047 | ||||||
chr15:73353059
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.786-9251G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353059 | ||||||
chr15:73353062
|
G | A | 15 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.786-9254C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353062 | ||||||
chr15:73353478
|
C | T | 290 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(287): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.786-9670G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353478 | ||||||
chr15:73353519
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-9711C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353519 | ||||||
chr15:73353897
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-10089G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353897 | ||||||
chr15:73353901
|
A | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-10093T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353901 | ||||||
chr15:73353936
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.786-10128G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353936 | ||||||
chr15:73354005
|
C | T | 2 | a0001c0003t0009g0238a0001c0003t0009g0239 | 2 | HG00280.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.786-10197G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354005 | ||||||
chr15:73354079
|
A | C | 1 | a0001c0001t0015g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.786-10271T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354079 | ||||||
chr15:73354083
|
C | T | 9 | a0001c0003t0001g0074a0001c0003t0001g0229a0001c0003t0001g0231others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-10275G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354083 | ||||||
chr15:73354146
|
A | C | 33 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(30): Show | 34 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.786-10338T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354146 | ||||||
chr15:73354175
|
A | G | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-10367T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354175 | ||||||
chr15:73354223
|
A | G | 1 | a0006c0018t0003g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786-10415T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354223 | ||||||
chr15:73354253
|
G | A | 15 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0207others(12): Show | 17 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-10445C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354253 | ||||||
chr15:73354429
|
C | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-10621G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354429 | ||||||
chr15:73354444
|
T | C | 4 | a0001c0006t0003g0008a0001c0006t0003g0058a0001c0006t0003g0059others(1): Show | 5 | HG02145.hp1 HG02622.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.786-10636A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354444 | ||||||
chr15:73354778
|
C | CCAT | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-10973_786-1097 others(7): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354778 | ||||||
chr15:73354787
|
T | G | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-10979A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354787 | ||||||
chr15:73355073
|
A | T | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-11265T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355073 | ||||||
chr15:73355216
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG01255.hp2 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-11408G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355216 | ||||||
chr15:73355242
|
G | A | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-11434C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355242 | ||||||
chr15:73355253
|
G | A | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-11445C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355253 | ||||||
chr15:73355326
|
T | C | 1 | a0001c0003t0001g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.786-11518A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355326 | ||||||
chr15:73355328
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0273a0001c0001t0002g0279others(2): Show | 6 | NA18944.hp1 NA18962.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.786-11520C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355328 | ||||||
chr15:73355401
|
T | TA | 13 | a0001c0001t0001g0233a0001c0003t0001g0074a0001c0003t0001g0229others(10): Show | 15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.786-11594dupT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355401 | ||||||
chr15:73355466
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.786-11658C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355466 | ||||||
chr15:73355522
|
C | T | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-11714G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355522 | ||||||
chr15:73355540
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.786-11732C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355540 | ||||||
chr15:73355734
|
A | G | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.785+11752T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355734 | ||||||
chr15:73355759
|
G | GCA | 7 | a0001c0001t0001g0255a0001c0001t0002g0026a0001c0001t0002g0169others(4): Show | 8 | HG01109.hp2 HG01433.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.785+11725_785+1172 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355759 | ||||||
chr15:73355761
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0181 | 3 | HG02056.hp1 NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.785+11725T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355761 | ||||||
chr15:73355811
|
T | C | 22 | a0001c0001t0001g0233a0001c0001t0003g0075a0001c0001t0003g0076others(19): Show | 24 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+11675A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355811 | ||||||
chr15:73356189
|
C | CT | 119 | a0001c0001t0001g0038a0001c0001t0001g0062a0001c0001t0001g0085others(116): Show | 131 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.785+11296dupA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356189 | ||||||
chr15:73356189
|
C | CTT | 7 | a0001c0001t0001g0274a0001c0001t0003g0243a0001c0001t0004g0285others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+11295_785+1129 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356189 | ||||||
chr15:73356189
|
CT | C | 21 | a0001c0001t0001g0215a0001c0001t0001g0233a0001c0001t0003g0075others(18): Show | 23 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.785+11296delA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356189 | ||||||
chr15:73356217
|
C | T | 1 | a0001c0002t0003g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.785+11269G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356217 | ||||||
chr15:73356232
|
G | T | 4 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0001t0004g0287others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+11254C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356232 | ||||||
chr15:73356241
|
T | C | 2 | a0005c0012t0001g0151a0005c0012t0001g0152 | 2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.785+11245A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356241 | ||||||
chr15:73356293
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 4 | HG01261.hp1 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+11193G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356293 | ||||||
chr15:73356320
|
T | C | 2 | a0001c0001t0004g0241a0001c0001t0005g0240 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.785+11166A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356320 | ||||||
chr15:73356323
|
G | A | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+11163C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356323 | ||||||
chr15:73356374
|
C | CT | 19 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0251others(16): Show | 21 | HG01106.hp2 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.785+11111dupA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356374 | ||||||
chr15:73356374
|
CT | C | 20 | a0001c0001t0002g0177a0001c0001t0002g0200a0001c0001t0002g0211others(17): Show | 21 | HG00558.hp2 HG00741.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.785+11111delA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356374 | ||||||
chr15:73356378
|
T | C | 3 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0004g0049 | 3 | HG02717.hp2 HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.785+11108A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356378 | ||||||
chr15:73356379
|
T | C | 7 | a0001c0006t0003g0008a0001c0006t0003g0056a0001c0006t0003g0057others(4): Show | 8 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.785+11107A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356379 | ||||||
chr15:73356573
|
T | C | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.785+10913A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356573 | ||||||
chr15:73356633
|
C | A | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.785+10853G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356633 | ||||||
chr15:73356648
|
G | C | 16 | a0001c0001t0001g0038a0001c0001t0001g0251a0001c0001t0001g0252others(13): Show | 17 | HG00280.hp1 HG01106.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.785+10838C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356648 | ||||||
chr15:73356739
|
C | T | 13 | a0001c0001t0001g0233a0001c0003t0001g0074a0001c0003t0001g0229others(10): Show | 15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+10747G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356739 | ||||||
chr15:73356751
|
A | G | 26 | a0001c0001t0001g0233a0001c0001t0003g0075a0001c0001t0003g0076others(23): Show | 28 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.785+10735T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356751 | ||||||
chr15:73356816
|
A | C | 1 | a0001c0001t0002g0244 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.785+10670T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356816 | ||||||
chr15:73356830
|
A | G | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.785+10656T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356830 | ||||||
chr15:73356925
|
G | A | 1 | a0001c0004t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.785+10561C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356925 | ||||||
chr15:73357004
|
A | G | 1 | a0001c0001t0022g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.785+10482T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357004 | ||||||
chr15:73357020
|
A | G | 38 | a0001c0001t0001g0038a0001c0001t0001g0085a0001c0001t0001g0251others(35): Show | 41 | HG00280.hp1 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.785+10466T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357020 | ||||||
chr15:73357054
|
G | A | 22 | a0001c0001t0001g0233a0001c0001t0003g0075a0001c0001t0003g0076others(19): Show | 24 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+10432C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357054 | ||||||
chr15:73357097
|
A | G | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+10389T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357097 | ||||||
chr15:73357252
|
C | T | 38 | a0001c0001t0001g0038a0001c0001t0001g0085a0001c0001t0001g0251others(35): Show | 41 | HG00280.hp1 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.785+10234G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357252 | ||||||
chr15:73357370
|
G | A | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+10116C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357370 | ||||||
chr15:73357425
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.785+10061C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357425 | ||||||
chr15:73357627
|
C | T | 1 | a0001c0002t0003g0087 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.785+9859G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357627 | ||||||
chr15:73357632
|
C | T | 1 | a0004c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.785+9854G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357632 | ||||||
chr15:73357698
|
TGGAG | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+9784_785+9787d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357698 | ||||||
chr15:73357981
|
G | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0004t0001g0253 | 3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+9505C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357981 | ||||||
chr15:73357984
|
T | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0004t0001g0253 | 3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+9502A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357984 | ||||||
chr15:73358039
|
G | A | 1 | a0001c0002t0003g0159 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.785+9447C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358039 | ||||||
chr15:73358065
|
A | G | 22 | a0001c0001t0001g0233a0001c0001t0003g0075a0001c0001t0003g0076others(19): Show | 24 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+9421T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358065 | ||||||
chr15:73358196
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.785+9290G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358196 | ||||||
chr15:73358206
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0004t0001g0253 | 3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+9280C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358206 | ||||||
chr15:73358380
|
T | G | 3 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0237 | 3 | HG00099.hp2 HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.785+9106A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358380 | ||||||
chr15:73358483
|
G | A | 48 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0185others(45): Show | 65 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.785+9003C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358483 | ||||||
chr15:73358497
|
T | C | 1 | a0001c0004t0001g0160 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.785+8989A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358497 | ||||||
chr15:73358542
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.785+8944C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358542 | ||||||
chr15:73358861
|
T | C | 13 | a0001c0001t0001g0233a0001c0003t0001g0074a0001c0003t0001g0229others(10): Show | 15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+8625A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358861 | ||||||
chr15:73358915
|
ACCT | A | 17 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0006g0063others(14): Show | 18 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.785+8568_785+8570d others(5): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358915 | ||||||
chr15:73359039
|
T | G | 13 | a0001c0001t0001g0233a0001c0003t0001g0074a0001c0003t0001g0229others(10): Show | 15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+8447A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359039 | ||||||
chr15:73359174
|
C | T | 5 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+8312G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359174 | ||||||
chr15:73359220
|
T | C | 1 | a0001c0001t0004g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.785+8266A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359220 | ||||||
chr15:73359253
|
G | A | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+8233C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359253 | ||||||
chr15:73359257
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.785+8229G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359257 | ||||||
chr15:73359259
|
A | T | 2 | a0001c0001t0002g0165a0001c0001t0002g0166 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.785+8227T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359259 | ||||||
chr15:73359306
|
G | C | 1 | a0001c0001t0002g0030 | 2 | HG00423.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.785+8180C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359306 | ||||||
chr15:73359615
|
G | A | 2 | a0001c0001t0003g0243a0001c0001t0021g0242 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.785+7871C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359615 | ||||||
chr15:73359697
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.785+7789G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359697 | ||||||
chr15:73359833
|
A | G | 67 | a0001c0001t0001g0062a0001c0001t0001g0202a0001c0001t0001g0206others(64): Show | 73 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.785+7653T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359833 | ||||||
chr15:73360061
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.785+7425G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360061 | ||||||
chr15:73360454
|
C | G | 290 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(287): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.785+7032G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360454 | ||||||
chr15:73360668
|
G | A | 68 | a0001c0001t0001g0171a0001c0001t0001g0182a0001c0001t0001g0184others(65): Show | 87 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.785+6818C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360668 | ||||||
chr15:73360802
|
G | T | 4 | a0002c0008t0002g0007a0002c0008t0002g0046a0002c0008t0002g0047others(1): Show | 5 | HG01070.hp1 HG01081.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+6684C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360802 | ||||||
chr15:73361114
|
C | T | 1 | a0001c0001t0012g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.785+6372G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361114 | ||||||
chr15:73361144
|
A | G | 115 | a0001c0001t0001g0038a0001c0001t0001g0062a0001c0001t0001g0085others(112): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.785+6342T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361144 | ||||||
chr15:73361161
|
T | C | 76 | a0001c0001t0001g0062a0001c0001t0001g0202a0001c0001t0001g0206others(73): Show | 82 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.785+6325A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361161 | ||||||
chr15:73361199
|
C | T | 15 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0006g0063others(12): Show | 16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.785+6287G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361199 | ||||||
chr15:73361525
|
C | T | 1 | a0001c0003t0009g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.785+5961G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361525 | ||||||
chr15:73361599
|
C | T | 3 | a0001c0002t0003g0081a0001c0002t0003g0083a0001c0014t0003g0082 | 3 | HG02886.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.785+5887G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361599 | ||||||
chr15:73361630
|
T | C | 50 | a0001c0001t0001g0062a0001c0001t0001g0202a0001c0001t0001g0206others(47): Show | 54 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.785+5856A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361630 | ||||||
chr15:73361749
|
G | A | 1 | a0001c0002t0003g0212 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.785+5737C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361749 | ||||||
chr15:73361782
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG01261.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.785+5704C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361782 | ||||||
chr15:73361786
|
C | T | 2 | a0001c0003t0001g0050a0001c0003t0001g0051 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.785+5700G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361786 | ||||||
chr15:73361922
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0002g0031 | 3 | NA18957.hp1 NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.785+5564C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361922 | ||||||
chr15:73362135
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.785+5351G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362135 | ||||||
chr15:73362501
|
G | A | 13 | a0001c0001t0001g0233a0001c0003t0001g0074a0001c0003t0001g0229others(10): Show | 15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+4985C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362501 | ||||||
chr15:73362558
|
G | A | 1 | a0001c0002t0003g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.785+4928C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362558 | ||||||
chr15:73362689
|
C | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+4797G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362689 | ||||||
chr15:73362895
|
C | A | 17 | a0001c0001t0001g0233a0001c0001t0004g0285a0001c0001t0004g0286others(14): Show | 19 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.785+4591G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362895 | ||||||
chr15:73362942
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.785+4544G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362942 | ||||||
chr15:73363067
|
C | T | 1 | a0001c0003t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.785+4419G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363067 | ||||||
chr15:73363210
|
C | T | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+4276G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363210 | ||||||
chr15:73363258
|
C | T | 8 | a0001c0001t0003g0055a0001c0001t0004g0049a0001c0006t0003g0008others(5): Show | 9 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+4228G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363258 | ||||||
chr15:73363367
|
T | A | 2 | a0001c0001t0002g0218a0001c0001t0002g0219 | 2 | HG00673.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.785+4119A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363367 | ||||||
chr15:73363556
|
T | A | 15 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0006g0063others(12): Show | 16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.785+3930A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363556 | ||||||
chr15:73363676
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.785+3810C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363676 | ||||||
chr15:73363822
|
A | G | 1 | a0001c0023t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.785+3664T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363822 | ||||||
chr15:73363920
|
G | A | 11 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(8): Show | 13 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.785+3566C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363920 | ||||||
chr15:73363921
|
C | A | 1 | a0001c0001t0002g0220 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.785+3565G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363921 | ||||||
chr15:73363966
|
G | A | 11 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0246others(8): Show | 13 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.785+3520C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363966 | ||||||
chr15:73363995
|
G | A | 2 | a0001c0003t0009g0238a0001c0003t0009g0239 | 2 | HG00280.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.785+3491C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363995 | ||||||
chr15:73364083
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.785+3403G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364083 | ||||||
chr15:73364194
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.785+3292C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364194 | ||||||
chr15:73364427
|
G | T | 41 | a0001c0001t0001g0062a0001c0001t0001g0233a0001c0001t0002g0066others(38): Show | 45 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.785+3059C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364427 | ||||||
chr15:73364437
|
A | G | 1 | a0001c0001t0007g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+3049T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364437 | ||||||
chr15:73364497
|
G | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0004t0001g0253 | 3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+2989C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364497 | ||||||
chr15:73364680
|
C | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2806G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364680 | ||||||
chr15:73364722
|
C | T | 48 | a0001c0001t0001g0062a0001c0001t0001g0233a0001c0001t0002g0066others(45): Show | 52 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.785+2764G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364722 | ||||||
chr15:73364763
|
A | C | 9 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0004g0049others(6): Show | 10 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.785+2723T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364763 | ||||||
chr15:73364780
|
T | A | 1 | a0008c0015t0007g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.785+2706A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364780 | ||||||
chr15:73364853
|
CA | C | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2632delT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364853 | ||||||
chr15:73364855
|
G | C | 7 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2631C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364855 | ||||||
chr15:73364926
|
T | G | 43 | a0001c0001t0001g0062a0001c0001t0001g0233a0001c0001t0002g0066others(40): Show | 47 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.785+2560A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364926 | ||||||
chr15:73364954
|
G | A | 19 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0003g0243others(16): Show | 20 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.785+2532C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364954 | ||||||
chr15:73364974
|
C | T | 1 | a0001c0001t0016g0040 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.785+2512G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364974 | ||||||
chr15:73364980
|
C | T | 2 | a0001c0001t0004g0285a0001c0001t0004g0286 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.785+2506G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364980 | ||||||
chr15:73364981
|
G | A | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+2505C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364981 | ||||||
chr15:73365277
|
A | T | 1 | a0001c0001t0002g0079 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.785+2209T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365277 | ||||||
chr15:73365489
|
A | C | 6 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0004g0077others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.785+1997T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365489 | ||||||
chr15:73365561
|
T | C | 1 | a0001c0001t0002g0244 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.785+1925A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365561 | ||||||
chr15:73365593
|
A | G | 1 | a0001c0003t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.785+1893T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365593 | ||||||
chr15:73365679
|
C | T | 1 | a0004c0011t0004g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.785+1807G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365679 | ||||||
chr15:73365689
|
T | C | 1 | a0001c0003t0001g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.785+1797A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365689 | ||||||
chr15:73365809
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.785+1677C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365809 | ||||||
chr15:73365836
|
A | G | 17 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0006g0063others(14): Show | 18 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.785+1650T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365836 | ||||||
chr15:73365841
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.785+1645C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365841 | ||||||
chr15:73366342
|
G | A | 1 | a0001c0001t0018g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+1144C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366342 | ||||||
chr15:73366360
|
T | C | 2 | a0001c0002t0010g0292a0006c0018t0003g0291 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.785+1126A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366360 | ||||||
chr15:73366403
|
G | A | 1 | a0001c0001t0004g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.785+1083C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366403 | ||||||
chr15:73366414
|
G | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0249 | 5 | NA18939.hp1 NA18942.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+1072C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366414 | ||||||
chr15:73366422
|
G | A | 1 | a0008c0015t0007g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.785+1064C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366422 | ||||||
chr15:73366465
|
C | T | 9 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0004g0049others(6): Show | 10 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.785+1021G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366465 | ||||||
chr15:73366466
|
C | G | 2 | a0001c0002t0003g0052a0001c0002t0003g0053 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.785+1020G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366466 | ||||||
chr15:73366773
|
G | A | 1 | a0001c0001t0002g0035 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.785+713C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366773 | ||||||
chr15:73366853
|
A | T | 259 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0018others(256): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.785+633T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366853 | ||||||
chr15:73366862
|
G | A | 4 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0001t0004g0287others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+624C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366862 | ||||||
chr15:73366941
|
G | C | 1 | a0001c0001t0006g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.785+545C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366941 | ||||||
chr15:73366999
|
G | A | 1 | a0001c0005t0005g0290 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.785+487C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366999 | ||||||
chr15:73367002
|
C | T | 2 | a0001c0003t0001g0050a0001c0003t0001g0051 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.785+484G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367002 | ||||||
chr15:73367003
|
G | A | 1 | a0001c0001t0002g0039 | 2 | NA18950.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.785+483C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367003 | ||||||
chr15:73367141
|
C | A | 2 | a0001c0002t0010g0292a0006c0018t0003g0291 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.785+345G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367141 | ||||||
chr15:73367166
|
G | C | 1 | a0001c0004t0001g0293 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.785+320C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367166 | ||||||
chr15:73367457
|
C | T | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+29G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367457 |