Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2181 | 167 | 78 | 36 | 26 | 8 | 17 | CTCF_chr16_67557526_67644177 | CTCF | ATGGA others(2176): Show |
chr16 | 67557526 | 67644177 | ||
| a0001c0002 | 0/0 | 2181 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | ATGGA others(2176): Show |
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 | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0002 | 0/0 | 3814 | 17 | 9 | 4 | 3 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0003 | 0/0 | 3814 | 7 | 4 | 0 | 0 | 0 | 3 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0004 | 0/0 | 3813 | 8 | 8 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3808): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0005 | 0/0 | 3814 | 4 | 0 | 3 | 0 | 1 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0006 | 0/0 | 3812 | 2 | 2 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3807): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0007 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0008 | 0/0 | 3814 | 2 | 0 | 0 | 2 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0009 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0010 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0011 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0012 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0001t0013 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
chr16 | 67557526 | 67644177 |
| a0001c0002t0003 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | CTCF_chr16_67557526_67644177 | CTCF | GACGC others(3809): Show |
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 | a0001 | c0001 | t0001 | g0119 | REF | REF | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0083 | REF | REF | CTCF_chr16_67557526_67644177 | CTCF | chr16 | 67557526 | 67644177 |
| view | 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 |
|---|
| view | 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 |
| view | 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 | a0001c0001t0005 a0001c0001t0013 |
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 | a0001c0001t0003 a0001c0002t0003 |
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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(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 |
| view | 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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | 12 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(9): Show |
12 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(9): 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 | a0001c0001t0001g0113 a0001c0001t0008g0128 |
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 | a0001c0001t0007g0129 a0001c0001t0007g0130 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0103 others(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 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0161 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0046 others(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 | a0001c0001t0002g0134 a0001c0001t0002g0147 a0001c0001t0002g0148 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
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 | a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0001g0017 a0001c0001t0004g0158 a0001c0001t0004g0159 others(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 | a0001c0001t0002g0168 a0001c0001t0009g0154 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0108 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0098 a0001c0001t0002g0144 a0001c0001t0002g0145 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0067 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0055 others(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 | a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0072 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0046 others(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 | a0001c0001t0002g0133 a0001c0001t0002g0145 a0001c0001t0004g0163 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0004 a0001c0001t0005g0041 a0001c0001t0005g0042 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(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 | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
23 | HG01074.hp1 HG01074.hp2 HG01243.hp1 others(20): 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 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0057 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0051 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0068 a0001c0001t0002g0134 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 others(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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0056 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0108 others(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 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0108 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0077 a0001c0001t0002g0148 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0037 a0001c0001t0002g0132 a0001c0001t0002g0133 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
7 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(4): 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 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0017 others(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 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0004g0158 others(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 | a0001c0001t0002g0155 a0001c0001t0004g0159 a0001c0001t0004g0163 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0053 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0001g0111 a0001c0001t0002g0153 a0001c0001t0004g0158 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0113 a0001c0001t0008g0128 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0063 a0001c0001t0001g0107 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0007g0129 a0001c0001t0007g0130 |
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 | a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0113 a0001c0001t0002g0155 a0001c0001t0002g0156 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0152 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0006g0135 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0012g0091 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0107 |
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 | 12 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(9): Show |
12 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(9): 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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0110 a0001c0001t0003g0139 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0073 a0001c0001t0001g0076 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0003g0139 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0019 a0001c0001t0002g0144 a0001c0001t0002g0145 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0055 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0002g0168 a0001c0001t0009g0154 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0111 a0001c0001t0005g0041 a0001c0001t0005g0042 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0156 a0001c0001t0004g0158 a0001c0001t0004g0159 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
160 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(157): 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 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0168 a0001c0001t0009g0154 |
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 | a0001c0001t0002g0150 a0001c0001t0002g0152 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0095 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0121 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0095 |
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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0123 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0004g0158 others(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 | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
69 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(66): 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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0006g0135 |
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 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0152 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0153 a0001c0001t0010g0166 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | 27 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(24): Show |
27 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(24): 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 | a0001c0001t0001g0116 a0001c0001t0002g0133 a0001c0001t0002g0144 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0002g0132 others(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 | a0001c0001t0002g0149 a0001c0001t0002g0150 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0104 a0001c0001t0007g0130 others(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 | a0001c0001t0001g0047 a0001c0001t0004g0162 a0001c0001t0004g0165 |
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 | a0001c0001t0007g0129 a0001c0001t0007g0130 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | 37 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0033 others(34): Show |
37 | HG00558.hp1 HG00639.hp2 HG01070.hp1 others(34): 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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0002g0132 others(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 | a0001c0001t0001g0099 a0001c0001t0002g0155 a0001c0001t0002g0156 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0077 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0078 others(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 | 6 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0088 others(3): Show |
6 | HG01175.hp1 HG01361.hp2 HG02486.hp2 others(3): 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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0141 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0003g0139 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0111 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0104 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0063 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0162 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0149 |
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 | a0001c0001t0002g0133 a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0153 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0146 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0036 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0055 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0003g0136 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(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 | a0001c0001t0002g0156 a0001c0001t0003g0136 a0001c0001t0003g0140 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0157 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0162 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0059 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0146 a0001c0001t0002g0147 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0062 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0004g0159 a0001c0001t0004g0163 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0002g0168 a0001c0001t0009g0154 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0112 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0108 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0162 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0060 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | a0001c0001t0002g0168 a0001c0001t0009g0154 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0162 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0006g0131 a0001c0001t0006g0135 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0003g0137 a0001c0001t0003g0141 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0057 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0113 a0001c0001t0005g0041 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0078 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0005g0042 a0001c0001t0005g0044 |
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 | a0001c0001t0001g0059 a0001c0001t0013g0045 |
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 | a0001c0001t0002g0150 a0001c0001t0002g0152 a0001c0001t0005g0041 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0002g0156 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0061 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0069 a0001c0001t0001g0070 |
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 | 8 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(5): 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 | a0001c0001t0002g0146 a0001c0001t0002g0149 a0001c0001t0002g0151 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0150 a0001c0001t0002g0152 others(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 | a0001c0001t0004g0160 a0001c0001t0009g0154 |
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 | a0001c0001t0002g0168 a0001c0001t0004g0158 a0001c0001t0004g0162 others(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 | a0001c0001t0004g0160 a0001c0001t0009g0154 |
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 | a0001c0001t0001g0095 a0001c0001t0002g0146 a0001c0001t0002g0149 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0150 a0001c0001t0002g0152 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0149 a0001c0001t0002g0151 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0002g0147 a0001c0001t0002g0168 a0001c0001t0004g0158 others(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 | a0001c0001t0001g0095 a0001c0001t0002g0147 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0157 a0001c0001t0004g0161 a0001c0001t0006g0131 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0113 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0095 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
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 | a0001c0001t0002g0168 a0001c0001t0009g0154 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0090 others(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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0120 |
3 | HG00639.hp2 HG01074.hp1 HG01515.hp2 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0108 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0081 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0082 a0001c0001t0001g0096 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0082 a0001c0001t0005g0044 a0001c0001t0013g0045 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0002g0132 others(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 | a0001c0001t0001g0034 a0001c0001t0002g0133 |
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 | a0001c0001t0001g0033 a0001c0001t0002g0147 a0001c0001t0007g0129 |
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 | a0001c0001t0002g0146 a0001c0001t0007g0130 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0002g0151 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0030 others(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 | a0001c0001t0003g0140 a0001c0002t0003g0142 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0088 |
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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0002g0148 others(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 | a0001c0001t0002g0133 a0001c0001t0002g0155 a0001c0001t0002g0156 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0151 others(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 | a0001c0001t0002g0168 a0001c0001t0007g0130 a0001c0001t0009g0154 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0002g0144 a0001c0001t0004g0158 a0001c0001t0004g0159 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0051 others(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 | 11 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(8): 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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0055 others(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 | a0001c0001t0007g0129 a0001c0001t0007g0130 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(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 | 20 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0027 others(17): Show |
20 | HG00438.hp1 HG01071.hp1 HG01109.hp2 others(17): 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 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0035 others(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 | a0001c0001t0002g0144 a0001c0001t0002g0155 a0001c0001t0002g0156 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(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 | a0001c0001t0002g0132 a0001c0001t0006g0131 |
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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0056 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
158 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(155): 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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0098 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0094 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0007g0129 a0001c0001t0007g0130 |
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 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0106 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | 46 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(43): Show |
46 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(43): 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 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(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 | a0001c0001t0004g0164 a0001c0001t0004g0165 |
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 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 |