| geneid | 610 |
|---|---|
| ensemblid | ENSG00000099822.3 |
| hgncid | 4846 |
| symbol | HCN2 |
| name | hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2 |
| refseq_nuc | NM_001194.4 |
| refseq_prot | NP_001185.3 |
| ensembl_nuc | ENST00000251287.3 |
| ensembl_prot | ENSP00000251287.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 589881 |
| end | 617159 |
| strand | + |
| ver | v1.2 |
| region | chr19:589881-617159 |
| region5000 | chr19:584881-622159 |
| regionname0 | HCN2_chr19_589881_617159 |
| regionname5000 | HCN2_chr19_584881_622159 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 889 | 265 | 76 | 47 | 106 | 3 | 32 | 75 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002 | 0/1 | 889 | 116 | 14 | 29 | 51 | 8 | 13 | 39 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0003 | 0/0 | 889 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0004 | 0/0 | 889 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0005 | 0/0 | 889 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0006 | 0/0 | 889 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0007 | 0/0 | 892 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0008 | 0/0 | 896 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0009 | 0/0 | 892 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0010 | 0/0 | 889 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0011 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0012 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0013 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0014 | 0/0 | 889 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0015 | 0/0 | 889 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0016 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0017 | 0/0 | 902 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0018 | 0/0 | 889 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0019 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2670 | 44 | 7 | 6 | 27 | 1 | 3 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0002 | 0/0 | 2670 | 29 | 0 | 2 | 25 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0003 | 0/0 | 2670 | 25 | 4 | 1 | 14 | 0 | 6 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0004 | 0/0 | 2670 | 24 | 2 | 3 | 14 | 1 | 4 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0005 | 0/0 | 2670 | 14 | 0 | 4 | 8 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0006 | 0/0 | 2670 | 12 | 4 | 2 | 4 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0007 | 0/0 | 2670 | 11 | 0 | 1 | 10 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0008 | 0/0 | 2670 | 11 | 7 | 0 | 1 | 0 | 3 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0009 | 0/0 | 2670 | 11 | 0 | 6 | 4 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0010 | 0/0 | 2670 | 9 | 1 | 1 | 7 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0011 | 0/0 | 2670 | 9 | 1 | 4 | 1 | 2 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0012 | 0/0 | 2670 | 9 | 3 | 0 | 5 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0013 | 0/0 | 2670 | 8 | 1 | 5 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0014 | 0/0 | 2670 | 7 | 1 | 0 | 6 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0015 | 0/0 | 2670 | 7 | 3 | 3 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0016 | 0/0 | 2670 | 6 | 1 | 1 | 4 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0017 | 0/0 | 2670 | 6 | 6 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0018 | 0/0 | 2670 | 6 | 4 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0019 | 0/0 | 2670 | 5 | 0 | 1 | 4 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0020 | 0/0 | 2670 | 5 | 4 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0021 | 0/0 | 2670 | 4 | 0 | 1 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0022 | 0/0 | 2670 | 4 | 0 | 1 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0023 | 0/0 | 2670 | 4 | 3 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0024 | 0/0 | 2670 | 4 | 1 | 2 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0025 | 0/0 | 2670 | 4 | 0 | 2 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0026 | 0/0 | 2670 | 4 | 2 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0027 | 0/0 | 2670 | 3 | 0 | 0 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0028 | 0/0 | 2670 | 3 | 0 | 2 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0029 | 0/0 | 2670 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0030 | 0/0 | 2670 | 3 | 1 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0031 | 0/0 | 2670 | 3 | 1 | 0 | 1 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0032 | 0/0 | 2670 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0033 | 1/0 | 2670 | 3 | 0 | 1 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0034 | 0/0 | 2670 | 3 | 2 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0035 | 0/0 | 2670 | 2 | 0 | 0 | 1 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0036 | 0/0 | 2670 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0037 | 0/0 | 2670 | 2 | 0 | 1 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0038 | 0/0 | 2670 | 2 | 1 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0039 | 0/0 | 2670 | 2 | 0 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0040 | 0/0 | 2670 | 2 | 0 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0041 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0042 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0043 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0044 | 0/0 | 2670 | 2 | 0 | 1 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0045 | 0/0 | 2670 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0046 | 0/0 | 2670 | 2 | 1 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0047 | 0/0 | 2670 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0048 | 0/0 | 2670 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0049 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0050 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0051 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0052 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0053 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0054 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0055 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0056 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0057 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0058 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0059 | 0/1 | 2670 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0060 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0061 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0062 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0063 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0064 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0065 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0066 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0067 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0068 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0069 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0070 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0071 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0072 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0073 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0074 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0075 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0076 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0077 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0078 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0079 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0080 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0081 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0082 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0083 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0084 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0085 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0086 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0087 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0088 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0089 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0090 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0091 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0092 | 0/0 | 2691 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0093 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0094 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0095 | 0/0 | 2679 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0096 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0097 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0098 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0099 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0100 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0101 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0102 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0103 | 0/0 | 2691 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0104 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0105 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0106 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0107 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0108 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0109 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0110 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0111 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0112 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0113 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0114 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0115 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0116 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0117 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0118 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0119 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0120 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0121 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| c0122 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 751 | 165 | 24 | 46 | 71 | 7 | 16 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0002 | 0/0 | 751 | 68 | 15 | 9 | 31 | 1 | 12 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0003 | 0/0 | 751 | 60 | 2 | 13 | 39 | 0 | 6 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0004 | 0/1 | 751 | 57 | 36 | 5 | 12 | 1 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0005 | 0/0 | 750 | 12 | 0 | 6 | 1 | 1 | 4 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0006 | 0/0 | 751 | 9 | 9 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0007 | 0/0 | 751 | 5 | 0 | 1 | 0 | 1 | 3 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0008 | 0/0 | 751 | 5 | 5 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0009 | 0/0 | 751 | 4 | 0 | 0 | 3 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0010 | 0/0 | 751 | 3 | 0 | 2 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0011 | 0/0 | 750 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0012 | 0/0 | 751 | 2 | 1 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0013 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0014 | 0/0 | 750 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0015 | 0/0 | 750 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0016 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0017 | 0/0 | 751 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0018 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0019 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0020 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0021 | 0/0 | 750 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0022 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0023 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0024 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0025 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0026 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| t0027 | 0/0 | 751 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| g0399 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2670 | 44 | 7 | 6 | 27 | 1 | 3 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0002 | 0/0 | 2670 | 29 | 0 | 2 | 25 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003 | 0/0 | 2670 | 25 | 4 | 1 | 14 | 0 | 6 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0006 | 0/0 | 2670 | 12 | 4 | 2 | 4 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0007 | 0/0 | 2670 | 11 | 0 | 1 | 10 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0008 | 0/0 | 2670 | 11 | 7 | 0 | 1 | 0 | 3 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0009 | 0/0 | 2670 | 11 | 0 | 6 | 4 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0013 | 0/0 | 2670 | 8 | 1 | 5 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0014 | 0/0 | 2670 | 7 | 1 | 0 | 6 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0015 | 0/0 | 2670 | 7 | 3 | 3 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0017 | 0/0 | 2670 | 6 | 6 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0018 | 0/0 | 2670 | 6 | 4 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0020 | 0/0 | 2670 | 5 | 4 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0022 | 0/0 | 2670 | 4 | 0 | 1 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0023 | 0/0 | 2670 | 4 | 3 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0024 | 0/0 | 2670 | 4 | 1 | 2 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0025 | 0/0 | 2670 | 4 | 0 | 2 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0026 | 0/0 | 2670 | 4 | 2 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0030 | 0/0 | 2670 | 3 | 1 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0031 | 0/0 | 2670 | 3 | 1 | 0 | 1 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0032 | 0/0 | 2670 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0033 | 1/0 | 2670 | 3 | 0 | 1 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0034 | 0/0 | 2670 | 3 | 2 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0039 | 0/0 | 2670 | 2 | 0 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0040 | 0/0 | 2670 | 2 | 0 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0041 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0042 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0044 | 0/0 | 2670 | 2 | 0 | 1 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0045 | 0/0 | 2670 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0046 | 0/0 | 2670 | 2 | 1 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0075 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0076 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0077 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0078 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0079 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0082 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0083 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0084 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0085 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0088 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0091 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0093 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0094 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0096 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0097 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0098 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0099 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0100 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0101 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0102 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0104 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0105 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0107 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0108 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0109 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0111 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0112 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0113 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0114 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0115 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0116 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0117 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0118 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0119 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004 | 0/0 | 2670 | 24 | 2 | 3 | 14 | 1 | 4 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0005 | 0/0 | 2670 | 14 | 0 | 4 | 8 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0010 | 0/0 | 2670 | 9 | 1 | 1 | 7 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0011 | 0/0 | 2670 | 9 | 1 | 4 | 1 | 2 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0012 | 0/0 | 2670 | 9 | 3 | 0 | 5 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0016 | 0/0 | 2670 | 6 | 1 | 1 | 4 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0019 | 0/0 | 2670 | 5 | 0 | 1 | 4 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0021 | 0/0 | 2670 | 4 | 0 | 1 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0027 | 0/0 | 2670 | 3 | 0 | 0 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0028 | 0/0 | 2670 | 3 | 0 | 2 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0035 | 0/0 | 2670 | 2 | 0 | 0 | 1 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0036 | 0/0 | 2670 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0037 | 0/0 | 2670 | 2 | 0 | 1 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0038 | 0/0 | 2670 | 2 | 1 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0050 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0051 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0052 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0053 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0054 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0055 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0057 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0058 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0059 | 0/1 | 2670 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0060 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0062 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0063 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0064 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0065 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0066 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0067 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0068 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0070 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0071 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0072 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0073 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0074 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0003c0029 | 0/0 | 2670 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0003c0089 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0004c0048 | 0/0 | 2670 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0004c0121 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0005c0043 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0005c0110 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0006c0047 | 0/0 | 2670 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0007c0095 | 0/0 | 2679 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0007c0106 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0008c0092 | 0/0 | 2691 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0008c0103 | 0/0 | 2691 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0009c0061 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0010c0069 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0011c0056 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0012c0081 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0013c0090 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0014c0087 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0015c0086 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0016c0080 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0017c0049 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0018c0120 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0019c0122 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3420 | 19 | 0 | 3 | 14 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0001t0002 | 0/0 | 3420 | 16 | 3 | 1 | 11 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0001t0004 | 0/0 | 3420 | 6 | 4 | 1 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0001t0009 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0001t0021 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0001t0027 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0002t0003 | 0/0 | 3420 | 22 | 0 | 2 | 19 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0002t0004 | 0/0 | 3420 | 5 | 0 | 0 | 4 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0002t0009 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0002t0019 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003t0001 | 0/0 | 3420 | 9 | 1 | 0 | 8 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003t0002 | 0/0 | 3420 | 11 | 0 | 1 | 6 | 0 | 4 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003t0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003t0007 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003t0010 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0003t0016 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0006t0001 | 0/0 | 3420 | 3 | 0 | 1 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0006t0002 | 0/0 | 3420 | 7 | 3 | 1 | 1 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0006t0004 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0006t0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0007t0001 | 0/0 | 3420 | 9 | 0 | 0 | 9 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0007t0002 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0007t0007 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0008t0001 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0008t0002 | 0/0 | 3420 | 3 | 1 | 0 | 1 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0008t0004 | 0/0 | 3420 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0008t0007 | 0/0 | 3420 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0008t0012 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0009t0001 | 0/0 | 3420 | 8 | 0 | 5 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0009t0002 | 0/0 | 3420 | 2 | 0 | 0 | 1 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0009t0010 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0013t0001 | 0/0 | 3420 | 7 | 1 | 5 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0013t0002 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0014t0003 | 0/0 | 3420 | 6 | 0 | 0 | 6 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0014t0024 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0015t0001 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0015t0002 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0015t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0015t0005 | 0/0 | 3419 | 3 | 0 | 3 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0017t0001 | 0/0 | 3420 | 5 | 5 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0017t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0018t0001 | 0/0 | 3420 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0018t0002 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0018t0020 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0018t0022 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0020t0003 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0020t0004 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0020t0008 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0022t0001 | 0/0 | 3420 | 4 | 0 | 1 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0023t0001 | 0/0 | 3420 | 3 | 2 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0023t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0024t0002 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0024t0003 | 0/0 | 3420 | 3 | 0 | 2 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0025t0001 | 0/0 | 3420 | 2 | 0 | 1 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0025t0004 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0025t0005 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0026t0002 | 0/0 | 3420 | 3 | 1 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0026t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0030t0004 | 0/0 | 3420 | 3 | 1 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0031t0001 | 0/0 | 3420 | 3 | 1 | 0 | 1 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0032t0004 | 0/0 | 3420 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0033t0001 | 1/0 | 3420 | 3 | 0 | 1 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0034t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0034t0005 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0034t0026 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0039t0001 | 0/0 | 3420 | 2 | 0 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0040t0003 | 0/0 | 3420 | 2 | 0 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0041t0001 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0042t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0042t0008 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0044t0001 | 0/0 | 3420 | 2 | 0 | 1 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0045t0003 | 0/0 | 3420 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0046t0001 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0046t0002 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0075t0004 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0076t0001 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0077t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0078t0008 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0079t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0082t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0083t0009 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0084t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0085t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0088t0002 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0091t0011 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0093t0003 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0094t0001 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0096t0003 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0097t0001 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0098t0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0099t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0100t0003 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0101t0008 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0102t0005 | 0/0 | 3419 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0104t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0105t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0107t0001 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0108t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0109t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0111t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0112t0014 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0113t0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0114t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0115t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0116t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0117t0015 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0118t0011 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0001c0119t0010 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004t0001 | 0/0 | 3420 | 12 | 0 | 1 | 8 | 0 | 3 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004t0002 | 0/0 | 3420 | 4 | 0 | 1 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004t0003 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004t0004 | 0/0 | 3420 | 4 | 1 | 0 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004t0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004t0007 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0004t0017 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0005t0003 | 0/0 | 3420 | 11 | 0 | 4 | 5 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0005t0004 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0005t0009 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0005t0025 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0010t0001 | 0/0 | 3420 | 6 | 1 | 0 | 5 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0010t0002 | 0/0 | 3420 | 3 | 0 | 1 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0011t0001 | 0/0 | 3420 | 9 | 1 | 4 | 1 | 2 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0012t0001 | 0/0 | 3420 | 6 | 1 | 0 | 4 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0012t0002 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0012t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0012t0013 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0016t0001 | 0/0 | 3420 | 5 | 0 | 1 | 4 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0016t0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0019t0003 | 0/0 | 3420 | 2 | 0 | 0 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0019t0004 | 0/0 | 3420 | 2 | 0 | 1 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0019t0018 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0021t0001 | 0/0 | 3420 | 3 | 0 | 1 | 2 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0021t0023 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0027t0003 | 0/0 | 3420 | 3 | 0 | 0 | 3 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0028t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0028t0004 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0028t0005 | 0/0 | 3419 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0035t0005 | 0/0 | 3419 | 2 | 0 | 0 | 1 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0036t0001 | 0/0 | 3420 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0037t0001 | 0/0 | 3420 | 2 | 0 | 1 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0038t0001 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0038t0005 | 0/0 | 3419 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0050t0002 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0051t0011 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0052t0001 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0053t0002 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0054t0004 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0055t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0057t0002 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0058t0012 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0059t0004 | 0/1 | 3420 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0060t0003 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0062t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0063t0001 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0064t0001 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0065t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0066t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0067t0001 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0068t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0070t0001 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0071t0002 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0072t0001 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0073t0001 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0002c0074t0002 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0003c0029t0002 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0003c0029t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0003c0089t0003 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0004c0048t0001 | 0/0 | 3420 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0004c0121t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0005c0043t0006 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0005c0110t0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0006c0047t0003 | 0/0 | 3420 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0007c0095t0001 | 0/0 | 3429 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0007c0106t0002 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0008c0092t0001 | 0/0 | 3441 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0008c0103t0001 | 0/0 | 3441 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0009c0061t0001 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0010c0069t0001 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0011c0056t0001 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0012c0081t0002 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0013c0090t0001 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0014c0087t0005 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0015c0086t0005 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0016c0080t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0017c0049t0001 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0018c0120t0002 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| a0019c0122t0004 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | copy fasta | chr19 | 584881 | 622159 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0002g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0004g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0009g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0021g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0001t0027g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0002t0019g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0007g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0010g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0003t0016g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0006t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0007t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0004g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0007g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0008t0012g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0001g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0009t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0001g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0013t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0014t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0014t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0014t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0014t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0014t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0014t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0014t0024g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0015t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0015t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0015t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0015t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0015t0005g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0015t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0017t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0017t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0017t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0017t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0018t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0018t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0018t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0018t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0018t0020g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0018t0022g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0020t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0020t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0020t0004g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0020t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0020t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0022t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0022t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0022t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0022t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0023t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0023t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0023t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0023t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0024t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0024t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0024t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0024t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0025t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0025t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0025t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0025t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0026t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0026t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0026t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0026t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0030t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0030t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0030t0004g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0031t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0031t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0031t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0032t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0032t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0032t0004g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0033t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0033t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0033t0001g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0034t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0034t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0034t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0039t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0039t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0040t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0040t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0041t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0041t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0042t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0042t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0044t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0044t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0045t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0046t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0046t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0075t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0076t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0077t0004g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0078t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0079t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0082t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0083t0009g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0084t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0085t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0088t0002g0399 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0091t0011g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0093t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0094t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0096t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0097t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0098t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0099t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0100t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0101t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0102t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0104t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0105t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0107t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0108t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0109t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0111t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0112t0014g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0113t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0114t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0115t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0116t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0117t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0118t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0001c0119t0010g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0004g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0006g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0007g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0004t0017g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0009g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0005t0025g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0010t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0011t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0012t0013g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0016t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0016t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0016t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0016t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0016t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0016t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0019t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0019t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0019t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0019t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0019t0018g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0021t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0021t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0021t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0021t0023g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0027t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0027t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0027t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0028t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0028t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0028t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0035t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0035t0005g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0036t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0037t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0037t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0038t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0038t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0050t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0051t0011g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0052t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0053t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0054t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0055t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0057t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0058t0012g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0059t0004g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0060t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0062t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0063t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0064t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0065t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0066t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0067t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0068t0004g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0070t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0071t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0072t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0073t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0002c0074t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0003c0029t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0003c0029t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0003c0029t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0003c0089t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0004c0048t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0004c0121t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0005c0043t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0005c0043t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0005c0110t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0006c0047t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0007c0095t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0007c0106t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0008c0092t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0008c0103t0001g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0009c0061t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0010c0069t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0011c0056t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0012c0081t0002g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0013c0090t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0014c0087t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0015c0086t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0016c0080t0004g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0017c0049t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0018c0120t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| a0019c0122t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0015 | c0086 | t0005 | g0133 | EUR | GBR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00099 | hp2 | a0001 | c0001 | t0021 | g0217 | EUR | GBR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00140 | hp1 | a0002 | c0037 | t0001 | g0323 | EUR | GBR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00140 | hp2 | a0002 | c0011 | t0001 | g0317 | EUR | GBR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00280 | hp1 | a0002 | c0067 | t0001 | g0255 | EUR | FIN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00280 | hp2 | a0002 | c0057 | t0002 | g0260 | EUR | FIN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00323 | hp1 | a0002 | c0011 | t0001 | g0318 | EUR | FIN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00323 | hp2 | a0001 | c0033 | t0001 | g0304 | EUR | FIN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00423 | hp1 | a0002 | c0027 | t0003 | g0351 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00423 | hp2 | a0001 | c0002 | t0009 | g0116 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00438 | hp1 | a0002 | c0021 | t0023 | g0288 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00438 | hp2 | a0002 | c0010 | t0001 | g0354 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00544 | hp1 | a0002 | c0010 | t0001 | g0253 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00609 | hp2 | a0011 | c0056 | t0001 | g0286 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0224 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00621 | hp2 | a0001 | c0014 | t0003 | g0096 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00639 | hp1 | a0001 | c0102 | t0005 | g0240 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00639 | hp2 | a0001 | c0109 | t0001 | g0034 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00642 | hp1 | a0002 | c0011 | t0001 | g0283 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00642 | hp2 | a0001 | c0085 | t0001 | g0221 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00673 | hp1 | a0002 | c0027 | t0003 | g0297 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00673 | hp2 | a0001 | c0040 | t0003 | g0195 | EAS | CHS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00733 | hp1 | a0002 | c0037 | t0001 | g0331 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00733 | hp2 | a0002 | c0065 | t0001 | g0285 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00735 | hp1 | a0001 | c0116 | t0001 | g0032 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00735 | hp2 | a0002 | c0004 | t0002 | g0279 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00738 | hp1 | a0002 | c0058 | t0012 | g0254 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00738 | hp2 | a0001 | c0046 | t0002 | g0037 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00741 | hp1 | a0001 | c0007 | t0007 | g0222 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG00741 | hp2 | a0002 | c0011 | t0001 | g0278 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01069 | hp1 | a0001 | c0006 | t0001 | g0213 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01069 | hp2 | a0001 | c0009 | t0001 | g0005 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01070 | hp1 | a0006 | c0047 | t0003 | g0002 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01070 | hp2 | a0001 | c0013 | t0001 | g0394 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01071 | hp1 | a0001 | c0009 | t0001 | g0005 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01071 | hp2 | a0006 | c0047 | t0003 | g0002 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0127 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01074 | hp2 | a0001 | c0022 | t0001 | g0242 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01081 | hp1 | a0002 | c0021 | t0001 | g0320 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01081 | hp2 | a0017 | c0049 | t0001 | g0311 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01099 | hp1 | a0002 | c0072 | t0001 | g0243 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01099 | hp2 | a0002 | c0010 | t0002 | g0319 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01106 | hp1 | a0002 | c0028 | t0001 | g0330 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01106 | hp2 | a0001 | c0044 | t0001 | g0209 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01109 | hp1 | a0001 | c0018 | t0001 | g0048 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01109 | hp2 | a0002 | c0004 | t0003 | g0341 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01167 | hp1 | a0001 | c0015 | t0005 | g0007 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01167 | hp2 | a0002 | c0038 | t0005 | g0338 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01168 | hp1 | a0002 | c0005 | t0003 | g0276 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01168 | hp2 | a0001 | c0030 | t0004 | g0234 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01169 | hp1 | a0001 | c0015 | t0005 | g0007 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01169 | hp2 | a0001 | c0030 | t0004 | g0235 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01175 | hp1 | a0002 | c0011 | t0001 | g0277 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01175 | hp2 | a0001 | c0006 | t0002 | g0166 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0372 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01192 | hp2 | a0001 | c0015 | t0005 | g0144 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01243 | hp1 | a0001 | c0018 | t0001 | g0040 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | PUR | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01255 | hp1 | a0002 | c0028 | t0005 | g0280 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0145 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01256 | hp1 | a0002 | c0036 | t0001 | g0008 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01256 | hp2 | a0002 | c0019 | t0004 | g0298 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01257 | hp1 | a0004 | c0048 | t0001 | g0003 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01258 | hp1 | a0004 | c0048 | t0001 | g0003 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01258 | hp2 | a0002 | c0036 | t0001 | g0008 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01261 | hp1 | a0002 | c0005 | t0003 | g0344 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01261 | hp2 | a0001 | c0111 | t0001 | g0033 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01358 | hp1 | a0002 | c0016 | t0001 | g0314 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01358 | hp2 | a0018 | c0120 | t0002 | g0160 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01361 | hp1 | a0002 | c0055 | t0001 | g0271 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01361 | hp2 | a0001 | c0033 | t0001 | g0233 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01496 | hp1 | a0002 | c0005 | t0003 | g0272 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01496 | hp2 | a0002 | c0011 | t0001 | g0365 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01515 | hp1 | a0002 | c0004 | t0007 | g0367 | EUR | IBS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01515 | hp2 | a0001 | c0031 | t0001 | g0146 | EUR | IBS | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01884 | hp1 | a0002 | c0012 | t0004 | g0256 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01884 | hp2 | a0001 | c0091 | t0011 | g0380 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01891 | hp1 | a0001 | c0003 | t0004 | g0012 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01891 | hp2 | a0001 | c0006 | t0006 | g0249 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01928 | hp1 | a0001 | c0013 | t0001 | g0389 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01928 | hp2 | a0002 | c0071 | t0002 | g0273 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01934 | hp1 | a0001 | c0009 | t0001 | g0395 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01934 | hp2 | a0002 | c0074 | t0002 | g0350 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01943 | hp1 | a0001 | c0105 | t0001 | g0121 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01943 | hp2 | a0001 | c0024 | t0003 | g0246 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01952 | hp1 | a0001 | c0009 | t0010 | g0120 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01952 | hp2 | a0002 | c0060 | t0003 | g0309 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01975 | hp1 | a0001 | c0013 | t0001 | g0129 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01975 | hp2 | a0002 | c0005 | t0003 | g0322 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01978 | hp1 | a0001 | c0013 | t0001 | g0391 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01978 | hp2 | a0001 | c0025 | t0004 | g0059 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01981 | hp1 | a0001 | c0013 | t0001 | g0131 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01981 | hp2 | a0008 | c0092 | t0001 | g0123 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0332 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01993 | hp2 | a0001 | c0104 | t0001 | g0176 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02004 | hp1 | a0001 | c0119 | t0010 | g0239 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02004 | hp2 | a0001 | c0009 | t0001 | g0388 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02015 | hp1 | a0002 | c0012 | t0013 | g0265 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02015 | hp2 | a0001 | c0075 | t0004 | g0200 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0192 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0203 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02040 | hp1 | a0002 | c0027 | t0003 | g0313 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02040 | hp2 | a0001 | c0009 | t0001 | g0114 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02055 | hp1 | a0001 | c0008 | t0001 | g0026 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02055 | hp2 | a0001 | c0032 | t0004 | g0100 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02056 | hp2 | a0002 | c0012 | t0001 | g0366 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02071 | hp1 | a0001 | c0022 | t0001 | g0152 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02074 | hp1 | a0001 | c0020 | t0003 | g0115 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02080 | hp2 | a0009 | c0061 | t0001 | g0356 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02083 | hp1 | a0002 | c0005 | t0009 | g0301 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02083 | hp2 | a0001 | c0007 | t0001 | g0190 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02129 | hp1 | a0001 | c0014 | t0003 | g0095 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02132 | hp1 | a0013 | c0090 | t0001 | g0118 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0205 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02135 | hp2 | a0002 | c0016 | t0001 | g0306 | EAS | KHV | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02145 | hp1 | a0003 | c0029 | t0002 | g0105 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02145 | hp2 | a0002 | c0012 | t0001 | g0359 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02148 | hp1 | a0002 | c0066 | t0001 | g0310 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02148 | hp2 | a0001 | c0025 | t0001 | g0036 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02155 | hp2 | a0002 | c0019 | t0003 | g0268 | EAS | CDX | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0074 | EAS | CDX | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02165 | hp2 | a0001 | c0040 | t0003 | g0191 | EAS | CDX | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02257 | hp1 | a0001 | c0041 | t0001 | g0019 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02257 | hp2 | a0001 | c0101 | t0008 | g0024 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02258 | hp1 | a0001 | c0018 | t0020 | g0058 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02258 | hp2 | a0001 | c0108 | t0004 | g0043 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02273 | hp1 | a0008 | c0103 | t0001 | g0393 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02280 | hp2 | a0002 | c0068 | t0004 | g0358 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02293 | hp1 | a0001 | c0009 | t0001 | g0218 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02293 | hp2 | a0001 | c0001 | t0027 | g0390 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02300 | hp1 | a0001 | c0024 | t0003 | g0177 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02451 | hp1 | a0001 | c0018 | t0002 | g0052 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02451 | hp2 | a0001 | c0003 | t0016 | g0384 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02572 | hp1 | a0001 | c0034 | t0026 | g0061 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02572 | hp2 | a0001 | c0015 | t0001 | g0373 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0396 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02602 | hp2 | a0002 | c0004 | t0017 | g0259 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02615 | hp1 | a0001 | c0017 | t0004 | g0023 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02615 | hp2 | a0001 | c0017 | t0001 | g0383 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02622 | hp1 | a0001 | c0041 | t0001 | g0099 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02622 | hp2 | a0001 | c0017 | t0001 | g0001 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02630 | hp1 | a0001 | c0113 | t0006 | g0042 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02630 | hp2 | a0001 | c0015 | t0001 | g0011 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02647 | hp1 | a0001 | c0098 | t0006 | g0064 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02647 | hp2 | a0001 | c0046 | t0001 | g0056 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02698 | hp1 | a0001 | c0013 | t0001 | g0198 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02698 | hp2 | a0002 | c0005 | t0003 | g0258 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02717 | hp1 | a0001 | c0076 | t0001 | g0029 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02717 | hp2 | a0001 | c0096 | t0003 | g0117 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02723 | hp1 | a0002 | c0004 | t0006 | g0353 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02723 | hp2 | a0002 | c0050 | t0002 | g0361 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02735 | hp1 | a0002 | c0004 | t0001 | g0342 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02735 | hp2 | a0001 | c0024 | t0003 | g0167 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02738 | hp1 | a0001 | c0117 | t0015 | g0063 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02738 | hp2 | a0001 | c0097 | t0001 | g0119 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02809 | hp1 | a0001 | c0003 | t0006 | g0201 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02809 | hp2 | a0016 | c0080 | t0004 | g0386 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02818 | hp1 | a0001 | c0023 | t0004 | g0247 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02818 | hp2 | a0001 | c0032 | t0004 | g0381 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0387 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02886 | hp2 | a0001 | c0008 | t0004 | g0385 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02895 | hp1 | a0001 | c0099 | t0004 | g0377 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02895 | hp2 | a0001 | c0017 | t0001 | g0001 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02896 | hp1 | a0001 | c0008 | t0004 | g0375 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02896 | hp2 | a0005 | c0043 | t0006 | g0108 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02897 | hp1 | a0005 | c0043 | t0006 | g0109 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02897 | hp2 | a0001 | c0017 | t0001 | g0001 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02922 | hp1 | a0003 | c0029 | t0004 | g0104 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02922 | hp2 | a0001 | c0078 | t0008 | g0031 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02965 | hp1 | a0003 | c0029 | t0002 | g0103 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02970 | hp1 | a0001 | c0023 | t0001 | g0370 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02976 | hp1 | a0001 | c0006 | t0002 | g0244 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03017 | hp1 | a0001 | c0006 | t0002 | g0073 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03017 | hp2 | a0001 | c0025 | t0001 | g0050 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03041 | hp1 | a0002 | c0062 | t0004 | g0362 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03041 | hp2 | a0001 | c0079 | t0004 | g0028 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03098 | hp1 | a0001 | c0015 | t0004 | g0021 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03130 | hp1 | a0001 | c0026 | t0002 | g0057 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03130 | hp2 | a0001 | c0084 | t0004 | g0101 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03139 | hp1 | a0001 | c0032 | t0004 | g0374 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03139 | hp2 | a0019 | c0122 | t0004 | g0102 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03195 | hp1 | a0001 | c0020 | t0004 | g0397 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03195 | hp2 | a0001 | c0017 | t0001 | g0376 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03209 | hp1 | a0001 | c0034 | t0004 | g0044 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03209 | hp2 | a0001 | c0118 | t0011 | g0060 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03225 | hp1 | a0001 | c0077 | t0004 | g0382 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03225 | hp2 | a0001 | c0006 | t0002 | g0107 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03239 | hp1 | a0001 | c0006 | t0002 | g0027 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03239 | hp2 | a0001 | c0112 | t0014 | g0047 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03453 | hp2 | a0001 | c0008 | t0002 | g0379 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03486 | hp1 | a0001 | c0030 | t0004 | g0378 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03486 | hp2 | a0001 | c0024 | t0002 | g0014 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03490 | hp1 | a0001 | c0008 | t0007 | g0004 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03490 | hp2 | a0001 | c0023 | t0001 | g0125 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03491 | hp1 | a0001 | c0045 | t0003 | g0006 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03491 | hp2 | a0001 | c0009 | t0002 | g0241 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03492 | hp1 | a0001 | c0008 | t0007 | g0004 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03492 | hp2 | a0001 | c0045 | t0003 | g0006 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03516 | hp1 | a0001 | c0020 | t0008 | g0010 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03516 | hp2 | a0001 | c0094 | t0001 | g0369 | AFR | ESN | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03540 | hp1 | a0001 | c0026 | t0004 | g0051 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03540 | hp2 | a0001 | c0115 | t0004 | g0062 | AFR | GWD | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03579 | hp1 | a0003 | c0089 | t0003 | g0106 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03579 | hp2 | a0001 | c0114 | t0004 | g0041 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03654 | hp1 | a0001 | c0008 | t0002 | g0128 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03654 | hp2 | a0001 | c0044 | t0001 | g0124 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03669 | hp1 | a0002 | c0073 | t0001 | g0291 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03669 | hp2 | a0001 | c0088 | t0002 | g0399 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0223 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03704 | hp1 | a0002 | c0005 | t0003 | g0326 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03704 | hp2 | a0002 | c0011 | t0001 | g0340 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03710 | hp2 | a0002 | c0004 | t0001 | g0303 | SAS | PJL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0219 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03831 | hp2 | a0002 | c0004 | t0001 | g0299 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03834 | hp1 | a0002 | c0070 | t0001 | g0315 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03834 | hp2 | a0001 | c0025 | t0005 | g0049 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03927 | hp1 | a0002 | c0035 | t0005 | g0349 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03927 | hp2 | a0007 | c0095 | t0001 | g0211 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03942 | hp1 | a0001 | c0003 | t0007 | g0067 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0078 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04115 | hp1 | a0001 | c0083 | t0009 | g0097 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04115 | hp2 | a0001 | c0013 | t0002 | g0197 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0210 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04184 | hp2 | a0014 | c0087 | t0005 | g0220 | SAS | BEB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04199 | hp1 | a0001 | c0003 | t0010 | g0196 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04199 | hp2 | a0010 | c0069 | t0001 | g0307 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04204 | hp1 | a0002 | c0054 | t0004 | g0250 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04204 | hp2 | a0002 | c0053 | t0002 | g0300 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0179 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG04228 | hp2 | a0002 | c0064 | t0001 | g0324 | SAS | STU | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18522 | hp1 | a0001 | c0020 | t0008 | g0013 | AFR | YRI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18522 | hp2 | a0001 | c0006 | t0002 | g0020 | AFR | YRI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18747 | hp1 | a0002 | c0005 | t0003 | g0281 | EAS | CHB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18747 | hp2 | a0001 | c0009 | t0001 | g0069 | EAS | CHB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18906 | hp1 | a0002 | c0012 | t0002 | g0346 | AFR | YRI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18906 | hp2 | a0001 | c0008 | t0012 | g0371 | AFR | YRI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18940 | hp1 | a0002 | c0011 | t0001 | g0289 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18940 | hp2 | a0001 | c0002 | t0019 | g0138 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18943 | hp1 | a0002 | c0010 | t0001 | g0262 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18944 | hp2 | a0001 | c0007 | t0001 | g0193 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18945 | hp1 | a0001 | c0007 | t0002 | g0086 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18945 | hp2 | a0001 | c0039 | t0001 | g0153 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18947 | hp1 | a0001 | c0007 | t0001 | g0088 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18947 | hp2 | a0002 | c0004 | t0001 | g0257 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0183 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18948 | hp2 | a0001 | c0014 | t0003 | g0071 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18950 | hp1 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18950 | hp2 | a0002 | c0004 | t0001 | g0261 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18951 | hp2 | a0001 | c0008 | t0002 | g0082 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18952 | hp1 | a0002 | c0004 | t0001 | g0316 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18953 | hp1 | a0002 | c0012 | t0001 | g0336 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18954 | hp1 | a0001 | c0107 | t0001 | g0054 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18960 | hp1 | a0002 | c0005 | t0003 | g0263 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18960 | hp2 | a0002 | c0021 | t0001 | g0287 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18961 | hp1 | a0001 | c0015 | t0002 | g0079 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18961 | hp2 | a0002 | c0004 | t0001 | g0347 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18962 | hp2 | a0001 | c0014 | t0003 | g0215 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18966 | hp2 | a0001 | c0014 | t0003 | g0076 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18967 | hp1 | a0001 | c0009 | t0001 | g0130 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18969 | hp2 | a0002 | c0052 | t0001 | g0305 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18970 | hp1 | a0001 | c0039 | t0001 | g0202 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18970 | hp2 | a0002 | c0012 | t0001 | g0345 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18971 | hp1 | a0001 | c0006 | t0001 | g0070 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18971 | hp2 | a0001 | c0001 | t0009 | g0143 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18973 | hp1 | a0001 | c0002 | t0004 | g0092 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18973 | hp2 | a0001 | c0007 | t0001 | g0212 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18979 | hp1 | a0002 | c0010 | t0002 | g0266 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18980 | hp1 | a0002 | c0004 | t0002 | g0355 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18980 | hp2 | a0002 | c0005 | t0004 | g0282 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18982 | hp1 | a0002 | c0004 | t0002 | g0329 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18982 | hp2 | a0001 | c0009 | t0002 | g0151 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18983 | hp1 | a0001 | c0014 | t0003 | g0204 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18983 | hp2 | a0002 | c0010 | t0002 | g0270 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0149 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18984 | hp2 | a0001 | c0006 | t0001 | g0214 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18985 | hp2 | a0012 | c0081 | t0002 | g0398 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0094 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18990 | hp2 | a0002 | c0019 | t0018 | g0269 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0174 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18995 | hp2 | a0002 | c0016 | t0001 | g0252 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18998 | hp1 | a0001 | c0026 | t0002 | g0045 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18999 | hp1 | a0002 | c0016 | t0001 | g0293 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19000 | hp2 | a0001 | c0006 | t0004 | g0072 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0111 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19009 | hp1 | a0001 | c0007 | t0001 | g0066 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19009 | hp2 | a0001 | c0022 | t0001 | g0075 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19011 | hp2 | a0002 | c0010 | t0001 | g0290 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19012 | hp1 | a0001 | c0100 | t0003 | g0171 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19012 | hp2 | a0002 | c0005 | t0003 | g0348 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19030 | hp1 | a0004 | c0121 | t0004 | g0236 | AFR | LWK | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19030 | hp2 | a0005 | c0110 | t0006 | g0046 | AFR | LWK | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19043 | hp1 | a0002 | c0016 | t0006 | g0292 | AFR | LWK | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | LWK | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19055 | hp2 | a0002 | c0005 | t0003 | g0251 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19057 | hp1 | a0001 | c0026 | t0002 | g0038 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19057 | hp2 | a0002 | c0012 | t0001 | g0294 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19063 | hp1 | a0001 | c0007 | t0001 | g0165 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19063 | hp2 | a0002 | c0004 | t0002 | g0328 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19064 | hp1 | a0002 | c0004 | t0004 | g0334 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19064 | hp2 | a0001 | c0022 | t0001 | g0227 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19065 | hp1 | a0002 | c0004 | t0001 | g0296 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19066 | hp1 | a0001 | c0031 | t0001 | g0173 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19066 | hp2 | a0001 | c0007 | t0001 | g0194 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0302 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19070 | hp2 | a0002 | c0021 | t0001 | g0267 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0110 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19074 | hp2 | a0007 | c0106 | t0002 | g0187 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19077 | hp1 | a0001 | c0007 | t0001 | g0189 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19077 | hp2 | a0002 | c0016 | t0001 | g0337 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19079 | hp1 | a0002 | c0004 | t0001 | g0295 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19080 | hp2 | a0002 | c0004 | t0004 | g0275 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19082 | hp1 | a0001 | c0006 | t0002 | g0216 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19082 | hp2 | a0002 | c0005 | t0003 | g0321 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19083 | hp1 | a0002 | c0019 | t0004 | g0368 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19083 | hp2 | a0002 | c0004 | t0001 | g0327 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19085 | hp1 | a0001 | c0007 | t0001 | g0089 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19085 | hp2 | a0002 | c0035 | t0005 | g0343 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19088 | hp1 | a0002 | c0019 | t0003 | g0333 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19089 | hp1 | a0002 | c0005 | t0025 | g0352 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19089 | hp2 | a0002 | c0010 | t0001 | g0308 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19090 | hp1 | a0002 | c0004 | t0004 | g0325 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19240 | hp1 | a0001 | c0014 | t0024 | g0248 | AFR | YRI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA19240 | hp2 | a0001 | c0008 | t0001 | g0022 | AFR | YRI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20129 | hp1 | a0001 | c0031 | t0001 | g0245 | AFR | ASW | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20129 | hp2 | a0002 | c0063 | t0001 | g0274 | AFR | ASW | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20752 | hp1 | a0002 | c0028 | t0004 | g0284 | EUR | TSI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20752 | hp2 | a0002 | c0012 | t0001 | g0264 | EUR | TSI | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20905 | hp1 | a0001 | c0002 | t0004 | g0184 | SAS | GIH | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20905 | hp2 | a0001 | c0034 | t0005 | g0035 | SAS | GIH | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01123 | hp1 | a0001 | c0093 | t0003 | g0159 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02109 | hp1 | a0001 | c0082 | t0004 | g0208 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02109 | hp2 | a0001 | c0023 | t0001 | g0122 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02486 | hp1 | a0001 | c0020 | t0004 | g0030 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02486 | hp2 | a0001 | c0018 | t0002 | g0053 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02559 | hp1 | a0002 | c0038 | t0001 | g0357 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG02559 | hp2 | a0002 | c0004 | t0004 | g0364 | AFR | ACB | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03471 | hp1 | a0002 | c0051 | t0011 | g0360 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG03471 | hp2 | a0001 | c0042 | t0008 | g0112 | AFR | MSL | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG06807 | hp1 | a0002 | c0011 | t0001 | g0312 | AFR | USA | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| HG06807 | hp2 | a0001 | c0008 | t0004 | g0228 | AFR | USA | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20300 | hp1 | a0002 | c0010 | t0001 | g0363 | AFR | USA | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA20300 | hp2 | a0001 | c0013 | t0001 | g0392 | AFR | USA | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA21309 | hp1 | a0001 | c0042 | t0004 | g0015 | AFR | LWK | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| NA21309 | hp2 | a0001 | c0018 | t0022 | g0039 | AFR | LWK | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0059 | t0004 | g0339 | REF | REF | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| homoSapiens_grch38 | hp1 | a0001 | c0033 | t0001 | g0335 | REF | REF | HCN2_chr19_584881_622159 | HCN2 | chr19 | 584881 | 622159 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:590004
|
C | G | 1 | a0019 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.59C>G | p.Pro20Arg | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 124/3420 | 59/2670 | 20/889 | chr19 | 590004 | ||
| chr19:590007
|
G | GGCCGCCG others(32): Show |
1 | a0017 | 1 | HG01081.hp2 | disruptive_inframe_insertion | MODERATE | c.95_133dupAACAGCAGC others(30): Show |
p.Gln32_Pro44dup | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 199/3420 | 134/2670 | 45/889 | INFO_REALIGN_3_PRIME | chr19 | 590007 | |
| chr19:590052
|
C | G | 1 | a0018 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.107C>G | p.Pro36Arg | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 172/3420 | 107/2670 | 36/889 | chr19 | 590052 | ||
| chr19:590052
|
C | T | 2 | a0004a0006 | 5 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(2): Show |
missense_variant | MODERATE | c.107C>T | p.Pro36Leu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 172/3420 | 107/2670 | 36/889 | chr19 | 590052 | ||
| chr19:590172
|
G | A | 5 | a0002a0009a0010others(2): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
missense_variant | MODERATE | c.227G>A | p.Arg76His | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 292/3420 | 227/2670 | 76/889 | chr19 | 590172 | ||
| chr19:590354
|
G | C | 1 | a0016 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.409G>C | p.Gly137Arg | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 474/3420 | 409/2670 | 137/889 | chr19 | 590354 | ||
| chr19:590527
|
G | C | 1 | a0012 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.582G>C | p.Glu194Asp | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 647/3420 | 582/2670 | 194/889 | chr19 | 590527 | ||
| chr19:590528
|
C | G | 1 | a0012 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.583C>G | p.Arg195Gly | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 648/3420 | 583/2670 | 195/889 | chr19 | 590528 | ||
| chr19:603639
|
C | T | 1 | a0006 | 2 | HG01070.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.728C>T | p.Pro243Leu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 793/3420 | 728/2670 | 243/889 | chr19 | 603639 | ||
| chr19:603749
|
G | A | 2 | a0003a0019 | 5 | HG02145.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
missense_variant | MODERATE | c.838G>A | p.Glu280Lys | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 903/3420 | 838/2670 | 280/889 | chr19 | 603749 | ||
| chr19:615946
|
C | CCCGCCGC others(2): Show |
2 | a0007a0009 | 3 | HG02080.hp2 HG03927.hp2 NA19074.hp2 |
disruptive_inframe_insertion | MODERATE | c.2156_2164dupCGCCGC others(3): Show |
p.Pro719_Pro721dup | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2230/3420 | 2165/2670 | 722/889 | INFO_REALIGN_3_PRIME | chr19 | 615946 | |
| chr19:616031
|
G | C | 1 | a0015 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2227G>C | p.Ala743Pro | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2292/3420 | 2227/2670 | 743/889 | chr19 | 616031 | ||
| chr19:616086
|
C | T | 1 | a0010 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.2282C>T | p.Pro761Leu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2347/3420 | 2282/2670 | 761/889 | chr19 | 616086 | ||
| chr19:616122
|
G | C | 1 | a0011 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.2318G>C | p.Gly773Ala | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2383/3420 | 2318/2670 | 773/889 | chr19 | 616122 | ||
| chr19:616132
|
C | CCCCGCCA others(14): Show |
1 | a0008 | 2 | HG01981.hp2 HG02273.hp1 |
disruptive_inframe_insertion | MODERATE | c.2342_2362dupCGGGCG others(15): Show |
p.Pro781_Pro787dup | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2428/3420 | 2363/2670 | 788/889 | INFO_REALIGN_3_PRIME | chr19 | 616132 | |
| chr19:616152
|
C | T | 1 | a0005 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.2348C>T | p.Ala783Val | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2413/3420 | 2348/2670 | 783/889 | chr19 | 616152 | ||
| chr19:616190
|
G | T | 1 | a0013 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.2386G>T | p.Gly796Cys | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2451/3420 | 2386/2670 | 796/889 | chr19 | 616190 | ||
| chr19:616323
|
C | A | 1 | a0014 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.2519C>A | p.Pro840Gln | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2584/3420 | 2519/2670 | 840/889 | chr19 | 616323 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:590095
|
G | T | 1 | a0001c0119 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.150G>T | p.Ala50Ala | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 215/3420 | 150/2670 | 50/889 | chr19 | 590095 | ||
| chr19:590158
|
G | T | 1 | a0001c0118 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.213G>T | p.Pro71Pro | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 278/3420 | 213/2670 | 71/889 | chr19 | 590158 | ||
| chr19:590165
|
C | A | 2 | a0002c0050a0002c0051 | 2 | HG02723.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.220C>A | p.Arg74Arg | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 285/3420 | 220/2670 | 74/889 | chr19 | 590165 | ||
| chr19:590224
|
G | A | 1 | a0001c0075 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.279G>A | p.Thr93Thr | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 344/3420 | 279/2670 | 93/889 | chr19 | 590224 | ||
| chr19:590305
|
G | A | 4 | a0001c0076a0001c0077a0001c0078others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.360G>A | p.Gly120Gly | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 425/3420 | 360/2670 | 120/889 | chr19 | 590305 | ||
| chr19:590323
|
G | T | 17 | a0001c0018a0001c0025a0001c0026others(14): Show | 31 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
synonymous_variant | LOW | c.378G>T | p.Ser126Ser | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 443/3420 | 378/2670 | 126/889 | chr19 | 590323 | ||
| chr19:590365
|
G | A | 4 | a0001c0076a0001c0077a0001c0078others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.420G>A | p.Pro140Pro | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | 485/3420 | 420/2670 | 140/889 | chr19 | 590365 | ||
| chr19:603625
|
T | C | 30 | a0001c0003a0001c0007a0001c0020others(27): Show | 91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
synonymous_variant | LOW | c.714T>C | p.Asp238Asp | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 779/3420 | 714/2670 | 238/889 | chr19 | 603625 | ||
| chr19:603634
|
T | C | 31 | a0001c0003a0001c0007a0001c0020others(28): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
synonymous_variant | LOW | c.723T>C | p.Thr241Thr | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 788/3420 | 723/2670 | 241/889 | chr19 | 603634 | ||
| chr19:603769
|
T | C | 31 | a0001c0003a0001c0007a0001c0020others(28): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
synonymous_variant | LOW | c.858T>C | p.Tyr286Tyr | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 923/3420 | 858/2670 | 286/889 | chr19 | 603769 | ||
| chr19:603826
|
C | T | 31 | a0001c0003a0001c0007a0001c0020others(28): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
synonymous_variant | LOW | c.915C>T | p.Phe305Phe | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 980/3420 | 915/2670 | 305/889 | chr19 | 603826 | ||
| chr19:603832
|
C | T | 15 | a0001c0009a0001c0013a0001c0045others(12): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
synonymous_variant | LOW | c.921C>T | p.Ile307Ile | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 986/3420 | 921/2670 | 307/889 | chr19 | 603832 | ||
| chr19:603874
|
C | T | 31 | a0001c0003a0001c0007a0001c0020others(28): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
synonymous_variant | LOW | c.963C>T | p.Arg321Arg | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 1028/3420 | 963/2670 | 321/889 | chr19 | 603874 | ||
| chr19:603934
|
A | G | 1 | a0001c0101 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1023A>G | p.Ser341Ser | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/8 | 1088/3420 | 1023/2670 | 341/889 | chr19 | 603934 | ||
| chr19:605090
|
C | T | 1 | a0002c0070 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1086C>T | p.Ser362Ser | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/8 | 1151/3420 | 1086/2670 | 362/889 | chr19 | 605090 | ||
| chr19:605093
|
G | A | 3 | a0002c0058a0002c0059a0013c0090 | 3 | HG00738.hp1 HG02132.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.1089G>A | p.Ala363Ala | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/8 | 1154/3420 | 1089/2670 | 363/889 | chr19 | 605093 | ||
| chr19:605147
|
C | T | 1 | a0001c0100 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.1143C>T | p.Asp381Asp | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/8 | 1208/3420 | 1143/2670 | 381/889 | chr19 | 605147 | ||
| chr19:605171
|
T | C | 65 | a0001c0001a0001c0002a0001c0006others(62): Show | 252 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(249): Show |
synonymous_variant | LOW | c.1167T>C | p.Pro389Pro | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/8 | 1232/3420 | 1167/2670 | 389/889 | chr19 | 605171 | ||
| chr19:607984
|
G | A | 1 | a0002c0064 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.1239G>A | p.Leu413Leu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/8 | 1304/3420 | 1239/2670 | 413/889 | chr19 | 607984 | ||
| chr19:607984
|
G | C | 28 | a0001c0006a0001c0014a0001c0018others(25): Show | 64 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(61): Show |
synonymous_variant | LOW | c.1239G>C | p.Leu413Leu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/8 | 1304/3420 | 1239/2670 | 413/889 | chr19 | 607984 | ||
| chr19:610273
|
G | A | 23 | a0001c0013a0001c0023a0001c0044others(20): Show | 36 | HG00280.hp1 HG01070.hp2 HG01099.hp1 others(33): Show |
synonymous_variant | LOW | c.1452G>A | p.Glu484Glu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/8 | 1517/3420 | 1452/2670 | 484/889 | chr19 | 610273 | ||
| chr19:613307
|
C | T | 36 | a0001c0002a0001c0014a0001c0015others(33): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(115): Show |
synonymous_variant | LOW | c.1644C>T | p.Ala548Ala | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/8 | 1709/3420 | 1644/2670 | 548/889 | chr19 | 613307 | ||
| chr19:613364
|
G | A | 1 | a0001c0109 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1701G>A | p.Pro567Pro | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/8 | 1766/3420 | 1701/2670 | 567/889 | chr19 | 613364 | ||
| chr19:613886
|
G | T | 2 | a0001c0112a0001c0117 | 2 | HG02738.hp1 HG03239.hp2 |
synonymous_variant | LOW | c.1860G>T | p.Ala620Ala | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/8 | 1925/3420 | 1860/2670 | 620/889 | chr19 | 613886 | ||
| chr19:613898
|
T | C | 96 | a0001c0001a0001c0002a0001c0003others(93): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(357): Show |
synonymous_variant | LOW | c.1872T>C | p.Ala624Ala | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/8 | 1937/3420 | 1872/2670 | 624/889 | chr19 | 613898 | ||
| chr19:616057
|
G | C | 23 | a0001c0002a0001c0014a0001c0024others(20): Show | 84 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(81): Show |
synonymous_variant | LOW | c.2253G>C | p.Ala751Ala | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2318/3420 | 2253/2670 | 751/889 | chr19 | 616057 | ||
| chr19:616175
|
C | A | 1 | a0002c0036 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.2371C>A | p.Arg791Arg | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2436/3420 | 2371/2670 | 791/889 | chr19 | 616175 | ||
| chr19:616241
|
C | T | 1 | a0001c0077 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.2437C>T | p.Leu813Leu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2502/3420 | 2437/2670 | 813/889 | chr19 | 616241 | ||
| chr19:616429
|
G | T | 7 | a0001c0032a0001c0041a0001c0077others(4): Show | 10 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
synonymous_variant | LOW | c.2625G>T | p.Leu875Leu | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 2690/3420 | 2625/2670 | 875/889 | chr19 | 616429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:589922
|
C | T | 1 | a0001c0001t0027 | 1 | HG02293.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/8 | chr19 | 589922 | ||||||
| chr19:616509
|
G | A | 39 | a0001c0001t0002a0001c0003t0002a0001c0003t0007others(36): Show | 83 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*35G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 35 | chr19 | 616509 | |||||
| chr19:616671
|
C | T | 8 | a0001c0003t0007a0001c0003t0010a0001c0007t0007others(5): Show | 9 | HG00741.hp1 HG01515.hp1 HG01952.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*197C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 197 | chr19 | 616671 | |||||
| chr19:616688
|
G | A | 23 | a0001c0001t0009a0001c0002t0003a0001c0002t0009others(20): Show | 67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*214G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 214 | chr19 | 616688 | |||||
| chr19:616701
|
G | A | 27 | a0001c0001t0009a0001c0002t0003a0001c0002t0009others(24): Show | 71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*227G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 227 | chr19 | 616701 | |||||
| chr19:616722
|
G | A | 1 | a0001c0001t0021 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 248 | chr19 | 616722 | |||||
| chr19:616876
|
G | C | 1 | a0002c0004t0017 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 402 | chr19 | 616876 | |||||
| chr19:616932
|
C | T | 8 | a0001c0003t0006a0001c0006t0006a0001c0098t0006others(5): Show | 9 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*458C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 458 | chr19 | 616932 | |||||
| chr19:616973
|
C | T | 5 | a0001c0020t0008a0001c0034t0026a0001c0042t0008others(2): Show | 6 | HG02257.hp2 HG02572.hp1 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*499C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 499 | chr19 | 616973 | |||||
| chr19:616996
|
G | C | 6 | a0001c0018t0022a0001c0020t0008a0001c0034t0026others(3): Show | 7 | HG02257.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*522G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 522 | chr19 | 616996 | |||||
| chr19:616999
|
A | G | 121 | a0001c0001t0002a0001c0001t0004a0001c0001t0021others(118): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*525A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 525 | chr19 | 616999 | |||||
| chr19:617001
|
G | C | 1 | a0002c0021t0023 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 527 | chr19 | 617001 | |||||
| chr19:617014
|
C | G | 1 | a0001c0002t0019 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*540C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 540 | chr19 | 617014 | |||||
| chr19:617023
|
CG | C | 12 | a0001c0001t0021a0001c0015t0005a0001c0025t0005others(9): Show | 15 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*556delG | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 556 | INFO_REALIGN_3_PRIME | chr19 | 617023 | ||||
| chr19:617030
|
G | A | 1 | a0002c0005t0025 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 556 | chr19 | 617030 | |||||
| chr19:617036
|
G | A | 3 | a0001c0003t0010a0001c0009t0010a0001c0119t0010 | 3 | HG01952.hp1 HG02004.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*562G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 562 | chr19 | 617036 | |||||
| chr19:617042
|
C | T | 1 | a0001c0117t0015 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 568 | chr19 | 617042 | |||||
| chr19:617052
|
G | T | 1 | a0002c0019t0018 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 578 | chr19 | 617052 | |||||
| chr19:617069
|
G | A | 2 | a0001c0003t0016a0001c0014t0024 | 2 | HG02451.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*595G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 595 | chr19 | 617069 | |||||
| chr19:617070
|
C | T | 2 | a0001c0003t0016a0001c0014t0024 | 2 | HG02451.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*596C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 596 | chr19 | 617070 | |||||
| chr19:617095
|
GC | G | 5 | a0001c0014t0024a0001c0034t0026a0001c0091t0011others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*627delC | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 8/8 | 627 | INFO_REALIGN_3_PRIME | chr19 | 617095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:591072
|
G | C | 1 | a0001c0002t0003g0009 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.632+495G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591072 | ||||||
| chr19:591115
|
C | G | 1 | a0012c0081t0002g0398 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.632+538C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591115 | ||||||
| chr19:591115
|
C | T | 1 | a0001c0088t0002g0399 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.632+538C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591115 | ||||||
| chr19:591116
|
G | C | 1 | a0012c0081t0002g0398 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.632+539G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591116 | ||||||
| chr19:591126
|
C | G | 2 | a0001c0001t0002g0396a0001c0020t0004g0397 | 2 | HG02602.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.632+549C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591126 | ||||||
| chr19:591208
|
G | A | 18 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0004g0017others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.632+631G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591208 | ||||||
| chr19:591355
|
G | A | 58 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0055others(55): Show | 60 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.632+778G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591355 | ||||||
| chr19:591461
|
C | T | 8 | a0001c0001t0027g0390a0001c0009t0001g0388a0001c0009t0001g0395others(5): Show | 8 | HG01070.hp2 HG01928.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.632+884C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591461 | ||||||
| chr19:591610
|
T | G | 1 | a0001c0098t0006g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.632+1033T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591610 | ||||||
| chr19:591630
|
C | G | 1 | a0012c0081t0002g0398 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.632+1053C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591630 | ||||||
| chr19:591631
|
G | C | 1 | a0012c0081t0002g0398 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.632+1054G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591631 | ||||||
| chr19:591642
|
G | A | 173 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.632+1065G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591642 | ||||||
| chr19:591649
|
G | C | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+1072G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591649 | ||||||
| chr19:591651
|
C | G | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+1074C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591651 | ||||||
| chr19:591698
|
T | G | 27 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0004g0017others(24): Show | 29 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.632+1121T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591698 | ||||||
| chr19:591979
|
C | T | 1 | a0001c0098t0006g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.632+1402C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591979 | ||||||
| chr19:591983
|
G | A | 1 | a0001c0007t0001g0066 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.632+1406G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 591983 | ||||||
| chr19:592054
|
G | A | 16 | a0001c0001t0001g0238a0001c0001t0002g0237a0001c0001t0027g0390others(13): Show | 18 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.632+1477G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592054 | ||||||
| chr19:592106
|
C | T | 14 | a0001c0001t0027g0390a0001c0009t0001g0005a0001c0009t0001g0388others(11): Show | 16 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.632+1529C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592106 | ||||||
| chr19:592107
|
G | A | 1 | a0002c0072t0001g0243 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.632+1530G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592107 | ||||||
| chr19:592229
|
C | T | 21 | a0001c0001t0004g0387a0001c0003t0002g0372a0001c0003t0016g0384others(18): Show | 23 | HG01192.hp1 HG01884.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.632+1652C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592229 | ||||||
| chr19:592368
|
G | T | 1 | a0002c0019t0004g0368 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.632+1791G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592368 | ||||||
| chr19:592458
|
G | A | 1 | a0001c0006t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.632+1881G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592458 | ||||||
| chr19:592471
|
G | A | 1 | a0001c0003t0007g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.632+1894G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592471 | ||||||
| chr19:592559
|
C | A | 11 | a0001c0003t0002g0372a0001c0008t0004g0375a0001c0008t0012g0371others(8): Show | 13 | HG01192.hp1 HG02572.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.632+1982C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592559 | ||||||
| chr19:592595
|
A | T | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+2018A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592595 | ||||||
| chr19:592596
|
T | G | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+2019T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592596 | ||||||
| chr19:592636
|
G | A | 4 | a0001c0001t0004g0068a0001c0015t0005g0007a0001c0024t0003g0246others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+2059G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592636 | ||||||
| chr19:592926
|
C | T | 1 | a0001c0003t0007g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.632+2349C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 592926 | ||||||
| chr19:593018
|
A | G | 81 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(78): Show | 86 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.632+2441A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593018 | ||||||
| chr19:593140
|
C | T | 5 | a0001c0001t0004g0387a0001c0003t0016g0384a0001c0008t0004g0385others(2): Show | 5 | HG02451.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+2563C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593140 | ||||||
| chr19:593142
|
C | T | 79 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(76): Show | 84 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.632+2565C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593142 | ||||||
| chr19:593145
|
C | T | 1 | a0001c0006t0002g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.632+2568C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593145 | ||||||
| chr19:593156
|
A | G | 79 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(76): Show | 84 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.632+2579A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593156 | ||||||
| chr19:593197
|
C | T | 1 | a0002c0004t0007g0367 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.632+2620C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593197 | ||||||
| chr19:593227
|
C | T | 1 | a0001c0006t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.632+2650C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593227 | ||||||
| chr19:593275
|
G | A | 16 | a0001c0001t0001g0238a0001c0001t0002g0237a0001c0001t0027g0390others(13): Show | 18 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.632+2698G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593275 | ||||||
| chr19:593319
|
T | C | 92 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(89): Show | 99 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.632+2742T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593319 | ||||||
| chr19:593344
|
C | T | 1 | a0001c0117t0015g0063 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.632+2767C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593344 | ||||||
| chr19:593345
|
A | G | 92 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(89): Show | 99 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.632+2768A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593345 | ||||||
| chr19:593347
|
C | T | 92 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(89): Show | 99 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.632+2770C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593347 | ||||||
| chr19:593382
|
T | C | 275 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(272): Show | 283 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.632+2805T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593382 | ||||||
| chr19:593391
|
C | T | 3 | a0001c0001t0001g0226a0001c0002t0003g0225a0001c0022t0001g0227 | 3 | NA18962.hp1 NA19056.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.632+2814C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593391 | ||||||
| chr19:593428
|
C | T | 92 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(89): Show | 99 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.632+2851C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593428 | ||||||
| chr19:593464
|
G | A | 92 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(89): Show | 99 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.632+2887G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593464 | ||||||
| chr19:593484
|
G | A | 1 | a0001c0008t0002g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632+2907G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593484 | ||||||
| chr19:593488
|
C | T | 1 | a0001c0008t0007g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.632+2911C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593488 | ||||||
| chr19:593490
|
A | G | 92 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(89): Show | 99 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.632+2913A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593490 | ||||||
| chr19:593543
|
C | T | 1 | a0002c0012t0001g0366 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.632+2966C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593543 | ||||||
| chr19:593556
|
G | A | 27 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(24): Show | 27 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.632+2979G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593556 | ||||||
| chr19:593570
|
A | C | 2 | a0001c0033t0001g0233a0002c0011t0001g0365 | 2 | HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.632+2993A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593570 | ||||||
| chr19:593580
|
G | C | 72 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0055others(69): Show | 76 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.632+3003G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593580 | ||||||
| chr19:593589
|
C | G | 2 | a0002c0004t0004g0364a0002c0010t0001g0363 | 2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.632+3012C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593589 | ||||||
| chr19:593609
|
G | A | 181 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.632+3032G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593609 | ||||||
| chr19:593619
|
C | CA | 13 | a0001c0001t0004g0387a0001c0002t0003g0094a0001c0003t0016g0384others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.632+3051dupA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 593619 | |||||
| chr19:593638
|
G | A | 90 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(87): Show | 97 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.632+3061G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593638 | ||||||
| chr19:593668
|
C | A | 1 | a0002c0010t0001g0253 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.632+3091C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593668 | ||||||
| chr19:593734
|
G | A | 2 | a0001c0001t0002g0396a0001c0020t0004g0397 | 2 | HG02602.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.632+3157G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593734 | ||||||
| chr19:593749
|
T | C | 5 | a0001c0001t0004g0387a0001c0003t0016g0384a0001c0008t0004g0385others(2): Show | 5 | HG02451.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+3172T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593749 | ||||||
| chr19:593757
|
G | A | 89 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0025others(86): Show | 96 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.632+3180G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593757 | ||||||
| chr19:593829
|
C | T | 1 | a0002c0062t0004g0362 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.632+3252C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593829 | ||||||
| chr19:593853
|
G | A | 5 | a0001c0030t0004g0234a0001c0030t0004g0235a0004c0048t0001g0003others(2): Show | 7 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.632+3276G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593853 | ||||||
| chr19:593854
|
C | T | 3 | a0001c0015t0005g0007a0001c0024t0003g0246a0001c0031t0001g0245 | 4 | HG01167.hp1 HG01169.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.632+3277C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593854 | ||||||
| chr19:593889
|
C | G | 273 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(270): Show | 281 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.632+3312C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593889 | ||||||
| chr19:593906
|
G | C | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+3329G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593906 | ||||||
| chr19:593907
|
C | A | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+3330C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593907 | ||||||
| chr19:593979
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+3402C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593979 | ||||||
| chr19:593980
|
A | C | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+3403A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593980 | ||||||
| chr19:593981
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.632+3404G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593981 | ||||||
| chr19:593986
|
C | T | 5 | a0001c0003t0002g0219a0001c0003t0002g0223a0001c0007t0007g0222others(2): Show | 5 | HG00642.hp2 HG00741.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+3409C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 593986 | ||||||
| chr19:594031
|
C | T | 2 | a0002c0050t0002g0361a0002c0051t0011g0360 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.632+3454C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594031 | ||||||
| chr19:594032
|
G | T | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.632+3455G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594032 | ||||||
| chr19:594065
|
AGGGGCTG others(56): Show |
A | 2 | a0001c0076t0001g0029a0001c0079t0004g0028 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.632+3500_632+3562d others(65): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 594065 | |||||
| chr19:594077
|
T | C | 1 | a0001c0023t0004g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.632+3500T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594077 | ||||||
| chr19:594107
|
G | A | 1 | a0001c0030t0004g0378 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.632+3530G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594107 | ||||||
| chr19:594147
|
A | G | 5 | a0001c0034t0026g0061a0001c0115t0004g0062a0002c0012t0001g0359others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+3570A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594147 | ||||||
| chr19:594180
|
G | A | 1 | a0002c0058t0012g0254 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.632+3603G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594180 | ||||||
| chr19:594218
|
CGGTG | C | 229 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.632+3642_632+3645d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594218 | ||||||
| chr19:594230
|
G | T | 1 | a0001c0006t0002g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.632+3653G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594230 | ||||||
| chr19:594272
|
C | G | 2 | a0001c0002t0003g0094a0001c0006t0002g0244 | 2 | HG02976.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.632+3695C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594272 | ||||||
| chr19:594272
|
C | T | 145 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.632+3695C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594272 | ||||||
| chr19:594283
|
C | T | 2 | a0002c0004t0002g0355a0009c0061t0001g0356 | 2 | HG02080.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.632+3706C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594283 | ||||||
| chr19:594327
|
A | T | 1 | a0001c0020t0004g0397 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.632+3750A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594327 | ||||||
| chr19:594382
|
GC | G | 10 | a0001c0003t0002g0372a0001c0008t0004g0375a0001c0008t0012g0371others(7): Show | 12 | HG01192.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.632+3807delC | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 594382 | |||||
| chr19:594393
|
G | A | 2 | a0001c0001t0002g0396a0001c0020t0004g0397 | 2 | HG02602.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.632+3816G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594393 | ||||||
| chr19:594533
|
G | A | 1 | a0001c0006t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.632+3956G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594533 | ||||||
| chr19:594583
|
G | A | 1 | a0001c0020t0008g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.632+4006G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594583 | ||||||
| chr19:594599
|
T | C | 255 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.632+4022T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594599 | ||||||
| chr19:594607
|
C | T | 1 | a0001c0001t0021g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.632+4030C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594607 | ||||||
| chr19:594621
|
G | C | 5 | a0001c0006t0002g0027a0001c0006t0002g0244a0001c0008t0001g0026others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+4044G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594621 | ||||||
| chr19:594643
|
G | A | 1 | a0001c0002t0003g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.632+4066G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594643 | ||||||
| chr19:594736
|
G | A | 6 | a0001c0001t0002g0016a0001c0003t0004g0012a0001c0020t0008g0010others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.632+4159G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594736 | ||||||
| chr19:594809
|
G | A | 3 | a0002c0004t0017g0259a0002c0005t0003g0258a0002c0057t0002g0260 | 3 | HG00280.hp2 HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.632+4232G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594809 | ||||||
| chr19:594937
|
A | T | 3 | a0001c0001t0002g0016a0002c0004t0004g0364a0002c0010t0001g0363 | 3 | HG02559.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.632+4360A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594937 | ||||||
| chr19:594952
|
G | C | 1 | a0001c0006t0002g0073 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.632+4375G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594952 | ||||||
| chr19:594954
|
A | C | 240 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.632+4377A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594954 | ||||||
| chr19:594965
|
C | T | 5 | a0001c0003t0004g0012a0001c0020t0008g0010a0001c0020t0008g0013others(2): Show | 5 | HG01891.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+4388C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594965 | ||||||
| chr19:594966
|
G | A | 2 | a0001c0023t0001g0370a0001c0094t0001g0369 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.632+4389G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 594966 | ||||||
| chr19:595071
|
G | A | 3 | a0001c0006t0006g0249a0001c0008t0002g0379a0001c0014t0024g0248 | 3 | HG01891.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.632+4494G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595071 | ||||||
| chr19:595137
|
G | GGCTGCAG others(17): Show |
1 | a0001c0023t0004g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.632+4561_632+4584d others(26): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 595137 | |||||
| chr19:595226
|
C | G | 5 | a0001c0006t0001g0213a0001c0006t0001g0214a0001c0006t0002g0216others(2): Show | 5 | HG01069.hp1 NA18962.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+4649C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595226 | ||||||
| chr19:595294
|
C | G | 5 | a0001c0001t0002g0091a0001c0002t0003g0093a0001c0002t0004g0092others(2): Show | 5 | HG02074.hp1 HG03927.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+4717C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595294 | ||||||
| chr19:595319
|
C | T | 1 | a0001c0003t0002g0210 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.632+4742C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595319 | ||||||
| chr19:595320
|
G | A | 1 | a0002c0012t0004g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.632+4743G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595320 | ||||||
| chr19:595358
|
C | G | 2 | a0001c0023t0004g0247a0001c0042t0008g0112 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.632+4781C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595358 | ||||||
| chr19:595401
|
C | G | 1 | a0002c0074t0002g0350 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.632+4824C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595401 | ||||||
| chr19:595409
|
C | G | 5 | a0001c0001t0004g0387a0001c0008t0004g0385a0001c0030t0004g0378others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+4832C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595409 | ||||||
| chr19:595516
|
C | T | 1 | a0001c0044t0001g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.632+4939C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595516 | ||||||
| chr19:595560
|
T | C | 103 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(100): Show | 104 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.632+4983T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595560 | ||||||
| chr19:595588
|
G | A | 1 | a0002c0012t0013g0265 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.632+5011G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595588 | ||||||
| chr19:595652
|
G | A | 1 | a0001c0006t0002g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.632+5075G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595652 | ||||||
| chr19:595663
|
G | A | 2 | a0001c0003t0001g0170a0001c0100t0003g0171 | 2 | NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.632+5086G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595663 | ||||||
| chr19:595719
|
G | C | 6 | a0001c0002t0009g0116a0001c0006t0001g0213a0001c0006t0001g0214others(3): Show | 6 | HG00423.hp2 HG01069.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.632+5142G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595719 | ||||||
| chr19:595812
|
C | G | 3 | a0001c0022t0001g0242a0002c0035t0005g0349a0004c0048t0001g0003 | 4 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.632+5235C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595812 | ||||||
| chr19:595827
|
C | T | 2 | a0002c0004t0001g0347a0002c0005t0003g0348 | 2 | NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.632+5250C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595827 | ||||||
| chr19:595828
|
G | A | 4 | a0001c0008t0001g0022a0001c0008t0012g0371a0001c0032t0004g0100others(1): Show | 4 | HG02055.hp2 HG03130.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.632+5251G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595828 | ||||||
| chr19:595833
|
G | A | 1 | a0001c0096t0003g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.632+5256G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595833 | ||||||
| chr19:595905
|
C | T | 2 | a0001c0082t0004g0208a0004c0121t0004g0236 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.632+5328C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595905 | ||||||
| chr19:595933
|
C | T | 1 | a0002c0012t0002g0346 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.632+5356C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595933 | ||||||
| chr19:595970
|
C | T | 1 | a0002c0012t0004g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.632+5393C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 595970 | ||||||
| chr19:596017
|
C | G | 1 | a0002c0012t0001g0345 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.632+5440C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596017 | ||||||
| chr19:596095
|
G | A | 18 | a0001c0001t0002g0077a0001c0001t0004g0172a0001c0002t0003g0098others(15): Show | 18 | HG00597.hp2 HG00609.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.632+5518G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596095 | ||||||
| chr19:596171
|
G | A | 8 | a0001c0001t0001g0081a0001c0001t0002g0065a0001c0002t0003g0078others(5): Show | 8 | HG02738.hp2 HG03017.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.632+5594G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596171 | ||||||
| chr19:596179
|
C | G | 5 | a0001c0006t0002g0244a0001c0020t0004g0397a0001c0030t0004g0378others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+5602C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596179 | ||||||
| chr19:596385
|
C | T | 1 | a0001c0101t0008g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.632+5808C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596385 | ||||||
| chr19:596418
|
G | A | 22 | a0001c0001t0002g0396a0001c0009t0001g0005a0001c0009t0001g0218others(19): Show | 23 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.632+5841G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596418 | ||||||
| chr19:596420
|
T | C | 326 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(323): Show | 332 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.632+5843T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596420 | ||||||
| chr19:596447
|
C | T | 1 | a0002c0004t0001g0316 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.632+5870C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596447 | ||||||
| chr19:596452
|
G | A | 1 | a0001c0008t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.632+5875G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596452 | ||||||
| chr19:596506
|
C | A | 1 | a0001c0091t0011g0380 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.632+5929C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596506 | ||||||
| chr19:596512
|
G | A | 1 | a0002c0051t0011g0360 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.632+5935G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596512 | ||||||
| chr19:596584
|
A | T | 1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.632+6007A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596584 | ||||||
| chr19:596663
|
G | C | 1 | a0001c0024t0003g0177 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.632+6086G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596663 | ||||||
| chr19:596891
|
AGGAGAGG others(8): Show |
A | 28 | a0001c0001t0027g0390a0001c0003t0004g0012a0001c0009t0001g0005others(25): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.632+6331_632+6345d others(17): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 596891 | |||||
| chr19:596942
|
G | A | 2 | a0002c0004t0001g0316a0002c0004t0004g0275 | 2 | NA18952.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.632+6365G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596942 | ||||||
| chr19:596962
|
C | A | 1 | a0001c0023t0004g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.632+6385C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 596962 | ||||||
| chr19:597021
|
C | G | 2 | a0002c0005t0003g0344a0002c0012t0001g0264 | 2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.632+6444C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597021 | ||||||
| chr19:597030
|
C | A | 1 | a0002c0005t0003g0276 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.632+6453C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597030 | ||||||
| chr19:597047
|
G | T | 1 | a0001c0002t0003g0093 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.632+6470G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597047 | ||||||
| chr19:597077
|
G | A | 1 | a0001c0002t0003g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.633-6467G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597077 | ||||||
| chr19:597240
|
G | A | 1 | a0002c0010t0002g0319 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.633-6304G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597240 | ||||||
| chr19:597444
|
G | A | 4 | a0001c0003t0004g0012a0001c0020t0008g0010a0001c0020t0008g0013others(1): Show | 4 | HG01891.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-6100G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597444 | ||||||
| chr19:597473
|
GGTGGTTT others(155): Show |
G | 3 | a0001c0078t0008g0031a0002c0012t0004g0256a0002c0064t0001g0324 | 3 | HG01884.hp1 HG02922.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.633-5982_633-5821d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 597473 | |||||
| chr19:597493
|
G | C | 1 | a0001c0018t0022g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633-6051G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597493 | ||||||
| chr19:597498
|
T | C | 2 | a0002c0011t0001g0277a0002c0011t0001g0278 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.633-6046T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597498 | ||||||
| chr19:597562
|
G | C | 317 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(314): Show | 324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.633-5982G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597562 | ||||||
| chr19:597571
|
C | T | 251 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.633-5973C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597571 | ||||||
| chr19:597576
|
C | CGGTTTCT others(13): Show |
3 | a0001c0001t0004g0387a0001c0008t0004g0385a0016c0080t0004g0386 | 3 | HG02809.hp2 HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.633-5954_633-5935d others(22): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 597576 | |||||
| chr19:597589
|
C | T | 3 | a0001c0003t0001g0170a0001c0039t0001g0202a0001c0100t0003g0171 | 3 | NA18970.hp1 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.633-5955C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597589 | ||||||
| chr19:597614
|
T | C | 1 | a0002c0012t0002g0346 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.633-5930T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597614 | ||||||
| chr19:597630
|
C | T | 1 | a0001c0046t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.633-5914C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597630 | ||||||
| chr19:597635
|
C | G | 307 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(304): Show | 314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.633-5909C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597635 | ||||||
| chr19:597711
|
TTCCTGGT others(13): Show |
T | 34 | a0001c0001t0027g0390a0001c0003t0002g0372a0001c0003t0004g0012others(31): Show | 36 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-5792_633-5773d others(22): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 597711 | |||||
| chr19:597771
|
C | T | 8 | a0001c0001t0001g0178a0001c0006t0006g0249a0001c0014t0024g0248others(5): Show | 9 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.633-5773C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597771 | ||||||
| chr19:597772
|
C | T | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633-5772C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597772 | ||||||
| chr19:597790
|
C | T | 260 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(257): Show | 262 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.633-5754C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597790 | ||||||
| chr19:597793
|
T | C | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633-5751T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597793 | ||||||
| chr19:597795
|
C | T | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633-5749C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597795 | ||||||
| chr19:597879
|
C | T | 3 | a0001c0003t0016g0384a0001c0018t0020g0058a0001c0025t0004g0059 | 3 | HG01978.hp2 HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.633-5665C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597879 | ||||||
| chr19:597937
|
T | C | 9 | a0001c0008t0004g0375a0001c0015t0001g0373a0001c0017t0001g0001others(6): Show | 11 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.633-5607T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597937 | ||||||
| chr19:597941
|
G | C | 1 | a0001c0008t0004g0385 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.633-5603G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597941 | ||||||
| chr19:597941
|
GGGGGAGG others(6): Show |
G | 9 | a0001c0008t0004g0375a0001c0015t0001g0373a0001c0017t0001g0001others(6): Show | 11 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.633-5600_633-5588d others(15): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 597941 | |||||
| chr19:597957
|
C | T | 7 | a0001c0001t0001g0178a0001c0006t0006g0249a0001c0014t0024g0248others(4): Show | 8 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-5587C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 597957 | ||||||
| chr19:598072
|
C | A | 5 | a0001c0006t0002g0027a0001c0008t0007g0004a0001c0014t0003g0095others(2): Show | 6 | HG00621.hp2 HG02129.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-5472C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598072 | ||||||
| chr19:598079
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.633-5465G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598079 | ||||||
| chr19:598358
|
G | A | 2 | a0002c0021t0001g0320a0006c0047t0003g0002 | 3 | HG01070.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.633-5186G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598358 | ||||||
| chr19:598391
|
C | T | 1 | a0001c0009t0001g0218 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.633-5153C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598391 | ||||||
| chr19:598405
|
C | T | 1 | a0002c0021t0001g0320 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.633-5139C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598405 | ||||||
| chr19:598463
|
C | T | 1 | a0002c0050t0002g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.633-5081C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598463 | ||||||
| chr19:598610
|
C | T | 1 | a0001c0022t0001g0227 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.633-4934C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598610 | ||||||
| chr19:598738
|
C | A | 51 | a0001c0001t0001g0178a0001c0001t0027g0390a0001c0003t0016g0384others(48): Show | 57 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.633-4806C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598738 | ||||||
| chr19:598751
|
G | A | 4 | a0001c0006t0002g0027a0001c0008t0007g0004a0001c0014t0003g0095others(1): Show | 5 | HG00621.hp2 HG02129.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-4793G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598751 | ||||||
| chr19:598798
|
CGG | C | 9 | a0001c0003t0002g0372a0001c0003t0004g0012a0001c0020t0004g0030others(6): Show | 9 | HG01192.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.633-4743_633-4742d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 598798 | |||||
| chr19:598859
|
C | T | 1 | a0001c0003t0016g0384 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.633-4685C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 598859 | ||||||
| chr19:599029
|
G | C | 2 | a0001c0006t0002g0244a0001c0078t0008g0031 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.633-4515G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599029 | ||||||
| chr19:599102
|
C | T | 7 | a0001c0001t0001g0178a0001c0006t0006g0249a0001c0014t0024g0248others(4): Show | 8 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.633-4442C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599102 | ||||||
| chr19:599294
|
C | T | 1 | a0001c0117t0015g0063 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.633-4250C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599294 | ||||||
| chr19:599309
|
C | T | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.633-4235C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599309 | ||||||
| chr19:599319
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.633-4225C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599319 | ||||||
| chr19:599321
|
G | T | 1 | a0002c0035t0005g0343 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.633-4223G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599321 | ||||||
| chr19:599414
|
CAGCATCT others(8): Show |
C | 1 | a0001c0001t0001g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.633-4127_633-4113d others(17): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599414 | |||||
| chr19:599505
|
C | T | 1 | a0001c0024t0003g0246 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.633-4039C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599505 | ||||||
| chr19:599528
|
C | G | 1 | a0001c0003t0007g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.633-4016C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599528 | ||||||
| chr19:599590
|
T | C | 4 | a0001c0006t0002g0027a0001c0008t0007g0004a0001c0014t0003g0095others(1): Show | 5 | HG00621.hp2 HG02129.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-3954T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599590 | ||||||
| chr19:599595
|
T | C | 1 | a0001c0003t0002g0205 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.633-3949T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599595 | ||||||
| chr19:599609
|
C | T | 2 | a0001c0082t0004g0208a0001c0118t0011g0060 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.633-3935C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599609 | ||||||
| chr19:599623
|
C | CA | 22 | a0001c0001t0001g0178a0001c0001t0002g0055a0001c0001t0002g0091others(19): Show | 23 | HG00673.hp1 HG00735.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.633-3906dupA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599623 | |||||
| chr19:599660
|
C | T | 3 | a0001c0001t0001g0085a0001c0007t0001g0089a0001c0107t0001g0054 | 3 | NA18954.hp1 NA18969.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.633-3884C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599660 | ||||||
| chr19:599665
|
A | G | 1 | a0002c0004t0006g0353 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.633-3879A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599665 | ||||||
| chr19:599687
|
G | C | 325 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(322): Show | 332 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.633-3857G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599687 | ||||||
| chr19:599688
|
T | C | 1 | a0001c0008t0002g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.633-3856T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599688 | ||||||
| chr19:599710
|
C | A | 206 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(203): Show | 209 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.633-3834C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599710 | ||||||
| chr19:599742
|
T | C | 93 | a0001c0001t0001g0178a0001c0001t0002g0396a0001c0001t0004g0229others(90): Show | 98 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.633-3802T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599742 | ||||||
| chr19:599804
|
A | G | 1 | a0001c0032t0004g0381 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.633-3740A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599804 | ||||||
| chr19:599847
|
C | CGT | 20 | a0001c0015t0005g0007a0001c0018t0002g0053a0001c0023t0001g0370others(17): Show | 21 | HG00280.hp2 HG00673.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.633-3648_633-3647d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
C | CGTGT | 15 | a0001c0001t0004g0168a0001c0001t0021g0217a0001c0006t0002g0244others(12): Show | 15 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.633-3650_633-3647d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
C | CGTGTGT | 14 | a0001c0006t0006g0249a0001c0017t0004g0023a0001c0018t0001g0040others(11): Show | 14 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.633-3652_633-3647d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
C | CGTGTGTG others(3): Show |
6 | a0001c0024t0003g0246a0002c0004t0001g0299a0002c0004t0001g0342others(3): Show | 6 | HG00280.hp1 HG01168.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.633-3656_633-3647d others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
C | CGTGTGTG others(5): Show |
1 | a0001c0113t0006g0042 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.633-3658_633-3647d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGT | C | 32 | a0001c0001t0002g0169a0001c0001t0002g0237a0001c0002t0003g0224others(29): Show | 32 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.633-3648_633-3647d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGT | C | 31 | a0001c0001t0001g0178a0001c0001t0002g0016a0001c0003t0002g0372others(28): Show | 34 | HG00621.hp2 HG01074.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.633-3650_633-3647d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGT | C | 27 | a0001c0001t0002g0055a0001c0001t0004g0017a0001c0001t0004g0068others(24): Show | 28 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.633-3652_633-3647d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGTG others(1): Show |
C | 11 | a0001c0003t0016g0384a0001c0008t0004g0385a0001c0009t0001g0218others(8): Show | 11 | HG01070.hp2 HG01928.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-3654_633-3647d others(10): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGTG others(3): Show |
C | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0199others(6): Show | 9 | HG01074.hp1 HG01257.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.633-3656_633-3647d others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGTG others(5): Show |
C | 20 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0158others(17): Show | 20 | HG01099.hp1 HG01123.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.633-3658_633-3647d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGTG others(6): Show |
C | 1 | a0001c0001t0001g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.633-3696_633-3684d others(15): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599847 | ||||||
| chr19:599847
|
CGTGTGTG others(7): Show |
C | 150 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0134others(147): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.633-3660_633-3647d others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0002g0065a0001c0003t0002g0232 | 2 | NA18950.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.633-3662_633-3647d others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0002g0396 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.633-3664_633-3647d others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599847
|
CGTGTGTG others(15): Show |
C | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.633-3668_633-3647d others(24): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 599847 | |||||
| chr19:599861
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.633-3683T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599861 | ||||||
| chr19:599920
|
G | A | 1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.633-3624G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599920 | ||||||
| chr19:599938
|
GGCTCAAG others(4): Show |
G | 6 | a0001c0001t0001g0178a0001c0022t0001g0242a0001c0082t0004g0208others(3): Show | 7 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.633-3605_633-3595d others(13): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 599938 | ||||||
| chr19:600103
|
G | A | 4 | a0002c0004t0001g0327a0002c0004t0002g0328a0002c0004t0002g0329others(1): Show | 4 | NA18982.hp1 NA19063.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-3441G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600103 | ||||||
| chr19:600153
|
G | C | 1 | a0001c0026t0002g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.633-3391G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600153 | ||||||
| chr19:600217
|
G | A | 1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.633-3327G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600217 | ||||||
| chr19:600241
|
C | CG | 3 | a0001c0018t0002g0052a0001c0026t0004g0051a0001c0076t0001g0029 | 3 | HG02451.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.633-3301dupG | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 600241 | |||||
| chr19:600246
|
C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0077a0001c0001t0004g0017others(36): Show | 39 | HG00423.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.633-3298C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600246 | ||||||
| chr19:600264
|
C | T | 46 | a0001c0001t0002g0016a0001c0001t0002g0077a0001c0001t0004g0017others(43): Show | 48 | HG00423.hp1 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.633-3280C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600264 | ||||||
| chr19:600271
|
C | G | 1 | a0002c0005t0003g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.633-3273C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600271 | ||||||
| chr19:600507
|
A | AT | 7 | a0001c0001t0001g0081a0001c0003t0001g0087a0001c0003t0002g0203others(4): Show | 7 | HG00544.hp1 HG02027.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.633-3026dupT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 600507 | |||||
| chr19:600573
|
T | C | 58 | a0001c0001t0002g0055a0001c0001t0002g0077a0001c0001t0004g0017others(55): Show | 60 | HG00609.hp1 HG00639.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.633-2971T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600573 | ||||||
| chr19:600628
|
A | C | 7 | a0001c0008t0002g0379a0001c0026t0002g0057a0001c0030t0004g0378others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.633-2916A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600628 | ||||||
| chr19:600669
|
C | T | 15 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0003t0001g0018others(12): Show | 15 | HG01978.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.633-2875C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600669 | ||||||
| chr19:600670
|
G | T | 4 | a0001c0001t0001g0178a0001c0022t0001g0242a0002c0035t0005g0349others(1): Show | 5 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-2874G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600670 | ||||||
| chr19:600675
|
T | G | 1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.633-2869T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600675 | ||||||
| chr19:600760
|
C | T | 12 | a0001c0003t0004g0012a0001c0008t0004g0385a0001c0020t0004g0030others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.633-2784C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600760 | ||||||
| chr19:600769
|
C | G | 83 | a0001c0001t0001g0188a0001c0001t0004g0017a0001c0003t0001g0087others(80): Show | 84 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.633-2775C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600769 | ||||||
| chr19:600799
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.633-2745G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600799 | ||||||
| chr19:600806
|
A | C | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.633-2738A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600806 | ||||||
| chr19:600868
|
G | A | 1 | a0001c0023t0001g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.633-2676G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600868 | ||||||
| chr19:600877
|
A | T | 2 | a0001c0001t0004g0229a0001c0001t0004g0387 | 2 | HG01243.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.633-2667A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600877 | ||||||
| chr19:600928
|
C | T | 1 | a0001c0023t0001g0125 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.633-2616C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600928 | ||||||
| chr19:600962
|
C | T | 2 | a0001c0018t0002g0052a0001c0076t0001g0029 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.633-2582C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600962 | ||||||
| chr19:600967
|
C | T | 3 | a0001c0009t0001g0005a0002c0074t0002g0350a0018c0120t0002g0160 | 4 | HG01069.hp2 HG01071.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-2577C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 600967 | ||||||
| chr19:601036
|
C | T | 4 | a0001c0003t0004g0012a0001c0020t0008g0010a0001c0020t0008g0013others(1): Show | 4 | HG01891.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-2508C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601036 | ||||||
| chr19:601056
|
G | T | 97 | a0001c0001t0001g0178a0001c0001t0002g0016a0001c0001t0002g0077others(94): Show | 103 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.633-2488G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601056 | ||||||
| chr19:601078
|
G | T | 9 | a0001c0003t0004g0012a0001c0020t0004g0030a0001c0020t0004g0397others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.633-2466G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601078 | ||||||
| chr19:601108
|
T | C | 2 | a0001c0008t0012g0371a0001c0032t0004g0100 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.633-2436T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601108 | ||||||
| chr19:601227
|
C | T | 1 | a0001c0001t0004g0387 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.633-2317C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601227 | ||||||
| chr19:601240
|
G | C | 6 | a0001c0006t0002g0027a0001c0014t0003g0095a0001c0014t0003g0096others(3): Show | 6 | HG00621.hp2 HG02129.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.633-2304G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601240 | ||||||
| chr19:601314
|
G | GA | 5 | a0001c0002t0003g0225a0001c0006t0004g0072a0001c0008t0001g0026others(2): Show | 5 | HG02055.hp1 HG02738.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-2221dupA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 601314 | |||||
| chr19:601373
|
G | A | 101 | a0001c0001t0001g0178a0001c0001t0002g0016a0001c0001t0002g0077others(98): Show | 105 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.633-2171G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601373 | ||||||
| chr19:601420
|
C | A | 4 | a0001c0001t0001g0178a0001c0022t0001g0242a0002c0035t0005g0349others(1): Show | 5 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-2124C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601420 | ||||||
| chr19:601514
|
G | A | 1 | a0001c0003t0001g0170 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.633-2030G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601514 | ||||||
| chr19:601526
|
G | GTGGTCA | 33 | a0001c0008t0004g0375a0001c0009t0001g0005a0001c0009t0001g0069others(30): Show | 37 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-2013_633-2012i others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 601526 | |||||
| chr19:601531
|
C | T | 4 | a0003c0029t0002g0103a0003c0029t0002g0105a0003c0029t0004g0104others(1): Show | 4 | HG02145.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-2013C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601531 | ||||||
| chr19:601534
|
C | T | 1 | a0001c0020t0004g0397 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.633-2010C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601534 | ||||||
| chr19:601538
|
C | T | 2 | a0001c0076t0001g0029a0001c0078t0008g0031 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.633-2006C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601538 | ||||||
| chr19:601572
|
TGTCGTCC others(34): Show |
T | 1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.633-1968_633-1928d others(43): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 601572 | |||||
| chr19:601614
|
G | A | 1 | a0001c0003t0002g0372 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.633-1930G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601614 | ||||||
| chr19:601617
|
C | T | 1 | a0002c0073t0001g0291 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.633-1927C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601617 | ||||||
| chr19:601646
|
T | C | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633-1898T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601646 | ||||||
| chr19:601708
|
G | A | 2 | a0001c0006t0006g0249a0001c0014t0024g0248 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.633-1836G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601708 | ||||||
| chr19:601739
|
G | A | 1 | a0001c0002t0003g0132 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.633-1805G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601739 | ||||||
| chr19:601813
|
C | A | 18 | a0001c0008t0002g0379a0001c0008t0004g0375a0001c0015t0001g0373others(15): Show | 20 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.633-1731C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601813 | ||||||
| chr19:601835
|
G | A | 1 | a0001c0001t0004g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.633-1709G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601835 | ||||||
| chr19:601848
|
C | T | 1 | a0001c0026t0004g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.633-1696C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601848 | ||||||
| chr19:601919
|
C | T | 1 | a0001c0009t0001g0395 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.633-1625C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 601919 | ||||||
| chr19:602044
|
G | A | 1 | a0002c0073t0001g0291 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.633-1500G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602044 | ||||||
| chr19:602052
|
C | T | 4 | a0001c0002t0003g0127a0001c0024t0003g0167a0001c0096t0003g0117others(1): Show | 4 | HG00733.hp2 HG01074.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-1492C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602052 | ||||||
| chr19:602072
|
C | CCCTCCTG others(214): Show |
2 | a0001c0018t0001g0040a0001c0114t0004g0041 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.633-1465_633-1464i others(223): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602072 | |||||
| chr19:602072
|
C | CCCTCCTG others(191): Show |
1 | a0002c0010t0001g0290 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.633-1426_633-1425i others(200): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602072 | |||||
| chr19:602072
|
CCCTCCTG others(59): Show |
C | 1 | a0001c0003t0001g0170 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.633-1464_633-1399d others(68): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602072 | |||||
| chr19:602073
|
C | CCTCCTGC others(331): Show |
1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.633-1465_633-1464i others(340): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602073 | |||||
| chr19:602080
|
T | C | 73 | a0001c0001t0001g0188a0001c0001t0004g0017a0001c0002t0003g0078others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.633-1464T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602080 | ||||||
| chr19:602094
|
T | TTCCTCCT others(247): Show |
2 | a0005c0043t0006g0108a0005c0043t0006g0109 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.633-1444_633-1443i others(256): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602094 | |||||
| chr19:602095
|
T | TCCTCCTC others(21): Show |
60 | a0001c0001t0001g0188a0001c0001t0004g0017a0001c0002t0003g0078others(57): Show | 61 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.633-1444_633-1443i others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602095 | |||||
| chr19:602095
|
T | TCCTCCTC others(54): Show |
1 | a0015c0086t0005g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.633-1444_633-1443i others(63): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602095 | |||||
| chr19:602095
|
T | TCCTCCTC others(529): Show |
1 | a0001c0101t0008g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.633-1444_633-1443i others(538): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602095 | |||||
| chr19:602095
|
T | TCCTCCTC others(115): Show |
1 | a0001c0003t0010g0196 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.633-1444_633-1443i others(124): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602095 | |||||
| chr19:602100
|
CCCTCT | C | 5 | a0001c0003t0001g0180a0001c0003t0002g0210a0001c0099t0004g0377others(2): Show | 5 | HG00544.hp2 HG02080.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-1439_633-1435d others(7): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602100 | |||||
| chr19:602101
|
C | CCTCTCCT others(468): Show |
3 | a0001c0001t0004g0229a0001c0008t0012g0371a0001c0032t0004g0100 | 3 | HG01243.hp2 HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.633-1323_633-1322i others(477): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602101 | |||||
| chr19:602101
|
C | CCTCTCCT others(506): Show |
1 | a0001c0006t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.633-1417_633-1416i others(515): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602101 | |||||
| chr19:602101
|
C | T | 66 | a0001c0001t0001g0188a0001c0001t0004g0017a0001c0002t0003g0078others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.633-1443C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602101 | ||||||
| chr19:602106
|
C | CCTCCTGC others(252): Show |
4 | a0001c0001t0001g0238a0002c0004t0001g0316a0002c0005t0003g0348others(1): Show | 4 | HG02083.hp1 HG02155.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-1384_633-1383i others(261): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602106 | |||||
| chr19:602106
|
C | CCTCCTGC others(252): Show |
1 | a0001c0001t0002g0237 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.633-1384_633-1383i others(261): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602106 | |||||
| chr19:602106
|
C | T | 5 | a0001c0003t0001g0180a0001c0003t0002g0210a0001c0099t0004g0377others(2): Show | 5 | HG00544.hp2 HG02080.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-1438C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602106 | ||||||
| chr19:602119
|
C | T | 55 | a0001c0001t0002g0016a0001c0001t0002g0077a0001c0001t0004g0068others(52): Show | 56 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.633-1425C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602119 | ||||||
| chr19:602128
|
C | T | 1 | a0001c0091t0011g0380 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633-1416C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602128 | ||||||
| chr19:602139
|
C | CCTCCTGC others(21): Show |
1 | a0001c0001t0002g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.633-1383_633-1356d others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602139 | |||||
| chr19:602161
|
T | C | 11 | a0001c0003t0001g0180a0001c0003t0002g0210a0001c0015t0001g0011others(8): Show | 11 | HG00099.hp1 HG00544.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.633-1383T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602161 | ||||||
| chr19:602167
|
T | TCTCCTGC others(26): Show |
3 | a0001c0001t0001g0188a0001c0003t0001g0230a0001c0003t0001g0231 | 3 | HG00597.hp2 HG03688.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.633-1223_633-1191d others(35): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(224): Show |
1 | a0002c0005t0003g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.633-1191_633-1190i others(233): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(445): Show |
1 | a0001c0006t0004g0072 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.633-1191_633-1190i others(454): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(252): Show |
2 | a0001c0109t0001g0034a0001c0111t0001g0033 | 2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.633-1130_633-1129i others(261): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(252): Show |
2 | a0001c0025t0001g0036a0001c0034t0005g0035 | 2 | HG02148.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.633-1355_633-1097d others(261): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(153): Show |
1 | a0001c0003t0001g0018 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.633-1257_633-1256i others(162): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(219): Show |
2 | a0001c0018t0020g0058a0002c0010t0001g0363 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.633-1257_633-1256i others(228): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(544): Show |
1 | a0002c0004t0004g0364 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.633-1290_633-1289i others(553): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(714): Show |
1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633-1290_633-1289i others(723): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(120): Show |
3 | a0001c0018t0002g0053a0001c0041t0001g0099a0001c0115t0004g0062 | 3 | HG02486.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.633-1323_633-1322i others(129): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCCTGC others(407): Show |
1 | a0001c0026t0002g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.633-1323_633-1322i others(416): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCTC | 11 | a0001c0003t0001g0180a0001c0003t0002g0210a0001c0006t0002g0107others(8): Show | 11 | HG00099.hp1 HG00544.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.633-1374_633-1373i others(7): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
T | TCTCTCCT others(780): Show |
1 | a0001c0015t0001g0011 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.633-1374_633-1373i others(789): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602167
|
TCTCCTGC others(59): Show |
T | 1 | a0001c0020t0004g0397 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.633-1256_633-1191d others(68): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602167 | |||||
| chr19:602189
|
C | CCCTCCTC others(892): Show |
1 | a0001c0006t0006g0249 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.633-1298_633-1297i others(901): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602189 | |||||
| chr19:602189
|
C | CCCTCCTC others(219): Show |
3 | a0001c0001t0021g0217a0002c0004t0001g0299a0010c0069t0001g0307 | 3 | HG00099.hp2 HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.633-1322_633-1097d others(228): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602189 | |||||
| chr19:602189
|
C | CCCTCCTC others(216): Show |
1 | a0002c0004t0001g0342 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.633-1149_633-1148i others(225): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602189 | |||||
| chr19:602189
|
C | CCCTCCTC others(351): Show |
1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.633-1290_633-1289i others(360): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602189 | |||||
| chr19:602189
|
C | CCCTCCTC others(313): Show |
1 | a0001c0001t0027g0390 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.633-1290_633-1289i others(322): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602189 | |||||
| chr19:602189
|
C | T | 7 | a0001c0002t0003g0078a0001c0003t0001g0180a0001c0003t0002g0210others(4): Show | 7 | HG00544.hp2 HG02080.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.633-1355C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602189 | ||||||
| chr19:602195
|
TCTCTC | T | 5 | a0001c0003t0001g0180a0001c0003t0002g0210a0001c0099t0004g0377others(2): Show | 5 | HG00544.hp2 HG02080.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-1345_633-1341d others(7): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602195 | |||||
| chr19:602200
|
C | CCTCCTGC others(186): Show |
1 | a0001c0013t0001g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.633-1191_633-1190i others(195): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602200 | |||||
| chr19:602200
|
C | CCTCCTGC others(572): Show |
1 | a0002c0028t0005g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.633-1163_633-1162i others(581): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602200 | |||||
| chr19:602200
|
C | CCTCCTGC others(374): Show |
1 | a0001c0001t0002g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.633-1290_633-1289i others(383): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602200 | |||||
| chr19:602200
|
C | CCTCCTGC others(21): Show |
1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.633-1323_633-1322i others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602200 | |||||
| chr19:602200
|
C | CCTCCTGC others(351): Show |
1 | a0001c0001t0001g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.633-1326_633-1325i others(360): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602200 | |||||
| chr19:602221
|
T | C | 2 | a0005c0043t0006g0108a0005c0043t0006g0109 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.633-1323T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602221 | ||||||
| chr19:602222
|
C | CCCTCCTC others(704): Show |
1 | a0001c0020t0008g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.633-1097_633-1096i others(713): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602222 | |||||
| chr19:602222
|
C | CCCTCCTC others(671): Show |
2 | a0001c0003t0004g0012a0001c0020t0008g0013 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.633-1097_633-1096i others(680): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602222 | |||||
| chr19:602222
|
C | CCCTCCTC others(313): Show |
1 | a0001c0014t0024g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.633-1224_633-1223i others(322): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602222 | |||||
| chr19:602222
|
C | CCCTCCTC others(87): Show |
1 | a0001c0025t0004g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.633-1257_633-1256i others(96): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602222 | |||||
| chr19:602222
|
C | CCCTCCTC others(445): Show |
1 | a0001c0001t0004g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.633-1290_633-1289i others(454): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602222 | |||||
| chr19:602222
|
C | T | 7 | a0001c0003t0006g0201a0001c0008t0001g0022a0001c0023t0004g0247others(4): Show | 8 | HG01256.hp1 HG01258.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-1322C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602222 | ||||||
| chr19:602228
|
T | C | 4 | a0001c0003t0006g0201a0001c0008t0001g0022a0001c0023t0004g0247others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-1316T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602228 | ||||||
| chr19:602233
|
C | CCTCCTGC others(54): Show |
1 | a0001c0008t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.633-1257_633-1256i others(63): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602233 | |||||
| chr19:602233
|
C | CCTCCTGC others(21): Show |
1 | a0002c0051t0011g0360 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.633-1290_633-1289i others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602233 | |||||
| chr19:602233
|
C | CCTCCTGC others(783): Show |
1 | a0001c0001t0004g0387 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.633-1290_633-1289i others(792): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602233 | |||||
| chr19:602233
|
CCTCCTGC others(120): Show |
C | 1 | a0004c0048t0001g0003 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.633-1256_633-1130d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602233 | |||||
| chr19:602255
|
C | CCCTCCTC others(120): Show |
1 | a0002c0012t0001g0366 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.633-1214_633-1213i others(129): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | CCCTCCTC others(313): Show |
1 | a0001c0009t0001g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.633-1191_633-1190i others(322): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | CCCTCCTC others(407): Show |
1 | a0001c0017t0001g0376 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.633-1120_633-1119i others(416): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | CCCTCCTC others(501): Show |
1 | a0001c0018t0022g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633-1224_633-1223i others(510): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | CCCTCCTC others(336): Show |
1 | a0016c0080t0004g0386 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.633-1224_633-1223i others(345): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | CCCTCCTC others(478): Show |
1 | a0001c0003t0016g0384 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.633-1257_633-1256i others(487): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | CCCTCCTC others(313): Show |
1 | a0001c0034t0026g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.633-1257_633-1256i others(322): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | CCCTCCTC others(384): Show |
1 | a0001c0041t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.633-1257_633-1256i others(393): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602255 | |||||
| chr19:602255
|
C | T | 7 | a0001c0001t0001g0081a0001c0001t0004g0068a0001c0002t0003g0078others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.633-1289C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602255 | ||||||
| chr19:602261
|
T | C | 1 | a0001c0015t0004g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.633-1283T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602261 | ||||||
| chr19:602266
|
C | CCTCCTGC others(501): Show |
1 | a0002c0004t0004g0275 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.633-1120_633-1119i others(510): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602266 | |||||
| chr19:602266
|
C | CCTCCTGC others(21): Show |
4 | a0001c0003t0006g0201a0001c0006t0002g0020a0002c0036t0001g0008others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-1257_633-1256i others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602266 | |||||
| chr19:602266
|
CCTCCTGC others(87): Show |
C | 1 | a0001c0084t0004g0101 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.633-1223_633-1130d others(96): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602266 | |||||
| chr19:602279
|
C | T | 1 | a0001c0015t0002g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.633-1265C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602279 | ||||||
| chr19:602280
|
G | T | 2 | a0001c0030t0004g0234a0001c0030t0004g0235 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.633-1264G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602280 | ||||||
| chr19:602287
|
T | C | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633-1257T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602287 | ||||||
| chr19:602288
|
C | CCCTCCTC others(87): Show |
1 | a0001c0097t0001g0119 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.633-1214_633-1213i others(96): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602288 | |||||
| chr19:602288
|
C | CCCTCCTC others(120): Show |
1 | a0011c0056t0001g0286 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.633-1223_633-1097d others(129): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602288 | |||||
| chr19:602288
|
C | CCCTCCTC others(120): Show |
1 | a0001c0002t0003g0078 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.633-1224_633-1223i others(129): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602288 | |||||
| chr19:602288
|
C | CCCTCCTC others(54): Show |
1 | a0001c0015t0004g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.633-1224_633-1223i others(63): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602288 | |||||
| chr19:602288
|
C | CCCTCCTC others(87): Show |
1 | a0001c0017t0004g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.633-1224_633-1223i others(96): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602288 | |||||
| chr19:602288
|
C | T | 10 | a0001c0001t0001g0081a0001c0001t0004g0068a0001c0006t0002g0020others(7): Show | 10 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.633-1256C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602288 | ||||||
| chr19:602294
|
TCTCTCCT others(92): Show |
T | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.633-1246_633-1148d others(101): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602294 | |||||
| chr19:602299
|
C | CCTCCTGC others(676): Show |
1 | a0001c0008t0002g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.633-1191_633-1190i others(685): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602299 | |||||
| chr19:602299
|
C | CCTCCTGC others(54): Show |
3 | a0001c0015t0001g0373a0001c0017t0001g0001a0002c0038t0001g0357 | 5 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-1180_633-1120d others(63): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602299 | |||||
| chr19:602320
|
T | C | 1 | a0001c0023t0004g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.633-1224T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602320 | ||||||
| chr19:602321
|
C | T | 12 | a0001c0017t0004g0023a0001c0018t0022g0039a0001c0023t0004g0247others(9): Show | 12 | HG02257.hp1 HG02615.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.633-1223C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602321 | ||||||
| chr19:602329
|
T | TCCTGCGT others(1408): Show |
1 | a0001c0030t0004g0378 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.633-1214_633-1213i others(1417): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602329 | |||||
| chr19:602332
|
CCTCCTGC others(21): Show |
C | 3 | a0001c0017t0001g0383a0002c0010t0002g0270a0009c0061t0001g0356 | 3 | HG02080.hp2 HG02615.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.633-1190_633-1163d others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602332 | |||||
| chr19:602354
|
T | C | 140 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(137): Show | 142 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.633-1190T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602354 | ||||||
| chr19:602360
|
T | TCTCCTGC others(346): Show |
2 | a0001c0018t0002g0053a0001c0041t0001g0099 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.633-1130_633-1129i others(355): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(699): Show |
1 | a0001c0008t0012g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.633-1130_633-1129i others(708): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(549): Show |
1 | a0002c0004t0001g0347 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.633-1120_633-1119i others(558): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(1085): Show |
1 | a0001c0003t0002g0372 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.633-1120_633-1119i others(1094): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(1057): Show |
1 | a0001c0008t0004g0375 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.633-1120_633-1119i others(1066): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(1306): Show |
1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.633-1120_633-1119i others(1315): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(1372): Show |
1 | a0001c0022t0001g0242 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.633-1120_633-1119i others(1381): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(1372): Show |
1 | a0002c0035t0005g0349 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.633-1120_633-1119i others(1381): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(351): Show |
1 | a0001c0018t0001g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.633-1120_633-1119i others(360): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(323): Show |
2 | a0001c0018t0001g0040a0001c0114t0004g0041 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.633-1097_633-1096i others(332): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(409): Show |
1 | a0019c0122t0004g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.633-1097_633-1096i others(418): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(577): Show |
1 | a0001c0008t0002g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.633-1097_633-1096i others(586): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(3078): Show |
1 | a0002c0068t0004g0358 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.633-1097_633-1096i others(3087): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(3375): Show |
1 | a0002c0012t0001g0359 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.633-1097_633-1096i others(3384): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(907): Show |
1 | a0002c0012t0004g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.633-1097_633-1096i others(916): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(186): Show |
2 | a0002c0010t0001g0262a0002c0010t0002g0266 | 2 | NA18943.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.633-1097_633-1096i others(195): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(92): Show |
2 | a0001c0018t0002g0052a0001c0076t0001g0029 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.633-1092_633-1091i others(101): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(379): Show |
2 | a0002c0058t0012g0254a0002c0059t0004g0339 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.633-1092_633-1091i others(388): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(1653): Show |
1 | a0001c0094t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.633-1092_633-1091i others(1662): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(316): Show |
1 | a0002c0005t0003g0276 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.633-1163_633-1162i others(325): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(59): Show |
2 | a0001c0018t0020g0058a0002c0010t0001g0363 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.633-1163_633-1162i others(68): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(92): Show |
1 | a0001c0003t0001g0018 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.633-1163_633-1162i others(101): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(318): Show |
1 | a0002c0004t0017g0259 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.633-1163_633-1162i others(327): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(582): Show |
1 | a0001c0031t0001g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.633-1163_633-1162i others(591): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(615): Show |
1 | a0001c0001t0002g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.633-1163_633-1162i others(624): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(318): Show |
6 | a0001c0046t0002g0037a0001c0093t0003g0159a0001c0116t0001g0032others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-1163_633-1162i others(327): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(582): Show |
1 | a0001c0001t0004g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.633-1163_633-1162i others(591): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(582): Show |
4 | a0001c0001t0002g0084a0001c0002t0003g0175a0001c0002t0004g0174others(1): Show | 4 | HG02080.hp1 NA18995.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-1163_633-1162i others(591): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCCTGC others(604): Show |
1 | a0001c0002t0003g0098 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.633-1163_633-1162i others(613): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTC | 53 | a0001c0001t0001g0081a0001c0001t0002g0055a0001c0001t0002g0077others(50): Show | 54 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.633-1181_633-1180i others(7): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(64): Show |
1 | a0002c0016t0001g0293 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(73): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(97): Show |
1 | a0001c0014t0003g0071 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(106): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(130): Show |
1 | a0001c0006t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(139): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(996): Show |
1 | a0001c0015t0001g0011 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(1005): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(163): Show |
1 | a0001c0113t0006g0042 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(172): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(460): Show |
1 | a0001c0006t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(469): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(323): Show |
1 | a0001c0008t0007g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.633-1181_633-1180i others(332): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(92): Show |
1 | a0001c0046t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(101): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(191): Show |
1 | a0018c0120t0002g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(200): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(539): Show |
1 | a0001c0115t0004g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(548): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(549): Show |
1 | a0001c0042t0008g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(558): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(64): Show |
1 | a0001c0013t0001g0394 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(73): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(689): Show |
1 | a0001c0032t0004g0374 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(698): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(1118): Show |
1 | a0002c0012t0002g0346 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(1127): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(628): Show |
1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(637): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(539): Show |
1 | a0002c0004t0006g0353 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(548): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(511): Show |
1 | a0004c0121t0004g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(520): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(572): Show |
1 | a0002c0016t0006g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(581): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(704): Show |
1 | a0001c0026t0004g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(713): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(59): Show |
1 | a0001c0009t0001g0114 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(68): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(319): Show |
1 | a0001c0002t0003g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(328): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(643): Show |
1 | a0001c0002t0003g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(652): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(352): Show |
1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(361): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(318): Show |
1 | a0001c0002t0003g0156 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(327): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(351): Show |
7 | a0001c0001t0001g0155a0001c0001t0002g0396a0001c0002t0003g0154others(4): Show | 7 | HG00735.hp2 HG01981.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.633-1181_633-1180i others(360): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(384): Show |
2 | a0001c0001t0001g0134a0001c0001t0002g0135 | 2 | NA19005.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.633-1181_633-1180i others(393): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(714): Show |
1 | a0001c0001t0002g0091 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(723): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(516): Show |
1 | a0001c0002t0009g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(525): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(318): Show |
2 | a0001c0002t0004g0183a0002c0004t0002g0355 | 2 | NA18948.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.633-1181_633-1180i others(327): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(351): Show |
42 | a0001c0001t0001g0083a0001c0001t0001g0141a0001c0001t0001g0157others(39): Show | 42 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.633-1181_633-1180i others(360): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(384): Show |
6 | a0001c0001t0001g0140a0001c0001t0002g0113a0001c0002t0003g0009others(3): Show | 6 | HG00408.hp2 HG00558.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-1181_633-1180i others(393): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(417): Show |
1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(426): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(450): Show |
3 | a0001c0001t0001g0182a0001c0008t0002g0082a0002c0004t0001g0261 | 3 | HG02300.hp2 NA18950.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.633-1181_633-1180i others(459): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(516): Show |
1 | a0001c0001t0001g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(525): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(714): Show |
2 | a0001c0001t0001g0136a0007c0095t0001g0211 | 2 | HG02129.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.633-1181_633-1180i others(723): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(643): Show |
2 | a0001c0001t0001g0199a0001c0006t0002g0166 | 2 | HG01175.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.633-1181_633-1180i others(652): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(224): Show |
1 | a0001c0001t0002g0126 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(233): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(351): Show |
1 | a0002c0028t0004g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.633-1181_633-1180i others(360): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
T | TCTCTCCT others(158): Show |
1 | a0001c0001t0002g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.633-1181_633-1180i others(167): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602360
|
TCTCCTGC others(26): Show |
T | 1 | a0001c0099t0004g0377 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.633-1162_633-1130d others(35): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602360 | |||||
| chr19:602373
|
C | T | 1 | a0001c0042t0008g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.633-1171C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602373 | ||||||
| chr19:602381
|
T | C | 3 | a0001c0001t0002g0055a0001c0077t0004g0382a0001c0113t0006g0042 | 3 | HG02630.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.633-1163T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602381 | ||||||
| chr19:602382
|
C | CCCTCCTC others(1547): Show |
1 | a0001c0091t0011g0380 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633-1130_633-1129i others(1556): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(473): Show |
1 | a0001c0001t0004g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.633-1130_633-1129i others(482): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(1060): Show |
1 | a0001c0001t0004g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.633-1130_633-1129i others(1069): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(26): Show |
3 | a0001c0002t0003g0132a0001c0105t0001g0121a0002c0050t0002g0361 | 3 | HG01943.hp1 HG02723.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.633-1124_633-1092d others(35): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(544): Show |
1 | a0001c0001t0004g0387 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.633-1120_633-1119i others(553): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(973): Show |
1 | a0001c0008t0004g0385 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.633-1097_633-1096i others(982): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(760): Show |
1 | a0003c0029t0002g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.633-1092_633-1091i others(769): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(826): Show |
2 | a0003c0029t0002g0103a0003c0089t0003g0106 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.633-1092_633-1091i others(835): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | CCCTCCTC others(793): Show |
1 | a0003c0029t0004g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.633-1092_633-1091i others(802): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602382
|
C | T | 22 | a0001c0001t0001g0137a0001c0001t0002g0016a0001c0001t0002g0055others(19): Show | 22 | HG00408.hp1 HG00544.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.633-1162C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602382 | ||||||
| chr19:602382
|
CCCTCCTC others(26): Show |
C | 2 | a0001c0020t0004g0030a0001c0034t0004g0044 | 2 | HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.633-1124_633-1092d others(35): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602382 | |||||
| chr19:602388
|
T | C | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.633-1156T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602388 | ||||||
| chr19:602393
|
C | CCTCCTGC others(247): Show |
1 | a0001c0032t0004g0100 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.633-1130_633-1129i others(256): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602393 | |||||
| chr19:602393
|
C | CCTCCTGC others(445): Show |
1 | a0001c0001t0002g0185 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.633-1130_633-1129i others(454): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602393 | |||||
| chr19:602393
|
C | CCTCCTGC others(21): Show |
1 | a0001c0097t0001g0119 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.633-1147_633-1120d others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602393 | |||||
| chr19:602414
|
T | TCCCTCCT others(506): Show |
1 | a0001c0008t0001g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.633-1130_633-1129i others(515): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602414 | ||||||
| chr19:602415
|
T | C | 7 | a0001c0001t0001g0137a0001c0001t0002g0185a0001c0003t0001g0180others(4): Show | 7 | HG00544.hp2 HG02071.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.633-1129T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602415 | ||||||
| chr19:602415
|
T | TCCTCCTC others(59): Show |
1 | a0001c0006t0001g0213 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.633-1097_633-1096i others(68): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602415 | |||||
| chr19:602415
|
T | TCCTCCTC others(445): Show |
1 | a0001c0108t0004g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.633-1097_633-1096i others(454): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602415 | |||||
| chr19:602415
|
T | TCCTCCTC others(1707): Show |
1 | a0001c0032t0004g0381 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.633-1097_633-1096i others(1716): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602415 | |||||
| chr19:602415
|
T | TCCTCCTC others(3134): Show |
1 | a0001c0098t0006g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.633-1097_633-1096i others(3143): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602415 | |||||
| chr19:602415
|
T | TCCTCCTC others(247): Show |
1 | a0005c0110t0006g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.633-1092_633-1091i others(256): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602415 | |||||
| chr19:602415
|
T | TCCTCCTC others(863): Show |
1 | a0001c0023t0001g0370 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.633-1092_633-1091i others(872): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602415 | |||||
| chr19:602513
|
C | A | 1 | a0017c0049t0001g0311 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.633-1031C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602513 | ||||||
| chr19:602532
|
G | A | 1 | a0002c0004t0001g0303 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.633-1012G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602532 | ||||||
| chr19:602587
|
C | T | 1 | a0001c0003t0002g0203 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.633-957C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602587 | ||||||
| chr19:602609
|
G | A | 1 | a0001c0032t0004g0381 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.633-935G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602609 | ||||||
| chr19:602662
|
C | T | 1 | a0001c0008t0001g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.633-882C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602662 | ||||||
| chr19:602673
|
T | C | 81 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0002g0055others(78): Show | 82 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.633-871T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602673 | ||||||
| chr19:602702
|
G | A | 1 | a0001c0008t0007g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.633-842G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602702 | ||||||
| chr19:602722
|
A | G | 1 | a0001c0002t0003g0093 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.633-822A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602722 | ||||||
| chr19:602726
|
T | A | 4 | a0001c0001t0001g0178a0001c0022t0001g0242a0002c0035t0005g0349others(1): Show | 5 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-818T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602726 | ||||||
| chr19:602769
|
C | G | 3 | a0001c0032t0004g0374a0001c0079t0004g0028a0002c0012t0002g0346 | 3 | HG03041.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.633-775C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602769 | ||||||
| chr19:602881
|
G | A | 23 | a0001c0003t0002g0219a0001c0003t0002g0223a0001c0003t0007g0067others(20): Show | 23 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.633-663G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602881 | ||||||
| chr19:602913
|
G | A | 1 | a0016c0080t0004g0386 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.633-631G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602913 | ||||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.633-583_633-582ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
1 | a0001c0091t0011g0380 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633-560_633-559ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
24 | a0001c0001t0004g0017a0001c0006t0002g0027a0001c0006t0006g0249others(21): Show | 24 | HG00621.hp2 HG01891.hp2 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.633-560_633-559ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
4 | a0001c0001t0001g0178a0001c0022t0001g0242a0002c0035t0005g0349others(1): Show | 5 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-560_633-559ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
4 | a0001c0017t0001g0383a0001c0032t0004g0374a0001c0079t0004g0028others(1): Show | 4 | HG02615.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-560_633-559ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(386): Show |
1 | a0001c0006t0002g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.633-560_633-559ins others(393): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
44 | a0001c0001t0002g0016a0001c0001t0002g0077a0001c0001t0004g0068others(41): Show | 45 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.633-560_633-559ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
2 | a0001c0001t0002g0055a0001c0001t0004g0387 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.633-560_633-559ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(465): Show |
1 | a0002c0016t0001g0306 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.633-560_633-559ins others(472): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
1 | a0001c0006t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.633-560_633-559ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
1 | a0001c0026t0002g0038 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.633-573_633-572ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
114 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0134others(111): Show | 117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.633-573_633-572ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(935): Show |
1 | a0001c0001t0001g0083 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.633-573_633-572ins others(942): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
1 | a0001c0002t0003g0093 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.633-573_633-572ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(465): Show |
1 | a0001c0002t0003g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.633-573_633-572ins others(472): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(464): Show |
2 | a0001c0001t0001g0226a0001c0002t0003g0225 | 2 | NA18962.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.633-573_633-572ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(307): Show |
4 | a0001c0001t0004g0229a0001c0008t0012g0371a0001c0026t0002g0057others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-573_633-572ins others(314): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGCGCC others(308): Show |
1 | a0001c0002t0004g0080 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.633-573_633-572ins others(315): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGTGCC others(464): Show |
1 | a0001c0003t0001g0231 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.633-600_633-599ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGTGCC others(464): Show |
86 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.633-600_633-599ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGTGCC others(464): Show |
1 | a0001c0003t0006g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.633-600_633-599ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGTGCC others(465): Show |
1 | a0001c0025t0004g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.633-600_633-599ins others(472): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602941
|
C | CAGGTGCC others(465): Show |
1 | a0001c0007t0001g0212 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.633-600_633-599ins others(472): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602941 | |||||
| chr19:602946
|
G | GCCTGGGG others(464): Show |
1 | a0002c0028t0001g0330 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.633-573_633-572ins others(471): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 602946 | |||||
| chr19:602972
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.633-572C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602972 | ||||||
| chr19:602985
|
C | T | 35 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0009t0001g0005others(32): Show | 37 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-559C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602985 | ||||||
| chr19:602987
|
T | C | 36 | a0001c0001t0001g0182a0001c0006t0001g0070a0001c0006t0004g0072others(33): Show | 38 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.633-557T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 602987 | ||||||
| chr19:603002
|
TGCCCGGG others(151): Show |
T | 1 | a0001c0001t0001g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.633-526_633-369del | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 603002 | |||||
| chr19:603007
|
G | GGGGCTGG others(71): Show |
31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-527_633-526ins others(78): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 603007 | |||||
| chr19:603007
|
G | GGGGCTGG others(71): Show |
4 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0014t0003g0071others(1): Show | 4 | HG02559.hp2 NA18948.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-527_633-526ins others(78): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 603007 | |||||
| chr19:603042
|
C | T | 1 | a0004c0121t0004g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.633-502C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603042 | ||||||
| chr19:603043
|
G | A | 35 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0009t0001g0005others(32): Show | 37 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-501G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603043 | ||||||
| chr19:603066
|
C | T | 2 | a0001c0001t0001g0155a0001c0002t0003g0154 | 2 | NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.633-478C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603066 | ||||||
| chr19:603084
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.633-460C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603084 | ||||||
| chr19:603124
|
T | C | 35 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0009t0001g0005others(32): Show | 37 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-420T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603124 | ||||||
| chr19:603135
|
GT | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-408delT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603135 | ||||||
| chr19:603136
|
T | C | 4 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0014t0003g0071others(1): Show | 4 | HG02559.hp2 NA18948.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-408T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603136 | ||||||
| chr19:603137
|
G | A | 4 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0014t0003g0071others(1): Show | 4 | HG02559.hp2 NA18948.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-407G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603137 | ||||||
| chr19:603137
|
G | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-407G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603137 | ||||||
| chr19:603138
|
C | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-406C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603138 | ||||||
| chr19:603138
|
C | CCCTTGCC others(71): Show |
4 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0014t0003g0071others(1): Show | 4 | HG02559.hp2 NA18948.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-404_633-403ins others(78): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 603138 | |||||
| chr19:603143
|
C | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-401C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603143 | ||||||
| chr19:603145
|
T | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-399T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603145 | ||||||
| chr19:603149
|
A | C | 35 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0009t0001g0005others(32): Show | 37 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-395A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603149 | ||||||
| chr19:603150
|
C | T | 43 | a0001c0001t0002g0016a0001c0001t0002g0077a0001c0001t0004g0068others(40): Show | 44 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.633-394C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603150 | ||||||
| chr19:603156
|
A | G | 35 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0009t0001g0005others(32): Show | 37 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-388A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603156 | ||||||
| chr19:603159
|
G | A | 4 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0014t0003g0071others(1): Show | 4 | HG02559.hp2 NA18948.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-385G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603159 | ||||||
| chr19:603160
|
G | T | 35 | a0001c0006t0001g0070a0001c0006t0004g0072a0001c0009t0001g0005others(32): Show | 37 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-384G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603160 | ||||||
| chr19:603164
|
C | T | 1 | a0002c0010t0002g0266 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.633-380C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603164 | ||||||
| chr19:603165
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-379G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603165 | ||||||
| chr19:603176
|
C | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-368C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603176 | ||||||
| chr19:603177
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-367A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603177 | ||||||
| chr19:603178
|
T | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-366T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603178 | ||||||
| chr19:603182
|
T | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-362T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603182 | ||||||
| chr19:603186
|
T | TG | 33 | a0001c0001t0001g0182a0001c0009t0001g0005a0001c0009t0001g0069others(30): Show | 35 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.633-353dupG | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 603186 | |||||
| chr19:603194
|
T | G | 125 | a0001c0001t0001g0182a0001c0003t0001g0018a0001c0003t0001g0087others(122): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.633-350T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603194 | ||||||
| chr19:603208
|
C | G | 32 | a0001c0001t0001g0182a0001c0009t0001g0005a0001c0009t0001g0069others(29): Show | 34 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.633-336C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603208 | ||||||
| chr19:603250
|
G | A | 1 | a0002c0010t0002g0319 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.633-294G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603250 | ||||||
| chr19:603264
|
TG | T | 121 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(118): Show | 124 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.633-274delG | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 603264 | |||||
| chr19:603293
|
G | GT | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-251_633-250ins others(1): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603293 | ||||||
| chr19:603294
|
C | G | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-250C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603294 | ||||||
| chr19:603295
|
A | C | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-249A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603295 | ||||||
| chr19:603300
|
C | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-244C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603300 | ||||||
| chr19:603302
|
C | T | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-242C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603302 | ||||||
| chr19:603306
|
C | A | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-238C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603306 | ||||||
| chr19:603313
|
G | A | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-231G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603313 | ||||||
| chr19:603316
|
A | G | 122 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(119): Show | 125 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.633-228A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603316 | ||||||
| chr19:603317
|
T | G | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-227T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603317 | ||||||
| chr19:603321
|
C | CGGGGCTG others(72): Show |
49 | a0001c0001t0002g0016a0001c0001t0002g0077a0001c0001t0004g0068others(46): Show | 50 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.633-145_633-144ins others(79): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 603321 | |||||
| chr19:603321
|
C | T | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.633-223C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603321 | ||||||
| chr19:603355
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.633-189C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603355 | ||||||
| chr19:603460
|
T | C | 90 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(87): Show | 91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.633-84T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603460 | ||||||
| chr19:603513
|
C | T | 123 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(120): Show | 126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.633-31C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | chr19 | 603513 | ||||||
| chr19:603971
|
A | G | 2 | a0001c0003t0010g0196a0002c0054t0004g0250 | 2 | HG04199.hp1 HG04204.hp1 |
splice_region_variant&intron_variant | LOW | c.1056+4A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 603971 | ||||||
| chr19:604021
|
C | T | 1 | a0001c0041t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1056+54C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604021 | ||||||
| chr19:604022
|
A | G | 175 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(172): Show | 181 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1056+55A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604022 | ||||||
| chr19:604027
|
C | T | 2 | a0001c0023t0004g0247a0001c0042t0004g0015 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1056+60C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604027 | ||||||
| chr19:604027
|
CGGGGCCA others(35): Show |
C | 1 | a0002c0027t0003g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1056+80_1056+121de others(43): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604027 | |||||
| chr19:604040
|
GCAGGGGC others(76): Show |
G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1056+80_1056+162de others(84): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604040 | |||||
| chr19:604040
|
GCAGGGGC others(506): Show |
G | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1056+89_1057-493de others(1): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604040 | |||||
| chr19:604046
|
GCGGGGCT others(117): Show |
G | 4 | a0001c0001t0001g0178a0001c0022t0001g0242a0002c0035t0005g0349others(1): Show | 5 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1056+80_1056+203de others(1): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604046 | ||||||
| chr19:604046
|
GCGGGGCT others(158): Show |
G | 1 | a0001c0023t0004g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1056+80_1056+244de others(1): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604046 | ||||||
| chr19:604069
|
T | C | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+102T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604069 | ||||||
| chr19:604071
|
G | C | 1 | a0002c0012t0004g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1056+104G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604071 | ||||||
| chr19:604082
|
GCAGGGGT others(157): Show |
G | 1 | a0001c0091t0011g0380 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1056+132_1056+295d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604082 | |||||
| chr19:604088
|
GTGGGGCT others(116): Show |
G | 125 | a0001c0001t0001g0083a0001c0001t0001g0155a0001c0001t0001g0158others(122): Show | 125 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1056+223_1056+345d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604088 | |||||
| chr19:604089
|
T | C | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+122T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604089 | ||||||
| chr19:604098
|
G | A | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+131G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604098 | ||||||
| chr19:604100
|
G | T | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+133G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604100 | ||||||
| chr19:604101
|
A | G | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+134A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604101 | ||||||
| chr19:604103
|
A | T | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+136A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604103 | ||||||
| chr19:604104
|
T | G | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+137T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604104 | ||||||
| chr19:604115
|
T | C | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+148T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604115 | ||||||
| chr19:604122
|
C | A | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+155C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604122 | ||||||
| chr19:604123
|
C | G | 2 | a0001c0001t0001g0141a0001c0002t0003g0156 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1056+156C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604123 | ||||||
| chr19:604129
|
GTGGGGCT others(75): Show |
G | 3 | a0001c0001t0001g0141a0001c0002t0003g0156a0006c0047t0003g0002 | 4 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056+173_1056+254d others(84): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604129 | |||||
| chr19:604140
|
G | A | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1056+173G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604140 | ||||||
| chr19:604140
|
GGAGATCT others(75): Show |
G | 148 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0134others(145): Show | 153 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.1056+203_1056+284d others(84): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604140 | |||||
| chr19:604149
|
GGTGGGGT others(34): Show |
G | 6 | a0001c0001t0001g0182a0001c0001t0002g0186a0001c0002t0003g0181others(3): Show | 6 | HG00408.hp1 HG02056.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1056+223_1056+263d others(43): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604149 | |||||
| chr19:604170
|
A | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1056+203A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604170 | ||||||
| chr19:604181
|
A | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1056+214A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604181 | ||||||
| chr19:604190
|
A | G | 46 | a0001c0001t0001g0178a0001c0001t0002g0016a0001c0001t0004g0068others(43): Show | 48 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1056+223A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604190 | ||||||
| chr19:604211
|
A | G | 49 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0002g0016others(46): Show | 51 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1056+244A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604211 | ||||||
| chr19:604222
|
A | G | 49 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0002g0016others(46): Show | 51 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1056+255A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604222 | ||||||
| chr19:604252
|
G | A | 41 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0002t0003g0074others(38): Show | 42 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1056+285G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604252 | ||||||
| chr19:604270
|
T | G | 1 | a0001c0001t0002g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1056+303T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604270 | ||||||
| chr19:604293
|
A | G | 60 | a0001c0001t0001g0083a0001c0001t0001g0155a0001c0001t0001g0158others(57): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1056+326A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604293 | ||||||
| chr19:604304
|
A | G | 60 | a0001c0001t0001g0083a0001c0001t0001g0155a0001c0001t0001g0158others(57): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1056+337A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604304 | ||||||
| chr19:604327
|
C | T | 9 | a0001c0001t0001g0178a0001c0001t0004g0017a0001c0017t0001g0383others(6): Show | 10 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1056+360C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604327 | ||||||
| chr19:604338
|
GGCTATGA others(15): Show |
G | 1 | a0002c0036t0001g0008 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1056+376_1056+397d others(24): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604338 | |||||
| chr19:604343
|
T | C | 1 | a0011c0056t0001g0286 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1056+376T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604343 | ||||||
| chr19:604441
|
A | G | 22 | a0001c0006t0002g0107a0001c0008t0001g0022a0001c0008t0001g0026others(19): Show | 24 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1056+474A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604441 | ||||||
| chr19:604443
|
G | C | 31 | a0001c0002t0003g0156a0001c0009t0001g0005a0001c0009t0001g0069others(28): Show | 33 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1056+476G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604443 | ||||||
| chr19:604520
|
A | C | 4 | a0001c0001t0004g0387a0001c0006t0002g0244a0001c0023t0004g0247others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-541A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604520 | ||||||
| chr19:604565
|
C | CTATGAGG others(35): Show |
2 | a0001c0023t0001g0370a0001c0094t0001g0369 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1057-479_1057-438d others(44): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604565 | |||||
| chr19:604565
|
C | CTATGAGG others(161): Show |
1 | a0002c0064t0001g0324 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1057-438_1057-437i others(170): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604565 | |||||
| chr19:604582
|
A | AGCGGGGT others(35): Show |
1 | a0002c0005t0003g0322 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1057-468_1057-427d others(44): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604582 | |||||
| chr19:604582
|
A | G | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-479A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604582 | ||||||
| chr19:604593
|
A | G | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-468A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604593 | ||||||
| chr19:604596
|
T | G | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-465T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604596 | ||||||
| chr19:604598
|
C | G | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-463C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604598 | ||||||
| chr19:604600
|
A | G | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-461A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604600 | ||||||
| chr19:604602
|
T | C | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-459T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604602 | ||||||
| chr19:604605
|
A | G | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-456A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604605 | ||||||
| chr19:604607
|
A | ATATGAGG others(36): Show |
5 | a0001c0001t0001g0136a0001c0006t0002g0244a0001c0009t0001g0114others(2): Show | 5 | HG02040.hp2 HG02129.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-432_1057-431i others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | ATATGAGG others(79): Show |
28 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0130others(25): Show | 30 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1057-432_1057-431i others(88): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | ATATGAGG others(165): Show |
1 | a0007c0106t0002g0187 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1057-432_1057-431i others(174): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | ATATGAGG others(36): Show |
7 | a0001c0003t0004g0012a0001c0006t0006g0249a0001c0014t0024g0248others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-420_1057-378d others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | ATATGAGG others(79): Show |
5 | a0001c0008t0012g0371a0001c0018t0002g0052a0001c0032t0004g0100others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-370_1057-369i others(88): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | ATATGAGG others(79): Show |
1 | a0001c0003t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1057-453_1057-368d others(88): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | ATATGAGG others(36): Show |
3 | a0002c0050t0002g0361a0005c0043t0006g0108a0005c0043t0006g0109 | 3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1057-421_1057-420i others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | ATATGAGG others(36): Show |
2 | a0001c0014t0003g0096a0001c0040t0003g0195 | 2 | HG00621.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.1057-421_1057-420i others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604607
|
A | C | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1057-454A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604607 | ||||||
| chr19:604607
|
ATATGAGG others(36): Show |
A | 3 | a0001c0003t0001g0018a0001c0042t0008g0112a0002c0063t0001g0274 | 3 | HG02970.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1057-420_1057-378d others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604607 | |||||
| chr19:604626
|
C | T | 39 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0006t0001g0070others(36): Show | 40 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1057-435C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604626 | ||||||
| chr19:604630
|
G | A | 89 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0182others(86): Show | 91 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1057-431G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604630 | ||||||
| chr19:604634
|
G | A | 91 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0182others(88): Show | 93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1057-427G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604634 | ||||||
| chr19:604641
|
A | AGGGCGGG others(36): Show |
1 | a0001c0039t0001g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1057-412_1057-370d others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604641 | |||||
| chr19:604641
|
A | AGGGCGGG others(79): Show |
24 | a0001c0002t0003g0224a0001c0003t0002g0219a0001c0003t0002g0223others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1057-368_1057-367i others(88): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604641 | |||||
| chr19:604641
|
A | G | 37 | a0001c0001t0001g0136a0001c0003t0006g0201a0001c0006t0002g0107others(34): Show | 39 | HG00621.hp2 HG00673.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1057-420A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604641 | ||||||
| chr19:604646
|
G | A | 10 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0140others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1057-415G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604646 | ||||||
| chr19:604649
|
A | ACTATGAG others(36): Show |
1 | a0001c0101t0008g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1057-410_1057-368d others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604649 | |||||
| chr19:604649
|
A | G | 3 | a0001c0006t0002g0107a0002c0012t0001g0359a0002c0068t0004g0358 | 3 | HG02145.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1057-412A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604649 | ||||||
| chr19:604650
|
C | CAATGCGG others(37): Show |
2 | a0002c0012t0001g0359a0002c0068t0004g0358 | 2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1057-411_1057-410i others(46): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604650 | ||||||
| chr19:604650
|
CTATGAGG others(80): Show |
C | 1 | a0001c0008t0004g0385 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1057-392_1057-306d others(89): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604650 | |||||
| chr19:604651
|
T | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-410T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604651 | ||||||
| chr19:604655
|
A | C | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-406A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604655 | ||||||
| chr19:604656
|
G | GGGTTGTG others(36): Show |
5 | a0001c0003t0002g0372a0001c0020t0004g0030a0001c0034t0004g0044others(2): Show | 5 | HG01192.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-378_1057-377i others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604656 | |||||
| chr19:604661
|
G | T | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-400G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604661 | ||||||
| chr19:604670
|
G | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-391G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604670 | ||||||
| chr19:604674
|
T | C | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-387T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604674 | ||||||
| chr19:604678
|
G | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-383G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604678 | ||||||
| chr19:604681
|
G | T | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-380G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604681 | ||||||
| chr19:604684
|
G | A | 4 | a0001c0032t0004g0381a0001c0098t0006g0064a0002c0012t0001g0359others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-377G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604684 | ||||||
| chr19:604688
|
C | T | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-373C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604688 | ||||||
| chr19:604692
|
G | A | 4 | a0001c0032t0004g0381a0001c0098t0006g0064a0002c0012t0001g0359others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-369G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604692 | ||||||
| chr19:604693
|
C | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-368C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604693 | ||||||
| chr19:604694
|
A | T | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-367A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604694 | ||||||
| chr19:604694
|
AATGCGGG others(37): Show |
A | 2 | a0001c0032t0004g0381a0001c0098t0006g0064 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1057-363_1057-320d others(46): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604694 | |||||
| chr19:604698
|
C | A | 3 | a0001c0006t0002g0107a0002c0012t0001g0359a0002c0068t0004g0358 | 3 | HG02145.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1057-363C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604698 | ||||||
| chr19:604699
|
G | T | 2 | a0002c0012t0001g0359a0002c0068t0004g0358 | 2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1057-362G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604699 | ||||||
| chr19:604704
|
T | G | 3 | a0001c0006t0002g0107a0002c0012t0001g0359a0002c0068t0004g0358 | 3 | HG02145.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1057-357T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604704 | ||||||
| chr19:604704
|
T | TTGCTGGG others(80): Show |
1 | a0001c0113t0006g0042 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1057-306_1057-305i others(89): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604704 | |||||
| chr19:604704
|
T | TTGCTGGG others(80): Show |
2 | a0001c0001t0001g0238a0001c0001t0002g0237 | 2 | HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1057-306_1057-305i others(89): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604704 | |||||
| chr19:604714
|
A | G | 3 | a0001c0006t0002g0107a0002c0012t0001g0359a0002c0068t0004g0358 | 3 | HG02145.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1057-347A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604714 | ||||||
| chr19:604716
|
G | T | 2 | a0002c0012t0001g0359a0002c0068t0004g0358 | 2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1057-345G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604716 | ||||||
| chr19:604717
|
G | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-344G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604717 | ||||||
| chr19:604718
|
C | CCAGACAT others(80): Show |
39 | a0001c0001t0002g0016a0001c0002t0004g0174a0001c0006t0001g0070others(36): Show | 40 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1057-306_1057-305i others(89): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604718 | |||||
| chr19:604718
|
C | CCAGACAT others(124): Show |
1 | a0002c0004t0001g0332 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1057-306_1057-305i others(133): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604718 | |||||
| chr19:604718
|
C | T | 3 | a0001c0006t0002g0107a0002c0012t0001g0359a0002c0068t0004g0358 | 3 | HG02145.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1057-343C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604718 | ||||||
| chr19:604721
|
G | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-340G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604721 | ||||||
| chr19:604722
|
A | G | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-339A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604722 | ||||||
| chr19:604725
|
T | G | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-336T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604725 | ||||||
| chr19:604728
|
G | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-333G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604728 | ||||||
| chr19:604732
|
T | C | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-329T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604732 | ||||||
| chr19:604736
|
G | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-325G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604736 | ||||||
| chr19:604737
|
A | C | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1057-324A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604737 | ||||||
| chr19:604738
|
T | A | 4 | a0001c0006t0002g0107a0001c0008t0004g0385a0002c0012t0001g0359others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-323T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604738 | ||||||
| chr19:604743
|
G | GGGTTGTG others(36): Show |
52 | a0001c0001t0004g0068a0001c0008t0001g0022a0001c0009t0001g0005others(49): Show | 56 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.1057-306_1057-305i others(45): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604743 | |||||
| chr19:604743
|
G | GGGTTGTG others(80): Show |
1 | a0001c0099t0004g0377 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1057-280_1057-279i others(89): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604743 | |||||
| chr19:604743
|
G | T | 6 | a0001c0006t0002g0107a0001c0008t0004g0385a0001c0032t0004g0381others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-318G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604743 | ||||||
| chr19:604791
|
T | G | 1 | a0001c0008t0002g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1057-270T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604791 | ||||||
| chr19:604795
|
G | GGGGGTCC others(93): Show |
1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-263_1057-262i others(102): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604795 | |||||
| chr19:604799
|
T | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-262T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604799 | ||||||
| chr19:604805
|
A | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-256A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604805 | ||||||
| chr19:604807
|
G | A | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-254G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604807 | ||||||
| chr19:604816
|
T | C | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-245T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604816 | ||||||
| chr19:604817
|
G | A | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-244G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604817 | ||||||
| chr19:604830
|
G | A | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-231G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604830 | ||||||
| chr19:604837
|
C | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-224C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604837 | ||||||
| chr19:604840
|
T | C | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-221T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604840 | ||||||
| chr19:604842
|
A | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-219A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604842 | ||||||
| chr19:604843
|
A | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-218A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604843 | ||||||
| chr19:604849
|
T | G | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-212T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604849 | ||||||
| chr19:604852
|
A | T | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-209A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604852 | ||||||
| chr19:604857
|
G | T | 1 | a0001c0042t0004g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057-204G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604857 | ||||||
| chr19:604858
|
G | GT | 6 | a0001c0003t0004g0012a0001c0020t0008g0010a0001c0020t0008g0013others(3): Show | 6 | HG01891.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-203_1057-202i others(3): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604858 | ||||||
| chr19:604859
|
C | CG | 235 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0134others(232): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1057-198dupG | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604859 | |||||
| chr19:604859
|
C | CGGGGGTC others(127): Show |
28 | a0001c0003t0002g0372a0001c0006t0002g0027a0001c0009t0001g0069others(25): Show | 29 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1057-198_1057-197i others(136): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604859 | |||||
| chr19:604859
|
C | CGGGGGTC others(128): Show |
1 | a0001c0009t0001g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1057-198_1057-197i others(137): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604859 | |||||
| chr19:604859
|
C | CGGGGGTC others(127): Show |
1 | a0002c0011t0001g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1057-198_1057-197i others(136): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604859 | |||||
| chr19:604859
|
C | CGGGGTCC others(126): Show |
4 | a0001c0009t0001g0005a0001c0105t0001g0121a0002c0074t0002g0350others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057-167_1057-166i others(135): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 604859 | |||||
| chr19:604859
|
C | G | 6 | a0001c0003t0004g0012a0001c0020t0008g0010a0001c0020t0008g0013others(3): Show | 6 | HG01891.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-202C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604859 | ||||||
| chr19:604859
|
C | T | 9 | a0001c0001t0002g0055a0001c0001t0004g0387a0001c0017t0004g0023others(6): Show | 9 | HG02615.hp1 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1057-202C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604859 | ||||||
| chr19:604890
|
A | T | 1 | a0002c0011t0001g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1057-171A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604890 | ||||||
| chr19:604895
|
G | A | 230 | a0001c0001t0001g0083a0001c0001t0001g0134a0001c0001t0001g0161others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1057-166G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604895 | ||||||
| chr19:604926
|
C | T | 1 | a0002c0027t0003g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1057-135C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604926 | ||||||
| chr19:604929
|
G | A | 32 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(29): Show | 34 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1057-132G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604929 | ||||||
| chr19:604934
|
C | T | 17 | a0001c0001t0001g0178a0001c0001t0004g0017a0001c0006t0002g0166others(14): Show | 19 | HG01074.hp2 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1057-127C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604934 | ||||||
| chr19:604940
|
G | C | 1 | a0001c0006t0001g0213 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1057-121G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604940 | ||||||
| chr19:604965
|
C | G | 2 | a0001c0023t0001g0370a0001c0094t0001g0369 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1057-96C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604965 | ||||||
| chr19:604988
|
G | A | 89 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0136others(86): Show | 91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1057-73G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604988 | ||||||
| chr19:604988
|
G | T | 115 | a0001c0001t0002g0169a0001c0001t0002g0396a0001c0001t0004g0168others(112): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1057-73G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 604988 | ||||||
| chr19:605045
|
C | T | 1 | a0003c0029t0004g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1057-16C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 2/7 | chr19 | 605045 | ||||||
| chr19:605228
|
C | T | 41 | a0001c0006t0001g0070a0001c0006t0002g0073a0001c0006t0002g0107others(38): Show | 41 | HG00423.hp1 HG00673.hp1 HG01109.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.1218+6C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605228 | ||||||
| chr19:605233
|
C | T | 7 | a0001c0001t0002g0055a0001c0001t0004g0387a0001c0006t0002g0027others(4): Show | 7 | HG02129.hp1 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+11C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605233 | ||||||
| chr19:605255
|
C | T | 208 | a0001c0001t0001g0178a0001c0001t0002g0016a0001c0001t0002g0169others(205): Show | 216 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1218+33C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605255 | ||||||
| chr19:605302
|
A | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+80A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605302 | ||||||
| chr19:605303
|
C | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+81C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605303 | ||||||
| chr19:605306
|
A | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+84A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605306 | ||||||
| chr19:605308
|
GGTTGAAC others(1): Show |
G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+87_1218+94del others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605308 | ||||||
| chr19:605315
|
C | A | 2 | a0001c0007t0001g0088a0001c0007t0001g0194 | 2 | NA18947.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1218+93C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605315 | ||||||
| chr19:605316
|
C | G | 21 | a0001c0003t0002g0219a0001c0003t0002g0223a0001c0003t0007g0067others(18): Show | 21 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1218+94C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605316 | ||||||
| chr19:605318
|
A | G | 26 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(23): Show | 28 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1218+96A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605318 | ||||||
| chr19:605319
|
A | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+97A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605319 | ||||||
| chr19:605320
|
GCCTTTCA others(201): Show |
G | 15 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0006t0002g0020others(12): Show | 16 | HG01256.hp1 HG01258.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+155_1218+362d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605320 | |||||
| chr19:605321
|
CCTT | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+100_1218+102d others(5): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605321 | ||||||
| chr19:605325
|
T | TCAGAGGT others(253): Show |
1 | a0001c0001t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1218+198_1218+199i others(262): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605325 | |||||
| chr19:605325
|
TCAGAGGT others(45): Show |
T | 80 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(77): Show | 82 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1218+155_1218+206d others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605325 | |||||
| chr19:605325
|
TCAGAGGT others(149): Show |
T | 47 | a0001c0001t0001g0136a0001c0001t0002g0091a0001c0006t0001g0070others(44): Show | 47 | HG00423.hp1 HG00673.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1218+155_1218+310d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605325 | |||||
| chr19:605328
|
GA | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+107delA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605328 | ||||||
| chr19:605332
|
T | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+110T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605332 | ||||||
| chr19:605332
|
T | TGGGGACC others(45): Show |
2 | a0001c0001t0002g0169a0001c0008t0002g0128 | 2 | HG01123.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1218+154_1218+155i others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605332 | |||||
| chr19:605332
|
TGGGGACC others(97): Show |
T | 79 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0134others(76): Show | 79 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1218+214_1218+317d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605332 | |||||
| chr19:605333
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+111G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605333 | ||||||
| chr19:605333
|
GGGGACCC others(96): Show |
G | 1 | a0001c0001t0002g0065 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1218+115_1218+217d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605333 | |||||
| chr19:605335
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+113G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605335 | ||||||
| chr19:605339
|
CCAG | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+118_1218+120d others(5): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605339 | ||||||
| chr19:605345
|
GCCCCC | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+124_1218+128d others(7): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605345 | ||||||
| chr19:605352
|
T | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+130T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605352 | ||||||
| chr19:605357
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+135A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605357 | ||||||
| chr19:605359
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+137G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605359 | ||||||
| chr19:605361
|
G | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+139G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605361 | ||||||
| chr19:605364
|
GACTC | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+143_1218+146d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605364 | ||||||
| chr19:605368
|
C | CGGGCCCT others(45): Show |
3 | a0001c0025t0001g0036a0001c0109t0001g0034a0001c0111t0001g0033 | 3 | HG00639.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1218+154_1218+155i others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605368 | |||||
| chr19:605371
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+149G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605371 | ||||||
| chr19:605375
|
TTACAGAG others(81): Show |
T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+154_1218+241d others(90): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605375 | ||||||
| chr19:605377
|
A | T | 45 | a0001c0001t0001g0081a0001c0001t0002g0055a0001c0001t0002g0169others(42): Show | 47 | HG00621.hp2 HG00639.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1218+155A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605377 | ||||||
| chr19:605377
|
ACAGAGGT others(149): Show |
A | 1 | a0002c0012t0004g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1218+214_1218+369d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605377 | |||||
| chr19:605377
|
ACAGAGGT others(201): Show |
A | 2 | a0001c0001t0004g0229a0001c0026t0004g0051 | 2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1218+207_1218+414d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605377 | |||||
| chr19:605384
|
T | C | 19 | a0001c0001t0002g0169a0001c0001t0004g0168a0001c0003t0002g0372others(16): Show | 19 | HG00639.hp2 HG00738.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1218+162T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605384 | ||||||
| chr19:605384
|
TGGGGACC others(45): Show |
T | 2 | a0001c0001t0002g0135a0001c0002t0003g0093 | 2 | NA18944.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1218+207_1218+258d others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605384 | |||||
| chr19:605416
|
G | C | 3 | a0001c0008t0004g0385a0001c0032t0004g0381a0001c0098t0006g0064 | 3 | HG02647.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1218+194G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605416 | ||||||
| chr19:605420
|
C | T | 5 | a0001c0003t0002g0372a0001c0007t0001g0089a0001c0017t0004g0023others(2): Show | 5 | HG01192.hp1 HG01361.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+198C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605420 | ||||||
| chr19:605421
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1218+199G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605421 | ||||||
| chr19:605423
|
GCCCTTTC others(98): Show |
G | 1 | a0002c0005t0003g0258 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1218+204_1218+308d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605423 | |||||
| chr19:605429
|
T | A | 8 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0002g0113others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218+207T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605429 | ||||||
| chr19:605429
|
T | TCAGAGGT others(45): Show |
1 | a0001c0023t0004g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1218+213_1218+214i others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605429 | |||||
| chr19:605429
|
T | TCAGAGGT others(409): Show |
2 | a0001c0001t0002g0055a0001c0001t0004g0387 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1218+213_1218+214i others(418): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605429 | |||||
| chr19:605429
|
T | TCAGAGGT others(149): Show |
2 | a0002c0012t0001g0359a0002c0068t0004g0358 | 2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1218+213_1218+214i others(158): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605429 | |||||
| chr19:605429
|
TCAGAGGC others(45): Show |
T | 15 | a0001c0001t0001g0178a0001c0001t0004g0017a0001c0006t0002g0166others(12): Show | 16 | HG01074.hp2 HG01175.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1218+214_1218+265d others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605429 | |||||
| chr19:605436
|
C | CGGGGACC others(773): Show |
1 | a0002c0011t0001g0365 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1218+310_1218+311i others(782): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605436 | |||||
| chr19:605436
|
C | T | 28 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0002g0055others(25): Show | 30 | HG00408.hp2 HG00558.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1218+214C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605436 | ||||||
| chr19:605436
|
CGGGGACC others(45): Show |
C | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1218+259_1218+310d others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605436 | |||||
| chr19:605436
|
CGGGGACC others(97): Show |
C | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1218+259_1218+362d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605436 | |||||
| chr19:605436
|
CGGGGACC others(149): Show |
C | 1 | a0001c0031t0001g0245 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1218+311_1218+466d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605436 | |||||
| chr19:605466
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+244A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605466 | ||||||
| chr19:605469
|
A | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+247A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605469 | ||||||
| chr19:605472
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+250C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605472 | ||||||
| chr19:605472
|
C | T | 32 | a0001c0003t0001g0018a0001c0003t0002g0219a0001c0003t0002g0223others(29): Show | 32 | HG00438.hp2 HG00642.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1218+250C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605472 | ||||||
| chr19:605473
|
G | A | 1 | a0001c0001t0002g0135 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1218+251G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605473 | ||||||
| chr19:605473
|
G | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+251G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605473 | ||||||
| chr19:605477
|
C | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+255C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605477 | ||||||
| chr19:605478
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+256C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605478 | ||||||
| chr19:605480
|
T | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+258T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605480 | ||||||
| chr19:605481
|
A | ACAGAGGT others(149): Show |
2 | a0001c0015t0001g0373a0001c0018t0022g0039 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1218+310_1218+311i others(158): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605481 | |||||
| chr19:605481
|
A | T | 165 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0155others(162): Show | 167 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1218+259A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605481 | ||||||
| chr19:605481
|
AC | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+260delC | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605481 | ||||||
| chr19:605481
|
ACAGAGGT others(97): Show |
A | 9 | a0001c0001t0001g0081a0001c0002t0004g0080a0001c0002t0004g0092others(6): Show | 9 | HG03453.hp2 NA18946.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+311_1218+414d others(2): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605481 | |||||
| chr19:605483
|
A | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+261A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605483 | ||||||
| chr19:605484
|
G | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+262G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605484 | ||||||
| chr19:605488
|
T | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+266T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605488 | ||||||
| chr19:605488
|
T | C | 91 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(88): Show | 93 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1218+266T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605488 | ||||||
| chr19:605491
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+269G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605491 | ||||||
| chr19:605494
|
C | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+272C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605494 | ||||||
| chr19:605495
|
C | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+273C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605495 | ||||||
| chr19:605497
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+275A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605497 | ||||||
| chr19:605499
|
G | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+277G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605499 | ||||||
| chr19:605501
|
GCCCCCTT | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+280_1218+286d others(9): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605501 | ||||||
| chr19:605509
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+287A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605509 | ||||||
| chr19:605513
|
A | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+291A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605513 | ||||||
| chr19:605515
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+293G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605515 | ||||||
| chr19:605517
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+295G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605517 | ||||||
| chr19:605518
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+296A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605518 | ||||||
| chr19:605520
|
G | C | 1 | a0002c0062t0004g0362 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1218+298G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605520 | ||||||
| chr19:605520
|
G | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+298G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605520 | ||||||
| chr19:605521
|
A | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+299A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605521 | ||||||
| chr19:605524
|
C | T | 3 | a0001c0017t0004g0023a0001c0099t0004g0377a0002c0011t0001g0340 | 3 | HG02615.hp1 HG02895.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1218+302C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605524 | ||||||
| chr19:605525
|
G | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+303G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605525 | ||||||
| chr19:605527
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+305G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605527 | ||||||
| chr19:605532
|
T | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+310T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605532 | ||||||
| chr19:605533
|
T | A | 33 | a0001c0001t0001g0134a0001c0001t0002g0055a0001c0001t0002g0135others(30): Show | 35 | HG00639.hp2 HG01109.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.1218+311T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605533 | ||||||
| chr19:605534
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+312C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605534 | ||||||
| chr19:605536
|
G | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+314G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605536 | ||||||
| chr19:605540
|
T | C | 97 | a0001c0001t0002g0065a0001c0003t0001g0018a0001c0003t0001g0087others(94): Show | 101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1218+318T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605540 | ||||||
| chr19:605540
|
T | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+318T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605540 | ||||||
| chr19:605541
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+319G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605541 | ||||||
| chr19:605544
|
G | C | 3 | a0001c0025t0001g0036a0001c0109t0001g0034a0001c0111t0001g0033 | 3 | HG00639.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1218+322G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605544 | ||||||
| chr19:605545
|
A | AGG | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+323_1218+324i others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605545 | ||||||
| chr19:605546
|
C | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+324C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605546 | ||||||
| chr19:605549
|
AG | A | 32 | a0001c0002t0003g0094a0001c0009t0001g0005a0001c0009t0001g0069others(29): Show | 34 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1218+329delG | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605549 | |||||
| chr19:605552
|
C | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+330C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605552 | ||||||
| chr19:605556
|
C | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+334C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605556 | ||||||
| chr19:605557
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+335C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605557 | ||||||
| chr19:605558
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+336C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605558 | ||||||
| chr19:605559
|
T | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+337T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605559 | ||||||
| chr19:605560
|
T | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+338T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605560 | ||||||
| chr19:605566
|
G | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+344G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605566 | ||||||
| chr19:605568
|
G | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+346G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605568 | ||||||
| chr19:605570
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+348A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605570 | ||||||
| chr19:605572
|
GACT | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+351_1218+353d others(5): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605572 | ||||||
| chr19:605575
|
T | A | 1 | a0001c0008t0002g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1218+353T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605575 | ||||||
| chr19:605576
|
C | T | 33 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(30): Show | 34 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1218+354C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605576 | ||||||
| chr19:605580
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+358C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605580 | ||||||
| chr19:605581
|
C | G | 32 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(29): Show | 34 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1218+359C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605581 | ||||||
| chr19:605583
|
TTTCA | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+362_1218+365d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605583 | ||||||
| chr19:605585
|
T | A | 245 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0134others(242): Show | 250 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1218+363T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605585 | ||||||
| chr19:605585
|
T | TCAGAGGT others(45): Show |
3 | a0002c0012t0001g0359a0002c0038t0005g0338a0002c0068t0004g0358 | 3 | HG01167.hp2 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1218+503_1218+554d others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605585 | |||||
| chr19:605585
|
TCAGAGGT others(45): Show |
T | 1 | a0002c0011t0001g0340 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1218+503_1218+554d others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605585 | |||||
| chr19:605589
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+367A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605589 | ||||||
| chr19:605592
|
T | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+370T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605592 | ||||||
| chr19:605592
|
T | C | 104 | a0001c0001t0004g0168a0001c0003t0001g0018a0001c0003t0001g0087others(101): Show | 108 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1218+370T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605592 | ||||||
| chr19:605592
|
T | TGGGGACC others(97): Show |
1 | a0002c0038t0001g0357 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1218+421_1218+422i others(106): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605592 | |||||
| chr19:605596
|
G | C | 1 | a0002c0055t0001g0271 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1218+374G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605596 | ||||||
| chr19:605598
|
C | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+376C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605598 | ||||||
| chr19:605599
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+377C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605599 | ||||||
| chr19:605602
|
G | C | 2 | a0002c0016t0001g0252a0009c0061t0001g0356 | 2 | HG02080.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1218+380G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605602 | ||||||
| chr19:605604
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1218+382C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605604 | ||||||
| chr19:605604
|
CGCCCCCT others(5): Show |
C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+383_1218+394d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605604 | ||||||
| chr19:605617
|
A | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+395A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605617 | ||||||
| chr19:605621
|
G | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+399G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605621 | ||||||
| chr19:605625
|
ACTCGG | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+404_1218+408d others(7): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605625 | ||||||
| chr19:605631
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+409G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605631 | ||||||
| chr19:605632
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+410C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605632 | ||||||
| chr19:605637
|
A | ACAGAGGT others(45): Show |
1 | a0001c0093t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1218+466_1218+467i others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605637 | |||||
| chr19:605637
|
A | T | 32 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(29): Show | 34 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1218+415A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605637 | ||||||
| chr19:605644
|
T | C | 105 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(102): Show | 109 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1218+422T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605644 | ||||||
| chr19:605644
|
T | TGGGGACC others(45): Show |
2 | a0001c0109t0001g0034a0001c0111t0001g0033 | 2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1218+456_1218+457i others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605644 | |||||
| chr19:605648
|
G | C | 18 | a0001c0003t0002g0219a0001c0003t0002g0223a0001c0003t0007g0067others(15): Show | 18 | HG00438.hp2 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1218+426G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605648 | ||||||
| chr19:605648
|
G | GACCCAGG others(45): Show |
1 | a0001c0025t0001g0036 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1218+473_1218+474i others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605648 | |||||
| chr19:605670
|
G | A | 4 | a0001c0008t0002g0379a0001c0008t0012g0371a0001c0032t0004g0100others(1): Show | 4 | HG02055.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+448G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605670 | ||||||
| chr19:605680
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1218+458C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605680 | ||||||
| chr19:605681
|
G | A | 1 | a0002c0004t0001g0332 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1218+459G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605681 | ||||||
| chr19:605689
|
A | T | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+467A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605689 | ||||||
| chr19:605696
|
T | C | 102 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(99): Show | 106 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1218+474T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605696 | ||||||
| chr19:605697
|
G | A | 1 | a0001c0083t0009g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1218+475G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605697 | ||||||
| chr19:605722
|
G | A | 5 | a0001c0006t0002g0027a0001c0006t0002g0244a0001c0014t0003g0095others(2): Show | 5 | HG00621.hp2 HG02129.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+500G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605722 | ||||||
| chr19:605725
|
GAGGACTC others(45): Show |
G | 3 | a0001c0002t0004g0184a0002c0053t0002g0300a0002c0055t0001g0271 | 3 | HG01361.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1218+526_1218+577d others(54): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605725 | |||||
| chr19:605731
|
T | A | 5 | a0001c0003t0002g0372a0001c0017t0004g0023a0001c0099t0004g0377others(2): Show | 5 | HG00639.hp2 HG01192.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218+509T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605731 | ||||||
| chr19:605748
|
T | C | 10 | a0001c0003t0002g0372a0001c0006t0002g0027a0001c0006t0002g0244others(7): Show | 10 | HG00621.hp2 HG00639.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+526T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605748 | ||||||
| chr19:605759
|
G | GCGCCCCC others(98): Show |
4 | a0001c0006t0002g0027a0001c0006t0002g0244a0001c0014t0003g0096others(1): Show | 4 | HG00621.hp2 HG02257.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+554_1218+555i others(107): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605759 | |||||
| chr19:605777
|
A | G | 324 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(321): Show | 332 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1218+555A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605777 | ||||||
| chr19:605783
|
T | A | 85 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(82): Show | 87 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1218+561T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605783 | ||||||
| chr19:605783
|
T | TCGGGCCC others(151): Show |
1 | a0001c0014t0003g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1218+590_1218+591i others(160): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605783 | |||||
| chr19:605784
|
C | T | 2 | a0001c0008t0012g0371a0001c0032t0004g0100 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1218+562C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605784 | ||||||
| chr19:605800
|
C | T | 20 | a0001c0001t0002g0016a0001c0001t0002g0055a0001c0001t0004g0068others(17): Show | 21 | HG01256.hp1 HG01258.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1218+578C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605800 | ||||||
| chr19:605808
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1218+586C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605808 | ||||||
| chr19:605813
|
C | T | 5 | a0001c0001t0002g0055a0001c0001t0004g0387a0001c0015t0001g0373others(2): Show | 5 | HG00323.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218+591C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605813 | ||||||
| chr19:605825
|
GGAGA | G | 4 | a0001c0001t0002g0055a0001c0001t0004g0387a0001c0015t0001g0373others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+606_1218+609d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 605825 | |||||
| chr19:605844
|
A | C | 1 | a0001c0084t0004g0101 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1218+622A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605844 | ||||||
| chr19:605860
|
C | A | 4 | a0001c0001t0002g0055a0001c0001t0004g0387a0001c0015t0001g0373others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+638C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605860 | ||||||
| chr19:605885
|
C | T | 100 | a0001c0001t0002g0016a0001c0001t0002g0055a0001c0001t0004g0068others(97): Show | 103 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(100): Show |
intron_variant | MODIFIER | c.1218+663C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605885 | ||||||
| chr19:605899
|
G | A | 96 | a0001c0001t0001g0134a0001c0003t0001g0018a0001c0003t0001g0087others(93): Show | 98 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1218+677G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605899 | ||||||
| chr19:605920
|
G | A | 7 | a0001c0001t0001g0199a0001c0030t0004g0234a0001c0030t0004g0235others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218+698G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605920 | ||||||
| chr19:605957
|
C | T | 3 | a0001c0006t0002g0027a0001c0014t0003g0095a0001c0014t0003g0096 | 3 | HG00621.hp2 HG02129.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1218+735C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605957 | ||||||
| chr19:605968
|
C | T | 47 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0009t0001g0005others(44): Show | 50 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.1218+746C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605968 | ||||||
| chr19:605985
|
A | G | 299 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(296): Show | 304 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1218+763A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 605985 | ||||||
| chr19:606021
|
C | T | 95 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(92): Show | 97 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1218+799C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606021 | ||||||
| chr19:606045
|
C | T | 6 | a0001c0001t0001g0178a0001c0006t0002g0166a0001c0018t0022g0039others(3): Show | 7 | HG01074.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+823C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606045 | ||||||
| chr19:606139
|
G | A | 1 | a0002c0005t0003g0263 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1218+917G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606139 | ||||||
| chr19:606140
|
C | T | 96 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0006t0001g0070others(93): Show | 99 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.1218+918C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606140 | ||||||
| chr19:606143
|
A | G | 96 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0006t0001g0070others(93): Show | 99 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.1218+921A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606143 | ||||||
| chr19:606155
|
A | G | 1 | a0002c0004t0004g0334 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1218+933A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606155 | ||||||
| chr19:606162
|
C | T | 1 | a0002c0012t0004g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1218+940C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606162 | ||||||
| chr19:606169
|
G | A | 90 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0006t0001g0070others(87): Show | 93 | HG00423.hp1 HG00673.hp1 HG01069.hp2 others(90): Show |
intron_variant | MODIFIER | c.1218+947G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606169 | ||||||
| chr19:606212
|
C | T | 154 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(151): Show | 157 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1218+990C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606212 | ||||||
| chr19:606258
|
A | G | 96 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0006t0001g0070others(93): Show | 99 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.1218+1036A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606258 | ||||||
| chr19:606290
|
G | A | 96 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0006t0001g0070others(93): Show | 99 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.1218+1068G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606290 | ||||||
| chr19:606299
|
C | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1218+1077C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606299 | ||||||
| chr19:606344
|
G | A | 1 | a0001c0098t0006g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1218+1122G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606344 | ||||||
| chr19:606380
|
C | T | 8 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0002g0126others(5): Show | 8 | HG01993.hp1 HG02273.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218+1158C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606380 | ||||||
| chr19:606450
|
G | A | 1 | a0002c0005t0009g0301 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1218+1228G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606450 | ||||||
| chr19:606466
|
G | T | 1 | a0001c0002t0003g0225 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1218+1244G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606466 | ||||||
| chr19:606473
|
T | C | 212 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(209): Show | 216 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1218+1251T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606473 | ||||||
| chr19:606531
|
T | A | 212 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(209): Show | 216 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1218+1309T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606531 | ||||||
| chr19:606627
|
C | T | 212 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(209): Show | 216 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1219-1337C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606627 | ||||||
| chr19:606681
|
C | T | 107 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(104): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1219-1283C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606681 | ||||||
| chr19:606720
|
C | T | 50 | a0001c0006t0001g0070a0001c0006t0001g0213a0001c0006t0001g0214others(47): Show | 50 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1219-1244C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606720 | ||||||
| chr19:606721
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1219-1243G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606721 | ||||||
| chr19:606722
|
C | T | 106 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(103): Show | 110 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1219-1242C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606722 | ||||||
| chr19:606723
|
G | A | 1 | a0002c0012t0013g0265 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1219-1241G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606723 | ||||||
| chr19:606728
|
T | A | 1 | a0002c0012t0004g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1219-1236T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606728 | ||||||
| chr19:606850
|
CA | C | 321 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(318): Show | 329 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.1219-1106delA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 606850 | |||||
| chr19:606855
|
A | G | 97 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(94): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1219-1109A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606855 | ||||||
| chr19:606893
|
C | T | 1 | a0001c0085t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1219-1071C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606893 | ||||||
| chr19:606920
|
C | T | 5 | a0001c0008t0004g0385a0001c0032t0004g0381a0001c0098t0006g0064others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-1044C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606920 | ||||||
| chr19:606934
|
G | A | 278 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(275): Show | 283 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.1219-1030G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606934 | ||||||
| chr19:606941
|
GT | G | 278 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(275): Show | 283 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.1219-1022delT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606941 | ||||||
| chr19:606943
|
G | C | 278 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(275): Show | 283 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.1219-1021G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606943 | ||||||
| chr19:606957
|
G | A | 1 | a0002c0016t0001g0293 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1219-1007G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606957 | ||||||
| chr19:606973
|
G | A | 95 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(92): Show | 97 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1219-991G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 606973 | ||||||
| chr19:607027
|
C | T | 170 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(167): Show | 171 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1219-937C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607027 | ||||||
| chr19:607041
|
G | A | 107 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(104): Show | 111 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1219-923G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607041 | ||||||
| chr19:607044
|
T | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1219-920T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607044 | ||||||
| chr19:607073
|
A | G | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1219-891A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607073 | ||||||
| chr19:607096
|
C | T | 3 | a0001c0006t0002g0107a0001c0042t0004g0015a0001c0042t0008g0112 | 3 | HG03225.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1219-868C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607096 | ||||||
| chr19:607108
|
C | T | 310 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(307): Show | 317 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.1219-856C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607108 | ||||||
| chr19:607126
|
G | A | 106 | a0001c0003t0001g0018a0001c0003t0001g0087a0001c0003t0001g0090others(103): Show | 110 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1219-838G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607126 | ||||||
| chr19:607152
|
CAA | C | 14 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0015t0001g0011others(11): Show | 15 | HG01256.hp1 HG01258.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1219-811_1219-810d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607152 | ||||||
| chr19:607284
|
G | C | 1 | a0001c0032t0004g0381 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1219-680G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607284 | ||||||
| chr19:607316
|
G | A | 119 | a0001c0001t0001g0178a0001c0001t0004g0017a0001c0001t0004g0229others(116): Show | 124 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1219-648G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607316 | ||||||
| chr19:607319
|
A | G | 14 | a0001c0001t0002g0016a0001c0001t0004g0068a0001c0015t0001g0011others(11): Show | 15 | HG01256.hp1 HG01258.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1219-645A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607319 | ||||||
| chr19:607335
|
G | A | 1 | a0001c0008t0002g0082 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1219-629G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607335 | ||||||
| chr19:607424
|
C | T | 2 | a0001c0006t0002g0107a0001c0042t0008g0112 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1219-540C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607424 | ||||||
| chr19:607426
|
C | G | 1 | a0001c0015t0001g0373 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1219-538C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607426 | ||||||
| chr19:607475
|
C | A | 1 | a0002c0010t0001g0253 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1219-489C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607475 | ||||||
| chr19:607587
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1219-377G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607587 | ||||||
| chr19:607604
|
C | T | 7 | a0001c0006t0002g0027a0001c0006t0002g0244a0001c0014t0003g0095others(4): Show | 7 | HG00621.hp2 HG02129.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1219-360C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607604 | ||||||
| chr19:607626
|
C | T | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219-338C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607626 | ||||||
| chr19:607628
|
A | G | 24 | a0001c0001t0027g0390a0001c0009t0001g0005a0001c0009t0001g0218others(21): Show | 26 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1219-336A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607628 | ||||||
| chr19:607637
|
C | A | 8 | a0001c0009t0001g0069a0001c0009t0001g0114a0001c0009t0001g0130others(5): Show | 8 | HG02040.hp2 HG02698.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-327C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607637 | ||||||
| chr19:607673
|
C | T | 4 | a0001c0006t0002g0027a0001c0014t0003g0095a0001c0014t0003g0096others(1): Show | 4 | HG00621.hp2 HG02129.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-291C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607673 | ||||||
| chr19:607735
|
A | G | 155 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(152): Show | 155 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1219-229A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607735 | ||||||
| chr19:607825
|
A | G | 107 | a0001c0001t0002g0055a0001c0001t0004g0387a0001c0006t0001g0070others(104): Show | 111 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(108): Show |
intron_variant | MODIFIER | c.1219-139A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607825 | ||||||
| chr19:607866
|
C | G | 3 | a0001c0001t0002g0055a0001c0001t0004g0387a0001c0015t0001g0373 | 3 | HG02572.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1219-98C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607866 | ||||||
| chr19:607894
|
G | C | 1 | a0001c0085t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1219-70G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607894 | ||||||
| chr19:607929
|
C | A | 2 | a0002c0004t0001g0316a0002c0004t0004g0275 | 2 | NA18952.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1219-35C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607929 | ||||||
| chr19:607941
|
C | T | 46 | a0001c0006t0001g0070a0001c0006t0001g0213a0001c0006t0001g0214others(43): Show | 46 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1219-23C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 3/7 | chr19 | 607941 | ||||||
| chr19:608332
|
G | T | 1 | a0002c0012t0001g0366 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1437+150G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608332 | ||||||
| chr19:608362
|
C | T | 2 | a0005c0043t0006g0108a0005c0043t0006g0109 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1437+180C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608362 | ||||||
| chr19:608415
|
T | A | 43 | a0001c0006t0001g0070a0001c0006t0001g0213a0001c0006t0001g0214others(40): Show | 43 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1437+233T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608415 | ||||||
| chr19:608444
|
G | A | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1437+262G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608444 | ||||||
| chr19:608445
|
C | T | 1 | a0001c0006t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1437+263C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608445 | ||||||
| chr19:608511
|
G | A | 126 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(123): Show | 127 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1437+329G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608511 | ||||||
| chr19:608563
|
C | T | 128 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(125): Show | 129 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1437+381C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608563 | ||||||
| chr19:608581
|
C | T | 128 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(125): Show | 129 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1437+399C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608581 | ||||||
| chr19:608622
|
A | G | 1 | a0002c0005t0003g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1437+440A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608622 | ||||||
| chr19:608626
|
G | GC | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1437+444_1437+445i others(3): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608626 | ||||||
| chr19:608635
|
G | C | 31 | a0001c0009t0001g0005a0001c0009t0001g0069a0001c0009t0001g0114others(28): Show | 33 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1437+453G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608635 | ||||||
| chr19:608668
|
C | T | 99 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(96): Show | 99 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1437+486C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608668 | ||||||
| chr19:608669
|
G | T | 1 | a0002c0005t0003g0258 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1437+487G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608669 | ||||||
| chr19:608676
|
C | T | 1 | a0001c0022t0001g0152 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1437+494C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608676 | ||||||
| chr19:608680
|
G | A | 2 | a0001c0003t0002g0372a0002c0012t0004g0256 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1437+498G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608680 | ||||||
| chr19:608753
|
A | G | 47 | a0001c0003t0002g0203a0001c0006t0001g0070a0001c0006t0001g0213others(44): Show | 47 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1437+571A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608753 | ||||||
| chr19:608811
|
C | T | 1 | a0002c0011t0001g0317 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1437+629C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608811 | ||||||
| chr19:608900
|
A | T | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437+718A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608900 | ||||||
| chr19:608904
|
T | A | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437+722T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608904 | ||||||
| chr19:608905
|
T | G | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437+723T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608905 | ||||||
| chr19:608906
|
G | T | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437+724G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608906 | ||||||
| chr19:608908
|
C | G | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437+726C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608908 | ||||||
| chr19:608911
|
T | G | 1 | a0001c0079t0004g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437+729T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608911 | ||||||
| chr19:608963
|
C | A | 5 | a0001c0009t0001g0114a0001c0009t0001g0130a0001c0013t0001g0198others(2): Show | 5 | HG02040.hp2 HG02698.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1437+781C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 608963 | ||||||
| chr19:609051
|
C | T | 3 | a0001c0020t0004g0030a0001c0034t0004g0044a0001c0077t0004g0382 | 3 | HG02486.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1437+869C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609051 | ||||||
| chr19:609180
|
C | T | 1 | a0002c0012t0001g0366 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1437+998C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609180 | ||||||
| chr19:609297
|
A | G | 54 | a0001c0001t0001g0157a0001c0001t0001g0238a0001c0001t0002g0025others(51): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.1438-962A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609297 | ||||||
| chr19:609341
|
G | A | 14 | a0001c0001t0001g0155a0001c0001t0001g0182a0001c0001t0002g0084others(11): Show | 14 | HG00408.hp1 HG02074.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1438-918G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609341 | ||||||
| chr19:609421
|
C | T | 27 | a0001c0006t0001g0070a0001c0006t0001g0213a0001c0006t0001g0214others(24): Show | 27 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1438-838C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609421 | ||||||
| chr19:609483
|
C | T | 1 | a0001c0008t0002g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1438-776C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609483 | ||||||
| chr19:609597
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1438-662C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609597 | ||||||
| chr19:609630
|
G | C | 6 | a0001c0017t0001g0383a0001c0023t0001g0370a0001c0094t0001g0369others(3): Show | 6 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1438-629G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609630 | ||||||
| chr19:609734
|
C | T | 18 | a0001c0009t0001g0005a0001c0009t0001g0388a0001c0009t0010g0120others(15): Show | 20 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1438-525C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609734 | ||||||
| chr19:609761
|
C | T | 3 | a0001c0007t0001g0088a0001c0007t0001g0194a0001c0112t0014g0047 | 3 | HG03239.hp2 NA18947.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1438-498C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609761 | ||||||
| chr19:609770
|
G | A | 1 | a0001c0101t0008g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1438-489G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609770 | ||||||
| chr19:609821
|
A | G | 2 | a0001c0003t0002g0372a0002c0012t0004g0256 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1438-438A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609821 | ||||||
| chr19:609901
|
G | GA | 12 | a0001c0006t0002g0020a0001c0018t0001g0040a0001c0018t0001g0048others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1438-348dupA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 609901 | |||||
| chr19:609934
|
T | TTCAACTT others(369): Show |
1 | a0002c0021t0023g0288 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1438-311_1438-310i others(378): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 609934 | |||||
| chr19:609941
|
T | C | 32 | a0001c0006t0002g0107a0001c0009t0001g0005a0001c0009t0001g0114others(29): Show | 34 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1438-318T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 609941 | ||||||
| chr19:610034
|
T | G | 222 | a0001c0001t0001g0238a0001c0001t0002g0016a0001c0001t0002g0055others(219): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1438-225T>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610034 | ||||||
| chr19:610072
|
G | A | 3 | a0001c0042t0004g0015a0001c0108t0004g0043a0002c0012t0004g0256 | 3 | HG01884.hp1 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1438-187G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610072 | ||||||
| chr19:610081
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1438-178C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610081 | ||||||
| chr19:610084
|
A | C | 32 | a0001c0001t0001g0178a0001c0001t0002g0055a0001c0001t0004g0017others(29): Show | 32 | HG00280.hp2 HG00733.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1438-175A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610084 | ||||||
| chr19:610102
|
G | A | 89 | a0001c0001t0001g0238a0001c0001t0002g0237a0001c0001t0004g0168others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1438-157G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610102 | ||||||
| chr19:610118
|
CACAAGCA others(62): Show |
C | 3 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0002t0003g0162 | 3 | NA18951.hp1 NA18952.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1438-126_1438-58de others(70): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 610118 | |||||
| chr19:610132
|
C | T | 1 | a0001c0100t0003g0171 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1438-127C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610132 | ||||||
| chr19:610140
|
C | T | 1 | a0002c0004t0002g0329 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1438-119C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610140 | ||||||
| chr19:610145
|
C | T | 2 | a0001c0076t0001g0029a0002c0016t0006g0292 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1438-114C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610145 | ||||||
| chr19:610150
|
TGGGGGCG others(62): Show |
T | 7 | a0001c0003t0016g0384a0001c0023t0001g0370a0001c0025t0004g0059others(4): Show | 7 | HG01978.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1438-78_1438-10del others(69): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 610150 | |||||
| chr19:610190
|
A | C | 1 | a0001c0002t0004g0174 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1438-69A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610190 | ||||||
| chr19:610243
|
C | G | 45 | a0001c0001t0004g0229a0001c0001t0021g0217a0001c0013t0001g0129others(42): Show | 46 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1438-16C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610243 | ||||||
| chr19:610244
|
G | A | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1438-15G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 4/7 | chr19 | 610244 | ||||||
| chr19:610412
|
C | T | 1 | a0002c0028t0004g0284 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.1584+7C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610412 | ||||||
| chr19:610417
|
G | A | 1 | a0001c0002t0003g0098 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1584+12G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610417 | ||||||
| chr19:610522
|
G | A | 1 | a0001c0025t0005g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1584+117G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610522 | ||||||
| chr19:610591
|
C | T | 24 | a0001c0003t0002g0372a0001c0006t0002g0020a0001c0006t0006g0249others(21): Show | 26 | HG01192.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1584+186C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610591 | ||||||
| chr19:610592
|
G | A | 2 | a0001c0003t0001g0230a0001c0003t0001g0231 | 2 | HG00597.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1584+187G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610592 | ||||||
| chr19:610600
|
C | T | 1 | a0001c0077t0004g0382 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1584+195C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610600 | ||||||
| chr19:610631
|
C | T | 2 | a0001c0013t0001g0198a0010c0069t0001g0307 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1584+226C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610631 | ||||||
| chr19:610644
|
T | C | 1 | a0001c0003t0002g0203 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1584+239T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610644 | ||||||
| chr19:610645
|
G | A | 252 | a0001c0001t0001g0083a0001c0001t0001g0134a0001c0001t0001g0136others(249): Show | 257 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(254): Show |
intron_variant | MODIFIER | c.1584+240G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610645 | ||||||
| chr19:610649
|
G | A | 1 | a0002c0035t0005g0349 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1584+244G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610649 | ||||||
| chr19:610665
|
A | C | 2 | a0001c0001t0002g0025a0001c0008t0002g0379 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1584+260A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610665 | ||||||
| chr19:610681
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1584+276G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610681 | ||||||
| chr19:610695
|
G | A | 2 | a0001c0024t0002g0014a0001c0101t0008g0024 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1584+290G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610695 | ||||||
| chr19:610729
|
A | G | 330 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(327): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1584+324A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610729 | ||||||
| chr19:610747
|
G | A | 1 | a0002c0011t0001g0365 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1584+342G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610747 | ||||||
| chr19:610770
|
C | G | 9 | a0001c0009t0001g0005a0001c0013t0001g0129a0001c0013t0001g0131others(6): Show | 10 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1584+365C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610770 | ||||||
| chr19:610770
|
C | T | 1 | a0001c0014t0003g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1584+365C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610770 | ||||||
| chr19:610811
|
G | A | 1 | a0002c0011t0001g0365 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1584+406G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610811 | ||||||
| chr19:610847
|
G | A | 159 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0158others(156): Show | 165 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1584+442G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610847 | ||||||
| chr19:610877
|
C | T | 1 | a0001c0094t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1584+472C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610877 | ||||||
| chr19:610914
|
A | AC | 15 | a0001c0001t0002g0025a0001c0002t0004g0174a0001c0003t0001g0018others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.1584+516dupC | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 610914 | |||||
| chr19:610919
|
C | G | 1 | a0001c0015t0004g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1584+514C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610919 | ||||||
| chr19:610922
|
G | A | 1 | a0001c0109t0001g0034 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1584+517G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610922 | ||||||
| chr19:610957
|
G | A | 1 | a0001c0009t0002g0241 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1584+552G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610957 | ||||||
| chr19:610980
|
T | C | 358 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(355): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1584+575T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 610980 | ||||||
| chr19:611035
|
C | G | 1 | a0001c0014t0003g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1584+630C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611035 | ||||||
| chr19:611051
|
T | C | 1 | a0003c0089t0003g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1584+646T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611051 | ||||||
| chr19:611073
|
G | A | 1 | a0002c0051t0011g0360 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1584+668G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611073 | ||||||
| chr19:611088
|
ACCCGGTT others(9): Show |
A | 4 | a0001c0003t0016g0384a0001c0018t0002g0053a0002c0010t0001g0363others(1): Show | 4 | HG02451.hp2 HG02486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+685_1584+700d others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 611088 | |||||
| chr19:611090
|
C | T | 2 | a0003c0029t0002g0103a0003c0029t0002g0105 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1584+685C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611090 | ||||||
| chr19:611100
|
G | A | 1 | a0002c0012t0013g0265 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1584+695G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611100 | ||||||
| chr19:611170
|
G | A | 5 | a0001c0001t0001g0137a0001c0002t0004g0080a0001c0022t0001g0075others(2): Show | 5 | HG02071.hp2 NA18945.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1584+765G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611170 | ||||||
| chr19:611188
|
C | T | 6 | a0001c0001t0002g0016a0001c0008t0012g0371a0001c0018t0001g0040others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584+783C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611188 | ||||||
| chr19:611244
|
G | A | 1 | a0002c0011t0001g0340 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1584+839G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611244 | ||||||
| chr19:611247
|
G | A | 3 | a0001c0018t0002g0052a0001c0026t0002g0057a0002c0012t0002g0346 | 3 | HG02451.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1584+842G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611247 | ||||||
| chr19:611253
|
G | A | 2 | a0001c0001t0002g0084a0001c0001t0002g0237 | 2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1584+848G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611253 | ||||||
| chr19:611308
|
C | T | 1 | a0002c0010t0001g0290 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1584+903C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611308 | ||||||
| chr19:611320
|
C | T | 1 | a0001c0003t0001g0170 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1584+915C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611320 | ||||||
| chr19:611321
|
G | A | 7 | a0001c0001t0002g0055a0001c0001t0004g0068a0001c0001t0004g0229others(4): Show | 7 | HG01243.hp2 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1584+916G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611321 | ||||||
| chr19:611372
|
G | T | 6 | a0001c0006t0002g0244a0001c0020t0004g0030a0001c0020t0004g0397others(3): Show | 6 | HG02486.hp1 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1584+967G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611372 | ||||||
| chr19:611373
|
C | T | 62 | a0001c0001t0001g0083a0001c0001t0001g0140a0001c0001t0001g0155others(59): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1584+968C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611373 | ||||||
| chr19:611389
|
G | A | 153 | a0001c0001t0001g0081a0001c0001t0001g0136a0001c0001t0001g0140others(150): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1584+984G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611389 | ||||||
| chr19:611390
|
T | C | 197 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0134others(194): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1584+985T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611390 | ||||||
| chr19:611391
|
G | A | 1 | a0003c0029t0002g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1584+986G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611391 | ||||||
| chr19:611403
|
C | G | 27 | a0001c0001t0001g0226a0001c0001t0002g0135a0001c0001t0002g0186others(24): Show | 28 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1584+998C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611403 | ||||||
| chr19:611469
|
G | A | 1 | a0001c0014t0003g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1584+1064G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611469 | ||||||
| chr19:611474
|
G | A | 7 | a0001c0001t0002g0055a0001c0001t0004g0068a0001c0001t0004g0229others(4): Show | 7 | HG01243.hp2 HG01978.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1584+1069G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611474 | ||||||
| chr19:611477
|
G | A | 1 | a0002c0016t0006g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1584+1072G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611477 | ||||||
| chr19:611507
|
G | A | 3 | a0001c0018t0022g0039a0001c0042t0008g0112a0001c0098t0006g0064 | 3 | HG02647.hp1 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1584+1102G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611507 | ||||||
| chr19:611534
|
G | A | 1 | a0001c0008t0004g0375 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1584+1129G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611534 | ||||||
| chr19:611574
|
G | A | 1 | a0001c0002t0003g0147 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1584+1169G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611574 | ||||||
| chr19:611660
|
C | T | 1 | a0001c0003t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1584+1255C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611660 | ||||||
| chr19:611738
|
C | T | 1 | a0001c0001t0021g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1584+1333C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611738 | ||||||
| chr19:611871
|
C | T | 1 | a0001c0020t0003g0115 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1585-1377C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611871 | ||||||
| chr19:611872
|
G | A | 6 | a0001c0002t0004g0080a0001c0002t0004g0092a0001c0002t0004g0174others(3): Show | 6 | NA18946.hp1 NA18973.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-1376G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611872 | ||||||
| chr19:611873
|
T | C | 1 | a0001c0020t0003g0115 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1585-1375T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611873 | ||||||
| chr19:611915
|
A | G | 138 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(135): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1585-1333A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611915 | ||||||
| chr19:611916
|
C | T | 87 | a0001c0001t0002g0084a0001c0001t0002g0237a0001c0001t0004g0172others(84): Show | 90 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1585-1332C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611916 | ||||||
| chr19:611943
|
C | T | 2 | a0001c0109t0001g0034a0002c0059t0004g0339 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1585-1305C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611943 | ||||||
| chr19:611973
|
C | T | 1 | a0002c0019t0018g0269 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1585-1275C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 611973 | ||||||
| chr19:612018
|
G | A | 1 | a0001c0045t0003g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1585-1230G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612018 | ||||||
| chr19:612025
|
A | G | 1 | a0001c0015t0004g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1585-1223A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612025 | ||||||
| chr19:612044
|
C | T | 6 | a0001c0023t0001g0370a0001c0042t0008g0112a0001c0082t0004g0208others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-1204C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612044 | ||||||
| chr19:612071
|
G | A | 138 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(135): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1585-1177G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612071 | ||||||
| chr19:612080
|
G | A | 4 | a0001c0099t0004g0377a0001c0114t0004g0041a0002c0012t0001g0264others(1): Show | 4 | HG02895.hp1 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1585-1168G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612080 | ||||||
| chr19:612090
|
A | G | 131 | a0001c0001t0002g0084a0001c0001t0002g0237a0001c0001t0004g0172others(128): Show | 135 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1585-1158A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612090 | ||||||
| chr19:612131
|
C | T | 89 | a0001c0001t0002g0084a0001c0001t0002g0237a0001c0001t0004g0172others(86): Show | 92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1585-1117C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612131 | ||||||
| chr19:612132
|
G | A | 2 | a0001c0076t0001g0029a0019c0122t0004g0102 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1585-1116G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612132 | ||||||
| chr19:612144
|
C | CA | 11 | a0001c0003t0001g0018a0001c0014t0024g0248a0001c0025t0004g0059others(8): Show | 11 | HG00733.hp1 HG00733.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1585-1091dupA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612144 | |||||
| chr19:612234
|
A | G | 58 | a0001c0001t0004g0017a0001c0001t0004g0387a0001c0001t0021g0217others(55): Show | 60 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1585-1014A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612234 | ||||||
| chr19:612311
|
A | G | 5 | a0001c0032t0004g0381a0001c0034t0026g0061a0001c0041t0001g0099others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585-937A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612311 | ||||||
| chr19:612375
|
C | A | 1 | a0004c0121t0004g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1585-873C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612375 | ||||||
| chr19:612393
|
G | GGT | 8 | a0001c0007t0001g0193a0001c0009t0002g0241a0001c0018t0001g0048others(5): Show | 9 | HG00735.hp2 HG01109.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585-821_1585-820d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGGGGG others(17): Show |
2 | a0001c0020t0008g0010a0001c0020t0008g0013 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1585-852_1585-851i others(26): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGGGTG others(11): Show |
2 | a0001c0001t0021g0217a0001c0030t0004g0234 | 2 | HG00099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1585-852_1585-851i others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGGGTG others(13): Show |
1 | a0001c0030t0004g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1585-852_1585-851i others(22): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGGGTG others(15): Show |
2 | a0002c0054t0004g0250a0016c0080t0004g0386 | 2 | HG02809.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1585-852_1585-851i others(24): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGT | 12 | a0001c0003t0016g0384a0001c0006t0002g0020a0001c0006t0002g0244others(9): Show | 12 | HG00738.hp2 HG02015.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.1585-823_1585-820d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGTGT | 18 | a0001c0001t0002g0169a0001c0003t0001g0206a0001c0003t0002g0110others(15): Show | 19 | HG00280.hp2 HG00738.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1585-825_1585-820d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGTGTG others(1): Show |
13 | a0001c0003t0001g0170a0001c0006t0002g0166a0001c0009t0001g0388others(10): Show | 13 | HG00438.hp2 HG00609.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1585-827_1585-820d others(10): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGTGTG others(3): Show |
10 | a0001c0001t0001g0136a0001c0003t0007g0067a0001c0007t0007g0222others(7): Show | 11 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1585-829_1585-820d others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGTGTG others(5): Show |
9 | a0001c0003t0001g0207a0001c0003t0001g0231a0001c0003t0002g0205others(6): Show | 9 | HG01515.hp1 HG01975.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585-831_1585-820d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGTGTG others(7): Show |
2 | a0001c0001t0001g0188a0001c0023t0001g0370 | 2 | HG02970.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1585-833_1585-820d others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGTGTG others(9): Show |
1 | a0002c0050t0002g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1585-835_1585-820d others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GGTGTGTG others(11): Show |
2 | a0001c0094t0001g0369a0001c0098t0006g0064 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1585-837_1585-820d others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
G | GTGTGTGT others(4): Show |
2 | a0001c0003t0001g0087a0002c0004t0001g0302 | 2 | NA19070.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1585-855_1585-854i others(13): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612393 | ||||||
| chr19:612393
|
GGT | G | 30 | a0001c0001t0002g0016a0001c0001t0002g0055a0001c0001t0004g0068others(27): Show | 32 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1585-821_1585-820d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
GGTGT | G | 9 | a0001c0008t0012g0371a0001c0032t0004g0381a0001c0034t0026g0061others(6): Show | 9 | HG01884.hp1 HG01952.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585-823_1585-820d others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
GGTGTGT | G | 6 | a0001c0003t0001g0018a0001c0008t0004g0385a0001c0014t0024g0248others(3): Show | 6 | HG02145.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-825_1585-820d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
GGTGTGTG others(1): Show |
G | 97 | a0001c0001t0002g0084a0001c0001t0002g0237a0001c0001t0004g0172others(94): Show | 100 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1585-827_1585-820d others(10): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0006t0002g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1585-829_1585-820d others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
GGTGTGTG others(7): Show |
G | 35 | a0001c0001t0002g0065a0001c0001t0002g0077a0001c0001t0002g0091others(32): Show | 35 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1585-833_1585-820d others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612393
|
GGTGTGTG others(13): Show |
G | 1 | a0001c0003t0001g0230 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1585-839_1585-820d others(22): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612393 | |||||
| chr19:612419
|
T | A | 1 | a0004c0121t0004g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1585-829T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612419 | ||||||
| chr19:612421
|
T | A | 2 | a0002c0012t0004g0256a0004c0121t0004g0236 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1585-827T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612421 | ||||||
| chr19:612423
|
T | A | 28 | a0001c0003t0001g0018a0001c0008t0004g0385a0001c0008t0012g0371others(25): Show | 30 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1585-825T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612423 | ||||||
| chr19:612423
|
T | TGA | 3 | a0001c0020t0004g0030a0001c0034t0004g0044a0014c0087t0005g0220 | 3 | HG02486.hp1 HG03209.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1585-824_1585-823i others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612423 | |||||
| chr19:612425
|
T | A | 37 | a0001c0003t0001g0018a0001c0008t0004g0385a0001c0008t0012g0371others(34): Show | 39 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1585-823T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612425 | ||||||
| chr19:612427
|
T | A | 142 | a0001c0001t0002g0084a0001c0001t0002g0237a0001c0001t0004g0172others(139): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1585-821T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612427 | ||||||
| chr19:612427
|
T | TGTGAGA | 3 | a0001c0001t0001g0199a0001c0008t0004g0228a0001c0013t0001g0131 | 3 | HG01257.hp2 HG01981.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1585-820_1585-819i others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGAGAG others(3): Show |
1 | a0001c0084t0004g0101 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1585-820_1585-819i others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGAG others(1): Show |
10 | a0001c0001t0001g0137a0001c0001t0001g0161a0001c0001t0001g0163others(7): Show | 10 | HG00438.hp1 HG02071.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(10): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGAG others(3): Show |
1 | a0001c0006t0006g0249 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1585-820_1585-819i others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGAG others(5): Show |
1 | a0001c0026t0004g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(3): Show |
4 | a0001c0022t0001g0075a0001c0115t0004g0062a0002c0016t0001g0252others(1): Show | 4 | HG02922.hp1 HG03540.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0004g0387a0001c0042t0004g0015 | 2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1585-820_1585-819i others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0004g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(3): Show |
2 | a0001c0008t0002g0128a0001c0042t0008g0112 | 2 | HG03471.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1585-820_1585-819i others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(5): Show |
12 | a0001c0002t0004g0080a0001c0002t0004g0092a0001c0002t0004g0184others(9): Show | 12 | HG01109.hp2 HG01515.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(7): Show |
4 | a0001c0001t0001g0155a0002c0011t0001g0277a0002c0011t0001g0278others(1): Show | 4 | HG00323.hp1 HG00741.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(9): Show |
1 | a0001c0008t0001g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(5): Show |
1 | a0001c0085t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1585-820_1585-819i others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(7): Show |
15 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0226others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(9): Show |
1 | a0001c0009t0001g0395 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(7): Show |
1 | a0002c0011t0001g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(16): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(9): Show |
22 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0001t0009g0143others(19): Show | 23 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0083a0001c0009t0001g0069 | 2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1585-820_1585-819i others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(9): Show |
1 | a0002c0011t0001g0340 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1585-820_1585-819i others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(11): Show |
18 | a0001c0001t0001g0085a0001c0001t0001g0141a0001c0001t0001g0157others(15): Show | 18 | HG00558.hp2 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(13): Show |
6 | a0001c0001t0001g0238a0001c0002t0004g0174a0001c0007t0001g0194others(3): Show | 6 | HG01099.hp1 HG02040.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1585-820_1585-819i others(22): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(19): Show |
1 | a0001c0018t0020g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(28): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(15): Show |
2 | a0001c0001t0001g0081a0002c0059t0004g0339 | 2 | NA19011.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1585-820_1585-819i others(24): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612427
|
T | TGTGTGTG others(19): Show |
1 | a0001c0003t0001g0090 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1585-820_1585-819i others(28): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612427 | |||||
| chr19:612429
|
A | T | 3 | a0001c0082t0004g0208a0001c0098t0006g0064a0002c0050t0002g0361 | 3 | HG02109.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1585-819A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612429 | ||||||
| chr19:612431
|
A | T | 1 | a0002c0050t0002g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1585-817A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612431 | ||||||
| chr19:612439
|
G | A | 9 | a0001c0001t0021g0217a0001c0020t0004g0030a0001c0020t0008g0010others(6): Show | 9 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-809G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612439 | ||||||
| chr19:612440
|
G | T | 3 | a0001c0099t0004g0377a0001c0114t0004g0041a0002c0012t0001g0264 | 3 | HG02895.hp1 HG03579.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1585-808G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612440 | ||||||
| chr19:612457
|
C | T | 1 | a0002c0016t0001g0314 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1585-791C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612457 | ||||||
| chr19:612459
|
G | A | 5 | a0001c0008t0012g0371a0001c0032t0004g0381a0001c0034t0026g0061others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585-789G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612459 | ||||||
| chr19:612548
|
G | C | 6 | a0001c0008t0012g0371a0001c0032t0004g0381a0001c0034t0026g0061others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-700G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612548 | ||||||
| chr19:612556
|
G | A | 9 | a0001c0003t0016g0384a0001c0006t0002g0107a0001c0006t0002g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585-692G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612556 | ||||||
| chr19:612571
|
A | G | 9 | a0001c0001t0021g0217a0001c0003t0016g0384a0001c0006t0002g0244others(6): Show | 9 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-677A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612571 | ||||||
| chr19:612575
|
A | G | 3 | a0001c0001t0021g0217a0001c0030t0004g0234a0001c0030t0004g0235 | 3 | HG00099.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1585-673A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612575 | ||||||
| chr19:612630
|
G | A | 1 | a0001c0082t0004g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1585-618G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612630 | ||||||
| chr19:612652
|
C | T | 1 | a0001c0033t0001g0233 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1585-596C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612652 | ||||||
| chr19:612658
|
A | G | 17 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0034t0005g0035others(14): Show | 19 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1585-590A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612658 | ||||||
| chr19:612717
|
A | T | 136 | a0001c0001t0001g0188a0001c0001t0002g0016a0001c0001t0002g0025others(133): Show | 139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1585-531A>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612717 | ||||||
| chr19:612733
|
C | CT | 15 | a0001c0003t0002g0205a0001c0008t0012g0371a0001c0013t0001g0198others(12): Show | 15 | HG00438.hp1 HG01928.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1585-500dupT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612733 | |||||
| chr19:612733
|
CT | C | 9 | a0001c0001t0001g0085a0001c0014t0024g0248a0001c0018t0020g0058others(6): Show | 9 | HG00438.hp2 HG01993.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585-500delT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612733 | |||||
| chr19:612733
|
CTT | C | 155 | a0001c0001t0001g0158a0001c0001t0002g0084a0001c0001t0002g0169others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1585-501_1585-500d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612733 | |||||
| chr19:612759
|
C | G | 18 | a0001c0002t0004g0080a0001c0002t0004g0092a0001c0002t0004g0174others(15): Show | 18 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1585-489C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612759 | ||||||
| chr19:612844
|
G | GT | 44 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0188others(41): Show | 44 | HG00408.hp1 HG00597.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1585-392dupT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612844 | |||||
| chr19:612844
|
GT | G | 47 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0055others(44): Show | 47 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.1585-392delT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 612844 | |||||
| chr19:612854
|
TTTC | T | 31 | a0001c0003t0016g0384a0001c0006t0002g0244a0001c0008t0004g0385others(28): Show | 33 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1585-393_1585-391d others(5): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612854 | ||||||
| chr19:612855
|
TTC | T | 94 | a0001c0001t0001g0158a0001c0001t0002g0084a0001c0001t0002g0164others(91): Show | 97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1585-392_1585-391d others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612855 | ||||||
| chr19:612938
|
C | T | 1 | a0001c0018t0022g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1585-310C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612938 | ||||||
| chr19:612939
|
G | A | 1 | a0001c0001t0004g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1585-309G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612939 | ||||||
| chr19:612940
|
C | A | 116 | a0001c0001t0002g0025a0001c0001t0002g0055a0001c0001t0002g0065others(113): Show | 119 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1585-308C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612940 | ||||||
| chr19:612957
|
C | T | 1 | a0002c0005t0003g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1585-291C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612957 | ||||||
| chr19:612959
|
C | G | 1 | a0002c0005t0003g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1585-289C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612959 | ||||||
| chr19:612960
|
G | T | 1 | a0002c0005t0003g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1585-288G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 612960 | ||||||
| chr19:613021
|
G | A | 1 | a0002c0050t0002g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1585-227G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 613021 | ||||||
| chr19:613026
|
T | C | 3 | a0001c0001t0002g0113a0001c0003t0002g0192a0001c0008t0002g0082 | 3 | HG00558.hp1 HG02027.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1585-222T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 613026 | ||||||
| chr19:613076
|
G | GT | 4 | a0001c0022t0001g0227a0001c0088t0002g0399a0002c0016t0001g0293others(1): Show | 4 | HG02896.hp2 HG03669.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1585-166dupT | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr19 | 613076 | |||||
| chr19:613091
|
C | T | 11 | a0001c0001t0004g0387a0001c0001t0021g0217a0001c0003t0004g0012others(8): Show | 11 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1585-157C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 613091 | ||||||
| chr19:613124
|
G | C | 1 | a0001c0018t0020g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1585-124G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 613124 | ||||||
| chr19:613242
|
C | G | 1 | a0002c0004t0001g0261 | 1 | NA18950.hp2 | splice_region_variant&intron_variant | LOW | c.1585-6C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 5/7 | chr19 | 613242 | ||||||
| chr19:613491
|
G | A | 5 | a0001c0033t0001g0304a0001c0109t0001g0034a0001c0111t0001g0033others(2): Show | 5 | HG00323.hp2 HG00639.hp2 HG01099.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1825+3G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613491 | ||||||
| chr19:613506
|
GCGCCTGG others(14): Show |
G | 19 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0034t0005g0035others(16): Show | 21 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1825+22_1825+42del others(21): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613506 | |||||
| chr19:613517
|
G | A | 6 | a0001c0001t0004g0168a0001c0008t0004g0228a0001c0008t0004g0375others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+29G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613517 | ||||||
| chr19:613554
|
G | GGGGGCT | 5 | a0001c0008t0004g0385a0001c0018t0020g0058a0001c0032t0004g0100others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+71_1825+72ins others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613554 | |||||
| chr19:613554
|
G | GGGGGCTG others(5): Show |
2 | a0001c0118t0011g0060a0002c0051t0011g0360 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1825+71_1825+72ins others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613554 | |||||
| chr19:613560
|
C | T | 142 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(139): Show | 144 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1825+72C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613560 | ||||||
| chr19:613571
|
C | A | 2 | a0002c0035t0005g0343a0002c0038t0005g0338 | 2 | HG01167.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1825+83C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613571 | ||||||
| chr19:613572
|
C | T | 2 | a0002c0035t0005g0343a0002c0038t0005g0338 | 2 | HG01167.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1825+84C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613572 | ||||||
| chr19:613572
|
CGGGGCCG others(23): Show |
C | 67 | a0001c0001t0001g0137a0001c0001t0002g0077a0001c0001t0002g0084others(64): Show | 67 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1825+143_1825+172d others(32): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613572 | |||||
| chr19:613572
|
CGGGGCCG others(53): Show |
C | 1 | a0007c0106t0002g0187 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1825+113_1825+172d others(62): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613572 | |||||
| chr19:613573
|
GGGGCCGG others(22): Show |
G | 1 | a0001c0001t0002g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1825+89_1825+117de others(30): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613573 | |||||
| chr19:613577
|
C | A | 2 | a0002c0035t0005g0343a0002c0038t0005g0338 | 2 | HG01167.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1825+89C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613577 | ||||||
| chr19:613578
|
C | T | 2 | a0002c0035t0005g0343a0002c0038t0005g0338 | 2 | HG01167.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1825+90C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613578 | ||||||
| chr19:613578
|
CGGGGAT | C | 17 | a0001c0001t0004g0068a0001c0001t0004g0229a0001c0003t0001g0170others(14): Show | 17 | HG00609.hp2 HG01243.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1825+113_1825+118d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613578 | |||||
| chr19:613578
|
CGGGGATG others(11): Show |
C | 24 | a0001c0001t0002g0169a0001c0003t0002g0210a0001c0003t0002g0232others(21): Show | 25 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1825+101_1825+118d others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613578 | |||||
| chr19:613578
|
CGGGGATG others(17): Show |
C | 10 | a0001c0002t0004g0080a0001c0002t0004g0174a0001c0002t0004g0184others(7): Show | 10 | HG01884.hp2 HG02809.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+95_1825+118de others(25): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613578 | |||||
| chr19:613578
|
CGGGGATG others(47): Show |
C | 2 | a0001c0024t0002g0014a0001c0093t0003g0159 | 2 | HG01123.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1825+95_1825+148de others(55): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613578 | |||||
| chr19:613583
|
A | C | 82 | a0001c0001t0004g0387a0001c0001t0021g0217a0001c0002t0003g0009others(79): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1825+95A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613583 | ||||||
| chr19:613584
|
T | C | 82 | a0001c0001t0004g0387a0001c0001t0021g0217a0001c0002t0003g0009others(79): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1825+96T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613584 | ||||||
| chr19:613584
|
TGGGGATG others(17): Show |
T | 5 | a0001c0001t0001g0136a0001c0034t0026g0061a0005c0043t0006g0108others(2): Show | 5 | HG02129.hp2 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1825+119_1825+142d others(26): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613584 | |||||
| chr19:613586
|
G | A | 2 | a0001c0118t0011g0060a0002c0051t0011g0360 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1825+98G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613586 | ||||||
| chr19:613589
|
A | C | 4 | a0001c0018t0022g0039a0001c0041t0001g0019a0001c0046t0002g0037others(1): Show | 4 | HG00738.hp2 HG02257.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+101A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613589 | ||||||
| chr19:613590
|
T | C | 4 | a0001c0018t0022g0039a0001c0041t0001g0019a0001c0046t0002g0037others(1): Show | 4 | HG00738.hp2 HG02257.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+102T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613590 | ||||||
| chr19:613590
|
T | TGGGGATG others(77): Show |
1 | a0002c0038t0005g0338 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1825+115_1825+116i others(86): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613590 | |||||
| chr19:613590
|
T | TGGGGATG others(83): Show |
1 | a0002c0035t0005g0343 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1825+118_1825+119i others(92): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613590 | |||||
| chr19:613590
|
T | TGGGGATG others(89): Show |
13 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0034t0005g0035others(10): Show | 15 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1825+118_1825+119i others(98): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613590 | |||||
| chr19:613590
|
T | TGGGGATG others(83): Show |
1 | a0002c0028t0004g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1825+118_1825+119i others(92): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613590 | |||||
| chr19:613590
|
TGGGGATG others(41): Show |
T | 1 | a0002c0005t0003g0326 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1825+119_1825+166d others(50): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613590 | |||||
| chr19:613595
|
A | C | 2 | a0001c0018t0022g0039a0001c0041t0001g0019 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1825+107A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613595 | ||||||
| chr19:613596
|
T | C | 2 | a0001c0018t0022g0039a0001c0041t0001g0019 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1825+108T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613596 | ||||||
| chr19:613596
|
TGGGGATG others(35): Show |
T | 1 | a0001c0046t0002g0037 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1825+119_1825+160d others(44): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613596 | |||||
| chr19:613601
|
A | C | 26 | a0001c0001t0002g0169a0001c0003t0002g0210a0001c0003t0002g0232others(23): Show | 27 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1825+113A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613601 | ||||||
| chr19:613602
|
T | C | 26 | a0001c0001t0002g0169a0001c0003t0002g0210a0001c0003t0002g0232others(23): Show | 27 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1825+114T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613602 | ||||||
| chr19:613602
|
TGGGGCC | T | 9 | a0001c0001t0004g0168a0001c0002t0004g0092a0001c0002t0009g0116others(6): Show | 9 | HG00423.hp2 HG02257.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1825+119_1825+124d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613602 | |||||
| chr19:613607
|
C | A | 16 | a0001c0003t0001g0018a0001c0018t0022g0039a0001c0020t0008g0010others(13): Show | 16 | HG01168.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1825+119C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613607 | ||||||
| chr19:613608
|
C | CGGGGATG others(5): Show |
1 | a0002c0028t0005g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1825+137_1825+148d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613608 | |||||
| chr19:613608
|
C | T | 16 | a0001c0003t0001g0018a0001c0018t0022g0039a0001c0020t0008g0010others(13): Show | 16 | HG01168.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1825+120C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613608 | ||||||
| chr19:613608
|
CGGGGAT | C | 19 | a0001c0001t0001g0188a0001c0001t0002g0016a0001c0001t0002g0025others(16): Show | 19 | HG02451.hp1 HG02602.hp1 HG02965.hp2 others(16): Show |
intron_variant | MODIFIER | c.1825+143_1825+148d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613608 | |||||
| chr19:613608
|
CGGGGATG others(5): Show |
C | 7 | a0001c0008t0004g0385a0001c0014t0024g0248a0001c0018t0020g0058others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+137_1825+148d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613608 | |||||
| chr19:613608
|
CGGGGATG others(29): Show |
C | 12 | a0001c0002t0003g0093a0001c0002t0003g0094a0001c0002t0003g0098others(9): Show | 13 | HG00597.hp1 HG01255.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+137_1825+172d others(38): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613608 | |||||
| chr19:613608
|
CGGGGATG others(35): Show |
C | 3 | a0001c0001t0004g0387a0001c0003t0004g0012a0001c0026t0004g0051 | 3 | HG01891.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1825+131_1825+172d others(44): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613608 | |||||
| chr19:613608
|
CGGGGATG others(53): Show |
C | 1 | a0001c0006t0006g0249 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1825+131_1826-174d others(62): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613608 | |||||
| chr19:613613
|
A | C | 3 | a0001c0003t0001g0018a0002c0012t0001g0359a0002c0051t0011g0360 | 3 | HG02145.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1825+125A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613613 | ||||||
| chr19:613614
|
T | C | 3 | a0001c0003t0001g0018a0002c0012t0001g0359a0002c0051t0011g0360 | 3 | HG02145.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1825+126T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613614 | ||||||
| chr19:613614
|
TGGGGATG others(17): Show |
T | 40 | a0001c0002t0003g0009a0001c0002t0003g0074a0001c0002t0003g0078others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1825+167_1826-174d others(26): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613614 | |||||
| chr19:613614
|
TGGGGATG others(41): Show |
T | 13 | a0001c0001t0002g0055a0001c0001t0021g0217a0001c0003t0016g0384others(10): Show | 13 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+143_1826-174d others(50): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613614 | |||||
| chr19:613619
|
A | C | 20 | a0001c0001t0004g0168a0001c0002t0004g0092a0001c0002t0009g0116others(17): Show | 20 | HG00423.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1825+131A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613619 | ||||||
| chr19:613620
|
T | C | 20 | a0001c0001t0004g0168a0001c0002t0004g0092a0001c0002t0009g0116others(17): Show | 20 | HG00423.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1825+132T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613620 | ||||||
| chr19:613620
|
T | TGGGGATG others(56): Show |
1 | a0002c0005t0003g0276 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1825+139_1825+140i others(65): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613620 | |||||
| chr19:613620
|
TGGGGATG others(35): Show |
T | 1 | a0001c0014t0003g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1825+161_1826-162d others(44): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613620 | |||||
| chr19:613625
|
A | C | 14 | a0001c0001t0004g0068a0001c0001t0004g0229a0001c0020t0004g0030others(11): Show | 14 | HG01243.hp2 HG01952.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.1825+137A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613625 | ||||||
| chr19:613626
|
T | C | 14 | a0001c0001t0004g0068a0001c0001t0004g0229a0001c0020t0004g0030others(11): Show | 14 | HG01243.hp2 HG01952.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.1825+138T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613626 | ||||||
| chr19:613631
|
A | C | 5 | a0001c0003t0006g0201a0001c0032t0004g0374a0001c0042t0004g0015others(2): Show | 5 | HG02809.hp1 HG03139.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+143A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613631 | ||||||
| chr19:613632
|
T | C | 5 | a0001c0003t0006g0201a0001c0032t0004g0374a0001c0042t0004g0015others(2): Show | 5 | HG02809.hp1 HG03139.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+144T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613632 | ||||||
| chr19:613632
|
TGGGGCC | T | 7 | a0001c0001t0004g0068a0001c0001t0004g0229a0001c0020t0004g0030others(4): Show | 7 | HG01243.hp2 HG01978.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1825+149_1825+154d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613632 | |||||
| chr19:613637
|
C | A | 5 | a0001c0032t0004g0374a0001c0041t0001g0019a0001c0042t0004g0015others(2): Show | 5 | HG02257.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+149C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613637 | ||||||
| chr19:613638
|
C | T | 5 | a0001c0032t0004g0374a0001c0041t0001g0019a0001c0042t0004g0015others(2): Show | 5 | HG02257.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+150C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613638 | ||||||
| chr19:613638
|
CGGGGAT | C | 35 | a0001c0001t0002g0065a0001c0001t0002g0126a0001c0001t0002g0169others(32): Show | 36 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1825+167_1825+172d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613638 | |||||
| chr19:613638
|
CGGGGATG others(5): Show |
C | 7 | a0001c0002t0009g0116a0001c0032t0004g0381a0001c0041t0001g0099others(4): Show | 7 | HG00423.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1825+161_1825+172d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613638 | |||||
| chr19:613638
|
CGGGGATG others(23): Show |
C | 3 | a0002c0005t0003g0251a0002c0060t0003g0309a0003c0089t0003g0106 | 3 | HG01952.hp2 HG03579.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1825+161_1826-174d others(32): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613638 | |||||
| chr19:613638
|
CGGGGATG others(29): Show |
C | 2 | a0001c0003t0006g0201a0002c0016t0006g0292 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1825+155_1826-174d others(38): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613638 | |||||
| chr19:613643
|
A | C | 1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1825+155A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613643 | ||||||
| chr19:613644
|
T | C | 1 | a0001c0078t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1825+156T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613644 | ||||||
| chr19:613644
|
TGGGGATG others(11): Show |
T | 1 | a0002c0073t0001g0291 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1826-179_1826-162d others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613644 | |||||
| chr19:613644
|
TGGGGATG others(29): Show |
T | 13 | a0001c0001t0001g0188a0001c0001t0002g0016a0001c0001t0002g0025others(10): Show | 13 | HG02451.hp1 HG02602.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+167_1826-162d others(38): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613644 | |||||
| chr19:613649
|
A | C | 64 | a0001c0001t0004g0068a0001c0001t0004g0168a0001c0001t0004g0229others(61): Show | 64 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1825+161A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613649 | ||||||
| chr19:613649
|
A | G | 1 | a0002c0005t0003g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1825+161A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613649 | ||||||
| chr19:613650
|
T | C | 65 | a0001c0001t0004g0068a0001c0001t0004g0168a0001c0001t0004g0229others(62): Show | 65 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1825+162T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613650 | ||||||
| chr19:613655
|
A | C | 13 | a0001c0002t0004g0080a0001c0002t0004g0092a0001c0002t0004g0174others(10): Show | 13 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.1825+167A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613655 | ||||||
| chr19:613656
|
T | C | 13 | a0001c0002t0004g0080a0001c0002t0004g0092a0001c0002t0004g0174others(10): Show | 13 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.1825+168T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613656 | ||||||
| chr19:613661
|
C | A | 9 | a0001c0002t0004g0080a0001c0002t0004g0174a0001c0002t0004g0184others(6): Show | 9 | HG02809.hp2 HG03516.hp1 NA18522.hp1 others(6): Show |
intron_variant | MODIFIER | c.1825+173C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613661 | ||||||
| chr19:613662
|
C | T | 9 | a0001c0002t0004g0080a0001c0002t0004g0174a0001c0002t0004g0184others(6): Show | 9 | HG02809.hp2 HG03516.hp1 NA18522.hp1 others(6): Show |
intron_variant | MODIFIER | c.1825+174C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613662 | ||||||
| chr19:613662
|
CGGGGAT | C | 39 | a0001c0001t0002g0065a0001c0001t0002g0126a0001c0001t0002g0169others(36): Show | 40 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1826-179_1826-174d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613662 | |||||
| chr19:613663
|
G | A | 1 | a0001c0018t0001g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1825+175G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613663 | ||||||
| chr19:613667
|
A | C | 74 | a0001c0001t0004g0168a0001c0001t0021g0217a0001c0002t0003g0009others(71): Show | 74 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1825+179A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613667 | ||||||
| chr19:613668
|
T | C | 74 | a0001c0001t0004g0168a0001c0001t0021g0217a0001c0002t0003g0009others(71): Show | 74 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1825+180T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613668 | ||||||
| chr19:613668
|
TGGGGATG others(5): Show |
T | 23 | a0001c0001t0001g0157a0001c0001t0001g0178a0001c0001t0001g0182others(20): Show | 23 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1826-143_1826-132d others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613668 | |||||
| chr19:613673
|
A | C | 104 | a0001c0001t0004g0068a0001c0001t0004g0168a0001c0001t0004g0229others(101): Show | 105 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1826-179A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613673 | ||||||
| chr19:613674
|
T | C | 104 | a0001c0001t0004g0068a0001c0001t0004g0168a0001c0001t0004g0229others(101): Show | 105 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1826-178T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613674 | ||||||
| chr19:613679
|
C | A | 16 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0034t0005g0035others(13): Show | 18 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1826-173C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613679 | ||||||
| chr19:613680
|
C | T | 16 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0034t0005g0035others(13): Show | 18 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1826-172C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613680 | ||||||
| chr19:613681
|
G | A | 1 | a0001c0002t0004g0080 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1826-171G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613681 | ||||||
| chr19:613685
|
A | C | 150 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1826-167A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613685 | ||||||
| chr19:613686
|
T | C | 147 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1826-166T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613686 | ||||||
| chr19:613686
|
TGGGGCC | T | 7 | a0001c0001t0002g0055a0001c0003t0016g0384a0001c0006t0002g0244others(4): Show | 7 | HG01358.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-161_1826-156d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613686 | |||||
| chr19:613687
|
G | C | 3 | a0002c0004t0002g0279a0002c0053t0002g0300a0002c0057t0002g0260 | 3 | HG00280.hp2 HG00735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1826-165G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613687 | ||||||
| chr19:613691
|
C | A | 13 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0018t0022g0039others(10): Show | 14 | HG00099.hp1 HG00639.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1826-161C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613691 | ||||||
| chr19:613691
|
CCGG | C | 8 | a0001c0001t0001g0081a0001c0003t0001g0090a0001c0006t0001g0214others(5): Show | 8 | HG01934.hp1 HG02148.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-160_1826-158d others(5): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613691 | ||||||
| chr19:613692
|
C | T | 18 | a0001c0008t0004g0228a0001c0008t0004g0375a0001c0015t0005g0007others(15): Show | 19 | HG00099.hp1 HG00639.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1826-160C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613692 | ||||||
| chr19:613697
|
A | C | 143 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1826-155A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613697 | ||||||
| chr19:613698
|
T | C | 71 | a0001c0001t0002g0169a0001c0001t0004g0387a0001c0001t0021g0217others(68): Show | 72 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1826-154T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613698 | ||||||
| chr19:613703
|
C | A | 10 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0096t0003g0117others(7): Show | 11 | HG00099.hp1 HG00639.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1826-149C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613703 | ||||||
| chr19:613704
|
C | T | 10 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0096t0003g0117others(7): Show | 11 | HG00099.hp1 HG00639.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1826-148C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613704 | ||||||
| chr19:613706
|
G | GCACCGGC others(3): Show |
5 | a0001c0034t0005g0035a0002c0005t0003g0272a0002c0005t0003g0322others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1826-146_1826-145i others(12): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613706 | ||||||
| chr19:613707
|
G | C | 14 | a0001c0001t0004g0387a0001c0001t0021g0217a0001c0030t0004g0234others(11): Show | 14 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1826-145G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613707 | ||||||
| chr19:613708
|
G | A | 10 | a0001c0001t0004g0387a0001c0030t0004g0378a0001c0032t0004g0100others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1826-144G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613708 | ||||||
| chr19:613708
|
G | GCA | 5 | a0001c0034t0005g0035a0002c0005t0003g0272a0002c0005t0003g0322others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1826-144_1826-143i others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613708 | ||||||
| chr19:613709
|
A | C | 150 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(147): Show | 153 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1826-143A>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613709 | ||||||
| chr19:613710
|
T | C | 150 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(147): Show | 153 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1826-142T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613710 | ||||||
| chr19:613712
|
G | GCACC | 4 | a0001c0032t0004g0374a0001c0077t0004g0382a0001c0079t0004g0028others(1): Show | 4 | HG03041.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-140_1826-139i others(6): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613712 | ||||||
| chr19:613713
|
G | C | 143 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(140): Show | 146 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1826-139G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613713 | ||||||
| chr19:613714
|
G | A | 127 | a0001c0001t0002g0169a0001c0001t0004g0168a0001c0001t0004g0387others(124): Show | 130 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1826-138G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613714 | ||||||
| chr19:613714
|
G | GATGGGGA others(47): Show |
1 | a0002c0035t0005g0343 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1826-138_1826-137i others(56): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613714 | ||||||
| chr19:613714
|
G | GCA | 4 | a0001c0032t0004g0374a0001c0077t0004g0382a0001c0079t0004g0028others(1): Show | 4 | HG03041.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-137_1826-136i others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613714 | |||||
| chr19:613718
|
G | GCACCGGC others(9): Show |
1 | a0002c0038t0005g0338 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1826-134_1826-133i others(18): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613718 | ||||||
| chr19:613719
|
G | C | 148 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(145): Show | 151 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1826-133G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613719 | ||||||
| chr19:613720
|
G | A | 148 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(145): Show | 151 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1826-132G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613720 | ||||||
| chr19:613720
|
G | GATGGGGA others(59): Show |
1 | a0002c0035t0005g0349 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1826-132_1826-131i others(68): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613720 | ||||||
| chr19:613720
|
G | GATGGGGC others(29): Show |
9 | a0001c0015t0005g0007a0001c0015t0005g0144a0001c0096t0003g0117others(6): Show | 10 | HG00099.hp1 HG00639.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-132_1826-131i others(38): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613720 | ||||||
| chr19:613720
|
G | GCA | 3 | a0001c0006t0006g0249a0001c0093t0003g0159a0002c0038t0005g0338 | 3 | HG01123.hp1 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1826-131_1826-130i others(4): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613720 | |||||
| chr19:613720
|
G | GCCGGCAC others(5): Show |
1 | a0001c0041t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1826-124_1826-123i others(14): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613720 | |||||
| chr19:613720
|
G | GCCGGCAC others(11): Show |
1 | a0001c0018t0022g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1826-124_1826-123i others(20): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613720 | |||||
| chr19:613782
|
C | T | 1 | a0002c0004t0002g0279 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1826-70C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613782 | ||||||
| chr19:613821
|
C | G | 2 | a0001c0006t0004g0072a0002c0004t0004g0325 | 2 | NA19000.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1826-31C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613821 | ||||||
| chr19:613827
|
AC | A | 68 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0229others(65): Show | 71 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1826-17delC | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr19 | 613827 | |||||
| chr19:613830
|
C | A | 1 | a0001c0003t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1826-22C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613830 | ||||||
| chr19:613832
|
C | G | 2 | a0001c0002t0003g0145a0001c0045t0003g0006 | 3 | HG01255.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1826-20C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 6/7 | chr19 | 613832 | ||||||
| chr19:614020
|
A | AGCGGGCC others(27): Show |
1 | a0002c0010t0001g0363 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1990+10_1990+43dup others(34): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 614020 | |||||
| chr19:614028
|
G | GGGGGCGT others(27): Show |
132 | a0001c0001t0002g0169a0001c0001t0004g0068a0001c0001t0004g0168others(129): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1990+24_1990+57dup others(34): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 614028 | |||||
| chr19:614028
|
G | GGGGGCGT others(27): Show |
2 | a0001c0006t0002g0166a0002c0012t0013g0265 | 2 | HG01175.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1990+45_1990+46ins others(34): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 614028 | |||||
| chr19:614028
|
G | GGGGGGCG others(28): Show |
1 | a0001c0002t0004g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1990+16_1990+17ins others(35): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 614028 | |||||
| chr19:614029
|
G | GGGGCGTG others(27): Show |
1 | a0001c0002t0003g0093 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1990+46_1990+47ins others(34): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 614029 | |||||
| chr19:614044
|
C | CGGGTGCC others(27): Show |
10 | a0001c0018t0022g0039a0001c0032t0004g0100a0001c0032t0004g0374others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1990+57_1990+58ins others(34): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 614044 | |||||
| chr19:614056
|
C | G | 2 | a0001c0001t0002g0164a0001c0002t0003g0132 | 2 | NA18989.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1990+40C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614056 | ||||||
| chr19:614135
|
G | A | 15 | a0001c0001t0004g0068a0001c0001t0004g0229a0001c0020t0004g0030others(12): Show | 15 | HG01243.hp2 HG01978.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1990+119G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614135 | ||||||
| chr19:614193
|
C | T | 1 | a0001c0008t0004g0385 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1990+177C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614193 | ||||||
| chr19:614222
|
G | A | 15 | a0001c0001t0004g0068a0001c0001t0004g0229a0001c0020t0004g0030others(12): Show | 15 | HG01243.hp2 HG01978.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1990+206G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614222 | ||||||
| chr19:614233
|
C | T | 1 | a0001c0007t0001g0194 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1990+217C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614233 | ||||||
| chr19:614345
|
G | C | 9 | a0001c0001t0004g0387a0001c0003t0004g0012a0001c0003t0006g0201others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1990+329G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614345 | ||||||
| chr19:614387
|
G | T | 2 | a0001c0009t0002g0241a0002c0004t0001g0342 | 2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1990+371G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614387 | ||||||
| chr19:614403
|
C | T | 1 | a0001c0018t0020g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1990+387C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614403 | ||||||
| chr19:614454
|
G | A | 2 | a0001c0039t0001g0153a0007c0106t0002g0187 | 2 | NA18945.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1990+438G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614454 | ||||||
| chr19:614530
|
G | A | 1 | a0001c0032t0004g0381 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1990+514G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614530 | ||||||
| chr19:614538
|
G | A | 103 | a0001c0001t0004g0168a0001c0001t0004g0387a0001c0002t0003g0009others(100): Show | 104 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1990+522G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614538 | ||||||
| chr19:614684
|
G | A | 1 | a0001c0023t0001g0370 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1990+668G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614684 | ||||||
| chr19:614741
|
G | A | 9 | a0001c0020t0008g0010a0001c0020t0008g0013a0001c0034t0026g0061others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1990+725G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614741 | ||||||
| chr19:614772
|
C | T | 6 | a0001c0030t0004g0234a0001c0030t0004g0235a0001c0030t0004g0378others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1990+756C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614772 | ||||||
| chr19:614778
|
G | A | 7 | a0001c0001t0004g0168a0001c0008t0004g0228a0001c0008t0004g0375others(4): Show | 7 | HG02895.hp1 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1990+762G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614778 | ||||||
| chr19:614805
|
C | T | 90 | a0001c0001t0004g0068a0001c0001t0004g0168a0001c0001t0004g0229others(87): Show | 91 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1990+789C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614805 | ||||||
| chr19:614815
|
G | A | 1 | a0001c0034t0005g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1990+799G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614815 | ||||||
| chr19:614865
|
C | T | 92 | a0001c0001t0004g0068a0001c0001t0004g0168a0001c0001t0004g0229others(89): Show | 93 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1990+849C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614865 | ||||||
| chr19:614967
|
T | C | 127 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0055others(124): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1991-828T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 614967 | ||||||
| chr19:615107
|
A | G | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1991-688A>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615107 | ||||||
| chr19:615112
|
T | A | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1991-683T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615112 | ||||||
| chr19:615113
|
G | C | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1991-682G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615113 | ||||||
| chr19:615114
|
T | A | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1991-681T>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615114 | ||||||
| chr19:615119
|
C | T | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1991-676C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615119 | ||||||
| chr19:615154
|
G | C | 10 | a0001c0018t0022g0039a0001c0032t0004g0100a0001c0032t0004g0374others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1991-641G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615154 | ||||||
| chr19:615241
|
GGCTCAC | G | 67 | a0001c0002t0003g0009a0001c0002t0003g0074a0001c0002t0003g0078others(64): Show | 68 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1991-551_1991-546d others(8): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 615241 | |||||
| chr19:615247
|
C | T | 18 | a0001c0001t0021g0217a0001c0015t0005g0007a0001c0015t0005g0144others(15): Show | 20 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1991-548C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615247 | ||||||
| chr19:615255
|
G | A | 2 | a0001c0023t0004g0247a0002c0062t0004g0362 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1991-540G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615255 | ||||||
| chr19:615262
|
C | T | 18 | a0001c0001t0021g0217a0001c0015t0005g0007a0001c0015t0005g0144others(15): Show | 20 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1991-533C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615262 | ||||||
| chr19:615281
|
G | C | 4 | a0001c0006t0002g0020a0001c0018t0002g0052a0001c0026t0002g0057others(1): Show | 4 | HG02451.hp1 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1991-514G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615281 | ||||||
| chr19:615291
|
C | T | 1 | a0001c0088t0002g0399 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1991-504C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615291 | ||||||
| chr19:615325
|
T | C | 1 | a0002c0004t0003g0341 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1991-470T>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615325 | ||||||
| chr19:615333
|
C | A | 1 | a0002c0004t0007g0367 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1991-462C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615333 | ||||||
| chr19:615345
|
T | TA | 30 | a0001c0001t0001g0136a0001c0001t0004g0068a0001c0001t0004g0168others(27): Show | 30 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1991-440dupA | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 615345 | |||||
| chr19:615358
|
C | T | 1 | a0001c0002t0003g0156 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1991-437C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615358 | ||||||
| chr19:615453
|
G | C | 2 | a0001c0041t0001g0019a0019c0122t0004g0102 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1991-342G>C | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615453 | ||||||
| chr19:615468
|
C | T | 2 | a0001c0001t0001g0081a0001c0003t0001g0090 | 2 | NA18990.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1991-327C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615468 | ||||||
| chr19:615475
|
C | T | 2 | a0001c0032t0004g0100a0001c0032t0004g0374 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1991-320C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615475 | ||||||
| chr19:615563
|
G | A | 1 | a0002c0027t0003g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1991-232G>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615563 | ||||||
| chr19:615568
|
C | G | 113 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0055others(110): Show | 114 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1991-227C>G | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615568 | ||||||
| chr19:615740
|
C | A | 1 | a0001c0018t0020g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1991-55C>A | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615740 | ||||||
| chr19:615770
|
C | T | 5 | a0001c0030t0004g0234a0001c0030t0004g0235a0002c0054t0004g0250others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1991-25C>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615770 | ||||||
| chr19:615791
|
G | T | 2 | a0001c0002t0003g0145a0001c0045t0003g0006 | 3 | HG01255.hp2 HG03491.hp1 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.1991-4G>T | HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 7/7 | chr19 | 615791 |