Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10664 |
|---|---|
| ensemblid | ENSG00000102974.16 |
| hgncid | 13723 |
| symbol | CTCF |
| name | CCCTC-binding factor |
| refseq_nuc | NM_006565.4 |
| refseq_prot | NP_006556.1 |
| ensembl_nuc | ENST00000264010.10 |
| ensembl_prot | ENSP00000264010.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 67562526 |
| end | 67639177 |
| strand | + |
| ver | v1.2 |
| region | chr16:67562526-67639177 |
| region5000 | chr16:67557526-67644177 |
| regionname0 | CTCF_chr16_67562526_67639177 |
| regionname5000 | CTCF_chr16_67557526_67644177 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 727 | 168 | 78 | 36 | 26 | 8 | 18 | 12 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1631 | 120 | 51 | 28 | 19 | 7 | 13 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0002 | 0/0 | 1631 | 17 | 9 | 4 | 3 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0003 | 0/0 | 1631 | 8 | 4 | 0 | 0 | 0 | 4 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0004 | 0/0 | 1630 | 8 | 8 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0005 | 0/0 | 1631 | 4 | 0 | 3 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0006 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0007 | 0/0 | 1631 | 2 | 2 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0008 | 0/0 | 1631 | 2 | 0 | 0 | 2 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0009 | 0/0 | 1631 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0010 | 0/0 | 1631 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0011 | 0/0 | 1631 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0012 | 0/0 | 1631 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| t0013 | 0/0 | 1631 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2184 | 167 | 78 | 36 | 26 | 8 | 17 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0002 | 0/0 | 2184 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3814 | 120 | 51 | 28 | 19 | 7 | 13 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0002 | 0/0 | 3814 | 17 | 9 | 4 | 3 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0003 | 0/0 | 3814 | 7 | 4 | 0 | 0 | 0 | 3 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0004 | 0/0 | 3813 | 8 | 8 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0005 | 0/0 | 3814 | 4 | 0 | 3 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0006 | 0/0 | 3812 | 2 | 2 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0007 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0008 | 0/0 | 3814 | 2 | 0 | 0 | 2 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0009 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0010 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0011 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0012 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0001t0013 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| a0001c0002t0003 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | copy fasta | chr16 | 67557526 | 67644177 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0012g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0001t0013g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0166 | EAS | CHS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0045 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02040 | hp2 | a0001 | c0001 | t0012 | g0091 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02074 | hp2 | a0001 | c0001 | t0008 | g0128 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0016 | EAS | KHV | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0102 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ESN | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0142 | SAS | PJL | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | STU | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0042 | EUR | TSI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | USA | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | USA | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | USA | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0083 | REF | REF | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67610850
|
C | T | 1 | a0001c0002 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.18C>T | p.Val6Val | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 3/12 | 343/3814 | 18/2184 | 6/727 | chr16 | 67610850 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67562579
|
C | G | 2 | a0001c0001t0005a0001c0001t0013 | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-272C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/12 | 48254 | chr16 | 67562579 | |||||
| chr16:67571222
|
G | A | 2 | a0001c0001t0003a0001c0002t0003 | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-52G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/12 | 39611 | chr16 | 67571222 | |||||
| chr16:67637892
|
G | A | 1 | a0001c0001t0009 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 20 | chr16 | 67637892 | |||||
| chr16:67637901
|
T | G | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*29T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 29 | chr16 | 67637901 | |||||
| chr16:67637925
|
C | T | 1 | a0001c0001t0013 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 53 | chr16 | 67637925 | |||||
| chr16:67637944
|
C | T | 1 | a0001c0001t0007 | 2 | HG02486.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*72C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 72 | chr16 | 67637944 | |||||
| chr16:67638270
|
G | C | 1 | a0001c0001t0011 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 398 | chr16 | 67638270 | |||||
| chr16:67638305
|
T | A | 1 | a0001c0001t0008 | 2 | HG02074.hp2 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*433T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 433 | chr16 | 67638305 | |||||
| chr16:67638318
|
CT | C | 1 | a0001c0001t0004 | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*449delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 449 | INFO_REALIGN_3_PRIME | chr16 | 67638318 | ||||
| chr16:67638398
|
G | A | 1 | a0001c0001t0010 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*526G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 526 | chr16 | 67638398 | |||||
| chr16:67638606
|
C | G | 1 | a0001c0001t0012 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*734C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 734 | chr16 | 67638606 | |||||
| chr16:67638914
|
CAT | C | 1 | a0001c0001t0006 | 2 | HG03209.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1043_*1044delAT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 12/12 | 1043 | chr16 | 67638914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67562856
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-127+132C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67562856 | ||||||
| chr16:67562912
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-127+188C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67562912 | ||||||
| chr16:67562921
|
ACGCC | A | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.-127+217_-127+220d others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67562921 | |||||
| chr16:67563046
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-127+322C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67563046 | ||||||
| chr16:67563171
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-127+447C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67563171 | ||||||
| chr16:67563181
|
C | T | 1 | a0001c0001t0010g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-127+457C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67563181 | ||||||
| chr16:67563300
|
C | T | 13 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(10): Show | 13 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-127+576C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67563300 | ||||||
| chr16:67563318
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0008g0128 | 2 | HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-127+594A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67563318 | ||||||
| chr16:67563321
|
T | C | 2 | a0001c0001t0007g0129a0001c0001t0007g0130 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-127+597T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67563321 | ||||||
| chr16:67563455
|
GGCTGGCT others(19): Show |
G | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-127+736_-127+761d others(28): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67563455 | |||||
| chr16:67564313
|
G | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-127+1589G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67564313 | ||||||
| chr16:67564371
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-127+1647A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67564371 | ||||||
| chr16:67564530
|
G | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(20): Show | 23 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-127+1806G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67564530 | ||||||
| chr16:67564541
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-127+1817C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67564541 | ||||||
| chr16:67564640
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-127+1916T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67564640 | ||||||
| chr16:67564732
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-127+2008A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67564732 | ||||||
| chr16:67565064
|
C | T | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-127+2340C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67565064 | ||||||
| chr16:67565293
|
C | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-127+2569C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67565293 | ||||||
| chr16:67565645
|
C | T | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-127+2921C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67565645 | ||||||
| chr16:67565666
|
CT | C | 63 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(60): Show | 63 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.-127+2944delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67565666 | |||||
| chr16:67565673
|
C | CA | 14 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 14 | HG01243.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-127+2970dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67565673 | |||||
| chr16:67565673
|
C | CAAA | 5 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(2): Show | 5 | HG01361.hp2 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+2968_-127+297 others(7): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67565673 | |||||
| chr16:67565756
|
G | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-127+3032G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67565756 | ||||||
| chr16:67565783
|
TCTAAGAG | T | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(8): Show | 11 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-127+3062_-127+306 others(11): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67565783 | |||||
| chr16:67565795
|
A | T | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(8): Show | 11 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-127+3071A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67565795 | ||||||
| chr16:67565897
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-127+3173G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67565897 | ||||||
| chr16:67565928
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-127+3204C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67565928 | ||||||
| chr16:67566125
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-127+3401C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67566125 | ||||||
| chr16:67566446
|
G | GTTGC | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+3723_-127+372 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67566446 | |||||
| chr16:67566515
|
T | TA | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(24): Show | 27 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-127+3816dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67566515 | |||||
| chr16:67566515
|
TA | T | 26 | a0001c0001t0001g0023a0001c0001t0001g0040a0001c0001t0001g0103others(23): Show | 26 | HG01109.hp1 HG01433.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-127+3816delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67566515 | |||||
| chr16:67566515
|
TAA | T | 7 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0161others(4): Show | 7 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127+3815_-127+381 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67566515 | |||||
| chr16:67566646
|
G | T | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-127+3922G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67566646 | ||||||
| chr16:67566805
|
T | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+4081T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67566805 | ||||||
| chr16:67566876
|
GGTTT | G | 8 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(5): Show | 8 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+4165_-127+416 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67566876 | |||||
| chr16:67567126
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-126-4022C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67567126 | ||||||
| chr16:67567305
|
T | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-126-3843T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67567305 | ||||||
| chr16:67567515
|
T | C | 1 | a0001c0001t0004g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-126-3633T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67567515 | ||||||
| chr16:67567705
|
T | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-126-3443T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67567705 | ||||||
| chr16:67567890
|
C | CT | 21 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0046others(18): Show | 21 | HG01070.hp1 HG01243.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-126-3233dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67567890 | |||||
| chr16:67567890
|
C | CTT | 9 | a0001c0001t0002g0134a0001c0001t0002g0147a0001c0001t0002g0148others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-126-3234_-126-323 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67567890 | |||||
| chr16:67567890
|
C | CTTT | 13 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152others(10): Show | 13 | HG00438.hp2 HG02027.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-3235_-126-323 others(7): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67567890 | |||||
| chr16:67567890
|
CT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(49): Show | 52 | HG00738.hp1 HG00741.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.-126-3233delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67567890 | |||||
| chr16:67568001
|
G | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-126-3147G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568001 | ||||||
| chr16:67568002
|
C | G | 24 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(21): Show | 24 | HG00438.hp2 HG00639.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-126-3146C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568002 | ||||||
| chr16:67568032
|
T | C | 1 | a0001c0001t0003g0143 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-126-3116T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568032 | ||||||
| chr16:67568077
|
C | T | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-3071C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568077 | ||||||
| chr16:67568092
|
A | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-3056A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568092 | ||||||
| chr16:67568094
|
T | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-126-3054T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568094 | ||||||
| chr16:67568233
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-126-2915C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568233 | ||||||
| chr16:67568316
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-126-2832G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568316 | ||||||
| chr16:67568420
|
C | T | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-2728C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568420 | ||||||
| chr16:67568718
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG02622.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-126-2430C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568718 | ||||||
| chr16:67568747
|
T | TTTGA | 2 | a0001c0001t0006g0131a0001c0001t0006g0135 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-126-2400_-126-239 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67568747 | |||||
| chr16:67568841
|
ACT | A | 9 | a0001c0001t0001g0017a0001c0001t0004g0158a0001c0001t0004g0159others(6): Show | 9 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-126-2304_-126-230 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67568841 | |||||
| chr16:67568876
|
T | C | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-126-2272T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568876 | ||||||
| chr16:67568909
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-126-2239C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67568909 | ||||||
| chr16:67569027
|
G | C | 2 | a0001c0001t0002g0168a0001c0001t0009g0154 | 2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-126-2121G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569027 | ||||||
| chr16:67569336
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-126-1812C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569336 | ||||||
| chr16:67569374
|
C | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-1774C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569374 | ||||||
| chr16:67569375
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-126-1773G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569375 | ||||||
| chr16:67569419
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108 | 3 | HG02109.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-126-1729C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569419 | ||||||
| chr16:67569544
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-126-1604C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569544 | ||||||
| chr16:67569637
|
T | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-126-1511T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569637 | ||||||
| chr16:67569683
|
T | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG01433.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-126-1465T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569683 | ||||||
| chr16:67569960
|
A | C | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-126-1188A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67569960 | ||||||
| chr16:67570076
|
A | AT | 11 | a0001c0001t0001g0098a0001c0001t0002g0144a0001c0001t0002g0145others(8): Show | 11 | HG00438.hp2 HG01109.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-126-1054dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67570076 | |||||
| chr16:67570076
|
AT | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0067a0001c0001t0001g0103others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-1054delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67570076 | |||||
| chr16:67570145
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-126-1003C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67570145 | ||||||
| chr16:67570170
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-126-978G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67570170 | ||||||
| chr16:67570285
|
T | G | 7 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0055others(4): Show | 7 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-863T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67570285 | ||||||
| chr16:67570341
|
A | G | 2 | a0001c0001t0006g0131a0001c0001t0006g0135 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-126-807A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67570341 | ||||||
| chr16:67570443
|
GTGTTT | G | 5 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(2): Show | 5 | HG01433.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-693_-126-689d others(7): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67570443 | |||||
| chr16:67570450
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0072 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-126-698G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67570450 | ||||||
| chr16:67570587
|
G | A | 4 | a0001c0001t0001g0050a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG01255.hp2 HG01975.hp2 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126-561G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67570587 | ||||||
| chr16:67570740
|
C | CT | 34 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0046others(31): Show | 34 | HG00438.hp2 HG00639.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.-126-387dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67570740 | |||||
| chr16:67570740
|
C | CTT | 5 | a0001c0001t0002g0133a0001c0001t0002g0145a0001c0001t0004g0163others(2): Show | 5 | HG01109.hp1 HG01433.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-388_-126-387d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 67570740 | |||||
| chr16:67570927
|
C | T | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-221C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 1/11 | chr16 | 67570927 | ||||||
| chr16:67571428
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10+164C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67571428 | ||||||
| chr16:67571603
|
A | G | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+339A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67571603 | ||||||
| chr16:67571891
|
C | T | 83 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(80): Show | 83 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.-10+627C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67571891 | ||||||
| chr16:67572405
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0005g0041a0001c0001t0005g0042others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+1141G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67572405 | ||||||
| chr16:67572944
|
C | CCCCG | 11 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0034others(8): Show | 11 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+1682_-10+1683i others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67572944 | |||||
| chr16:67572945
|
C | CCCG | 20 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0029others(17): Show | 20 | HG00438.hp1 HG01175.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+1682_-10+1683i others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67572945 | |||||
| chr16:67572946
|
C | CCG | 14 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0022others(11): Show | 14 | HG00438.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+1682_-10+1683i others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67572946 | ||||||
| chr16:67572947
|
G | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(55): Show | 58 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-10+1683G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67572947 | ||||||
| chr16:67572947
|
G | GC | 24 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(21): Show | 24 | HG01074.hp1 HG01074.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+1694dupC | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67572947 | |||||
| chr16:67572947
|
G | GCC | 33 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 33 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.-10+1693_-10+1694d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67572947 | |||||
| chr16:67572947
|
G | GCCC | 15 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0067others(12): Show | 15 | HG01346.hp1 HG01975.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1692_-10+1694d others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67572947 | |||||
| chr16:67572947
|
G | GCCCC | 11 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0057others(8): Show | 11 | HG01496.hp2 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+1691_-10+1694d others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67572947 | |||||
| chr16:67572949
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-10+1685C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67572949 | ||||||
| chr16:67572979
|
G | A | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+1715G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67572979 | ||||||
| chr16:67573319
|
C | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+2055C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67573319 | ||||||
| chr16:67573384
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0051 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-10+2120A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67573384 | ||||||
| chr16:67573887
|
C | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+2623C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67573887 | ||||||
| chr16:67573945
|
C | T | 24 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(21): Show | 24 | HG00438.hp2 HG00639.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+2681C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67573945 | ||||||
| chr16:67573992
|
C | G | 1 | a0001c0001t0005g0044 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-10+2728C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67573992 | ||||||
| chr16:67574084
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(1): Show | 4 | HG01175.hp1 HG01515.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2820A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574084 | ||||||
| chr16:67574198
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-10+2934C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574198 | ||||||
| chr16:67574495
|
C | G | 1 | a0001c0001t0013g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-10+3231C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574495 | ||||||
| chr16:67574650
|
C | CT | 18 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0046others(15): Show | 18 | HG00741.hp1 HG01109.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10+3412dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67574650 | |||||
| chr16:67574650
|
CT | C | 15 | a0001c0001t0001g0037a0001c0001t0001g0068a0001c0001t0002g0134others(12): Show | 15 | HG02027.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10+3412delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67574650 | |||||
| chr16:67574695
|
G | A | 1 | a0001c0001t0007g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-10+3431G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574695 | ||||||
| chr16:67574777
|
G | A | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+3513G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574777 | ||||||
| chr16:67574882
|
C | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-10+3618C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574882 | ||||||
| chr16:67574936
|
C | T | 16 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(13): Show | 16 | HG00438.hp2 HG00639.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10+3672C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574936 | ||||||
| chr16:67574945
|
C | G | 1 | a0001c0001t0002g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10+3681C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67574945 | ||||||
| chr16:67575032
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-10+3768G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67575032 | ||||||
| chr16:67575197
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-10+3933C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67575197 | ||||||
| chr16:67575403
|
TGGGCA | T | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+4146_-10+4150d others(7): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67575403 | |||||
| chr16:67575540
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-10+4276G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67575540 | ||||||
| chr16:67575596
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-10+4332C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67575596 | ||||||
| chr16:67575989
|
T | TA | 10 | a0001c0001t0001g0022a0001c0001t0001g0068a0001c0001t0001g0095others(7): Show | 10 | HG01175.hp1 HG01175.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+4746dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67575989 | |||||
| chr16:67575989
|
TA | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(4): Show | 7 | HG00738.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+4746delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67575989 | |||||
| chr16:67576015
|
G | A | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+4751G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67576015 | ||||||
| chr16:67576038
|
G | A | 2 | a0001c0001t0006g0131a0001c0001t0006g0135 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-10+4774G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67576038 | ||||||
| chr16:67576140
|
T | TA | 36 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0024others(33): Show | 36 | HG00438.hp1 HG01109.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10+4898dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67576140 | |||||
| chr16:67576140
|
T | TAA | 7 | a0001c0001t0002g0133a0001c0001t0002g0134a0001c0001t0002g0146others(4): Show | 7 | HG01433.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+4897_-10+4898d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67576140 | |||||
| chr16:67576152
|
A | AC | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+4888_-10+4889i others(3): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67576152 | ||||||
| chr16:67576163
|
C | A | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+4899C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67576163 | ||||||
| chr16:67576324
|
G | A | 1 | a0001c0001t0007g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-10+5060G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67576324 | ||||||
| chr16:67576550
|
G | GT | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0022others(40): Show | 43 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-10+5307dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67576550 | |||||
| chr16:67576550
|
G | GTT | 8 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0104others(5): Show | 8 | HG01361.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+5306_-10+5307d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67576550 | |||||
| chr16:67576550
|
GT | G | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108others(5): Show | 8 | HG00741.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5307delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67576550 | |||||
| chr16:67576556
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-10+5292T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67576556 | ||||||
| chr16:67576944
|
G | A | 4 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+5680G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67576944 | ||||||
| chr16:67577051
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-10+5787G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577051 | ||||||
| chr16:67577144
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108 | 3 | HG02109.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-10+5880C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577144 | ||||||
| chr16:67577145
|
G | A | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5881G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577145 | ||||||
| chr16:67577329
|
A | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0121 | 3 | HG01192.hp2 HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-10+6065A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577329 | ||||||
| chr16:67577357
|
C | CA | 9 | a0001c0001t0001g0060a0001c0001t0001g0077a0001c0001t0002g0148others(6): Show | 9 | HG00639.hp1 HG02027.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+6110dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67577357 | |||||
| chr16:67577357
|
CA | C | 14 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(11): Show | 14 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+6110delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67577357 | |||||
| chr16:67577435
|
CT | C | 40 | a0001c0001t0001g0037a0001c0001t0002g0132a0001c0001t0002g0133others(37): Show | 40 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10+6184delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67577435 | |||||
| chr16:67577531
|
G | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+6267G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577531 | ||||||
| chr16:67577540
|
T | C | 83 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(80): Show | 83 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.-10+6276T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577540 | ||||||
| chr16:67577636
|
G | A | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+6372G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577636 | ||||||
| chr16:67577698
|
C | T | 8 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+6434C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577698 | ||||||
| chr16:67577740
|
C | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG03017.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6476C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577740 | ||||||
| chr16:67577975
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-10+6711G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67577975 | ||||||
| chr16:67578325
|
C | CT | 13 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG00609.hp1 HG00609.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10+7086dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67578325 | |||||
| chr16:67578325
|
CT | C | 60 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0021others(57): Show | 60 | HG00639.hp2 HG00738.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.-10+7086delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67578325 | |||||
| chr16:67578350
|
T | G | 1 | a0001c0001t0001g0096 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-10+7086T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67578350 | ||||||
| chr16:67578461
|
T | G | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+7197T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67578461 | ||||||
| chr16:67579015
|
G | C | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+7751G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67579015 | ||||||
| chr16:67579223
|
A | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+7959A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67579223 | ||||||
| chr16:67579299
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10+8035G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67579299 | ||||||
| chr16:67579503
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+8239C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67579503 | ||||||
| chr16:67579768
|
G | A | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+8504G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67579768 | ||||||
| chr16:67580056
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG01433.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-10+8792C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67580056 | ||||||
| chr16:67580330
|
C | G | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+9066C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67580330 | ||||||
| chr16:67580772
|
A | AT | 19 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(16): Show | 19 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10+9531dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67580772 | |||||
| chr16:67580772
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-10+9518_-10+9531d others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67580772 | |||||
| chr16:67580772
|
A | ATTTTTTT others(8): Show |
5 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0004g0158others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+9517_-10+9531d others(17): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67580772 | |||||
| chr16:67580772
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0002g0155a0001c0001t0004g0159a0001c0001t0004g0163others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+9516_-10+9531d others(18): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67580772 | |||||
| chr16:67580772
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0004g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10+9514_-10+9531d others(20): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67580772 | |||||
| chr16:67580772
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0004g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10+9512_-10+9531d others(22): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67580772 | |||||
| chr16:67580772
|
AT | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0053others(30): Show | 33 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-10+9531delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67580772 | |||||
| chr16:67580905
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-10+9641C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67580905 | ||||||
| chr16:67580950
|
A | G | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+9686A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67580950 | ||||||
| chr16:67580967
|
C | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+9703C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67580967 | ||||||
| chr16:67581054
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-10+9790G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67581054 | ||||||
| chr16:67581212
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10+9948G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67581212 | ||||||
| chr16:67581328
|
C | CT | 6 | a0001c0001t0001g0111a0001c0001t0002g0153a0001c0001t0004g0158others(3): Show | 6 | HG01109.hp2 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+10078dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67581328 | |||||
| chr16:67581504
|
T | A | 1 | a0001c0001t0001g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-10+10240T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67581504 | ||||||
| chr16:67581505
|
A | T | 1 | a0001c0001t0001g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-10+10241A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67581505 | ||||||
| chr16:67581648
|
C | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031others(8): Show | 11 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+10384C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67581648 | ||||||
| chr16:67581945
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-10+10681C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67581945 | ||||||
| chr16:67582210
|
C | CA | 7 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0069others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+10963dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67582210 | |||||
| chr16:67582210
|
CA | C | 15 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0002g0155others(12): Show | 15 | HG01361.hp2 HG02559.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+10963delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67582210 | |||||
| chr16:67582243
|
A | G | 1 | a0001c0001t0002g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-10+10979A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67582243 | ||||||
| chr16:67582567
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-10+11303C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67582567 | ||||||
| chr16:67582635
|
G | T | 1 | a0001c0001t0002g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10+11371G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67582635 | ||||||
| chr16:67582700
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-10+11436T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67582700 | ||||||
| chr16:67582885
|
G | A | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+11621G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67582885 | ||||||
| chr16:67582928
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0008g0128 | 2 | HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-10+11664A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67582928 | ||||||
| chr16:67582983
|
C | CT | 13 | a0001c0001t0001g0039a0001c0001t0001g0063a0001c0001t0001g0107others(10): Show | 13 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+11734dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67582983 | |||||
| chr16:67583283
|
A | G | 44 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(41): Show | 44 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-10+12019A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67583283 | ||||||
| chr16:67583574
|
C | T | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+12310C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67583574 | ||||||
| chr16:67583587
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+12323C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67583587 | ||||||
| chr16:67583697
|
A | C | 2 | a0001c0001t0007g0129a0001c0001t0007g0130 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-10+12433A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67583697 | ||||||
| chr16:67583775
|
G | A | 2 | a0001c0001t0006g0131a0001c0001t0006g0135 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-10+12511G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67583775 | ||||||
| chr16:67584043
|
T | TTGTGTGC others(8): Show |
44 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(41): Show | 44 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-10+12789_-10+1280 others(19): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584043 | |||||
| chr16:67584082
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-10+12818C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584082 | ||||||
| chr16:67584150
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-10+12886C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584150 | ||||||
| chr16:67584334
|
C | CGTCTTCT others(3): Show |
1 | a0001c0001t0002g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-10+13070_-10+1307 others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584334 | ||||||
| chr16:67584334
|
C | CGTCTTCT others(4): Show |
1 | a0001c0001t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10+13070_-10+1307 others(15): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584334 | ||||||
| chr16:67584334
|
C | CGTCTTTT others(23): Show |
1 | a0001c0001t0002g0144 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10+13070_-10+1307 others(34): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584334 | ||||||
| chr16:67584337
|
C | CTT | 7 | a0001c0001t0001g0113a0001c0001t0002g0155a0001c0001t0002g0156others(4): Show | 7 | HG03041.hp1 HG03225.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+13093_-10+1309 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584337 | |||||
| chr16:67584337
|
C | CTTCTTTT others(3): Show |
7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0152others(4): Show | 7 | HG00639.hp1 HG02027.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+13075_-10+1307 others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584337 | |||||
| chr16:67584337
|
C | CTTCTTTT others(4): Show |
3 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0006g0135 | 3 | HG03098.hp2 HG03209.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-10+13075_-10+1307 others(15): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584337 | |||||
| chr16:67584337
|
C | CTTCTTTT others(5): Show |
1 | a0001c0001t0002g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10+13075_-10+1307 others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584337 | |||||
| chr16:67584337
|
C | CTTCTTTT others(6): Show |
2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+13075_-10+1307 others(17): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584337 | |||||
| chr16:67584337
|
C | T | 4 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0146others(1): Show | 4 | HG01109.hp1 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+13073C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584337 | ||||||
| chr16:67584337
|
CT | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(19): Show | 22 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-10+13094delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584337 | |||||
| chr16:67584338
|
T | TTC | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+13075_-10+1307 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67584338 | |||||
| chr16:67584340
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-10+13076T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584340 | ||||||
| chr16:67584389
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-10+13125G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584389 | ||||||
| chr16:67584431
|
C | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0012g0091 | 3 | HG02040.hp2 NA19007.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-10+13167C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584431 | ||||||
| chr16:67584615
|
C | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0112 | 3 | HG02809.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-10+13351C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584615 | ||||||
| chr16:67584630
|
T | G | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+13366T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67584630 | ||||||
| chr16:67585330
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-10+14066G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585330 | ||||||
| chr16:67585353
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-10+14089A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585353 | ||||||
| chr16:67585473
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-10+14209C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585473 | ||||||
| chr16:67585512
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-10+14248C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585512 | ||||||
| chr16:67585536
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0030 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-10+14272A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585536 | ||||||
| chr16:67585613
|
T | C | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+14349T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585613 | ||||||
| chr16:67585831
|
GGTTAT | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0107 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-10+14571_-10+1457 others(9): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67585831 | |||||
| chr16:67585844
|
G | T | 13 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(10): Show | 13 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+14580G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585844 | ||||||
| chr16:67585882
|
C | G | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+14618C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67585882 | ||||||
| chr16:67586364
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-10+15100G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67586364 | ||||||
| chr16:67586598
|
G | A | 9 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(6): Show | 9 | HG01433.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+15334G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67586598 | ||||||
| chr16:67586780
|
A | G | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+15516A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67586780 | ||||||
| chr16:67586803
|
G | GT | 4 | a0001c0001t0001g0065a0001c0001t0001g0110a0001c0001t0003g0139others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+15547dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67586803 | |||||
| chr16:67586898
|
A | G | 1 | a0001c0001t0007g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-10+15634A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67586898 | ||||||
| chr16:67587099
|
C | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+15835C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67587099 | ||||||
| chr16:67587100
|
A | AT | 24 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0001t0001g0076others(21): Show | 24 | HG00609.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-10+15859dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67587100 | |||||
| chr16:67587100
|
A | ATT | 10 | a0001c0001t0002g0132a0001c0001t0002g0149a0001c0001t0002g0150others(7): Show | 10 | HG00438.hp2 HG00639.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+15858_-10+1585 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67587100 | |||||
| chr16:67587100
|
A | ATTT | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0003g0139others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+15857_-10+1585 others(7): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67587100 | |||||
| chr16:67587100
|
AT | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(20): Show | 23 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-10+15859delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67587100 | |||||
| chr16:67587100
|
ATT | A | 13 | a0001c0001t0001g0019a0001c0001t0002g0144a0001c0001t0002g0145others(10): Show | 13 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10+15858_-10+1585 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67587100 | |||||
| chr16:67587390
|
C | G | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+16126C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67587390 | ||||||
| chr16:67587530
|
G | GT | 15 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0055others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+16278dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67587530 | |||||
| chr16:67588517
|
G | A | 1 | a0001c0001t0004g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10+17253G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67588517 | ||||||
| chr16:67588586
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+17322A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67588586 | ||||||
| chr16:67588693
|
A | ATATAT | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+17431_-10+1743 others(9): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67588693 | |||||
| chr16:67588861
|
A | AT | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+17606dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67588861 | |||||
| chr16:67589034
|
A | G | 1 | a0001c0001t0004g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10+17770A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589034 | ||||||
| chr16:67589052
|
G | T | 2 | a0001c0001t0002g0168a0001c0001t0009g0154 | 2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10+17788G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589052 | ||||||
| chr16:67589185
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-10+17921T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589185 | ||||||
| chr16:67589322
|
A | G | 1 | a0001c0001t0010g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-10+18058A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589322 | ||||||
| chr16:67589431
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(1): Show | 4 | HG01175.hp1 HG01515.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+18167T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589431 | ||||||
| chr16:67589760
|
G | T | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-10+18496G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589760 | ||||||
| chr16:67589815
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-10+18551G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589815 | ||||||
| chr16:67589824
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-10+18560C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589824 | ||||||
| chr16:67589916
|
A | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-10+18652A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67589916 | ||||||
| chr16:67590043
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+18779C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67590043 | ||||||
| chr16:67590113
|
C | CT | 6 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(3): Show | 6 | HG02055.hp1 HG03041.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+18865dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67590113 | |||||
| chr16:67590113
|
CT | C | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0118others(5): Show | 8 | HG00741.hp2 HG01070.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+18865delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67590113 | |||||
| chr16:67590279
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0015 | 2 | HG00609.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-10+19015G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67590279 | ||||||
| chr16:67590520
|
G | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-10+19256G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67590520 | ||||||
| chr16:67590616
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10+19352C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67590616 | ||||||
| chr16:67590617
|
G | A | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+19353G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67590617 | ||||||
| chr16:67590674
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-10+19410C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67590674 | ||||||
| chr16:67590960
|
C | CA | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00738.hp2 HG01175.hp2 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+19719dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67590960 | |||||
| chr16:67590960
|
C | CAA | 6 | a0001c0001t0001g0111a0001c0001t0005g0041a0001c0001t0005g0042others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+19718_-10+1971 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67590960 | |||||
| chr16:67590960
|
CA | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(34): Show | 37 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-10+19719delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67590960 | |||||
| chr16:67590960
|
CAA | C | 10 | a0001c0001t0002g0156a0001c0001t0004g0158a0001c0001t0004g0159others(7): Show | 10 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+19718_-10+1971 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67590960 | |||||
| chr16:67591551
|
G | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG01433.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-9-19273G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67591551 | ||||||
| chr16:67591714
|
C | CT | 14 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(11): Show | 14 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-19103dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67591714 | |||||
| chr16:67591723
|
G | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-19101G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67591723 | ||||||
| chr16:67591724
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-19100G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67591724 | ||||||
| chr16:67591759
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-19065A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67591759 | ||||||
| chr16:67591763
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-19061A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67591763 | ||||||
| chr16:67591894
|
A | G | 80 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(77): Show | 80 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.-9-18930A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67591894 | ||||||
| chr16:67591969
|
T | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.-9-18855T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67591969 | ||||||
| chr16:67592164
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9-18660C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67592164 | ||||||
| chr16:67592289
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9-18535G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67592289 | ||||||
| chr16:67592291
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 161 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.-9-18533G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67592291 | ||||||
| chr16:67592327
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9-18497G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67592327 | ||||||
| chr16:67592442
|
A | G | 10 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(7): Show | 10 | HG02647.hp1 HG02809.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-18382A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67592442 | ||||||
| chr16:67593026
|
G | GA | 24 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(21): Show | 24 | HG00438.hp2 HG00639.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-9-17788dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67593026 | |||||
| chr16:67593151
|
G | A | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-17673G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67593151 | ||||||
| chr16:67593343
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9-17481G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67593343 | ||||||
| chr16:67593377
|
A | G | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-17447A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67593377 | ||||||
| chr16:67593470
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0009g0154 | 2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-17354G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67593470 | ||||||
| chr16:67593575
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0152 | 2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-9-17249C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67593575 | ||||||
| chr16:67593732
|
G | T | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-17092G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67593732 | ||||||
| chr16:67593869
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-16955A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67593869 | ||||||
| chr16:67594041
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9-16783C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67594041 | ||||||
| chr16:67594517
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-9-16307A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67594517 | ||||||
| chr16:67594576
|
C | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-16248C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67594576 | ||||||
| chr16:67594945
|
G | T | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9-15879G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67594945 | ||||||
| chr16:67595269
|
T | C | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9-15555T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67595269 | ||||||
| chr16:67595333
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9-15491C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67595333 | ||||||
| chr16:67595549
|
GTCT | G | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-15270_-9-15268d others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67595549 | |||||
| chr16:67595614
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9-15210T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67595614 | ||||||
| chr16:67595963
|
C | CT | 9 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9-14852dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67595963 | |||||
| chr16:67596055
|
G | T | 1 | a0001c0001t0002g0144 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-9-14769G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67596055 | ||||||
| chr16:67596151
|
A | C | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9-14673A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67596151 | ||||||
| chr16:67596159
|
G | A | 1 | a0001c0001t0010g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-9-14665G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67596159 | ||||||
| chr16:67596341
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-9-14483G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67596341 | ||||||
| chr16:67596511
|
ATGGT | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0055 | 2 | HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-9-14309_-9-14306d others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67596511 | |||||
| chr16:67596526
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-9-14298C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67596526 | ||||||
| chr16:67596670
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-9-14154C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67596670 | ||||||
| chr16:67596815
|
G | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-14009G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67596815 | ||||||
| chr16:67597120
|
A | G | 1 | a0001c0001t0002g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-9-13704A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597120 | ||||||
| chr16:67597172
|
C | T | 5 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(2): Show | 5 | HG01433.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-13652C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597172 | ||||||
| chr16:67597187
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-13637A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597187 | ||||||
| chr16:67597220
|
T | G | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-13604T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597220 | ||||||
| chr16:67597221
|
T | A | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-13603T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597221 | ||||||
| chr16:67597286
|
T | C | 2 | a0001c0001t0006g0131a0001c0001t0006g0135 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-13538T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597286 | ||||||
| chr16:67597401
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0095 | 2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.-9-13423G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597401 | ||||||
| chr16:67597494
|
A | G | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-9-13330A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597494 | ||||||
| chr16:67597548
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-9-13276A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597548 | ||||||
| chr16:67597698
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-9-13126G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597698 | ||||||
| chr16:67597998
|
A | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0121 | 3 | HG01192.hp2 HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-9-12826A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67597998 | ||||||
| chr16:67598167
|
G | A | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-12657G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67598167 | ||||||
| chr16:67598259
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-9-12565G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67598259 | ||||||
| chr16:67598509
|
GTTA | G | 2 | a0001c0001t0006g0131a0001c0001t0006g0135 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-12308_-9-12306d others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67598509 | |||||
| chr16:67599118
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0095 | 2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.-9-11706C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67599118 | ||||||
| chr16:67599207
|
C | G | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-11617C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67599207 | ||||||
| chr16:67599360
|
G | A | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-11464G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67599360 | ||||||
| chr16:67599386
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-11438A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67599386 | ||||||
| chr16:67599403
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-9-11421A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67599403 | ||||||
| chr16:67599407
|
G | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-11417G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67599407 | ||||||
| chr16:67599808
|
T | G | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9-11016T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67599808 | ||||||
| chr16:67600571
|
G | GTC | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-10250_-9-10249d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67600571 | |||||
| chr16:67600632
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-9-10192C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67600632 | ||||||
| chr16:67600804
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-9-10020A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67600804 | ||||||
| chr16:67600843
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-9-9981G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67600843 | ||||||
| chr16:67600872
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-9-9952G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67600872 | ||||||
| chr16:67601139
|
T | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-9685T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601139 | ||||||
| chr16:67601217
|
G | GGT | 3 | a0001c0001t0001g0059a0001c0001t0001g0084a0001c0001t0001g0123 | 3 | HG01071.hp1 HG03017.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-9-9570_-9-9569dup others(2): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601217 | |||||
| chr16:67601217
|
G | GGTGT | 8 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0004g0158others(5): Show | 8 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-9572_-9-9569dup others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601217 | |||||
| chr16:67601217
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-9578_-9-9569dup others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601217 | |||||
| chr16:67601217
|
GGT | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(67): Show | 70 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-9-9570_-9-9569del others(2): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601217 | |||||
| chr16:67601217
|
GGTGT | G | 31 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0024others(28): Show | 31 | HG01257.hp1 HG01433.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.-9-9572_-9-9569del others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601217 | |||||
| chr16:67601217
|
GGTGTGT | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0080a0001c0001t0006g0135 | 3 | HG01975.hp1 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-9-9574_-9-9569del others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601217 | |||||
| chr16:67601217
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9-9578_-9-9569del others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601217 | |||||
| chr16:67601252
|
G | GTGTTT | 3 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0152 | 3 | HG00639.hp1 HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-9-9560_-9-9556dup others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601252 | |||||
| chr16:67601252
|
G | GTTT | 3 | a0001c0001t0002g0148a0001c0001t0002g0153a0001c0001t0010g0166 | 3 | HG00438.hp2 HG03491.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-9-9571_-9-9570ins others(3): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601252 | |||||
| chr16:67601252
|
GTGTTT | G | 6 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(3): Show | 6 | HG02145.hp1 HG02602.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-9560_-9-9556del others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601252 | |||||
| chr16:67601256
|
T | G | 1 | a0001c0001t0003g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-9-9568T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601256 | ||||||
| chr16:67601257
|
T | G | 1 | a0001c0001t0003g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9-9567T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601257 | ||||||
| chr16:67601259
|
G | T | 7 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-9565G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601259 | ||||||
| chr16:67601280
|
TCTCA | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-9540_-9-9537del others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601280 | |||||
| chr16:67601294
|
C | CGT | 28 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(25): Show | 28 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-9-9487_-9-9486dup others(2): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
C | CGTGT | 6 | a0001c0001t0001g0116a0001c0001t0002g0133a0001c0001t0002g0144others(3): Show | 6 | HG01346.hp2 HG01361.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-9489_-9-9486dup others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
C | CGTGTGT | 6 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0002g0132others(3): Show | 6 | HG00438.hp2 HG01496.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-9491_-9-9486dup others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-9-9495_-9-9486dup others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
C | CGTGTGTG others(5): Show |
2 | a0001c0001t0002g0149a0001c0001t0002g0150 | 2 | HG00639.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-9-9497_-9-9486dup others(12): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
CGT | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0017others(33): Show | 36 | HG00558.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9-9487_-9-9486del others(2): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
CGTGT | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0034others(22): Show | 25 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-9-9489_-9-9486del others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
CGTGTGT | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0104a0001c0001t0007g0130others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-9491_-9-9486del others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-9-9499_-9-9486del others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601294
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0001g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-9-9501_-9-9486del others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601294 | |||||
| chr16:67601335
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-9-9489G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601335 | ||||||
| chr16:67601338
|
T | TG | 3 | a0001c0001t0001g0047a0001c0001t0004g0162a0001c0001t0004g0165 | 3 | HG02486.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-9-9486_-9-9485ins others(1): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601338 | ||||||
| chr16:67601352
|
T | G | 2 | a0001c0001t0007g0129a0001c0001t0007g0130 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-9-9472T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601352 | ||||||
| chr16:67601564
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9-9260G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601564 | ||||||
| chr16:67601577
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-9-9247C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601577 | ||||||
| chr16:67601810
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-9-9014C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601810 | ||||||
| chr16:67601848
|
C | T | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-8976C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601848 | ||||||
| chr16:67601864
|
A | AT | 38 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0033others(35): Show | 38 | HG00558.hp1 HG00639.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.-9-8943dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601864 | |||||
| chr16:67601864
|
AT | A | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-8943delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67601864 | |||||
| chr16:67601965
|
G | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-8859G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67601965 | ||||||
| chr16:67602226
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-9-8598T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602226 | ||||||
| chr16:67602322
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-9-8502G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602322 | ||||||
| chr16:67602509
|
T | C | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9-8315T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602509 | ||||||
| chr16:67602614
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-9-8210G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602614 | ||||||
| chr16:67602670
|
T | C | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-8154T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602670 | ||||||
| chr16:67602734
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-9-8090G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602734 | ||||||
| chr16:67602842
|
C | CA | 5 | a0001c0001t0001g0013a0001c0001t0001g0071a0001c0001t0002g0132others(2): Show | 5 | HG01361.hp2 HG01433.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-7963dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67602842 | |||||
| chr16:67602842
|
CA | C | 8 | a0001c0001t0001g0099a0001c0001t0002g0155a0001c0001t0002g0156others(5): Show | 8 | HG01070.hp1 HG03041.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-7963delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67602842 | |||||
| chr16:67602858
|
A | G | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-7966A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602858 | ||||||
| chr16:67602864
|
G | A | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-7960G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602864 | ||||||
| chr16:67602867
|
G | T | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-7957G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602867 | ||||||
| chr16:67602868
|
A | C | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-7956A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602868 | ||||||
| chr16:67602928
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9-7896G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67602928 | ||||||
| chr16:67603325
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-9-7499C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67603325 | ||||||
| chr16:67603364
|
C | G | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-7460C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67603364 | ||||||
| chr16:67603660
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-7164C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67603660 | ||||||
| chr16:67603681
|
C | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0077 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-9-7143C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67603681 | ||||||
| chr16:67603809
|
T | A | 1 | a0001c0001t0003g0136 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-9-7015T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67603809 | ||||||
| chr16:67603824
|
C | CA | 21 | a0001c0001t0001g0030a0001c0001t0001g0054a0001c0001t0001g0078others(18): Show | 21 | HG01109.hp1 HG01361.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9-6983dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67603824 | |||||
| chr16:67604124
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-9-6700G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604124 | ||||||
| chr16:67604128
|
C | CA | 7 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0088others(4): Show | 7 | HG01175.hp1 HG01361.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-6679dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604128 | |||||
| chr16:67604177
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-6647G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604177 | ||||||
| chr16:67604319
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-6505A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604319 | ||||||
| chr16:67604539
|
C | T | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9-6285C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604539 | ||||||
| chr16:67604584
|
A | G | 4 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0141others(1): Show | 4 | HG02602.hp2 HG02735.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-6240A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604584 | ||||||
| chr16:67604610
|
G | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6214G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604610 | ||||||
| chr16:67604688
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-9-6136C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604688 | ||||||
| chr16:67604730
|
G | GT | 11 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-6080dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604730 | |||||
| chr16:67604730
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-9-6092_-9-6080dup others(13): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604730 | |||||
| chr16:67604730
|
GT | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 19 | HG02280.hp1 HG02280.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.-9-6080delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604730 | |||||
| chr16:67604734
|
TTTTTTTT others(11): Show |
T | 1 | a0001c0001t0003g0143 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9-6079_-9-6062del others(18): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604734 | |||||
| chr16:67604735
|
TTTTTTTT others(10): Show |
T | 6 | a0001c0001t0003g0137a0001c0001t0003g0138a0001c0001t0003g0139others(3): Show | 6 | HG02055.hp1 HG02602.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-6079_-9-6063del others(17): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604735 | |||||
| chr16:67604736
|
TTTTTTTT others(9): Show |
T | 1 | a0001c0001t0003g0136 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-9-6079_-9-6064del others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604736 | |||||
| chr16:67604738
|
T | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0111 | 2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-9-6086T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604738 | ||||||
| chr16:67604739
|
T | TG | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0104 | 3 | HG02630.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-6085_-9-6084ins others(1): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604739 | ||||||
| chr16:67604739
|
TTTTTTGT others(6): Show |
T | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG03041.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9-6079_-9-6067del others(13): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604739 | |||||
| chr16:67604740
|
T | G | 6 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0097others(3): Show | 6 | HG01070.hp1 HG01175.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-6084T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604740 | ||||||
| chr16:67604740
|
T | TG | 6 | a0001c0001t0001g0020a0001c0001t0001g0049a0001c0001t0001g0063others(3): Show | 6 | HG01192.hp2 HG01243.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-6084_-9-6083ins others(1): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604740 | ||||||
| chr16:67604740
|
TTTTTG | T | 7 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0162others(4): Show | 7 | HG02622.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-6079_-9-6075del others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604740 | |||||
| chr16:67604741
|
T | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(20): Show | 23 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-6083T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604741 | ||||||
| chr16:67604742
|
TTTGTTTT others(3): Show |
T | 2 | a0001c0001t0002g0144a0001c0001t0002g0149 | 2 | HG00639.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-6079_-9-6070del others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604742 | |||||
| chr16:67604744
|
TGTTTTTT others(1): Show |
T | 3 | a0001c0001t0002g0133a0001c0001t0006g0131a0001c0001t0006g0135 | 3 | HG01433.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-6079_-9-6072del others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604744 | ||||||
| chr16:67604745
|
G | T | 5 | a0001c0001t0002g0148a0001c0001t0002g0151a0001c0001t0002g0153others(2): Show | 5 | HG00438.hp2 HG01361.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-6079G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604745 | ||||||
| chr16:67604752
|
G | T | 22 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0146others(19): Show | 22 | HG00438.hp2 HG01361.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9-6072G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604752 | ||||||
| chr16:67604759
|
T | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0060others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-6065T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67604759 | ||||||
| chr16:67604964
|
A | AT | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(41): Show | 44 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-9-5832dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604964 | |||||
| chr16:67604964
|
A | ATT | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(32): Show | 35 | HG00438.hp2 HG00609.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9-5833_-9-5832dup others(2): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604964 | |||||
| chr16:67604964
|
A | ATTT | 16 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0036others(13): Show | 16 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-5834_-9-5832dup others(3): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67604964 | |||||
| chr16:67605058
|
C | T | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-5766C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67605058 | ||||||
| chr16:67605210
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-9-5614T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67605210 | ||||||
| chr16:67605219
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-9-5605C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67605219 | ||||||
| chr16:67605246
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9-5578T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67605246 | ||||||
| chr16:67605365
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-9-5459C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67605365 | ||||||
| chr16:67605417
|
A | G | 15 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0055others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-5407A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67605417 | ||||||
| chr16:67605526
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-5298C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67605526 | ||||||
| chr16:67606278
|
C | T | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-9-4546C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67606278 | ||||||
| chr16:67606334
|
G | A | 4 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0146others(1): Show | 4 | HG01109.hp1 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-4490G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67606334 | ||||||
| chr16:67606533
|
G | A | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-4291G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67606533 | ||||||
| chr16:67606756
|
G | GT | 53 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0014others(50): Show | 53 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-9-4048dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67606756 | |||||
| chr16:67606756
|
G | GTT | 5 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0003g0136others(2): Show | 5 | HG00438.hp2 HG02486.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-4049_-9-4048dup others(2): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67606756 | |||||
| chr16:67606790
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-9-4034A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67606790 | ||||||
| chr16:67606797
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-9-4027T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67606797 | ||||||
| chr16:67606857
|
G | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-3967G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67606857 | ||||||
| chr16:67607038
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-3786C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607038 | ||||||
| chr16:67607232
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-9-3592C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607232 | ||||||
| chr16:67607612
|
C | A | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-9-3212C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607612 | ||||||
| chr16:67607639
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-3185T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607639 | ||||||
| chr16:67607645
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9-3179G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607645 | ||||||
| chr16:67607657
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9-3167G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607657 | ||||||
| chr16:67607735
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-9-3089C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607735 | ||||||
| chr16:67607879
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-2945T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67607879 | ||||||
| chr16:67608005
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-9-2819C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67608005 | ||||||
| chr16:67608018
|
C | CA | 47 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(44): Show | 47 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.-9-2791dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67608018 | |||||
| chr16:67608018
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-2798_-9-2791dup others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67608018 | |||||
| chr16:67608018
|
C | CAAAAAAA others(2): Show |
20 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(17): Show | 20 | HG00438.hp2 HG02027.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9-2799_-9-2791dup others(9): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67608018 | |||||
| chr16:67608018
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0156a0001c0001t0003g0136a0001c0001t0003g0140others(2): Show | 5 | HG02145.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-2800_-9-2791dup others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67608018 | |||||
| chr16:67608018
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0155a0001c0001t0002g0157 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9-2801_-9-2791dup others(11): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67608018 | |||||
| chr16:67608217
|
G | C | 1 | a0001c0001t0002g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9-2607G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67608217 | ||||||
| chr16:67608278
|
C | T | 5 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0162others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-2546C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67608278 | ||||||
| chr16:67608346
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-9-2478A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67608346 | ||||||
| chr16:67608447
|
T | C | 1 | a0001c0001t0004g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9-2377T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67608447 | ||||||
| chr16:67608457
|
A | C | 1 | a0001c0001t0001g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-9-2367A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67608457 | ||||||
| chr16:67608735
|
G | GT | 79 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(76): Show | 79 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9-2078dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67608735 | |||||
| chr16:67608795
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-9-2029A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67608795 | ||||||
| chr16:67609032
|
C | T | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-1792C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67609032 | ||||||
| chr16:67609563
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-9-1261T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67609563 | ||||||
| chr16:67609569
|
A | G | 1 | a0001c0001t0012g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-9-1255A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67609569 | ||||||
| chr16:67609624
|
C | CT | 13 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0024others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-1183dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67609624 | |||||
| chr16:67609699
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-1125C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67609699 | ||||||
| chr16:67609783
|
C | T | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1041C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67609783 | ||||||
| chr16:67610270
|
G | A | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-554G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610270 | ||||||
| chr16:67610350
|
C | CT | 11 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0059others(8): Show | 11 | HG01071.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-454dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67610350 | |||||
| chr16:67610350
|
C | CTT | 6 | a0001c0001t0002g0132a0001c0001t0002g0146a0001c0001t0002g0147others(3): Show | 6 | HG00438.hp2 HG02257.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-455_-9-454dupTT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67610350 | |||||
| chr16:67610350
|
C | CTTT | 5 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG00639.hp1 HG02027.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-456_-9-454dupTT others(1): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67610350 | |||||
| chr16:67610350
|
CT | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0062others(3): Show | 6 | HG01109.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-454delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67610350 | |||||
| chr16:67610388
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-436T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610388 | ||||||
| chr16:67610439
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9-385G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610439 | ||||||
| chr16:67610460
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9-364C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610460 | ||||||
| chr16:67610546
|
G | A | 9 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(6): Show | 9 | HG01433.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9-278G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610546 | ||||||
| chr16:67610597
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-227G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610597 | ||||||
| chr16:67610598
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-226C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610598 | ||||||
| chr16:67610660
|
GGTT | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-160_-9-158delGT others(1): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 67610660 | |||||
| chr16:67610801
|
A | G | 1 | a0001c0001t0007g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9-23A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610801 | ||||||
| chr16:67610813
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-9-11C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 2/11 | chr16 | 67610813 | ||||||
| chr16:67611654
|
T | C | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781+41T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 3/11 | chr16 | 67611654 | ||||||
| chr16:67611687
|
T | C | 1 | a0001c0001t0012g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.781+74T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 3/11 | chr16 | 67611687 | ||||||
| chr16:67611883
|
TTTAAGA | T | 2 | a0001c0001t0004g0159a0001c0001t0004g0163 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.782-64_782-59delAG others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 67611883 | |||||
| chr16:67612234
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.952+113T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67612234 | ||||||
| chr16:67612408
|
G | A | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.952+287G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67612408 | ||||||
| chr16:67612462
|
C | T | 1 | a0001c0001t0008g0016 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.952+341C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67612462 | ||||||
| chr16:67612493
|
G | T | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.952+372G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67612493 | ||||||
| chr16:67612568
|
C | G | 1 | a0001c0001t0010g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.952+447C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67612568 | ||||||
| chr16:67613136
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.952+1015A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67613136 | ||||||
| chr16:67613188
|
C | T | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+1067C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67613188 | ||||||
| chr16:67613409
|
T | C | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.952+1288T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67613409 | ||||||
| chr16:67613456
|
G | A | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.952+1335G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67613456 | ||||||
| chr16:67613917
|
C | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.952+1796C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67613917 | ||||||
| chr16:67614053
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.952+1932C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614053 | ||||||
| chr16:67614076
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.952+1955G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614076 | ||||||
| chr16:67614176
|
G | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.952+2055G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614176 | ||||||
| chr16:67614204
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.952+2083G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614204 | ||||||
| chr16:67614207
|
C | T | 21 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.952+2086C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614207 | ||||||
| chr16:67614346
|
C | CA | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0110others(5): Show | 8 | HG00438.hp2 HG01109.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+2247dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 67614346 | |||||
| chr16:67614346
|
CA | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(5): Show | 8 | HG01361.hp2 HG02922.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.952+2247delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 67614346 | |||||
| chr16:67614368
|
A | G | 2 | a0001c0001t0002g0168a0001c0001t0009g0154 | 2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.952+2247A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614368 | ||||||
| chr16:67614576
|
AC | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0112 | 3 | HG02809.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.953-2168delC | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614576 | ||||||
| chr16:67614801
|
C | T | 1 | a0001c0001t0002g0150 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.953-1944C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614801 | ||||||
| chr16:67614863
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.953-1882A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614863 | ||||||
| chr16:67614895
|
G | A | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.953-1850G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67614895 | ||||||
| chr16:67615108
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.953-1637C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615108 | ||||||
| chr16:67615190
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108 | 3 | HG02109.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.953-1555T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615190 | ||||||
| chr16:67615349
|
T | A | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-1396T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615349 | ||||||
| chr16:67615381
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.953-1364C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615381 | ||||||
| chr16:67615414
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.953-1331G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615414 | ||||||
| chr16:67615682
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.953-1063C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615682 | ||||||
| chr16:67615705
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.953-1040C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615705 | ||||||
| chr16:67615758
|
G | C | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-987G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615758 | ||||||
| chr16:67615902
|
T | C | 5 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0162others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.953-843T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67615902 | ||||||
| chr16:67616354
|
C | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0060others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.953-391C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67616354 | ||||||
| chr16:67616477
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.953-268A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67616477 | ||||||
| chr16:67616654
|
C | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.953-91C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 4/11 | chr16 | 67616654 | ||||||
| chr16:67617018
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1086+140G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617018 | ||||||
| chr16:67617137
|
G | A | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1086+259G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617137 | ||||||
| chr16:67617207
|
A | G | 1 | a0001c0001t0013g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1086+329A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617207 | ||||||
| chr16:67617225
|
C | G | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1086+347C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617225 | ||||||
| chr16:67617523
|
T | C | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086+645T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617523 | ||||||
| chr16:67617580
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1086+702G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617580 | ||||||
| chr16:67617731
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1086+853C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617731 | ||||||
| chr16:67617976
|
G | A | 65 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(62): Show | 65 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1086+1098G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67617976 | ||||||
| chr16:67618009
|
A | G | 11 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031others(8): Show | 11 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1086+1131A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67618009 | ||||||
| chr16:67618162
|
T | C | 2 | a0001c0001t0002g0168a0001c0001t0009g0154 | 2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1086+1284T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67618162 | ||||||
| chr16:67618272
|
T | C | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1086+1394T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67618272 | ||||||
| chr16:67618290
|
G | A | 5 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0162others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1086+1412G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67618290 | ||||||
| chr16:67618295
|
G | A | 1 | a0001c0001t0012g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1086+1417G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67618295 | ||||||
| chr16:67618724
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1086+1846A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67618724 | ||||||
| chr16:67618930
|
T | C | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-1767T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67618930 | ||||||
| chr16:67619163
|
C | T | 2 | a0001c0001t0006g0131a0001c0001t0006g0135 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1087-1534C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619163 | ||||||
| chr16:67619165
|
G | T | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG03041.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1087-1532G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619165 | ||||||
| chr16:67619261
|
C | T | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-1436C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619261 | ||||||
| chr16:67619310
|
C | T | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1087-1387C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619310 | ||||||
| chr16:67619422
|
C | T | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-1275C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619422 | ||||||
| chr16:67619435
|
CAAAA | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG00738.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087-1257_1087-125 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 67619435 | |||||
| chr16:67619444
|
C | A | 14 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0053others(11): Show | 14 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1087-1253C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619444 | ||||||
| chr16:67619593
|
G | C | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1087-1104G>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619593 | ||||||
| chr16:67619880
|
T | C | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-817T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67619880 | ||||||
| chr16:67620211
|
C | CT | 16 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(13): Show | 16 | HG00438.hp2 HG00639.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1087-477dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 67620211 | |||||
| chr16:67620211
|
C | CTT | 7 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1087-478_1087-477d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 67620211 | |||||
| chr16:67620492
|
G | A | 2 | a0001c0001t0003g0137a0001c0001t0003g0141 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1087-205G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67620492 | ||||||
| chr16:67620561
|
G | T | 1 | a0001c0001t0002g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1087-136G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67620561 | ||||||
| chr16:67620609
|
C | G | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-88C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67620609 | ||||||
| chr16:67620660
|
T | G | 1 | a0001c0001t0011g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1087-37T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 5/11 | chr16 | 67620660 | ||||||
| chr16:67621051
|
T | G | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG03041.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1207+234T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 6/11 | chr16 | 67621051 | ||||||
| chr16:67621093
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG02622.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1207+276A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 6/11 | chr16 | 67621093 | ||||||
| chr16:67621230
|
T | C | 44 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(41): Show | 44 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1208-212T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 6/11 | chr16 | 67621230 | ||||||
| chr16:67621748
|
C | CT | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(60): Show | 63 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.1357+176dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67621748 | |||||
| chr16:67621748
|
C | CTT | 20 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0057others(17): Show | 20 | HG00438.hp2 HG01109.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1357+175_1357+176d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67621748 | |||||
| chr16:67621957
|
C | T | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357+366C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67621957 | ||||||
| chr16:67622248
|
C | T | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+657C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622248 | ||||||
| chr16:67622268
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1357+677A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622268 | ||||||
| chr16:67622318
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1357+727C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622318 | ||||||
| chr16:67622344
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1357+753C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622344 | ||||||
| chr16:67622355
|
C | CA | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357+776dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67622355 | |||||
| chr16:67622641
|
CT | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0005g0041others(6): Show | 9 | HG00741.hp2 HG01071.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357+1069delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67622641 | |||||
| chr16:67622805
|
G | A | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1357+1214G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622805 | ||||||
| chr16:67622811
|
A | AT | 21 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0078others(18): Show | 21 | HG00558.hp1 HG00558.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1357+1241dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67622811 | |||||
| chr16:67622835
|
ATTTTTTA others(50): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1357+1245_1357+130 others(61): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622835 | ||||||
| chr16:67622891
|
A | T | 1 | a0001c0001t0001g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1357+1300A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622891 | ||||||
| chr16:67622954
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(2): Show | 5 | HG01433.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357+1363G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622954 | ||||||
| chr16:67622969
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1357+1378G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67622969 | ||||||
| chr16:67623146
|
G | A | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+1555G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67623146 | ||||||
| chr16:67623379
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1357+1788G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67623379 | ||||||
| chr16:67623491
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1357+1900C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67623491 | ||||||
| chr16:67623642
|
A | G | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357+2051A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67623642 | ||||||
| chr16:67623673
|
C | A | 1 | a0001c0001t0012g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1357+2082C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67623673 | ||||||
| chr16:67623791
|
T | G | 1 | a0001c0001t0002g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1357+2200T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67623791 | ||||||
| chr16:67624047
|
CA | C | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1357+2473delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624047 | |||||
| chr16:67624065
|
TTA | T | 2 | a0001c0001t0005g0042a0001c0001t0005g0044 | 2 | HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1357+2480_1357+248 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624065 | |||||
| chr16:67624069
|
A | ATG | 2 | a0001c0001t0001g0059a0001c0001t0013g0045 | 2 | HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1357+2479_1357+248 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624069 | |||||
| chr16:67624069
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1357+2478A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624069 | ||||||
| chr16:67624069
|
ATATGTG | A | 4 | a0001c0001t0002g0150a0001c0001t0002g0152a0001c0001t0005g0041others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+2480_1358-247 others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624069 | |||||
| chr16:67624069
|
ATATGTGT others(25): Show |
A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1357+2480_1358-245 others(36): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624069 | |||||
| chr16:67624069
|
ATATGTGT others(27): Show |
A | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357+2480_1358-245 others(38): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624069 | |||||
| chr16:67624071
|
A | ATG | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(25): Show | 28 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1358-2440_1358-243 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
A | ATGTG | 18 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0019others(15): Show | 18 | HG00558.hp1 HG00609.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.1358-2442_1358-243 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
A | ATGTGTG | 15 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0021others(12): Show | 15 | HG01109.hp2 HG02074.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1358-2444_1358-243 others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
A | ATGTGTGT others(1): Show |
4 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0002g0156others(1): Show | 4 | HG00558.hp2 HG02083.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-2446_1358-243 others(12): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0061 | 2 | HG01496.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1358-2448_1358-243 others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0059others(3): Show | 6 | HG01071.hp1 HG01192.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1357+2480A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624071 | ||||||
| chr16:67624071
|
ATG | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0013others(3): Show | 6 | HG00609.hp2 HG01257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-2440_1358-243 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
ATGTG | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0035others(4): Show | 7 | HG02647.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-2442_1358-243 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
ATGTGTG | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0071others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-2444_1358-243 others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG02622.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1358-2448_1358-243 others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624071
|
ATGTGTGT others(5): Show |
A | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(6): Show | 9 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1358-2450_1358-243 others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624071 | |||||
| chr16:67624075
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1358-2480G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624075 | ||||||
| chr16:67624103
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1358-2452G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624103 | ||||||
| chr16:67624105
|
G | A | 5 | a0001c0001t0002g0146a0001c0001t0002g0149a0001c0001t0002g0151others(2): Show | 5 | HG00438.hp2 HG00639.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358-2450G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624105 | ||||||
| chr16:67624107
|
G | A | 4 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0152others(1): Show | 4 | HG02027.hp1 HG02895.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-2448G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624107 | ||||||
| chr16:67624107
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1358-2436_1358-242 others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624107 | |||||
| chr16:67624109
|
G | A | 2 | a0001c0001t0004g0160a0001c0001t0009g0154 | 2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1358-2446G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624109 | ||||||
| chr16:67624111
|
G | A | 1 | a0001c0001t0004g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1358-2444G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624111 | ||||||
| chr16:67624113
|
G | A | 6 | a0001c0001t0002g0168a0001c0001t0004g0158a0001c0001t0004g0162others(3): Show | 6 | HG01361.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-2442G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624113 | ||||||
| chr16:67624113
|
GTGTA | G | 2 | a0001c0001t0004g0160a0001c0001t0009g0154 | 2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1358-2438_1358-243 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624113 | |||||
| chr16:67624115
|
G | A | 10 | a0001c0001t0001g0095a0001c0001t0002g0146a0001c0001t0002g0149others(7): Show | 10 | HG00438.hp2 HG00639.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1358-2440G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624115 | ||||||
| chr16:67624117
|
A | G | 19 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0032others(16): Show | 19 | HG01361.hp2 HG02027.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1358-2438A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624117 | ||||||
| chr16:67624117
|
ATGTGTG | A | 4 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0152others(1): Show | 4 | HG02027.hp1 HG02895.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-2434_1358-242 others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624117 | |||||
| chr16:67624117
|
ATGTGTGT others(1): Show |
A | 5 | a0001c0001t0002g0146a0001c0001t0002g0149a0001c0001t0002g0151others(2): Show | 5 | HG00438.hp2 HG00639.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358-2436_1358-242 others(12): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624117 | |||||
| chr16:67624121
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-2434G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624121 | ||||||
| chr16:67624123
|
G | A | 10 | a0001c0001t0002g0147a0001c0001t0002g0168a0001c0001t0004g0158others(7): Show | 10 | HG01361.hp2 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1358-2432G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624123 | ||||||
| chr16:67624125
|
G | A | 19 | a0001c0001t0001g0095a0001c0001t0002g0147a0001c0001t0002g0148others(16): Show | 19 | HG01361.hp2 HG02027.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1358-2430G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624125 | ||||||
| chr16:67624127
|
A | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-2428A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624127 | ||||||
| chr16:67624129
|
A | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-2426A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624129 | ||||||
| chr16:67624131
|
A | ATATG | 16 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(13): Show | 16 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1358-2422_1358-241 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624131 | |||||
| chr16:67624131
|
A | ATG | 4 | a0001c0001t0002g0157a0001c0001t0004g0161a0001c0001t0006g0131others(1): Show | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-2423_1358-242 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624131 | |||||
| chr16:67624131
|
A | G | 19 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(16): Show | 19 | HG00438.hp2 HG00639.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1358-2424A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624131 | ||||||
| chr16:67624133
|
A | ATG | 2 | a0001c0001t0001g0082a0001c0001t0001g0113 | 2 | HG00558.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1358-2410_1358-240 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624133 | |||||
| chr16:67624133
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0095 | 2 | HG02027.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1358-2422A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624133 | ||||||
| chr16:67624133
|
ATGTG | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG00738.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-2412_1358-240 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624133 | |||||
| chr16:67624135
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-2420G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624135 | ||||||
| chr16:67624137
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-2418G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624137 | ||||||
| chr16:67624139
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1358-2402_1358-239 others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624139 | |||||
| chr16:67624145
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1358-2410G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624145 | ||||||
| chr16:67624157
|
G | GTA | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358-2388_1358-238 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67624157 | |||||
| chr16:67624554
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1358-2001T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624554 | ||||||
| chr16:67624833
|
A | G | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1358-1722A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624833 | ||||||
| chr16:67624948
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1358-1607G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624948 | ||||||
| chr16:67624965
|
C | T | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG03041.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1358-1590C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67624965 | ||||||
| chr16:67625123
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1358-1432C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67625123 | ||||||
| chr16:67625259
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1358-1296T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67625259 | ||||||
| chr16:67625441
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1358-1114C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67625441 | ||||||
| chr16:67625486
|
C | T | 2 | a0001c0001t0002g0168a0001c0001t0009g0154 | 2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1358-1069C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | chr16 | 67625486 | ||||||
| chr16:67626283
|
CAAAAATA | C | 7 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1358-259_1358-253d others(9): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67626283 | |||||
| chr16:67626452
|
C | CA | 10 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0085others(7): Show | 10 | HG01192.hp1 HG01361.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1358-82dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67626452 | |||||
| chr16:67626452
|
CA | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0090others(4): Show | 7 | HG00609.hp2 HG01433.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-82delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67626452 | |||||
| chr16:67626452
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0003g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1358-92_1358-82del others(11): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 67626452 | |||||
| chr16:67626792
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1518+77A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67626792 | ||||||
| chr16:67626999
|
G | A | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518+284G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67626999 | ||||||
| chr16:67627037
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG00639.hp2 HG01074.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518+322C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627037 | ||||||
| chr16:67627217
|
G | A | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1518+502G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627217 | ||||||
| chr16:67627230
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1518+515C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627230 | ||||||
| chr16:67627231
|
G | A | 1 | a0001c0001t0007g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1518+516G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627231 | ||||||
| chr16:67627262
|
G | A | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG03041.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1518+547G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627262 | ||||||
| chr16:67627423
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108 | 3 | HG02109.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1518+708G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627423 | ||||||
| chr16:67627442
|
G | A | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1518+727G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627442 | ||||||
| chr16:67627455
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0078a0001c0001t0001g0081 | 3 | HG02145.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1518+740C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627455 | ||||||
| chr16:67627636
|
T | TA | 17 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0078others(14): Show | 17 | HG01433.hp1 HG01433.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1519-722dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 67627636 | |||||
| chr16:67627670
|
C | T | 7 | a0001c0001t0001g0050a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 7 | HG00558.hp2 HG01255.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519-700C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627670 | ||||||
| chr16:67627872
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1519-498G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627872 | ||||||
| chr16:67627922
|
C | CA | 18 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0049others(15): Show | 18 | HG00438.hp2 HG00609.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1519-426dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 67627922 | |||||
| chr16:67627922
|
CA | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0082a0001c0001t0001g0096others(7): Show | 10 | HG00558.hp2 HG01433.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1519-426delA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 67627922 | |||||
| chr16:67627977
|
C | G | 5 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(2): Show | 5 | HG01433.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1519-393C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67627977 | ||||||
| chr16:67628073
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1519-297C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67628073 | ||||||
| chr16:67628081
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1519-289C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67628081 | ||||||
| chr16:67628089
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1519-281C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67628089 | ||||||
| chr16:67628127
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1519-243G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67628127 | ||||||
| chr16:67628278
|
A | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG03017.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519-92A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67628278 | ||||||
| chr16:67628306
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1519-64G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 8/11 | chr16 | 67628306 | ||||||
| chr16:67628912
|
T | A | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1701+360T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 9/11 | chr16 | 67628912 | ||||||
| chr16:67629051
|
C | CA | 9 | a0001c0001t0001g0023a0001c0001t0001g0063a0001c0001t0001g0067others(6): Show | 9 | HG00741.hp2 HG01071.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1702-331dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr16 | 67629051 | |||||
| chr16:67629388
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0030 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1702-10T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 9/11 | chr16 | 67629388 | ||||||
| chr16:67629593
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1837+60G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629593 | ||||||
| chr16:67629733
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1837+200G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629733 | ||||||
| chr16:67629736
|
C | T | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1837+203C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629736 | ||||||
| chr16:67629745
|
CCTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1837+213_1837+232d others(22): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629745 | ||||||
| chr16:67629746
|
C | CTT | 7 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0024others(4): Show | 7 | HG00738.hp1 HG01243.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837+258_1837+259d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
C | CTTT | 8 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0025others(5): Show | 8 | HG01433.hp2 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837+257_1837+259d others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
C | CTTTTTT | 5 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0038others(2): Show | 5 | HG00738.hp2 HG01975.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1837+254_1837+259d others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1837+250_1837+259d others(12): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0082a0001c0001t0005g0044a0001c0001t0013g0045 | 3 | HG00558.hp2 HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1837+249_1837+259d others(13): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1837+248_1837+259d others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1837+246_1837+259d others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1837+242_1837+259d others(20): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CT | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0115others(5): Show | 8 | HG01074.hp1 HG01192.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837+259delT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTT | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0068others(6): Show | 9 | HG00639.hp2 HG01071.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837+258_1837+259d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTT | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(12): Show | 15 | HG00609.hp1 HG00609.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1837+257_1837+259d others(5): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTT | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(13): Show | 16 | HG00438.hp1 HG01255.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1837+256_1837+259d others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTT | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0053a0001c0001t0001g0056others(11): Show | 14 | HG00558.hp1 HG01109.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1837+255_1837+259d others(7): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTT | C | 9 | a0001c0001t0001g0048a0001c0001t0001g0065a0001c0001t0001g0077others(6): Show | 9 | HG01361.hp2 HG02055.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837+254_1837+259d others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT | C | 6 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0057others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837+253_1837+259d others(9): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1837+249_1837+259d others(13): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0002g0132others(2): Show | 5 | HG03098.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1837+248_1837+259d others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0034a0001c0001t0002g0133 | 2 | HG01433.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1837+247_1837+259d others(15): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0033a0001c0001t0002g0147a0001c0001t0007g0129 | 3 | HG02257.hp2 HG02895.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1837+246_1837+259d others(16): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0002g0146a0001c0001t0007g0130 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1837+245_1837+259d others(17): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0002g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1837+244_1837+259d others(18): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0002g0145 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1837+243_1837+259d others(19): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0002g0144 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1837+242_1837+259d others(20): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(12): Show |
C | 5 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0002g0151others(2): Show | 5 | HG00438.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1837+241_1837+259d others(21): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(13): Show |
C | 8 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0030others(5): Show | 8 | HG00639.hp1 HG02027.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837+240_1837+259d others(22): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0003g0140a0001c0002t0003g0142 | 2 | HG03486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1837+239_1837+259d others(23): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(15): Show |
C | 5 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(2): Show | 5 | HG02145.hp1 HG02602.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1837+238_1837+259d others(24): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629746
|
CTTTTTTT others(19): Show |
C | 2 | a0001c0001t0001g0078a0001c0001t0001g0088 | 2 | HG02145.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1837+234_1837+259d others(28): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67629746 | |||||
| chr16:67629797
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1837+264C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629797 | ||||||
| chr16:67629798
|
G | A | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837+265G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629798 | ||||||
| chr16:67629814
|
G | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1837+281G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629814 | ||||||
| chr16:67629916
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1837+383A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67629916 | ||||||
| chr16:67630019
|
G | A | 1 | a0001c0001t0008g0016 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1837+486G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67630019 | ||||||
| chr16:67630178
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1837+645C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67630178 | ||||||
| chr16:67630219
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1837+686A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67630219 | ||||||
| chr16:67631154
|
G | GT | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0002g0148others(4): Show | 7 | HG00438.hp1 HG00741.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837+1631dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631154 | |||||
| chr16:67631154
|
G | GTT | 8 | a0001c0001t0002g0133a0001c0001t0002g0155a0001c0001t0002g0156others(5): Show | 8 | HG01433.hp1 HG02055.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837+1630_1837+163 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631154 | |||||
| chr16:67631154
|
G | GTTT | 7 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0151others(4): Show | 7 | HG02145.hp1 HG02735.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837+1629_1837+163 others(7): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631154 | |||||
| chr16:67631154
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0002g0168a0001c0001t0007g0130a0001c0001t0009g0154 | 3 | HG01361.hp2 HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1837+1631_1837+163 others(15): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631154 | |||||
| chr16:67631154
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0007g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1837+1631_1837+163 others(19): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631154 | |||||
| chr16:67631164
|
T | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1837+1631T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631164 | ||||||
| chr16:67631164
|
TG | T | 7 | a0001c0001t0002g0144a0001c0001t0004g0158a0001c0001t0004g0159others(4): Show | 7 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837+1632delG | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631164 | ||||||
| chr16:67631165
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 115 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1837+1632G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631165 | ||||||
| chr16:67631167
|
T | G | 28 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(25): Show | 28 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1837+1634T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631167 | ||||||
| chr16:67631168
|
T | G | 17 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0051others(14): Show | 17 | HG01496.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1837+1635T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631168 | ||||||
| chr16:67631172
|
G | GT | 12 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(9): Show | 12 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1837+1649dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631172 | |||||
| chr16:67631172
|
G | T | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1837+1639G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631172 | ||||||
| chr16:67631176
|
T | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 6 | HG01496.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837+1643T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631176 | ||||||
| chr16:67631177
|
T | G | 20 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0055others(17): Show | 20 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1837+1644T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631177 | ||||||
| chr16:67631294
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1837+1761A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631294 | ||||||
| chr16:67631561
|
A | G | 2 | a0001c0001t0007g0129a0001c0001t0007g0130 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1837+2028A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631561 | ||||||
| chr16:67631672
|
T | TC | 10 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0054others(7): Show | 10 | HG00438.hp2 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1837+2146dupC | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631672 | |||||
| chr16:67631680
|
A | AC | 56 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(53): Show | 56 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1837+2158dupC | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631680 | |||||
| chr16:67631680
|
A | ACC | 21 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0027others(18): Show | 21 | HG00438.hp1 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1837+2157_1837+215 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631680 | |||||
| chr16:67631680
|
AC | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0035others(17): Show | 20 | HG01070.hp2 HG01109.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1837+2158delC | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631680 | |||||
| chr16:67631680
|
ACC | A | 10 | a0001c0001t0002g0144a0001c0001t0002g0155a0001c0001t0002g0156others(7): Show | 10 | HG01361.hp2 HG02622.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1837+2157_1837+215 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67631680 | |||||
| chr16:67631691
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1837+2158C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631691 | ||||||
| chr16:67631692
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1837+2159T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67631692 | ||||||
| chr16:67632049
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1837+2516G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67632049 | ||||||
| chr16:67632060
|
C | A | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837+2527C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67632060 | ||||||
| chr16:67632074
|
C | CAAAAAAA | 21 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(18): Show | 21 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1837+2550_1837+255 others(11): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67632074 | |||||
| chr16:67632074
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0132a0001c0001t0006g0131 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1837+2547_1837+255 others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67632074 | |||||
| chr16:67632092
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1837+2559G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67632092 | ||||||
| chr16:67632125
|
T | TTCAGAAA | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1837+2594_1837+260 others(11): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67632125 | |||||
| chr16:67632192
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0022 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1837+2659T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67632192 | ||||||
| chr16:67632208
|
C | T | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1837+2675C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67632208 | ||||||
| chr16:67632325
|
G | GAAGCATC others(51): Show |
1 | a0001c0001t0001g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1837+2793_1837+285 others(62): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67632325 | |||||
| chr16:67632389
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0056others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837+2856G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67632389 | ||||||
| chr16:67632650
|
C | CT | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837+3121dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67632650 | |||||
| chr16:67632654
|
T | TC | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 159 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.1837+3126dupC | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67632654 | |||||
| chr16:67632952
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1837+3419G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67632952 | ||||||
| chr16:67633207
|
CTA | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108 | 3 | HG02109.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1838-3480_1838-347 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67633207 | |||||
| chr16:67633260
|
G | T | 1 | a0001c0001t0012g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1838-3430G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67633260 | ||||||
| chr16:67633260
|
GGT | G | 84 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(81): Show | 84 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.1838-3427_1838-342 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67633260 | |||||
| chr16:67633607
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1838-3083A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67633607 | ||||||
| chr16:67633700
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1838-2990C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67633700 | ||||||
| chr16:67633781
|
G | GAC | 15 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(12): Show | 15 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1838-2876_1838-287 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67633781 | |||||
| chr16:67633781
|
G | GACAC | 22 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0024others(19): Show | 22 | HG00609.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.1838-2878_1838-287 others(8): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67633781 | |||||
| chr16:67633781
|
G | GACACAC | 2 | a0001c0001t0001g0094a0001c0001t0001g0098 | 2 | HG02602.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1838-2880_1838-287 others(10): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67633781 | |||||
| chr16:67633781
|
G | GACACACA others(3): Show |
1 | a0001c0001t0002g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1838-2884_1838-287 others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67633781 | |||||
| chr16:67633781
|
GAC | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0105a0001c0001t0001g0109others(30): Show | 33 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1838-2876_1838-287 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67633781 | |||||
| chr16:67633814
|
A | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG01433.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1838-2876A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67633814 | ||||||
| chr16:67633950
|
G | A | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1838-2740G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67633950 | ||||||
| chr16:67634480
|
T | A | 1 | a0001c0001t0009g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1838-2210T>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67634480 | ||||||
| chr16:67634516
|
C | CT | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.1838-2153dupT | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67634516 | |||||
| chr16:67634516
|
C | CTT | 20 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0094others(17): Show | 20 | HG00438.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1838-2154_1838-215 others(6): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67634516 | |||||
| chr16:67634606
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1838-2084C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67634606 | ||||||
| chr16:67634620
|
C | G | 7 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG00438.hp2 HG00639.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1838-2070C>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67634620 | ||||||
| chr16:67635147
|
G | A | 2 | a0001c0001t0007g0129a0001c0001t0007g0130 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1838-1543G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67635147 | ||||||
| chr16:67635152
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1838-1538G>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67635152 | ||||||
| chr16:67635552
|
G | A | 5 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1838-1138G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67635552 | ||||||
| chr16:67635681
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0106 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1838-1009G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67635681 | ||||||
| chr16:67635732
|
A | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1838-958A>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67635732 | ||||||
| chr16:67635911
|
C | A | 1 | a0001c0001t0001g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1838-779C>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67635911 | ||||||
| chr16:67635998
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1838-692G>A | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67635998 | ||||||
| chr16:67636214
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1838-476A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67636214 | ||||||
| chr16:67636373
|
A | T | 1 | a0001c0001t0003g0136 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1838-317A>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67636373 | ||||||
| chr16:67636544
|
T | C | 8 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1838-146T>C | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | chr16 | 67636544 | ||||||
| chr16:67636545
|
C | CA | 27 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0056others(24): Show | 27 | HG01433.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1838-132dupA | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67636545 | |||||
| chr16:67636569
|
G | GTA | 47 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 47 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1838-101_1838-100d others(4): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67636569 | |||||
| chr16:67636569
|
G | GTATATAT others(3): Show |
6 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(3): Show | 6 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1838-109_1838-100d others(12): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67636569 | |||||
| chr16:67636569
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0004g0164a0001c0001t0004g0165 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1838-111_1838-100d others(14): Show |
CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 67636569 | |||||
| chr16:67637199
|
T | G | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0155others(12): Show | 15 | HG01109.hp1 HG01361.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1999+348T>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 11/11 | chr16 | 67637199 | ||||||
| chr16:67637456
|
C | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG01361.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.2000-232C>T | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 11/11 | chr16 | 67637456 | ||||||
| chr16:67637622
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2000-66A>G | CTCF | ENSG00000102974.16 | transcript | ENST00000264010.10 | protein_coding | 11/11 | chr16 | 67637622 |