Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 29915 |
|---|---|
| ensemblid | ENSG00000111727.12 |
| hgncid | 24972 |
| symbol | HCFC2 |
| name | host cell factor C2 |
| refseq_nuc | NM_013320.3 |
| refseq_prot | NP_037452.1 |
| ensembl_nuc | ENST00000229330.9 |
| ensembl_prot | ENSP00000229330.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 104064531 |
| end | 104106524 |
| strand | + |
| ver | v1.2 |
| region | chr12:104064531-104106524 |
| region5000 | chr12:104059531-104111524 |
| regionname0 | HCFC2_chr12_104064531_104106524 |
| regionname5000 | HCFC2_chr12_104059531_104111524 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 792 | 375 | 91 | 62 | 168 | 14 | 38 | 132 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0002 | 0/0 | 792 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0003 | 0/0 | 792 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0004 | 0/0 | 792 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0005 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2379 | 372 | 89 | 62 | 167 | 14 | 38 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| c0002 | 0/0 | 2379 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| c0003 | 0/0 | 2379 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| c0004 | 0/0 | 2379 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| c0005 | 0/0 | 2379 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| c0006 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| c0007 | 0/0 | 2379 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3282 | 154 | 54 | 45 | 32 | 8 | 14 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0002 | 0/0 | 3282 | 58 | 1 | 4 | 47 | 0 | 6 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0003 | 0/0 | 3282 | 56 | 13 | 3 | 35 | 1 | 4 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0004 | 0/0 | 3283 | 52 | 14 | 7 | 22 | 3 | 6 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0005 | 0/0 | 3282 | 11 | 0 | 0 | 11 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0006 | 0/0 | 3283 | 11 | 0 | 3 | 8 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0007 | 0/1 | 3284 | 8 | 0 | 1 | 0 | 2 | 4 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0008 | 0/0 | 3284 | 5 | 1 | 0 | 2 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0009 | 0/0 | 3282 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0010 | 0/0 | 3281 | 4 | 2 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0011 | 0/0 | 3282 | 4 | 0 | 0 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0012 | 0/0 | 3281 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0013 | 0/0 | 3282 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0014 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0015 | 0/0 | 3285 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0016 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0017 | 0/0 | 3283 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0018 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0019 | 0/0 | 3281 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0020 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0021 | 0/0 | 3284 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| t0022 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 14 | 1 | 7 | 4 | 1 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0002 | 0/0 | 14 | 1 | 0 | 13 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0003 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0004 | 0/0 | 10 | 1 | 2 | 7 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0006 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0007 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0017 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0019 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0023 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0042 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2379 | 372 | 89 | 62 | 167 | 14 | 38 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0002 | 0/0 | 2379 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0006 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0002c0003 | 0/0 | 2379 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0003c0004 | 0/0 | 2379 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0004c0005 | 0/0 | 2379 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0005c0007 | 0/0 | 2379 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5660 | 148 | 49 | 44 | 32 | 8 | 14 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0002 | 0/0 | 5660 | 58 | 1 | 4 | 47 | 0 | 6 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0003 | 0/0 | 5660 | 56 | 13 | 3 | 35 | 1 | 4 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0004 | 0/0 | 5661 | 52 | 14 | 7 | 22 | 3 | 6 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0005 | 0/0 | 5660 | 11 | 0 | 0 | 11 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0006 | 0/0 | 5661 | 10 | 0 | 2 | 8 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0007 | 0/1 | 5662 | 7 | 0 | 1 | 0 | 2 | 3 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0008 | 0/0 | 5662 | 4 | 1 | 0 | 1 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0009 | 0/0 | 5660 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0010 | 0/0 | 5659 | 4 | 2 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0011 | 0/0 | 5660 | 4 | 0 | 0 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0012 | 0/0 | 5659 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0013 | 0/0 | 5660 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0014 | 0/0 | 5661 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0016 | 0/0 | 5660 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0017 | 0/0 | 5661 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0018 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0019 | 0/0 | 5659 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0020 | 0/0 | 5661 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0021 | 0/0 | 5662 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0001t0022 | 0/0 | 5660 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0002t0001 | 0/0 | 5660 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0001c0006t0008 | 0/0 | 5662 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0002c0003t0001 | 0/0 | 5660 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0003c0004t0001 | 0/0 | 5660 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0004c0005t0007 | 0/0 | 5662 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0004c0005t0015 | 0/0 | 5663 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| a0005c0007t0006 | 0/0 | 5661 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | copy fasta | chr12 | 104059531 | 104111524 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 1 | 7 | 4 | 1 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0007 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0004 | 0/0 | 9 | 1 | 2 | 6 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0002 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0042 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0009g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0011g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0011g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0013g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0014g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0017g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0018g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0019g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0021g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0022g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0002t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0006t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0002c0003t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0003c0004t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0004c0005t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0004c0005t0015g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0005c0007t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0017 | EUR | GBR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0202 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0195 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00673 | hp1 | a0001 | c0001 | t0012 | g0083 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0201 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01168 | hp1 | a0001 | c0001 | t0022 | g0164 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0204 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0026 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0026 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0062 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01928 | hp1 | a0005 | c0007 | t0006 | g0005 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0137 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0071 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02074 | hp1 | a0001 | c0001 | t0012 | g0084 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02080 | hp1 | a0001 | c0006 | t0008 | g0002 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02129 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CDX | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02257 | hp1 | a0001 | c0001 | t0021 | g0056 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0200 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02523 | hp1 | a0001 | c0001 | t0016 | g0034 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02683 | hp2 | a0001 | c0001 | t0019 | g0079 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0042 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02698 | hp2 | a0001 | c0001 | t0013 | g0040 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02738 | hp2 | a0004 | c0005 | t0015 | g0141 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0036 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0136 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0178 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0206 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0191 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0017 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03834 | hp2 | a0004 | c0005 | t0007 | g0140 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0139 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0138 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04204 | hp2 | a0001 | c0001 | t0013 | g0040 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18612 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0058 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18985 | hp1 | a0001 | c0001 | t0010 | g0113 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19000 | hp2 | a0001 | c0001 | t0011 | g0122 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19059 | hp1 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19059 | hp2 | a0001 | c0001 | t0012 | g0085 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19065 | hp2 | a0001 | c0001 | t0011 | g0118 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19076 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19083 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ASW | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0044 | EUR | TSI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02486 | hp1 | a0003 | c0004 | t0001 | g0036 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0042 | REF | REF | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0124 | REF | REF | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104067989
|
C | T | 1 | a0004 | 2 | HG02738.hp2 HG03834.hp2 |
missense_variant | MODERATE | c.355C>T | p.Pro119Ser | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/15 | 385/5660 | 355/2379 | 119/792 | chr12 | 104067989 | ||
| chr12:104082535
|
G | C | 1 | a0002 | 2 | HG01081.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.803G>C | p.Gly268Ala | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 6/15 | 833/5660 | 803/2379 | 268/792 | chr12 | 104082535 | ||
| chr12:104093474
|
C | T | 1 | a0005 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1373C>T | p.Thr458Met | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/15 | 1403/5660 | 1373/2379 | 458/792 | chr12 | 104093474 | ||
| chr12:104093484
|
T | A | 1 | a0003 | 2 | HG02486.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.1383T>A | p.Asn461Lys | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/15 | 1413/5660 | 1383/2379 | 461/792 | chr12 | 104093484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104066276
|
T | G | 1 | a0001c0002 | 2 | HG03225.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.273T>G | p.Val91Val | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/15 | 303/5660 | 273/2379 | 91/792 | chr12 | 104066276 | ||
| chr12:104098363
|
A | G | 1 | a0001c0006 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1761A>G | p.Pro587Pro | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/15 | 1791/5660 | 1761/2379 | 587/792 | chr12 | 104098363 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104103823
|
A | T | 1 | a0001c0001t0009 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*550A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 550 | chr12 | 104103823 | |||||
| chr12:104103885
|
G | T | 1 | a0001c0001t0022 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 612 | chr12 | 104103885 | |||||
| chr12:104104591
|
A | G | 5 | a0001c0001t0003a0001c0001t0006a0001c0001t0021others(2): Show | 69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1318A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 1318 | chr12 | 104104591 | |||||
| chr12:104105195
|
T | TA | 5 | a0001c0001t0007a0001c0001t0014a0001c0001t0021others(2): Show | 11 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1926dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 1927 | INFO_REALIGN_3_PRIME | chr12 | 104105195 | ||||
| chr12:104105299
|
T | C | 4 | a0001c0001t0002a0001c0001t0012a0001c0001t0016others(1): Show | 63 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2026T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2026 | chr12 | 104105299 | |||||
| chr12:104105545
|
A | G | 1 | a0001c0001t0020 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2272A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2272 | chr12 | 104105545 | |||||
| chr12:104105579
|
A | AT | 8 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(5): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2322dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2323 | INFO_REALIGN_3_PRIME | chr12 | 104105579 | ||||
| chr12:104105579
|
A | ATT | 3 | a0001c0001t0008a0001c0006t0008a0004c0005t0015 | 6 | HG02080.hp1 HG02738.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2321_*2322dupTT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2323 | INFO_REALIGN_3_PRIME | chr12 | 104105579 | ||||
| chr12:104105579
|
AT | A | 3 | a0001c0001t0010a0001c0001t0012a0001c0001t0019 | 8 | HG00673.hp1 HG01884.hp2 HG02074.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2322delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2322 | INFO_REALIGN_3_PRIME | chr12 | 104105579 | ||||
| chr12:104105583
|
T | A | 1 | a0001c0001t0018 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2310T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2310 | chr12 | 104105583 | |||||
| chr12:104106107
|
A | T | 2 | a0001c0001t0013a0001c0001t0019 | 3 | HG02683.hp2 HG02698.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2834A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2834 | chr12 | 104106107 | |||||
| chr12:104106113
|
T | C | 1 | a0001c0001t0011 | 4 | NA18612.hp1 NA19000.hp2 NA19065.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2840T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2840 | chr12 | 104106113 | |||||
| chr12:104106361
|
T | C | 1 | a0001c0001t0005 | 11 | NA18945.hp2 NA18954.hp2 NA18959.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3088T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 3088 | chr12 | 104106361 | |||||
| chr12:104106432
|
T | A | 1 | a0001c0001t0016 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3159T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 3159 | chr12 | 104106432 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104064742
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.163+19C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064742 | ||||||
| chr12:104064776
|
G | T | 1 | a0001c0001t0004g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163+53G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064776 | ||||||
| chr12:104064919
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.163+196C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064919 | ||||||
| chr12:104064965
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.163+242C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064965 | ||||||
| chr12:104065300
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.163+577G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065300 | ||||||
| chr12:104065382
|
G | T | 9 | a0001c0001t0001g0051a0001c0001t0001g0232a0001c0001t0001g0233others(6): Show | 11 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+659G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065382 | ||||||
| chr12:104065386
|
G | C | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.163+663G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065386 | ||||||
| chr12:104065446
|
T | C | 3 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0007g0026 | 4 | HG01516.hp2 HG01517.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-721T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065446 | ||||||
| chr12:104065667
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.164-500A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065667 | ||||||
| chr12:104065828
|
G | A | 1 | a0001c0001t0021g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.164-339G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065828 | ||||||
| chr12:104065947
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-220G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065947 | ||||||
| chr12:104066033
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(42): Show | 59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-134A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104066033 | ||||||
| chr12:104066124
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-43C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104066124 | ||||||
| chr12:104066127
|
T | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(42): Show | 59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-40T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104066127 | ||||||
| chr12:104066389
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.312+74A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066389 | ||||||
| chr12:104066404
|
T | C | 1 | a0001c0001t0010g0058 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.312+89T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066404 | ||||||
| chr12:104066434
|
GTATTATT others(9): Show |
G | 44 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0023others(41): Show | 69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.312+134_312+149del others(16): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 104066434 | |||||
| chr12:104066450
|
C | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(35): Show | 61 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.312+135C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066450 | ||||||
| chr12:104066502
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.312+187T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066502 | ||||||
| chr12:104066593
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.312+278T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066593 | ||||||
| chr12:104066772
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0004g0059 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.312+457T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066772 | ||||||
| chr12:104066856
|
C | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+541C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066856 | ||||||
| chr12:104066873
|
C | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+558C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066873 | ||||||
| chr12:104067133
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0239a0001c0001t0010g0019 | 4 | HG00323.hp1 HG00738.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-814G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067133 | ||||||
| chr12:104067156
|
T | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(126): Show | 191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.313-791T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067156 | ||||||
| chr12:104067459
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG01109.hp2 HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.313-488C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067459 | ||||||
| chr12:104067551
|
A | G | 1 | a0001c0001t0003g0173 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.313-396A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067551 | ||||||
| chr12:104067604
|
T | G | 1 | a0001c0001t0014g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-343T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067604 | ||||||
| chr12:104067689
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.313-258A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067689 | ||||||
| chr12:104067762
|
C | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0130others(3): Show | 9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-185C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067762 | ||||||
| chr12:104068159
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(43): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.473+52C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068159 | ||||||
| chr12:104068402
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0175 | 4 | HG02723.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+295T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068402 | ||||||
| chr12:104068596
|
A | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(35): Show | 61 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.473+489A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068596 | ||||||
| chr12:104068636
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.473+529T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068636 | ||||||
| chr12:104069038
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0064others(4): Show | 11 | HG00642.hp2 HG01192.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.473+931G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069038 | ||||||
| chr12:104069115
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 5 | HG02109.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+1008G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069115 | ||||||
| chr12:104069525
|
TA | T | 43 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0024others(40): Show | 58 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.473+1433delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104069525 | |||||
| chr12:104069604
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0004g0017a0001c0001t0004g0176others(5): Show | 9 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+1497G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069604 | ||||||
| chr12:104069720
|
T | C | 1 | a0001c0001t0004g0181 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.473+1613T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069720 | ||||||
| chr12:104070027
|
A | G | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+1920A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070027 | ||||||
| chr12:104070035
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.473+1928T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070035 | ||||||
| chr12:104070093
|
T | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(247): Show | 373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.473+1986T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070093 | ||||||
| chr12:104070130
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.473+2023C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070130 | ||||||
| chr12:104070260
|
CCT | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+2155_473+2156d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104070260 | |||||
| chr12:104070769
|
T | A | 1 | a0001c0001t0002g0069 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.473+2662T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070769 | ||||||
| chr12:104070801
|
C | CT | 50 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(47): Show | 74 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.473+2715dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104070801 | |||||
| chr12:104071007
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0114others(7): Show | 14 | HG01074.hp1 HG01256.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.473+2900C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071007 | ||||||
| chr12:104071024
|
T | A | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.473+2917T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071024 | ||||||
| chr12:104071049
|
G | A | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+2942G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071049 | ||||||
| chr12:104071276
|
C | A | 1 | a0001c0001t0002g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.473+3169C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071276 | ||||||
| chr12:104071360
|
A | G | 1 | a0001c0001t0003g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.473+3253A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071360 | ||||||
| chr12:104071571
|
CCTAA | C | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+3468_473+3471d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104071571 | |||||
| chr12:104071576
|
CTATTTTA others(3): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.473+3486_473+3495d others(12): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104071576 | |||||
| chr12:104071679
|
C | A | 1 | a0001c0001t0002g0027 | 2 | NA18971.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.473+3572C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071679 | ||||||
| chr12:104072046
|
A | G | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+3939A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072046 | ||||||
| chr12:104072198
|
C | T | 1 | a0001c0001t0001g0025 | 3 | NA18612.hp2 NA18950.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.473+4091C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072198 | ||||||
| chr12:104072270
|
G | C | 1 | a0001c0001t0003g0142 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.473+4163G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072270 | ||||||
| chr12:104072368
|
TA | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(73): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.473+4278delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104072368 | |||||
| chr12:104072443
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.473+4336A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072443 | ||||||
| chr12:104072502
|
G | A | 1 | a0001c0001t0004g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.473+4395G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072502 | ||||||
| chr12:104072523
|
A | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01071.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.473+4416A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072523 | ||||||
| chr12:104072608
|
T | C | 29 | a0001c0001t0003g0003a0001c0001t0003g0043a0001c0001t0003g0142others(26): Show | 46 | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.473+4501T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072608 | ||||||
| chr12:104072700
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.473+4593T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072700 | ||||||
| chr12:104072733
|
C | G | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.473+4626C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072733 | ||||||
| chr12:104072787
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0130others(3): Show | 9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+4680C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072787 | ||||||
| chr12:104072869
|
C | T | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+4762C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072869 | ||||||
| chr12:104072889
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.473+4782C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072889 | ||||||
| chr12:104073109
|
T | G | 4 | a0001c0001t0004g0086a0001c0001t0012g0083a0001c0001t0012g0084others(1): Show | 4 | HG00408.hp1 HG00673.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+5002T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073109 | ||||||
| chr12:104073110
|
C | G | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+5003C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073110 | ||||||
| chr12:104073167
|
C | CT | 24 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0021others(21): Show | 42 | HG00438.hp1 HG00544.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.473+5075dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104073167 | |||||
| chr12:104073167
|
CTTT | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+5073_473+5075d others(5): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104073167 | |||||
| chr12:104073187
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(34): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.473+5080C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073187 | ||||||
| chr12:104073291
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(174): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.473+5184G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073291 | ||||||
| chr12:104073405
|
C | T | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+5298C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073405 | ||||||
| chr12:104073410
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0010g0062 | 2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.473+5303G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073410 | ||||||
| chr12:104073417
|
C | A | 1 | a0001c0001t0003g0044 | 2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.473+5310C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073417 | ||||||
| chr12:104073723
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(41): Show | 58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.473+5616C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073723 | ||||||
| chr12:104073742
|
G | A | 1 | a0001c0001t0002g0020 | 3 | HG00558.hp2 HG04228.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.473+5635G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073742 | ||||||
| chr12:104073834
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.474-5611A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073834 | ||||||
| chr12:104074041
|
C | G | 1 | a0001c0001t0011g0118 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.474-5404C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074041 | ||||||
| chr12:104074278
|
G | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG01109.hp2 HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.474-5167G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074278 | ||||||
| chr12:104074529
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.474-4916G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074529 | ||||||
| chr12:104074791
|
A | T | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.474-4654A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074791 | ||||||
| chr12:104075090
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG02486.hp2 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.474-4355C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075090 | ||||||
| chr12:104075195
|
T | TA | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(179): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.474-4238dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075195 | |||||
| chr12:104075195
|
T | TAA | 4 | a0001c0001t0003g0023a0001c0001t0003g0044a0001c0001t0003g0163others(1): Show | 7 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-4239_474-4238d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075195 | |||||
| chr12:104075289
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-4156T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075289 | ||||||
| chr12:104075298
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-4147C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075298 | ||||||
| chr12:104075304
|
A | G | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-4141A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075304 | ||||||
| chr12:104075457
|
C | CT | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(146): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.474-3970dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075457 | |||||
| chr12:104075457
|
C | CTT | 37 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(34): Show | 56 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.474-3971_474-3970d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075457 | |||||
| chr12:104075584
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.474-3861G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075584 | ||||||
| chr12:104075651
|
G | A | 2 | a0001c0001t0004g0182a0001c0001t0004g0204 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.474-3794G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075651 | ||||||
| chr12:104075659
|
C | A | 1 | a0001c0001t0002g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.474-3786C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075659 | ||||||
| chr12:104075826
|
AT | A | 5 | a0001c0001t0006g0005a0001c0001t0006g0144a0001c0001t0006g0145others(2): Show | 10 | HG01123.hp2 HG01928.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-3610delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075826 | |||||
| chr12:104075835
|
T | G | 5 | a0001c0001t0006g0005a0001c0001t0006g0144a0001c0001t0006g0145others(2): Show | 10 | HG01123.hp2 HG01928.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-3610T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075835 | ||||||
| chr12:104075939
|
G | T | 1 | a0001c0001t0002g0121 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.474-3506G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075939 | ||||||
| chr12:104075940
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.474-3505C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075940 | ||||||
| chr12:104076433
|
A | AT | 129 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(126): Show | 191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.474-3010dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104076433 | |||||
| chr12:104076477
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.474-2968G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076477 | ||||||
| chr12:104076655
|
T | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-2790T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076655 | ||||||
| chr12:104076693
|
TCTGCATT others(85): Show |
T | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0217others(7): Show | 14 | HG00558.hp1 HG02015.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-2721_474-2630d others(94): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104076693 | |||||
| chr12:104076879
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.474-2566T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076879 | ||||||
| chr12:104076944
|
A | C | 1 | a0001c0001t0002g0106 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.474-2501A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076944 | ||||||
| chr12:104076983
|
C | T | 3 | a0001c0001t0002g0105a0004c0005t0007g0140a0004c0005t0015g0141 | 3 | HG02738.hp2 HG03834.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.474-2462C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076983 | ||||||
| chr12:104077074
|
A | G | 2 | a0001c0001t0004g0201a0001c0001t0004g0202 | 2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.474-2371A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077074 | ||||||
| chr12:104077103
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.474-2342G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077103 | ||||||
| chr12:104077252
|
T | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-2193T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077252 | ||||||
| chr12:104077263
|
G | A | 1 | a0001c0001t0014g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.474-2182G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077263 | ||||||
| chr12:104077550
|
G | GT | 6 | a0001c0001t0001g0066a0001c0001t0002g0104a0001c0001t0004g0198others(3): Show | 6 | HG00438.hp2 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-1878dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104077550 | |||||
| chr12:104077550
|
G | GTTT | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-1880_474-1878d others(5): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104077550 | |||||
| chr12:104077550
|
GT | G | 50 | a0001c0001t0001g0232a0001c0001t0002g0089a0001c0001t0002g0090others(47): Show | 75 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.474-1878delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104077550 | |||||
| chr12:104077567
|
T | A | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-1878T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077567 | ||||||
| chr12:104077568
|
A | T | 1 | a0001c0001t0010g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474-1877A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077568 | ||||||
| chr12:104077840
|
A | T | 1 | a0001c0001t0020g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.474-1605A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077840 | ||||||
| chr12:104077885
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(185): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.474-1560C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077885 | ||||||
| chr12:104077939
|
G | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-1506G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077939 | ||||||
| chr12:104078067
|
T | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-1378T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078067 | ||||||
| chr12:104078161
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 7 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-1284G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078161 | ||||||
| chr12:104078281
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0003g0165 | 2 | HG02818.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.474-1164G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078281 | ||||||
| chr12:104078283
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.474-1162G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078283 | ||||||
| chr12:104078339
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 6 | HG01081.hp2 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-1106G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078339 | ||||||
| chr12:104078343
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-1102A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078343 | ||||||
| chr12:104078397
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-1048A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078397 | ||||||
| chr12:104078554
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0121 | 3 | HG02523.hp2 NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.474-891A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078554 | ||||||
| chr12:104078587
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-858A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078587 | ||||||
| chr12:104078678
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.474-767T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078678 | ||||||
| chr12:104078786
|
G | A | 5 | a0001c0001t0003g0011a0001c0001t0003g0054a0001c0001t0003g0055others(2): Show | 9 | HG01943.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-659G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078786 | ||||||
| chr12:104078855
|
C | T | 9 | a0001c0001t0001g0051a0001c0001t0001g0232a0001c0001t0001g0233others(6): Show | 11 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.474-590C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078855 | ||||||
| chr12:104078918
|
C | A | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-527C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078918 | ||||||
| chr12:104078995
|
C | A | 1 | a0001c0001t0002g0106 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.474-450C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078995 | ||||||
| chr12:104078996
|
A | G | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-449A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078996 | ||||||
| chr12:104079088
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.474-357A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104079088 | ||||||
| chr12:104079125
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.474-320G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104079125 | ||||||
| chr12:104079333
|
G | A | 1 | a0001c0001t0010g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.474-112G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104079333 | ||||||
| chr12:104079696
|
A | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0130others(6): Show | 12 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+43A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104079696 | ||||||
| chr12:104079769
|
C | A | 1 | a0001c0001t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.682+116C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104079769 | ||||||
| chr12:104079941
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(39): Show | 71 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.682+288A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104079941 | ||||||
| chr12:104080218
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 5 | HG02109.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-528A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080218 | ||||||
| chr12:104080221
|
T | C | 3 | a0001c0001t0014g0136a0004c0005t0007g0140a0004c0005t0015g0141 | 3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.683-525T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080221 | ||||||
| chr12:104080392
|
G | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(35): Show | 61 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.683-354G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080392 | ||||||
| chr12:104080585
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.683-161G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080585 | ||||||
| chr12:104080952
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.767+122G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104080952 | ||||||
| chr12:104081067
|
G | C | 1 | a0001c0001t0001g0028 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.767+237G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081067 | ||||||
| chr12:104081102
|
T | G | 1 | a0001c0001t0004g0183 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.767+272T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081102 | ||||||
| chr12:104081600
|
G | GT | 18 | a0001c0001t0001g0051a0001c0001t0001g0232a0001c0001t0001g0233others(15): Show | 26 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.767+786dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081600 | |||||
| chr12:104081600
|
GT | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0064others(10): Show | 16 | HG01257.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.767+786delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081600 | |||||
| chr12:104081624
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.767+794C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081624 | ||||||
| chr12:104081852
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(38): Show | 55 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.768-648C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081852 | ||||||
| chr12:104081904
|
C | CA | 9 | a0001c0001t0001g0080a0001c0001t0001g0114a0001c0001t0002g0109others(6): Show | 9 | HG00621.hp2 HG00673.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-575dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081904 | |||||
| chr12:104081904
|
CA | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(33): Show | 57 | HG00323.hp2 HG00558.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.768-575delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081904 | |||||
| chr12:104081904
|
CAA | C | 9 | a0001c0001t0004g0228a0001c0001t0007g0026a0001c0001t0007g0042others(6): Show | 11 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.768-576_768-575del others(2): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081904 | |||||
| chr12:104081939
|
TA | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-550delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081939 | |||||
| chr12:104082167
|
A | G | 1 | a0001c0001t0003g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.768-333A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082167 | ||||||
| chr12:104082399
|
C | T | 4 | a0001c0001t0004g0195a0001c0001t0004g0201a0001c0001t0004g0202others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-101C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082399 | ||||||
| chr12:104082477
|
G | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0209a0001c0001t0001g0212 | 8 | HG00735.hp1 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.768-23G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082477 | ||||||
| chr12:104082486
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(34): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.768-14T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082486 | ||||||
| chr12:104082675
|
G | A | 10 | a0001c0001t0003g0011a0001c0001t0003g0023a0001c0001t0003g0044others(7): Show | 17 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.875-38G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 6/14 | chr12 | 104082675 | ||||||
| chr12:104083044
|
T | C | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+143T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083044 | ||||||
| chr12:104083291
|
G | A | 1 | a0004c0005t0007g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1063+390G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083291 | ||||||
| chr12:104083497
|
C | T | 1 | a0004c0005t0015g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1063+596C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083497 | ||||||
| chr12:104083554
|
T | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0134 | 2 | HG01106.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1063+653T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083554 | ||||||
| chr12:104083615
|
A | G | 44 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0023others(41): Show | 69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1063+714A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083615 | ||||||
| chr12:104083892
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0004g0049 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063+991C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083892 | ||||||
| chr12:104083896
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(35): Show | 61 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1063+995T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083896 | ||||||
| chr12:104083963
|
A | G | 4 | a0001c0001t0004g0195a0001c0001t0004g0201a0001c0001t0004g0202others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+1062A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083963 | ||||||
| chr12:104083971
|
T | G | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1063+1070T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083971 | ||||||
| chr12:104084036
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1063+1135G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084036 | ||||||
| chr12:104084103
|
G | A | 5 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(2): Show | 7 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063+1202G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084103 | ||||||
| chr12:104084178
|
T | C | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+1277T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084178 | ||||||
| chr12:104084638
|
G | C | 1 | a0001c0001t0004g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1063+1737G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084638 | ||||||
| chr12:104084965
|
A | G | 1 | a0004c0005t0007g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1064-1882A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084965 | ||||||
| chr12:104085012
|
A | G | 44 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0023others(41): Show | 69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1064-1835A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085012 | ||||||
| chr12:104085122
|
A | C | 1 | a0001c0001t0003g0043 | 2 | NA18988.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1064-1725A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085122 | ||||||
| chr12:104085287
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(42): Show | 59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1064-1560A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085287 | ||||||
| chr12:104085736
|
T | TTG | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(243): Show | 369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1064-1110_1064-110 others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104085736 | |||||
| chr12:104085885
|
C | G | 1 | a0001c0001t0004g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1064-962C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085885 | ||||||
| chr12:104085995
|
A | AT | 34 | a0001c0001t0001g0038a0001c0001t0001g0072a0001c0001t0001g0081others(31): Show | 42 | HG00673.hp2 HG01081.hp2 HG01361.hp2 others(39): Show |
intron_variant | MODIFIER | c.1064-832dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104085995 | |||||
| chr12:104085995
|
AT | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0095a0001c0001t0004g0178others(4): Show | 9 | HG01496.hp1 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1064-832delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104085995 | |||||
| chr12:104086050
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1064-797T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086050 | ||||||
| chr12:104086058
|
T | TG | 26 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0025others(23): Show | 38 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1064-788dupG | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086058 | |||||
| chr12:104086127
|
A | G | 3 | a0001c0001t0014g0136a0004c0005t0007g0140a0004c0005t0015g0141 | 3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1064-720A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086127 | ||||||
| chr12:104086484
|
C | G | 1 | a0001c0001t0003g0044 | 2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1064-363C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086484 | ||||||
| chr12:104086619
|
A | AAAAT | 80 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0021others(77): Show | 115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1064-194_1064-191d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | |||||
| chr12:104086619
|
A | AAAATAAA others(1): Show |
45 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0077others(42): Show | 75 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1064-198_1064-191d others(10): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | |||||
| chr12:104086619
|
A | AAAATAAA others(5): Show |
5 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0003g0146others(2): Show | 6 | HG01516.hp2 HG01517.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064-202_1064-191d others(14): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | |||||
| chr12:104086619
|
AAAAT | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(33): Show | 53 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1064-194_1064-191d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | |||||
| chr12:104086619
|
AAAATAAA others(5): Show |
A | 10 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0080others(7): Show | 24 | HG00438.hp1 HG00544.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1064-202_1064-191d others(14): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | |||||
| chr12:104086714
|
A | G | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1064-133A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086714 | ||||||
| chr12:104086716
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0175 | 4 | HG02723.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-131C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086716 | ||||||
| chr12:104087121
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1231+107G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087121 | ||||||
| chr12:104087249
|
G | A | 1 | a0003c0004t0001g0036 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1231+235G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087249 | ||||||
| chr12:104087352
|
TA | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(180): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1231+355delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087352 | |||||
| chr12:104087375
|
A | G | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+361A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087375 | ||||||
| chr12:104087402
|
C | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231+388C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087402 | ||||||
| chr12:104087409
|
ACGTG | A | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+396_1231+399d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087409 | ||||||
| chr12:104087410
|
CGT | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(86): Show | 127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1231+427_1231+428d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | |||||
| chr12:104087410
|
CGTGT | C | 50 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0092others(47): Show | 77 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1231+425_1231+428d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | |||||
| chr12:104087410
|
CGTGTGT | C | 8 | a0001c0001t0002g0069a0001c0001t0003g0165a0001c0001t0003g0167others(5): Show | 10 | HG00423.hp1 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231+423_1231+428d others(8): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | |||||
| chr12:104087410
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0003g0142a0001c0001t0014g0136a0004c0005t0007g0140others(1): Show | 4 | HG02738.hp2 HG03209.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231+421_1231+428d others(10): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | |||||
| chr12:104087410
|
CGTGTGTG others(3): Show |
C | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 63 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1231+419_1231+428d others(12): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | |||||
| chr12:104087410
|
CGTGTGTG others(15): Show |
C | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1231+407_1231+428d others(24): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | |||||
| chr12:104087414
|
T | A | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+400T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087414 | ||||||
| chr12:104087437
|
G | A | 2 | a0001c0001t0007g0138a0001c0001t0007g0139 | 2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1231+423G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087437 | ||||||
| chr12:104087439
|
GTGTA | G | 3 | a0001c0001t0001g0223a0001c0001t0007g0138a0001c0001t0007g0139 | 3 | HG00673.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1231+429_1231+432d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087439 | |||||
| chr12:104087443
|
A | G | 10 | a0001c0001t0001g0061a0001c0001t0005g0012a0001c0001t0005g0210others(7): Show | 14 | HG01884.hp2 HG02257.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1231+429A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087443 | ||||||
| chr12:104087443
|
ATG | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(17): Show | 33 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1231+439_1231+440d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087443 | |||||
| chr12:104087445
|
G | A | 10 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0005g0012others(7): Show | 14 | HG00673.hp2 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1231+431G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087445 | ||||||
| chr12:104087447
|
G | A | 1 | a0001c0001t0010g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1231+433G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087447 | ||||||
| chr12:104087455
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0010g0062 | 2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1231+441A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087455 | ||||||
| chr12:104087457
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0010g0062 | 2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1231+443A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087457 | ||||||
| chr12:104087466
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1231+452C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087466 | ||||||
| chr12:104087466
|
CAT | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0029others(57): Show | 87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1231+469_1231+470d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087466 | |||||
| chr12:104087466
|
CATAT | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(150): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1231+467_1231+470d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087466 | |||||
| chr12:104087466
|
CATATAT | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(27): Show | 47 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.1231+465_1231+470d others(8): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087466 | |||||
| chr12:104087467
|
A | ATG | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1231+454_1231+455i others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087467 | |||||
| chr12:104087468
|
T | TATATATA others(15): Show |
1 | a0001c0001t0002g0031 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1231+468_1231+469i others(24): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087468 | |||||
| chr12:104087470
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1231+456T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087470 | ||||||
| chr12:104087470
|
T | TATATATA others(17): Show |
1 | a0001c0001t0007g0137 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1231+466_1231+467i others(26): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087470 | |||||
| chr12:104087470
|
T | TATATATA others(45): Show |
1 | a0001c0001t0022g0164 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1231+466_1231+467i others(54): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087470 | |||||
| chr12:104087471
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+470_1231+483d others(16): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087471 | |||||
| chr12:104087472
|
T | C | 1 | a0001c0001t0010g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1231+458T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087472 | ||||||
| chr12:104087479
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1231+465A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087479 | ||||||
| chr12:104087484
|
T | C | 1 | a0001c0001t0002g0031 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1231+470T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087484 | ||||||
| chr12:104087496
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1231+482T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087496 | ||||||
| chr12:104087652
|
T | C | 3 | a0001c0001t0012g0083a0001c0001t0012g0084a0001c0001t0012g0085 | 3 | HG00673.hp1 HG02074.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.1232-334T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087652 | ||||||
| chr12:104087716
|
G | A | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1232-270G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087716 | ||||||
| chr12:104087913
|
T | C | 4 | a0001c0001t0004g0195a0001c0001t0004g0201a0001c0001t0004g0202others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1232-73T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087913 | ||||||
| chr12:104088150
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1284+112C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088150 | ||||||
| chr12:104088232
|
T | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(39): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1284+194T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088232 | ||||||
| chr12:104088463
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(79): Show | 119 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1284+425G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088463 | ||||||
| chr12:104088520
|
T | C | 1 | a0001c0001t0020g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1284+482T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088520 | ||||||
| chr12:104088599
|
G | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(34): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1284+561G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088599 | ||||||
| chr12:104088769
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1284+731G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088769 | ||||||
| chr12:104088919
|
G | C | 1 | a0001c0001t0002g0096 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1284+881G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088919 | ||||||
| chr12:104089015
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1284+977T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089015 | ||||||
| chr12:104089043
|
A | C | 1 | a0001c0001t0005g0210 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1284+1005A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089043 | ||||||
| chr12:104089103
|
C | T | 3 | a0001c0001t0014g0136a0004c0005t0007g0140a0004c0005t0015g0141 | 3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1284+1065C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089103 | ||||||
| chr12:104089104
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG01109.hp2 HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+1066G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089104 | ||||||
| chr12:104089143
|
C | A | 1 | a0001c0001t0004g0189 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1284+1105C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089143 | ||||||
| chr12:104089171
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1284+1133G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089171 | ||||||
| chr12:104089448
|
G | A | 2 | a0001c0001t0004g0185a0001c0001t0004g0192 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1284+1410G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089448 | ||||||
| chr12:104089649
|
C | T | 1 | a0001c0001t0014g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1284+1611C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089649 | ||||||
| chr12:104089659
|
T | G | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+1621T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089659 | ||||||
| chr12:104089795
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0010g0019 | 3 | HG00738.hp2 HG03490.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1284+1757T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089795 | ||||||
| chr12:104089816
|
C | G | 1 | a0001c0001t0010g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1284+1778C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089816 | ||||||
| chr12:104089837
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1284+1799C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089837 | ||||||
| chr12:104089850
|
A | T | 1 | a0001c0001t0003g0155 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1284+1812A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089850 | ||||||
| chr12:104090022
|
G | A | 5 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(2): Show | 7 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284+1984G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090022 | ||||||
| chr12:104090164
|
T | A | 5 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(2): Show | 7 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284+2126T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090164 | ||||||
| chr12:104090198
|
A | G | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284+2160A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090198 | ||||||
| chr12:104090268
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1284+2230A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090268 | ||||||
| chr12:104090284
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1284+2246C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090284 | ||||||
| chr12:104090497
|
C | CT | 36 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(33): Show | 55 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1284+2469dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 104090497 | |||||
| chr12:104090698
|
C | CA | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(35): Show | 61 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1284+2665dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 104090698 | |||||
| chr12:104090942
|
G | T | 2 | a0001c0001t0004g0182a0001c0001t0004g0204 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1285-2444G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090942 | ||||||
| chr12:104090960
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1285-2426T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090960 | ||||||
| chr12:104090986
|
T | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(39): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1285-2400T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090986 | ||||||
| chr12:104091014
|
G | A | 1 | a0001c0001t0004g0047 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1285-2372G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091014 | ||||||
| chr12:104091026
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(39): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1285-2360G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091026 | ||||||
| chr12:104091190
|
A | G | 3 | a0001c0001t0003g0023a0001c0001t0003g0163a0001c0001t0022g0164 | 5 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285-2196A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091190 | ||||||
| chr12:104091449
|
C | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-1937C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091449 | ||||||
| chr12:104091500
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1285-1886G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091500 | ||||||
| chr12:104091592
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(41): Show | 58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1285-1794G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091592 | ||||||
| chr12:104091744
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1285-1642T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091744 | ||||||
| chr12:104091984
|
A | C | 1 | a0001c0001t0001g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1285-1402A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091984 | ||||||
| chr12:104092151
|
G | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-1235G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104092151 | ||||||
| chr12:104092185
|
C | T | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-1201C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104092185 | ||||||
| chr12:104092255
|
C | G | 1 | a0001c0001t0003g0150 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1285-1131C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104092255 | ||||||
| chr12:104093026
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1285-360C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104093026 | ||||||
| chr12:104093270
|
G | A | 1 | a0001c0001t0004g0186 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1285-116G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104093270 | ||||||
| chr12:104093621
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1462+58G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093621 | ||||||
| chr12:104093776
|
A | AT | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(233): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1462+227dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 104093776 | |||||
| chr12:104093779
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1462+216T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093779 | ||||||
| chr12:104093799
|
G | GCTGTTAC others(370): Show |
1 | a0001c0001t0001g0132 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1462+237_1462+238i others(379): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 104093799 | |||||
| chr12:104093827
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1462+264A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093827 | ||||||
| chr12:104093946
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1462+383C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093946 | ||||||
| chr12:104093968
|
C | G | 2 | a0001c0001t0002g0033a0001c0001t0002g0102 | 3 | NA18947.hp2 NA19004.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1462+405C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093968 | ||||||
| chr12:104094058
|
G | A | 1 | a0001c0001t0003g0148 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1462+495G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094058 | ||||||
| chr12:104094102
|
T | C | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1462+539T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094102 | ||||||
| chr12:104094172
|
A | G | 1 | a0001c0001t0020g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1462+609A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094172 | ||||||
| chr12:104094200
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1462+637C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094200 | ||||||
| chr12:104094214
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1462+651T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094214 | ||||||
| chr12:104094380
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0004g0059 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1462+817C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094380 | ||||||
| chr12:104094403
|
C | A | 2 | a0001c0001t0001g0061a0001c0001t0010g0062 | 2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1462+840C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094403 | ||||||
| chr12:104094692
|
A | G | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463-668A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094692 | ||||||
| chr12:104095100
|
AT | A | 43 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0023others(40): Show | 68 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1463-257delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 104095100 | |||||
| chr12:104095128
|
C | T | 5 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(2): Show | 7 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463-232C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095128 | ||||||
| chr12:104095147
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0130others(3): Show | 9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463-213G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095147 | ||||||
| chr12:104095149
|
A | G | 4 | a0001c0001t0003g0023a0001c0001t0003g0044a0001c0001t0003g0163others(1): Show | 7 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463-211A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095149 | ||||||
| chr12:104095187
|
C | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0130others(3): Show | 9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463-173C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095187 | ||||||
| chr12:104095243
|
G | C | 1 | a0001c0001t0007g0138 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1463-117G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095243 | ||||||
| chr12:104095342
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(42): Show | 59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1463-18T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095342 | ||||||
| chr12:104095623
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1666+60C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104095623 | ||||||
| chr12:104095884
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0209a0001c0001t0001g0212 | 8 | HG00735.hp1 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1666+321C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104095884 | ||||||
| chr12:104095925
|
A | G | 1 | a0001c0001t0004g0047 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1666+362A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104095925 | ||||||
| chr12:104096267
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1667-93C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104096267 | ||||||
| chr12:104096287
|
A | G | 1 | a0002c0003t0001g0039 | 2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1667-73A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104096287 | ||||||
| chr12:104096563
|
A | C | 1 | a0001c0001t0009g0010 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1740+130A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096563 | ||||||
| chr12:104096814
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1740+381G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096814 | ||||||
| chr12:104096824
|
A | C | 1 | a0001c0001t0001g0212 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1740+391A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096824 | ||||||
| chr12:104096875
|
G | A | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1740+442G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096875 | ||||||
| chr12:104096891
|
A | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0130others(6): Show | 12 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1740+458A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096891 | ||||||
| chr12:104096929
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(39): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1740+496G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096929 | ||||||
| chr12:104097014
|
A | G | 1 | a0001c0001t0010g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1740+581A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097014 | ||||||
| chr12:104097130
|
T | G | 10 | a0001c0001t0001g0022a0001c0001t0001g0133a0001c0001t0007g0026others(7): Show | 14 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1740+697T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097130 | ||||||
| chr12:104097200
|
C | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 310 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.1740+767C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097200 | ||||||
| chr12:104097266
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1740+833C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097266 | ||||||
| chr12:104097496
|
CT | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(41): Show | 58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1741-837delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 104097496 | |||||
| chr12:104097512
|
TAA | T | 50 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0037others(47): Show | 74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1741-829_1741-828d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 104097512 | |||||
| chr12:104097770
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1741-573G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097770 | ||||||
| chr12:104098070
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1741-273A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104098070 | ||||||
| chr12:104098169
|
C | G | 4 | a0001c0001t0002g0009a0001c0001t0002g0088a0001c0001t0002g0091others(1): Show | 8 | NA18951.hp2 NA18973.hp2 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741-174C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104098169 | ||||||
| chr12:104098225
|
A | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0029others(62): Show | 94 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1741-118A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104098225 | ||||||
| chr12:104098321
|
AT | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0232a0001c0001t0001g0233others(2): Show | 6 | HG02615.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741-13delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 104098321 | |||||
| chr12:104098682
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1878+202G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098682 | ||||||
| chr12:104098691
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0095 | 2 | HG01496.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1878+211G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098691 | ||||||
| chr12:104098857
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(83): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1878+377A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098857 | ||||||
| chr12:104098860
|
C | T | 5 | a0001c0001t0001g0115a0001c0001t0003g0023a0001c0001t0003g0044others(2): Show | 8 | HG00639.hp2 HG01074.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1878+380C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098860 | ||||||
| chr12:104098935
|
G | A | 1 | a0001c0001t0003g0154 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1878+455G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098935 | ||||||
| chr12:104099161
|
T | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1878+681T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099161 | ||||||
| chr12:104099269
|
T | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0004g0017others(9): Show | 13 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1878+789T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099269 | ||||||
| chr12:104099301
|
C | T | 65 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0029others(62): Show | 94 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1878+821C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099301 | ||||||
| chr12:104099403
|
A | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(5): Show | 10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1878+923A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099403 | ||||||
| chr12:104099437
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 7 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1878+957C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099437 | ||||||
| chr12:104099516
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1878+1036G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099516 | ||||||
| chr12:104099617
|
T | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0018others(72): Show | 108 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1878+1137T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099617 | ||||||
| chr12:104099908
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1878+1428C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099908 | ||||||
| chr12:104100040
|
C | T | 3 | a0001c0001t0014g0136a0004c0005t0007g0140a0004c0005t0015g0141 | 3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1878+1560C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100040 | ||||||
| chr12:104100074
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1878+1594A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100074 | ||||||
| chr12:104100084
|
A | T | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1878+1604A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100084 | ||||||
| chr12:104100197
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1878+1717C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100197 | ||||||
| chr12:104100316
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1879-1652C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100316 | ||||||
| chr12:104100320
|
C | T | 1 | a0001c0001t0002g0032 | 2 | NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1879-1648C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100320 | ||||||
| chr12:104100377
|
G | A | 5 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(2): Show | 7 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1879-1591G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100377 | ||||||
| chr12:104100518
|
G | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0121 | 3 | HG02523.hp2 NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1879-1450G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100518 | ||||||
| chr12:104100558
|
A | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1879-1410A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100558 | ||||||
| chr12:104100593
|
T | C | 1 | a0001c0001t0021g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1879-1375T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100593 | ||||||
| chr12:104100648
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1879-1320C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100648 | ||||||
| chr12:104100757
|
G | C | 5 | a0001c0001t0007g0026a0001c0001t0007g0042a0001c0001t0007g0137others(2): Show | 7 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1879-1211G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100757 | ||||||
| chr12:104101056
|
CTCTG | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(26): Show | 46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1879-908_1879-905d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 104101056 | |||||
| chr12:104101135
|
G | A | 1 | a0001c0001t0011g0122 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1879-833G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104101135 | ||||||
| chr12:104101506
|
G | A | 3 | a0001c0001t0014g0136a0004c0005t0007g0140a0004c0005t0015g0141 | 3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1879-462G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104101506 | ||||||
| chr12:104102496
|
A | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(77): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2064+343A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102496 | ||||||
| chr12:104102505
|
G | C | 3 | a0001c0001t0014g0136a0004c0005t0007g0140a0004c0005t0015g0141 | 3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2064+352G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102505 | ||||||
| chr12:104102584
|
T | C | 1 | a0004c0005t0007g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2065-375T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102584 | ||||||
| chr12:104102649
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2065-310G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102649 | ||||||
| chr12:104102844
|
T | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 7 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2065-115T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102844 | ||||||
| chr12:104102942
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2065-17T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102942 | ||||||
| chr12:104102943
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0174 | 3 | HG01074.hp1 HG02818.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2065-16T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102943 | ||||||
| chr12:104102943
|
T | TC | 35 | a0001c0001t0001g0041a0001c0001t0001g0130a0001c0001t0001g0131others(32): Show | 53 | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(50): Show |
splice_region_variant&intron_variant | LOW | c.2065-7dupC | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 104102943 | |||||
| chr12:104102946
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0049others(39): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2065-13C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102946 | ||||||
| chr12:104102949
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2065-10C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102949 |